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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Shhtm1Chg
targeted mutation 1, Chin Chiang
MGI:1857796
Summary 39 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Shhtm1Chg/Shhtm1Chg involves: 129S1/Sv * 129X1/SvJ MGI:2173405
hm2
Shhtm1Chg/Shhtm1Chg involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5298540
hm3
Shhtm1Chg/Shhtm1Chg involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3028973
hm4
Shhtm1Chg/Shhtm1Chg involves: C57BL/6 MGI:3042793
ht5
ShhDsh/Shhtm1Chg involves: 101 * 129S1/Sv * 129X1/SvJ * C3H * C57BL/10Rl MGI:3583816
cn6
Shhtm1Chg/Shhtm2Amc
Nkx2-5tm1(cre)Rjs/Nkx2-5+
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ MGI:4843919
cn7
Shhtm1Chg/Shhtm2Chg
Tg(Mef2c-cre)2Blk/0
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ MGI:4843920
cn8
Shhtm1Chg/Shhtm2Chg
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:3687543
cx9
Gli2tm2.1Alj/Gli2+
Shhtm1Chg/Shhtm1Chg
either: (involves: 129) or (involves: 129 * Black Swiss) MGI:3846351
cx10
Gli2tm2.1Alj/Gli2tm2.1Alj
Shhtm1Chg/Shhtm1Chg
either: (involves: 129) or (involves: 129 * Black Swiss) MGI:2173463
cx11
Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj
Shhtm1Chg/Shhtm1Chg
either: (involves: 129) or (involves: 129 * Black Swiss) MGI:3846352
cx12
Rr29tm1.1Bobh/Rr29+
Shhtm1Chg/Shh+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:5613161
cx13
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
Shhtm1Chg/Shhtm1Chg
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3717155
cx14
Shhtm1Chg/Shh+
Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg
Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 MGI:3812210
cx15
HhatTg(TFAP2A-cre)1Will/Hhat+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ MGI:5447986
cx16
Rr26tm1Svok/Rr26tm1Svok
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ MGI:5562302
cx17
Shhtm1Chg/Shhtm1Chg
Zic2Ku/Zic2Ku
involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH MGI:5827501
cx18
Shh+/Shhtm1Chg
Zic2Ku/Zic2+
involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH MGI:5827502
cx19
Shhtm1Chg/Shh+
Vps25m1Lis/Vps25m1Lis
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J MGI:5751502
cx20
Ift122sopb/Ift122sopb
Shhtm1Chg/Shhtm1Chg
involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J MGI:4888266
cx21
Shhtm1Chg/Shhtm1Chg
Tmem107schlei/Tmem107schlei
involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J MGI:5433094
cx22
Shhtm1Chg/Shhtm1Chg
Tulp3hhkr/Tulp3hhkr
involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6 MGI:3842141
cx23
Ndst1tm1.1Grob/Ndst1tm1.1Grob
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3589448
cx24
Six3tm3.1Gco/Six3+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3814907
cx25
Ihhtm1Amc/Ihhtm1Amc
Shhtm1Chg/Shhtm1Chg
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3818879
cx26
Gli2tm1Blnw/Gli2tm1Blnw
Shhtm1Chg/Shhtm1Chg
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3834148
cx27
Gas1tm1Fan/Gas1tm1Fan
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:7386875
cx28
Ndst1tm1.1Grob/Ndst1+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3589447
cx29
Gas1tm1Fan/Gas1tm1Fan
Shhtm1Chg/Shhtm1Chg
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:7386876
cx30
Rr45tm1.1Tshir/Rr45+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/JNCrlj MGI:6144003
cx31
Shhtm1Chg/Shhtm1Chg
Tg(Prrx1-Sox9,-lacZ)1Haak/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 MGI:3840967
cx32
Gli3tm2Blnw/Gli3+
Shhtm1Chg/Shhtm1Chg
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N MGI:3711913
cx33
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3711884
cx34
Gas1tm2Fan/Gas1+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3711885
cx35
Rr115em1Bobh/Rr115+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:7367584
cx36
Shhtm1Chg/Shh+
Tg(Shh)#Dje/0
involves: 129S1/Sv * 129X1/SvJ * Swiss Webster MGI:3665550
cx37
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shhtm1Chg
involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3711878
cx38
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shh+
involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3711877
cx39
Fkbp8tm1Tili/Fkbp8tm1Tili
Shhtm1Chg/Shhtm1Chg
involves: C57BL/6 MGI:3042780


Genotype
MGI:2173405
hm1
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most die at or just before birth

embryo
• indistinct midline at E8.5
• the ventral lips of the cephalic folds are fused and the floor and roof of the neural tube are almost in contact with each other at the mesencephalic/diencephalic junction at E9.5
• absent floor plate at E9.5, with the ventral region of the neural tube consisting instead of a thick epithelium (J:35802)
• at E10.5 (J:73074)
• rostral-to-caudal loss of notochord tissue

nervous system
• the ventral lips of the cephalic folds are fused and the floor and roof of the neural tube are almost in contact with each other at the mesencephalic/diencephalic junction at E9.5
• absent floor plate at E9.5, with the ventral region of the neural tube consisting instead of a thick epithelium (J:35802)
• at E10.5 (J:73074)
• size is reduced
• ventral forebrain structures are lost
• most of the diencephalon as an identifiable structure is absent
• the bilateral lobes of the telencephalon are fused to form a single midline structure
• absent motor neurons
• absent from the spinal cord at E10.5

skeleton
• absence or fusion of the paired distal limb bones
• have a bony extension of the humerus in the forelimb
• the fibula is absent in the hindlimb
• the tibia is absent in the hindlimb
• most sclerotomal derivatives are absent
• craniofacial bones are severely affected and almost entirely absent
• most of the ribs are absent, with only 5-6 rib cartilages remaining
• most sclerotomal derivatives including the entire vertebral column are absent, with only 5-6 rib cartilages remaining
• cartilage is absent at the elbow joint

limbs/digits/tail
• have a bony extension of the humerus in the forelimb
• lack distinct forelimbs at E15.5
• the fibula is absent in the hindlimb
• the tibia is absent in the hindlimb
• lack distinct hindlimbs at E15.5
• distal truncations of the forelimb skeleton and loss of the autopod at E14.5

vision/eye
• there is no invagination to form the double-layered optic cups
• the optic stalks are deficient or absent
• optic vesicles are fused at the midline at E9.5, the optic stalks are deficient or absent, and there is no invagination to form the double-layered optic cups
• at E10.5 (J:73074)

craniofacial
• normal facial features such as the eyes, nose, and oral structures are not identifiable by E15.5
• craniofacial bones are severely affected and almost entirely absent
• have a single nasal pit at the midline instead of bilateral pits at E10.5

cardiovascular system
• abnormalities in the heart although asymmetry or early heart looping appears normal

renal/urinary system

respiratory system
• have a single nasal pit at the midline instead of bilateral pits at E10.5

digestive/alimentary system

growth/size/body
• exhibit severe growth retardation throughout most of the embryo by E15.5

cellular
• in the neural tube and somites

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
holoprosencephaly 3 DOID:0110875 OMIM:142945
J:35802




Genotype
MGI:5298540
hm2
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• at E16.5, the forelimb autopod is presented by a single cartilage element
• at E16.5, the forelimb zeugopod is presented by a single bone element
• at E16.5, the hindlimb zeugopod is presented by a single small cartilage with a single digit




Genotype
MGI:3028973
hm3
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• a delay in resorption of epithelia in the prospective superior and posterior semicircular canals is observed at E12.5
• absence of Shh affects development of periotic and condensing mesenchyme during otic vesicle development
• completely absent from inner ear at E15.5; in place of this structure is a rudimentary structure resembling the otocyst
• lateral canal is absent at E15.5
• canal is poorly formed at E15.5
• ampulla is not developed
• canal is poorly formed at E15.5
• ampulla is not developed
• no distinct development is noted at E15.5
• no distinct development is noted at E15.5
• absent at E15.5

nervous system
• fails to form in mutants




Genotype
MGI:3042793
hm4
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• many markers of dorsal and lateral cell fates are expressed across the ventral midline
• by E11.5 homozygotes display severe growth retardation
• at E11.5 ventral cell types are missing in the neural tube in homozygous mutants
• by E11.5 - E12.5 the somites in homozygotes are abnormally shaped
• by E11.5 - E12.5 the somites in homozygotes are smaller compared to wild-type embryos

growth/size/body
• by E11.5 homozygotes display severe growth retardation

limbs/digits/tail
• by E11.5 - E12.5 the limbs fail to grow out along the proximodistal axis

vision/eye
• at E11.5 homozygotes have a single ventrally positioned eye

nervous system
• at E11.5 ventral cell types are missing in the neural tube in homozygous mutants
• at E11.5 homozygotes display severe holoprosencephaly
• motor neurons and their progenitors are absent in homozygous mutants

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
holoprosencephaly 3 DOID:0110875 OMIM:142945
J:89364




Genotype
MGI:3583816
ht5
Allelic
Composition
ShhDsh/Shhtm1Chg
Genetic
Background
involves: 101 * 129S1/Sv * 129X1/SvJ * C3H * C57BL/10Rl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ShhDsh mutation (0 available); any Shh mutation (45 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• have midline defects that are seen in the single homozygous Shh mutants

limbs/digits/tail
• have limb malformations that are nearly identical to that of single homozygous Shh mutants




Genotype
MGI:4843919
cn6
Allelic
Composition
Shhtm1Chg/Shhtm2Amc
Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic
Background
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nkx2-5tm1(cre)Rjs mutation (1 available); any Nkx2-5 mutation (21 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Shhtm2Amc mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E10.5 and E18.5, mice exhibit abnormal arch-artery patterning compared to in wild-type mice
• at E10.5, mice exhibit short outflow tract compared with wild-type mice
• mice exhibit cell death in the anterior heart field unlike in wild-type mice

embryo
• mice exhibit cell death in neural crest cells unlike in wild-type mice
• mice exhibit abnormal neural crest cells localization and septation defects compared with wild-type mice

cellular
• mice exhibit cell death in neural crest cells unlike in wild-type mice
• mice exhibit abnormal neural crest cells localization and septation defects compared with wild-type mice




Genotype
MGI:4843920
cn7
Allelic
Composition
Shhtm1Chg/Shhtm2Chg
Tg(Mef2c-cre)2Blk/0
Genetic
Background
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Shhtm2Chg mutation (0 available); any Shh mutation (45 available)
Tg(Mef2c-cre)2Blk mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• mice exhibit normal outflow tracts
• at E18.5, 4 of 16 mice exhibit abnormal arch-artery patterning compared with wild-type mice
• in 14 of 16 mice
• however, mice exhibit normal outflow tract length with no increase in apoptosis




Genotype
MGI:3687543
cn8
Allelic
Composition
Shhtm1Chg/Shhtm2Chg
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (42 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Shhtm2Chg mutation (0 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

limbs/digits/tail
• exhibit defective development of the carpal and tarsal bones in the central digit
• in the forelimb, digit 2 is replaced with a biphalangeal digit characteristic of digit 1
• in the hindlimb, digit 1 is replaced by digits with more posterior characteristics
• exhibit defective development of the carpal and tarsal bones in the central digit

skeleton
• exhibit defective development of the carpal and tarsal bones in the central digit
• exhibit defective development of the carpal and tarsal bones in the central digit




Genotype
MGI:3846351
cx9
Allelic
Composition
Gli2tm2.1Alj/Gli2+
Shhtm1Chg/Shhtm1Chg
Genetic
Background
either: (involves: 129) or (involves: 129 * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm2.1Alj mutation (1 available); any Gli2 mutation (169 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo

nervous system
• fused telencephalic vesicles are seen at E10.5
• loss of many ventral tissues is seen at E10.5

growth/size/body




Genotype
MGI:2173463
cx10
Allelic
Composition
Gli2tm2.1Alj/Gli2tm2.1Alj
Shhtm1Chg/Shhtm1Chg
Genetic
Background
either: (involves: 129) or (involves: 129 * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm2.1Alj mutation (1 available); any Gli2 mutation (169 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E10.5
• absent from the spinal cord at E10.5

vision/eye
• at E10.5

embryo
• at E10.5




Genotype
MGI:3846352
cx11
Allelic
Composition
Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj
Shhtm1Chg/Shhtm1Chg
Genetic
Background
either: (involves: 129) or (involves: 129 * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm2.1Alj mutation (1 available); any Gli2 mutation (169 available)
Gli2tm3.1(Gli1)Alj mutation (0 available); any Gli2 mutation (169 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E10.5
• in about half of mice development of the diencephalic vesicles is partially rescued with partial separation into 2 vesicles seen at E10.5 or E11.5
• absent from the spinal cord at E10.5
• absence of V3 interneurons at E10.5

embryo
• at E10.5

growth/size/body
• head size is increased compared to mice homozygous null for Shh alone




Genotype
MGI:5613161
cx12
Allelic
Composition
Rr29tm1.1Bobh/Rr29+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rr29tm1.1Bobh mutation (0 available); any Rr29 mutation (2 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• range of limb phenotypes similar to mice homozygous for Rr29tm1.1Bobh
• 40% of mice have 4 digits, 30% have 4 phalanges and 3 metatarsels, 10% have 3 digits and 20% have 3 sets of phalanges and 2 metatarsels




Genotype
MGI:3717155
cx13
Allelic
Composition
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Tctn1Gt(KST296)Byg mutation (0 available); any Tctn1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• forebrains are larger than in Shhtm1Chg




Genotype
MGI:3812210
cx14
Allelic
Composition
Shhtm1Chg/Shh+
Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg
Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Sulf1Gt(XM190)Byg mutation (0 available); any Sulf1 mutation (110 available)
Sulf2Gt(PST111)Byg mutation (1 available); any Sulf2 mutation (176 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• agnathic mice exhibit a narrow craniofacial region
• in 3 of 126 mice age E14.5 to E18.5
• in 2 of 126 mice age E14.5 to E18.5

vision/eye
• agnathic mice exhibit small or absent eyes
• agnathic mice exhibit small or absent eyes

skeleton
• in 3 of 126 mice age E14.5 to E18.5
• in 2 of 126 mice age E14.5 to E18.5




Genotype
MGI:5447986
cx15
Allelic
Composition
HhatTg(TFAP2A-cre)1Will/Hhat+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
HhatTg(TFAP2A-cre)1Will mutation (1 available); any Hhat mutation (26 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• E17.5-18.5 embryos have craniofacial defects that are not consistent with holoprosencephaly showing that the transgene did not insert into Shh.




Genotype
MGI:5562302
cx16
Allelic
Composition
Rr26tm1Svok/Rr26tm1Svok
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rr26tm1Svok mutation (0 available); any Rr26 mutation (0 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
N
• mice exhibit normal hands and feet




Genotype
MGI:5827501
cx17
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Zic2Ku/Zic2Ku
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Zic2Ku mutation (4 available); any Zic2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• embryos exhibit a heart defect

embryo

growth/size/body

nervous system
• the forebrain is severely truncated at E9.5
• by E10.5, the forebrain forms a fluid-filled, cyst-like structure




Genotype
MGI:5827502
cx18
Allelic
Composition
Shh+/Shhtm1Chg
Zic2Ku/Zic2+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Zic2Ku mutation (4 available); any Zic2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• trans-heterozygotes do not exhibit any defects characteristic of either single homozygote




Genotype
MGI:5751502
cx19
Allelic
Composition
Shhtm1Chg/Shh+
Vps25m1Lis/Vps25m1Lis
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Vps25m1Lis mutation (0 available); any Vps25 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• as in Vps25m1Lis homozygotes
• stunted as in Vps25m1Lis homozygotes
• as in Vps25m1Lis homozygotes

growth/size/body
• stunted as in Vps25m1Lis homozygotes
• as in Vps25m1Lis homozygotes

limbs/digits/tail
• partial rescue of polydactyly observed in Vps25m1Lis homozygotes

skeleton
• as in Vps25m1Lis homozygotes

hearing/vestibular/ear
• as in Vps25m1Lis homozygotes




Genotype
MGI:4888266
cx20
Allelic
Composition
Ift122sopb/Ift122sopb
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift122sopb mutation (0 available); any Ift122 mutation (52 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• at E10.5 the neural tube is ventralized similar to the phenotype in mice homozygous for Ift122sopb alone

nervous system
• at E10.5 the neural tube is ventralized similar to the phenotype in mice homozygous for Ift122sopb alone




Genotype
MGI:5433094
cx21
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Tmem107schlei/Tmem107schlei
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Tmem107schlei mutation (0 available); any Tmem107 mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• absence of ventral cell types (V3) in the floor plate
• however, ventral neuron specification defects of V2 interneurons and motor neurons observed in Smobnb homozygotes is partially rescued

limbs/digits/tail
N
• increased apoptosis observed in the limb bud of Smobnb homozygotes is rescued
• reduced digit number observed in Smobnb homozygotes is rescued to four or five digits

embryo
• absence of ventral cell types (V3) in the floor plate
• however, ventral neuron specification defects of V2 interneurons and motor neurons observed in Smobnb homozygotes is partially rescued




Genotype
MGI:3842141
cx22
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Tulp3hhkr/Tulp3hhkr
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Tulp3hhkr mutation (1 available); any Tulp3 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• expression of neural tube markers is ventralized compared to in wild-type mice

limbs/digits/tail
• mice exhibit two digits on fore limbs and four digits on the hind limbs unlike in wild-type mice

homeostasis/metabolism

embryo
• expression of neural tube markers is ventralized compared to in wild-type mice




Genotype
MGI:3589448
cx23
Allelic
Composition
Ndst1tm1.1Grob/Ndst1tm1.1Grob
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndst1tm1.1Grob mutation (0 available); any Ndst1 mutation (46 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 3-times fewer than expected mutants are produced

craniofacial
• 4 of 5 mutants display severely hypoplastic frontonasal prominences similar to defects seen in severely affected Ndst1tm1.1Grob single homozygotes
• 4 of 5 mutants display severely hypoplastic maxillary prominences similar to defects seen in severely affected Ndst1tm1.1Grob single homozygotes

nervous system
• all mutants display collapse of the midbrain
• all mutants display collapse of the forebrain




Genotype
MGI:3814907
cx24
Allelic
Composition
Six3tm3.1Gco/Six3+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Six3tm3.1Gco mutation (0 available); any Six3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 75% display a phenotype typical of holoprosencephaly after one backcross to C57BL/6
• after five backcrosses to C57BL/6, 100% show a holoprosencephaly phenotype
• a single ganglionic eminence
• telencephalon is smaller at E10.5 than in controls
• reduced apoptosis in the ventral midline at E10.5
• increased apoptosis in the lateral dorsal telencephalon
• cerebral hemispheres fused rostrally

craniofacial
• defective separation of the medial nasal prominence at E11.5
• fusion defects in the secondary palate
• absence of philtrum at E17.5
• no cartilaginous nasal septum at E17.5

respiratory system
• no cartilaginous nasal septum at E17.5

vision/eye
• reduced apoptosis at E10.5
• shorter distance between the eyes at E11.5

digestive/alimentary system
• fusion defects in the secondary palate

growth/size/body
• fusion defects in the secondary palate
• absence of philtrum at E17.5
• no cartilaginous nasal septum at E17.5
• at E11.5

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
holoprosencephaly 2 DOID:0110872 OMIM:157170
J:140315




Genotype
MGI:3818879
cx25
Allelic
Composition
Ihhtm1Amc/Ihhtm1Amc
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ihhtm1Amc mutation (1 available); any Ihh mutation (22 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• yolk sacs are essentially avascular
• embryos is in primitive unturned position at E9.5
• yolk sacs are thin and transparent
• at E9.5 yolk sac mesoderm is a thin lining of inner yolk sac surface which adheres to mesodermal layer of amnion in some embryos

cardiovascular system
• yolk sacs are essentially avascular




Genotype
MGI:3834148
cx26
Allelic
Composition
Gli2tm1Blnw/Gli2tm1Blnw
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm1Blnw mutation (0 available); any Gli2 mutation (169 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
N
• normal levels of apoptotic cells in the neural tube

nervous system
N
• normal sized neural tube




Genotype
MGI:7386875
cx27
Allelic
Composition
Gas1tm1Fan/Gas1tm1Fan
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm1Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

craniofacial
• perinatal skulls show exacerbated neurocranial, splanchnocranial, and dermatocranial defects relative to the single Gas1tm1Fan homozygotes
• midline craniofacial phenotype is significantly worsened relative to that in single Gas1tm1Fan homozygotes
• Meckels cartilage is truncated and lacks a malleal end; the proximal end is slightly bifurcated
• perinatal skull size is reduced
• neurocranial base development is severely disrupted: the trabecular basal plate, which runs from the rostral basisphenoid, presphenoid, and ethmoid through the nasal septum, is discontinuous and cleft
• all lateral extensions from the neurocranial base are disrupted: the ala temporali are hypoplastic, the lamina obturans fail to invest the cartilage of the ala, and ectopic preotic cartilaginous pillars extend toward the crista parotica of the otic capsule
• at E18.5, 75% of mice exhibit clefting of the basisphenoid
• the ala temporali are hypoplastic
• squamosal bones are repatterned and separated into distinct retrotympanic and squamosal portions
• at E18.5, 25% of mice show fusion of the premaxillary incisors, 75% of mice show premaxillary incisor agenesis, and 75% show fusion of the mandibular incisors
• at E18.5, the distal dentary contains a single lower incisor
• at E18.5, the duplicated proximal dentary includes an alveolus containing an ectopic molar
• at E18.5, the proximal dentary appears to be duplicated and includes a secondary cartilage-containing condylar process and an alveolus containing an ectopic molar
• the distal dentary is synostotic across the midline and contains a single lower incisor
• at E18.5, the distal dentary lacks a symphysis as it is synostotic across the midline; 75% of mice exhibit a synostotic mandible/symphysis phenotype
• at E18.5, premaxillaries are hypoplastic, synostotic, and lack incisor teeth
• gonial bones fail to form
• a vestigial stapes is observed
• nasal capsules and associated dermal ossifications are severely reduced, without proper midline manifestations
• at E18.5, all (100%) of mice exhibit complete secondary cleft palate
• mice survive to birth but only have a single external nostril

growth/size/body
• at E18.5, 25% of mice show fusion of the premaxillary incisors, 75% of mice show premaxillary incisor agenesis, and 75% show fusion of the mandibular incisors
• at E18.5, the distal dentary contains a single lower incisor
• at E18.5, the duplicated proximal dentary includes an alveolus containing an ectopic molar
• nasal capsules and associated dermal ossifications are severely reduced, without proper midline manifestations
• at E18.5, all (100%) of mice exhibit complete secondary cleft palate
• mice survive to birth but only have a single external nostril

nervous system
• mice exhibit a more severe holoprosencephaly phenotype than single Gas1tm1Fan homozygotes

respiratory system
• nasal capsules and associated dermal ossifications are severely reduced, without proper midline manifestations
• mice survive to birth but only have a single external nostril

skeleton
• perinatal skulls show exacerbated neurocranial, splanchnocranial, and dermatocranial defects relative to the single Gas1tm1Fan homozygotes
• midline craniofacial phenotype is significantly worsened relative to that in single Gas1tm1Fan homozygotes
• Meckels cartilage is truncated and lacks a malleal end; the proximal end is slightly bifurcated
• perinatal skull size is reduced
• neurocranial base development is severely disrupted: the trabecular basal plate, which runs from the rostral basisphenoid, presphenoid, and ethmoid through the nasal septum, is discontinuous and cleft
• all lateral extensions from the neurocranial base are disrupted: the ala temporali are hypoplastic, the lamina obturans fail to invest the cartilage of the ala, and ectopic preotic cartilaginous pillars extend toward the crista parotica of the otic capsule
• at E18.5, 75% of mice exhibit clefting of the basisphenoid
• the ala temporali are hypoplastic
• squamosal bones are repatterned and separated into distinct retrotympanic and squamosal portions
• at E18.5, 25% of mice show fusion of the premaxillary incisors, 75% of mice show premaxillary incisor agenesis, and 75% show fusion of the mandibular incisors
• at E18.5, the distal dentary contains a single lower incisor
• at E18.5, the duplicated proximal dentary includes an alveolus containing an ectopic molar
• at E18.5, the proximal dentary appears to be duplicated and includes a secondary cartilage-containing condylar process and an alveolus containing an ectopic molar
• the distal dentary is synostotic across the midline and contains a single lower incisor
• at E18.5, the distal dentary lacks a symphysis as it is synostotic across the midline; 75% of mice exhibit a synostotic mandible/symphysis phenotype
• at E18.5, premaxillaries are hypoplastic, synostotic, and lack incisor teeth
• gonial bones fail to form
• a vestigial stapes is observed
• nasal capsules and associated dermal ossifications are severely reduced, without proper midline manifestations
• at E18.5, 100% of premaxillaries are synostotic
• no patent sutures between the frontal and parietal ossifications are observed

hearing/vestibular/ear
• middle ear-associated splanchnocranial elements either fail to develop (malleus and incus) or are represented by a cartilaginous remnant (stapes)
• dermatocranial elements (ectotympanic and gonial bones) fail to form
• gonial bones fail to form
• a vestigial stapes is observed
• ectotympanic bones fail to form

digestive/alimentary system
• at E18.5, all (100%) of mice exhibit complete secondary cleft palate




Genotype
MGI:3589447
cx28
Allelic
Composition
Ndst1tm1.1Grob/Ndst1+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndst1tm1.1Grob mutation (0 available); any Ndst1 mutation (46 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• at E15.5, 4 of 8 mutants display hyploplastic lower jaws
• at E15.5, 4 of 8 mutants display hypoplastic frontonasal or maxillary processes
• at E15.5, 4 of 8 mutants display hypoplastic frontonasal or maxillary processes
• at E15.5, 4 of 8 mutants lack a tongue
• at E15.5, 4 of 8 mutants lack olfactory epithelium
• surviving mutants generally have a smaller snout

vision/eye
• at E15.5, 4 of 8 mutants display absent or hypoplastic eye lenses
• at E15.5, 4 of 8 mutants display severe eye developmental defects
• surviving mutants generally have smaller eyes

digestive/alimentary system
• at E15.5, 4 of 8 mutants lack a tongue

taste/olfaction
• at E15.5, 4 of 8 mutants lack olfactory epithelium

skeleton
• at E15.5, 4 of 8 mutants display hyploplastic lower jaws

respiratory system
• at E15.5, 4 of 8 mutants lack olfactory epithelium

growth/size/body
• at E15.5, 4 of 8 mutants lack a tongue
• at E15.5, 4 of 8 mutants lack olfactory epithelium
• surviving mutants generally have a smaller snout




Genotype
MGI:7386876
cx29
Allelic
Composition
Gas1tm1Fan/Gas1tm1Fan
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm1Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice only survive to around E9.5

craniofacial
• mice exhibit severe craniofacial defects




Genotype
MGI:6144003
cx30
Allelic
Composition
Rr45tm1.1Tshir/Rr45+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rr45tm1.1Tshir mutation (2 available); any Rr45 mutation (2 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype



Genotype
MGI:3840967
cx31
Allelic
Composition
Shhtm1Chg/Shhtm1Chg
Tg(Prrx1-Sox9,-lacZ)1Haak/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Tg(Prrx1-Sox9,-lacZ)1Haak mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• at E13.5 limb bud morphology is the same as that in null mice that do not express the transgene

embryo
• at E13.5 limb bud morphology is the same as that in null mice that do not express the transgene




Genotype
MGI:3711913
cx32
Allelic
Composition
Gli3tm2Blnw/Gli3+
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm2Blnw mutation (0 available); any Gli3 mutation (80 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• limb phenotypes are indistinguishable to those seen in Gli3tm2Blnw homozygotes
• digit identity is partially restored with 3 or 4 digits clearly mimicking digits 2 to 4 or 2 to 5 identities
• limb phenotypes are indistinguishable to those seen in Gli3tm2Blnw homozygotes
• limb phenotypes are indistinguishable to those seen in Gli3tm2Blnw homozygotes
• some digits have shortened phalanges
• digit 1 is sometimes duplicated

skeleton
• some digits have shortened phalanges




Genotype
MGI:3711884
cx33
Allelic
Composition
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm2Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• digit 2 or 3 is absent from the forelimbs
• however, long bones are normal

craniofacial
• cranio-skeletal defects are more significant than those seen in Gas1tm2Fan homozygotes
• profound truncation
• at E18.5, complete fusion of medial nasal processes

nervous system
• floor plate cells adopt more dorsal fates, as shown by marker staining, than Gas1tm2Fan homozygotes
• axonal projections are misrouted through the Isl1/2+ motor column
• vp3 interneuron progenitors are reduced further compared to Gas1tm2Fan homozygotes
• pMN motorneuron progenitors are dramatically reduced although their relative dorsal position to vp3 interneuron progenitors is preserved
• however, pMN specification occurs normally

skeleton
• profound truncation
• partial fusion of intervertebral discs
• reduction in the ossification centers

respiratory system
• at E18.5, complete fusion of medial nasal processes

growth/size/body
• at E18.5, complete fusion of medial nasal processes

embryo
• floor plate cells adopt more dorsal fates, as shown by marker staining, than Gas1tm2Fan homozygotes




Genotype
MGI:3711885
cx34
Allelic
Composition
Gas1tm2Fan/Gas1+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm2Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• pMN motorneuron progenitor cell numbers are increased




Genotype
MGI:7367584
cx35
Allelic
Composition
Rr115em1Bobh/Rr115+
Shhtm1Chg/Shh+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rr115em1Bobh mutation (0 available); any Rr115 mutation (0 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• reduced in size or absent in E17.5 embryos
• in E17.5 embryos
• excessively fused or absent in E17.5 embryos
• reduced length in E17.5 embryos
• in E17.5 embryos

endocrine/exocrine glands
• absent oxytocin and vasopressin expressing cells in paraventricular nucleus (PVN) in E15.5 embryos
• absent oxytocin, tyrosine hydroxylase (TH1) and vasopressin expressing cells in paraventricular nucleus (PVN) in E15.5 embryos
• mislocated in E17.5 embryos, intercepting the basisphenoid bone
• shifted ventrally in E11.5 embryos
• severely malformed in E13.5 embryos
• less separation of infundibulum from neuroectodermal tissue in E13.5 embryos
• undergoing apoptosis in E17.5 embryos
• infundibulum shifted ventrally in E11.5 embryos, remaining ectopic in E15.5 embryos

growth/size/body
• reduced length in E17.5 embryos
• in E17.5 embryos

mortality/aging
• expected Mendelian ratios at stage E17.5
• premature death by age P4

nervous system
• mislocated in E17.5 embryos, intercepting the basisphenoid bone
• shifted ventrally in E11.5 embryos
• severely malformed in E13.5 embryos
• less separation of infundibulum from neuroectodermal tissue in E13.5 embryos
• undergoing apoptosis in E17.5 embryos
• infundibulum shifted ventrally in E11.5 embryos, remaining ectopic in E15.5 embryos
• midline hypothalamic brain tissue absent in E17.5 embryos
• absent oxytocin and vasopressin expressing cells in paraventricular nucleus (PVN) in E15.5 embryos
• absent oxytocin, tyrosine hydroxylase (TH1) and vasopressin expressing cells in paraventricular nucleus (PVN) in E15.5 embryos

respiratory system
• reduced length in E17.5 embryos

skeleton
• reduced in size or absent in E17.5 embryos
• in E17.5 embryos
• excessively fused or absent in E17.5 embryos




Genotype
MGI:3665550
cx36
Allelic
Composition
Shhtm1Chg/Shh+
Tg(Shh)#Dje/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Swiss Webster
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
Tg(Shh)#Dje mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• partial loss of Shh partially rescues Tg(Shh)#Dje phenotype; at E18.5, in some animals, cerebellum is slightly smaller than that of transgenics alone
• IGL is not as thick or irregular as that of Shh transgenic mice and overall size is reduced




Genotype
MGI:3711878
cx37
Allelic
Composition
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm2Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die after E9.5 and are all dead at E13.5

embryo
• at E9.5, embryos fail to undergo proper turning
• at E9.5, double-kink in the body axis or an L-shaped body axis
• development arrests at E9.5

growth/size/body

cardiovascular system
• at E9.5, hearts are linear or mostly linear

homeostasis/metabolism
• at E9.5, severe cardiac edema




Genotype
MGI:3711877
cx38
Allelic
Composition
Gas1tm2Fan/Gas1tm2Fan
Shhtm1Chg/Shh+
Genetic
Background
involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gas1tm2Fan mutation (0 available); any Gas1 mutation (14 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• 16% of forelimbs have 4.5 digits, 84% of forelimbs and 100% of hindlimbs are missing digit 2
• no digit forms at the digit 2 position

nervous system
• mild, with a narrowing and fusion of the midline facial structures

respiratory system
• single nostril

craniofacial
• single nostril

growth/size/body
• single nostril




Genotype
MGI:3042780
cx39
Allelic
Composition
Fkbp8tm1Tili/Fkbp8tm1Tili
Shhtm1Chg/Shhtm1Chg
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fkbp8tm1Tili mutation (0 available); any Fkbp8 mutation (22 available)
Shhtm1Chg mutation (1 available); any Shh mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• there is a general ventralization of neural cell fates in cells posterior to the prospective spinal cord similar to that seen in Fkbp8tm1Tili homozygotes
• at E12.5 double homozygotes have dilated caudal neural tubes similar to Fkbp8tm1Tili homozygotes
• by E12.5 the somites in double homozygotes are abnormally shaped similar to Shhtm1Chg homozygotes
• by E12.5 the somites in double homozygotes are small similar to Shhtm1Chg homozygotes

limbs/digits/tail
• by E12.5 the limbs fail to grow out along the proximodistal axis similar to Shhtm1Chg homozygotes

vision/eye
• double homozygotes are rescued from cyclopia seen in Shhtm1Chg homozygotes

nervous system
• at E12.5 double homozygotes have dilated caudal neural tubes similar to Fkbp8tm1Tili homozygotes





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory