Bmp4tm1.1Jlch/Bmp4+
B6.129-Bmp4tm1.1Jlch
|
decreased primordial germ cell number |
J:108516
|
Bmp4tm1.1Jlch/Bmp4tm1.1Jlch
B6.129-Bmp4tm1.1Jlch
|
abnormal forelimb morphology |
J:108516
|
|
decreased primordial germ cell number |
J:108516
|
|
decreased rib number |
J:108516
|
|
preaxial polydactyly |
J:108516
|
|
seminiferous tubule degeneration |
J:108516
|
|
short ribs |
J:108516
|
|
small testis |
J:108516
|
Bmp4tm1.1Jlch/Bmp4tm2Blh
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
|
abnormal allantois morphology |
J:108516
|
|
abnormal chorion morphology |
J:108516
|
|
abnormal forelimb morphology |
J:108516
|
|
anophthalmia |
J:108516
|
|
failure of ventral body wall closure |
J:108516
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:108516
|
|
microphthalmia |
J:108516
|
|
omphalocele |
J:108516
|
|
perimembraneous ventricular septal defect |
J:108516
|
|
polydactyly |
J:108516
|
|
postnatal lethality, incomplete penetrance |
J:108516
|
|
small allantois |
J:108516
|
|
split xiphoid process |
J:108516
|
Bmp4tm1b(EUCOMM)Hmgu/Bmp4+
C57BL/6N-Bmp4tm1b(EUCOMM)Hmgu/Bay
|
abnormal eye anterior chamber depth |
J:211773
|
|
abnormal iris morphology |
J:211773
|
|
abnormal optic disk morphology |
J:211773
|
|
abnormal retina inner nuclear layer morphology |
J:211773
|
|
abnormal retina morphology |
J:211773
|
|
abnormal retina outer nuclear layer morphology |
J:211773
|
|
decreased anxiety-related response |
J:211773
|
|
decreased total retina thickness |
J:211773
|
|
eyelids fail to open |
J:211773
|
|
hyperactivity |
J:211773
|
|
increased cornea thickness |
J:211773
|
|
increased grip strength |
J:211773
|
|
microphthalmia |
J:211773
|
Bmp4tm1b(EUCOMM)Hmgu/Bmp4tm1b(EUCOMM)Hmgu
C57BL/6N-Bmp4tm1b(EUCOMM)Hmgu/Bay
|
abnormal allantois morphology |
J:211773
|
|
abnormal embryo development |
J:211773
|
|
abnormal embryo size |
J:211773
|
|
abnormal embryo turning |
J:211773
|
|
abnormal forebrain development |
J:211773
|
|
abnormal heart morphology |
J:211773
|
|
abnormal hindbrain development |
J:211773
|
|
abnormal midbrain development |
J:211773
|
|
abnormal neural tube closure |
J:211773
|
|
embryonic growth retardation |
J:211773
|
|
embryonic lethality prior to tooth bud stage |
J:211773
|
|
preweaning lethality, complete penetrance |
J:211773
|
Bmp4tm1Blh/Bmp4+
B6.129S2-Bmp4tm1Blh
|
abnormal anterior eye segment morphology |
J:82877
|
|
abnormal canal of Schlemm morphology |
J:82877
|
|
abnormal cornea morphology |
J:82877
|
|
abnormal eye electrophysiology |
J:82877
|
|
abnormal eye morphology |
J:82877
|
|
abnormal eye size |
J:42445
|
|
abnormal fertility/fecundity |
J:118380
|
|
abnormal iridocorneal angle |
J:82877
|
|
abnormal line of Schwalbe morphology |
J:82877
|
|
abnormal male reproductive system morphology |
J:42445
|
|
abnormal optic disk morphology |
J:82877
|
|
abnormal optic nerve morphology |
J:82877
|
|
abnormal organ of Corti morphology |
J:118380
|
|
abnormal placement of pupils |
J:82877
|
|
abnormal posterior eye segment morphology |
J:82877
|
|
abnormal prostate gland anterior lobe morphology |
J:42445
|
|
abnormal retina blood vessel pattern |
J:82877
|
|
abnormal retina morphology |
J:82877
|
|
abnormal retina photoreceptor layer morphology |
J:82877
|
|
abnormal seminiferous tubule morphology |
J:42445
|
|
abnormal sensory neuron innervation pattern |
J:118380
|
|
abnormal vestibulocollic reflex |
J:118380
|
|
abnormal vitreous body morphology |
J:82877
|
|
absent optic nerve |
J:82877
|
|
absent Schlemm's canal |
J:82877
|
|
absent trabecular meshwork |
J:82877
|
|
anophthalmia |
J:42445
|
|
anterior cortical cataract |
J:82877
|
|
anterior iris synechia |
J:82877
|
|
anterior subcapsular cataract |
J:82877
|
|
cataract |
J:82877
|
|
circling |
J:118380
|
|
corneal opacity |
J:82877
|
|
decreased cornea thickness |
J:82877
|
|
decreased litter size |
J:118380
|
|
decreased vestibular hair cell stereocilia number |
J:118380
|
|
hydronephrosis |
J:42445
|
|
hypoplastic trabecular meshwork |
J:82877
|
|
impaired hearing |
J:118380
|
|
increased opacity of vitreous body |
J:82877
|
|
increased or absent threshold for auditory brainstem response |
J:118380
|
|
iris hypoplasia |
J:82877
|
|
irregularly shaped pupil |
J:82877
|
|
kidney atrophy |
J:42445
|
|
kidney cyst |
J:42445
|
|
microphthalmia |
J:42445
|
|
ocular hypertension |
J:82877
|
|
perinatal lethality, incomplete penetrance |
J:42445
|
|
persistence of hyaloid vascular system |
J:82877
|
|
polydactyly |
J:42445
|
|
reduced female fertility |
J:118380
|
|
retina detachment |
J:82877
|
|
short frontal bone |
J:42445
|
|
short nasal bone |
J:42445
|
|
single kidney |
J:42445
|
|
thin retina ganglion layer |
J:82877
|
|
thin retina inner nuclear layer |
J:82877
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * 129S6/SvEvTac
|
abnormal eye morphology |
J:82877
|
|
abnormal iris morphology |
J:82877
|
|
decreased primordial germ cell number |
J:53311
|
|
persistence of hyaloid vascular system |
J:82877
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss
|
normal
behavior/neurological phenotype |
J:136636
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * BALB/cJ
|
persistence of hyaloid vascular system |
J:82877
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * C3Hf/HeA * C57BL/LiA
|
abnormal anterior eye segment morphology |
J:82877
|
|
abnormal iridocorneal angle |
J:82877
|
|
buphthalmos |
J:82877
|
|
mydriasis |
J:82877
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * C57BL/6
|
abnormal ear development |
J:159227
|
|
abnormal lateral semicircular canal morphology |
J:159227
|
|
abnormal renal glomerulus morphology |
J:173500
|
|
absent lateral semicircular canal |
J:159227
|
|
circling |
J:159227
|
|
decreased body weight |
J:173500
|
|
decreased lateral semicircular canal size |
J:159227
|
|
normal
hearing/vestibular/ear phenotype |
J:159227
|
|
increased circulating glucose level |
J:173500
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * C57BL/6 * CBA
|
abnormal lateral semicircular canal morphology |
J:159227
|
|
circling |
J:159227
|
|
decreased primordial germ cell number |
J:53311,
J:199855
|
Bmp4tm1Blh/Bmp4+
involves: 129S2/SvPas * CAST/Ei
|
cataract |
J:82877
|
Bmp4tm1Blh/Bmp4+
Tg(Prdm14-Venus)1Sait/0
involves: 129S2/SvPas
|
decreased primordial germ cell number |
J:138571
|
Bmp4tm1Blh/Bmp4tm1Blh
129S2/SvPas-Bmp4tm1Blh
|
abnormal extraembryonic mesoderm development |
J:28717
|
|
abnormal visceral yolk sac morphology |
J:28717
|
|
absent visceral yolk sac blood islands |
J:28717
|
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:28717
|
|
failure of primitive streak formation |
J:28717
|
Bmp4tm1Blh/Bmp4tm1Blh
B6.129S2-Bmp4tm1Blh
|
abnormal extraembryonic mesoderm development |
J:28717
|
|
abnormal visceral yolk sac morphology |
J:28717
|
|
absent visceral yolk sac blood islands |
J:28717
|
|
decreased erythrocyte cell number |
J:28717
|
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:28717
|
|
failure of primitive streak formation |
J:28717
|
Bmp4tm1Blh/Bmp4tm1Blh
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss
|
abnormal amniotic cavity morphology |
J:79391
|
|
abnormal heart looping |
J:79391
|
|
abnormal lateral plate mesoderm morphology |
J:79391
|
|
abnormal mesoderm development |
J:79391
|
|
abnormal posterior primitive streak morphology |
J:79391
|
|
abnormal primitive node morphology |
J:79391
|
Bmp4tm1Blh/Bmp4tm1Blh
involves: 129S2/SvPas * Black Swiss
|
abnormal lens induction |
J:51570
|
|
absent allantois |
J:53311
|
|
absent primordial germ cells |
J:53311
|
|
absent Rathke's pouch |
J:50517
|
|
embryonic growth retardation |
J:51570,
J:53311
|
|
embryonic lethality during organogenesis, complete penetrance |
J:51570
|
Bmp4tm1Blh/Bmp4tm1Blh
involves: 129S2/SvPas * C57BL/6
|
abnormal extraembryonic mesoderm development |
J:28717
|
|
abnormal rostral-caudal axis patterning |
J:28717
|
|
abnormal visceral yolk sac mesenchyme morphology |
J:28717
|
|
abnormal visceral yolk sac morphology |
J:28717
|
|
absent visceral yolk sac blood islands |
J:28717
|
|
embryonic growth retardation |
J:28717
|
|
embryonic lethality, complete penetrance |
J:28717
|
Bmp4tm1Blh/Bmp4tm1Blh
involves: 129S2/SvPas * C57BL/6 * CBA
|
absent allantois |
J:53311
|
|
absent primordial germ cells |
J:53311
|
|
embryonic growth retardation |
J:53311
|
|
prenatal lethality, complete penetrance |
J:53311
|
Bmp4tm1Blh/Bmp4tm1Blh
involves: 129S2/SvPas * ICR
|
embryonic growth retardation |
J:28717
|
|
embryonic lethality during organogenesis, complete penetrance |
J:28717
|
Bmp4tm1Blh/Bmp4tm3.1Blh
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss
|
abnormal eye morphology |
J:75136
|
|
eyelids fail to open |
J:75136
|
|
perinatal lethality, complete penetrance |
J:75136
|
Bmp4tm1Blh/Bmp4tm3.1Blh
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss * ICR
|
abnormal eye morphology |
J:86001
|
|
normal
cardiovascular system phenotype |
J:86001
|
|
ostium primum atrial septal defect |
J:86001
|
|
partial atrioventricular septal defect |
J:86001
|
|
postnatal lethality, complete penetrance |
J:86001
|
Bmp4tm1Blh/Bmp4tm3.1Blh
Tg(Tnnt2-cre)5Blh/0
involves: 129S/Sv * Black Swiss * C57BL/6 * DBA/2 * ICR
|
abnormal atrioventricular cushion morphology |
J:86001
|
|
common atrioventricular valve |
J:86001
|
|
complete atrioventricular septal defect |
J:86001
|
|
double outlet right ventricle |
J:86001
|
|
perinatal lethality, complete penetrance |
J:86001
|
Bmp4tm1Blh/Bmp4tm4Blh
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss * C57BL/6 * SJL
|
abnormal semicircular canal morphology |
J:136636
|
Bmp4tm1Blh/Bmp4tm4Blh
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * Black Swiss * C57BL/6 * SJL
|
abnormal endolymphatic duct morphology |
J:136636
|
|
abnormal scala media morphology |
J:136636
|
|
abnormal semicircular canal ampulla morphology |
J:136636
|
|
abnormal semicircular canal morphology |
J:136636
|
|
abnormal utricle morphology |
J:136636
|
|
abnormal vestibular saccule morphology |
J:136636
|
|
absent semicircular canals |
J:136636
|
Bmp4tm1Blh/Bmp4tm4Blh
Tg(Pax2-cre)1Dje/0
involves: 129S2/SvPas * 129S6/SvEvTac * Black Swiss * C57BL/6 * SJL
|
abnormal inner ear morphology |
J:136636
|
|
abnormal semicircular canal morphology |
J:136636
|
|
abnormal utricle morphology |
J:136636
|
|
abnormal vestibular saccule morphology |
J:136636
|
Bmp4tm1Jfm/Bmp4tm1.1Jfm
Nkx2-5tm1(cre)Rjs/Nkx2-5+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd
|
abnormal aortic arch and aortic arch branch attachment |
J:89237
|
|
abnormal conotruncal ridge morphology |
J:89237
|
|
abnormal heart development |
J:89237
|
|
abnormal pharyngeal arch artery morphology |
J:89237
|
|
abnormal pulmonary artery morphology |
J:89237
|
|
aortopulmonary window |
J:89237
|
|
conotruncal ridge hypoplasia |
J:89237
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:89237
|
|
hydrops fetalis |
J:89237
|
|
interrupted aortic arch, type b |
J:89237
|
|
pericardial effusion |
J:89237
|
|
perimembraneous ventricular septal defect |
J:89237
|
|
persistent truncus arteriosus |
J:89237
|
|
semilunar valve hypoplasia |
J:89237
|
Bmp4tm1Jfm/Bmp4tm1.1Jfm
Tg(Prrx1-cre)1Cjt/0
involves: 129S4/SvJaeSor
|
conotruncal ridge hypoplasia |
J:89237
|
Bmp4tm1Jfm/Bmp4tm1Jfm
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S4/SvJaeSor * C57BL/6J * CBA/J
|
abnormal mandible morphology |
J:181229
|
|
impaired osteoblast differentiation |
J:181229
|
|
large anterior fontanelle |
J:181229
|
|
small interparietal bone |
J:181229
|
Bmp4tm1Jfm/Bmp4tm1Jfm
Tg(Mef2c-cre)2Blk/0
involves: 129S4/SvJaeSor
|
abnormal cardiac outflow tract development |
J:169047
|
|
abnormal heart and great artery attachment |
J:169047
|
|
abnormal truncus arteriosus septation |
J:169047
|
Bmp4tm1Jfm/Bmp4tm1Jfm
Tg(Prrx1-cre)1Cjt/0
involves: 129S4/SvJaeSor * C57BL/6 * SJL
|
polydactyly |
J:118257
|
Bmp4tm2(tetO-Bmp4,lacZ)Jfm/Bmp4tm2(tetO-Bmp4,lacZ)Jfm
involves: 129S4/SvJaeSor
|
abnormal cardiac mesenchyme morphology |
J:181229
|
|
abnormal head mesenchyme morphology |
J:181229
|
Bmp4tm2Blh/Bmp4+
B6.129S6-Bmp4tm2Blh
|
abnormal vertebral spinous process morphology |
J:108516
|
|
anophthalmia |
J:108516
|
|
cervical vertebral fusion |
J:108516
|
|
decreased rib number |
J:108516
|
|
enlarged kidney |
J:108516
|
|
microphthalmia |
J:108516
|
|
perimembraneous ventricular septal defect |
J:108516
|
|
polycystic kidney |
J:108516
|
|
postnatal lethality, incomplete penetrance |
J:108516
|
|
short ribs |
J:108516
|
|
thoracic vertebral fusion |
J:108516
|
Bmp4tm2Blh/Bmp4+
involves: 129S6/SvEvTac * Black Swiss
|
decreased primordial germ cell number |
J:53311
|
Bmp4tm2Blh/Bmp4+
involves: 129S6/SvEvTac * Black Swiss * C57BL/6J
|
abnormal kidney development |
J:61482
|
|
abnormal kidney mesenchyme morphology |
J:61482
|
|
abnormal metanephric mesenchyme morphology |
J:82895
|
|
abnormal nephrogenic zone morphology |
J:61482,
J:82895
|
|
abnormal renal/urinary system morphology |
J:61482
|
|
abnormal ureter development |
J:61482,
J:82895
|
|
abnormal ureter morphology |
J:61482
|
|
abnormal ureter smooth muscle morphology |
J:82895
|
|
abnormal ureteral orifice morphology |
J:61482
|
|
abnormal ureteric bud elongation |
J:61482
|
|
abnormal ureterovesical junction morphology |
J:61482
|
|
abnormal Wolffian duct morphology |
J:61482
|
|
bifid ureter |
J:61482
|
|
dilated kidney calyx |
J:61482
|
|
dilated ureter |
J:61482
|
|
duplex kidney |
J:61482
|
|
ectopic ureter |
J:61482
|
|
ectopic ureteric bud |
J:61482
|
|
hydronephrosis |
J:61482
|
|
hydroureter |
J:61482
|
|
increased metanephric mesenchyme apoptosis |
J:82895
|
|
kidney cyst |
J:61482
|
|
renal hypoplasia |
J:61482
|
|
small kidney |
J:61482
|
Bmp4tm2Blh/Bmp4+
involves: 129S6/SvEvTac * ICR
|
abnormal angiogenesis |
J:112335
|
|
abnormal artery morphology |
J:112335
|
|
abnormal heart right ventricle pressure |
J:112335
|
|
abnormal vascular endothelial cell physiology |
J:112335
|
|
abnormal vascular smooth muscle morphology |
J:112335
|
|
heart right ventricle hypertrophy |
J:112335
|
Bmp4tm2Blh/Bmp4tm2Blh
involves: 129S6/SvEvTac * Black Swiss
|
abnormal foregut morphology |
J:71204
|
|
abnormal liver bud morphology |
J:71204
|
|
absent allantois |
J:53311
|
|
absent primordial germ cells |
J:53311
|
|
delayed hepatic development |
J:71204
|
|
embryonic growth retardation |
J:53311
|
|
embryonic lethality during organogenesis, complete penetrance |
J:71204
|
Bmp4tm3.1Blh/Bmp4+
Tg(Sftpc-cre)1Blh/0
involves: 129S6/SvEvTac * C57BL/6 * DBA/2
|
abnormal lung morphology |
J:106392
|
|
abnormal respiratory system physiology |
J:106392
|
Bmp4tm3.1Blh/Bmp4tm3.1Blh
involves: 129S6/SvEvTac * Black Swiss
|
abnormal eye morphology |
J:75136
|
Bmp4tm3.1Blh/Bmp4tm3.1Blh
Tg(Tnnt2-cre)5Blh/0
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * ICR
|
atrial septal defect |
J:86001
|
|
normal
cardiovascular system phenotype |
J:86001
|
|
perinatal lethality |
J:86001
|
Bmp4tm3Blh/Bmp4+
involves: 129S6/SvEvTac
|
prenatal lethality, incomplete penetrance |
J:83123
|
Bmp4tm3Blh/Bmp4+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac
|
prenatal lethality, incomplete penetrance |
J:83123
|
Bmp4tm3Blh/Bmp4tm3Blh
involves: 129S6/SvEvTac
|
abnormal eye development |
J:83123
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:83123
|
Bmp4tm3Blh/Bmp4tm3Blh
involves: 129S6/SvEvTac * Black Swiss
|
abnormal eye morphology |
J:75136
|
|
circling |
J:75136
|
|
eyelids fail to open |
J:75136
|
|
postnatal lethality |
J:75136
|
Bmp4tm3Blh/Bmp4tm3Blh
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac
|
abnormal eye development |
J:83123
|
|
abnormal face development |
J:83123
|
|
abnormal snout morphology |
J:83123
|
|
embryonic lethality during organogenesis, complete penetrance |
J:83123
|
|
normal
nervous system phenotype |
J:83123
|
|
retrognathia |
J:83123
|
Bmp4tm4Blh/Bmp4tm4Blh
Isl1tm1(cre)Sev/Isl1+
involves: 129 * 129S6/SvEvTac
|
abnormal embryonic cloaca development |
J:192045
|
|
abnormal external female genitalia morphology |
J:192045
|
|
abnormal fibula morphology |
J:192045
|
|
abnormal hindlimb bud morphology |
J:192045
|
|
abnormal limb development |
J:192045
|
|
abnormal renal/urinary system morphology |
J:192045
|
|
absent urinary bladder |
J:192045
|
|
anal stenosis |
J:192045
|
|
external male genitalia hypoplasia |
J:192045
|
|
renal hypoplasia |
J:192045
|
|
sirenomelia |
J:192045
|
Bmp4tm5.1Bhr/Bmp4tm2.1Blh
involves: 129S6/SvEvTac * C57BL/6 * CBA * Swiss Webster
|
embryonic growth retardation |
J:159629
|
|
prenatal lethality, complete penetrance |
J:159629
|
Bmp4tm5.1Bhr/Bmp4tm5.1Bhr
involves: 129S6/SvEvTac * C57BL/6 * CBA * Swiss Webster
|
embryonic growth retardation |
J:159629
|
|
prenatal lethality, complete penetrance |
J:159629
|
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(CAG-Bmp4,-EGFP)1Ypc/0
involves: C57BL/6J * CBA/J * CD-1
|
abnormal jaw morphology |
J:214763
|
|
abnormal secondary palate development |
J:214763
|
|
abnormal temporomandibular joint morphology |
J:214763
|
|
absent mandibular angle |
J:214763
|
|
absent mandibular condyloid process |
J:214763
|
|
absent mandibular coronoid process |
J:214763
|
|
absent outer ear |
J:214763
|
|
agnathia |
J:214763
|
|
cleft palate |
J:214763
|
|
decreased palatal shelf size |
J:214763
|
|
enhanced osteoblast differentiation |
J:214763
|
|
eyelids open at birth |
J:214763
|
|
frontal bone hypoplasia |
J:214763
|
|
mandible hypoplasia |
J:214763
|
|
maxilla hypoplasia |
J:214763
|
|
nasal bone hypoplasia |
J:214763
|
|
palatal shelf fusion with tongue or mandible |
J:214763
|
|
short snout |
J:214763
|
|
syngnathia |
J:214763
|
Osr2tm2(cre)Jian/Osr2+
Tg(CAG-Bmp4,-EGFP)1Ypc/0
involves: 129S1/Sv * C57BL/6J * CD-1
|
cleft palate |
J:214763
|
|
palatal shelf fusion with tongue or mandible |
J:214763
|
|
palatal shelves fail to meet at midline |
J:214763
|
Tg(Actb-GFP,-Bmp4)1Csk/0
Tg(CAG-cre/Esr1*)67Csk/0
C57BL/6-Tg(Actb-GFP,-Bmp4)1Csk Tg(CAG-cre/Esr1*)67Csk
|
abnormal renal glomerulus morphology |
J:173500
|
|
albuminuria |
J:173500
|
|
glomerulosclerosis |
J:173500
|
Tg(Eno2-Bmp4)3Jake/0
involves: BALB/c * C57BL/6
|
abnormal gait |
J:93682
|
|
abnormal motor capabilities/coordination/movement |
J:93682
|
|
abnormal muscle fiber morphology |
J:93682
|
|
abnormal muscle morphology |
J:93682
|
|
abnormal radial glial cell morphology |
J:82446
|
|
abnormal trabecular bone morphology |
J:93682
|
|
decreased oligodendrocyte number |
J:82446
|
|
ectopic bone |
J:93682
|
|
increased astrocyte number |
J:82446
|
|
kyphoscoliosis |
J:93682
|
|
kyphosis |
J:93682
|
|
limb grasping |
J:93682
|
|
scoliosis |
J:93682
|
Tg(Krt14-Bmp4)#Jake/0
involves: BALB/c * C57BL/6
|
normal
limbs/digits/tail phenotype |
J:78767
|
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