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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hes5tm1Fgu
targeted mutation 1, Francois Guillemot
MGI:2149674
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hes5tm1Fgu/Hes5tm1Fgu involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:2172826
cn2
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Fgu/Hes1tm1Hojo
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:3713199
cn3
Hes1tm1Kag/Hes1tm1Kag
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
Tg(Nes-cre/ERT2)5-1Kag/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:3808127
cn4
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Kag/Hes1tm1Kag
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:3808125
cx5
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129S1/Sv * 129X1/SvJ MGI:3808126
cx6
Hes1tm1Fgu/Hes1+
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3617616
cx7
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5+
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3617615
cx8
Hes1tm1Fgu/Hes1tm1Fgu
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3526895
cx9
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5tm1Fgu
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:2172828


Genotype
MGI:2172826
hm1
Allelic
Composition
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• somehat reduced density of Muller glial cells at 7 and 14 days of age as well as in adults
• density reduction of about 30-40%
• no increase in apoptosis

hearing/vestibular/ear
• doublets of inner hair cells interspersed along the single row
• many areas with four outer hair cell rows rather than 3
• significant increase of hair cells on sensory epithelium of utricle and saccule (but to a lesser extent)

nervous system
• somehat reduced density of Muller glial cells at 7 and 14 days of age as well as in adults
• density reduction of about 30-40%
• no increase in apoptosis
• more Map2+ neurons in the brain and expression of Map2 by neurons was premature
• doublets of inner hair cells interspersed along the single row
• many areas with four outer hair cell rows rather than 3
• significant increase of hair cells on sensory epithelium of utricle and saccule (but to a lesser extent)




Genotype
MGI:3713199
cn2
Allelic
Composition
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Fgu/Hes1tm1Hojo
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Ito mutation (1 available); any Emx1 mutation (34 available)
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes1tm1Hojo mutation (0 available); any Hes1 mutation (21 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• pituitary gland is sphere-shaped
• gland is composed of round cells only and lacks columnar cells
• cells expressing proopiomelanocortin (POMC) are all round, characteristic of pituitary anterior lobe cells whereas in wild-type, both round and columnar cells (in intermediate lobe) express POMC
• growth hormone-producing cells are slightly increased in number
• at E18, neurohypophysis is lost in mutants, but is formed normally in wild-type and Hes1-null animals
• at E12.5, evagination of the infundibulum is affected compared to control embryos
• at E18, there are decreased numbers of pituitary gland progenitor cells compared to wild-type, shown by proliferation assays
• no apoptosis is observed
• lumen of Rathke's pouch is absent
• at E18, pituitary gland is severely hypoplastic
• intermediate lobe is absent

nervous system
• pituitary gland is sphere-shaped
• gland is composed of round cells only and lacks columnar cells
• cells expressing proopiomelanocortin (POMC) are all round, characteristic of pituitary anterior lobe cells whereas in wild-type, both round and columnar cells (in intermediate lobe) express POMC
• growth hormone-producing cells are slightly increased in number
• at E18, neurohypophysis is lost in mutants, but is formed normally in wild-type and Hes1-null animals
• at E12.5, evagination of the infundibulum is affected compared to control embryos
• at E18, there are decreased numbers of pituitary gland progenitor cells compared to wild-type, shown by proliferation assays
• no apoptosis is observed
• lumen of Rathke's pouch is absent
• at E18, pituitary gland is severely hypoplastic
• intermediate lobe is absent




Genotype
MGI:3808127
cn3
Allelic
Composition
Hes1tm1Kag/Hes1tm1Kag
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
Tg(Nes-cre/ERT2)5-1Kag/0
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Kag mutation (2 available); any Hes1 mutation (21 available)
Hes3tm1Kag mutation (2 available); any Hes3 mutation (18 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
Tg(Nes-cre/ERT2)5-1Kag mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit no change in Cajal-Retzius cell number




Genotype
MGI:3808125
cn4
Allelic
Composition
Emx1tm1(cre)Ito/Emx1+
Hes1tm1Kag/Hes1tm1Kag
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Emx1tm1(cre)Ito mutation (1 available); any Emx1 mutation (34 available)
Hes1tm1Kag mutation (2 available); any Hes1 mutation (21 available)
Hes3tm1Kag mutation (2 available); any Hes3 mutation (18 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit accelerated differentiation of neurons compared to in wild-type mice, including Cajal-Retzius cells in the dorsal telencephalon
• unlike in wild-type mice, at E11.5 and E12.5 dorsal midline cells do not flatten and remain pseudostratified
• mice exhibit mild abnormalities in the cortical hem and cortical neuroepithelium
• at E11.5 and E12.5, the number of Cajal-Retzius cells in the marginal zone of the piriform cortex is increased compared to in wild-type mice

embryo
• unlike in wild-type mice, at E11.5 and E12.5 dorsal midline cells do not flatten and remain pseudostratified

cellular
• mice exhibit accelerated differentiation of neurons compared to in wild-type mice, including Cajal-Retzius cells in the dorsal telencephalon




Genotype
MGI:3808126
cx5
Allelic
Composition
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E10.5, the choroid plexus of the fourth ventricle is hypoplastic




Genotype
MGI:3617616
cx6
Allelic
Composition
Hes1tm1Fgu/Hes1+
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• significantly increased outer hair cell numbers relative to homozygotes or controls

nervous system
• significantly increased outer hair cell numbers relative to homozygotes or controls




Genotype
MGI:3617615
cx7
Allelic
Composition
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• significantly increased inner hair cell numbers relative to homozygotes or controls

nervous system
• significantly increased inner hair cell numbers relative to homozygotes or controls




Genotype
MGI:3526895
cx8
Allelic
Composition
Hes1tm1Fgu/Hes1tm1Fgu
Hes3tm1Kag/Hes3tm1Kag
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes3tm1Kag mutation (2 available); any Hes3 mutation (18 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E8.5 many differentiated neurons have already formed unlike in Hes1, Hes5 double mutants where premature differentiation is not seen until E9.5
• at E9.5 almost all cells are neurons in the ventral spinal cord and at E10.0 virtually all radial glial cells have differentiated

cellular
• at E8.5 many differentiated neurons have already formed unlike in Hes1, Hes5 double mutants where premature differentiation is not seen until E9.5
• at E9.5 almost all cells are neurons in the ventral spinal cord and at E10.0 virtually all radial glial cells have differentiated




Genotype
MGI:2172828
cx9
Allelic
Composition
Hes1tm1Fgu/Hes1tm1Fgu
Hes5tm1Fgu/Hes5tm1Fgu
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1Fgu mutation (1 available); any Hes1 mutation (21 available)
Hes5tm1Fgu mutation (1 available); any Hes5 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• at E9.5 and E10.5 radial glial cells prematurely differentiate into neurons resulting in failure of later born cells (oligodendrocytes, astrocytes, and ependymal cells) to be generated
• at E9.5 and E10.5 prematurely differentiated neurons are found in the regions where the optic vesicles should develop
• neural tube defects in 71.2% of embryos (J:62024)
• at E10.5 the cells of the neural tube are disorganized with many cells scattered across the lumen rather in contrast to the radial morphology seen in wild-type mice (J:94391)
• also at E10.5 the outer boundary of the neural tube is irregular and ambiguous (J:94391)
• the forebrain monotonous tube
• ependymal cells are absent
• astrocytes are absent
• oligodendrocytes are absent
• the ganglionic eminences are not properly formed due to premature neuronal differentiation
• even greater neuron density in double homozygotes
• neurons of the spinal cord and dorsal root ganglia are intermingled
• the basal lamina is missing from the ventral spinal cord and neurons of the spinal cord and dorsal root ganglia are intermingled

vision/eye
• at E9.5 and E10.5 the optic vesicles are absent; instead, differentiated neurons are found in the region that would normally become the optic vesicle

taste/olfaction
• increased numbers of neurons in olfactory placodes at E10.5

growth/size/body

embryo
• neural tube defects in 71.2% of embryos (J:62024)
• at E10.5 the cells of the neural tube are disorganized with many cells scattered across the lumen rather in contrast to the radial morphology seen in wild-type mice (J:94391)
• also at E10.5 the outer boundary of the neural tube is irregular and ambiguous (J:94391)

respiratory system
• increased numbers of neurons in olfactory placodes at E10.5

craniofacial
• increased numbers of neurons in olfactory placodes at E10.5

cellular
• at E9.5 and E10.5 radial glial cells prematurely differentiate into neurons resulting in failure of later born cells (oligodendrocytes, astrocytes, and ependymal cells) to be generated
• at E9.5 and E10.5 prematurely differentiated neurons are found in the regions where the optic vesicles should develop





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory