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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Zeb1+
wild type
MGI:1857516
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Zeb1Tw/Zeb1+ B6.Cg-Zeb1Tw MGI:5295198
ht2
Zeb1tm1Yhi/Zeb1+ involves: 129P2/OlaHsd * C57BL/6 MGI:3812429
ht3
Zeb1tm2Yhi/Zeb1+ involves: 129S1/Sv * 129X1/SvJ MGI:3653687
ht4
Zeb1Tw/Zeb1+ involves: C57BL/6J MGI:2654860
ht5
Zeb1Tw/Zeb1+ STOCK PCS MGI:2654856
cx6
Zeb1tm2Yhi/Zeb1+
Zeb2tm1.2Yhi/Zeb2+
involves: 129S1/Sv * 129X1/SvJ * ICR MGI:3653728


Genotype
MGI:5295198
ht1
Allelic
Composition
Zeb1Tw/Zeb1+
Genetic
Background
B6.Cg-Zeb1Tw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1Tw mutation (1 available); any Zeb1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Inner ear morphology, hearing thresholds, and otoconia of Zeb1Tw/Zeb1+ and Zeb1Tw/Zeb1Tw mice

behavior/neurological
• starting at 7 weeks of age mice consume 15 - 20% more food

growth/size/body
• in adults

adipose tissue

homeostasis/metabolism
• slight glucose intolerance in females at 15 weeks of age
• in females at 15 weeks of age
• elevated in the serum

hearing/vestibular/ear
• average length of the cochlear duct is 91% that of wild-type controls
• the contours of the canals are irregular due to small bulges and projections
• the non-ampullated ends are irregular or constricted
• utricles have giant otoconia visible by scanning electron microscopy
• increase in the binaural average ABR thresholds at 1 month of age

hematopoietic system
• in adults
• decrease in the number of polymorphonuclear neutrophils in adults
• in adults

immune system
• in adults
• decrease in the number of polymorphonuclear neutrophils in adults
• in adults

endocrine/exocrine glands
• in adults




Genotype
MGI:3812429
ht2
Allelic
Composition
Zeb1tm1Yhi/Zeb1+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1tm1Yhi mutation (2 available); any Zeb1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• iridocorneal adhesions lead to loss of the iridocorneal angle
• iridocorneal adhesions are observed in 4 month old mice
• corneolenticular and iridolenticular adhesions are also evident
• the cornea of 4 month old mice is more than twice as thick as controls
• there number of keratocytes found in the cornea are doubled in 4 month old mice compared to age-matched controls




Genotype
MGI:3653687
ht3
Allelic
Composition
Zeb1tm2Yhi/Zeb1+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1tm2Yhi mutation (1 available); any Zeb1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• exhibit exaggerated neointima formation after artery injury compared to controls

homeostasis/metabolism
• exhibit exaggerated neointima formation after artery injury compared to controls




Genotype
MGI:2654860
ht4
Allelic
Composition
Zeb1Tw/Zeb1+
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1Tw mutation (1 available); any Zeb1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• heterozygotes display hyperactivity, twirling around the cage in periodic spurts
• heterozygotes exhibit bidirectional "twirling" or circling behavior

growth/size/body
• most male and female heterozygotes become obese as they reach maturity
• onset of obesity varies from 2 months to 3 months of age in some heterozygotes
• young heterozygotes remain smaller than wild-type, despite normal feeding

reproductive system
• a less than 1:1 ratio of heterozygous (43.6%) to wild-type (56.4%) pups is obtained from matings of heterozygous males with wild-type females, suggesting increased lethality either in utero or prior to genotyping at 10 days after birth
• obese female heterozygotes tend to become sterile
• obese male heterozygotes breed at a reduced rate

hearing/vestibular/ear
• heterozygotes display inner ear defects (not shown)

pigmentation
• most heterozygotes display a lighter coat color than wild-type mice

integument
• most heterozygotes display a lighter coat color than wild-type mice
• most heterozygotes have sparse hair




Genotype
MGI:2654856
ht5
Allelic
Composition
Zeb1Tw/Zeb1+
Genetic
Background
STOCK PCS
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1Tw mutation (1 available); any Zeb1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• when allowed to grow up together, 2-month old male heterozygotes often begin to fight to such an extent that they must be either separated or sacrificed
• when lifted by the tail, heterozygotes flex their back, tuck their head under, and draw their limbs backwards
• in response to a downward falling movement, heterozygotes fail to thrust their forelimbs forward, indicating absence of a landing reaction
• heterozygotes display vertical head shaking less often than horizontal head shaking
• heterozygotes display head shaking in a horizontal plane, often combined with circling
• heterozygotes often exhibit circling combined with horizontal head shaking
• some heterozygous parents of both sexes are prone to attacking and killing their young during the first week of life, esp. after being stressed in some way

hearing/vestibular/ear
N
• heterozygotes are not deaf and generally display a normal cochlea
• 2 of 9 heterozygotes displayed abnormal cochlear duct morphology
• in one of these 2 heterozygotes, the left cochlear duct was normal but the right was hydropic, the organ of Corti was disorganized, and the stria vascularis was missing
• in the other, both cochlear ducts were affected, the apical region was hydropic, the organ of Corti was abnormal, and the stria vascularis was missing form the right ear
• heterozygotes show a highly variable reduction or absence of the horizontal canal along with absence of otoliths and uneven contours of the vertical canals
• at the very least, the horizontal canal is present and only slightly decreased in length, while the otolith number is sometimes reduced
• however, the horizontal canal and ampulla are never entirely absent
• at the very least, the posterior vertical canal displays an abnormal contour
• the uneveness of outline progresses to formation of projections from the walls of the canal
• in severe cases, these projections form branches or duplications running from the canal to the utriculus or the common crus
• the horizontal ampulla is located more posteriorly than in normal mice
• the horizontal crista is always abnormal in shape and lies lateral to rather than anterior to the utricle macula
• in contrast, the ampullae and cristae of the vertical canals are normal
• the epithelium forming the horizontal crista is folded inwards rather than upwards, forming a pit instead of a ridge in the ventromedial part of the ampulla
• at the very least, the anterior vertical canal displays an abnormal contour
• the uneveness of outline progresses to formation of projections from the walls of the canal
• in severe cases, these projections form branches or duplications running from the canal to the utriculus or the common crus
• the arcuate fossa may be variably obliterated by branches from the anterior vertical canal
• in some ears, the lumen of the endolymphatic ducts is sligtly dilated, suggesting some excess of endolymphatic fluid
• when present, otoliths are often thinner than normal
• a reduction in otolith number is sometimes observed along with a slightly reduced lateral canal
• complete loss of otoliths is associated with severe reduction of the lateral canal and increasingly shortened and branched vertical canals
• 9 of 18 heterozygous ears lack both saccular and utricular otoliths, 7 show a normal saccular otolith with a thin utricular otolith in 3 cases, and the remaining 2 ears show a thin saccular otolith only

growth/size/body
• starting at 3 months of age, adult heterozygotes display a tendency to become obese
• however, some heterozygotes exhibit a normal breeding life and remain slim
• a few heterozygotes lag behind their wild-type littermates in growth
• however, the growth of young heterozygotes is usually normal

adipose tissue
• obese heterozygotes display increased deposition of subcutaneous fat in the inguinal and neck regions and between the shoulder blades
• obese heterozygotes display increased abdominal fat deposition in the mesentery and around the kidneys, ovaries, and testes
• obese heterozygotes display increased deposition of subcutaneous fat in the inguinal region

reproductive system
• both sexes are fertile but become sterile if obesity sets in




Genotype
MGI:3653728
cx6
Allelic
Composition
Zeb1tm2Yhi/Zeb1+
Zeb2tm1.2Yhi/Zeb2+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Zeb1tm2Yhi mutation (1 available); any Zeb1 mutation (67 available)
Zeb2tm1.2Yhi mutation (1 available); any Zeb2 mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

reproductive system
• 70% exhibit closure of the vaginal orifice





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last database update
12/30/2025
MGI 6.24
The Jackson Laboratory