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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tyr+
wild type
MGI:2432472
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Tyrc-26DVT/Tyr+ involves: 101/Rl * C3H/Rl * T-stock MGI:5293748
ht2
Tyrc-ch83R/Tyr+ involves: 101/Rl * C3H/Rl * T-stock MGI:5294374
ht3
Tyrc-25H/Tyr+ involves: AKR * STOCK Tyrc-25H/Tyrc-ch MGI:3691584
ht4
Tyrc-25H/Tyr+ involves: SM/J * STOCK Tyrc-h/Tyrc-25H MGI:3691849
cx5
Tyrc-ch/Del(7)Tyrc-3H involves: 101/H * C3H/HeH MGI:4431256
cx6
Tyrc/Del(7)Tyrc-3H involves: 101/H * C3H/HeH MGI:4431254
cx7
Tyrc-ch/Del(7)Tyrc-6H involves: 101/H * C3H/HeH MGI:4843178
cx8
Tenm4l7Rn3-4R/Tyrc-26DVT involves: 101/Rl * BALB/cRl * C3H/Rl * C57BL/10Rl * T-stock MGI:3789295


Genotype
MGI:5293748
ht1
Allelic
Composition
Tyrc-26DVT/Tyr+
Genetic
Background
involves: 101/Rl * C3H/Rl * T-stock
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tyrc-26DVT mutation (2 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:5294374
ht2
Allelic
Composition
Tyrc-ch83R/Tyr+
Genetic
Background
involves: 101/Rl * C3H/Rl * T-stock
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tyrc-ch83R mutation (0 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• appears wild-type




Genotype
MGI:3691584
ht3
Allelic
Composition
Tyrc-25H/Tyr+
Genetic
Background
involves: AKR * STOCK Tyrc-25H/Tyrc-ch
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tyrc-25H mutation (0 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• this allele includes a deletion, detected in banded mitotic chromosomes, comprising 1-6cM, representing about 7.6% of Chr 7




Genotype
MGI:3691849
ht4
Allelic
Composition
Tyrc-25H/Tyr+
Genetic
Background
involves: SM/J * STOCK Tyrc-h/Tyrc-25H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tyrc-25H mutation (0 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• an induced, associated deletion involves, minimally, the MOD2 structural locus




Genotype
MGI:4431256
cx5
Allelic
Composition
Tyrc-ch/Del(7)Tyrc-3H
Genetic
Background
involves: 101/H * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(7)Tyrc-3H mutation (0 available); any Del(7)Tyrc-3H mutation (0 available)
Tyrc-ch mutation (79 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• the coat color is intermediate between that expected for an albino mouse and a mouse homozygous for chinchilla

integument
• the coat color is intermediate between that expected for an albino mouse and a mouse homozygous for chinchilla




Genotype
MGI:4431254
cx6
Allelic
Composition
Tyrc/Del(7)Tyrc-3H
Genetic
Background
involves: 101/H * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(7)Tyrc-3H mutation (0 available); any Del(7)Tyrc-3H mutation (0 available)
Tyrc mutation (79 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• this mouse is albino

integument
• this mouse is albino




Genotype
MGI:4843178
cx7
Allelic
Composition
Tyrc-ch/Del(7)Tyrc-6H
Genetic
Background
involves: 101/H * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(7)Tyrc-6H mutation (1 available); any Del(7)Tyrc-6H mutation (0 available)
Tyrc-ch mutation (79 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• these mice are noticeably lighter in color than mice that are homozygous chinchilla

integument
• these mice are noticeably lighter in color than mice that are homozygous chinchilla




Genotype
MGI:3789295
cx8
Allelic
Composition
Tenm4l7Rn3-4R/Tyrc-26DVT
Genetic
Background
involves: 101/Rl * BALB/cRl * C3H/Rl * C57BL/10Rl * T-stock
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tenm4l7Rn3-4R mutation (0 available); any Tenm4 mutation (302 available)
Tyrc-26DVT mutation (2 available); any Tyr mutation (375 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• when the Odz4l7Rn3-4R allele is inherited from the father, animals survive to adulthood
• when the Odz4l7Rn3-4R allele is inherited from the mother, animals die as embryos between E8.5 and E17.5

cardiovascular system
• when the Odz4l7Rn3-4R allele is inherited from the mother, defects in vascularization are seen

embryo
• when the Odz4l7Rn3-4R allele is inherited from the mother, developmental delay is seen
• when the Odz4l7Rn3-4R allele is inherited from the mother, abnormalities in limb bud elongation are seen
• when the Odz4l7Rn3-4R allele is inherited from the mother, kinky neural tubes are observed

growth/size/body
• when the Odz4l7Rn3-4R allele is inherited from the mother, developmental delay is seen
• when the Odz4l7Rn3-4R allele is inherited from the father, 30% of animals appear runted and scruffy at weaning

limbs/digits/tail
• when the Odz4l7Rn3-4R allele is inherited from the mother, abnormalities in limb bud elongation are seen

nervous system
• when the Odz4l7Rn3-4R allele is inherited from the mother, kinky neural tubes are observed

skeleton
• when the Odz4l7Rn3-4R allele is inherited from the father, 27% of mutant animals display lumbar and/or thoracic vertebral fusions
• when the Odz4l7Rn3-4R allele is inherited from the father, an aberrant spinous process is observed in 18% of mutant animals
• when the Odz4l7Rn3-4R allele is inherited from the father, 27% of mutant animals display lumbar and/or thoracic vertebral fusions





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory