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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tal1Hpt
hair patches
MGI:1859843
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tal1Hpt/Tal1Hpt (C57BL/6J x C3FeLe.B6-a/a)F1 MGI:3608700
hm2
Tal1Hpt/Tal1Hpt HPT/Le MGI:3608708
ht3
Tal1Hpt/Tal1+ (C57BL/6J x C3FeLe.B6-a/a)F1 MGI:3608691
ht4
Tal1Hpt/Tal1+ HPT/Le MGI:3608965


Genotype
MGI:3608700
hm1
Allelic
Composition
Tal1Hpt/Tal1Hpt
Genetic
Background
(C57BL/6J x C3FeLe.B6-a/a)F1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tal1Hpt mutation (2 available); any Tal1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation

integument
• coat appearance of a homozygote can be discerned from a heterozygote only by breeding tests
• the permanent coat may be normal with a few bare patches
• some homozygotes have a sparse permanent coat with extensive bare patches




Genotype
MGI:3608708
hm2
Allelic
Composition
Tal1Hpt/Tal1Hpt
Genetic
Background
HPT/Le
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tal1Hpt mutation (2 available); any Tal1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• death is associated with abnormalities of ectodermal derivatives




Genotype
MGI:3608691
ht3
Allelic
Composition
Tal1Hpt/Tal1+
Genetic
Background
(C57BL/6J x C3FeLe.B6-a/a)F1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tal1Hpt mutation (2 available); any Tal1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• the skin is littered with heavily pigmented debris

integument
• permanent coat of some may be normal but have a few bare patches
• the permanent coat of some heterozygotes is sparse with extensive bare patches
• the skin is littered with heavily pigmented debris




Genotype
MGI:3608965
ht4
Allelic
Composition
Tal1Hpt/Tal1+
Genetic
Background
HPT/Le
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tal1Hpt mutation (2 available); any Tal1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• model for mechanisms of progressive noninflammatory renal disease
• disorganization, swelling, and fusion of the foot processes
• condition is progressive and by 6 months of age most glomeruli show advanced sclerosis
• results from progressive glomerulosclerosis

cardiovascular system
• increased systolic pressure by 3 months of age

pigmentation
• mosaicism for pigmented and unpigmented areas is observed a few days after birth

hematopoietic system
• occurs by 40 weeks of age
• assumed secondary to renal failure
• before one year of age counts are normal
• at 68 weeks of age the leukocyte count is significanlty decreased with a slight decrease in lymphocytes and increase in neutrophils

growth/size/body
• mutants at all ages are smaller than age and sex-matched controls

immune system
• before one year of age counts are normal
• at 68 weeks of age the leukocyte count is significanlty decreased with a slight decrease in lymphocytes and increase in neutrophils

integument
• patchy absence of hair throughout life
• pigmented and unpigmented areas observed soon after birth correspond to future areas of abnormal and normal hair growth respectively
• follicles may not produce hairs or hairs may not erupt
• keratin plugs follicles
• abnormal follicles are larger than normal
• reduced numbers of normal follicles can be detected as early as E14
• mosaicism for pigmented and unpigmented areas is observed a few days after birth

muscle





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory