About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory