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Phenotypes Associated with This Genotype
Genotype
MGI:5641692
Allelic
Composition
Mysm1tm1a(KOMP)Wtsi/Mysm1tm1a(KOMP)Wtsi
Genetic
Background
C57BL/6-Mysm1tm1a(KOMP)Wtsi
Cell Lines EPD0019_1_A05
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mysm1tm1a(KOMP)Wtsi mutation (2 available); any Mysm1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• abnormalities in the hair follicles
• abnormal hair follicle patterning, with hair follicles no longer arranged as staggered rows of triplets (J:209956)
• defects in hair follicle organization and associated structures (J:232539)
• the hair follicle cycle is disturbed, with most hair follicles in telogen
• abnormalities in the interfollicular epidermis
• within the interfollicular epidermis, the scale pattern is completely disrupted, although regions of scale differentiation lacking the granular layer can still be seen
• foot pad hyperpigmentation
• white tails (J:209956)

limbs/digits/tail
• foot pad hyperpigmentation
• white tails (J:209956)

pigmentation
• foot pad hyperpigmentation
• white tails (J:209956)


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
12/17/2024
MGI 6.24
The Jackson Laboratory