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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Acer1tm1(KOMP)Vlcg
targeted mutation 1, Velocigene
MGI:5085811
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Acer1tm1(KOMP)Vlcg/Acer1tm1(KOMP)Vlcg C57BL/6-Acer1tm1(KOMP)Vlcg MGI:6116829
cx2
Acer1tm1(KOMP)Vlcg/Acer1tm1(KOMP)Vlcg
Acer2em1Mvw/Acer2em1Mvw
involves: C57BL/6J * C57BL/6NTac MGI:6116840


Genotype
MGI:6116829
hm1
Allelic
Composition
Acer1tm1(KOMP)Vlcg/Acer1tm1(KOMP)Vlcg
Genetic
Background
C57BL/6-Acer1tm1(KOMP)Vlcg
Cell Lines 18475A-H9
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Acer1tm1(KOMP)Vlcg mutation (2 available); any Acer1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• red oil O staining shows decreased staining on the surface of the skin but increased accumulation of lipids in the hair follicle pilary canal indicative of impaired lipid secretion from the sebaceous gland to the skin surface

growth/size/body
• although normal weight when younger, at 13 and 18 months of age homozygotes have decreased body weight relative to wild-type or heterozygous controls

homeostasis/metabolism
• skin of homozygotes has very low alkaline ceramidase activity on very-long-acyl-chain ceramide C24:1 ceramide, but only a moderate reduction in alkaline ceramidase activity on long chain ceramide C18:1 ceramide

mortality/aging
N
• intercrosses of heterozygotes yields normal Mendelian ratio of homozygotes, heterozygotes and wild-type offspring

integument
• red oil O staining shows decreased staining on the surface of the skin but increased accumulation of lipids in the hair follicle pilary canal indicative of impaired lipid secretion from the sebaceous gland to the skin surface
• progressive hair loss begins at 2 to 3 months of age
• accumulation of lipids in the opening of the pilary canal may be responsible for the dilation of the infundibulum
• the pilary canal in the hair follicle infundibulum region is wider and morphologically irregular
• the first telogen to anagen transition is delayed and then both telogen and anagen cycles are shorter than normal
• hair follicle stem cells have decreased maintenance of quiescence, thus there are fewer than normal hair follicle stem cells in adults and this deficiency worsens with age
• increased cell proliferation and apoptosis with decreased cell differentiation in the epidermis
• increased cell proliferation and apoptosis with decreased cell differentiation in the epidermis




Genotype
MGI:6116840
cx2
Allelic
Composition
Acer1tm1(KOMP)Vlcg/Acer1tm1(KOMP)Vlcg
Acer2em1Mvw/Acer2em1Mvw
Genetic
Background
involves: C57BL/6J * C57BL/6NTac
Cell Lines 18475A-H9
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Acer1tm1(KOMP)Vlcg mutation (2 available); any Acer1 mutation (18 available)
Acer2em1Mvw mutation (1 available); any Acer2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• double homozygotes have the same alopecia phenotype as that found in Acer1 null homozygotes





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory