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Trappc6amhyp
Spontaneous Allele Detail
Summary
Symbol: Trappc6amhyp
Name: trafficking protein particle complex 6A; mosaic hypopigmentation
MGI ID: MGI:3688725
Gene: Trappc6a  Location: Chr7:19242595-19250070 bp, + strand  Genetic Position: Chr7, 9.92 cM, cytoband A2
Alliance: Trappc6amhyp page
Mutation
origin
Strain of Origin:  MEV/1TyJ
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutation:    Viral insertion
 
Mutation detailsThis mutation is a viral DNA sequence insertion into intron 1 of the gene. Northern blot analysis showed that the expression of the gene was absent in the kidney and skin of homozygous mice. (J:114372)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Trappc6a Mutation:  18 strains or lines available
References
Original:  J:114372 Gwynn B, et al., A mouse TRAPP-related protein is involved in pigmentation. Genomics. 2006 Aug;88(2):196-203
All:  1 reference(s)

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