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Relbshep
Spontaneous Allele Detail
Nomenclature
Symbol: Relbshep
Name: avian reticuloendotheliosis viral (v-rel) oncogene related B; spontaneous hepatitis
MGI ID: MGI:5002714
Gene: Relb  Location: Chr7:19340142-19363363 bp, - strand  Genetic Position: Chr7, 9.93 cM
Reduced body size in Relbshep/Relbshep mice

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  BALB/cJ x A/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis spontaneous mutation has a G-to-T mutation at chromosome 7 position 19,612,646 (GRCm38) which causes a single amino acid change of glutamine to lysine at residue 331 (p.Q331K). (J:176116, J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Relb Mutation:  26 strains or lines available
References
Original:  J:171971 Harris B, et al., Spontaneous hepatitis: A new liver disease model exhibiting hepatitis maps to Chromosome 7. MGI Direct Data Submission. 2011;
All:  3 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
11/23/2021
MGI 6.17
The Jackson Laboratory