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Allele : Gpr179<nob5> G protein-coupled receptor 179; no b wave 5
Primary Identifier  MGI:5431477 Allele Type  Spontaneous
Gene  Gpr179 Inheritance Mode  Recessive
Strain of Origin  C3H Is Recombinase  false
Is Wild Type  false
description  This mutation has been found in C3H/HeN, but is absent from C3H/HeJ, C3H/HeOuJ, C3HeB/FeJ, C3H/HeSnJ (J:224435) and C3H/HeH (J:211946).
molecularNote  The ERV2 retroviral transposon inserted into intron 1. RT-PCR confirmed reduced transcript expression in the retina.
  • mutations:
  • Transposon insertion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

17 Publication categories





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