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Allele : Golga1<awag> golgin A1; ages with abnormal gait

Primary Identifier  MGI:3510600 Allele Type  Spontaneous
Gene  Golga1 Inheritance Mode  Recessive
Strain of Origin  B6(Cg)-Tyr<c-2J>/J Is Recombinase  false
Is Wild Type  false
molecularNote  This spontaneous mutation was discovered in 1998 at The Jackson Laboratory. The molecular lesion is a small intragenic deletion of TTCACAC at 39,023,425-431 (GRCm38) in the gene. This causes a frame shift and premature termination.
  • mutations:
  • Intragenic deletion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

3 Publication categories