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Allele : Crx<rd23> cone-rod homeobox; retinal degeneration 23

Primary Identifier  MGI:7640120 Allele Type  Spontaneous
Attribute String  Null/knockout Gene  Crx
Inheritance Mode  Recessive Strain of Origin  B6;SJL-Tnfrsf14<tm1.1Kro>/J
Is Recombinase  false Is Wild Type  false
molecularNote  This spontaneous single G to C point substitution in the splicing zone 5 base pairs after the end of exon 2, at Chr 7:15,605,064 (GRCm39), results in the loss of exon 2 and a frameshift that leads to a stop codon at amino acid 202.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

3 Publication categories