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Allele : Prkcq<rpea1> protein kinase C, theta; retinal pigment epithelium atrophy 1

Primary Identifier  MGI:5639127 Allele Type  Spontaneous
Attribute String  Null/knockout Gene  Prkcq
Inheritance Mode  Recessive Strain of Origin  ABJ/LeJ
Is Recombinase  false Is Wild Type  false
molecularNote  A G-to-A transition in the fifth base in intron 6 (GTAAG to GTAAA) affects the splice donor site causes skipping of exon 6, a frameshift, and premature stop codon. Protein was not detected by western blot analysis on extracts of eye, indicating that this is a null allele.
  • mutations:
  • Single point mutation
  • synonyms:
  • nm3342,
  • nm3342
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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

5 Publication categories