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Allele : Mctp1<dwnd> multiple C2 domains, transmembrane 1; deaf wanderer

Primary Identifier  MGI:6192114 Allele Type  Spontaneous
Attribute String  Modified regulatory region, Null/knockout Gene  Mctp1
Inheritance Mode  Recessive Strain of Origin  C57BL/10SnJ
Is Recombinase  false Is Wild Type  false
molecularNote  This 53,008 bp deletion, spanning from Chr 13: 76,815,703 bp to 76,868,709 bp deletes all of exons 11-15, 7,270 bp of flanking intron 10-11 and 40,908 bp of flanking intron 15-16, and is expected to eliminate the third C2 deomain and the two transmembrane helices, in addition to disrupting an enhancer of Nr2f1.
  • mutations:
  • Intragenic deletion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele