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Allele : Ccdc136<Gt(373F8)Cmhd> coiled-coil domain containing 136; gene trap 373F8, Centre for Modeling Human Disease

Primary Identifier  MGI:4965479 Allele Type  Gene trapped
Gene  Ccdc136 Transmission  Germline
Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+> Is Recombinase  false
Is Wild Type  false
molecularNote  The gene was disrupted by the insertion of a pUPA GFP reporter vector 3' to exon 2 in the gene. The detection of low levels of potentially functional transcripts in homozygous mice raised the possibility that this mutation is not a null allele.
  • mutations:
  • Insertion of gene trap vector
  • synonyms:
  • Ccdc136<GFP>,
  • MGI:3884678,
  • Ccdc136<GFP>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories

Trail: Allele