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Allele : Hc<0> hemolytic complement; deficient

Primary Identifier  MGI:3027637 Allele Type  Spontaneous
Gene  Hc Strain of Origin  multiple strains
Is Recombinase  false Is Wild Type  false
description 

This is an allele characteristic of various inbred mouse strains including the following: A/HeJ, A/J, AKR/J, DBA/2J, NZB/B1NJ, SWR/J, B10.D2/oSnJ

Hc was identified as a candidate gene for Abhr2 in a microarray analysis of lung mRNA from A/J, C3H/HeJ, and (A/J x C3H/HeJ)F1 x A/J backcross animals. Hc genotype shows statistically significant correlation to allergen-induced bronchial hyperresponsive phenotype. The A/J allele contains a 2 bp deletion resulting in deficient Hc mRNA and protein production and is associated with susceptibility to allergen-induced bronchial hyperresponsiveness. (J:108211)

molecularNote  A 2 base "TA" deletion at positions 62 and 63 of an 83 base pair exon near the 5' end of the gene is found in the following mouse strains: A/HeJ, A/J, AKR/J, DBA/2J, I/LnJ, KK/HlJ, MOLF/EiJ, NZB/B1NJ, RF/J, ST/bJ SWR/J, B10.D2/oSnJ. The consequence of this deletion is the creation of a stop codon starting four bases after the deletion. A truncated product of 216 amino acids is predicted as a result although contradictory reports exist that a larger pro-C5 protein may be synthesized. Nevertheless, macrophages from mouse strains carrying this allele do not secrete complement 5.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • hc<o>,
  • C5-def,
  • C5-d,
  • hc<o>,
  • C5-,
  • Hc<Hfib2>,
  • C5-deficient,
  • C5-d,
  • Hc<Hfib2>,
  • C5-def,
  • C5-,
  • C5-deficient
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

32 Carried By

Trail: Allele

0 Driven By

158 Publication categories

Trail: Allele