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Allele : Alb<Mhdabcl001> albumin; bone calcium low mutant 001

Primary Identifier  MGI:5424985 Allele Type  Chemically induced (ENU)
Attribute String  Not Specified Gene  Alb
Strain of Origin  C3HeB/FeJ Is Recombinase  false
Is Wild Type  false
molecularNote  This ENU-induced mutation was isolated in a screen for metabolic bone disease as part of the Munich ENU Mutagenesis Project. It has been identified as a T-to-C transition at nucleotide position 829 of the cDNA sequence, in exon 6 of the gene, resulting in replacement of cysteine by arginine at amino acid position 277 of the protein (C277R; Cys277Arg).
  • mutations:
  • Single point mutation
  • synonyms:
  • BCL001,
  • Mhdabcl001,
  • Mhdabcl001,
  • BCL001
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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

2 Publication categories