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Allele : Nelfa<m1Mhda> negative elongation factor complex member A, Whsc2; mutation 1, Martin Hrabe de Angelis

Primary Identifier  MGI:5818776 Allele Type  Chemically induced (ENU)
Attribute String  Not Specified Gene  Nelfa
Strain of Origin  C3HeB/FeJ Is Recombinase  false
Is Wild Type  false
molecularNote  The molecular lesion is a T-to-A missense mutation (236T>A) in codon 79 in exon 2. This is predicted to alter amino acid 79 from an isoleucine to an asparagine (Ile79Asn) in the encoded protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • Whsc2<I79NMhda>,
  • Whsc2<I79NMhda>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

2 Publication categories

Trail: Allele