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Allele : Srebf2<lop13> sterol regulatory element binding factor 2; lens opacity 13

Primary Identifier  MGI:1856940 Allele Type  Spontaneous
Attribute String  Hypomorph Gene  Srebf2
Inheritance Mode  Recessive Strain of Origin  129T1/Sv-Dnd1<Ter>
Is Recombinase  false Is Wild Type  false
molecularNote  A C-to-T mutation at coding nucleotide 3112 in exon 18 results in an arginine to cysteine substitution at amino acid 1038 (p.R1038C).
  • mutations:
  • Single point mutation
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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

5 Publication categories

Trail: Allele