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Allele : Slc25a13<hspn> solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13; hyperspin

Primary Identifier  MGI:5514275 Allele Type  Spontaneous
Attribute String  Dominant negative, Null/knockout Gene  Slc25a13
Inheritance Mode  Recessive Strain of Origin  SJL/J
Is Recombinase  false Is Wild Type  false
molecularNote  The hyperspin mutation is a spontaneous 123.6 kb deletion of Chromosome 6: 5.86-6.66 Mb (GRCm38) that begins in intron 3 of Slc25a13 and ends in exon 17, an interval that includes an enhancer of Dlx5 and, in addition to creating a null allele of Slc25a13, diminishes otocyst expression of Dlx5.
  • mutations:
  • Intragenic deletion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele