| Name: dystrobrevin alpha |
| Aliases:
Dtn,
RIKEN cDNA 2210407P21 gene,
adbn,
87K protein,
2210407P21Rik,
a-DB-1,
alpha-dystrobrevin,
A0,
dystrobrevin
|
| Description: PHENOTYPE: Homozygous targeted mutants exhibit skeletal and cardiac myopathies. Neuromuscular junctions appear to form normally, but their postnatal maturation is compromised. Dtna mutations do not increase the severity of Dmd or Utrn mutants whose products are also part of the dystrophin-glycoprotein complex. [provided by MGI curators] |
| Crossreferences:
MGI:106039,
UniProtKB:Q3V0M6,
UniProtKB:Q8CFR5,
UniProtKB:A0A1Y7VK79,
UniProtKB:Q9D2N4,
UniProtKB:Q3UHJ2,
UniProtKB:A0A1Y7VL34,
UniProtKB:A0A1Y7VLZ6,
UniProtKB:Q8BSY4,
NCBI_Gene:13527,
UniProtKB:Q3UHP1,
UniProtKB:A0A1Y7VJN9,
ENSEMBL:ENSMUSG00000024302,
UniProtKB:I6L9D6,
UniProtKB:Q8BTD9
|
| This information is supplied by the AllianceGenome.org API. |