SAMD9L wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SAMD9L wild-type allele is located in the vicinity of 7q21.2 and is approximately 18 kb in length. This allele, which encodes sterile alpha motif domain-containing protein 9-like protein, plays a role in signaling regulation, tumor suppression and endocytosis. Mutations in the gene are associated with myeloid disorders, hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome.

**Synonyms:** - ATXPC - C7orf6 - Chromosome 7 Open Reading Frame 6 Gene - DRIF2 - FLJ39885 - KIAA2005 - M7MLS1 - MLSM7 - SCA49 - Sterile Alpha Motif Domain Containing 9 Like wt Allele - Sterile Alpha Motif Domain Containing 9-Like Gene - UEF - UEF1