SAMD9 gene

sterile alpha motif domain containing 9

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a sterile alpha motif domain-containing protein. The encoded protein localizes to the cytoplasm and may play a role in regulating cell proliferation and apoptosis. Mutations in this gene are the cause of normophosphatemic familial tumoral calcinosis. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Jul 2010]

From UniProt:

May play a role in the inflammatory response to tissue injury and the control of extra-osseous calcification, acting as a downstream target of TNF-alpha signaling. Involved in the regulation of EGR1, in coordination with RGL2. May be involved in endosome fusion.

From NCBI Gene:

  • Tumoral calcinosis, familial, normophosphatemic
  • Mirage syndrome

From UniProt:

MIRAGE syndrome (MIRAGE): A form of syndromic adrenal hypoplasia characterized by myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy. [MIM:617053]

Tumoral calcinosis, normophosphatemic, familial (NFTC): An uncommon, life-threatening disorder characterized by progressive deposition of calcified masses in cutaneous and subcutaneous tissues. Serum phosphate levels are normal. Clinical features include painful calcified ulcerative lesions and massive calcium deposition in the mid- and lower dermis, severe skin and bone infections, erythematous papular skin eruption in infancy, conjunctivitis, and gingivitis. NFTC shows a striking resemblance to acquired dystrophic calcinosis, in which tissue calcification occurs as a consequence of tissue injury/inflammation. [MIM:610455]

Cytogenetic Location: 7q21.2, which is the long (q) arm of chromosome 7 at position 21.2

Molecular Location: base pairs 93,099,513 to 93,118,023 on chromosome 7 (Homo sapiens Updated Annotation Release 109.20190905, GRCh38.p13) (NCBI)

Cytogenetic Location: 7q21.2, which is the long (q) arm of chromosome 7 at position 21.2
  • C7orf5
  • DRIF1
  • NFTC
  • OEF1
  • OEF2