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Gene : TRPM6 Homo sapiens

Name  ? transient receptor potential cation channel subfamily M member 6 Cytological Location  9q21.13
Brief Description  transient receptor potential cation channel subfamily M member 6
description  This gene is predominantly expressed in the kidney and colon, and encodes a protein containing an ion channel domain and a protein kinase domain. It is crucial for magnesium homeostasis, and plays an essential role in epithelial magnesium transport and in the active magnesium absorption in the gut and kidney. Mutations in this gene are associated with hypomagnesemia with secondary hypocalcemia. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Apr 2010]
  • synonyms:
  • HMGX,
  • hypomagnesemia, secondary hypocalcemia,
  • transient receptor potential cation channel, subfamily M, member 6,
  • FLJ22628,
  • OTTHUMG00000020027,
  • TRPM6,
  • HGNC:17995,
  • HOMG,
  • HSH,
  • HOMG,
  • NM_017662,
  • CHAK2,
  • uc004ajl.1,
  • AK026281,
  • HSH,
  • HOMG1,
  • CHAK2
  • identifiers:
  • 140803,
  • ENSG00000119121,
  • TRPM6

Genome feature

Region: gene ? Length: 165600  
Location: 9:74722495-74888094 reverse strand Cyto location: 9q21.13

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1 Diseases

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92 SN Ps

4 Cross References

18 Data Sets

18 Homologues

0 Located Features

90 Rna Seq Results