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Gene : TRPM7 Homo sapiens

Name  ? transient receptor potential cation channel subfamily M member 7 Cytological Location  15q21.2
Brief Description  transient receptor potential cation channel subfamily M member 7
description  This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017]
  • synonyms:
  • transient receptor potential cation channel, subfamily M, member 7,
  • ALSPDC,
  • LTRPC7,
  • LTrpC-7,
  • uc001zyt.5,
  • TRPM7,
  • LTRPC7,
  • CHAK,
  • CHAK1,
  • CHAK1,
  • AF346629,
  • NM_017672,
  • OTTHUMG00000172449,
  • HGNC:17994,
  • TRP-PLIK,
  • TRP-PLIK
  • identifiers:
  • 54822,
  • ENSG00000092439,
  • TRPM7

Genome feature

Region: gene ? Length: 129658  
Location: 15:50557158-50686815 reverse strand Cyto location: 15q21.2


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1 Diseases

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429 SN Ps

5 Cross References

18 Data Sets

17 Homologues

0 Located Features

90 Rna Seq Results