TRPM6

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

TRPM6 is a transient receptor potential ion channel associated with hypomagnesemia with secondary hypocalcemia.[5]

AliasesTRPM6, CHAK2, HMGX, HOMG, HOMG1, HSH, transient receptor potential cation channel subfamily M member 6
End74,888,094 bp[1]
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TRPM6
Identifiers
AliasesTRPM6, CHAK2, HMGX, HOMG, HOMG1, HSH, transient receptor potential cation channel subfamily M member 6
External IDsOMIM: 607009; MGI: 2675603; HomoloGene: 9767; GeneCards: TRPM6; OMA:TRPM6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001177310
NM_001177311
NM_017662

NM_153417

RefSeq (protein)

NP_001170781
NP_001170782
NP_060132

NP_700466

Location (UCSC)Chr 9: 74.72 – 74.89 MbChr 19: 18.73 – 18.87 Mb
PubMed search[3][4]
Wikidata
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