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TRPM6

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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
View/Edit HumanView/Edit Mouse

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

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000119121Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024727Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Schlingmann KP, Weber S, Peters M, et al. (2002). "Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family". Nat. Genet. 31 (2): 166–70. doi:10.1038/ng889. PMID 12032568. S2CID 40990544.

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.