MCOLN2

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

MCOLN2

Mucolipin-2 also known as TRPML2 (transient receptor potential cation channel, mucolipin subfamily, member 2) is a protein that in humans is encoded by the MCOLN2 gene.[5] It is a member of the small family of the TRPML channels, a subgroup of the large protein family of TRP ion channels.

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MCOLN2
Identifiers
AliasesMCOLN2, TRP-ML2, TRPML2, mucolipin 2, mucolipin TRP cation channel 2
External IDsOMIM: 607399; MGI: 1915529; HomoloGene: 12258; GeneCards: MCOLN2; OMA:MCOLN2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_153259
NM_001330647

NM_001005846
NM_026656

RefSeq (protein)

NP_001317576
NP_694991

NP_001005846
NP_080932

Location (UCSC)Chr 1: 84.93 – 85 MbChr 3: 145.86 – 145.9 Mb
PubMed search[3][4]
Wikidata
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TRPML2 is associated with the Arf6-regulated trafficking pathway and is involved in the intracellular transport of membranes and membrane proteins.[6]

See also

  • transient receptor potential cation channel, mucolipin subfamily, member 1 (MCOLN1)
  • transient receptor potential cation channel, mucolipin subfamily, member 3 (MCOLN3)
  • TRPML

References

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