MCOLN1
Mucolipin 1 | |||||||||||||
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Identifiers | |||||||||||||
Symbols | MCOLN1 ; MG-2; ML4; MLIV; MST080; TRP-ML1; TRPM-L1; TRPML1 | ||||||||||||
External IDs | OMIM: 605248 MGI: 1890498 HomoloGene: 10744 IUPHAR: 501 GeneCards: MCOLN1 Gene | ||||||||||||
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Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 57192 | 94178 | |||||||||||
Ensembl | ENSG00000090674 | ENSMUSG00000004567 | |||||||||||
UniProt | Q9GZU1 | Q99J21 | |||||||||||
RefSeq (mRNA) | NM_020533 | NM_053177 | |||||||||||
RefSeq (protein) | NP_065394 | NP_444407 | |||||||||||
Location (UCSC) | Chr 19: 7.59 – 7.6 Mb | Chr 8: 3.5 – 3.52 Mb | |||||||||||
PubMed search | |||||||||||||
Mucolipin-1 also known as TRPML1 (transient receptor potential cation channel, mucolipin subfamily, member 1) is a protein that in humans is encoded by the MCOLN1 gene.[1] It is a member of the small family of the TRPML channels, a subgroup of the large protein family of TRP ion channels.
TRPML1 is a 65 kDa protein associated with mucolipidosis type IV. Its predicted structure includes six transmembrane domains, a transient receptor potential (TRP) cation-channel domain, and an internal channel pore.[2] TRPML1 is believed to channel iron ions across the endosome/lysosome membrane into the cell and so its malfunction causes cellular iron deficiency.[3]
See also
- transient receptor potential cation channel, mucolipin subfamily, member 2 (MCOLN2)
- transient receptor potential cation channel, mucolipin subfamily, member 3 (MCOLN3)
- mucolipidosis type IV
- TRPML
References
- ↑ Clapham DE, Julius D, Montell C, Schultz G (December 2005). "International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels". Pharmacol. Rev. 57 (4): 427–50. doi:10.1124/pr.57.4.6. PMID 16382100.
- ↑ Venugopal B, Browning MF, Curcio-Morelli C, Varro A, Michaud N, Nanthakumar N, Walkley SU, Pickel J, Slaugenhaupt SA (November 2007). "Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IV". Am. J. Hum. Genet. 81 (5): 1070–83. doi:10.1086/521954. PMC 2265643. PMID 17924347.
- ↑ Dong, X, Cheng, X., Mills, E., Delling, M., Wang, F., Kurz, T. and Xu, H. (2008). "The Type IV Mucolipidosis-Associated Protein TRPML1 is an Endo-lysosomal Iron Release Channel". Nature 455 (7215): 992–6. doi:10.1038/nature07311. PMID 18794901.
External links
- GeneReviews/NIH/NCBI/UW entry on Mucolipidosis IV
- mucolipin-1 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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