MCOLN3
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| Mucolipin 3 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||
| Symbols | MCOLN3 ; TRP-ML3; TRPML3 | ||||||||||||
| External IDs | OMIM: 607400 MGI: 1890500 HomoloGene: 10118 IUPHAR: 503 GeneCards: MCOLN3 Gene | ||||||||||||
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| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 55283 | 171166 | |||||||||||
| Ensembl | ENSG00000055732 | ENSMUSG00000036853 | |||||||||||
| UniProt | Q8TDD5 | Q8R4F0 | |||||||||||
| RefSeq (mRNA) | NM_001253693 | NM_134160 | |||||||||||
| RefSeq (protein) | NP_001240622 | NP_598921 | |||||||||||
| Location (UCSC) | Chr 1: 85.02 – 85.05 Mb |
Chr 3: 146.12 – 146.14 Mb |
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| PubMed search | [1] | [2] | |||||||||||
Mucolipin-3 also known as TRPML3 (transient receptor potential cation channel, mucolipin subfamily, member 3) is a protein that in humans is encoded by the MCOLN3 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.[2]
Contents
Gene
In human, the MCOLN3 gene resides on the short arm of chromosome 1 at 1p22.3. The gene is split in 12 exons, which entail the open reading frame of 1659 nucleotides. The encoded protein, TRPML3, has 553 amino acid with a predicted molecular weight of ≈64 kDa. Computational analyses of the secondary structure predict the presence of six transmembrane domains, an ion transport motif (PF00520) and a transient receptor potential motif (PS50272). In the mouse, Mcoln3, is located on the distal end of chromosome 3 at cytogenetic band qH2. Human and mouse TRPML3 proteins share 91% sequence identity.[3] All vertebrate species, for which a genomic sequence is available, harbor the MCOLN3 gene. Homologs of MCOLN3 are also present in the genome of insects (Drosophila melanogaster), nematodes (Caenorhabditis elegans), sea urchin (Strongylocentrotus purpuratus) and lower organisms including Hydra and Dictyostelium.
Expression
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Function
TRPML3 is an inwardly-rectifying cation channel.[1]
Genetics
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Phenotypes
Mutations of the MCOLN3 gene in mice result in auditory hair cell death and deafness.[4]
See also
- transient receptor potential cation channel, mucolipin subfamily, member 1 (MCOLN1)
- transient receptor potential cation channel, mucolipin subfamily, member 2 (MCOLN2)
References
Further reading
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External links
- MCOLN3 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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