SLC16A8 (solute carrier family 16 member 8)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23539 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Solute carrier family 16 member 8 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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SLC16A8 |
SynonymsGene synonyms aliases
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MCT3, REMP |
ChromosomeChromosome number
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22 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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22q13.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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SLC16A8 is a member of a family of proton-coupled monocarboxylate transporters that mediate lactate transport across cell membranes (Yoon et al., 1999 [PubMed 10493836]).[supplied by OMIM, Apr 2010] |
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
O95907 |
Protein name |
Monocarboxylate transporter 3 (MCT 3) (Solute carrier family 16 member 8) |
Protein function |
Probable retinal pigment epithelium (RPE)-specific proton-coupled L-lactate transporter (By similarity). May facilitate transport of lactate and H(+) out of the retina and could therefore play a role in pH and ion homeostasis of the outer retina |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF07690 |
MFS_1 |
20 → 329 |
Major Facilitator Superfamily |
Family |
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Sequence |
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Sequence length |
504 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Glioblastoma |
Glioblastoma, Glioblastoma Multiforme |
rs121913500, rs886042842, rs1555138291, rs1558518449, rs1567176006, rs1558650888 |
28346443 |
Glioma |
Glioma |
rs121909219, rs121909224, rs587776667, rs587776671, rs121909239, rs121909241, rs28933368, rs121913500, rs55863639, rs786201995, rs786202517, rs786201044, rs398123317, rs1057518425, rs121913499, rs1060500122, rs781647403, rs1060500126, rs1554897889, rs1114167629, rs1114167656, rs587782603, rs1554893824, rs1554900615, rs1564568660, rs786204900, rs762518389, rs1339631701 |
28346443 |
Age-related macular degeneration |
Age related macular degeneration |
rs2133900556, rs199474657, rs2274700, rs1410996, rs61750120, rs1800728, rs62654397, rs61749423, rs61751412, rs61749439, rs61751398, rs61752417, rs62645946, rs1801269, rs62646860, rs61750142, rs61750145, rs61750152, rs61751377, rs61753029, rs61751407, rs61751389, rs61750645, rs61750648, rs879255520, rs752147871, rs886044750, rs886044749, rs746541266, rs756840095, rs886044725, rs749526785, rs1057518955, rs1057518767, rs371489809, rs1064793014, rs1571264574, rs1659524475 |
26691988, 23455636 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Central nervous system neoplasms |
Central Nervous System Neoplasms |
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28346443 |
Exudative macular degeneration |
Exudative age-related macular degeneration, exudative macular degeneration |
|
26691988 |
Geographic atrophy |
Geographic Atrophy |
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26691988 |
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