Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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8111
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Gene name
Gene Name - the full gene name approved by the HGNC.
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G protein-coupled receptor 68 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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GPR68 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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AI2A6, GPR12A, OGR1 |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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AI2A6 |
Chromosome
Chromosome number
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14 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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14q32.11 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a G protein-coupled receptor for sphingosylphosphorylcholine. The encoded protein is a proton-sensing receptor, inactive at pH 7.8 but active at pH 6.8. Mutations in this gene are a cause of amelogenesis imperfecta. [pr |
UniProt ID |
Q15743
|
Protein name |
G-protein coupled receptor 68 (G-protein coupled receptor 12A) (GPR12A) (Ovarian cancer G-protein coupled receptor 1) (OGR-1) |
Protein function |
Proton-sensing G-protein coupled receptor activated by extracellular pH, which is required to monitor pH changes and generate adaptive reactions (PubMed:12955148, PubMed:29677517, PubMed:32865988, PubMed:33478938, PubMed:39753132). The receptor |
PDB |
9BHM
,
9BI6
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00001
|
7tm_1 |
38 → 286 |
7 transmembrane receptor (rhodopsin family) |
Family |
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Tissue specificity |
TISSUE SPECIFICITY: Found at low level in a wide range of tissues, but significantly expressed in lung, kidney, bone and nervous system. {ECO:0000269|PubMed:12955148}. |
Sequence |
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Sequence length |
365 |
Interactions |
View interactions
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Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Amelogenesis imperfecta |
Amelogenesis Imperfecta hypomaturation type, AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6 |
rs267607178, rs143816093, rs606231351, rs137854435, rs137854440, rs137854441, rs137854444, rs587776587, rs121908109, rs587776588, rs140213840, rs104894704, rs387906487, rs387906488, rs387906489, rs104894733, rs104894734, rs104894736, rs387906490, rs387906491, rs104894737, rs104894738, rs144411158, rs587776911, rs587776912, rs587776913, rs587776914, rs387907215, rs866941536, rs1560562738, rs1560562630, rs146645381, rs1560558455, rs587777515, rs587777516, rs587777530, rs139620139, rs587777531, rs587777535, rs587777536, rs587777537, rs606231462, rs1553275034, rs869320671, rs786201004, rs140015315, rs730882118, rs730880297, rs730880298, rs786204825, rs786204826, rs1555409827, rs1057517671, rs1057517672, rs556734208, rs146238585, rs202073531, rs1057519277, rs767907487, rs779823931, rs1060499539, rs1085307111, rs546603773, rs1553275070, rs1553275195, rs752102959, rs1554623490, rs1553888384, rs770804941, rs1553887511, rs557128345, rs1568724130, rs199527325, rs1603038146, rs773117913, rs1560973571, rs1560782372, rs1560980659, rs1560973467, rs772929908, rs762816338, rs1565222166, rs1595312054, rs1866200282, rs2086254952 View all (70 more) |
27693231 |
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Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Breast Cancer |
Breast Cancer |
Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients |
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GWAS, CBGDA |
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