Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8111
Gene name Gene Name - the full gene name approved by the HGNC.
G protein-coupled receptor 68
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPR68
Synonyms (NCBI Gene) Gene synonyms aliases
AI2A6, GPR12A, OGR1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
AI2A6
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q32.11
Summary Summary of gene provided in NCBI Entrez Gene.
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
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1057517671 TT>- Pathogenic Frameshift variant, coding sequence variant
rs1057517672 A>G Pathogenic Missense variant, coding sequence variant
rs1555409827 TTGAAGCTGGTGAGCAGGAGGGAGAAGTGGTAGGCGTTGAAAACGCCCTTGGCGAAGTCGCAGCTGGCCTCCCAGACGCTGCGCACCAGCAGCAACACGTGGTAGGGCAGGAAGCAGGCCAGGAAGATGACCACGGTGCTGAGCACCAGCCGCTGGATCTGGTCCTTGCGGCTCTTCTGGGTGCCGTGGCTCCGGCGCACGGCGCGCAGGATGCCCTGGTAGGACGCCAGCAGCAGGCAGATGGGGAAGAGGAAG Pathogenic Inframe deletion, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1031769 hsa-miR-145 CLIP-seq
MIRT1031770 hsa-miR-3166 CLIP-seq
MIRT1031771 hsa-miR-3678-3p CLIP-seq
MIRT1031772 hsa-miR-3922-5p CLIP-seq
MIRT1031773 hsa-miR-4494 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane TAS 8661159
GO:0006954 Process Inflammatory response TAS 7498459
GO:0007186 Process G protein-coupled receptor signaling pathway TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601404 4519 ENSG00000119714
Protein
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
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
Sequence length 365
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Class A/1 (Rhodopsin-like receptors)
G alpha (q) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
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
View all (70 more)
27693231
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 GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Amelogenesis Imperfecta Associate 32279993
Asthma Associate 22145625
Breast Neoplasms Associate 35545051
Carcinoma Hepatocellular Associate 31236404
Carcinoma Pancreatic Ductal Stimulate 29092903
Colitis Associate 31996710, 39768215
Dry Eye Syndromes Stimulate 36503812
Fibrosis Associate 36010617
Idiopathic Pulmonary Fibrosis Inhibit 36010617
Inflammation Associate 26206859, 36010617, 36503812, 39768215