Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
27201
Gene name Gene Name - the full gene name approved by the HGNC.
G protein-coupled receptor 78
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPR78
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the G protein-coupled receptor family, which contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. This is an orphan receptor, which displays significant level of
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT007057 hsa-miR-30d-5p Luciferase reporter assay 23085757
MIRT007058 hsa-miR-181a-5p Luciferase reporter assay 23085757
MIRT007061 hsa-miR-199a-5p Luciferase reporter assay 23085757
MIRT618547 hsa-miR-8485 HITS-CLIP 23824327
MIRT618546 hsa-miR-329-3p HITS-CLIP 23824327
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 IBA 21873635
GO:0004930 Function G protein-coupled receptor activity IDA 17363172
GO:0005515 Function Protein binding IPI 26940976
GO:0005886 Component Plasma membrane IEA
GO:0007186 Process G protein-coupled receptor signaling pathway IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606921 4528 ENSG00000155269
Protein
UniProt ID Q96P69
Protein name G-protein coupled receptor 78
Protein function Orphan receptor. Displays a significant level of constitutive activity. Its effect is mediated by G(s)-alpha protein that stimulate adenylate cyclase, resulting in an elevation of intracellular cAMP.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 22 294 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: High level of expression in placenta. Expressed throughout the brain at low level. No expression detected in skeletal muscle, lung, heart, liver, pancreas, or kidney. {ECO:0000269|PubMed:17363172}.
Sequence
Sequence length 363
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Neuroblastoma Neuroblastoma rs113994087, rs113994089, rs281864719, rs863225285, rs863225284, rs863225283, rs281864720, rs863225282, rs863225281, rs1057519698, rs915983602, rs1469271544 28545128
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
16389273
Unknown
Disease term Disease name Evidence References Source
Systemic lupus erythematosus Systemic lupus erythematosus GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 35301432
Carcinoma Non Small Cell Lung Associate 35986740, 36239568
Hypoxia Associate 35301432