Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
387509
Gene name Gene Name - the full gene name approved by the HGNC.
G protein-coupled receptor 153
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPR153
Synonyms (NCBI Gene) Gene synonyms aliases
PGR1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an integral membrane protein that belongs to the Class A rhodopsin superfamily of G protein coupled receptors. The encoded protein is expressed primarily in the central nervous system. A knockdown of the orthologous gene in rat is associ
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs776061422 G>A,T Likely-pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018324 hsa-miR-335-5p Microarray 18185580
MIRT487782 hsa-miR-132-5p PAR-CLIP 23592263
MIRT487781 hsa-miR-1254 PAR-CLIP 23592263
MIRT487780 hsa-miR-3116 PAR-CLIP 23592263
MIRT487779 hsa-miR-661 PAR-CLIP 23592263
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 IEA
GO:0007186 Process G protein-coupled receptor signaling pathway IEA
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614269 23618 ENSG00000158292
Protein
UniProt ID Q6NV75
Protein name Probable G-protein coupled receptor 153 (G-protein coupled receptor PGR1)
Protein function Orphan receptor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 24 297 7 transmembrane receptor (rhodopsin family) Family
Sequence
MSDERRLPGSAVGWLVCGGLSLLANAWGILSVGAKQKKWKPLEFLLCTLAATHMLNVAVP
IATYSVVQLRRQRPDFEWNEGLCKVFVSTFYTLTLATCFSVTSLSYHRMWMVCWPVNYRL
SNAKKQAVHTVMGIWMVSFILSALPAVGWHDTSERFYTHGCRFIVAEIGLGFGVCFLLLV
GGSVAMGVICTAIALFQTLAVQVGRQADRRAFTVPTIVVEDAQGKRRSSIDGSEPAKTSL
QTTGLVTTIVFIYDCLMGFPVLVVSFSSLRADASAPWMALCVLWCSVAQALLLPVFL
WAC
DRYRADLKAVREKCMALMANDEESDDETSLEGGISPDLVLERSLDYGYGGDFVALDRMAK
YEISALEGGLPQLYPLRPLQEDKMQYLQVPPTRRFSHDDADVWAAVPLPAFLPRWGSGED
LAALAHLVLPAGPERRRASLLAFAEDAPPSRARRRSAESLLSLRPSALDSGPRGARDSPP
GSPRRRPGPGPRSASASLLPDAFALTAFECEPQALRRPPGPFPAAPAAPDGADPGEAPTP
PSSAQRSPGPRPSAHSHAGSLRPGLSASWGEPGGLRAAGGGGSTSSFLSSPSESSGYATL
HSDSLGSAS
Sequence length 609
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia, Schizophrenia, Childhood rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
21822266, 26508570
Associations from Text Mining
Disease Name Relationship Type References
Mental Disorders Associate 26508570
Schizophrenia Childhood Associate 26508570