GPR141 (G protein-coupled receptor 141)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
353345
Gene name Gene Name - the full gene name approved by the HGNC.
G protein-coupled receptor 141
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPR141
Synonyms (NCBI Gene) Gene synonyms aliases
PGR13
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p14.1
Summary Summary of gene provided in NCBI Entrez Gene.
GPR141 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003 [PubMed 14623098]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(34)
miRTarBase ID miRNA Experiments Reference
MIRT563020 hsa-miR-5683 PAR-CLIP 20371350
MIRT563019 hsa-miR-6871-5p PAR-CLIP 20371350
MIRT563018 hsa-miR-205-3p PAR-CLIP 20371350
MIRT563017 hsa-miR-6729-3p PAR-CLIP 20371350
MIRT563016 hsa-miR-4740-3p PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(9)
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005515 Function Protein binding IPI 32814053
GO:0005886 Component Plasma membrane IEA
GO:0006954 Process Inflammatory response IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
609045 19997 ENSG00000187037
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q7Z602
Protein name Probable G-protein coupled receptor 141 (G-protein coupled receptor PGR13)
Protein function Orphan receptor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 33 → 281 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 305
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Periodontitis Periodontitis N/A N/A GWAS
Show/Hide Text Mining Associations (4)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 37204251
Hereditary Breast and Ovarian Cancer Syndrome Associate 37204251
Neoplasm Metastasis Associate 37204251
Neoplasms Associate 37204251