Gene Gene information from NCBI Gene database.
Entrez ID 124222
Gene name Progestin and adipoQ receptor family member 4
Gene symbol PAQR4
Synonyms (NCBI Gene)
-
Chromosome 16
Chromosome location 16p13.3
miRNA miRNA information provided by mirtarbase database.
244
miRTarBase ID miRNA Experiments Reference
MIRT029666 hsa-miR-26b-5p Microarray 19088304
MIRT048738 hsa-miR-96-5p CLASH 23622248
MIRT1213368 hsa-miR-1207-5p CLIP-seq
MIRT1213369 hsa-miR-122 CLIP-seq
MIRT738866 hsa-miR-1225-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IDA 32291319
GO:0000139 Component Golgi membrane IEA
GO:0005794 Component Golgi apparatus IEA
GO:0016020 Component Membrane IEA
GO:0050821 Process Protein stabilization IDA 38961186
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614578 26386 ENSG00000162073
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N4S7
Protein name Progestin and adipoQ receptor family member 4 (Progestin and adipoQ receptor family member IV)
Protein function Plays a role in maintaining adipose tissue function through the regulation of ceramide levels (PubMed:32291319, PubMed:38961186). Mediates the stability of ceramide synthetases, CERS2 and CERS5, and their activities (Probable). {ECO:0000269|PubM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03006 HlyIII 43 254 Haemolysin-III related Family
Tissue specificity TISSUE SPECIFICITY: Relatively widely expressed in a range of tissues. Expressed in subcutaneous white adipose tissue (PubMed:38961186). {ECO:0000269|PubMed:16044242, ECO:0000269|PubMed:38961186}.
Sequence
Sequence length 273
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Uncertain significance rs376908274 RCV005932581
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Stimulate 36573110
Carcinogenesis Associate 36481756
Carcinoma Hepatocellular Stimulate 35240821
Carcinoma Renal Cell Associate 36481756
Neoplasms Associate 30322804, 36573110
Neoplasms Stimulate 36481756
Stomach Neoplasms Associate 30322804
Urinary Bladder Neoplasms Stimulate 36481756