Gene Gene information from NCBI Gene database.
Entrez ID 79706
Gene name PRKR interacting protein 1
Gene symbol PRKRIP1
Synonyms (NCBI Gene)
C114KRBOX3
Chromosome 7
Chromosome location 7q22.1
miRNA miRNA information provided by mirtarbase database.
106
miRTarBase ID miRNA Experiments Reference
MIRT036381 hsa-miR-1229-3p CLASH 23622248
MIRT720792 hsa-miR-584-3p HITS-CLIP 19536157
MIRT720791 hsa-miR-1224-3p HITS-CLIP 19536157
MIRT720790 hsa-miR-6734-3p HITS-CLIP 19536157
MIRT720789 hsa-miR-3667-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0003014 Process Renal system process IDA 21183621
GO:0003725 Function Double-stranded RNA binding IBA
GO:0003725 Function Double-stranded RNA binding IEA
GO:0003725 Function Double-stranded RNA binding ISS
GO:0004860 Function Protein kinase inhibitor activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617458 21894 ENSG00000128563
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H875
Protein name PRKR-interacting protein 1
Protein function Required for pre-mRNA splicing as component of the spliceosome (PubMed:28502770, PubMed:30705154). Binds double-stranded RNA. Inhibits EIF2AK2 kinase activity (By similarity). {ECO:0000250|UniProtKB:Q9CWV6, ECO:0000269|PubMed:28502770, ECO:00002
PDB 5XJC , 6ICZ , 6QDV , 7W5A , 7W5B , 8C6J , 9FMD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06658 DUF1168 42 178 Protein of unknown function (DUF1168) Family
Sequence
Sequence length 184
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations