Gene Gene information from NCBI Gene database.
Entrez ID 8899
Gene name Pre-mRNA processing factor kinase PRP4K
Gene symbol PRP4K
Synonyms (NCBI Gene)
PR4HPRP4PRP4HPRPF4BPrp4BdJ1013A10.1
Chromosome 6
Chromosome location 6p25.2
miRNA miRNA information provided by mirtarbase database.
467
miRTarBase ID miRNA Experiments Reference
MIRT028664 hsa-miR-30a-5p Proteomics 18668040
MIRT053285 hsa-miR-371a-5p qRT-PCRWestern blot 23466643
MIRT053285 hsa-miR-371a-5p qRT-PCRWestern blot 23466643
MIRT654725 hsa-miR-4502 HITS-CLIP 23824327
MIRT654724 hsa-miR-3192-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000244 Process Spliceosomal tri-snRNP complex assembly IDA 20118938
GO:0000387 Process Spliceosomal snRNP assembly IDA 12077342
GO:0000398 Process MRNA splicing, via spliceosome IC 11991638
GO:0000775 Component Chromosome, centromeric region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602338 17346 ENSG00000112739
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q13523
Protein name Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog)
Protein function Serine/threonine kinase involved in spliceosomal assembly as well as mitosis and signaling regulation (PubMed:10799319, PubMed:12077342, PubMed:17513757, PubMed:17998396). Connects chromatin mediated regulation of transcription and pre-mRNA spli
PDB 4IAN , 4IFC , 4IIR , 4IJP , 6CNH , 6PJJ , 6PK6 , 6QX9 , 8H6E , 8H6J , 8QXD , 8R08 , 8R0A , 8Y6O
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 687 1003 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
MAAAETQSLREQPEMEDANSEKSINEENGEVSEDQSQNKHSRHKKKKHKHRSKHKKHKHS
SEEDKDKKHKHKHKHKKHKRKEIIDASDKEGMSPAKRTKLDDLALLEDLEKQRALIKAEL
DNELMEGKVQSGMGLILQGYESGSEEEGEIHEKARNGNRSSTRSSSTKGKLELVDNKITT
KKRSKSRSKERTRHRSDKKKSKGGIEIVKEKTTRSKSKERKKSKSPSKRSKSQDQARKSK
SPTLRRRSQEKIGKARSPTDDKVKIEDKSKSKDRKKSPIINESRSRDRGKKSRSPVDLRG
KSKDRRSRSKERKSKRSETDKEKKPIKSPSKDASSGKENRSPSRRPGRSPKRRSLSPKPR
DKSRRSRSPLLNDRRSKQSKSPSRTLSPGRRAKSRSLERKRREPERRRLSSPRTRPRDDI
LSRRERSKDASPINRWSPTRRRSRSPIRRRSRSPLRRSRSPRRRSRSPRRRDRGRRSRSR
LRRRSRSRGGRRRRSRSKVKEDKFKGSLSEGMKVEQESSSDDNLEDFDVEEEDEEALIEQ
RRIQRQAIVQKYKYLAEDSNMSVPSEPSSPQSSTRTRSPSPDDILERVAADVKEYERENV
DTFEASVKAKHNLMTVEQNNGSSQKKLLAPDMFTESDDMFAAYFDSARLRAAGIGKDFKE
NPNLRDNWTDAEGYYRVNIGEVLDKRYNVYGYTGQGVFSNVVRARDNARANQEVAVKIIR
NNELMQKTGLKELEFLKKLNDADPDDKFHCLRLFRHFYHKQHLCLVFEPLSMNLREVLKK
YGKDVGLHIKAVRSYSQQLFLALKLLKRCNILHADIKPDNILVNESKTILKLCDFGSASH
VADNDITPYLVSRFYRAPEIIIGKSYDYGIDMWSVGCTLYELYTGKILFPGKTNNHMLKL
AMDLKGKMPNKMIRKGVFKDQHFDQNLNFMYIEVDKVTEREKVTVMSTINPTKDLLADLI
GCQRLPEDQRKKVHQLKDLLDQILMLDPAKRISINQALQHAFI
QEKI
Sequence length 1007
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Likely benign rs148856086 RCV005927426
Clear cell carcinoma of kidney Likely benign rs148856086 RCV005927427
Gastric cancer Likely benign rs148856086 RCV005927428
Ovarian serous cystadenocarcinoma Likely benign rs148856086 RCV005927429