Gene Gene information from NCBI Gene database.
Entrez ID 6733
Gene name SRSF protein kinase 2
Gene symbol SRPK2
Synonyms (NCBI Gene)
SFRSK2
Chromosome 7
Chromosome location 7q22.3
miRNA miRNA information provided by mirtarbase database.
320
miRTarBase ID miRNA Experiments Reference
MIRT020912 hsa-miR-155-5p Proteomics 18668040
MIRT025155 hsa-miR-181a-5p Microarray 17612493
MIRT030965 hsa-miR-21-5p Microarray 18591254
MIRT653145 hsa-miR-548c-3p HITS-CLIP 23824327
MIRT653144 hsa-miR-4282 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
59
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000245 Process Spliceosomal complex assembly IBA
GO:0000245 Process Spliceosomal complex assembly IDA 9472028
GO:0000245 Process Spliceosomal complex assembly IEA
GO:0000287 Function Magnesium ion binding IDA 9472028
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602980 11306 ENSG00000135250
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P78362
Protein name SRSF protein kinase 2 (EC 2.7.11.1) (SFRS protein kinase 2) (Serine/arginine-rich protein-specific kinase 2) (SR-protein-specific kinase 2) [Cleaved into: SRSF protein kinase 2 N-terminal; SRSF protein kinase 2 C-terminal]
Protein function Serine/arginine-rich protein-specific kinase which specifically phosphorylates its substrates at serine residues located in regions rich in arginine/serine dipeptides, known as RS domains and is involved in the phosphorylation of SR splicing fac
PDB 2X7G , 5MYV , 7ZKX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 81 230 Protein kinase domain Domain
PF00069 Pkinase 511 686 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain, moderately expressed in heart and skeletal muscle and at low levels in lung, liver, and kidney. {ECO:0000269|PubMed:9472028}.
Sequence
MSVNSEKSSSSERPEPQQKAPLVPPPPPPPPPPPPPLPDPTPPEPEEEILGSDDEEQEDP
ADYCKGGYHPVKIGDLFNGRYHVIRKLGWGHFSTVWLCWDMQGKRFVAMKVVKSAQHYTE
TALDEIKLLKCVRESDPSDPNKDMVVQLIDDFKISGMNGIHVCMVFEVLGHHLLKWIIKS
NYQGLPVRCVKSIIRQVLQGLDYLHSKCKIIHTDIKPENILMCVDDAYVR
RMAAEATEWQ
KAGAPPPSGSAVSTAPQQKPIGKISKNKKKKLKKKQKRQAELLEKRLQEIEELEREAERK
IIEENITSAAPSNDQDGEYCPEVKLKTTGLEEAAEAETAKDNGEAEDQEEKEDAEKENIE
KDEDDVDQELANIDPTWIESPKTNGHIENGPFSLEQQLDDEDDDEEDCPNPEEYNLDEPN
AESDYTYSSSYEQFNGELPNGRHKIPESQFPEFSTSLFSGSLEPVACGSVLSEGSPLTEQ
EESSPSHDRSRTVSASSTGDLPKAKTRAADLLVNPLDPRNADKIRVKIADLGNACWVHKH
FTEDIQTRQYRSIEVLIGAGYSTPADIWSTACMAFELATGDYLFEPHSGEDYSRDEDHIA
HIIELLGSIPRHFALSGKYSREFFNRRGELRHITKLKPWSLFDVLVEKYGWPHEDAAQFT
DFLIPMLEMVPEKRASAGECLRHPWL
NS
Sequence length 688
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
13
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Benign rs56318802 RCV005913041
Hepatocellular carcinoma Benign rs56318802 RCV005913039
Malignant tumor of esophagus Benign rs56318802 RCV005913040
SRPK2-related disorder Likely benign; Benign rs758052569, rs190731348, rs371115678, rs56172322, rs146307731, rs56666353, rs56318802, rs1380771554 RCV003923957
RCV003911821
RCV003927299
RCV003959345
RCV003924285
RCV003905874
RCV003905875
RCV003983809
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 23071587
Autism Spectrum Disorder Associate 37907504
Carcinoma Non Small Cell Lung Associate 23071587
Carcinoma Squamous Cell Stimulate 23071587
Cholangiocarcinoma Associate 39344395
Colorectal Neoplasms Associate 31898732
COVID 19 Associate 35967328
Infertility Male Associate 31103287
Leukemia Associate 18559500, 26244849
Leukemia Myeloid Acute Associate 18559500