Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54039
Gene name Gene Name - the full gene name approved by the HGNC.
Poly(rC) binding protein 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PCBP3
Synonyms (NCBI Gene) Gene synonyms aliases
ALPHA-CP3, PCBP3-OT1, PCBP3OT
Chromosome Chromosome number
21
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
21q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the KH-domain protein subfamily. Proteins of this subfamily, also referred to as alpha-CPs, bind to RNA with a specificity for C-rich pyrimidine regions. Alpha-CPs play important roles in post-transcriptional activities and h
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018087 hsa-miR-335-5p Microarray 18185580
MIRT029600 hsa-miR-26b-5p Microarray 19088304
MIRT1216541 hsa-miR-338-5p CLIP-seq
MIRT1216542 hsa-miR-4263 CLIP-seq
MIRT1216543 hsa-miR-4799-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0003723 Function RNA binding HDA 22658674
GO:0003723 Function RNA binding NAS 10936052
GO:0003729 Function MRNA binding IBA 21873635
GO:0005634 Component Nucleus HDA 16780588
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608502 8651 ENSG00000183570
Protein
UniProt ID P57721
Protein name Poly(rC)-binding protein 3 (Alpha-CP3) (PCBP3-overlapping transcript) (PCBP3-overlapping transcript 1)
Protein function Single-stranded nucleic acid binding protein that binds preferentially to oligo dC.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00013 KH_1 47 109 KH domain Domain
PF00013 KH_1 131 195 KH domain Domain
PF00013 KH_1 295 359 KH domain Domain
Sequence
MGEGDAFWAPSVLPHSTLSTLSHHPQPQFGRRMESKVSEGGLNVTLTIRLLMHGKEVGSI
IGKKGETVKKMREESGARINISEGNCPERIVTITGPTDAIFKAFAMIAY
KFEEDIINSMS
NSPATSKPPVTLRLVVPASQCGSLIGKGGSKIKEIRESTGAQVQVAGDMLPNSTERAVTI
SGTPDAIIQCVKQIC
VVMLESPPKGATIPYRPKPASTPVIFAGGQAYTIQGQYAIPHPDQ
LTKLHQLAMQQTPFPPLGQTNPAFPGEKLPLHSSEEAQNLMGQSSGLDASPPASTHELTI
PNDLIGCIIGRQGTKINEIRQMSGAQIKIANATEGSSERQITITGTPANISLAQYLINA
R
LTSEVTGMGTL
Sequence length 371
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Myopia Myopia GWAS
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Chromosome 21 monosomy Associate 35361402
Pancreatic Neoplasms Associate 35920801
Pulmonary Disease Chronic Obstructive Associate 30694715
Sarcoma Kaposi Associate 40016701