Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10391
Gene name Gene Name - the full gene name approved by the HGNC.
Coronin 2B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CORO2B
Synonyms (NCBI Gene) Gene synonyms aliases
CLIPINC
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q23
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004703 hsa-miR-185-5p Flow, Immunoblot, Microarray, qRT-PCR 19688090
MIRT017553 hsa-miR-335-5p Microarray 18185580
MIRT024407 hsa-miR-215-5p Microarray 19074876
MIRT026427 hsa-miR-192-5p Microarray 19074876
MIRT904706 hsa-miR-106a CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003093 Process Regulation of glomerular filtration IEA
GO:0003779 Function Actin binding NAS 10224093
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005925 Component Focal adhesion IDA 29162887
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605002 2256 ENSG00000103647
Protein
UniProt ID Q9UQ03
Protein name Coronin-2B (Coronin-like protein C) (Clipin-C) (Protein FC96)
Protein function May play a role in the reorganization of neuronal actin structure.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08953 DUF1899 10 75 Domain of unknown function (DUF1899) Domain
PF00400 WD40 78 116 WD domain, G-beta repeat Repeat
PF00400 WD40 170 208 WD domain, G-beta repeat Repeat
PF16300 WD40_4 350 392 Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in brain.
Sequence
MTVTKMSWRPQYRSSKFRNVYGKVANREHCFDGIPITKNVHDNHFCAVNTRFLAIVTESA
GGGSFLVIPLEQTGR
IEPNYPKVCGHQGNVLDIKWNPFIDNIIASCSEDTSVRIWEIPEG
GLKRNMTEALLELHGHSRRVGLVEWHPTTNNILFSAGYDYKVLIWNLDVGEPVKMIDCHT
DVILCMSFNTDGSLLTTTCKDKKLRVIE
PRSGRVLQEANCKNHRVNRVVFLGNMKRLLTT
GVSRWNTRQIALWDQEDLSMPLIEEEIDGLSGLLFPFYDADTHMLYLAGKGDGNIRYYEI
STEKPYLSYLMEFRSPAPQKGLGVMPKHGLDVSACEVFRFYKLVTLKGLIEPISMIVPRR
SDSYQEDIYPMTPGTEPALTPDEWLGGINRDP
VLMSLKEGYKKSSKMVFKAPIKEKKSVV
VNGIDLLENVPPRTENELLRMFFRQQDEIRRLKEELAQKDIRIRQLQLELKNLRNSPKNC
Sequence length 480
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
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
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Ciliopathies Associate 28800606
Diabetic Nephropathies Inhibit 31221975
Kidney Diseases Associate 31221975