Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79585
Gene name Gene Name - the full gene name approved by the HGNC.
Coronin 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CORO7
Synonyms (NCBI Gene) Gene synonyms aliases
0610011B16Rik, CRN7, POD1
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the coronin protein family. However, unlike other coronin proteins, it is not an actin-binding protein but rather functions as an F-actin regulator directing anterograde Golgi to endosome transport. The encoded protein has tw
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018155 hsa-miR-335-5p Microarray 18185580
MIRT049245 hsa-miR-92a-3p CLASH 23622248
MIRT696403 hsa-miR-606 HITS-CLIP 23313552
MIRT696402 hsa-miR-4781-3p HITS-CLIP 23313552
MIRT696401 hsa-miR-4716-5p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0003779 Function Actin binding IDA 24768539
GO:0005515 Function Protein binding IPI 21130766, 24768539
GO:0005794 Component Golgi apparatus ISS
GO:0005802 Component Trans-Golgi network IDA 24768539
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611668 26161 ENSG00000262246
Protein
UniProt ID P57737
Protein name Coronin-7 (Crn7) (70 kDa WD repeat tumor rejection antigen homolog)
Protein function F-actin regulator involved in anterograde Golgi to endosome transport: upon ubiquitination via 'Lys-33'-linked ubiquitin chains by the BCR(KLHL20) E3 ubiquitin ligase complex, interacts with EPS15 and localizes to the trans-Golgi network, where
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08953 DUF1899 2 65 Domain of unknown function (DUF1899) Domain
PF00400 WD40 67 106 WD domain, G-beta repeat Repeat
PF00400 WD40 158 196 WD domain, G-beta repeat Repeat
PF16300 WD40_4 338 380 Repeat
PF08953 DUF1899 468 532 Domain of unknown function (DUF1899) Domain
PF00400 WD40 584 623 WD domain, G-beta repeat Repeat
PF00400 WD40 629 665 WD domain, G-beta repeat Repeat
PF16300 WD40_4 808 852 Repeat
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Expressed in the spleen, peripheral leukocytes, testes, brain, thymus and small intestine. {ECO:0000269|PubMed:21130766}.
Sequence
MNRFRVSKFRHTEARPPRRESWISDIRAGTAPSCRNHIKSSCSLIAFNSDRPGVLGIVPL
QGQGE
DKRRVAHLGCHSDLVTDLDFSPFDDFLLATGSADRTVKLWRLPGPGQALPSAPGV
VLGPEDLPVEVLQFHPTSDGILVSAAGTTVKVWDAAKQQPLTELAAHGDLVQSAVWSRDG
ALVGTACKDKQLRIFD
PRTKPRASQSTQAHENSRDSRLAWMGTWEHLVSTGFNQMREREV
KLWDTRFFSSALASLTLDTSLGCLVPLLDPDSGLLVLAGKGERQLYCYEVVPQQPALSPV
TQCVLESVLRGAALVPRQALAVMSCEVLRVLQLSDTAIVPIGYHVPRKAVEFHEDLFPDT
AGCVPATDPHSWWAGDNQQV
QKVSLNPACRPHPSFTSCLVPPAEPLPDTAQPAVMETPVG
DADASEGFSSPPSSLTSPSTPSSLGPSLSSTSGIGTSPSLRSLQSLLGPSSKFRHAQGTV
LHRDSHITNLKGLNLTTPGESDGFCANKLRVAVPLLSSGGQVAVLELRKPGR
LPDTALPT
LQNGAAVTDLAWDPFDPHRLAVAGEDARIRLWRVPAEGLEEVLTTPETVLTGHTEKICSL
RFHPLAANVLASSSYDLTVRIWD
LQAGADRLKLQGHQDQIFSLAWSPDGQQLATVCKDGR
VRVYR
PRSGPEPLQEGPGPKGGRGARIVWVCDGRCLLVSGFDSQSERQLLLYEAEALAGG
PLAVLGLDVAPSTLLPSYDPDTGLVLLTGKGDTRVFLYELLPESPFFLECNSFTSPDPHK
GLVLLPKTECDVREVELMRCLRLRQSSLEPVAFRLPRVRKEFFQDDVFPDTAVIWEPVLS
AEAWLQGANGQP
WLLSLQPPDMSPVSQAPREAPARRAPSSAQYLEEKSDQQKKEELLNAM
VAKLGNREDPLPQDSFEGVDEDEWD
Sequence length 925
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
28991256, 30285260
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes 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
Coronary Heart Disease Coronary Heart Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Pancreatic Ductal Associate 37239355
Squamous Cell Carcinoma of Head and Neck Associate 34884487