Gene Gene information from NCBI Gene database.
Entrez ID 79585
Gene name Coronin 7
Gene symbol CORO7
Synonyms (NCBI Gene)
0610011B16RikCRN7POD1
Chromosome 16
Chromosome location 16p13.3
Summary 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.
84
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0003779 Function Actin binding IDA 24768539
GO:0003779 Function Actin binding IEA
GO:0005515 Function Protein binding IPI 21130766, 24768539
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611668 26161 ENSG00000262246
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Acute megakaryoblastic leukemia Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CUTANEOUS MELANOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Mediastinal germ cell tumor Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations