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CORO7 (coronin 7)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79585
Gene nameGene Name - the full gene name approved by the HGNC.
Coronin 7
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
CORO7
SynonymsGene synonyms aliases
0610011B16Rik, CRN7, POD1
ChromosomeChromosome number
16
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p13.3
SummarySummary 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
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
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
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 28991256, 30285260

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