Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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79585 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Coronin 7 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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CORO7 |
SynonymsGene synonyms aliases
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0610011B16Rik, CRN7, POD1 |
ChromosomeChromosome number
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16 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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16p13.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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 |
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Repeat |
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Sequence |
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Sequence length |
925 |
Interactions |
View interactions |
Associated diseases
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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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