Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
22820
Gene name Gene Name - the full gene name approved by the HGNC.
Coat protein complex I subunit gamma 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
COPG1
Synonyms (NCBI Gene) Gene synonyms aliases
COPG, IMD128
Disease Acronyms (UniProt) Disease acronyms from UniProt database
IMD128
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q21.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017439 hsa-miR-335-5p Microarray 18185580
MIRT023687 hsa-miR-1-3p Proteomics 18668040
MIRT023687 hsa-miR-1-3p Proteomics;Microarray 18668037
MIRT032263 hsa-let-7b-5p Proteomics 18668040
MIRT051586 hsa-let-7e-5p CLASH 23622248
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 IBA 21873635
GO:0000139 Component Golgi membrane ISS
GO:0000139 Component Golgi membrane TAS
GO:0005198 Function Structural molecule activity IEA
GO:0005515 Function Protein binding IPI 14527956, 19039328, 25036637
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615525 2236 ENSG00000181789
Protein
UniProt ID Q9Y678
Protein name Coatomer subunit gamma-1 (Gamma-1-coat protein) (Gamma-1-COP)
Protein function The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi ne
PDB 1R4X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01602 Adaptin_N 23 539 Adaptin N terminal region Family
PF08752 COP-gamma_platf 611 759 Coatomer gamma subunit appendage platform subdomain Domain
PF16381 Coatomer_g_Cpla 761 873 Coatomer subunit gamma-1 C-terminal appendage platform Domain
Sequence
MLKKFDKKDEESGGGSNPFQHLEKSAVLQEARVFNETPINPRKCAHILTKILYLINQGEH
LGTTEATEAFFAMTKLFQSNDPTLRRMCYLTIKEMSCIAEDVIIVTSSLTKDMTGKEDNY
RGPAVRALCQITDSTMLQAIERYMKQAIVDKVPSVSSSALVSSLHLLKCSFDVVKRWVNE
AQEAASSDNIMVQYHALGLLYHVRKNDRLAVNKMISKVTRHGLKSPFAYCMMIRVASKQL
EEEDGSRDSPLFDFIESCLRNKHEMVVYEAASAIVNLPGCSAKELAPAVSVLQLFCSSPK
AALRYAAVRTLNKVAMKHPSAVTACNLDLENLVTDSNRSIATLAITTLLKTGSESSIDRL
MKQISSFMSEISDEFKVVVVQAISALCQKYPRKHAVLMNFLFTMLREEGGFEYKRAIVDC
IISIIEENSESKETGLSHLCEFIEDCEFTVLATRILHLLGQEGPKTTNPSKYIRFIYNRV
VLEHEEVRAGAVSALAKFGAQNEEMLPSILVLLKRCVMDDDNEVRDRATFYLNVLEQKQ
K
ALNAGYILNGLTVSIPGLERALQQYTLEPSEKPFDLKSVPLATAPMAEQRTESTPITAVK
QPEKVAATRQEIFQEQLAAVPEFRGLGPLFKSSPEPVALTESETEYVIRCTKHTFTNHMV
FQFDCTNTLNDQTLENVTVQMEPTEAYEVLCYVPARSLPYNQPGTCYTLVALPKEDPTAV
ACTFSCMMKFTVKDCDPTTGETDDEGYEDEYVLEDLEVT
VADHIQKVMKLNFEAAWDEVG
DEFEKEETFTLSTIKTLEEAVGNIVKFLGMHPCERSDKVPDNKNTHTLLLAGVFRGGHDI
LVRSRLLLLDTVTMQVTARSLEELPVDIILASV
G
Sequence length 874
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    COPI-mediated anterograde transport
COPI-dependent Golgi-to-ER retrograde traffic
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Severe combined immunodeficiency disease non-severe combined immunodeficiency due to COPG1 deficiency GenCC
Diabetes Diabetes GWAS
Atrial Fibrillation Atrial Fibrillation GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Renal Cell Associate 33850477