Gene Gene information from NCBI Gene database.
Entrez ID 51614
Gene name ERGIC and golgi 3
Gene symbol ERGIC3
Synonyms (NCBI Gene)
C20orf47C2orf47CGI-54Erv46NY-BR-84PRO0989SDBCAG84dJ477O4.2
Chromosome 20
Chromosome location 20q11.22
miRNA miRNA information provided by mirtarbase database.
62
miRTarBase ID miRNA Experiments Reference
MIRT007115 hsa-miR-490-3p GFP reporter assay 23212913
MIRT007115 hsa-miR-490-3p GFP reporter assay 23212913
MIRT032333 hsa-let-7b-5p Proteomics 18668040
MIRT968941 hsa-miR-1275 CLIP-seq
MIRT968942 hsa-miR-140-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0005515 Function Protein binding IPI 15308636, 31142615, 32296183, 33961781
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616971 15927 ENSG00000125991
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y282
Protein name Endoplasmic reticulum-Golgi intermediate compartment protein 3 (Serologically defined breast cancer antigen NY-BR-84)
Protein function Possible role in transport between endoplasmic reticulum and Golgi. Positively regulates trafficking of the secretory proteins SERPINA1/alpha1-antitrypsin and HP/haptoglobin (PubMed:31142615).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13850 ERGIC_N 7 97 Endoplasmic Reticulum-Golgi Intermediate Compartment (ERGIC) Domain
PF07970 COPIIcoated_ERV 145 363 Endoplasmic reticulum vesicle transporter Family
Sequence
Sequence length 383
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Developmental disorder Likely pathogenic rs2515204602 RCV003441161
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Malignant tumor of urinary bladder Uncertain significance rs113718222 RCV005909289
See cases Uncertain significance rs113718222 RCV001374376
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 23212913, 35602902
Carcinoma Non Small Cell Lung Associate 26177443
Lung Neoplasms Associate 23374247, 26177443
Neoplasm Metastasis Stimulate 35602902
Neoplasms Associate 35602902