Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10328
Gene name Gene Name - the full gene name approved by the HGNC.
ER membrane protein complex subunit 8
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EMC8
Synonyms (NCBI Gene) Gene synonyms aliases
C16orf2, C16orf4, COX4NB, FAM158B, NOC4
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q24.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT041833 hsa-miR-484 CLASH 23622248
MIRT688409 hsa-miR-140-3p HITS-CLIP 23313552
MIRT688408 hsa-miR-483-5p HITS-CLIP 23313552
MIRT688407 hsa-miR-7845-5p HITS-CLIP 23313552
MIRT688406 hsa-miR-654-3p 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:0005515 Function Protein binding IPI 16189514, 22119785, 26496610, 28514442, 30021884, 32296183, 32439656, 33961781, 35271311
GO:0005737 Component Cytoplasm IDA 22119785
GO:0005783 Component Endoplasmic reticulum IDA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604886 7864 ENSG00000131148
Protein
UniProt ID O43402
Protein name ER membrane protein complex subunit 8 (Neighbor of COX4) (Protein FAM158B)
Protein function Part of the endoplasmic reticulum membrane protein complex (EMC) that enables the energy-independent insertion into endoplasmic reticulum membranes of newly synthesized membrane proteins (PubMed:29242231, PubMed:29809151, PubMed:30415835, PubMed
PDB 6WW7 , 7ADO , 7ADP , 8EOI , 8J0N , 8J0O , 8S9S , 9C7V
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03665 UPF0172 3 202 Uncharacterised protein family (UPF0172) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in liver, pancreas, heart, lung, kidney, brain, skeletal muscle, and placenta. Expression levels are highest in pancreas and moderate in heart, skeletal muscle, and placenta.
Sequence
Sequence length 210
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Severe insulin-deficient type 2 diabetes N/A N/A GWAS