Gene Gene information from NCBI Gene database.
Entrez ID 5412
Gene name Ubiquitin like 3
Gene symbol UBL3
Synonyms (NCBI Gene)
HCG-1PNSC1
Chromosome 13
Chromosome location 13q12.3
miRNA miRNA information provided by mirtarbase database.
604
miRTarBase ID miRNA Experiments Reference
MIRT024892 hsa-miR-215-5p Microarray 19074876
MIRT026728 hsa-miR-192-5p Microarray 19074876
MIRT028556 hsa-miR-30a-5p Proteomics 18668040
MIRT029836 hsa-miR-26b-5p Microarray 19088304
MIRT045013 hsa-miR-186-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0070062 Component Extracellular exosome HDA 19056867
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604711 12504 ENSG00000122042
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95164
Protein name Ubiquitin-like protein 3 (Membrane-anchored ubiquitin-fold protein) (HsMUB) (MUB) (Protein HCG-1)
PDB 2GOW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13881 Rad60-SLD_2 8 114 Ubiquitin-2 like Rad60 SUMO-like Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:10375635}.
Sequence
Sequence length 117
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BRCAX BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Hemochromatosis Hemochromatosis BEFREE 8490624
★☆☆☆☆
Found in Text Mining only
HEMOCHROMATOSIS, TYPE 1 Hemochromatosis BEFREE 8490624
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 30323354
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Pancreatic neoplasm Pubtator 35035831 Associate
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 33542925 Associate
★☆☆☆☆
Found in Text Mining only