Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11236
Gene name Gene Name - the full gene name approved by the HGNC.
Ring finger protein 139
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RNF139
Synonyms (NCBI Gene) Gene synonyms aliases
HRCA1, RCA1, TRC8
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q24.13
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT038108 hsa-miR-423-5p CLASH 23622248
MIRT726730 hsa-miR-27a-3p HITS-CLIP 22473208
MIRT726729 hsa-miR-27b-3p HITS-CLIP 22473208
MIRT1310177 hsa-miR-101 CLIP-seq
MIRT1310178 hsa-miR-1276 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002020 Function Protease binding IPI 25239945
GO:0004842 Function Ubiquitin-protein transferase activity IDA 17016439
GO:0004842 Function Ubiquitin-protein transferase activity IMP 19720873
GO:0004842 Function Ubiquitin-protein transferase activity TAS 10500182
GO:0005515 Function Protein binding IPI 12032852, 19706601, 19720873, 23223569, 25239945, 32814053
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603046 17023 ENSG00000170881
Protein
UniProt ID Q8WU17
Protein name E3 ubiquitin-protein ligase RNF139 (EC 2.3.2.27) (RING finger protein 139) (RING-type E3 ubiquitin transferase RNF139) (Translocation in renal carcinoma on chromosome 8 protein)
Protein function E3-ubiquitin ligase; acts as a negative regulator of cell proliferation through mechanisms involving G2/M arrest and cell death (PubMed:10500182, PubMed:12032852, PubMed:17016439). Required for MHC class I ubiquitination in cells expressing the
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13705 TRC8_N 19 516 TRC8 N-terminal domain Domain
PF13639 zf-RING_2 545 586 Ring finger domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in testis, placenta and adrenal gland. Moderate expression in heart, brain, liver, skeletal muscle and pancreas, and low expression in lung and kidney. {ECO:0000269|PubMed:9689122}.
Sequence
Sequence length 664
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    ER Quality Control Compartment (ERQC)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Papillary renal carcinoma Papillary Renal Cell Carcinoma rs5030823, rs2137087134, rs121913668, rs121913669, rs121913670, rs121913671, rs121913673, rs121913243, rs786202724
Renal carcinoma Renal Cell Carcinoma, Conventional (Clear Cell) Renal Cell Carcinoma, Sarcomatoid Renal Cell Carcinoma, Collecting Duct Carcinoma of the Kidney rs121913668, rs121913670, rs121913243, rs786202724
Unknown
Disease term Disease name Evidence References Source
Chromophobe carcinoma Chromophobe Renal Cell Carcinoma ClinVar
Hereditary renal carcinoma Hereditary clear cell renal cell carcinoma ClinVar
Papillary Renal Carcinoma nonpapillary renal cell carcinoma GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 25228972
Barrett Esophagus Stimulate 25228972
Breast Neoplasms Associate 36077333
Carcinoma Basal Cell Associate 19642973
Carcinoma Hepatocellular Associate 24346768
Carcinoma Renal Cell Associate 19642973, 9689122
Dysgerminoma Associate 19642973
Esophageal Neoplasms Associate 25228972
Glioblastoma Associate 19642973
Glioma Inhibit 34106407