RNF139, ring finger protein 139, 11236

N. diseases: 36; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206734
Disease: Hemangioblastoma
Hemangioblastoma
0.010 GeneticVariation disease BEFREE A Novel RNF139 Mutation in Hemangioblastomas: Case Report. 31031691 2019
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
0.010 Biomarker group BEFREE The effect of RNF139 on tumorigenicity of tongue cancer cells was analyzed by xenograft model on immunodeficient Balb/c nude mice. 28662643 2017
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 GeneticVariation disease BEFREE As the tumor suppressor gene TRC8/RNF139 is disrupted by constitutional t(8;22)(q24.13;q11.21) in dysgerminoma, it may be associated with the onset of CML. 27686674 2017
CUI: C0153349
Disease: Malignant neoplasm of tongue
Malignant neoplasm of tongue
0.010 Biomarker disease BEFREE The effect of RNF139 on tumorigenicity of tongue cancer cells was analyzed by xenograft model on immunodeficient Balb/c nude mice. 28662643 2017
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 Biomarker group BEFREE In order to find the oral cancer related E3 ubiquitin ligases, we screened the human E3 ubiquitin ligase library and found that RING finger protein 139 (RNF139) regulated the biological behavior of tongue cancer cells. 28662643 2017
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 Biomarker disease BEFREE In order to find the oral cancer related E3 ubiquitin ligases, we screened the human E3 ubiquitin ligase library and found that RING finger protein 139 (RNF139) regulated the biological behavior of tongue cancer cells. 28662643 2017
CUI: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma
0.010 AlteredExpression disease BEFREE While human tongue cancer tissues had low expression of RNF139. 28662643 2017
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 AlteredExpression disease BEFREE The expression of the HCV core protein alters endoplasmic reticulum (ER) distribution and induces ER stress in SPP/TRC8 double-knockout cells. 27142248 2016
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus
0.010 AlteredExpression disease BEFREE Among these proteins, the RNF32 and RNF121 expression in BE was 20.3-fold and 16.4-fold higher, respectively, than that in NE, and the expression of RNF24, RNF130, RNF141, RNF139, RNF11, RNF14, and RNF159 was upregulated more than 2-fold compared with NE. 25228972 2014
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 Biomarker group BEFREE These results highlight the tumorigenic role of HO-1 and the importance of TRC8-mediated HO-1 degradation in the control of cancer growth. 22689053 2013
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 Biomarker phenotype BEFREE TRC8 suppresses tumorigenesis through targeting heme oxygenase-1 for ubiquitination and degradation. 22689053 2013
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 AlteredExpression phenotype BEFREE Ectopic TRC8 expression suppresses HO-1-induced cancer cell growth and migration/invasion. 22689053 2013
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 Biomarker group BEFREE These results highlight the tumorigenic role of HO-1 and the importance of TRC8-mediated HO-1 degradation in the control of cancer growth. 22689053 2013
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 Biomarker disease BEFREE TRC8 has the potential to act in a novel regulatory relationship linking the cholesterol/lipid biosynthetic pathway with cellular growth control and has been identified in families with hereditary renal (RCC) and thyroid cancers. 19642973 2009
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 Biomarker disease BEFREE RNF139/TRC8 is a potential tumor suppressor gene with similarity to PTCH, a tumor suppressor implicated in basal cell carcinomas and glioblastomas. 19642973 2009
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.010 Biomarker disease BEFREE TRC8 has the potential to act in a novel regulatory relationship linking the cholesterol/lipid biosynthetic pathway with cellular growth control and has been identified in families with hereditary renal (RCC) and thyroid cancers. 19642973 2009
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma
0.010 Biomarker disease BEFREE TRC8 encodes an E3-ubiquitin ligase disrupted in a family with hereditary renal cell carcinoma (RCC). 15735686 2005
CUI: C2826323
Disease: Refractory Cytopenia of Childhood
Refractory Cytopenia of Childhood
0.010 Biomarker disease BEFREE TRC8 encodes an E3-ubiquitin ligase disrupted in a family with hereditary renal cell carcinoma (RCC). 15735686 2005
CUI: C0238462
Disease: Medullary carcinoma of thyroid
Medullary carcinoma of thyroid
0.010 GeneticVariation disease BEFREE We previously reported that the TRC8 gene was interrupted by a t(3;8) translocation in a family with hereditary renal and non-medullary thyroid cancer. 12032852 2002
Experimental Organism Basal Cell Carcinoma
0.010 Biomarker phenotype BEFREE We now show that the 8q24.1 breakpoint region encodes a 664-aa multiple membrane spanning protein, TRC8, with similarity to the hereditary basal cell carcinoma/segment polarity gene, patched. 9689122 1998
CUI: C0023521
Disease: Globoid cell leukodystrophy
Globoid cell leukodystrophy
0.010 Biomarker disease BEFREE Ultrastructurally immunogold deposits only of RCA-I and WGA in the typical Krabbe's inclusions have been clearly demonstrated. 1335383 1993
HEREDITARY RENAL CANCER ASSOCIATED 1
0.010 Biomarker disease BEFREE We have identified a gene, referred to as HRCA1 (hereditary renal cancer associated 1), that maps immediately adjacent to the breakpoint. 7690964 1993
CUI: C0013377
Disease: Dysgerminoma
Dysgerminoma
0.020 GeneticVariation disease BEFREE As the tumor suppressor gene TRC8/RNF139 is disrupted by constitutional t(8;22)(q24.13;q11.21) in dysgerminoma, it may be associated with the onset of CML. 27686674 2017
CUI: C0013377
Disease: Dysgerminoma
Dysgerminoma
0.020 Biomarker disease BEFREE TRC8 was strongly underexpressed in the dysgerminoma. 19642973 2009
Clear-cell metastatic renal cell carcinoma
0.020 GeneticVariation disease BEFREE Haploinsufficiency of TRC8 may facilitate development of clear cell-RCC in association with VHL mutations, and may increase risk for other tumor types. 19642973 2009