INHBB, inhibin subunit beta B, 3625

N. diseases: 22; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0342549
Disease: Familial Testotoxicosis
Familial Testotoxicosis
0.300 Biomarker disease CTD_human Activating mutations in the luteinizing hormone receptor gene: a human model of non-follicle-stimulating hormone-dependent inhibin production and germ cell maturation. 16684832 2006
CUI: C0006110
Disease: Brain Death
Brain Death
0.200 Biomarker phenotype RGD Gene expression profile in rat renal isografts from brain dead donors. 15808645 2005
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0.200 Biomarker disease RGD Developmental expression of testis messenger ribonucleic acids in the rat following propylthiouracil-induced neonatal hypothyroidism. 7819453 1994
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism
0.200 Biomarker disease RGD Developmental expression of testis messenger ribonucleic acids in the rat following propylthiouracil-induced neonatal hypothyroidism. 7819453 1994
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 Biomarker disease BEFREE THBS2, INHBB and BGN are prognostic markers and potential therapeutic targets for CRC. 28424419 2017
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 PosttranslationalModification disease BEFREE The aim of the present study was to examine the presence of DNA sequences of five human DNA viruses (assessed by PCR): JC polyoma virus (JCV), human adenovirus (AdV), Epstein-Barr virus (EBV), Kaposi sarcoma-associated herpesvirus (KSHV/HHV8) and human papillomavirus (HPV) in a cohort of 186 sporadic colorectal cancers (CRCs) and related these data with the methylation status of six CpG island methylator phenotype (CIMP)-specific genes (MLH1, CACNA1G, NEUROG1, IGF2, SOCS1, RUNX3) and seven cancer-related genes markers (p16, MINT1, MINT2, MINT31, EN1, SCTR and INHBB) assessed by methylation-specific PCR in 186 and 134 CRC cases, respectively. 21625944 2011
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 Biomarker disease BEFREE Given that the number of hypermethylated loci at 2q14.2 likely affects the range of silenced flanking genes, high frequency of simultaneous hypermethylation of three CpG islands (EN1, SCTR, and INHBB) may have potential influence on specific characteristics of CIMP+ colorectal cancers. 18403637 2008
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 Biomarker group BEFREE Inhibin-βA might be important during progression of CIN, whereas the inhibin-βB subunit could exert a substantial function during differentiation of cervical carcinomas. 21475087 2010
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 Biomarker group BEFREE Hypermethylation of at least one of the CpG islands analysed (EN1, SCTR, INHBB) occurred in most carcinomas (90%), with EN1 methylated in 73 and 40% of carcinomas and adenomas, respectively. 19384295 2009
CUI: C2699510
Disease: Split-Hand/Foot Malformation
Split-Hand/Foot Malformation
0.020 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 Biomarker disease LHGDN High serum concentration of total inhibin in polycystic ovary syndrome. 18423626 2008
CUI: C2699510
Disease: Split-Hand/Foot Malformation
Split-Hand/Foot Malformation
0.020 GeneticVariation disease BEFREE To investigate whether mutation of a gene in proximity to the chromosome 2 breakpoint underlies the SHFLD, we sought independent evidence of mutations in GLI2, INHBB and two other genes (RALB and FLJ14816) in 44 unrelated patients with SHFM, SHFLD or isolated long bone deficiency. 17569090 2007
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 Biomarker disease LHGDN Luteal-phase inhibin A and follicular-phase inhibin B levels are not characteristic of patients with an elevated LH-to-FSH ratio. 16758344 2006
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 GeneticVariation disease BEFREE INHBB is an established locus for ER-negative breast cancer, and HABP2 and LINC01483 represent putative new breast cancer susceptibility loci, because both loci were associated with breast cancer in available meta-analysis data including 122,977 breast cancer cases and 105,974 control subjects (P < 0.05). h<sup>2</sup><sub>SNP</sub> (SE) estimates for percent dense, absolute dense, and nondense volume were 0.29 (0.07), 0.31 (0.07), and 0.25 (0.07), respectively. 29665850 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 GeneticVariation disease BEFREE INHBB is an established locus for ER-negative breast cancer, and HABP2 and LINC01483 represent putative new breast cancer susceptibility loci, because both loci were associated with breast cancer in available meta-analysis data including 122,977 breast cancer cases and 105,974 control subjects (P < 0.05). h<sup>2</sup><sub>SNP</sub> (SE) estimates for percent dense, absolute dense, and nondense volume were 0.29 (0.07), 0.31 (0.07), and 0.25 (0.07), respectively. 29665850 2018
estrogen receptor-negative breast cancer
0.010 GeneticVariation disease BEFREE INHBB is an established locus for ER-negative breast cancer, and HABP2 and LINC01483 represent putative new breast cancer susceptibility loci, because both loci were associated with breast cancer in available meta-analysis data including 122,977 breast cancer cases and 105,974 control subjects (P < 0.05). h<sup>2</sup><sub>SNP</sub> (SE) estimates for percent dense, absolute dense, and nondense volume were 0.29 (0.07), 0.31 (0.07), and 0.25 (0.07), respectively. 29665850 2018
Secondary malignant neoplasm of lymph node
0.010 Biomarker disease BEFREE Several upregulated miR-34 targets displayed elevated expression in primary human colorectal cancers that was associated with lymph-node metastases (<i>INHBB, AXL, FGFR1,</i> and <i>PDFGRB</i>) and upregulation of <i>INHBB</i> and <i>AXL</i> in primary colorectal cancer was associated with poor patient survival. 28363996 2017
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 AlteredExpression disease BEFREE Histopathological studies suggest that elevated expression of activin/inhibin βB subunit is associated with reduced survival in non-endometrioid endometrial cancers (type II, mostly serous). 26384307 2015
CUI: C0036220
Disease: Kaposi Sarcoma
Kaposi Sarcoma
0.010 GeneticVariation disease BEFREE The aim of the present study was to examine the presence of DNA sequences of five human DNA viruses (assessed by PCR): JC polyoma virus (JCV), human adenovirus (AdV), Epstein-Barr virus (EBV), Kaposi sarcoma-associated herpesvirus (KSHV/HHV8) and human papillomavirus (HPV) in a cohort of 186 sporadic colorectal cancers (CRCs) and related these data with the methylation status of six CpG island methylator phenotype (CIMP)-specific genes (MLH1, CACNA1G, NEUROG1, IGF2, SOCS1, RUNX3) and seven cancer-related genes markers (p16, MINT1, MINT2, MINT31, EN1, SCTR and INHBB) assessed by methylation-specific PCR in 186 and 134 CRC cases, respectively. 21625944 2011
CUI: C0001430
Disease: Adenoma
Adenoma
0.010 PosttranslationalModification group BEFREE Hypermethylation of at least one of the CpG islands analysed (EN1, SCTR, INHBB) occurred in most carcinomas (90%), with EN1 methylated in 73 and 40% of carcinomas and adenomas, respectively. 19384295 2009
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly
0.010 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009
CUI: C2931019
Disease: Split hand foot deformity 1
Split hand foot deformity 1
0.010 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 AlteredExpression group LHGDN Activin and estrogen crosstalk regulates transcription in human breast cancer cells. 17914098 2007
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
0.010 Biomarker disease LHGDN Relationship of estradiol and inhibin to the follicle-stimulating hormone variability in hypergonadotropic hypogonadism or premature ovarian failure. 15562017 2005
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.010 Biomarker disease LHGDN Relationship of estradiol and inhibin to the follicle-stimulating hormone variability in hypergonadotropic hypogonadism or premature ovarian failure. 15562017 2005