CGB5 (chorionic gonadotropin subunit beta 5)

Gene Gene information from NCBI Gene database.
Gene Transcription factors Other IDs Pathways Associated diseases
Entrez ID 93659
Gene name Chorionic gonadotropin subunit beta 5
Gene symbol CGB5
Synonyms (NCBI Gene)
CGBHCGhCGB
Chromosome 19
Chromosome location 19q13.33
Summary This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 5 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biologi
Transcription factors Transcription factors information provided by TRRUST V2 database.
4
Gene Transcription factors Other IDs Pathways Associated diseases
Show/Hide all (4)
Transcription factor Regulation Reference
KLF6 Activation 21799854
MTA3 Repression 23510993
PPARA Unknown 11564716
RXRA Unknown 11564716
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene Transcription factors Other IDs Pathways Associated diseases
MIM HGNC e!Ensembl
608825 16452 ENSG00000189052
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene Transcription factors Other IDs Pathways Associated diseases
  Reactome
    Glycoprotein hormones
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene Transcription factors Other IDs Pathways Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
POLYCYSTIC OVARY SYNDROME — CTD
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (99)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute Promyelocytic Leukemia Promyelocytic Leukemia BEFREE 9002938
★★★★★
★☆☆☆☆
Found in Text Mining only
Adenoma Adenoma BEFREE 1923947
★★★★★
★☆☆☆☆
Found in Text Mining only
Adrenal Gland Neoplasms Adrenal neoplasia BEFREE 19636197
★★★★★
★☆☆☆☆
Found in Text Mining only
Adrenal Gland Pheochromocytoma Adrenal Gland Pheochromocytoma BEFREE 31490776
★★★★★
★☆☆☆☆
Found in Text Mining only
Adrenal hyperplasia Adrenal hyperplasia BEFREE 16249277
★★★★★
★☆☆☆☆
Found in Text Mining only
Anorexia Nervosa Anorexia BEFREE 26428446
★★★★★
★☆☆☆☆
Found in Text Mining only
Benign Prostatic Hyperplasia Benign Prostatic Hyperplasia BEFREE 9002634
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 12602911, 14633660, 18758818, 9516957
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 15044447, 24753159 Inhibit
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 19047151, 33572731 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only