Pituitary Dwarfism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of reduced stature with normal proportions related to dysfunction of the pituitary gland related to either an isolated defect in the secretion of growth hormone or to panhypopituitarism, i.e., a deficit of all the anterior pituitary hormones. (Human Phenotype Ontology, HP_0000839)
External Link https://www.disgenet.org/browser/0/1/0/C0013338
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Genes

40 genes associated with the disease Pituitary Dwarfism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALB albumin
BRD2 bromodomain containing 2
BTK Bruton agammaglobulinemia tyrosine kinase
CSHL1 chorionic somatomammotropin hormone-like 1
FBRS fibrosin
FBXO8 F-box protein 8
GH1 growth hormone 1
GHR growth hormone receptor
GHRH growth hormone releasing hormone
GHRHR growth hormone releasing hormone receptor
GHSR growth hormone secretagogue receptor
GLI2 GLI family zinc finger 2
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
GPR101 G protein-coupled receptor 101
HESX1 HESX homeobox 1
HGH1 HGH1 homolog (S. cerevisiae)
IGF1 insulin-like growth factor 1 (somatomedin C)
IGFBP3 insulin-like growth factor binding protein 3
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
MMUT methylmalonyl-CoA mutase
NR5A1 nuclear receptor subfamily 5, group A, member 1
OTX2 orthodenticle homeobox 2
PAX6 paired box 6
PHEX phosphate regulating endopeptidase homolog, X-linked
POMC proopiomelanocortin
POU1F1 POU class 1 homeobox 1
PRL prolactin
PROP1 PROP paired-like homeobox 1
RNPC3 RNA-binding region (RNP1, RRM) containing 3
SDS serine dehydratase
SHBG sex hormone-binding globulin
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SOAT1 sterol O-acyltransferase 1
SOX3 SRY (sex determining region Y)-box 3
TACR3 tachykinin receptor 3
TG thyroglobulin