Turner Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description No OMIM mapping, confirmed by DO. [LS]. (Human Disease Ontology, DOID_3491)
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Genes

21 genes associated with the Turner Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
AKT1 v-akt murine thymoma viral oncogene homolog 1
EFHC2 EF-hand domain (C-terminal) containing 2
ESR1 estrogen receptor 1
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GHR growth hormone receptor
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IGFBP3 insulin-like growth factor binding protein 3
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KRAS Kirsten rat sarcoma viral oncogene homolog
LHX4 LIM homeobox 4
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYOD1 myogenic differentiation 1
PTPN1 protein tyrosine phosphatase, non-receptor type 1
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SCN5A sodium channel, voltage gated, type V alpha subunit
SOCS2 suppressor of cytokine signaling 2
SOS2 son of sevenless homolog 2 (Drosophila)
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor