Abnormality Of Female Internal Genitalia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the female internal genitalia. (Human Phenotype Ontology, HP_0000008)
External Link https://www.disgenet.org/browser/0/1/0/C4025900
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Genes

30 genes associated with the disease Abnormality Of Female Internal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
CTC1 CTS telomere maintenance complex component 1
CXCR4 chemokine (C-X-C motif) receptor 4
DKC1 dyskeratosis congenita 1, dyskerin
DLL3 delta-like 3 (Drosophila)
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FGF20 fibroblast growth factor 20
GLI1 GLI family zinc finger 1
GREB1L growth regulation by estrogen in breast cancer-like
HES7 hes family bHLH transcription factor 7
HOXD13 homeobox D13
ITGA8 integrin, alpha 8
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PARN poly(A)-specific ribonuclease
RET ret proto-oncogene
RIPPLY2 ripply transcriptional repressor 2
RTEL1 regulator of telomere elongation helicase 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
TBX6 T-box 6
TERT telomerase reverse transcriptase
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
USB1 U6 snRNA biogenesis 1
WRAP53 WD repeat containing, antisense to TP53