Streak Ovary Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A developmental disorder characterized by the progressive loss of primordial germ cells in the developing ovaries of an embryo, leading to hypoplastic ovaries composed of wavy connective tissue with occasional clumps of granulosa cells, and frequently mesonephric or hilar cells. (Human Phenotype Ontology, HP_0010464)
External Link https://www.disgenet.org/browser/0/1/0/C0266371
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Genes

21 genes associated with the disease Streak Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BMP15 bone morphogenetic protein 15
DCAF17 DDB1 and CUL4 associated factor 17
DHH desert hedgehog
DMRT3 doublesex and mab-3 related transcription factor 3
FSHR follicle stimulating hormone receptor
GATA4 GATA binding protein 4
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
MRPS22 mitochondrial ribosomal protein S22
NR0B1 nuclear receptor subfamily 0, group B, member 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
NUP107 nucleoporin 107kDa
PAX6 paired box 6
PSMC3IP PSMC3 interacting protein
SETBP1 SET binding protein 1
SOX9 SRY (sex determining region Y)-box 9
SPIDR scaffolding protein involved in DNA repair
SRY sex determining region Y
VAMP7 vesicle-associated membrane protein 7
WT1 Wilms tumor 1
WWOX WW domain containing oxidoreductase
ZFPM2 zinc finger protein, FOG family member 2