Persistent Hyperplastic Primary Vitreous Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060282)
External Link https://www.disgenet.org/browser/0/1/0/C0266568
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Genes

33 genes associated with the disease Persistent Hyperplastic Primary Vitreous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ATOH7 atonal homolog 7 (Drosophila)
BCOR BCL6 corepressor
CADPS2 Ca++-dependent secretion activator 2
CCND3 cyclin D3
CDK6 cyclin-dependent kinase 6
CDKN2A cyclin-dependent kinase inhibitor 2A
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
COL11A2 collagen, type XI, alpha 2
COL18A1 collagen, type XVIII, alpha 1
COL4A1 collagen, type IV, alpha 1
CRYBA1 crystallin, beta A1
EGFR epidermal growth factor receptor
FOXQ1 forkhead box Q1
FZD4 frizzled class receptor 4
GAPDH glyceraldehyde-3-phosphate dehydrogenase
GFAP glial fibrillary acidic protein
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
ISPD isoprenoid synthase domain containing
KDR kinase insert domain receptor
MKI67 marker of proliferation Ki-67
NDP Norrie disease (pseudoglioma)
PARP1 poly (ADP-ribose) polymerase 1
PAX6 paired box 6
PCNA proliferating cell nuclear antigen
PPARD peroxisome proliferator-activated receptor delta
RMDN1 regulator of microtubule dynamics 1
RMDN2 regulator of microtubule dynamics 2
RMDN3 regulator of microtubule dynamics 3
SETD2 SET domain containing 2
SYBU syntabulin (syntaxin-interacting)
TGFB2 transforming growth factor, beta 2
TSPAN12 tetraspanin 12