Abnormal Nasolacrimal System Morphology Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4025835
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Genes

23 genes associated with the disease Abnormal Nasolacrimal System Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BCL10 B-cell CLL/lymphoma 10
BIRC3 baculoviral IAP repeat containing 3
COX7B cytochrome c oxidase subunit VIIb
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FOXP1 forkhead box P1
GJB6 gap junction protein, beta 6, 30kDa
HCCS holocytochrome c synthase
IGH immunoglobulin heavy locus
KAT6B K(lysine) acetyltransferase 6B
KIF11 kinesin family member 11
KRAS Kirsten rat sarcoma viral oncogene homolog
MALT1 MALT1 paracaspase
MBTPS2 membrane-bound transcription factor peptidase, site 2
NDUFB11 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa
PEX1 peroxisomal biogenesis factor 1
PEX6 peroxisomal biogenesis factor 6
PHGDH phosphoglycerate dehydrogenase
PSAT1 phosphoserine aminotransferase 1
PTDSS1 phosphatidylserine synthase 1
SIX1 SIX homeobox 1
TWIST1 twist family bHLH transcription factor 1