Lymphedema, Microcephaly And Chorioretinopathy Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1835265
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Genes

7 genes associated with the disease Lymphedema, Microcephaly And Chorioretinopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APTX aprataxin
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KIF11 kinesin family member 11
KIF1A kinesin family member 1A
SETX senataxin
SPTBN2 spectrin, beta, non-erythrocytic 2