Symmetrical Dyschromatosis Of Extremities Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0406775
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Genes

20 genes associated with the disease Symmetrical Dyschromatosis Of Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
ACE angiotensin I converting enzyme
ADA adenosine deaminase
ADAR adenosine deaminase, RNA-specific
ANPEP alanyl (membrane) aminopeptidase
APCS amyloid P component, serum
ARSH arylsulfatase family, member H
BAG3 BCL2-associated athanogene 3
CHAF1A chromatin assembly factor 1, subunit A (p150)
COL18A1 collagen, type XVIII, alpha 1
CTR9 CTR9, Paf1/RNA polymerase II complex component
ELP1 elongator acetyltransferase complex subunit 1
GRB2 growth factor receptor-bound protein 2
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
PIK3R4 phosphoinositide-3-kinase, regulatory subunit 4
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila)
SH2D1A SH2 domain containing 1A
TOR1A torsin family 1, member A (torsin A)