Duane Retraction Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_12557)
External Link https://www.disgenet.org/browser/0/1/0/C0751083
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Genes

31 genes associated with the disease Duane Retraction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARX aristaless related homeobox
BHLHE22 basic helix-loop-helix family, member e22
CDH2 cadherin 2, type 1, N-cadherin (neuronal)
CHD7 chromodomain helicase DNA binding protein 7
CHN1 chimerin 1
COL25A1 collagen, type XXV, alpha 1
CPA6 carboxypeptidase A6
CREBBP CREB binding protein
CSPP1 centrosome and spindle pole associated protein 1
DNM1L dynamin 1-like
DVL1 dishevelled segment polarity protein 1
ECEL1 endothelin converting enzyme-like 1
EP300 E1A binding protein p300
EYA1 EYA transcriptional coactivator and phosphatase 1
FAM58A family with sequence similarity 58, member A
FOXL2 forkhead box L2
HOXA1 homeobox A1
HOXD3 homeobox D3
KIAA0586 KIAA0586
KIF21A kinesin family member 21A
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
OMA1 OMA1 zinc metallopeptidase
OPA1 optic atrophy 1 (autosomal dominant)
PIEZO2 piezo-type mechanosensitive ion channel component 2
PTPRN2 protein tyrosine phosphatase, receptor type, N polypeptide 2
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
TGFB1 transforming growth factor, beta 1
WFDC1 WAP four-disulfide core domain 1
WNT5A wingless-type MMTV integration site family, member 5A