Sjogren-Larsson Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_14501)
External Link https://www.disgenet.org/browser/0/1/0/C0037231
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Genes

20 genes associated with the disease Sjogren-Larsson Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide
ALDH3A1 aldehyde dehydrogenase 3 family, member A1
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
CD59 CD59 molecule, complement regulatory protein
DNAJC13 DnaJ (Hsp40) homolog, subfamily C, member 13
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
FANCA Fanconi anemia, complementation group A
HSD17B6 hydroxysteroid (17-beta) dehydrogenase 6
IQCB1 IQ motif containing B1
KRT18 keratin 18, type I
MLH1 mutL homolog 1
MRC1 mannose receptor, C type 1
MSH2 mutS homolog 2
NPHP3 nephronophthisis 3 (adolescent)
NXPH3 neurexophilin 3
POLD1 polymerase (DNA directed), delta 1, catalytic subunit
POLE polymerase (DNA directed), epsilon, catalytic subunit
SCLT1 sodium channel and clathrin linker 1
TXNRD1 thioredoxin reductase 1
WDR19 WD repeat domain 19