Wolf-Hirschhorn 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_0050460)
External Link https://www.disgenet.org/browser/0/1/0/C1956097
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Genes

29 genes associated with the disease Wolf-Hirschhorn Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALB albumin
C4ORF48 chromosome 4 open reading frame 48
CDK2AP2 cyclin-dependent kinase 2 associated protein 2
CDKN2A cyclin-dependent kinase inhibitor 2A
CPLX1 complexin 1
CTBP1 C-terminal binding protein 1
DRD5 dopamine receptor D5
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FGFR3 fibroblast growth factor receptor 3
FGFRL1 fibroblast growth factor receptor-like 1
GH1 growth hormone 1
IL33R interleukin 33 receptor
LAMTOR2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
LAP3 leucine aminopeptidase 3
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
MSX1 msh homeobox 1
NELFA negative elongation factor complex member A
NSD2 nuclear receptor binding SET domain protein 2
OXA1L oxidase (cytochrome c) assembly 1-like
RBPJ recombination signal binding protein for immunoglobulin kappa J region
RPP14 ribonuclease P/MRP 14kDa subunit
S100A9 S100 calcium binding protein A9
SET SET nuclear proto-oncogene
SF3B6 splicing factor 3b, subunit 6, 14kDa
SLBP stem-loop binding protein
SUB1 SUB1 homolog (S. cerevisiae)
TACC3 transforming, acidic coiled-coil containing protein 3
WFS1 Wolfram syndrome 1 (wolframin)
ZNF141 zinc finger protein 141