Congenital Hypoplasia Of Radius Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0685381
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Genes

37 genes associated with the disease Congenital Hypoplasia Of Radius in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALG12 ALG12, alpha-1,6-mannosyltransferase
APC adenomatous polyposis coli
CHN1 chimerin 1
COL25A1 collagen, type XXV, alpha 1
DHODH dihydroorotate dehydrogenase (quinone)
DONSON downstream neighbor of SON
EIF4A3 eukaryotic translation initiation factor 4A3
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FAM58A family with sequence similarity 58, member A
FANCB Fanconi anemia, complementation group B
FANCI Fanconi anemia, complementation group I
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GDF5 growth differentiation factor 5
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
IFT81 intraflagellar transport 81
IHH indian hedgehog
LRP4 low density lipoprotein receptor-related protein 4
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
NIPBL Nipped-B homolog (Drosophila)
NPR2 natriuretic peptide receptor 2
PDE4D phosphodiesterase 4D, cAMP-specific
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
RAD51C RAD51 paralog C
RBM10 RNA binding motif protein 10
RECQL4 RecQ protein-like 4
RFWD3 ring finger and WD repeat domain 3
RPL26 ribosomal protein L26
RPS19 ribosomal protein S19
SALL4 spalt-like transcription factor 4
SELENON selenoprotein N
SF3B4 splicing factor 3b, subunit 4, 49kDa
SHOX short stature homeobox
TBX3 T-box 3
TRIP11 thyroid hormone receptor interactor 11
WNT7A wingless-type MMTV integration site family, member 7A