aplasia/hypoplasia of the ulna Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the ulna. (Human Phenotype Ontology, HP_0006495)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006495
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Genes

28 genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B2M beta-2-microglobulin
BMPR1B bone morphogenetic protein receptor, type IB
CHD7 chromodomain helicase DNA binding protein 7
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
DHODH dihydroorotate dehydrogenase (quinone)
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
GDF5 growth differentiation factor 5
IHH indian hedgehog
JAG1 jagged 1
LMBR1 limb development membrane protein 1
LRP4 low density lipoprotein receptor-related protein 4
PIGT phosphatidylinositol glycan anchor biosynthesis, class T
RBM8A RNA binding motif protein 8A
RECQL4 RecQ protein-like 4
RPL26 ribosomal protein L26
SALL4 spalt-like transcription factor 4
SCARF2 scavenger receptor class F, member 2
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SHOX short stature homeobox
TBX3 T-box 3
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB16 zinc finger and BTB domain containing 16