radioulnar synostosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9827)
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Genes

27 genes co-occuring with the disease radioulnar synostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ATRNL1 attractin-like 1 1.84272
HOXA11 homeobox A11 1.76728
SF3B4 splicing factor 3b, subunit 4, 49kDa 1.57512
FGFRL1 fibroblast growth factor receptor-like 1 1.35638
ATRN attractin 1.29964
EFTUD2 elongation factor Tu GTP binding domain containing 2 1.28479
TBX4 T-box 4 1.26168
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6 1.05976
LRP4 low density lipoprotein receptor-related protein 4 1.02819
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor) 0.998658
GREM1 gremlin 1, DAN family BMP antagonist 0.992752
BCOR BCL6 corepressor 0.963309
FGFR2 fibroblast growth factor receptor 2 0.932484
TBX5 T-box 5 0.871234
FGFR1 fibroblast growth factor receptor 1 0.812642
LMX1B LIM homeobox transcription factor 1, beta 0.81018
SHFM1 split hand/foot malformation (ectrodactyly) type 1 0.804026
RECQL4 RecQ protein-like 4 0.789672
IGFBP5 insulin-like growth factor binding protein 5 0.728547
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2 0.696306
POR P450 (cytochrome) oxidoreductase 0.687891
FGF19 fibroblast growth factor 19 0.642221
NOG noggin 0.595233
RUNX2 runt-related transcription factor 2 0.416521
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) 0.385193
FGFR3 fibroblast growth factor receptor 3 0.372587
LDLR low density lipoprotein receptor 0.226952