vacterl association Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. (Human Disease Ontology, DOID_14679)
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Genes

57 genes co-occuring with the disease vacterl association in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TEF thyrotrophic embryonic factor 1.83863
SHH sonic hedgehog 1.72183
MTHFSD methenyltetrahydrofolate synthetase domain containing 1.71408
TADA2A transcriptional adaptor 2A 1.62067
SPATA17 spermatogenesis associated 17 1.52996
HOXA3 homeobox A3 1.52864
HOXC4 homeobox C4 1.46979
HOXD3 homeobox D3 1.42849
HOXB3 homeobox B3 1.36814
PARP10 poly (ADP-ribose) polymerase family, member 10 1.3603
IFT172 intraflagellar transport 172 1.32891
HOXD13 homeobox D13 1.2909
PTF1A pancreas specific transcription factor, 1a 1.22735
FOXF1 forkhead box F1 1.22388
SALL1 spalt-like transcription factor 1 1.14093
HOXA5 homeobox A5 1.12614
TRAP1 TNF receptor-associated protein 1 1.11898
GPR35 G protein-coupled receptor 35 1.09167
LPP LIM domain containing preferred translocation partner in lipoma 1.05681
GLI2 GLI family zinc finger 2 1.05093
FOXL1 forkhead box L1 1.01427
PCSK5 proprotein convertase subtilisin/kexin type 5 1.00246
ZIC3 Zic family member 3 1.00203
HOXB5 homeobox B5 0.97086
EFNB2 ephrin-B2 0.947435
GLI1 GLI family zinc finger 1 0.877376
GLI3 GLI family zinc finger 3 0.860999
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase 0.853221
AATF apoptosis antagonizing transcription factor 0.847488
ZC3H12D zinc finger CCCH-type containing 12D 0.792131
LIG3 ligase III, DNA, ATP-dependent 0.749644
PLEC plectin 0.716021
EPHB3 EPH receptor B3 0.687891
UPK3A uroplakin 3A 0.663181
FOXC2 forkhead box C2 0.636708
SHOX short stature homeobox 0.613183
FGF10 fibroblast growth factor 10 0.603811
EPHB2 EPH receptor B2 0.582773
CHD7 chromodomain helicase DNA binding protein 7 0.572662
FGF8 fibroblast growth factor 8 (androgen-induced) 0.52343
CAPN10 calpain 10 0.503824
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) 0.490072
IHH indian hedgehog 0.460129
FGF19 fibroblast growth factor 19 0.41727
KLF10 Kruppel-like factor 10 0.368149
FANCA Fanconi anemia, complementation group A 0.365562
HNF1B HNF1 homeobox B 0.358551
MECOM MDS1 and EVI1 complex locus 0.33944
FANCD2 Fanconi anemia, complementation group D2 0.306672
PAX6 paired box 6 0.263722
GLS2 glutaminase 2 (liver, mitochondrial) 0.24715
HMGA2 high mobility group AT-hook 2 0.238752
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B 0.237357
PTEN phosphatase and tensin homolog 0.221108
GSK3B glycogen synthase kinase 3 beta 0.220081
PRRC2A proline-rich coiled-coil 2A 0.201308
SRY sex determining region Y 0.173571