klippel-feil syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A physical disorder that has_material_basis_in abnormal segmentation of the vertebra during fetal development which results_in fusion located_in cervical vertebra. (Human Disease Ontology, DOID_10426)
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Genes

24 genes co-occuring with the disease klippel-feil syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GDF6 growth differentiation factor 6 2.34426
MEOX1 mesenchyme homeobox 1 2.10807
PAX1 paired box 1 1.89221
RPS26P6 ribosomal protein S26 pseudogene 6 1.67006
GDF3 growth differentiation factor 3 1.6171
ADCK2 aarF domain containing kinase 2 1.60145
TBX6 T-box 6 1.46144
GDF1 growth differentiation factor 1 1.40439
RPS26 ribosomal protein S26 1.18453
CHN1 chimerin 1 1.1194
RNF34 ring finger protein 34, E3 ubiquitin protein ligase 1.01638
HOXA1 homeobox A1 0.799923
GALNS galactosamine (N-acetyl)-6-sulfatase 0.730976
SALL4 spalt-like transcription factor 4 0.698715
UBE2S ubiquitin-conjugating enzyme E2S 0.668345
UBE2K ubiquitin-conjugating enzyme E2K 0.624535
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 0.516494
HLA-DRB4 major histocompatibility complex, class II, DR beta 4 0.515725
HLA-DRB5 major histocompatibility complex, class II, DR beta 5 0.495411
BMP2 bone morphogenetic protein 2 0.340906
CBS cystathionine-beta-synthase 0.312102
FLAD1 flavin adenine dinucleotide synthetase 1 0.292975
COMT catechol-O-methyltransferase 0.24996
PPARA peroxisome proliferator-activated receptor alpha 0.198709