scimitar syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
CORIN corin, serine peptidase 1.55026
CECR1 cat eye syndrome chromosome region, candidate 1 1.4711
ANKRD1 ankyrin repeat domain 1 (cardiac muscle) 1.29877
VIPR1 vasoactive intestinal peptide receptor 1 1.02692
KLK11 kallikrein-related peptidase 11 1.02271
HEY2 hes-related family bHLH transcription factor with YRPW motif 2 0.998236
YARS tyrosyl-tRNA synthetase 0.977165
PDLIM1 PDZ and LIM domain 1 0.97044
GREM2 gremlin 2, DAN family BMP antagonist 0.921323
SNRPN small nuclear ribonucleoprotein polypeptide N 0.894589
TBX1 T-box 1 0.877376
OR10T2 olfactory receptor, family 10, subfamily T, member 2 0.739488
FBN1 fibrillin 1 0.60264
MBTPS1 membrane-bound transcription factor peptidase, site 1 0.583941
NOTCH1 notch 1 0.578494
NPPA natriuretic peptide A 0.569163
TPM1 tropomyosin 1 (alpha) 0.529608
PDGFRA platelet-derived growth factor receptor, alpha polypeptide 0.439034
GJA1 gap junction protein, alpha 1, 43kDa 0.434899
LDLR low density lipoprotein receptor 0.311014
TNNT2 troponin T type 2 (cardiac) 0.250311
DMD dystrophin 0.204263