charcot-marie-tooth disease type 1 Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050538)
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Genes

18 genes co-occuring with the disease charcot-marie-tooth disease type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MPZ myelin protein zero 2.69738
PMP22 peripheral myelin protein 22 2.38867
EGR2 early growth response 2 1.95159
GJB1 gap junction protein, beta 1, 32kDa 1.61665
LITAF lipopolysaccharide-induced TNF factor 1.35681
NAB1 NGFI-A binding protein 1 (EGR1 binding protein 1) 1.27911
SULT2B1 sulfotransferase family, cytosolic, 2B, member 1 0.926692
MAG myelin associated glycoprotein 0.856905
NAB2 NGFI-A binding protein 2 (EGR1 binding protein 2) 0.775341
ACKR1 atypical chemokine receptor 1 (Duffy blood group) 0.705949
KLF10 Kruppel-like factor 10 0.700321
MECOM MDS1 and EVI1 complex locus 0.669538
MTMR2 myotubularin related protein 2 0.66755
NEFL neurofilament, light polypeptide 0.606933
HTN3 histatin 3 0.562169
MFN2 mitofusin 2 0.386679
SOX10 SRY (sex determining region Y)-box 10 0.378885
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1 0.247501