brachial plexus lesion Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A brachial plexus neuropathy characterized by an abnormality, usually caused by disease or trauma, located in the brachial plexus. (Human Disease Ontology, DOID_8443)
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Genes

17 genes co-occuring with the disease brachial plexus lesion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
KCNK6 potassium channel, two pore domain subfamily K, member 6 1.30357
SEMA3F sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F 1.22735
IGLL5 immunoglobulin lambda-like polypeptide 5 1.05976
SRPX2 sushi-repeat containing protein, X-linked 2 1.03662
CRLF1 cytokine receptor-like factor 1 0.97296
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A 0.906086
GDNF glial cell derived neurotrophic factor 0.871643
CST7 cystatin F (leukocystatin) 0.861818
AMD1 adenosylmethionine decarboxylase 1 0.823718
NRP1 neuropilin 1 0.794181
WDFY2 WD repeat and FYVE domain containing 2 0.748424
GAL galanin/GMAP prepropeptide 0.663578
CAMP cathelicidin antimicrobial peptide 0.591337
CALCA calcitonin-related polypeptide alpha 0.472604
NF1 neurofibromin 1 0.437154
BDNF brain-derived neurotrophic factor 0.321909
TAC1 tachykinin, precursor 1 0.279011