squamous cell neoplasm Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A cell type benign neoplasm composed_of epithelial cells located_in the ectodermal or endodermal cells linking body cavities. (Human Disease Ontology, DOID_3168)
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Genes

15 genes co-occuring with the disease squamous cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CLEC2A C-type lectin domain family 2, member A 1.68906
KRT10 keratin 10, type I 0.909787
HPD 4-hydroxyphenylpyruvate dioxygenase 0.881472
KRT1 keratin 1, type II 0.860999
MSH2 mutS homolog 2 0.626888
PTGER4 prostaglandin E receptor 4 (subtype EP4) 0.595623
MLH1 mutL homolog 1 0.585108
KRT14 keratin 14, type I 0.582384
MIB1 mindbomb E3 ubiquitin protein ligase 1 0.567609
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae) 0.543542
PCNA proliferating cell nuclear antigen 0.497321
CABIN1 calcineurin binding protein 1 0.494648
KRT5 keratin 5, type II 0.45447
MSH6 mutS homolog 6 0.42364
KRT7 keratin 7, type II 0.335046