artemis deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A severe combined immunodeficiency that is caused when the DCLREI1, DNA cross-link repair 1C gene contains mutations resulting in the inability to repair DNA. (Human Disease Ontology, DOID_0060006)
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9 genes co-occuring with the disease artemis deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
DCLRE1C DNA cross-link repair 1C 1.93421
SEPT4 septin 4 1.53568
PRKDC protein kinase, DNA-activated, catalytic polypeptide 1.50272
RAG1 recombination activating gene 1 1.43727
LIG4 ligase IV, DNA, ATP-dependent 0.938704
EFNA5 ephrin-A5 0.450324
IL2RA interleukin 2 receptor, alpha 0.350084
FOXP3 forkhead box P3 0.28294
PI3 peptidase inhibitor 3, skin-derived 0.212271