coronin-1a 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 an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs. (Human Disease Ontology, DOID_0060019)
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Genes

6 genes co-occuring with the disease coronin-1a deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CORO1A coronin, actin binding protein, 1A 1.99364
CORO1B coronin, actin binding protein, 1B 1.46671
CORO1C coronin, actin binding protein, 1C 1.26473
NT5C 5', 3'-nucleotidase, cytosolic 1.23777
BRWD1 bromodomain and WD repeat domain containing 1 0.97002
CD4 CD4 molecule 0.174093