acquired immunodeficiency syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A Human immunodeficiency virus infectious disease that results_in reduction in the numbers of CD4-bearing helper T cells below 200 per ┬ÁL of blood or 14% of all lymphocytes thereby rendering the subject highly vulnerable to life-threatening infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted_by sexual contact, transmitted_by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted_by congenital method, and transmitted_by contaminated needles. Opportunistic infections are common in people with AIDS. (Human Disease Ontology, DOID_635)
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Genes

19 genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CCR2 chemokine (C-C motif) receptor 2
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CX3CR1 chemokine (C-X3-C motif) receptor 1
CXCL12 chemokine (C-X-C motif) ligand 12
CXCR6 chemokine (C-X-C motif) receptor 6
DGKI diacylglycerol kinase, iota
DOC2B double C2-like domains, beta
HCP5 HLA complex P5 (non-protein coding)
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1R1 interleukin 1 receptor, type I
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
NBPF15 neuroblastoma breakpoint family, member 15
PARD3B par-3 family cell polarity regulator beta
RXRG retinoid X receptor, gamma
SOX5 SRY (sex determining region Y)-box 5
TGFBRAP1 transforming growth factor, beta receptor associated protein 1
ZNRD1 zinc ribbon domain containing 1