Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
1981 to 1990 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1981
C-C motif chemokine ligand 27
ALP, CTACK, CTAK, ESKINE, ILC, PESKY, SCYA27
Contact dermatitis, Mesothelioma

1982
C-C motif chemokine ligand 28
CCK1, MEC, SCYA28
Alzheimer disease, Breast cancer

1983
C-C motif chemokine ligand 3
G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI, SCYA3
Atherosclerosis, Brain ischemia, Hepatocellular carcinoma, Colonic neoplasms, Color vision deficiency, Glomerulonephritis, Hypersensitivity, Mesothelioma, Myocardial ischemia, Pulmonary fibrosis, Status epilepticus

1984
C-C motif chemokine ligand 3 like 3
464.2, D17S1718, G0S19-2, LD78, LD78BETA, SCYA3L, SCYA3L1
Skin disease

1985
C-C motif chemokine ligand 4
ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4
Atherosclerosis, Brain ischemia, Color vision deficiency, Dermatologic disorder, Glomerulonephritis, Hypersensitivity, Myocardial ischemia, Pulmonary fibrosis, Skin disease

1986
C-C motif chemokine ligand 5
D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP
Asthma, Autoimmune hepatitis, Biliary cirrhosis, Atopic dermatitis, Diabetes mellitus type 1, Glomerulonephritis, Alcoholic hepatitis, Hyperoxaluria, Liver cirrhosis, Mesothelioma, Pancreatitis, Biliary cholangitis, Pulmonary fibrosis

1987
C-C motif chemokine ligand 7
FIC, MARC, MCP-3, MCP3, NC28, SCYA6, SCYA7
Cholelithiasis, Crohn disease, Glomerulonephritis, Hypersensitivity, Inflammatory bowel disease, Mesothelioma, Multiple sclerosis, Ulcerative colitis

1988
C-C motif chemokine ligand 8
HC14, MCP-2, MCP2, SCYA10, SCYA8
Rheumatoid arthritis, Hypersensitivity, Inflammatory bowel disease, Ulcerative colitis

1989
CCM2 scaffold protein
C7orf22, OSM, PP10187
Cavernous malformations of cns, Cerebral cavernous malformation, Colorectal cancer, Congenital cerebral aneurysm, Congenital malformation of cerebral vessels, Coronary artery disease, Vascular dementia, Developmental venous anomaly, Cerebral cavernous malformations, Myocardial infarction, Diabetes mellitus type 2, Vasculitis

1990
CCM2 like scaffold protein
C20orf160, dJ310O13.5
Alzheimer disease, Migraine