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
2091 to 2100 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2091
CD46 molecule
AHUS2, MCP, MIC10, TLX, TRA2.10
Hemolytic anemia, Hemolytic uremic syndrome, Breast cancer, Contact dermatitis, Macular and posterior pole degeneration, Atypical hemolytic uremic syndrome, Kidney disease, Macular degeneration, Mesangiocapillary glomerulonephritis, Multiple sclerosis, Obesity, Prostatic neoplasms, Retinal degeneration, Retinopathy

2092
CD47 molecule
IAP, MER6, OA3
Bipolar disorder, Bipolar depression, Oligodendroglioma, Schizophrenia, Tourette syndrome

2093
CD48 molecule
BCM1, BLAST, BLAST1, MEM-102, SLAMF2, hCD48, mCD48
Hypothyroidism, Lung cancer, Multiple sclerosis, Squamous cell carcinoma

2094
CD5 molecule
LEU1, T1
Rheumatoid arthritis, Hypothyroidism, Lymphocytic b-cell leukemia

2095
CD53 molecule
MOX44, TSPAN25
Gastro-entero-pancreatic neuroendocrine tumor, Kidney disease, Obesity

2096
CD55 molecule (Cromer blood group)
CHAPLE, CR, CROM, DAF, TC
Alzheimer disease, Amphetamine or sympathomimetic abuse, Autism, Endometriosis

2097
CD58 molecule
LFA-3, LFA3, ag3
B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Multiple sclerosis, Biliary cholangitis, Systemic lupus erythematosus

2098
CD59 molecule (CD59 blood group)
16.3A5, 1F5, EJ16, EJ30, EL32, G344, HRF-20, HRF20, MAC-IP, MACIF, MEM43, MIC11, MIN1, MIN2, MIN3, MIRL, MSK21, p18-20
Hemolytic anemia, Kidney disease, Oligodendroglioma

2099
CD5 molecule like
AIM, API6, CT-2, PRO229, SP-ALPHA, Spalpha, hAIM
Hepatocellular carcinoma, Color vision deficiency, Multiple myeloma

2100
CD6 molecule
TP120
Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Multiple sclerosis, Prostate cancer, Psoriasis, Sclerosing cholangitis, Scoliosis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis