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
3201 to 3210 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3201
Cytochrome b reductase 1
CYB561A2, DCYTB, FRRS3
Asthma, Breast cancer, Cancer, Colorectal cancer, Dementia, Estrogen-receptor negative breast cancer, Hereditary hemochromatosis, Lung cancer, Metabolic syndrome, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Diabetes mellitus type 2

3202
Cytochrome c1
MC3DN6, UQCR4
Mitochondrial complex deficiency, Mitochondrial disease

3203
Cytochrome c, somatic
CYC, HCS, THC4
Alzheimer disease, Thrombocytopenia with normal platelets, Brain ischemia, Chloracne, Fatty liver, Fatty liver, alcoholic, Methylmalonic acidemia, Obesity, Systemic lupus erythematosus, Thrombocytopenia, Transient ischemic attack

3204
Cytoplasmic FMR1 interacting protein 1
P140SRA-1, SHYC, SRA-1, SRA1
Eczema, Atrial septal defect, Autism, Post-traumatic stress disorder, Schizophrenia, Strabismus

3205
Cytoplasmic FMR1 interacting protein 2
DEE65, EIEE65, PIR121
Asthma, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Respiratory system disease

3206
Cytoglobin
HGB, NOD, STAP
Biliary cirrhosis, Cholelithiasis, Diabetic neuropathy, Hepatic insufficiency, Hepatomegaly, Liver cirrhosis, Biliary cholangitis, Retinitis pigmentosa, Diabetes mellitus type 2

3207
Cylicin 1
CYCL1, SPGFX8
Spermatogenic failure, x-linked

3208
Cylicin 2
-
Alzheimer disease, Autism, Obesity, Obsessive-compulsive disorder, Tourette syndrome

3209
CYLD lysine 63 deubiquitinase
BRSS, CDMT, CYLD1, CYLDI, EAC, FTDALS8, MFT, MFT1, SBS, TEM, USPL2
Amyotrophic lateral sclerosis, Asthma, Brooke-spiegler syndrome, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Crohn disease, Familial cylindromatosis, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Multiple familial trichoepithelioma, Ulcerative colitis, Uterine neoplasms

3210
Cytochrome P450 family 11 subfamily A member 1
CYP11A, CYPXIA1, P450SCC
Autism, Congenital adrenal hyperplasia, 46, xy disorder of sex development, Endometrial neoplasms, Seizures, Squamous cell carcinoma