Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
761 to 770 of 1338 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
Mitochondrially encoded cytochrome b
MTCYB
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss

762
CEA cell adhesion molecule 6
CD66c, CEAL, NCA, NCA-50/90
Astrocytoma, Cystic fibrosis, Parkinson disease

763
CCR4-NOT transcription complex subunit 2
CDC36, HSPC131, IDNADFS, NOT2, NOT2H
12q15q21 microdeletion syndrome, Amyotrophic lateral sclerosis, Intellectual developmental disorder dysmorphic skeletal, Intellectual developmental disorder dysmorphic speech skeletal, Neurodevelopmental disorders, Osteoarthritis, Ovarian cancer

764
CCR4-NOT transcription complex subunit 3
IDDSADF, LENG2, NOT3, NOT3H
Neurodevelopmental disorder, Intellectual developmental disorder speech autism dysmorphic, Non-specific syndromic intellectual disability, Prostatic neoplasm

765
CCR4-NOT transcription complex subunit 4
CLONE243, NOT4, NOT4H
Cannabis abuse, Major depressive disorder, Peripheral arterial disease, Schizophrenia

766
Cytochrome c oxidase assembly factor 5
6330578E17Rik, C2orf64, CEMCOX3, MC4DN9, Pet191
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Central nervous system cancer, Glioma, Mitochondrial complex deficiency

767
CDGSH iron sulfur domain 2
ERIS, Miner1, NAF-1, WFS2, ZCD2
Atrial fibrillation, Autism, Diabetes mellitus type 2, Schizophrenia, Wolfram syndrome

768
Cornulin
C1orf10, DRC1, PDRC1, SEP53

769
Claudin 11
HLD22, OSP, OTM
Bipolar disorder, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Multiple sclerosis, Prostate cancer, Willis-ekbom disease, Schizophrenia

770
CD207 molecule
CLEC4K
Eczema, Birbeck granule deficiency, Narcolepsy, Schizophrenia, Seasonal allergic rhinitis