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
2761 to 2770 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

2761
Contactin associated protein family member 5
caspr5
Alzheimer disease, Anxiety disorder, Attention deficit hyperactivity disorder, Neurodevelopmental disorder, Essential tremor, Gastroesophageal reflux disease, Hoarding disorder, Insomnia, Lung cancer, Major depressive disorder, Movement disorder, Non-specific syndromic intellectual disability, Ovarian cancer, Periodic limb movement disorder, Post-traumatic stress disorder
View all (4 more)

2762
Centriolin
CEP1, CEP110, FAN, bA165P4.1
Breast cancer, Prostate cancer, Urticaria, Vitreous body disease

2763
Centrobin, centriole duplication and spindle assembly protein
LIP8, PP1221
Oligodendroglioma, Polycystic ovary syndrome, Polycythemia, Psoriasis

2764
Cytochrome c oxidase assembly factor 1
C7orf44, MITRAC15
Patellar tendinitis

2765
Cytochrome c oxidase assembly factor 3
CCDC56, COX25, HSPC009, MC4DN14, MITRAC12, hCOA3
Basal cell carcinoma, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

2766
Cytochrome c oxidase assembly factor 5
6330578E17Rik, C2orf64, CEMCOX3, MC4DN9, Pet191
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Central nervous system cancer, Cytochrome c oxidase deficiency, Glioma, Mitochondrial complex deficiency

2767
Cytochrome c oxidase assembly factor 6
C1orf31, CEMCOX4, MC4DN13
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency

2768
Cytochrome c oxidase assembly factor 7
C1orf163, RESA1, SCAN3, SELRC1
Basal cell carcinoma, Mitochondrial disease, Spinocerebellar ataxia

2769
Cytochrome c oxidase assembly factor 8
APOP, APOP1, APOPT1, C14orf153, MC4DN17
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Insomnia, Major depressive disorder, Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Obsessive-compulsive disorder, Schizophrenia

2770
Coenzyme A synthase
DPCK, NBIA6, NBP, PCH12, PPAT, UKR1, pOV-2
Coasy protein-associated neurodegeneration, Coenzyme a synthase protein associated neurodegeneration, Hallervorden spatz syndrome, Metabolic syndrome, Mucopolysaccharidosis, Neurodegeneration with brain iron accumulation, Pontocerebellar hypoplasia, Diabetes mellitus type 2