Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2661 to 2670 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2661
Clock circadian regulator
KAT13D, bHLHe8
Alzheimer disease, Androgenetic alopecia, Bipolar disorder, Coronary artery disease, Major depressive disorder, Mood disorder, Schizophrenia, Seasonal affective disorder, Depression

2662
Cleavage factor polyribonucleotide kinase subunit 1
HEAB, hClp1
Congenital pontocerebellar hypoplasia, Liver cirrhosis, Major depressive disorder, Pontocerebellar hypoplasia

2663
ClpB family mitochondrial disaggregase
ANKCLB, ANKCLP, HSP78, MEGCANN, MGCA7, MGCA7A, SCN9, SKD3
3-methylglutaconic aciduria, Severe congenital neutropenia, Leigh syndrome, Microcytic anemia, Neutropenia, Obesity, Scoliosis, Congenital neutropenia

2664
Caseinolytic mitochondrial matrix peptidase proteolytic subunit
DFNB81, PRLTS3
Alzheimer disease, Gonadal dysgenesis, Peripheral arterial disease, Perrault syndrome, Xq27.3 q28 duplication syndrome

2665
Colipase
-
Diabetes mellitus type 2

2666
CLPTM1 regulator of GABA type A receptor forward trafficking
-
Alzheimer disease, Iga nephropathy, Metabolic syndrome, Pancreatic neoplasms, Diabetes mellitus type 2

2667
CLPTM1 like
CRR9
Basal cell carcinoma, Benign prostatic hyperplasia, Non-small-cell lung carcinoma, Cervical cancer, Cervical intraepithelial neoplasia, Lymphocytic leukemia, Colorectal cancer, Melanoma, Head and neck cancer, Keratinocyte carcinoma, Lung cancer, Lung neoplasms, Mouth neoplasms, Nasopharyngeal neoplasms, Non-melanoma skin carcinoma
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2668
Caseinolytic mitochondrial matrix peptidase chaperone subunit X
EPP2
Alzheimer disease, Dementia, Erythropoietic protoporphyria

2669
Clarin 1
RP61, USH3, USH3A
Branchiootorenal syndrome, Hearing impairment, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome

2670
Clarin 2
DFNB117
Isolated sensorineural deafness, Deafness, Hearing loss, Nonsyndromic hearing loss