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
Showing genes starting with "C"
1171 to 1180 of 1806 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1171
Cleavage factor polyribonucleotide kinase subunit 1
HEAB, hClp1
Congenital pontocerebellar hypoplasia, Liver cirrhosis, Major depressive disorder, Pontocerebellar hypoplasia

1172
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

1173
Caseinolytic mitochondrial matrix peptidase proteolytic subunit
DFNB81, PRLTS3
Alzheimer disease, Gonadal dysgenesis, Peripheral arterial disease, Perrault syndrome, Xq27.3 q28 duplication syndrome

1174
Colipase
-
Diabetes mellitus type 2

1175
CLPTM1 regulator of GABA type A receptor forward trafficking
-
Alzheimer disease, Iga nephropathy, Metabolic syndrome, Pancreatic neoplasms, Diabetes mellitus type 2

1176
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
View all (16 more)

1177
Caseinolytic mitochondrial matrix peptidase chaperone subunit X
EPP2
Alzheimer disease, Dementia, Erythropoietic protoporphyria

1178
Clarin 1
RP61, USH3, USH3A
Branchiootorenal syndrome, Hearing impairment, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome

1179
Clarin 2
DFNB117
Isolated sensorineural deafness, Deafness, Hearing loss, Nonsyndromic hearing loss

1180
Clarin 3
TMEM12, USH3AL1
Parkinson disease