Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
1151 to 1160 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1151
CAP-Gly domain containing linker protein family member 4
RSNL2
Lung cancer

1152
CDC like kinase 1
CLK, CLK/STY, STY
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Non-melanoma skin carcinoma, Ovarian cancer, Ovarian serous carcinoma
View all (3 more)

1153
CDC like kinase 2
-
Alzheimer disease, Diabetes mellitus type 2

1154
CDC like kinase 3
PHCLK3, PHCLK3/152
Urinary bladder cancer

1155
Calmin
-
Alzheimer disease, Venous thromboembolism

1156
CXADR like cell adhesion molecule
ACAM, ASAM, CSBM, CSBS
Breast cancer, Central nervous system cancer, Colorectal cancer, Congenital short bowel syndrome, Glaucoma, Glioblastoma, Glioma, Hemorrhoid, Intestinal obstruction, Oligodendroglioma, Partial epilepsy, Post-operative acute kidney injury

1157
CLN3 lysosomal/endosomal transmembrane protein, battenin
BTN1, BTS, JNCL, SLC29B1
Asthma, Bipolar disorder, Bullous pemphigoid, Neuronal ceroid lipofuscinosis, Cone-rod dystrophy, Crohn disease, Progressive myoclonic epilepsy, Hypothyroidism, Inflammatory bowel disease, Intellectual developmental disorder, Retinitis pigmentosa, Stomach neoplasms, Diabetes mellitus type 1, Diabetes mellitus type 2, Visual disorder

1158
CLN5 lysosomal BMP synthase
-
Neuronal ceroid lipofuscinosis, Neurodevelopmental disorder, Pontocerebellar hypoplasia, Visual disorder

1159
CLN6 transmembrane ER protein
CLN4A, CLN6A, HsT18960, nclf
Atrophy, Neuronal ceroid lipofuscinosis, Congenital neurologic anomalies, Cystic fibrosis, Motor skills disorder, Neurodevelopmental disorder, Spastic ataxia, Visual disorder

1160
CLN8 transmembrane ER and ERGIC protein
C8orf61, EPMR, TLCD6
Autism, Neuronal ceroid lipofuscinosis, Gaucher disease, Intellectual developmental disorder, Major depressive disorder