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"
1231 to 1240 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1231
Connector enhancer of kinase suppressor of Ras 2
CNK2, KSR2, MAGUIN, MRXSHG
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Diabetes mellitus type 2, Insomnia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, X-linked intellectual disability, Post-traumatic stress disorder, Psychiatric disorders, Schizophrenia, X-linked complex neurodevelopmental disorder

1232
CNKSR family member 3
CNK3, CNK3/IPCEF1, MAGI1
Color vision deficiency, Osteonecrosis of the femoral head, Parkinson disease

1233
Calponin 2
-
Alzheimer disease, Asthma, Atrophic macular degeneration, Renal cell carcinoma, Congenital pulmonary artery atresia, Age-related macular degeneration

1234
Calponin 3
-
Carcinoma, Prostatic neoplasms

1235
Cyclin and CBS domain divalent metal cation transport mediator 1
ACDP1, CLP-1, SLC70A1
Melanoma, Peripheral arterial disease, Scoliosis, Tooth disease

1236
Cyclin and CBS domain divalent metal cation transport mediator 2
ACDP2, HOMG6, HOMGSMR, SLC70A2
Anorexia nervosa, Cardiac arrhythmias, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brain aneurysm, Cardiac arrhythmia, Coronary artery disease, Disorder of magnesium metabolism, Hypertension, Gout, Insomnia, Kidney disease, Large artery stroke
View all (13 more)

1237
Cyclin and CBS domain divalent metal cation transport mediator 3
ACDP3, SLC70A3
Bipolar disorder, Crohn disease, Erectile dysfunction, Prostate cancer, Schizophrenia

1238
Cyclin and CBS domain divalent metal cation transport mediator 4
ACDP4, SLC70A4
Amaurosis hypertrichosis, Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Obsessive-compulsive disorder, Retinitis pigmentosa, Schizophrenia, Tourette syndrome

1239
CCR4-NOT transcription complex subunit 1
AD-005, CDC39, HPE12, NOT1, NOT1H, VIBOS
Autism, Neurodevelopmental disorder, Holoprosencephaly, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Obesity, Schizophrenia, Vissers-bodmer syndrome

1240
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 disorder, Osteoarthritis, Ovarian cancer