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"
1261 to 1270 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1261
Contactin 1
CMYO12, CMYP12, F3, GP135, MYPCN
Alzheimer disease, Astrocytoma, Bipolar disorder, Central nervous system cancer, Compton-north congenital myopathy, Congenital lethal myopathy , Congenital myopathy, Dementia, Dry eye syndrome, Glioma, Major depressive disorder, Parkinson disease, Schizophrenia, Spondylosis

1262
Contactin 2
AXT, EPEO5, FAME5, TAG-1, TAX, TAX1
Benign myoclonic epilepsy, Neurodevelopmental disorder, Diabetes mellitus, Early onset epilepsy with developmental delay, Familial adult myoclonic epilepsy, Adult myoclonic epilepsy, Gout, Non-specific syndromic intellectual disability, Periodontitis, Schizophrenia, Diabetes mellitus type 2

1263
Contactin 3
BIG-1, PANG, PCS
Attention deficit hyperactivity disorder, Autism, Cannabis abuse, Colorectal cancer, Allergic contact dermatitis, Gestational diabetes, Peripheral arterial disease, Substance abuse

1264
Contactin 4
AXCAM, BIG-2
Amyotrophic lateral sclerosis, Anorexia nervosa, Attention deficit hyperactivity disorder, Atypical femoral fracture, Autism, B-cell acute lymphoblastic leukemia, Bipolar disorder, Neurodevelopmental disorder, Craniofacial abnormalities, Developmental disability, Gallbladder neoplasms, Growth disorder, Major depressive disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder
View all (7 more)

1265
Contactin 5
HNB-2s, NB-2
Anxiety disorder, Astrocytoma, Atrial fibrillation, Basal cell carcinoma, Behcet disease, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Circadian rhythm sleep disorder, Liver cirrhosis, Color vision deficiency, Colorectal cancer, Crohn disease, Dementia, Diabetic ketoacidosis
View all (19 more)

1266
Contactin 6
NB3
Autism, Bipolar disorder, Adenoid cystic carcinoma, Color vision deficiency, Neurodevelopmental disorder, Cutaneous mastocytosis, Tourette syndrome, Non-specific syndromic intellectual disability, Ocular hypotension, Oligodendroglioma, Prostate cancer, Schizophrenia, Systemic lupus erythematosus

1267
Contactin associated protein 1
CASPR, CHN3, CNTNAP, NRXN4, P190
Arthrogryposis multiplex congenita, Distal arthrogryposis, Breast cancer, Charcot-marie-tooth disease, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Lethal congenital contracture syndrome, Major depressive disorder, Neuropathy, congenital hypomyelinating, Pena-shokeir syndrome

1268
Contactin associated protein 2
AUTS15, CASPR2, CDFE, NRXN4, PTHSL1
Alzheimer disease, Asthma, Autism, Bipolar disorder, Breast cancer, Cataract, Charcot-marie-tooth disease, Developmental and epileptic encephalopathy, Colorectal cancer, Colonic neoplasms, Neurodevelopmental disorder, Cortical dysplasia-focal epilepsy syndrome, Crohn disease, Dementia, Diabetic neuropathy
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1269
Contactin associated protein family member 4
CASPR4
Alzheimer disease, Hepatocellular carcinoma, Color vision deficiency, Melanoma, Prostate cancer

1270
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)