Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2561 to 2570 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2561
CDGSH iron sulfur domain 1
C10orf70, MDS029, ZCD1, mitoNEET
Alzheimer disease

2562
CDGSH iron sulfur domain 2
ERIS, Miner1, NAF-1, WFS2, ZCD2
Atrial fibrillation, Autism, Diabetes mellitus type 2, Schizophrenia, Wolfram syndrome

2563
CDGSH iron sulfur domain 3
MiNT, Miner2
Turnpenny-fry syndrome, Wolfram syndrome

2564
Cytokine inducible SH2 containing protein
BACTS2, CIS, CIS-1, G18, SOCS
Allergic contact dermatitis, Tuberculoma

2565
Citron rho-interacting serine/threonine kinase
CITK, CRIK, MCPH17, STK21
Atrial fibrillation, Primary microcephaly, Congenital microcephaly, Crohn disease, Inflammatory bowel disease, Long qt syndrome, Microcephaly, Migraine, Respiratory system infectious disease, Scoliosis, Diabetes mellitus type 2, Ulcerative colitis

2566
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 1
MSG1
Autism, Willis-ekbom disease

2567
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2
ASD8, MRG-1, MRG1, P35SRJ, VSD2
Atrial septal defect, Congenital heart disease, Congenital septal defect of heart, Congenital heart septal defect, Obesity, Tetralogy of fallot, Ventricular septal defect

2568
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4
-
Androgenetic alopecia, Breast cancer

2569
CDKN1A interacting zinc finger protein 1
LSFR1, NP94, ZNF356
Cerebellar ataxia, Cervical dystonia, Developmental and epileptic encephalopathy, Dystonia, Global developmental delay, Prostatic neoplasms, Sarcoma, Torsion dystonia, Diabetes mellitus type 2

2570
Cytoskeleton associated protein 2 like
-
Hepatocellular carcinoma, Desbuquois syndrome, Endometriosis, Hypogonadism, Intellectual developmental disorder