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
1691 to 1700 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1691
Calcium voltage-gated channel auxiliary subunit gamma 2
MRD10
Nonsyndromic intellectual disability, Neurodevelopmental disorder, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia

1692
Calcium voltage-gated channel auxiliary subunit gamma 3
-
Asthma, Macular degeneration, Metabolic syndrome, Oligodendroglioma, Orofacial cleft, Prostate cancer, Diabetes mellitus type 2

1693
Calcium voltage-gated channel auxiliary subunit gamma 4
-
Astrocytoma, Bipolar disorder, Major depressive disorder, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Schizophrenia, Scoliosis

1694
Calcium voltage-gated channel auxiliary subunit gamma 5
-
Bipolar disorder, Insomnia, Schizophrenia

1695
Calcium voltage-gated channel auxiliary subunit gamma 7
-
Alzheimer disease, Intellectual developmental disorder

1696
Calcium voltage-gated channel auxiliary subunit gamma 8
-
Alzheimer disease, Schizophrenia

1697
Cactin, spliceosome C complex subunit
C19orf29, NY-REN-24, fSAPc
Obesity

1698
CDK2 associated cullin domain 1
C10orf46, CAC1
Atrial fibrillation, Colorectal neoplasms, Obesity

1699
Calcyclin binding protein
GIG5, PNAS-107, S100A6BP, SIP
Metabolic syndrome, Psychiatric disorders, Diabetes mellitus type 2

1700
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
CDG1Z, DEE50, EIEE50, GATD4
Hypoplastic anemia, Sickle cell anemia, Beta thalassemia, Carbamoyl phosphate synthetase deficiency, Congenital facial anomaly, Congenital hypoplastic anemia, Aplastic anemia, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Intellectual developmental disorder, Meniere disease, Spherocytosis