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
Showing genes starting with "C"
1341 to 1350 of 1796 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

1341
Coat protein complex I subunit alpha
AIAISD, AILJK, HEP-COP, alpha-COP
Ankylosing spondylitis, Arthritis, Autoimmune disease, Autoimmune interstitial lung disease-arthritis syndrome, Autoinflammation and autoimmunity, systemic, with immune dysregulation 1, Lung disease

1342
Coat protein complex I subunit beta 1
BARMACS, COPB
Baralle-macken syndrome, Cataract, Intellectual developmental disorder dysmorphic microcephaly, Multiple sclerosis, Intellectual disability, Skeletal dysplasia, Diabetes mellitus type 2

1343
Coat protein complex I subunit beta 2
MCPH19, OPDD, beta'-COP
Primary microcephaly, Bone fragility with contractures, arterial rupture, and deafness, Microcephaly, Obesity, Osteoporosis, Osteoporosis-pseudoglioma syndrome

1344
Coat protein complex I subunit gamma 1
COPG, IMD128
Atrial fibrillation, Immunodeficiency, Mesothelioma, Diabetes mellitus type 2

1345
Coordinator of PRMT5 and differentiation stimulator
C17orf79, COPR5, HSA272196, TTP1
Prostate cancer

1346
COP9 signalosome subunit 2
ALIEN, CSN2, SGN2, TRIP15
Endometriosis, Lung cancer, Non-small cell lung carcinoma, Squamous cell carcinoma

1347
COP9 signalosome subunit 3
CSN3, SGN3
Hepatomegaly

1348
COP9 signalosome subunit 5
CSN5, JAB1, MOV-34, SGN5
Hepatocellular carcinoma, Colorectal cancer, Stevens-johnson syndrome

1349
COP9 signalosome subunit 7A
CSN7, CSN7A, SGN7a
Insomnia, Stomach neoplasms

1350
COP9 signalosome subunit 7B
CSN7B, SGN7b
Scoliosis