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
2821 to 2830 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2821
COMM domain containing 4
-
Gout, Diabetes mellitus type 2

2822
COMM domain containing 7
C20orf92, dJ1085F17.3
Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Prostate cancer, Psoriasis, Sclerosing cholangitis, Toxic nodular goiter, Diabetes mellitus type 2, Ulcerative colitis

2823
COMM domain containing 8
-
Hemolytic anemia, Uterine fibroid

2824
Cartilage oligomeric matrix protein
CTS2, EDM1, EPD1, MED, PSACH, THBS5, TSP-5, TSP5
Attention deficit hyperactivity disorder, Carpal tunnel syndrome, Comp-related skeletal dysplasia, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Osteoarthritis, Osteochondrodysplasias

2825
Catechol-O-methyltransferase
HEL-S-98n
22q11.2 deletion syndrome, Amphetamine or sympathomimetic abuse, Anhedonia, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Bipolar disorder, Breast neoplasms, Bulimia, Cannabis abuse, Hepatocellular carcinoma, Dilated cardiomyopathy, Cardiomyopathy, Cognition disorder, Delirium, dementia, and cognitive disorders
View all (27 more)

2826
COP1 E3 ubiquitin ligase
CFAP78, FAP78, RFWD2, RNF200
Alzheimer disease, Autism, Bipolar disorder, Endometriosis, Irritable bowel syndrome, Major depressive disorder, Obesity, Schizophrenia

2827
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

2828
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

2829
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

2830
Coat protein complex I subunit gamma 1
COPG, IMD128
Atrial fibrillation, Immunodeficiency, Mesothelioma, Diabetes mellitus type 2