Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1641 to 1650 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1641
Complement C9
ARMD15, C9D
Atrophic macular degeneration, C1 esterase inhibitor deficiency, C9 deficiency, Hepatocellular carcinoma, Cardiac embolism, Cardioembolic stroke, Central nervous system cancer, Complement component deficiency, Macular and posterior pole degeneration, Dermatomyositis, Glioblastoma, Glioma, Macular degeneration, Age-related macular degeneration, Mesothelioma
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1642
Chromosome 9 open reading frame 152
bA470J20.2
Alzheimer disease, Prostate cancer

1643
Chromosome 9 open reading frame 40
-
Gout

1644
Chromosome 9 open reading frame 57
-
Metabolic syndrome, Schizophrenia, Scoliosis, Diabetes mellitus type 2

1645
C9orf72-SMCR8 complex subunit
ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1
Amyotrophic lateral sclerosis, Juvenile arthritis, Autism, Eye disorder, Eye disease, Frontotemporal dementia, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Huntington disease, Juvenile idiopathic arthritis, Non-organic psychosis, Oligoarticular juvenile idiopathic arthritis, Progressive myoclonic epilepsy, Psychotic disorders, Schizoaffective disorder
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1646
Carbonic anhydrase 1
CA-I, CAB, Car1, HEL-S-11
Biliary cirrhosis, Congestive ophthalmopathy, Esophageal squamous cell carcinoma, Graves ophthalmopathy, Systemic lupus erythematosus, Myopathic ophthalmopathy, Biliary cholangitis, Rheumatoid arthritis, Rickets, Sjogren syndrome, Stomach neoplasms

1647
Carbonic anhydrase 10
CA-RPX, CARPX, HUCEP-15
Asthma, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Color vision deficiency, Dementia, Gastritis, Gastroesophageal reflux disease, Insomnia, Lung cancer, Myocardial infarction, Peptic ulcer disease, Willis-ekbom disease, Scoliosis, Substance abuse
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1648
Carbonic anhydrase 12
CA-XII, CAXII, HsT18816, T18816
Alzheimer disease, Dental caries, Gout, Lung neoplasms, Neuroblastoma

1649
Carbonic anhydrase 2
CA-II, CAC, CAII, Car2, HEL-76, HEL-S-282
Autism, Autoimmune pancreatitis, Osteopetrosis, Biliary cirrhosis, Hepatocellular carcinoma, Cholangitis, Desbuquois syndrome, Esophageal squamous cell carcinoma, Systemic lupus erythematosus, Osteoporosis, Pancreatitis, Biliary cholangitis, Rheumatoid arthritis, Sjogren syndrome, Stomach neoplasms

1650
Carbonic anhydrase 3
CAIII, Car3
Fatty liver, Fatty liver, alcoholic, Obesity