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
8501 to 8510 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8501
N-deacetylase and N-sulfotransferase 4
N-HSST, N-HSST 4, NDST-4, NHSST4
Alzheimer disease, Liver cirrhosis, Dementia, Osteoarthritis, Prostatic neoplasms, Willis-ekbom disease

8502
NADH:ubiquinone oxidoreductase subunit A1
CI-MWFE, MC1DN12, MWFE, ZNF183
Leigh syndrome, Mitochondrial complex deficiency

8503
NADH:ubiquinone oxidoreductase subunit A10
CI-42KD, CI-42k, MC1DN22
Alzheimer disease, Appendicitis, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Essential tremor, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Schizophrenia

8504
NADH:ubiquinone oxidoreductase subunit A11
B14.7, CI-B14.7, MC1DN14
Mitochondrial complex deficiency, Mitochondrial disease

8505
NADH:ubiquinone oxidoreductase subunit A12
B17.2, DAP13, MC1DN23
Alzheimer disease, Color vision deficiency, Coronary artery disease, Gallstones, Insomnia, Leigh syndrome, Mitochondrial complex deficiency, Myocardial infarction, Schizophrenia

8506
NADH:ubiquinone oxidoreductase subunit A13
B16.6, CDA016, CGI-39, GRIM-19, GRIM19, MC1DN28
Differentiated thyroid carcinoma, Hypertrophic cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Nystagmus, Hurthle cell thyroid cancer, Thyroid carcinoma

8507
NADH:ubiquinone oxidoreductase subunit A2
B8, CD14, CIB8, MC1DN13
Attention deficit hyperactivity disorder, Autism, Cystic leukoencephalopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Stomach neoplasms

8508
NADH:ubiquinone oxidoreductase subunit A3
B9, CI-B9
Leigh syndrome

8509
NADH:ubiquinone oxidoreductase subunit A6
B14, CI-B14, LYRM6, MC1DN33, NADHB14
Mitochondrial complex deficiency, Mitochondrial disease

8510
NADH:ubiquinone oxidoreductase subunit A8
CI-19KD, CI-PGIV, MC1DN37, PGIV
Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Scoliosis