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
8521 to 8530 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8521
NADH:ubiquinone oxidoreductase subunit B10
MC1DN35, PDSW
Mitochondrial complex deficiency, Mitochondrial disease

8522
NADH:ubiquinone oxidoreductase subunit B11
CI-ESSS, ESSS, MC1DN30, NP17.3, Np15, P17.3
Microphthalmia, Mitochondrial complex deficiency, Mitochondrial disease, Neurodevelopmental disorder

8523
NADH:ubiquinone oxidoreductase subunit B2
AGGG, CI-AGGG
Diabetes mellitus type 2

8524
NADH:ubiquinone oxidoreductase subunit B3
B12, CI-B12, MC1DN25
Congenital cataract, Developmental regression, Mitochondrial complex deficiency, Mitochondrial disease

8525
NADH:ubiquinone oxidoreductase subunit B4
B15, CI-B15
Obesity, Rheumatoid arthritis

8526
NADH:ubiquinone oxidoreductase subunit B7
B18, CI-B18, MC1DN39
Hepatolenticular degeneration, Mitochondrial complex deficiency

8527
NADH:ubiquinone oxidoreductase subunit B8
ASHI, CI-ASHI, MC1DN32
Dermatologic disorder, Leigh syndrome, Mitochondrial complex deficiency, Skin disease

8528
NADH:ubiquinone oxidoreductase subunit B9
B22, CI-B22, LYRM3, MC1DN24, UQOR22
Malignant glioma, Mitochondrial complex deficiency, Peripheral arterial disease

8529
NADH:ubiquinone oxidoreductase subunit C2
B14.5b, CI-B14.5b, HLC-1, MC1DN36, NADHDH2
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

8530
NDUFC2-KCTD14 readthrough
-
Mitochondrial complex deficiency, Mitochondrial disease, Pelvic organ prolapse