Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6111 to 6120 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6111
Isocitrate dehydrogenase (NADP(+)) 2
D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP, IDPM, mNADP-IDH
Anaplastic astrocytoma, Anaplastic oligoastrocytoma, Anaplastic oligodendroglioma, Cardiomegaly, Cardiomyopathy, Central nervous system disease, Cholangiocarcinoma, Chordoma, Combined d-2- and l-2-hydroxyglutaric aciduria, Craniofacial abnormalities, D-2-hydroxyglutaric aciduria, Desbuquois syndrome, Gemistocytic astrocytoma, Gout, Growth disorder
View all (12 more)

6112
Isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha
RP90
Osteoarthritis, Osteoporosis, Retinitis pigmentosa

6113
Isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta
RP46
Optic atrophy, Retinitis pigmentosa, Stomach neoplasms

6114
Isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit gamma
H-IDHG, RP99
Retinitis pigmentosa

6115
Isopentenyl-diphosphate delta isomerase 2
IPPI2
Kidney disease

6116
Indoleamine 2,3-dioxygenase 1
IDO, IDO-1, INDO
Anhedonia, Breast neoplasms, Depression, Degenerative disorder, Major depressive disorder, Endometriosis, Neurodegenerative disorder, Obesity

6117
Indoleamine 2,3-dioxygenase 2
INDOL1
Bipolar disorder, Liver cirrhosis, Major depressive disorder, Multinodular goiter, Schizophrenia

6118
Iduronate 2-sulfatase
ID2S, MPS2, SIDS
Colonic neoplasms, Colorectal cancer, Desbuquois syndrome, Epidermolysis bullosa, Aplastic anemia, Kidney disease, Lung neoplasms, Mucopolysaccharidosis, Scoliosis

6119
Alpha-L-iduronidase
IDA, MPS1, MPSI
Alzheimer disease, Atrial fibrillation, Desbuquois syndrome, Developmental and epileptic encephalopathy, Gitelman syndrome, Hyperoxaluria, Mucopolysaccharidosis, Nephrolithiasis, Pfaundler-hurler syndrome, Diabetes mellitus type 2

6120
Immediate early response 2
CHX1, ETR101
Lung neoplasms, Venous thromboembolism