Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3731 to 3740 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3731
Dedicator of cytokinesis 8
HEL-205, HIES2, MRD2, ZIR8
Androgenetic alopecia, Autism, Nonsyndromic intellectual disability, Combined immunodeficiency disease, Neurodevelopmental disorder, Coronary artery disease, Crohn disease, Melanoma, Atopic dermatitis, Developmental disability, Hepatitis b, Hyper-ige recurrent infection syndrome, Inflammatory bowel disease, Diabetes mellitus type 1, Intellectual developmental disorder
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3732
Dedicator of cytokinesis 9
ZIZ1, ZIZIMIN1
Bipolar disorder, Corneal astigmatism, Coronary artery disease, Irritable bowel syndrome, Keratoconus, Moyamoya disease, Myocardial infarction, Pelvic organ prolapse

3733
Deoxyhypusine hydroxylase
HLRC1, NEDMVIC, hDOHH
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

3734
Docking protein 1
P62DOK, pp62
Bell's palsy, Lung neoplasms, Myopia, Ovarian neoplasms

3735
Docking protein 2
p56DOK, p56dok-2
Eczema, Crohn disease, Heart failure, Lung neoplasms, Pancreatic cancer, Respiratory system disease

3736
Docking protein 3
DOKL
Coronary artery disease, Lung neoplasms

3737
Docking protein 4
IRS-5, IRS5
Myositis, Psoriasis

3738
Docking protein 5
C20orf180, IRS-6, IRS6
Bipolar disorder, Celiac disease, Lung cancer, Scoliosis, Diabetes mellitus type 2, Vascular disease

3739
Docking protein 6
DOK5L, HsT3226
Autism, Adrenal gland neoplasms, Bone fracture, Breast cancer, Central nervous system cancer, Dementia, Glioblastoma, Glioma, Glomerulonephritis, Insomnia, Myocardial infarction, Osteoporosis, Stroke, Urinary bladder cancer, Venous thromboembolism

3740
Docking protein 7
C4orf25, CMS10, CMS1B, FADS3
Congenital cardiovascular anomaly, Congenital myasthenic syndrome, Coronary artery disease, Fetal akinesia deformation sequence, Gallstones, Hyperlipidemia, Insomnia, Metabolic syndrome, Moyamoya disease, Myasthenic syndrome, Pena-shokeir syndrome , Peripheral vascular disease, Postsynaptic congenital myasthenic syndrome, Rett syndrome, Spondylosis