Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3511 to 3520 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3511
Deoxyguanosine kinase
MTDPS3, NCPH, NCPH1, PEOB4, dGK
Cerebral atrophy, Deoxyguanosine kinase deficiency, Mitochondrial dna depletion syndrome, Portal hypertension, Memory disorders, Migraine, Mitochondrial disease

3512
24-dehydrocholesterol reductase
DCE, Nbla03646, SELADIN1, seladin-1
Alzheimer disease, Autism, Desbuquois syndrome, Desmosterolosis, Non-immune hydrops fetalis, Melanoma, Schizophrenia

3513
7-dehydrocholesterol reductase
SLOS
Syndactyly of the toes, Autism, Behcet disease, Bone disease, Bullous pemphigoid, Congenital microcephaly, Promyelocytic leukemia, Liver cirrhosis, Metabolic bone disorder, Smith-lemli-opitz syndrome

3514
Dehydrodolichyl diphosphate synthase subunit
CIT, CPT, DEDSM, DS, HDS, RP59, hCIT
Alzheimer disease, Congenital disorder of glycosylation, Developmental delay and seizures, Developmental and epileptic encephalopathy, Retinitis pigmentosa

3515
Dihydrodiol dehydrogenase
2DD, HUM2DD
Oligodendroglioma, Prostatic neoplasms

3516
Dihydrofolate reductase
DHFR1, DHFRP1, DYR
Megaloblastic anemia, Rheumatoid arthritis, Autism, Breast neoplasms, Colorectal neoplasms, Adenomatous polyposis, Folic acid deficiency, Female infertility, Nervous system disease, Osteosarcoma, Pancytopenia

3517
Desert hedgehog signaling molecule
GDMN, GDXYM, HHG-3, SRXY7
46,xy gonadal dysgenesis, Attention deficit hyperactivity disorder, Bipolar disorder, Gonadal dysgenesis, Swyer syndrome

3518
Dihydroorotate dehydrogenase (quinone)
DHOdehase, POADS, URA1
Sickle cell anemia, Beta thalassemia, Coronary artery disease, Desbuquois syndrome, Miller-dieker syndrome, Postaxial acrofacial dysostosis, Spherocytosis

3519
Deoxyhypusine synthase
DHS, DS, MIG13, NEDSSWI
Neurodevelopmental disorder

3520
Dehydrogenase/reductase 1
SDR19C1
Autism