Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3391 to 3400 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3391
Defective in cullin neddylation 1 domain containing 4
DCNL4
Metabolic syndrome, Squamous cell carcinoma, Diabetes mellitus type 2

3392
Defective in cullin neddylation 1 domain containing 5
DCNL5, SCCRO5
Cardiovascular disease

3393
Doublecortin
DBCN, DC, LISX, SCLH, XLIS
Lissencephaly, Congenital neurologic anomalies, Lissencephaly, x-linked, Neurodevelopmental disorder

3394
Dicarbonyl and L-xylulose reductase
DCR, HCR2, HCRII, KIDCR, P34H, PNTSU, SDR20C1, XR
Cancer, Essential pentosuria, Liver cirrhosis, Obesity, Prostatic neoplasms

3395
DET1 and DDB1 associated 1
C19orf58, PCIA1
Rheumatoid arthritis

3396
Dimethylarginine dimethylaminohydrolase 1
DDAH, DDAH-1, DDAHI, HEL-S-16
Alzheimer disease, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Eosinophilia, Hypertension, Liver disease, Multiple sclerosis, Myocardial ischemia

3397
DDAH family member 2, ADMA-independent
DDAH, DDAHII, G6a, HEL-S-277, NG30
Ischemic heart disease, Coronary artery disease, Myocardial ischemia, Preeclampsia

3398
Damage specific DNA binding protein 1
DDBA, UV-DDB1, WHIKERS, XAP1, XPCE, XPE, XPE-BF
Congenital heart defects, Stomach neoplasms, White-kernohan syndrome

3399
Damage specific DNA binding protein 2
DDBB, UV-DDB2, XPE
Attention deficit hyperactivity disorder, Cardiomyopathy, Hypertension, Major depressive disorder, Metabolic syndrome, Mood disorder, Schizophrenia, Substance abuse, Diabetes mellitus type 2, Venous thromboembolism, Xeroderma pigmentosum

3400
Dopa decarboxylase
AADC
Bipolar disorder, Lymphoblastic leukemia, Aromatic l-amino-acid decarboxylase deficiency, Bipolar depression, Exostoses, Global developmental delay, Liver cirrhosis, Major depressive disorder, Metabolic syndrome, Parkinson disease, Pheochromocytoma, Diabetes mellitus type 2, Depression