Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "D"
71 to 80 of 594 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Deoxycytidine kinase
-
Central nervous system cancer, Glioblastoma, Glioma

72
Doublecortin like kinase 1
CL1, CLICK1, DCAMKL1, DCDC3A, DCLK
Androgenetic alopecia, Angioedema, Asthma, Bipolar disorder, Liver cirrhosis, Color vision deficiency, Colorectal neoplasms, Lipoma, Metabolic syndrome, Nonalcoholic fatty liver disease, Obesity, Ovarian cancer, Ovarian serous carcinoma, Retinopathy of prematurity, Schizophrenia
View all (3 more)

73
Doublecortin like kinase 2
CL2, CLICK-II, CLICK2, CLIK2, DCAMKL2, DCDC3, DCDC3B, DCK2
Alzheimer disease, Breast cancer, Coronary artery disease, Dementia, Major depressive disorder, Metabolic syndrome, Mood disorder, Myocardial infarction, Nonalcoholic fatty liver disease, Osteoarthritis, Diabetes mellitus type 2

74
Doublecortin like kinase 3
CLR, DCAMKL3, DCDC3C, DCK3
Major depressive disorder

75
DNA cross-link repair 1A
PSO2, SNM1, SNM1A
Basal cell carcinoma, Upper aerodigestive tract neoplasm

76
DNA cross-link repair 1B
APOLLO, DKCB8, SNM1B, SNMIB
Breast cancer, Cardiovascular disease, Coronary artery disease, Melanoma, Dyskeratosis congenita, Fanconi anemia, Hoyeraal hreidarsson syndrome, Myocardial infarction, Non-melanoma skin carcinoma, Rheumatoid arthritis, Spastic paraplegia, Hereditary spastic paraplegia, Diabetes mellitus type 1

77
DNA cross-link repair 1C
A-SCID, DCLREC1C, RS-SCID, SCIDA, SNM1C
Common variable immunodeficiency, Ehlers-danlos syndrome, Migraine, Omenn syndrome, Severe combined immunodeficiency

78
Decorin
CSCD, DSPG2, PG40, PGII, PGS2, SLRR1B
Hepatocellular carcinoma, Congenital stromal corneal dystrophy, Corneal dystrophy, Endometrial neoplasms, Myocardial ischemia

79
Decapping mRNA 1B
DCP1
Basal cell carcinoma, Obesity, Pancreatic cancer

80
Decapping enzyme, scavenger
ARS, DCS1, HINT-5, HINT5, HSL1, HSPC015
Al-raqad syndrome, Nonsyndromic intellectual disability