Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
3351 to 3360 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3351
Dachsous cadherin-related 1
CDH19, CDH25, CDHR6, FIB1, MMVP2, MVP2, PCDH16, VMLDS1
Cardiomyopathy, Cerebrofacioarticular syndrome, Congenital heart disease, Dry eye syndrome, Periventricular nodular heterotopia, Lymphedema, Mitral valve prolapse, Tetralogy of fallot, Van maldergem syndrome

3352
Dachsous cadherin-related 2
CDH27, CDHJ, CDHR7, PCDH23, PCDHJ
Alzheimer disease, Eczema, Auditory system disease, Bipolar disorder, Obstructive pulmonary disease, Coronary artery disease, Dry eye syndrome, Dupuytren contracture, Glioma, Graves disease, Hypertension, Major depressive disorder, Obesity, Oligodendroglioma, Schizophrenia
View all (5 more)

3353
Deoxycytidine kinase
-
Central nervous system cancer, Glioblastoma, Glioma

3354
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)

3355
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

3356
Doublecortin like kinase 3
CLR, DCAMKL3, DCDC3C, DCK3
Major depressive disorder

3357
DNA cross-link repair 1A
PSO2, SNM1, SNM1A
Basal cell carcinoma, Upper aerodigestive tract neoplasm

3358
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

3359
DNA cross-link repair 1C
A-SCID, DCLREC1C, RS-SCID, SCIDA, SNM1C
Common variable immunodeficiency, Ehlers-danlos syndrome, Migraine, Omenn syndrome, Severe combined immunodeficiency

3360
Decorin
CSCD, DSPG2, PG40, PGII, PGS2, SLRR1B
Hepatocellular carcinoma, Congenital stromal corneal dystrophy, Corneal dystrophy, Endometrial neoplasms, Myocardial ischemia