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
3571 to 3580 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3571
Disco interacting protein 2 homolog C
KIAA0934
Colorectal cancer, Neurodevelopmental disorder, Migraine, Neurotic disorder, Non-specific syndromic intellectual disability, Obesity, Prostate cancer, Scoliosis, Small cell lung carcinoma

3572
Divergent protein kinase domain 1A
FAM69A
Diamond-blackfan anemia, Aplastic anemia, Atrial septal defect, Bipolar disorder, Ovarian agenesis, Endometriosis, Erythroid hypoplasia, Auricle malformation, Major depressive disorder, Multiple sclerosis, Prostate cancer, Pulmonary arterial hypertension, Schizophrenia, Testicular hydrocele

3573
Divergent protein kinase domain 1C
C18orf51, FAM69C, FNCAD
Sjogren syndrome

3574
Divergent protein kinase domain 2A
C3orf58, DIA1, GoPro49, HASF
Autism, Colorectal cancer, Liver cirrhosis

3575
Divergent protein kinase domain 2B
4930578C19Rik, CXorf36, DIA1R, EPQL1862, PRO3743, bA435K1.1
Autism, Hepatocellular carcinoma, X-linked intellectual disability

3576
DIRAS family GTPase 2
Di-Ras2
Alzheimer disease, Bladder exstrophy

3577
DIRAS family GTPase 3
ARHI, NOEY2
Hepatocellular carcinoma

3578
DIS3 exosome endoribonuclease and 3''-5'' exoribonuclease
2810028N01Rik, EXOSC11, KIAA1008, RRP44, dis3p
Prostate cancer

3579
DIS3 like exosome 3'-5' exoribonuclease
DIS3L1
Metabolic syndrome, Diabetes mellitus type 2

3580
DIS3 like 3'-5' exoribonuclease 2
FAM6A, PRLMNS, hDIS3L2
Androgenetic alopecia, Diabetic neuropathy, Neurodevelopmental disorder, Osteoarthritis, Perlman syndrome