Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3561 to 3570 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3561
DIRAS family GTPase 3
ARHI, NOEY2
Hepatocellular carcinoma

3562
DIS3 exosome endoribonuclease and 3''-5'' exoribonuclease
2810028N01Rik, EXOSC11, KIAA1008, RRP44, dis3p
Prostate cancer

3563
DIS3 like exosome 3'-5' exoribonuclease
DIS3L1
Metabolic syndrome, Diabetes mellitus type 2

3564
DIS3 like 3'-5' exoribonuclease 2
FAM6A, PRLMNS, hDIS3L2
Androgenetic alopecia, Diabetic neuropathy, Neurodevelopmental disorder, Osteoarthritis, Perlman syndrome

3565
DISC1 scaffold protein
C1orf136, SCZD9
Alzheimer disease, Amyotrophic lateral sclerosis, Anhedonia, Anxiety disorder, Asperger syndrome, Autism, Bell's palsy, Bipolar disorder, Fatigue syndrome, Color vision deficiency, Colorectal cancer, Bipolar depression, Major depressive disorder, Developmental coordination disorder, Peritoneal disease
View all (9 more)

3566
Dispatched RND transporter family member 1
DISPA, HPE10
Colorectal cancer, Esophageal atresia, Gastrointestinal stromal tumor, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Myocardial infarction, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly

3567
Dispatched RND transporter family member 2
C15orf36, DISPB, HsT16908, LINC00594
Digestive system disease, Diverticular disease

3568
Dispatched RND transporter family member 3
PTCHD2
Attention deficit hyperactivity disorder, Glaucoma

3569
DIX domain containing 1
CCD1
Anxiety disorder, Autism, Bipolar disorder, Bipolar depression, Major depressive disorder, Obesity, Schizophrenia

3570
Dyskerin pseudouridine synthase 1
CBF5, CHINE1, DKC, DKCX, NAP57, NOLA4, XAP101
Aplastic anemia, Cataract-multisystem syndrome, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Dkc1-related disorder, Dyskeratosis congenita, Hoyeraal hreidarsson syndrome, X-linked dyskeratosis congenita