Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3691 to 3700 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3691
Deoxyribonuclease 2 beta
DLAD
Prostate cancer, Psychiatric disorders

3692
Delta/notch like EGF repeat containing
UNQ26, bet
Breast cancer, Carpal tunnel syndrome, Cerebral amyloid angiopathy, Obstructive pulmonary disease, Dementia, Estrogen-receptor negative breast cancer, Oligodendroglioma, Diabetes mellitus type 2

3693
Dynein heavy chain domain 1
C11orf47, CCDC35, DHCD1, DNHD1L, SPGF65
Asthma, Renal cell carcinoma, Obstructive asthma, Essential tremor, Male infertility large polyploid spermatozoa, Male infertility single gene azoospermia, Male infertility spermatogenesis disorder, Scoliosis, Spermatogenic failure

3694
DNL-type zinc finger
C9orf151, HEP, HEP1, TIMM15, ZIM17, bA413M3.2
Inflammatory bowel disease

3695
Dynamin 1
DEE31, DEE31A, DEE31B, DNM, EIEE31
Asthma, Attention deficit hyperactivity disorder, Cerebellar ataxia, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Global developmental delay, Insomnia, Lennox-gastaut syndrome, Neurodevelopmental disorder, Retinopathy of prematurity, Schizophrenia, West syndrome

3696
Dynamin 1 like
DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1, HDYNIV, OPA5
Optic atrophy, Encephalopathy due to mitochondrial and peroxisomal fission defect, Leigh syndrome, Microcephaly, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy with sideroblastic anemia, Myocardial ischemia, Obesity, Parkinson disease, Spastic paraplegia

3697
Dynamin 2
CMT2M, CMTDI1, CMTDIB, DI-CMTB, DYN2, DYNII, LCCS5
Centronuclear myopathy, Charcot-marie-tooth disease, Obstructive pulmonary disease, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital structural myopathy, Hyperlipidemia, Irritable bowel syndrome, Lethal congenital contracture syndrome, Moyamoya angiopathy
View all (9 more)

3698
Dynamin 3
Dyna III
Astrocytoma, Breast cancer, Endometriosis, Kidney neoplasms, Metabolic syndrome, Moyamoya disease, Neurotic disorder, Nonalcoholic fatty liver disease, Open angle glaucoma, Ovarian cancer, Diabetes mellitus type 2, Uterine fibroid

3699
Dynamin binding protein
ARHGEF36, CTRCT48, TUBA
Cataract, Congenital total cataract, Nonalcoholic fatty liver disease, Scoliosis

3700
DNA methyltransferase 1
ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT, m.HsaI
Anxiety disorder, Asthma, Autism, Cerebellar ataxia with deafness and narcolepsy, Beckwith-wiedemann syndrome, Bipolar disorder, Breast neoplasms, Carcinoma, Pancreatic ductal carcinoma, Cardiovascular disease, Cerebellar ataxia, Cerebellar ataxia, deafness, and narcolepsy, Cerebellar atrophy, Cerebral atrophy, Charcot-marie-tooth disease
View all (23 more)