Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3791 to 3800 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3791
DNA replication and sister chromatid cohesion 1
DCC1
Venous thromboembolism

3792
Dermatan sulfate epimerase
DS-epi1, DSEP, DSEPI, EDSMC2, SART-2, SART2
Desbuquois syndrome, Ehlers-danlos syndrome, Nephrotic syndrome, Systemic lupus erythematosus, Ulcerative colitis

3793
Dermatan sulfate epimerase like
C18orf4, DE-epi2
Dementia, Hearing loss, Major depressive disorder, Mood disorder, Multiple myeloma

3794
Desmoglein 1
CDHF4, DG1, DSG, EPKHE, EPKHIA, PPKS1, SPPK1
Bicuspid aortic valve, Dermatitis, Diffuse palmoplantar keratoderma, Eosinophilia, Congenital erythroderma with palmoplantar keratoderma, hypotrichosis, and hyper-ige, Focal palmoplantar keratoderma with joint keratoses, Hypersensitivity, Insomnia, Keratosis palmoplantaris striata, Metabolic syndrome

3795
Desmoglein 2
CDHF5, HDGC
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiac arrest, Cardiomyopathy, Dilated cardiomyopathy, Conduction disorder of the heart, Arrhythmogenic right ventricular dysplasia, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Ventricular fibrillation, Catecholaminergic polymorphic ventricular tachycardia

3796
Desmoglein 3
ABOLM, CDHF6, PVA
Acantholytic blistering of oral and laryngeal mucosa, Colonic neoplasms, Colorectal cancer, Parkinson disease

3797
Desmoglein 4
CDGF13, CDHF13, HYPT6, LAH
Hypotrichosis, Hypotrichosis simplex

3798
Desmoplakin
DCWHKTA, DP
Amyloidosis, Arrhythmogenic right ventricular cardiomyopathy, Bicuspid aortic valve, Brugada syndrome, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Carvajal syndrome, Obstructive airway disease, Obstructive pulmonary disease, Conduction disorder of the heart, Ectodermal dysplasia, Junctional epidermolysis bullosa, Erythrokeratodermia-cardiomyopathy syndrome
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3799
Dentin sialophosphoprotein
DFNA39, DGI1, DMP3, DPP, DSP
Bone fragility with contractures, arterial rupture, and deafness, Squamous cell carcinoma, Autosomal dominant sensorineural deafness, Dentin dysplasia, Dentinogenesis imperfecta, Hearing impairment, Mouth neoplasms, Osteoporosis-pseudoglioma syndrome

3800
Dystonin
BP240, BPA, BPAG1, CATX-15, CATX15, D6S1101, DMH, DT, EBS3, EBSB2, HSAN6, MACF2
Alzheimer disease, Atrial fibrillation, Autism, Cardiomyopathy, Charcot-marie-tooth disease, Congenital joint contractures, Distal spinal muscular atrophy, Dominantly inherited sensory neuropathy, Epidermolysis bullosa, Esophageal atresia, Global developmental delay, Gout, Hereditary sensory and autonomic neuropathy, Moyamoya angiopathy, Multiple sclerosis
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