Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
331 to 340 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

331
SET domain containing 4
C21orf18, C21orf27
Mitral valve prolapse

332
SET domain containing 5
MRD23, SETD5A
Attention deficit hyperactivity disorder, Autism, Congenital heart disease, Developmental disability, Global developmental delay, Hearing impairment, Hyperphosphatasia with intellectual disability syndrome, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic facial, Irritable bowel syndrome, Metabolic syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Polymicrogyria, Diabetes mellitus type 2
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333
SET domain containing 6, protein lysine methyltransferase
-
Autism, Colorectal cancer, Schizophrenia

334
SET domain containing 7, histone lysine methyltransferase
KMT7, SET7, SET7/9, SET9
Alzheimer disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Schizophrenia

335
SET domain containing 9
C5orf35
Breast cancer, Coronary artery disease, Metabolic syndrome, Diabetes mellitus type 2

336
SET domain bifurcated histone lysine methyltransferase 1
ESET, H3-K9-HMTase4, KG1T, KMT1E, TDRD21
Alzheimer disease, Anhedonia, Autism, Color vision deficiency, Melanoma, Mesothelioma, Myocardial infarction, Prostatic neoplasms, Schizophrenia, Skin disease

337
SET domain bifurcated histone lysine methyltransferase 2
C13orf4, CLLD8, CLLL8, KMT1F
Dyslexia

338
SET and mariner transposase domain methyltransferase
METNASE, Mar1
Spondylosis

339
SET like protein
SETP18
Intellectual developmental disorder

340
Senataxin
ALS4, AOA2, SCAN2, SCAR1, STEX, Sen1, bA479K20.2
Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia with oculomotor apraxia, Distal hereditary motor neuropathy, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Charcot-marie-tooth disease, Dementia, Distal spinal muscular atrophy, Frontotemporal dementia, Hereditary motor and sensory neuropathies, Motor neuron disease, Nystagmus, Proximal spinal muscular atrophy
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