Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11831 to 11840 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11831
SET domain containing 1B, histone lysine methyltransferase
IDDSELD, KMT2G, Set1B
Nonsyndromic intellectual disability, Color vision deficiency, Neurodevelopmental disorder, Coronary artery disease, Developmental delay, Epilepsy, Intellectual developmental disorder seizures language, Major depressive disorder, Non-specific syndromic intellectual disability, Obesity

11832
SET domain containing 2, histone lysine methyltransferase
HBP231, HIF-1, HIP-1, HSPC069, HYPB, KMT3A, LLS, MRD70, RAPAS, SET2, p231HBP
Autism, Breast neoplasms, Adenoid cystic carcinoma, Renal cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Dandy-walker syndrome, Desbuquois syndrome, Idiopathic pulmonary fibrosis, Intellectual developmental disorder, Leukemia, Mesothelioma, Neurodevelopmental disorder, Prostatic neoplasms, Rhabdomyosarcoma, Sotos syndrome

11833
SET domain containing 3, actin N3(tau)-histidine methyltransferase
C14orf154, hSETD3
Color vision deficiency, Colorectal cancer, Insomnia, Oligodendroglioma, Willis-ekbom disease, Schizophrenia

11834
SET domain containing 4
C21orf18, C21orf27
Mitral valve prolapse

11835
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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11836
SET domain containing 6, protein lysine methyltransferase
-
Autism, Colorectal cancer, Schizophrenia

11837
SET domain containing 7, histone lysine methyltransferase
KMT7, SET7, SET7/9, SET9
Alzheimer disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Schizophrenia

11838
SET domain containing 9
C5orf35
Breast cancer, Coronary artery disease, Metabolic syndrome, Diabetes mellitus type 2

11839
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

11840
SET domain bifurcated histone lysine methyltransferase 2
C13orf4, CLLD8, CLLL8, KMT1F
Dyslexia