Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11771 to 11780 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11771
Sestrin 2
HI95, SES2, SEST2
Colorectal neoplasms, Gout, Hepatomegaly

11772
Sestrin 3
SEST3
Prostatic neoplasms

11773
SEC14 and spectrin domain containing 1
Solo
Atrial fibrillation, Bipolar disorder, Dental caries, Alzheimer disease, Migraine, Scoliosis

11774
SET nuclear proto-oncogene
2PP2A, I2PP2A, IGAAD, IPP2A2, MRD58, PHAPII, TAF-I, TAF-IBETA
Nonsyndromic intellectual disability, Intellectual developmental disorder, Necrosis

11775
SET binding protein 1
MRD29, SEB
Androgenetic alopecia, Arthrogryposis multiplex congenita, Atrial septal defect, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Breast neoplasms, Bundle branch block, Basal cell carcinoma, Cerebral amyloid angiopathy, Cerebral atrophy, Color vision deficiency, Neurodevelopmental disorder, Congenital neurologic anomalies, Coronary aneurysm
View all (22 more)

11776
SET domain containing 1A, histone lysine methyltransferase
EPEDD, EPEO2, KMT2F, NEDSID, Set1, Set1A
Ankylosing spondylitis, Autism, Obstructive pulmonary disease, Crohn disease, Developmental disability, Early onset epilepsy with developmental delay, Graves disease, Intellectual developmental disorder, Multiple sclerosis, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Parkinson disease, Psoriasis, Psoriasis vulgaris, Schizophrenia
View all (2 more)

11777
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

11778
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

11779
SET domain containing 3, actin N3(tau)-histidine methyltransferase
C14orf154, hSETD3
Color vision deficiency, Colorectal cancer, Insomnia, Oligodendroglioma, Willis-ekbom disease, Schizophrenia

11780
SET domain containing 4
C21orf18, C21orf27
Mitral valve prolapse