Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11511 to 11520 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11511
Spliceosome associated factor 3, U4/U6 recycling protein
DSAP1, P100, RP11-13G14, TIP110, p110, p110(nrb)
Neurodevelopmental disorder, Disseminated superficial actinic porokeratosis, Non-specific syndromic intellectual disability, Open angle glaucoma, Porokeratosis

11512
SAM and SH3 domain containing 1
CAPOK, DUH, DUH1, SH3D6A, dJ323M4.1
Alzheimer disease, Autoimmune disease, Autoimmune thyroid disease, Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma, Colorectal cancer, Diabetic neuropathy, Dilated cardiomyopathy, Dyschromatosis, Dyschromatosis symmetrica hereditaria, Esophageal cancer, Esophageal disease, Esophageal ulcer, Gastric cancer, Glioma, Hepatolenticular degeneration
View all (9 more)

11513
SAM and SH3 domain containing 3
753P9, CXorf9, HACS2, IMD102, SH3D6C, SLY
Combined immunodeficiency, x-linked, Immunodeficiency, X-linked combined immunodeficiency diseases

11514
SAS-6 centriolar assembly protein
MCPH14, SAS-6, SAS6
Primary microcephaly, Microcephaly

11515
Spermidine/spermine N1-acetyltransferase 1
DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1
Anxiety disorder, Bipolar disorder, Major depressive disorder, Allergic contact dermatitis, Keratosis follicularis spinulosa decalvans, Mood disorder, Non-organic psychosis, Obesity, Psychotic disorders, Schizoaffective disorder, Systemic lupus erythematosus, Depression

11516
SATB homeobox 1
DEFDA, DHDBV, KTZSL
Eczema, Autism, Breast cancer, Neurodevelopmental disorder, Den hoed-de boer-voisin syndrome, Developmental delay with dysmorphic facies and dental anomalies, Duchenne muscular dystrophy, Hyperaldosteronism, Intellectual developmental disorder seizures extrapyramidal, Lung cancer, Non-specific syndromic intellectual disability, Venous thromboembolism

11517
SATB homeobox 2
C2DELq32q33, DEL2Q32Q33, GLSS
Autism, Cancer, Cerebellar ataxia, Chromosome 2q32-q33 deletion syndrome, Cleft palate, Clinodactyly, Colorectal cancer, Colorectal neoplasms, Craniofacial abnormalities, Desbuquois syndrome, Developmental disability, Dyslexia, Gastroesophageal reflux disease, Glass syndrome, Global developmental delay
View all (10 more)

11518
Salvador family WW domain containing protein 1
SAV, WW45, WWP4
Astrocytoma

11519
Stabilizer of axonemal microtubules 1
C9orf138, FAM154A
Asthma, Neoplasms, Ovarian neoplasms, Non-small cell lung carcinoma, Diabetes mellitus type 2

11520
Stabilizer of axonemal microtubules 4
C11orf66, IIIG9, PPP1R32
Cardiovascular disease, Hypertension, Metabolic syndrome, Diabetes mellitus type 2