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"
381 to 390 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

381
SAGA complex associated factor 29
CCDC101, STAF36, TDRD29
Asthma, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Diabetic retinopathy, Inflammatory bowel disease

382
SH3GL interacting endocytic adaptor 1
-
Anorexia nervosa, Attention deficit hyperactivity disorder, Heart failure, Inflammatory bowel disease, Major depressive disorder, Neuroblastoma, Obesity, Substance abuse, Diabetes mellitus type 2

383
Serum/glucocorticoid regulated kinase 1
SGK
Alzheimer disease, Eczema, Brain infarction, Carcinoma, Cerebral amyloid angiopathy, Color vision deficiency, Dementia, Diabetic neuropathy, Hypertension, Myeloid leukemia, Lewy body disease, Major depressive disorder, Pelvic organ prolapse, Schizophrenia, Scoliosis
View all (2 more)

384
Serum/glucocorticoid regulated kinase 2
H-SGK2, dJ138B7.2
Liver cirrhosis

385
Serum/glucocorticoid regulated kinase family member 3
CISK, SGK2, SGKL
Alzheimer disease, Hypophosphatemic rickets, Major depressive disorder

386
Sphingomyelin synthase 1
MOB, MOB1, SMS1, TMEM23, hmob33
Attention deficit hyperactivity disorder, Neurodevelopmental disorder, Estrogen-receptor negative breast cancer, Multiple sclerosis, Schizophrenia, Scoliosis, Squamous cell carcinoma, Substance abuse

387
Sphingomyelin synthase 2
CDL, SMS2
Bone fragility with contractures, arterial rupture, and deafness, Calvarial doughnut lesions with bone fragility, Desbuquois syndrome, Doughnut lesion of calvaria and bone fragility syndrome, Osteoporosis-pseudoglioma syndrome

388
Shugoshin 1
CAID, NY-BR-85, SGO, SGOL1
Cardiac arrhythmias, Cardiac arrhythmia, Atrial and intestinal dysrhythmia, Chronobiology disorder, Intestinal disease

389
Shugoshin 2
SGOL2, TRIPIN
Gonadal dysgenesis, Premature ovarian failure, Perrault syndrome

390
Sphingosine-1-phosphate lyase 1
NPHS14, RENI, S1PL, SPL
Eczema, Attention deficit hyperactivity disorder, Charcot-marie-tooth disease, Digestive system disease, Hyperopia, Multiple myeloma, Nephrotic syndrome, Obesity, Willis-ekbom disease, Scoliosis, Seborrheic dermatitis, Substance abuse, Diabetes mellitus type 2, Uveal melanoma