Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
11831 to 11840 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11831
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
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11832
Serum/glucocorticoid regulated kinase family member 3
CISK, SGK2, SGKL
Alzheimer disease, Hypophosphatemic rickets, Major depressive disorder

11833
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

11834
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

11835
Shugoshin 1
CAID, NY-BR-85, SGO, SGOL1
Cardiac arrhythmias, Cardiac arrhythmia, Atrial and intestinal dysrhythmia, Chronobiology disorder, Intestinal disease

11836
Shugoshin 2
SGOL2, TRIPIN
Gonadal dysgenesis, Premature ovarian failure, Perrault syndrome

11837
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

11838
Sphingosine-1-phosphate phosphatase 2
SPP2, SPPase2
Anorexia nervosa, Eating disorder, Major depressive disorder, Tourette syndrome

11839
N-sulfoglucosamine sulfohydrolase
HSS, MPS3A, SFMD
Autoinflammatory syndrome, Central nervous system cancer, Desbuquois syndrome, Developmental regression, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Mucopolysaccharidosis, Nystagmus, Psoriasis, Sanfilippo syndrome

11840
Small G protein signaling modulator 1
RUTBC2
Hypertension, Sclerosing cholangitis, Diabetes mellitus type 2