Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11881 to 11890 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11881
Sarcoglycan epsilon
DYT11, ESG, epsilon-SG
Major depressive disorder, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Insomnia, Movement disorder, Myoclonic dystonia, Schizophrenia

11882
Sarcoglycan gamma
35DAG, A4, DAGA4, DMDA, DMDA1, LGMD2C, LGMDR5, MAM, SCARMD2, gamma-SG
Asthma, Limb girdle muscular dystrophy, Diabetes mellitus type 2, Gastric cancer, Limb-girdle muscular dystrophy, Major depressive disorder, Ovarian epithelial cancer, Muscular dystrophy, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Sarcoglycanopathies

11883
Sarcoglycan zeta
ZSG1
Amphetamine or sympathomimetic abuse, Attention deficit hyperactivity disorder, Autism, Color vision deficiency, Corneal astigmatism, Coronary artery disease, Coronary stenosis, Dermatologic disorder, Differentiated thyroid carcinoma, Endometrial cancer, Hypertension, Insomnia, Major depressive disorder, Ovarian epithelial cancer, Metabolic syndrome
View all (14 more)

11884
SAGA complex associated factor 29
CCDC101, STAF36, TDRD29
Asthma, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Diabetic retinopathy, Inflammatory bowel disease

11885
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

11886
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)

11887
Serum/glucocorticoid regulated kinase 2
H-SGK2, dJ138B7.2
Liver cirrhosis

11888
Serum/glucocorticoid regulated kinase family member 3
CISK, SGK2, SGKL
Alzheimer disease, Hypophosphatemic rickets, Major depressive disorder

11889
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

11890
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