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
Showing genes starting with "S"
201 to 210 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
SEC23 homolog A, COPII component
CLSD, hSec23A
Craniolenticulosutural dysplasia, Insomnia, Osteoarthritis

202
SEC23 homolog B, COPII component
CDA-II, CDAII, CDAN2, CWS7, HEMPAS, hSec23B
Congenital dyserythropoietic anemia, Central nervous system cancer, Cowden disease, Glioblastoma, Glioma, Neurotic disorder

203
SEC23 interacting protein
MSTP053, P125, P125A, iPLA1A, iPLA1beta
Lymphocytic leukemia, Parkinson disease, Diabetes mellitus type 2

204
SEC24 homolog A, COPII component
-
Schizophrenia

205
SEC24 homolog B, COPII component
SEC24
Alzheimer disease

206
SEC24 homolog C, COPII component
-
22q11.2 deletion syndrome, Bipolar disorder, Developmental and epileptic encephalopathy, Digeorge syndrome, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2, Depression

207
SEC24 homolog D, COPII component
CLCRP2
Bone fragility with contractures, arterial rupture, and deafness, Cole-carpenter syndrome, Desbuquois syndrome, Epilepsy, Intellectual developmental disorder, Myocardial infarction, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Hypertension

208
SEC31 homolog A, COPII component
ABP125, ABP130, HPBKS, HSPC275, HSPC334, NEDSOSB, SEC31L1
Asthma, Diffuse large b-cell lymphoma, Neurodevelopmental disorder, Oligodendroglioma

209
SEC61 translocon subunit alpha 1
ADTKD5, CVID15, HNFJ4, HSEC61, SEC61, SEC61A
Tubulointerstitial kidney disease, Common variable immunodeficiency, Craniofacial abnormalities, Hyperuricemic nephropathy, Neutropenia, Severe congenital neutropenia, Polycystic liver disease, Prostate cancer, Congenital neutropenia

210
SEC61 translocon subunit alpha 2
-
Prostate cancer, Diabetes mellitus type 2