Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1491 to 1500 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1491
Syntaxin 18
Ufe1
Scoliosis

1492
Syntaxin 1A
HPC-1, P35-1, STX1, SYN1A
Autism, Neurodevelopmental disorder, Creutzfeldt-jakob disease, Cystic fibrosis, Hirschsprung disease, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Williams syndrome

1493
Syntaxin 1B
GEFSP9, STX1B1, STX1B2
Epilepsy, Generalized epilepsy, Developmental and epileptic encephalopathy, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Neurodevelopmental disorder, Neurotic disorder, Parkinson disease, Psoriasis, Psoriasis vulgaris, Seizures, Diabetes mellitus, type 2

1494
Syntaxin 2
EPIM, EPM, STX2A, STX2B, STX2C
Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Male infertility, Renal pelvis neoplasm, Spermatogenic failure, Venous thromboembolism

1495
Syntaxin 3
DIAR12, MVID2, RDMVID, STX3A
Color vision deficiency, Microvillus inclusion disease

1496
Syntaxin 4
DFNB123, STX4A, p35-2
Isolated sensorineural deafness, Deafness, Hearing loss, Psoriasis, Nonsyndromic hearing loss, Diabetes mellitus, type 2

1497
Syntaxin 5
CDG2AA, SED5, STX5A
Congenital disorder of glycosylation

1498
Syntaxin 6
-
Neuronal ceroid lipofuscinosis, Insomnia, Nonalcoholic fatty liver disease, Progressive supranuclear palsy, Creutzfeldt-jakob disease, Diabetes mellitus, type 2

1499
Syntaxin 7
-
Cutaneous leishmaniasis, Cortical development malformation

1500
Syntaxin 8
CARB
Alzheimer disease, Central nervous system cancer, Diabetic neuropathy, Glioblastoma, Glioma, Hyperopia, Obstructive sleep apnea syndrome