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"
1481 to 1490 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1481
Syntaxin 11
FHL4, HLH4, HPLH4
Autoinflammatory syndrome, Developmental disorder, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Scoliosis

1482
Syntaxin 12
STX13, STX14
Diabetes mellitus type 2

1483
Syntaxin 16
SYN-16, SYN16
Pseudohypoparathyroidism

1484
Syntaxin 17
-
Insomnia, Melanoma

1485
Syntaxin 18
Ufe1
Scoliosis

1486
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

1487
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

1488
Syntaxin 2
EPIM, EPM, STX2A, STX2B, STX2C
Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Male infertility, Renal pelvis neoplasms, Spermatogenic failure, Venous thromboembolism

1489
Syntaxin 3
DIAR12, MVID2, RDMVID, STX3A
Color vision deficiency, Microvillus inclusion disease

1490
Syntaxin 4
DFNB123, STX4A, p35-2
Isolated sensorineural deafness, Deafness, Hearing loss, Psoriasis, Nonsyndromic hearing loss, Diabetes mellitus type 2