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
12931 to 12940 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12931
Syntaxin 11
FHL4, HLH4, HPLH4
Autoinflammatory syndrome, Developmental disorder, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Scoliosis

12932
Syntaxin 12
STX13, STX14
Diabetes mellitus type 2

12933
Syntaxin 16
SYN-16, SYN16
Pseudohypoparathyroidism

12934
Syntaxin 17
-
Insomnia, Melanoma

12935
Syntaxin 18
Ufe1
Scoliosis

12936
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

12937
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

12938
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

12939
Syntaxin 3
DIAR12, MVID2, RDMVID, STX3A
Color vision deficiency, Microvillus inclusion disease

12940
Syntaxin 4
DFNB123, STX4A, p35-2
Isolated sensorineural deafness, Deafness, Hearing loss, Psoriasis, Nonsyndromic hearing loss, Diabetes mellitus type 2