Detailed description page of humcfs

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STX1A details
Primary information
gene_nameSTX1A
Humcfs IdHumcfs_2234
chromosome_numberchromosome7
nameFRA7J
chrlocation59900001-77500000
cytoband7q11
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000106089
havana_transcript_idOTTHUMT00000268431
gene_location73700729-73719657
gene_orientation-
exon_idENSE00001827783, ENSE00001520737, ENSE00003486867, ENSE00003488858, ENSE00003597685, ENSE00003577314, ENSE00003657220, ENSE00003519598, ENSE00001928326
exon_number9
gene_descriptionsyntaxin 1A (brain)
disease_descriptionAsymptomatic Infections,Overweight,Shigella Infections,Autistic Disorder,High-functioning autism,Hemolytic-Uremic Syndrome,Malignant neoplasm of pancreas,Benign neonatal epilepsy,Attention deficit hyperactivity disorder,Adenoma,Hemorrhagic diarrhea,Cystic Fibrosis,Mental Retardation,Cocaine Dependence,Uremia syndrome,Diabetes Mellitus, Non-Insulin-Dependent,Diabetes,Parathyroid Neoplasms,Diarrhea,Pancreatic carcinoma,Williams Syndrome,Enteritis due to specified virus,Diabetes Mellitus,Obesity,Kidney Failure, Chronic,Disease caused by Shigella dysenteriae,Epilepsy,Familial benign neonatal epilepsy,Impaired glucose tolerance,Schizophrenia,Alzheimer's Disease,Diarrhea-associated hemolytic uremic syndrome,Tumor necrosis,Migraine Disorders,Hereditary pancreatitis
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID16236432
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