Homo sapiens (human): 6804 Help Entry 6804              CDS       T01001                                  Symbol STX1A, HPC-1, P35-1, STX1, SYN1A Name (RefSeq) syntaxin 1A   KO K04560   syntaxin 1A Organism hsa  Homo sapiens (human) Pathway hsa04130   SNARE interactions in vesicular transport hsa04721   Synaptic vesicle cycle hsa04911   Insulin secretion hsa05016   Huntington disease hsa05022   Pathways of neurodegeneration - multiple diseases hsa05031   Amphetamine addiction Network nt06410  Calcium signaling nt06461  Huntington disease   Element N00986   Mutation-caused aberrant Htt to VGCC-Ca2+ -apoptotic pathway Disease H01439   Williams-Beuren syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    04130 SNARE interactions in vesicular transport     6804 (STX1A)  09150 Organismal Systems   09152 Endocrine system    04911 Insulin secretion     6804 (STX1A)   09156 Nervous system    04721 Synaptic vesicle cycle     6804 (STX1A)  09160 Human Diseases   09164 Neurodegenerative disease    05016 Huntington disease     6804 (STX1A)    05022 Pathways of neurodegeneration - multiple diseases     6804 (STX1A)   09165 Substance dependence    05031 Amphetamine addiction     6804 (STX1A)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:hsa04131]     6804 (STX1A) Membrane trafficking [BR:hsa04131]  SNARE   Syntaxin (Qa)    Stx-PM     6804 (STX1A) BRITE hierarchyBRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Syntaxin SNARE Syntaxin_2 AAA_13 Ferritin GNVR PspA_IM30 DUF5856 Prominin DUF6664 Laminin_II FAD_binding_1 DUF1910 FlgN Syntaxin-6_N Lzipper-MIP1 SIMPL ANIS5_cation-bd FapA Lipoprotein_2 Motif Other DBs NCBI-GeneID:  6804 NCBI-ProteinID:  NP_004594 OMIM:  186590 HGNC:  11433 Ensembl:  ENSG00000106089 Pharos:  Q16623(Tbio) UniProt:  Q16623 Q75ME0 LinkDB All DBs Position 7:complement(73699210..73719669) Genome browser AA seq 288 aa AA seqDB search MKDRTQELRTAKDSDDDDDVAVTVDRDRFMDEFFEQVEEIRGFIDKIAENVEEVKRKHSA ILASPNPDEKTKEELEELMSDIKKTANKVRSKLKSIEQSIEQEEGLNRSSADLRIRKTQH STLSRKFVEVMSEYNATQSDYRERCKGRIQRQLEITGRTTTSEELEDMLESGNPAIFASG IIMDSSISKQALSEIETRHSEIIKLENSIRELHDMFMDMAMLVESQGEMIDRIEYNVEHA VDYVERAVSDTKKAVKYQSKARRKKIMIIICCVILGIVIASTVGGIFA NT seq 867 nt NT seq  +upstreamnt  +downstreamnt atgaaggaccgaacccaggagctccgcacggccaaggacagcgatgatgatgatgatgtc gctgtcaccgtggaccgagaccgcttcatggatgagttctttgagcaggtggaggagatt cgaggcttcattgacaagatcgcagagaacgtggaggaggtgaagcggaagcacagtgcc atcctggcatcccccaaccccgatgagaagacgaaggaggagctggaagaactcatgtcc gacataaagaagacagcaaacaaagttcgttccaagttaaagagcatcgagcagtccatc gagcaagaggaaggcctgaaccgctcctccgctgacctgaggatccggaagacacagcac tccacgctgtccagaaagtttgtggaggtcatgtcggagtacaacgccacgcagtccgac taccgcgagcgctgcaaaggccgcatccagaggcagctggagatcaccggcaggaccacg accagtgaggagctggaggacatgctggagagtgggaaccccgccatctttgcctctggg atcatcatggactccagcatctcgaagcaggctctgagcgagattgagacgcggcacagt gagatcatcaagctggagaacagcatccgtgagctacacgacatgttcatggacatggcc atgctcgtggagagccagggagagatgattgacaggatcgagtacaatgtggaacacgcg gtagactatgtggagagggccgtgtctgacaccaagaaggccgtcaagtaccagagcaag gcgcgccggaagaaaatcatgatcatcatctgctgtgtgatcctgggcatcgtcatcgcc tccactgttgggggcatcttcgcctag

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