syntaxin-binding protein 2 isoform a [Homo sapiens] - Protein (original) (raw)
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Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More... - Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More... - Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.
Articles about the STXBP2 gene
- STXBP2-R190C Variant in a Patient With Neonatal Hemophagocytic Lymphohistiocytosis (HLH) and G6PD Deficiency Reveals a Critical Role of STXBP2 Domain 2 on Granule Exocytosis. [Front Immunol. 2020]
STXBP2-R190C Variant in a Patient With Neonatal Hemophagocytic Lymphohistiocytosis (HLH) and G6PD Deficiency Reveals a Critical Role of STXBP2 Domain 2 on Granule Exocytosis.
Benavides N, Spessott WA, Sanmillan ML, Vargas M, Livingston MS, Erickson N, Pozos TC, McCormick ME, Scharrig E, Messinger YH, et al. Front Immunol. 2020; 11:545414. Epub 2020 Oct 8. - MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. [Hum Mutat. 2018]
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.
Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, et al. Hum Mutat. 2018 Mar; 39(3):333-344. Epub 2018 Jan 17. - Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations. [JCI Insight. 2017]
Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations.
Vogel GF, van Rijn JM, Krainer IM, Janecke AR, Posovszky C, Cohen M, Searle C, Jantchou P, Escher JC, Patey N, et al. JCI Insight. 2017 Jul 20; 2(14). Epub 2017 Jul 20.
More about the STXBP2 gene
Related information
- BioProject
Proteins related to BioProjects - Nucleotide
Nucleotide sequence from coding region - PubMed
PubMed articles cited by protein sequence record - Taxonomy
Taxonomy sequences associated with protein record - BioSystems
BioSystems - CCDS
Link to Consensus CDS - CDD Search Results
Display conserved domains within a protein - Conserved Domains (Concise)
Link to a concise list of conserved domains in a protein - Conserved Domains (Full)
Link to conserved domains within a protein - Domain Relatives
Display proteins with similar conserved domain architecture - Encoding mRNA
Link from protein to encoding mRNA - Full text in PMC
Free full text articles in PMC - Gene
Link to related Genes - Genome
Genome record encoding protein sequence - Identical Structures
3D structures for identical protein sequences - OMIM
OMIM records associated with protein sequence - Protein (UniProtKB)
Protein gi (refseq) to protein gi (UniProtKB) - PubMed (RefSeq)
Link to RefSeq PubMed articles - PubMed (Weighted)
Links to pubmed - Related Structures (List)
List of related structures - SNP
Related SNPs
LinkOut to external resources
- Ensembl [Ensembl]
Ensembl - OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource - Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System - reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome - Find Quality Antibodies [GeneTex Inc]
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Finds sub-sequence or patterns in the sequence and highlights the matching region. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences.
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