STXBP2 (syntaxin binding protein 2)

2016-10-01  

Identity

HGNC
LOCATION
19p13.2
LOCUSID
ALIAS
FHL5,Hunc18b,MUNC18-2,UNC18-2,UNC18B,pp10122
FUSION GENES

Other Information

Locus ID:

NCBI: 6813
MIM: 601717
HGNC: 11445
Ensembl: ENSG00000076944

Variants:

dbSNP: 6813
ClinVar: 6813
TCGA: ENSG00000076944
COSMIC: STXBP2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000076944ENST00000221283Q15833
ENSG00000076944ENST00000414284Q15833
ENSG00000076944ENST00000441779Q15833
ENSG00000076944ENST00000593535M0QZ54
ENSG00000076944ENST00000595950M0R0D4
ENSG00000076944ENST00000597068M0R0M7
ENSG00000076944ENST00000599400M0R376
ENSG00000076944ENST00000599737M0R118
ENSG00000076944ENST00000600702M0R1A1
ENSG00000076944ENST00000602355R4GMY7
ENSG00000076944ENST00000612033A0A087WUN8

Expression (GTEx)

0
50
100
150
200
250
300

Pathways

PathwaySourceExternal ID
HemostasisREACTOMER-HSA-109582
Platelet activation, signaling and aggregationREACTOMER-HSA-76002
Response to elevated platelet cytosolic Ca2+REACTOMER-HSA-76005
Platelet degranulationREACTOMER-HSA-114608

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA166182763emapalumabChemicalLabelAnnotationassociated

References

Pubmed IDYearTitleCitations
343395482021Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis.3
343395482021Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis.3
316517262020Different Clinical Presentation of 3 Children With Familial Hemophagocytic Lymphohistiocytosis With 2 Novel Mutations.2
331629742020STXBP2-R190C Variant in a Patient With Neonatal Hemophagocytic Lymphohistiocytosis (HLH) and G6PD Deficiency Reveals a Critical Role of STXBP2 Domain 2 on Granule Exocytosis.5
316517262020Different Clinical Presentation of 3 Children With Familial Hemophagocytic Lymphohistiocytosis With 2 Novel Mutations.2
331629742020STXBP2-R190C Variant in a Patient With Neonatal Hemophagocytic Lymphohistiocytosis (HLH) and G6PD Deficiency Reveals a Critical Role of STXBP2 Domain 2 on Granule Exocytosis.5
295997802018Bi-Allelic Mutations in STXBP2 Reveal a Complementary Role for STXBP1 in Cytotoxic Lymphocyte Killing.12
303647842018Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2-Deficient Intestinal Organoids.16
295997802018Bi-Allelic Mutations in STXBP2 Reveal a Complementary Role for STXBP1 in Cytotoxic Lymphocyte Killing.12
303647842018Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2-Deficient Intestinal Organoids.16
277813872017Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study.29
281630422017Munc18b Increases Insulin Granule Fusion, Restoring Deficient Insulin Secretion in Type-2 Diabetes Human and Goto-Kakizaki Rat Islets with Improvement in Glucose Homeostasis.11
283804452017Identification of STXBP2 as a novel susceptibility locus for myocardial infarction in Japanese individuals by an exome-wide association study.9
290442932017Down Regulation of the Munc18b-syntaxin-11 Complex and β1-tubulin Impairs Secretion and Spreading in Neonatal Platelets.16
277813872017Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study.29

Citation

Dessen P

STXBP2 (syntaxin binding protein 2)

Atlas Genet Cytogenet Oncol Haematol. 2016-10-01

Online version: http://atlasgeneticsoncology.org/gene/56387/favicon/js/lib/popper.js