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Stx11 Gene Detail
Summary
  • Symbol
    Stx11
  • Name
    syntaxin 11
  • Synonyms
    5830405C08Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1921982
    NCBI Gene: 74732
  • Alliance
    gene page
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:12813953-12840042 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 10, 4.54 cM, cytoband A2
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1159 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1921982
 protein coding gene Chr10:12813953-12840242 (-)
129S1/SvImJ MGP_129S1SvImJ_G0017016
 protein coding gene Chr10:10327801-10354856 (-)
A/J MGP_AJ_G0016994
 protein coding gene Chr10:9938554-9962608 (-)
AKR/J MGP_AKRJ_G0016958
 protein coding gene Chr10:10170118-10195691 (-)
BALB/cJ MGP_BALBcJ_G0016952
 protein coding gene Chr10:9941139-9965126 (-)
C3H/HeJ MGP_C3HHeJ_G0016777
 protein coding gene Chr10:10323082-10351937 (-)
C57BL/6NJ MGP_C57BL6NJ_G0017414
 protein coding gene Chr10:10614484-10637967 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0015119
 protein coding gene Chr10:9214597-9238825 (-)
CAST/EiJ MGP_CASTEiJ_G0016359
 protein coding gene Chr10:10182066-10208284 (-)
CBA/J MGP_CBAJ_G0016749
 protein coding gene Chr10:10994429-11023627 (-)
DBA/2J MGP_DBA2J_G0016857
 protein coding gene Chr10:9842229-9871803 (-)
FVB/NJ MGP_FVBNJ_G0016852
 protein coding gene Chr10:9690733-9715044 (-)
LP/J MGP_LPJ_G0016932
 protein coding gene Chr10:10183967-10213358 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0016882
 protein coding gene Chr10:10914830-10939523 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0017452
 protein coding gene Chr10:10054849-10080182 (-)
PWK/PhJ MGP_PWKPhJ_G0016144
 protein coding gene Chr10:9727380-9753157 (-)
SPRET/EiJ MGP_SPRETEiJ_G0015927
 protein coding gene Chr10:10171975-10203710 (-)
WSB/EiJ MGP_WSBEiJ_G0016421
 protein coding gene Chr10:10082675-10113606 (-)



Homology
more
  • Human Ortholog
    STX11, syntaxin 11
  • Vertebrate Orthologs
    5
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    STX11, syntaxin 11
  • Synonyms
    FHL4, HLH4, HPLH4
  • Links
    NCBI Gene ID: 8676
    neXtProt AC: NX_O75558
    UniProt: O75558

  • Chr Location
    6q24.2; chr6:144139963-144191939 (+)  GRCh38
Human Diseases
more
  • Diseases
    1 with Stx11 mouse models; 1 with human STX11 associations

Human Disease Mouse Models
      
IDs
 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    32 phenotypes from 3 alleles in 3 genetic backgrounds
    14 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for a knock-out allele exhibit defective CTL degranulation and symptoms of hemophagocytic lymphohistiocytosis following infection with LMCV.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    22
  • GO References
    7
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    811
  • Tissues
    14
  • cDNA Data
    18
  • Literature Summary
    3
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000039232 Ensembl Gene Model | MGI Sequence Detail 26090 C57BL/6J ±  kb
    transcript ENSMUST00000163425 Ensembl | MGI Sequence Detail 4032 Not Applicable  
    polypeptide ENSMUSP00000132758 Ensembl | MGI Sequence Detail 287 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 20
      cDNA 18
      Primer pair 2

      Microarray probesets 4
    References
    more
    • Summaries
      All 42
      Developmental Gene Expression 3
      Diseases 1
      Gene Ontology 7
      Phenotypes 14
    • Earliest
      J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
    • Latest
      J:348041 Kogl T, et al., Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect. J Exp Med. 2024 Jul 1;221(7)
    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
    Citing These Resources
    Funding Information
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    Send questions and comments to User Support.     		last database update
    11/12/2024
    MGI 6.24     		The Jackson Laboratory