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Slc2a4 Gene Detail
Summary
  • Symbol
    Slc2a4
  • Name
    solute carrier family 2 (facilitated glucose transporter), member 4
  • Synonyms
    Glut4, Glut-4, twgy
  • Feature Type
    protein coding gene
  • IDs
    MGI:95758
    NCBI Gene: 20528
  • Alliance
    gene page
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:69833365-69839014 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 11, 42.93 cM, cytoband C-E1
  • Mapping Data
    11 experiments
Strain
Comparison
more
  • SNPs within 2kb
    61 from dbSNP Build 142
  • Strain Annotations
    18
  • PCR
    3
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_95758
 protein coding gene Chr11:69833112-69839040 (-)
129S1/SvImJ MGP_129S1SvImJ_G0018571
 protein coding gene Chr11:70431076-70436713 (-)
A/J MGP_AJ_G0018539
 protein coding gene Chr11:67764217-67769853 (-)
AKR/J MGP_AKRJ_G0018508
 protein coding gene Chr11:69786550-69792184 (-)
BALB/cJ MGP_BALBcJ_G0018511
 protein coding gene Chr11:68096183-68101819 (-)
C3H/HeJ MGP_C3HHeJ_G0018324
 protein coding gene Chr11:69823901-69829537 (-)
C57BL/6NJ MGP_C57BL6NJ_G0018962
 protein coding gene Chr11:72557771-72563407 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0016607
 protein coding gene Chr11:64692939-64698577 (-)
CAST/EiJ MGP_CASTEiJ_G0017879
 protein coding gene Chr11:70066712-70072358 (-)
CBA/J MGP_CBAJ_G0018296
 protein coding gene Chr11:75810322-75816217 (-)
DBA/2J MGP_DBA2J_G0018406
 protein coding gene Chr11:67350244-67355892 (-)
FVB/NJ MGP_FVBNJ_G0018396
 protein coding gene Chr11:66995831-67001464 (-)
LP/J MGP_LPJ_G0018476
 protein coding gene Chr11:71014090-71019727 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0018419
 protein coding gene Chr11:76400830-76406466 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0019004
 protein coding gene Chr11:70059747-70065383 (-)
PWK/PhJ MGP_PWKPhJ_G0017653
 protein coding gene Chr11:68002344-68008065 (-)
SPRET/EiJ MGP_SPRETEiJ_G0017443
 protein coding gene Chr11:69875742-69881383 (-)
WSB/EiJ MGP_WSBEiJ_G0017933
 protein coding gene Chr11:69723847-69729490 (-)



Homology
more
  • Human Ortholog
    SLC2A4, solute carrier family 2 member 4
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLC2A4, solute carrier family 2 member 4
  • Synonyms
    GLUT4
  • Links
    NCBI Gene ID: 6517
    neXtProt AC: NX_P14672
    UniProt: P14672

  • Chr Location
    17p13.1; chr17:7281718-7288257 (+)  GRCh38
Human Diseases
more
  • Diseases
    1 with Slc2a4 mouse models; 1 with human SLC2A4 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
    57 phenotypes from 3 alleles in 11 genetic backgrounds
    5 phenotypes from multigenic genotypes
    65 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.
Homozygous inactivation of this gene causes impaired glucose metabolism in skeletal muscle and adipose tissue. Mice homozygous for a knock-out allele show premature death associated with cardiac hypertrophy, growth retardation, insulin resistance, reduced adipose tissue deposits, and muscle fatigue.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    76
  • GO References
    35
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
non-membrane-bounded 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
    998
  • Tissues
    184
  • cDNA Data
    50
  • Literature Summary
    38
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000018566 Ensembl Gene Model | MGI Sequence Detail 5650 C57BL/6J ±  kb
    transcript ENSMUST00000018710 Ensembl | MGI Sequence Detail 2524 Not Applicable  
    polypeptide ENSMUSP00000018710 Ensembl | MGI Sequence Detail 509 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 67
      Genomic 2
      cDNA 52
      Primer pair 8
      Other 5

      Microarray probesets 4
    Other
    Accession IDs
    less
    MGD-MRK-10158, MGD-MRK-10162, MGI:3588496
    References
    more
    • Summaries
      All 338
      Developmental Gene Expression 38
      Diseases 1
      Gene Ontology 35
      Phenotypes 65
    • Earliest
      J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
    • Latest
      J:331835 Salazar-Petres E, et al., Placental structure, function, and mitochondrial phenotype relate to fetal size in each fetal sex in mice. Biol Reprod. 2022 Jun 13;106(6):1292-1311
    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
    04/16/2024
    MGI 6.23     		The Jackson Laboratory