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Slc16a11 Gene Detail
Summary
  • Symbol
    Slc16a11
  • Name
    solute carrier family 16 (monocarboxylic acid transporters), member 11
  • Synonyms
    MNCb-2717
  • Feature Type
    protein coding gene
  • IDs
    MGI:2663709
    NCBI Gene: 216867
  • Alliance
  • Transcription Start Sites
    9 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:70104717-70107239 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 11, 42.99 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    42 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2663709
protein coding gene Chr11:70103578-70107243 (+)
129S1/SvImJ MGP_129S1SvImJ_G0018584
protein coding gene Chr11:70733291-70736956 (+)
A/J MGP_AJ_G0018552
protein coding gene Chr11:68044607-68048272 (+)
AKR/J MGP_AKRJ_G0018521
protein coding gene Chr11:70075088-70078753 (+)
BALB/cJ MGP_BALBcJ_G0018524
protein coding gene Chr11:68367385-68371050 (+)
C3H/HeJ MGP_C3HHeJ_G0018337
protein coding gene Chr11:70113418-70117083 (+)
C57BL/6NJ MGP_C57BL6NJ_G0018975
protein coding gene Chr11:72831359-72835024 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0016620
protein coding gene Chr11:64962884-64966533 (+)
CAST/EiJ MGP_CASTEiJ_G0017892
protein coding gene Chr11:70358829-70362488 (+)
CBA/J MGP_CBAJ_G0018309
protein coding gene Chr11:76139519-76143184 (+)
DBA/2J MGP_DBA2J_G0018419
protein coding gene Chr11:67620332-67623994 (+)
FVB/NJ MGP_FVBNJ_G0018409
protein coding gene Chr11:67275852-67279517 (+)
LP/J MGP_LPJ_G0018489
protein coding gene Chr11:71302973-71306638 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0018432
protein coding gene Chr11:76708668-76712333 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0019017
protein coding gene Chr11:70346891-70350556 (+)
PWK/PhJ MGP_PWKPhJ_G0017666
protein coding gene Chr11:68273672-68277399 (+)
SPRET/EiJ MGP_SPRETEiJ_G0017456
protein coding gene Chr11:70144282-70147969 (+)
WSB/EiJ MGP_WSBEiJ_G0017946
protein coding gene Chr11:70009784-70013444 (+)



Homology
more
  • Human Ortholog
    SLC16A11, solute carrier family 16 member 11
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLC16A11, solute carrier family 16 member 11
  • Synonyms
    MCT 11, MCT11
  • Links
    NCBI Gene ID: 162515
    neXtProt AC: NX_Q8NCK7
    UniProt: Q8NCK7

  • Chr Location
    17p13.1; chr17:7041621-7044092 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    19 phenotype references
Homozygous null mice show no significant metabolic defects.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
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
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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
  • Tissues
  • cDNA Data
  • Literature Summary
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 216867 NCBI Gene Model | MGI Sequence Detail 2523 C57BL/6J ±  kb
transcript NM_001416062 RefSeq | MGI Sequence Detail 1680 C57BL/6  
polypeptide Q5NC32 UniProt | EBI | MGI Sequence Detail 447 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 10
    cDNA 9
    Primer pair 1

    Microarray probesets 3
References
more
  • Summaries
    All 42
    Developmental Gene Expression 2
    Gene Ontology 5
    Phenotypes 19
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:348785 Zhang D, et al., Maternal Ezh1/2 deficiency impairs the function of mitochondria in mouse oocytes and early embryos. J Cell Physiol. 2024 Mar 26;

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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory