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Slc22a20 Gene Detail
Summary
  • Symbol
    Slc22a20
  • Name
    solute carrier family 22 (organic anion transporter), member 20
  • Synonyms
    LOC381203, mOAT6
Location &
Maps
more
  • Sequence Map
    Chr19:6020262-6036171 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 19, 4.34 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    524 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2685809
 protein coding gene Chr19:6020262-6036171 (-)
129S1/SvImJ ENSMUSG00200045320
 protein coding gene Chr19:2782672-2798588 (-)
A/J ENSMUSG00195046000
 protein coding gene Chr19:3177990-3193913 (-)
AKR/J ENSMUSG00220046624
 protein coding gene Chr19:2951121-2967024 (-)
BALB/cJ ENSMUSG00180036956
 protein coding gene Chr19:3552707-3568632 (-)
C3H/HeJ ENSMUSG00175011146
 protein coding gene Chr19:2802886-2818803 (-)
C57BL/6NJ ENSMUSG00215044015
 protein coding gene Chr19:3020991-3036917 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0022581
 protein coding gene Chr19:2751661-2768781 (-)
CAST/EiJ ENSTCUG00005042463
 protein coding gene Chr19:2939141-2954716 (-)
CBA/J ENSMUSG00210033213
 protein coding gene Chr19:2805633-2821539 (-)
DBA/2J ENSMUSG00185043635
 protein coding gene Chr19:3182122-3198024 (-)
FVB/NJ ENSMUSG00205046645
 protein coding gene Chr19:3188186-3204074 (-)
JF1/MsJ ENSUMUG00000049314
 protein coding gene Chr19:3156623-3172261 (-)
LP/J ENSMUSG00230052760
 protein coding gene Chr19:4089568-4105474 (-)
NOD/ShiLtJ ENSMUSG00190028197
 protein coding gene Chr19:2712488-2728380 (-)
NZO/HlLtJ ENSMUSG00225024910
 protein coding gene Chr19:7798374-7814284 (-)
PWK/PhJ ENSLUMG00010005189
 protein coding gene Chr19:2922408-2937992 (-)
SPRET/EiJ ENSMSPG00010044637
 protein coding gene Chr19:2913184-2928070 (-)
WSB/EiJ ENSIUOG00005038533
 protein coding gene Chr19:2825843-2841721 (-)



Homology
more
  • Human Ortholog
    SLC22A20P, solute carrier family 22 member 20, pseudogene
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLC22A20P, solute carrier family 22 member 20, pseudogene
  • Synonyms
    Oat6, SLC22A20
  • Links
    NCBI Gene ID: 440044
    UniProt: A6NK97

  • Chr Location
    11q13.1; chr11:65213840-65242757 (+)  GRCh38
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    10
  • GO References
    5
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
    611
  • Tissues
    11
  • cDNA Data
    6
  • Literature Summary
    2
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 381203 NCBI Gene Model | MGI Sequence Detail 15910 C57BL/6J ±  kb
transcript NM_198650 RefSeq | MGI Sequence Detail 1897 C57BL/6  
polypeptide Q80UJ1 UniProt | EBI | MGI Sequence Detail 556 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR005828 Major facilitator, sugar transporter-like
    IPR020846 Major facilitator superfamily domain
    IPR036259 MFS transporter superfamily
  • GlyGen
    Q80UJ1 4 sites
Molecular
Reagents
less
  • All nucleic 8
    cDNA 6
    Primer pair 2

    Microarray probesets 1
References
more
  • Summaries
    All 27
    Developmental Gene Expression 2
    Gene Ontology 5
    Phenotypes 4
  • Earliest
    J:86696 Zambrowicz BP, et al., Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14109-14
  • Latest
    J:153498 Diez-Roux G, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582
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
09/08/2026
MGI 6.24 		The Jackson Laboratory