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Slco3a1 Gene Detail
Summary
  • Symbol
    Slco3a1
  • Name
    solute carrier organic anion transporter family, member 3a1
  • Synonyms
    5830414C08Rik, Anr1, MJAM, OATP-D, Slc21a11
  • Feature Type
    protein coding gene
  • IDs
    MGI:1351867
    NCBI Gene: 108116
  • Alliance
  • Transcription Start Sites
    29 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:73925167-74204528 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 7, 42.95 cM, cytoband D1
  • Mapping Data
    3 experiments
Strain
Comparison
more
  • SNPs within 2kb
    9068 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1351867
protein coding gene Chr7:73925166-74204528 (-)
129S1/SvImJ ENSMUSG00200011593
protein coding gene Chr7:60703107-60989288 (-)
A/J ENSMUSG00195013798
protein coding gene Chr7:65101012-65386806 (-)
AKR/J ENSMUSG00220020325
protein coding gene Chr7:58646739-58932535 (-)
BALB/cJ ENSMUSG00180013225
protein coding gene Chr7:61806544-62092351 (-)
C3H/HeJ ENSMUSG00175020318
protein coding gene Chr7:62604193-62890361 (-)
C57BL/6NJ ENSMUSG00215024979
protein coding gene Chr7:61727231-62006754 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0029863
protein coding gene Chr7:76774886-77058655 (-)
CAST/EiJ ENSTCUG00005004025
protein coding gene Chr7:65229487-65517175 (-)
CBA/J ENSMUSG00210023782
protein coding gene Chr7:62462721-62748879 (-)
DBA/2J ENSMUSG00185000925
protein coding gene Chr7:66785504-67071673 (-)
FVB/NJ ENSMUSG00205017424
protein coding gene Chr7:62432622-62717168 (-)
JF1/MsJ ENSUMUG00000024331
protein coding gene Chr7:71522475-71803325 (-)
LP/J ENSMUSG00230011070
protein coding gene Chr7:72840204-73125954 (-)
NOD/ShiLtJ ENSMUSG00190016331
protein coding gene Chr7:62557590-62843171 (-)
NZO/HlLtJ ENSMUSG00225041947
protein coding gene Chr7:71101771-71387494 (-)
PWK/PhJ ENSLUMG00010015711
protein coding gene Chr7:61078154-61358617 (-)
SPRET/EiJ ENSMSPG00010020052
protein coding gene Chr7:61491329-61775310 (-)
WSB/EiJ ENSIUOG00005018383
protein coding gene Chr7:62939982-63238725 (-)



Homology
more
  • Human Ortholog
    SLCO3A1, solute carrier organic anion transporter family member 3A1
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLCO3A1, solute carrier organic anion transporter family member 3A1
  • Synonyms
    OATP3A1, OATP-D, OATPD, OATP-RP3, OATPRP3, SLC21A11
  • Links
    NCBI Gene ID: 28232
    UniProt: Q9UIG8

  • Chr Location
    15q26.1; chr15:91853708-92172435 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    5 phenotypes from 1 allele in 1 genetic background
    15 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 for a null endonuclease-mediated mutation exhibit shorter survival times, increased hepatic levels of bile acid, and develop more liver injury after induction of cholestasis.
Gene Ontology
(GO)
Classifications
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  • 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
  • Comparison Matrix
  • Sequences &
    Gene Models
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    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000025790 Ensembl Gene Model | MGI Sequence Detail 279362 C57BL/6J ±  kb
    transcript ENSMUST00000026897 Ensembl | MGI Sequence Detail 4589 Not Applicable  
    polypeptide ENSMUSP00000026897 Ensembl | MGI Sequence Detail 710 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 90
      cDNA 88
      Primer pair 2

      Microarray probesets 4
    Other
    Accession IDs
    less
    MGI:1328325, MGI:1926070, MGI:2142386
    References
    more
    • Summaries
      All 58
      Developmental Gene Expression 5
      Gene Ontology 10
      Phenotypes 15
    • Earliest
      J:88307 Giometti CS, et al., The analysis of recessive lethal mutations in mice by using two-dimensional gel electrophoresis of liver proteins. Mutat Res. 1990 Sep;242(1):47-55
    • Latest
      J:284228 Ikegami K, et al., Effect of expression alteration in flanking genes on phenotypes of St8sia2-deficient mice. Sci Rep. 2019 Sep 20;9(1):13634

    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)
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    Funding Information
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    last database update
    09/08/2026
    MGI 6.24
    The Jackson Laboratory