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Slc4a3 Gene Detail
Summary
  • Symbol
    Slc4a3
  • Name
    solute carrier family 4 (anion exchanger), member 3
  • Synonyms
    A930038D23Rik, Ae3
  • Feature Type
    protein coding gene
  • IDs
    MGI:109350
    NCBI Gene: 20536
  • Alliance
  • Transcription Start Sites
    7 TSS
Location &
Maps
more
  • Sequence Map
    Chr1:75522688-75536075 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 1, 39.16 cM, cytoband C3
  • Mapping Data
    5 experiments
Strain
Comparison
more
  • SNPs within 2kb
    334 from dbSNP Build 142
  • Strain Annotations
    27
  • RFLP
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_109350
protein coding gene Chr1:75522688-75538816 (+)
129S1/SvImJ ENSMUSGG00200054403
protein coding gene Chr1:73189886-73192539 (+)
129S1/SvImJ ENSMUSG00200035044
protein coding gene Chr1:73187059-73188325 (+)
A/J ENSMUSG00195008197
protein coding gene Chr1:72611310-72612576 (+)
A/J ENSMUSGG00195054903
protein coding gene Chr1:72614137-72616790 (+)
AKR/J ENSMUSG00220010061
protein coding gene Chr1:72762087-72763353 (+)
AKR/J ENSMUSGG00220054586
protein coding gene Chr1:72764914-72767567 (+)
BALB/cJ ENSMUSG00180019357
protein coding gene Chr1:72873220-72874486 (+)
BALB/cJ ENSMUSGG00180055337
protein coding gene Chr1:72876047-72878700 (+)
C3H/HeJ ENSMUSGG00175054703
protein coding gene Chr1:73014508-73017161 (+)
C3H/HeJ ENSMUSG00175017669
protein coding gene Chr1:73011681-73012947 (+)
C57BL/6NJ ENSMUSGG00215055718
protein coding gene Chr1:72921373-72924026 (+)
C57BL/6NJ ENSMUSG00215013598
protein coding gene Chr1:72918546-72919812 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0014306
protein coding gene Chr1:69032067-69049602 (+)
CAST/EiJ no annotation
CBA/J ENSMUSG00210032378
protein coding gene Chr1:72701545-72702811 (+)
CBA/J ENSMUSGG00210054932
protein coding gene Chr1:72704372-72707025 (+)
DBA/2J ENSMUSGG00185057695
protein coding gene Chr1:73793320-73795973 (+)
DBA/2J ENSMUSG00185031031
protein coding gene Chr1:73790493-73791759 (+)
FVB/NJ ENSMUSGG00205054252
protein coding gene Chr1:72376370-72379023 (+)
FVB/NJ ENSMUSG00205026473
protein coding gene Chr1:72373543-72374809 (+)
JF1/MsJ no annotation
LP/J ENSMUSG00230009235
protein coding gene Chr1:73780467-73781733 (+)
LP/J ENSMUSGG00230055577
protein coding gene Chr1:73783294-73785947 (+)
NOD/ShiLtJ ENSMUSG00190037427
protein coding gene Chr1:72926973-72928239 (+)
NOD/ShiLtJ ENSMUSGG00190055054
protein coding gene Chr1:72929800-72932453 (+)
NZO/HlLtJ ENSMUSGG00225055253
protein coding gene Chr1:76998038-77000691 (+)
NZO/HlLtJ ENSMUSG00225038491
protein coding gene Chr1:76995211-76996477 (+)
PWK/PhJ no annotation
SPRET/EiJ ENSMSPG00010019521
protein coding gene Chr1:74353042-74368973 (+)
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    SLC4A3, solute carrier family 4 member 3
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLC4A3, solute carrier family 4 member 3
  • Synonyms
    AE3, CAE3/BAE3, SLC2C, SQT7
  • Links
    NCBI Gene ID: 6508
    UniProt: P48751

  • Chr Location
    2q35; chr2:219627011-219641980 (+)  GRCh38

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    9 phenotypes from 2 alleles in 2 genetic backgrounds
    15 phenotypes from multigenic genotypes
    1 images
    33 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.
Homozygotes for one knock-out allele show inner retina defects including selective ERG b-wave depression, optic nerve and retinal vessel anomalies, sheathing of retinal vessels and late onset photoreceptor death. Homozygotes for another knock-out allele are more sensitive to seizure-inducing agents.
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
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 20536 NCBI Gene Model | MGI Sequence Detail 13388 C57BL/6J ±  kb
    transcript NM_009208 RefSeq | MGI Sequence Detail 4441 ZRU/MplStud  
    polypeptide P16283 UniProt | EBI | MGI Sequence Detail 1227 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 71
      Genomic 3
      cDNA 67
      Primer pair 1
      Antibodies 1

      Microarray probesets 4
    Other
    Accession IDs
    less
    MGD-MRK-1169, MGD-MRK-38395, MGI:1925074
    References
    more
    • Summaries
      All 75
      Developmental Gene Expression 5
      Diseases 1
      Gene Ontology 10
      Phenotypes 33
    • Earliest
      J:134667 Roderick TH, et al., Two radiation-induced chromosomal inversions in mice (Mus musculus). Proc Natl Acad Sci U S A. 1970 Oct;67(2):961-7
    • Latest
      J:358138 Morikawa R, et al., The sodium-bicarbonate cotransporter Slc4a5 mediates feedback at the first synapse of vision. Neuron. 2024 Sep 18;

    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