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Slc36a3os Gene Detail
Summary
  • Symbol
    Slc36a3os
  • Name
    solute carrier family 36 (proton/amino acid symporter), member 3, opposite strand
  • Synonyms
    Gm12233
Location &
Maps
more
  • Sequence Map
    Chr11:55137044-55140193 bp, + strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 11, 32.13 cM
Strain
Comparison
more
  • SNPs within 2kb
    23 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3651340
antisense lncRNA gene Chr11:55131316-55140193 (+)
129S1/SvImJ MGP_129S1SvImJ_G0002962
antisense lncRNA gene Chr11:54650946-54653909 (+)
A/J MGP_AJ_G0002939
antisense lncRNA gene Chr11:52611509-52614570 (+)
AKR/J MGP_AKRJ_G0002920
antisense lncRNA gene Chr11:54331049-54334151 (+)
BALB/cJ MGP_BALBcJ_G0002927
antisense lncRNA gene Chr11:52950983-52954106 (+)
C3H/HeJ MGP_C3HHeJ_G0002882
antisense lncRNA gene Chr11:54271086-54274049 (+)
C57BL/6NJ MGP_C57BL6NJ_G0003068
antisense lncRNA gene Chr11:56307593-56311882 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0002611
antisense lncRNA gene Chr11:50047060-50049842 (+)
CAST/EiJ MGP_CASTEiJ_G0002853
antisense lncRNA gene Chr11:54314492-54317442 (+)
CBA/J MGP_CBAJ_G0002879
antisense lncRNA gene Chr11:58991848-58994811 (+)
DBA/2J MGP_DBA2J_G0002886
antisense lncRNA gene Chr11:52308900-52312043 (+)
FVB/NJ MGP_FVBNJ_G0002904
antisense lncRNA gene Chr11:51971607-51974572 (+)
LP/J MGP_LPJ_G0002961
antisense lncRNA gene Chr11:55103560-55106523 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0002892
antisense lncRNA gene Chr11:60190602-60193565 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0003072
antisense lncRNA gene Chr11:54351436-54354400 (+)
PWK/PhJ MGP_PWKPhJ_G0002811
antisense lncRNA gene Chr11:52873435-52876307 (+)
SPRET/EiJ MGP_SPRETEiJ_G0002760
antisense lncRNA gene Chr11:54151146-54154121 (+)
WSB/EiJ MGP_WSBEiJ_G0002882
antisense lncRNA gene Chr11:53989918-53993025 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    7 phenotype references
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
  • cDNA Data
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000085531 Ensembl Gene Model | MGI Sequence Detail 3150 C57BL/6J ±  kb
transcript ENSMUST00000155883 Ensembl | MGI Sequence Detail 520 Not Applicable  
For the selected sequence
Molecular
Reagents
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  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 13
    Diseases 1
    Phenotypes 7
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:155870 Barlow JL, et al., A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome. Nat Med. 2010 Jan;16(1):59-66

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
07/07/2020
MGI 6.15
The Jackson Laboratory