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Gm10369 Gene Detail
Summary
  • Symbol
    Gm10369
  • Name
    predicted gene 10369
  • Feature Type
    lncRNA gene
  • IDs
    MGI:3642774
    NCBI Gene: 100038504
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr5:134676490-134680145 bp, + strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 5, 74.74 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    89 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3642774
lncRNA gene Chr5:134676118-134680145 (+)
129S1/SvImJ MGP_129S1SvImJ_G0004195
antisense lncRNA gene Chr5:139110949-139114604 (+)
A/J MGP_AJ_G0004174
antisense lncRNA gene Chr5:133198535-133202199 (+)
AKR/J MGP_AKRJ_G0004155
antisense lncRNA gene Chr5:137515197-137518861 (+)
BALB/cJ MGP_BALBcJ_G0004160
antisense lncRNA gene Chr5:134552395-134556050 (+)
C3H/HeJ MGP_C3HHeJ_G0004108
antisense lncRNA gene Chr5:138069942-138073597 (+)
C57BL/6NJ MGP_C57BL6NJ_G0004308
antisense lncRNA gene Chr5:144348214-144351869 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0003785
antisense lncRNA gene Chr5:127484683-127488382 (+)
CAST/EiJ MGP_CASTEiJ_G0004070
antisense lncRNA gene Chr5:137496974-137500629 (+)
CBA/J MGP_CBAJ_G0004102
antisense lncRNA gene Chr5:149978553-149982208 (+)
DBA/2J MGP_DBA2J_G0004118
antisense lncRNA gene Chr5:133091736-133095391 (+)
FVB/NJ MGP_FVBNJ_G0004134
antisense lncRNA gene Chr5:132223247-132226911 (+)
LP/J MGP_LPJ_G0004196
antisense lncRNA gene Chr5:139581755-139585410 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0004124
antisense lncRNA gene Chr5:153023032-153026687 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0004306
antisense lncRNA gene Chr5:137248239-137251894 (+)
PWK/PhJ MGP_PWKPhJ_G0004024
antisense lncRNA gene Chr5:132127830-132131534 (+)
SPRET/EiJ MGP_SPRETEiJ_G0003967
antisense lncRNA gene Chr5:134827535-134831169 (+)
WSB/EiJ MGP_WSBEiJ_G0004106
antisense lncRNA gene Chr5:138000871-138004528 (+)



Homology
less
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
  • UniProt
  • UniGene
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000072573 Ensembl Gene Model | MGI Sequence Detail 3656 C57BL/6J ±  kb
transcript ENSMUST00000100641 Ensembl | MGI Sequence Detail 1148 Not Applicable  
polypeptide Q3UQI0 UniProt | EBI | MGI Sequence Detail 159 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2

    Microarray probesets 1
References
more
  • Summaries
    All 13
    Diseases 2
    Phenotypes 4
  • Earliest
    J:182796 Li HH, et al., Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice. EMBO Mol Med. 2009 Apr;1(1):50-65
  • Latest
    J:216195 Segura-Puimedon M, et al., Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder. Hum Mol Genet. 2014 Dec 15;23(24):6481-94

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
02/18/2020
MGI 6.14
The Jackson Laboratory