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Gm10369 Gene Detail
Summary
  • Symbol
    Gm10369
  • Name
    predicted gene 10369
Location &
Maps
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  • 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
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  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    6 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
Interactions
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Sequences &
Gene Models
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  • 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
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  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2

    Microarray probesets 1
References
more
  • Summaries
    All 15
    Diseases 2
    Phenotypes 6
  • 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:287750 Jimenez-Altayo F, et al., Stenosis coexists with compromised alpha1-adrenergic contractions in the ascending aorta of a mouse model of Williams-Beuren syndrome. Sci Rep. 2020 Jan 21;10(1):889

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
01/12/2021
MGI 6.16
The Jackson Laboratory