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Gm11146 Gene Detail
Summary
  • Symbol
    Gm11146
  • Name
    predicted gene 11146
  • Feature Type
    protein coding gene
  • IDs
    MGI:3779400
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr16:77588578-77602094 bp, - strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 44.71 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    87 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3779400
protein coding gene Chr16:77588578-77602094 (-)
129S1/SvImJ MGP_129S1SvImJ_G0022958
protein coding gene Chr16:77717776-77732488 (-)
A/J MGP_AJ_G0022926
protein coding gene Chr16:74286356-74300422 (-)
AKR/J MGP_AKRJ_G0022896
protein coding gene Chr16:76520304-76533824 (-)
BALB/cJ MGP_BALBcJ_G0022928
protein coding gene Chr16:74683132-74696883 (-)
C3H/HeJ MGP_C3HHeJ_G0022690
protein coding gene Chr16:76974393-76989747 (-)
C57BL/6NJ MGP_C57BL6NJ_G0023376
protein coding gene Chr16:80206902-80221549 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0020879
protein coding gene Chr16:72752220-72766494 (-)
CAST/EiJ MGP_CASTEiJ_G0022213
protein coding gene Chr16:77381126-77395336 (-)
CBA/J MGP_CBAJ_G0022660
protein coding gene Chr16:83630275-83643757 (-)
DBA/2J MGP_DBA2J_G0022793
protein coding gene Chr16:74133213-74146693 (-)
FVB/NJ MGP_FVBNJ_G0022768
protein coding gene Chr16:73490293-73503723 (-)
LP/J MGP_LPJ_G0022863
protein coding gene Chr16:77458086-77471741 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0022787
protein coding gene Chr16:86829620-86857350 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0023394
protein coding gene Chr16:76855810-76870251 (-)
PWK/PhJ MGP_PWKPhJ_G0021955
protein coding gene Chr16:74330228-74345356 (-)
SPRET/EiJ MGP_SPRETEiJ_G0021785
protein coding gene Chr16:76471760-76486219 (-)
WSB/EiJ MGP_WSBEiJ_G0022260
protein coding gene Chr16:77074833-77088756 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    7 phenotype references
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
Sequences &
Gene Models
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  • All Sequences
  • UniProt
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000079546 Ensembl Gene Model | MGI Sequence Detail 13517 C57BL/6J ±  kb
transcript ENSMUST00000114231 Ensembl | MGI Sequence Detail 96 Not Applicable  
polypeptide ENSMUSP00000109869 Ensembl | MGI Sequence Detail 32 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
References
more
  • Summaries
    All 11
    Diseases 1
    Phenotypes 7
  • Earliest
    J:202375 Herault Y, et al., Tackling the complexity of the genotype-phenotype relationship in the Down syndrome with the mouse aneuploidy zoo: a resource of new models to study aneuploidies involving human chromosome 21. 2009;:Abstr
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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
09/22/2020
MGI 6.16
The Jackson Laboratory