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Gm56188 Gene Detail
Summary
  • Symbol
    Gm56188
  • Name
    predicted gene, 56188
Location &
Maps
more
  • Sequence Map
    Chr2:74531350-74531486 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 2, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    36 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_6848834
miRNA gene Chr2:74531350-74531486 (-)
129S1/SvImJ ENSMUSG00200004108
miRNA gene Chr2:71579982-71580118 (-)
A/J ENSMUSG00195019774
miRNA gene Chr2:71726686-71726822 (-)
AKR/J ENSMUSG00220002351
miRNA gene Chr2:71691319-71691455 (-)
BALB/cJ ENSMUSG00180007081
miRNA gene Chr2:71680341-71680477 (-)
C3H/HeJ ENSMUSG00175011204
miRNA gene Chr2:71806236-71806372 (-)
C57BL/6NJ ENSMUSG00215031277
miRNA gene Chr2:71643183-71643319 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005031328
miRNA gene Chr2:71120092-71120228 (-)
CBA/J ENSMUSG00210002415
miRNA gene Chr2:71848892-71849028 (-)
DBA/2J ENSMUSG00185011869
miRNA gene Chr2:71684737-71684873 (-)
FVB/NJ ENSMUSG00205020863
miRNA gene Chr2:71136717-71136853 (-)
JF1/MsJ ENSUMUG00000044083
miRNA gene Chr2:71361911-71362047 (-)
LP/J ENSMUSG00230026168
miRNA gene Chr2:73479570-73479706 (-)
NOD/ShiLtJ ENSMUSG00190010879
miRNA gene Chr2:71759445-71759581 (-)
NZO/HlLtJ ENSMUSG00225015234
miRNA gene Chr2:81243637-81243773 (-)
PWK/PhJ ENSLUMG00010032652
miRNA gene Chr2:71600235-71600371 (-)
SPRET/EiJ ENSMSPG00010022292
miRNA gene Chr2:73000208-73000343 (-)
WSB/EiJ ENSIUOG00005011413
miRNA gene Chr2:71802718-71802854 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00002076500 Ensembl Gene Model | MGI Sequence Detail 137 C57BL/6J ±  kb
transcript ENSMUST00020182558 Ensembl | MGI Sequence Detail 137 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:308920 Bolt CC, et al., Mesomelic dysplasias associated with the HOXD locus are caused by regulatory reallocations. Nat Commun. 2021 Aug 18;12(1):5013

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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last database update
09/08/2026
MGI 6.24
The Jackson Laboratory