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Gm56191 Gene Detail
Summary
  • Symbol
    Gm56191
  • Name
    predicted gene, 56191
Location &
Maps
more
  • Sequence Map
    Chr2:74765759-74765858 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
    161 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_6848840
rRNA gene Chr2:74765759-74765858 (-)
129S1/SvImJ ENSMUSG00200004452
rRNA gene Chr2:71814595-71814694 (-)
A/J ENSMUSG00195021323
rRNA gene Chr2:71961354-71961453 (-)
AKR/J ENSMUSG00220002563
rRNA gene Chr2:71926010-71926109 (-)
BALB/cJ ENSMUSG00180007054
rRNA gene Chr2:71915029-71915128 (-)
C3H/HeJ ENSMUSG00175011408
rRNA gene Chr2:72040960-72041059 (-)
C57BL/6NJ ENSMUSG00215030640
rRNA gene Chr2:71877790-71877889 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005031779
rRNA gene Chr2:71362413-71362512 (-)
CBA/J ENSMUSG00210002669
rRNA gene Chr2:72083599-72083698 (-)
DBA/2J ENSMUSG00185011759
rRNA gene Chr2:71919467-71919566 (-)
FVB/NJ ENSMUSG00205019895
rRNA gene Chr2:71371370-71371469 (-)
JF1/MsJ ENSUMUG00000043369
rRNA gene Chr2:71595189-71595288 (-)
LP/J ENSMUSG00230027259
rRNA gene Chr2:73714206-73714305 (-)
NOD/ShiLtJ ENSMUSG00190011426
rRNA gene Chr2:71994064-71994163 (-)
NZO/HlLtJ ENSMUSG00225015690
rRNA gene Chr2:81478217-81478316 (-)
PWK/PhJ ENSLUMG00010032878
rRNA gene Chr2:71833831-71833930 (-)
SPRET/EiJ ENSMSPG00010023591
rRNA gene Chr2:73232395-73232494 (-)
WSB/EiJ ENSIUOG00005011965
rRNA gene Chr2:72037453-72037552 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00002076952 Ensembl Gene Model | MGI Sequence Detail 100 C57BL/6J ±  kb
transcript ENSMUST00020183135 Ensembl | MGI Sequence Detail 100 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