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Gm52973 Pseudogene Detail
Summary
  • Symbol
    Gm52973
  • Name
    predicted gene, 52973
Location &
Maps
more
  • Sequence Map
    Chr18:50367705-50367911 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 18, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    121 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_6388855
pseudogene Chr18:50367705-50367911 (+)
129S1/SvImJ ENSMUSG00200031090
pseudogene Chr18:47411170-47411376 (+)
A/J ENSMUSG00195025672
pseudogene Chr18:47561217-47561423 (+)
AKR/J ENSMUSG00220021768
pseudogene Chr18:47507373-47507579 (+)
BALB/cJ ENSMUSG00180007842
pseudogene Chr18:48092878-48093084 (+)
C3H/HeJ ENSMUSG00175011337
pseudogene Chr18:47691481-47691687 (+)
C57BL/6NJ ENSMUSG00215009862
pseudogene Chr18:47097990-47098196 (+)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005014459
pseudogene Chr18:46971086-46971292 (+)
CBA/J ENSMUSG00210022626
pseudogene Chr18:47650485-47650691 (+)
DBA/2J ENSMUSG00185028512
pseudogene Chr18:47551460-47551666 (+)
FVB/NJ ENSMUSG00205015993
pseudogene Chr18:47027667-47027873 (+)
JF1/MsJ ENSUMUG00000030264
pseudogene Chr18:47524829-47525035 (+)
LP/J ENSMUSG00230029909
pseudogene Chr18:49587774-49587980 (+)
NOD/ShiLtJ ENSMUSG00190028664
pseudogene Chr18:47335317-47335523 (+)
NZO/HlLtJ ENSMUSG00225027844
pseudogene Chr18:49490506-49490712 (+)
PWK/PhJ ENSLUMG00010022270
pseudogene Chr18:47669666-47669872 (+)
SPRET/EiJ ENSMSPG00010013460
pseudogene Chr18:47974799-47975005 (+)
WSB/EiJ no annotation



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
Expression
less
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000118595 Ensembl Gene Model | MGI Sequence Detail 207 C57BL/6J ±  kb
transcript ENSMUST00000239331 Ensembl | MGI Sequence Detail 207 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67

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
09/15/2026
MGI 6.29
The Jackson Laboratory