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Gm8437 Pseudogene Detail
Summary
  • Symbol
    Gm8437
  • Name
    predicted gene 8437
Location &
Maps
more
  • Sequence Map
    Chr17:31512095-31513177 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 17, 16.02 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    113 from dbSNP Build 142
  • Strain Annotations
    23
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3642987
pseudogene Chr17:31512095-31513177 (-)
129S1/SvImJ ENSMUSG00200054168
pseudogene Chr17:27197586-27201154 (-)
A/J ENSMUSG00195054572
pseudogene Chr17:28130419-28133984 (-)
AKR/J ENSMUSG00220053904
pseudogene Chr17:27158468-27162033 (-)
BALB/cJ ENSMUSG00180051500
pseudogene Chr17:27473131-27476699 (-)
C3H/HeJ ENSMUSG00175053840
pseudogene Chr17:27039636-27043201 (-)
C57BL/6NJ ENSMUSG00215054486
pseudogene Chr17:27029849-27033417 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005052148
pseudogene Chr17:27907195-27908269 (-)
CAST/EiJ ENSTCUG00005051787
pseudogene Chr17:27963518-27964593 (-)
CAST/EiJ ENSTCUG00005052152
pseudogene Chr17:28032028-28033112 (-)
CBA/J ENSMUSG00210051031
pseudogene Chr17:26866582-26870147 (-)
DBA/2J ENSMUSG00185054689
pseudogene Chr17:29483611-29487179 (-)
FVB/NJ ENSMUSG00205053733
pseudogene Chr17:27340311-27343879 (-)
JF1/MsJ ENSUMUG00000058009
pseudogene Chr17:28715591-28719147 (-)
JF1/MsJ ENSUMUG00000058104
pseudogene Chr17:28778246-28781181 (-)
JF1/MsJ ENSUMUG00000058103
pseudogene Chr17:28659928-28662865 (-)
LP/J ENSMUSG00230055233
pseudogene Chr17:30596122-30599690 (-)
NOD/ShiLtJ ENSMUSG00190054340
pseudogene Chr17:26983389-26986953 (-)
NZO/HlLtJ ENSMUSG00225055062
pseudogene Chr17:32633150-32636718 (-)
PWK/PhJ ENSLUMG00010053678
pseudogene Chr17:26466883-26469813 (-)
PWK/PhJ ENSLUMG00010053603
pseudogene Chr17:26585952-26589515 (-)
SPRET/EiJ ENSMSPG00010050404
pseudogene Chr17:27735703-27739275 (-)
WSB/EiJ ENSIUOG00005051943
pseudogene Chr17:27748075-27751640 (-)



Homology
less
Human Diseases
less
  • References
    3 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    28 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
  • cDNA Data
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000118295 Ensembl Gene Model | MGI Sequence Detail 1083 C57BL/6J ±  kb
transcript ENSMUST00000235710 Ensembl | MGI Sequence Detail 889 Not Applicable  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 33
    Diseases 3
    Phenotypes 28
  • Earliest
    J:154298 Pereira PL, et al., A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome. Hum Mol Genet. 2009 Dec 15;18(24):4756-4769
  • Latest
    J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

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