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Gm8492 Pseudogene Detail
Summary
  • Symbol
    Gm8492
  • Name
    predicted gene 8492
Location &
Maps
more
  • Sequence Map
    Chr17:9539227-9540213 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 17, 6.83 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    100 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3643249
pseudogene Chr17:9539028-9540229 (-)
129S1/SvImJ ENSMUSG00200034677
pseudogene Chr17:5775394-5776380 (-)
A/J ENSMUSG00195023597
pseudogene Chr17:5984082-5985068 (-)
AKR/J ENSMUSG00220029450
pseudogene Chr17:6046235-6047221 (-)
BALB/cJ ENSMUSG00180025981
pseudogene Chr17:5630745-5631731 (-)
C3H/HeJ ENSMUSG00175034829
pseudogene Chr17:5774470-5775456 (-)
C57BL/6NJ ENSMUSG00215030948
pseudogene Chr17:5782666-5783652 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0010150
pseudogene Chr17:7562784-7563783 (+)
CAST/EiJ ENSTCUG00005023061
pseudogene Chr17:6018060-6019046 (-)
CBA/J ENSMUSG00210039472
pseudogene Chr17:5441273-5442259 (-)
DBA/2J ENSMUSG00185024664
pseudogene Chr17:6533935-6534921 (-)
FVB/NJ ENSMUSG00205009528
pseudogene Chr17:5846716-5847702 (-)
JF1/MsJ ENSUMUG00000040347
pseudogene Chr17:6131704-6132690 (-)
LP/J ENSMUSG00230034447
pseudogene Chr17:7966247-7967233 (-)
NOD/ShiLtJ ENSMUSG00190036788
pseudogene Chr17:5979910-5980896 (-)
NZO/HlLtJ ENSMUSG00225029208
pseudogene Chr17:9886538-9887524 (-)
PWK/PhJ ENSLUMG00010020115
pseudogene Chr17:5950348-5951334 (-)
SPRET/EiJ ENSMSPG00010038185
pseudogene Chr17:7724041-7725027 (+)
WSB/EiJ ENSIUOG00005014296
pseudogene Chr17:5834460-5835446 (-)



Homology
less
Human Diseases
less
  • References
    6 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    379 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
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000097958 Ensembl Gene Model | MGI Sequence Detail 987 C57BL/6J ±  kb
transcript ENSMUST00000182375 Ensembl | MGI Sequence Detail 987 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 384
    Diseases 6
    Phenotypes 379
  • Earliest
    J:7073 Washburn LL, et al., Sex reversal in XY mice caused by dominant mutation on chromosome 17. Nature. 1983 May 26;303(5915):338-40
  • Latest
    J:391449 Thibodeau J, et al., Loss of cystathionine-beta-synthase contributes to elevated OXPHOS, a vulnerability in Ara-C-resistant Myeloid Leukemia in Down syndrome. Biochem Pharmacol. 2026 Feb 13;247:117815

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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Funding Information
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last database update
09/15/2026
MGI 6.29
The Jackson Laboratory