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Gm8682 Pseudogene Detail
Summary
  • Symbol
    Gm8682
  • Name
    predicted gene 8682
  • Feature Type
    pseudogene
  • IDs
    MGI:3643679
    NCBI Gene: 667524
  • Alliance
Location &
Maps
more
  • Sequence Map
    ChrX:158819317-158819814 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 73.95 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    9 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3643679
pseudogene ChrX:158819317-158819996 (+)
129S1/SvImJ MGP_129S1SvImJ_G0014978
pseudogene ChrX:157950062-157950559 (+)
A/J MGP_AJ_G0014967
pseudogene ChrX:157232282-157232779 (+)
AKR/J MGP_AKRJ_G0014909
pseudogene ChrX:162222499-162222996 (+)
BALB/cJ MGP_BALBcJ_G0014922
pseudogene ChrX:155302210-155302706 (+)
C3H/HeJ MGP_C3HHeJ_G0014760
pseudogene ChrX:158357659-158358156 (+)
C57BL/6NJ MGP_C57BL6NJ_G0015408
pseudogene ChrX:162651847-162652344 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0013030
pseudogene ChrX:148492548-148493045 (+)
CAST/EiJ MGP_CASTEiJ_G0014365
pseudogene ChrX:137379596-137380092 (+)
CBA/J MGP_CBAJ_G0014744
pseudogene ChrX:167288367-167288864 (+)
DBA/2J MGP_DBA2J_G0014829
pseudogene ChrX:156206097-156206594 (+)
FVB/NJ MGP_FVBNJ_G0014812
pseudogene ChrX:155314660-155315157 (+)
LP/J MGP_LPJ_G0014930
pseudogene ChrX:159132403-159132900 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0014856
pseudogene ChrX:175979082-175979578 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0015392
pseudogene ChrX:157504237-157504734 (+)
PWK/PhJ MGP_PWKPhJ_G0014157
pseudogene ChrX:134256094-134256590 (+)
SPRET/EiJ MGP_SPRETEiJ_G0013947
pseudogene ChrX:137806833-137807330 (+)
WSB/EiJ MGP_WSBEiJ_G0014445
pseudogene ChrX:155464074-155464571 (+)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
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
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  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000082810 Ensembl Gene Model | MGI Sequence Detail 498 C57BL/6J ±  kb
transcript ENSMUST00000121310 Ensembl | MGI Sequence Detail 498 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 5
    Phenotypes 1
  • Earliest
    J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55

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
04/16/2024
MGI 6.23
The Jackson Laboratory