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Gm15192 Pseudogene Detail
Summary
  • Symbol
    Gm15192
  • Name
    predicted gene 15192
  • Feature Type
    pseudogene
  • IDs
    MGI:3705866
  • Alliance
Location &
Maps
more
  • Sequence Map
    ChrX:159081474-159081766 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 73.95 cM
Strain
Comparison
more
  • SNPs within 2kb
    98 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3705866
pseudogene ChrX:159081474-159081766 (+)
129S1/SvImJ MGP_129S1SvImJ_G0040719
pseudogene ChrX:158222018-158222310 (+)
A/J MGP_AJ_G0040716
pseudogene ChrX:157492912-157493204 (+)
AKR/J MGP_AKRJ_G0040641
pseudogene ChrX:162483548-162483840 (+)
BALB/cJ MGP_BALBcJ_G0040709
pseudogene ChrX:155559093-155559385 (+)
C3H/HeJ MGP_C3HHeJ_G0040341
pseudogene ChrX:158619374-158619666 (+)
C57BL/6NJ MGP_C57BL6NJ_G0041412
pseudogene ChrX:162941517-162941809 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0037527
pseudogene ChrX:148735515-148735829 (+)
CAST/EiJ MGP_CASTEiJ_G0039382
pseudogene ChrX:137642297-137642589 (+)
CBA/J MGP_CBAJ_G0040311
pseudogene ChrX:167572098-167572390 (+)
DBA/2J MGP_DBA2J_G0040526
pseudogene ChrX:156456838-156457130 (+)
FVB/NJ MGP_FVBNJ_G0040448
pseudogene ChrX:155571997-155572289 (+)
LP/J MGP_LPJ_G0040566
pseudogene ChrX:159403365-159403657 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0040453
pseudogene ChrX:176270487-176270779 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0041462
pseudogene ChrX:157775401-157775693 (+)
PWK/PhJ MGP_PWKPhJ_G0039030
pseudogene ChrX:134514869-134515161 (+)
SPRET/EiJ MGP_SPRETEiJ_G0038747
pseudogene ChrX:138054603-138054895 (+)
WSB/EiJ MGP_WSBEiJ_G0039630
pseudogene ChrX:155727536-155727828 (+)



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
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000083318 Ensembl Gene Model | MGI Sequence Detail 293 C57BL/6J ±  kb
transcript ENSMUST00000121005 Ensembl | MGI Sequence Detail 293 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 4
    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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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory