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Gm15190 Pseudogene Detail
Summary
  • Symbol
    Gm15190
  • Name
    predicted gene 15190
  • Synonyms
    ENSMUSG00000043469
Location &
Maps
more
  • Sequence Map
    ChrX:158367779-158368054 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 73.61 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    60 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3705630
pseudogene ChrX:158367396-158368108 (-)
129S1/SvImJ MGP_129S1SvImJ_G0014975
pseudogene ChrX:157490053-157490328 (-)
A/J MGP_AJ_G0014964
pseudogene ChrX:156767078-156767353 (-)
AKR/J MGP_AKRJ_G0014906
pseudogene ChrX:161750648-161750923 (-)
BALB/cJ MGP_BALBcJ_G0014919
pseudogene ChrX:154850345-154850620 (-)
C3H/HeJ MGP_C3HHeJ_G0014757
pseudogene ChrX:157887327-157887602 (-)
C57BL/6NJ MGP_C57BL6NJ_G0015405
pseudogene ChrX:162183654-162183929 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0009907
pseudogene Chr13:103452890-103453165 (+)
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0014741
pseudogene ChrX:166809849-166810124 (-)
DBA/2J MGP_DBA2J_G0014826
pseudogene ChrX:155752310-155752585 (-)
FVB/NJ MGP_FVBNJ_G0014809
pseudogene ChrX:154870548-154870823 (-)
LP/J MGP_LPJ_G0014927
pseudogene ChrX:158661167-158661442 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0014853
pseudogene ChrX:175494101-175494376 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0015389
pseudogene ChrX:157036385-157036660 (-)
PWK/PhJ MGP_PWKPhJ_G0014154
pseudogene ChrX:133800844-133801119 (-)
SPRET/EiJ MGP_SPRETEiJ_G0013944
pseudogene ChrX:137353538-137353813 (-)
WSB/EiJ MGP_WSBEiJ_G0014442
pseudogene ChrX:155002589-155002864 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotype references
Expression
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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 ENSMUSG00000082693 Ensembl Gene Model | MGI Sequence Detail 276 C57BL/6J ±  kb
transcript ENSMUST00000120855 Ensembl | MGI Sequence Detail 276 Not Applicable  
For the selected sequence
Other
Accession IDs
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MGI:3704518
References
more
  • Summaries
    All 9
    Phenotypes 3
  • 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
11/12/2024
MGI 6.24
The Jackson Laboratory