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Gm15019 Pseudogene Detail
Summary
  • Symbol
    Gm15019
  • Name
    predicted gene 15019
  • Feature Type
    pseudogene
  • IDs
    MGI:3705840
  • Alliance
Location &
Maps
more
  • Sequence Map
    ChrX:134627747-134630223 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 57.26 cM
Strain
Comparison
more
  • SNPs within 2kb
    35 from dbSNP Build 142
  • Strain Annotations
    7
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3705840
pseudogene ChrX:134627747-134630223 (+)
129S1/SvImJ MGP_129S1SvImJ_G0040707
pseudogene ChrX:133071986-133074462 (+)
A/J no annotation
AKR/J MGP_AKRJ_G0040631
pseudogene ChrX:136707494-136709983 (+)
BALB/cJ no annotation
C3H/HeJ MGP_C3HHeJ_G0040331
pseudogene ChrX:133050086-133052326 (+)
C57BL/6NJ MGP_C57BL6NJ_G0041401
pseudogene ChrX:136862619-136866467 (+)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0040302
pseudogene ChrX:141074584-141078363 (+)
DBA/2J no annotation
FVB/NJ no annotation
LP/J MGP_LPJ_G0040554
pseudogene ChrX:133989205-133991681 (+)
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 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
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000084330 Ensembl Gene Model | MGI Sequence Detail 2477 C57BL/6J ±  kb
transcript ENSMUST00000120148 Ensembl | MGI Sequence Detail 434 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 5
    Diseases 1
    Phenotypes 2
  • Earliest
    J:199138 Zhou J, et al., A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice. Biol Reprod. 2013 Jun;88(6):159
  • Latest
    J:210663 Zhou J, et al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet. 2014 Jul 15;23(14):3823-9

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
05/07/2024
MGI 6.23
The Jackson Laboratory