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Gm15016 Pseudogene Detail
Summary
  • Symbol
    Gm15016
  • Name
    predicted gene 15016
Location &
Maps
more
  • Sequence Map
    ChrX:134889296-134890015 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 57.35 cM
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_3705629
pseudogene ChrX:134889296-134890015 (+)
129S1/SvImJ MGP_129S1SvImJ_G0014836
pseudogene ChrX:133344093-133344812 (+)
A/J MGP_AJ_G0014832
pseudogene ChrX:132749982-132750701 (+)
AKR/J MGP_AKRJ_G0014769
pseudogene ChrX:137003899-137004618 (+)
BALB/cJ MGP_BALBcJ_G0014784
pseudogene ChrX:131132787-131133506 (+)
C3H/HeJ MGP_C3HHeJ_G0014616
pseudogene ChrX:133339088-133339807 (+)
C57BL/6NJ MGP_C57BL6NJ_G0015268
pseudogene ChrX:137174044-137174763 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0012923
pseudogene ChrX:124752832-124753657 (+)
CAST/EiJ MGP_CASTEiJ_G0014236
pseudogene ChrX:114257627-114258451 (+)
CBA/J MGP_CBAJ_G0014609
pseudogene ChrX:141395697-141396416 (+)
DBA/2J MGP_DBA2J_G0014695
pseudogene ChrX:132076266-132076985 (+)
FVB/NJ MGP_FVBNJ_G0014675
pseudogene ChrX:131262952-131263671 (+)
LP/J MGP_LPJ_G0014791
pseudogene ChrX:134270392-134271111 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0014722
pseudogene ChrX:148758548-148759267 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0015248
pseudogene ChrX:132693061-132693780 (+)
PWK/PhJ MGP_PWKPhJ_G0014035
pseudogene ChrX:111169478-111170302 (+)
SPRET/EiJ MGP_SPRETEiJ_G0013827
pseudogene ChrX:114894574-114895386 (+)
WSB/EiJ MGP_WSBEiJ_G0014318
pseudogene ChrX:131032015-131032734 (+)



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 ENSMUSG00000083223 Ensembl Gene Model | MGI Sequence Detail 720 C57BL/6J ±  kb
transcript ENSMUST00000117300 Ensembl | MGI Sequence Detail 720 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 6
    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
03/19/2024
MGI 6.23
The Jackson Laboratory