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Gm15020 Gene Detail
Summary
  • Symbol
    Gm15020
  • Name
    predicted gene 15020
  • Feature Type
    lncRNA gene
  • IDs
    MGI:3708106
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:134023627-134053345 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 56.57 cM
Strain
Comparison
more
  • Strain Annotations
    8
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3708106
 lncRNA gene ChrX:134023627-134053345 (-)
129S1/SvImJ no annotation
A/J no annotation
AKR/J MGP_AKRJ_G0015731
 unclassified non-coding RNA gene ChrX:136249293-136257644 (+)
BALB/cJ MGP_BALBcJ_G0015729
 unclassified non-coding RNA gene ChrX:130185298-130222123 (-)
C3H/HeJ no annotation
C57BL/6NJ MGP_C57BL6NJ_G0016185
 unclassified non-coding RNA gene ChrX:136454228-136474957 (+)
CAROLI/EiJ no annotation
CAST/EiJ MGP_CASTEiJ_G0015106
 unclassified non-coding RNA gene ChrX:113520465-113782612 (+)
CBA/J MGP_CBAJ_G0015529
 unclassified non-coding RNA gene ChrX:140335260-140416088 (-)
DBA/2J no annotation
FVB/NJ no annotation
LP/J no annotation
NOD/ShiLtJ MGP_NODShiLtJ_G0015656
 unclassified non-coding RNA gene ChrX:148179667-148256664 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0016229
 unclassified non-coding RNA gene ChrX:131974254-132006133 (+)
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
Gene Ontology
(GO)
Classifications
less
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
    706
Sequences &
Gene Models
less
  • All Sequences
    10
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000085556 Ensembl Gene Model | MGI Sequence Detail 29719 C57BL/6J ±  kb
transcript ENSMUST00000147142 Ensembl | MGI Sequence Detail 636 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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory