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Gm26684 Gene Detail
Summary
  • Symbol
    Gm26684
  • Name
    predicted gene, 26684
  • Feature Type
    lncRNA gene
  • IDs
    MGI:5477178
    NCBI Gene: 102638507
  • Alliance
    gene page
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:54816344-54834101 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 15, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    495 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5477178
 lncRNA gene Chr15:54815466-54834488 (+)
129S1/SvImJ MGP_129S1SvImJ_G0005601
 lincRNA gene Chr15:54016858-54028475 (+)
A/J MGP_AJ_G0005587
 lincRNA gene Chr15:51874577-51887056 (+)
AKR/J MGP_AKRJ_G0005566
 lincRNA gene Chr15:53343639-53355290 (+)
BALB/cJ MGP_BALBcJ_G0005568
 lincRNA gene Chr15:52099433-52111113 (+)
C3H/HeJ MGP_C3HHeJ_G0005515
 lincRNA gene Chr15:53430277-53441909 (+)
C57BL/6NJ MGP_C57BL6NJ_G0005725
 lincRNA gene Chr15:56114984-56130332 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0005091
 lincRNA gene Chr15:49113471-49124423 (+)
CAST/EiJ MGP_CASTEiJ_G0005458
 lincRNA gene Chr15:54014736-54025957 (+)
CBA/J MGP_CBAJ_G0005505
 lincRNA gene Chr15:58109642-58121307 (+)
DBA/2J MGP_DBA2J_G0005520
 lincRNA gene Chr15:51769782-51781537 (+)
FVB/NJ MGP_FVBNJ_G0005546
 lincRNA gene Chr15:50890020-50901835 (+)
LP/J MGP_LPJ_G0005604
 lincRNA gene Chr15:53806121-53824006 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0005531
 lincRNA gene Chr15:63194467-63206835 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0005725
 lincRNA gene Chr15:53690325-53703654 (+)
PWK/PhJ MGP_PWKPhJ_G0005408
 lincRNA gene Chr15:51839134-51850679 (+)
SPRET/EiJ MGP_SPRETEiJ_G0005326
 lincRNA gene Chr15:53433118-53449412 (+)
WSB/EiJ MGP_WSBEiJ_G0005508
 lincRNA gene Chr15:53674466-53686861 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    11 phenotype references
  • All Mutations and Alleles
    4
  • Chemically induced (other)
    3
  • Radiation induced
    1
  • Genomic Mutations
    4 involving Gm26684
  • Find Mice (IMSR)
    0 strains or lines available
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
  • cDNA Data
    1
Sequences &
Gene Models
less
  • All Sequences
    27
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic 102638507 NCBI Gene Model | MGI Sequence Detail 17758 C57BL/6J ±  kb
transcript NR_155354 RefSeq | MGI Sequence Detail 1136 ZRU/MplStud  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 15
    Diseases 1
    Phenotypes 11
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:155838 Katayama K, et al., Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities. BMC Genet. 2009;10:60
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
11/19/2024
MGI 6.24 		The Jackson Laboratory