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1700094J05Rik Gene Detail
Summary
  • Symbol
    1700094J05Rik
  • Name
    RIKEN cDNA 1700094J05 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1914773
    NCBI Gene: 67523
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:76224849-76237341 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 10, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    312 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1914773
lncRNA gene Chr10:76224644-76237590 (+)
129S1/SvImJ ENSMUSG00200050062
lncRNA gene Chr10:72901956-72914452 (+)
A/J ENSMUSG00195049526
lncRNA gene Chr10:73238580-73251073 (+)
AKR/J ENSMUSG00220049055
lncRNA gene Chr10:72898297-72910793 (+)
BALB/cJ ENSMUSG00180052894
lncRNA gene Chr10:73253040-73265531 (+)
C3H/HeJ ENSMUSG00175052957
lncRNA gene Chr10:73124311-73136807 (+)
C57BL/6NJ ENSMUSG00215052943
lncRNA gene Chr10:72861940-72874433 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0002520
antisense lncRNA gene Chr10:70428924-70440091 (+)
CAST/EiJ ENSTCUG00005052100
lncRNA gene Chr10:72744045-72756537 (+)
CBA/J ENSMUSG00210050521
lncRNA gene Chr10:72980512-72993004 (+)
DBA/2J ENSMUSG00185053354
lncRNA gene Chr10:73322784-73335279 (+)
FVB/NJ ENSMUSG00205051030
lncRNA gene Chr10:73015441-73027934 (+)
JF1/MsJ ENSUMUG00000056342
lncRNA gene Chr10:74464918-74477736 (+)
LP/J ENSMUSG00230051247
lncRNA gene Chr10:75092345-75104837 (+)
NOD/ShiLtJ ENSMUSG00190052222
lncRNA gene Chr10:73300281-73312771 (+)
NZO/HlLtJ ENSMUSG00225048163
lncRNA gene Chr10:79389037-79401531 (+)
PWK/PhJ ENSLUMG00010052525
lncRNA gene Chr10:72861151-72873955 (+)
SPRET/EiJ ENSMSPG00010048683
lncRNA gene Chr10:74651677-74664374 (+)
WSB/EiJ ENSIUOG00005051312
lncRNA gene Chr10:72904972-72917514 (+)



Homology
less
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    35 phenotype references
  • All Mutations and Alleles
    6
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Targeted
    4
  • Genomic Mutations
    5 involving 1700094J05Rik
  • Find Mice (IMSR)
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
  • cDNA Data
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 67523 NCBI Gene Model | MGI Sequence Detail 12493 C57BL/6J ±  kb
transcript NR_040580 RefSeq | MGI Sequence Detail 997 ZRU/MplStud  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2
References
more
  • Summaries
    All 42
    Diseases 2
    Phenotypes 35
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

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
09/08/2026
MGI 6.24
The Jackson Laboratory