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1600023N17Rik Gene Detail
Summary
  • Symbol
    1600023N17Rik
  • Name
    RIKEN cDNA 1600023N17 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1917038
    NCBI Gene: 69788
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr5:45668702-45669708 bp, - strand
  • From Ensembl annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 5, Syntenic
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    49 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1917038
lncRNA gene Chr5:45668701-45669708 (-)
129S1/SvImJ MGP_129S1SvImJ_G0001483
unclassified gene Chr5:44381524-44382530 (-)
A/J MGP_AJ_G0001465
unclassified gene Chr5:42845003-42846009 (-)
AKR/J MGP_AKRJ_G0001451
unclassified gene Chr5:44322692-44323698 (-)
BALB/cJ MGP_BALBcJ_G0001461
unclassified gene Chr5:43315124-43316130 (-)
C3H/HeJ MGP_C3HHeJ_G0001438
unclassified gene Chr5:44336653-44337659 (-)
C57BL/6NJ MGP_C57BL6NJ_G0001578
unclassified gene Chr5:46468836-46469842 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0001271
unclassified gene Chr5:39996717-39997735 (-)
CAST/EiJ MGP_CASTEiJ_G0001414
unclassified gene Chr5:43483611-43484617 (-)
CBA/J MGP_CBAJ_G0001429
unclassified gene Chr5:47749972-47750978 (-)
DBA/2J MGP_DBA2J_G0001434
unclassified gene Chr5:42911788-42912794 (-)
FVB/NJ MGP_FVBNJ_G0001442
unclassified gene Chr5:42341133-42342139 (-)
LP/J MGP_LPJ_G0001488
unclassified gene Chr5:44873821-44874827 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0001428
unclassified gene Chr5:48481825-48482831 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0001566
unclassified gene Chr5:43850223-43851229 (-)
PWK/PhJ MGP_PWKPhJ_G0001370
unclassified gene Chr5:42038543-42039549 (-)
SPRET/EiJ MGP_SPRETEiJ_G0001340
unclassified gene Chr5:43308424-43309430 (-)
WSB/EiJ MGP_WSBEiJ_G0001431
unclassified gene Chr5:43912780-43913786 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    18 phenotype references
  • All Mutations and Alleles
    5
  • Chemically induced (other)
    2
  • Radiation induced
    2
  • Spontaneous
    1
  • Genomic Mutations
    5 involving 1600023N17Rik
  • Find Mice (IMSR)
Expression
less
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000104986 Ensembl Gene Model | MGI Sequence Detail 1007 C57BL/6J ±  kb
transcript NR_073433 RefSeq | MGI Sequence Detail 1008 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2

    Microarray probesets 2
Other
Accession IDs
less
MGI:2141117
References
more
  • Summaries
    All 30
    Diseases 1
    Phenotypes 18
  • Earliest
    J:5021 Batchelor AL, et al., A comparison of the mutagenic effectiveness of chronic neutron- and gamma-irradiation of mouse spermatogonia. Mutat Res. 1966 Jun;3(3):218-29
  • Latest
    J:125425 Howell GR, et al., Mutation of a ubiquitously expressed mouse transmembrane protein (Tapt1) causes specific skeletal homeotic transformations. Genetics. 2007 Feb;175(2):699-707

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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last database update
09/05/2019
MGI 6.14
The Jackson Laboratory