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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
    gene page
Location &
Maps
more
  • Sequence Map
    Chr5:45826044-45827050 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • 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 Chr5:45826043-45827050 (-)
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)
    1 strains or lines available
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
  • cDNA Data
    2
Sequences &
Gene Models
less
  • All Sequences
    25
  • RefSeq
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000104986 Ensembl Gene Model | MGI Sequence Detail 1007 C57BL/6J ±  kb
transcript NR_073433 RefSeq | MGI Sequence Detail 1008 ZRU/MplStud  
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 29
    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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory