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1700009J07Rik Gene Detail
Summary
  • Symbol
    1700009J07Rik
  • Name
    RIKEN cDNA 1700009J07 gene
  • Synonyms
    4930535B06Rik
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1914938
    NCBI Gene: 75188
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:77893420-77896111 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 10, 39.72 cM, cytoband C1
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    43 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1914938
lncRNA gene Chr10:77893417-77896114 (+)
129S1/SvImJ MGP_129S1SvImJ_G0005132
lincRNA gene Chr10:78291289-78293986 (+)
A/J MGP_AJ_G0005115
lincRNA gene Chr10:75586008-75588705 (+)
AKR/J MGP_AKRJ_G0005093
lincRNA gene Chr10:77607708-77610405 (+)
BALB/cJ MGP_BALBcJ_G0005096
lincRNA gene Chr10:75760310-75763007 (+)
C3H/HeJ MGP_C3HHeJ_G0005045
lincRNA gene Chr10:77693810-77696507 (+)
C57BL/6NJ MGP_C57BL6NJ_G0005246
lincRNA gene Chr10:81076747-81079444 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0004652
lincRNA gene Chr10:71937911-71940637 (+)
CAST/EiJ MGP_CASTEiJ_G0004992
lincRNA gene Chr10:78019518-78022191 (+)
CBA/J MGP_CBAJ_G0005035
lincRNA gene Chr10:84146855-84149552 (+)
DBA/2J MGP_DBA2J_G0005054
lincRNA gene Chr10:74827101-74829798 (+)
FVB/NJ MGP_FVBNJ_G0005076
lincRNA gene Chr10:74002276-74004973 (+)
LP/J MGP_LPJ_G0005133
lincRNA gene Chr10:78735836-78738533 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0005059
lincRNA gene Chr10:86152356-86155053 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0005253
lincRNA gene Chr10:77643318-77646031 (+)
PWK/PhJ MGP_PWKPhJ_G0004943
lincRNA gene Chr10:74712098-74714787 (+)
SPRET/EiJ MGP_SPRETEiJ_G0004868
lincRNA gene Chr10:76861813-76864531 (+)
WSB/EiJ MGP_WSBEiJ_G0005039
lincRNA gene Chr10:77624421-77627134 (+)



Homology
less
Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    19 phenotype references
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
  • UniProt
  • UniGene
Representative SequencesLengthStrain/SpeciesFlank
genomic 75188 NCBI Gene Model | MGI Sequence Detail 2692 C57BL/6J ±  kb
transcript NR_015547 RefSeq | MGI Sequence Detail 914 C57BL/6  
polypeptide Q9D4Z3 UniProt | EBI | MGI Sequence Detail 125 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 10
    cDNA 10

    Microarray probesets 2
Other
Accession IDs
less
MGI:1922438
References
more
  • Summaries
    All 33
    Diseases 2
    Phenotypes 19
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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
09/10/2019
MGI 6.14
The Jackson Laboratory