About   Help   FAQ
9330117O12Rik Gene Detail
Summary
  • Symbol
    9330117O12Rik
  • Name
    RIKEN cDNA 9330117O12 gene
Location &
Maps
more
  • Sequence Map
    Chr18:54744816-54772942 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 18, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    873 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_5439411
lncRNA gene Chr18:54744781-54772944 (+)
129S1/SvImJ ENSMUSG00200034035
lncRNA gene Chr18:51781751-51809838 (+)
A/J ENSMUSG00195005405
lncRNA gene Chr18:51929605-51957689 (+)
AKR/J ENSMUSG00220016345
lncRNA gene Chr18:51916920-51945021 (+)
BALB/cJ ENSMUSG00180012583
lncRNA gene Chr18:52497535-52525643 (+)
C3H/HeJ ENSMUSG00175036975
lncRNA gene Chr18:52111892-52140003 (+)
C57BL/6NJ ENSMUSG00215039604
lncRNA gene Chr18:51472947-51501078 (+)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005027544
lncRNA gene Chr18:51320528-51352357 (+)
CBA/J ENSMUSG00210032815
lncRNA gene Chr18:52044697-52072821 (+)
DBA/2J ENSMUSG00185016016
lncRNA gene Chr18:51964753-51992873 (+)
FVB/NJ ENSMUSG00205018135
lncRNA gene Chr18:51406519-51434642 (+)
JF1/MsJ ENSUMUG00000035322
lncRNA gene Chr18:51876408-51908194 (+)
LP/J ENSMUSG00230011567
lncRNA gene Chr18:53961019-53989104 (+)
NOD/ShiLtJ ENSMUSG00190032626
lncRNA gene Chr18:51674624-51702732 (+)
NZO/HlLtJ ENSMUSG00225035389
lncRNA gene Chr18:53862992-53891111 (+)
PWK/PhJ ENSLUMG00010008642
lncRNA gene Chr18:52015593-52044301 (+)
SPRET/EiJ ENSMSPG00010018928
lncRNA gene Chr18:52390040-52419719 (+)
WSB/EiJ ENSIUOG00005009725
lncRNA gene Chr18:51596902-51625013 (+)



Homology
more
  • Human Ortholog
    LINC01170, long independently transcribed non-coding RNA 1170
  • Vertebrate Orthologs
    1
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    LINC01170, long independently transcribed non-coding RNA 1170
  • Links
    NCBI Gene ID: 103724389

  • Chr Location
    5q23.2; chr5:124059664-124438655 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
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
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 328957 NCBI Gene Model | MGI Sequence Detail 28127 C57BL/6J ±  kb
transcript NR_045400 RefSeq | MGI Sequence Detail 1840 ZRU/MplStud  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 1
    cDNA 1
References
more
  • Summaries
    All 5
    Phenotypes 1
  • Earliest
    J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67

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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
09/15/2026
MGI 6.29
The Jackson Laboratory