About   Help   FAQ
4833422M21Rik Gene Detail
Summary
  • Symbol
    4833422M21Rik
  • Name
    RIKEN cDNA 4833422M21 gene
  • Synonyms
    4933406G12Rik
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1923018
    NCBI Gene: 75768
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr15:96231870-96254684 bp, - strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 15, 52.34 cM, cytoband F2
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    199 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1923018
lncRNA gene Chr15:96231870-96254684 (-)
129S1/SvImJ MGP_129S1SvImJ_G0005621
lincRNA gene Chr15:97799450-97822855 (-)
A/J MGP_AJ_G0005608
lincRNA gene Chr15:93977743-94001233 (-)
AKR/J MGP_AKRJ_G0005587
lincRNA gene Chr15:96794921-96819849 (-)
BALB/cJ MGP_BALBcJ_G0005588
lincRNA gene Chr15:94175220-94198826 (-)
C3H/HeJ MGP_C3HHeJ_G0005535
lincRNA gene Chr15:96843884-96871389 (-)
C57BL/6NJ MGP_C57BL6NJ_G0005746
lincRNA gene Chr15:101425543-101449858 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0005110
lincRNA gene Chr15:89969491-89992741 (-)
CAST/EiJ MGP_CASTEiJ_G0005479
lincRNA gene Chr15:97703909-97728958 (-)
CBA/J MGP_CBAJ_G0005525
lincRNA gene Chr15:104802954-104829136 (-)
DBA/2J MGP_DBA2J_G0005540
lincRNA gene Chr15:93420184-93444628 (-)
FVB/NJ MGP_FVBNJ_G0005567
lincRNA gene Chr15:92413258-92431290 (-)
LP/J MGP_LPJ_G0005624
lincRNA gene Chr15:97916289-97948599 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0005552
lincRNA gene Chr15:109020941-109043244 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0005746
lincRNA gene Chr15:96920729-96944832 (-)
PWK/PhJ MGP_PWKPhJ_G0005428
lincRNA gene Chr15:93495667-93519908 (-)
SPRET/EiJ MGP_SPRETEiJ_G0005346
lincRNA gene Chr15:96709420-96739854 (-)
WSB/EiJ MGP_WSBEiJ_G0005529
lincRNA gene Chr15:97422766-97450630 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    19 phenotype references
  • All Mutations and Alleles
    3
  • Chemically induced (other)
    1
  • Radiation induced
    2
  • Genomic Mutations
    3 involving 4833422M21Rik
  • Find Mice (IMSR)
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 75768 NCBI Gene Model | MGI Sequence Detail 22815 C57BL/6J ±  kb
transcript NR_130160 RefSeq | MGI Sequence Detail 1365 Not Specified  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 7
    cDNA 7

    Microarray probesets 2
Other
Accession IDs
less
MGI:1921317
References
more
  • Summaries
    All 30
    Diseases 1
    Phenotypes 19
  • Earliest
    J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
  • Latest
    J:233611 Hirata A, et al., Homeobox family Hoxc localization during murine palate formation. Congenit Anom (Kyoto). 2016 Jul;56(4):172-9

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 & Copyright Notice
Send questions and comments to User Support.
last database update
09/10/2019
MGI 6.14
The Jackson Laboratory