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4930578M01Rik Gene Detail
Summary
  • Symbol
    4930578M01Rik
  • Name
    RIKEN cDNA 4930578M01 gene
  • Synonyms
    3010001K12Rik
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1923201
    NCBI Gene: 75951
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr15:98985965-98989281 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 15, 55.43 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    48 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1923201
lncRNA gene Chr15:98983348-98996446 (+)
129S1/SvImJ MGP_129S1SvImJ_G0005623
lincRNA gene Chr15:100768343-100771673 (+)
A/J MGP_AJ_G0005610
lincRNA gene Chr15:96778104-96781432 (+)
AKR/J MGP_AKRJ_G0005589
lincRNA gene Chr15:99762402-99765732 (+)
BALB/cJ MGP_BALBcJ_G0005590
lincRNA gene Chr15:96974040-96977352 (+)
C3H/HeJ MGP_C3HHeJ_G0005537
lincRNA gene Chr15:99813766-99817094 (+)
C57BL/6NJ MGP_C57BL6NJ_G0005748
lincRNA gene Chr15:104517877-104521228 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0005113
lincRNA gene Chr15:92696390-92700151 (+)
CAST/EiJ MGP_CASTEiJ_G0005481
lincRNA gene Chr15:100670083-100673869 (+)
CBA/J MGP_CBAJ_G0005527
lincRNA gene Chr15:108071484-108074816 (+)
DBA/2J MGP_DBA2J_G0005542
lincRNA gene Chr15:96224797-96228127 (+)
FVB/NJ MGP_FVBNJ_G0005569
lincRNA gene Chr15:95206203-95209521 (+)
LP/J MGP_LPJ_G0005626
lincRNA gene Chr15:100911348-100914674 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0005554
lincRNA gene Chr15:112049016-112052325 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0005748
lincRNA gene Chr15:99847382-99850693 (+)
PWK/PhJ MGP_PWKPhJ_G0005430
lincRNA gene Chr15:96348676-96352041 (+)
SPRET/EiJ MGP_SPRETEiJ_G0005348
lincRNA gene Chr15:99712080-99715386 (+)
WSB/EiJ MGP_WSBEiJ_G0005531
lincRNA gene Chr15:100389962-100393294 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    22 phenotype references
  • All Mutations and Alleles
    82
  • Chemically induced (other)
    1
  • Gene trapped
    79
  • Radiation induced
    2
  • Genomic Mutations
    3 involving 4930578M01Rik
  • Find Mice (IMSR)
Expression
less
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 75951 NCBI Gene Model | MGI Sequence Detail 3317 C57BL/6J ±  kb
transcript NR_045991 RefSeq | MGI Sequence Detail 907 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 7
    cDNA 7

    Microarray probesets 2
Other
Accession IDs
less
MGI:1917460
References
more
  • Summaries
    All 36
    Diseases 1
    Phenotypes 22
  • 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
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory