About   Help   FAQ
2610037D02Rik Gene Detail
Summary
  • Symbol
    2610037D02Rik
  • Name
    RIKEN cDNA 2610037D02 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1917290
    NCBI Gene: 70040
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:96190474-96197974 bp, - strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 15, 51.93 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    154 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1917290
lncRNA gene Chr15:96134819-96284495 (-)
129S1/SvImJ MGP_129S1SvImJ_G0005620
lincRNA gene Chr15:97691794-97858862 (-)
A/J MGP_AJ_G0005607
lincRNA gene Chr15:93879030-94031515 (-)
AKR/J MGP_AKRJ_G0005586
lincRNA gene Chr15:96693582-96850814 (-)
BALB/cJ MGP_BALBcJ_G0005587
lincRNA gene Chr15:94077798-94229072 (-)
C3H/HeJ MGP_C3HHeJ_G0005534
lincRNA gene Chr15:96742672-96901190 (-)
C57BL/6NJ MGP_C57BL6NJ_G0005745
lincRNA gene Chr15:101317979-101482881 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0005111
lincRNA gene Chr15:90020720-90023697 (-)
CAST/EiJ MGP_CASTEiJ_G0005478
lincRNA gene Chr15:97598029-97765032 (-)
CBA/J MGP_CBAJ_G0005524
lincRNA gene Chr15:104696763-104860946 (-)
DBA/2J MGP_DBA2J_G0005539
lincRNA gene Chr15:93322117-93475015 (-)
FVB/NJ MGP_FVBNJ_G0005566
lincRNA gene Chr15:92315768-92460890 (-)
LP/J MGP_LPJ_G0005623
lincRNA gene Chr15:97814287-97978751 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0005551
lincRNA gene Chr15:108921119-109075730 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0005745
lincRNA gene Chr15:96820281-96976384 (-)
PWK/PhJ MGP_PWKPhJ_G0005427
lincRNA gene Chr15:93395808-93550787 (-)
SPRET/EiJ MGP_SPRETEiJ_G0005345
lincRNA gene Chr15:96609123-96775275 (-)
WSB/EiJ MGP_WSBEiJ_G0005528
lincRNA gene Chr15:97322474-97480823 (-)



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 2610037D02Rik
  • Find Mice (IMSR)
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 70040 NCBI Gene Model | MGI Sequence Detail 7501 C57BL/6J ±  kb
transcript NR_040423 RefSeq | MGI Sequence Detail 3631 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 4
    cDNA 4

    Microarray probesets 5
Other
Accession IDs
less
MGI:2146147
References
more
  • Summaries
    All 32
    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