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2410124H12Rik Gene Detail
Summary
  • Symbol
    2410124H12Rik
  • Name
    RIKEN cDNA 2410124H12 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1924035
    NCBI Gene: 76785
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:92275630-92294258 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 16, 53.64 cM, cytoband C4
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    747 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1924035
lncRNA gene Chr16:92267791-92294268 (+)
129S1/SvImJ MGP_129S1SvImJ_G0037108
sense overlapping lncRNA gene Chr16:93564215-93583300 (+)
A/J MGP_AJ_G0037095
sense overlapping lncRNA gene Chr16:89183686-89203154 (+)
AKR/J MGP_AKRJ_G0037043
sense overlapping lncRNA gene Chr16:91906704-91930854 (+)
BALB/cJ MGP_BALBcJ_G0037086
sense overlapping lncRNA gene Chr16:89712965-89731971 (+)
C3H/HeJ MGP_C3HHeJ_G0036773
sense overlapping lncRNA gene Chr16:92444126-92463673 (+)
C57BL/6NJ MGP_C57BL6NJ_G0037600
sense overlapping lncRNA gene Chr16:96557423-96577179 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0034643
sense overlapping lncRNA gene Chr16:86865581-86885906 (+)
CAST/EiJ MGP_CASTEiJ_G0035960
sense overlapping lncRNA gene Chr16:93034706-93057573 (+)
CBA/J MGP_CBAJ_G0036748
sense overlapping lncRNA gene Chr16:100701288-100722299 (+)
DBA/2J MGP_DBA2J_G0036923
sense overlapping lncRNA gene Chr16:89091123-89110418 (+)
FVB/NJ MGP_FVBNJ_G0036873
sense overlapping lncRNA gene Chr16:88215194-88234665 (+)
LP/J MGP_LPJ_G0036970
sense overlapping lncRNA gene Chr16:93259304-93279085 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0036881
sense overlapping lncRNA gene Chr16:105200335-105221134 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0037717
sense overlapping lncRNA gene Chr16:92407489-92426059 (+)
PWK/PhJ MGP_PWKPhJ_G0035654
sense overlapping lncRNA gene Chr16:89288028-89308880 (+)
SPRET/EiJ MGP_SPRETEiJ_G0035461
sense overlapping lncRNA gene Chr16:91979080-92000650 (+)
WSB/EiJ MGP_WSBEiJ_G0036162
sense overlapping lncRNA gene Chr16:92652633-92673544 (+)



Homology
less
Human Diseases
less
  • References
    4 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    69 phenotype references
Gene Ontology
(GO)
Classifications
less
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
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Representative SequencesLengthStrain/SpeciesFlank
genomic 76785 NCBI Gene Model | MGI Sequence Detail 18629 C57BL/6J ±  kb
transcript NR_165041 RefSeq | MGI Sequence Detail 710 C57BL/6  
polypeptide Q9CWF8 UniProt | EBI | MGI Sequence Detail 123 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2

    Microarray probesets 1
References
more
  • Summaries
    All 81
    Diseases 4
    Phenotypes 69
  • Earliest
    J:42265 Huang TT, et al., Superoxide-mediated cytotoxicity in superoxide dismutase-deficient fetal fibroblasts. Arch Biochem Biophys. 1997 Aug 15;344(2):424-32
  • Latest
    J:335294 Redhead Y, et al., Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes. Development. 2023 Apr 15;150(8):dev201077

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)
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Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory