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5031425E22Rik Gene Detail
Summary
  • Symbol
    5031425E22Rik
  • Name
    RIKEN cDNA 5031425E22 gene
  • Synonyms
    BC050254
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1923227
    NCBI Gene: 269630
  • Alliance
    gene page
  • Transcription Start Sites
    16 TSS
Location &
Maps
more
  • Sequence Map
    Chr5:23587300-23639351 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 5, 10.33 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1267 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1923227
 lncRNA gene Chr5:23557556-23639396 (-)
129S1/SvImJ MGP_129S1SvImJ_G0006590
 lincRNA gene Chr5:21045727-21084398 (-)
A/J MGP_AJ_G0006583
 lincRNA gene Chr5:20374767-20409214 (-)
AKR/J MGP_AKRJ_G0006553
 lincRNA gene Chr5:21167835-21203277 (-)
BALB/cJ MGP_BALBcJ_G0006558
 lincRNA gene Chr5:20857454-20894468 (-)
C3H/HeJ MGP_C3HHeJ_G0006505
 lincRNA gene Chr5:21254151-21289465 (-)
C57BL/6NJ MGP_C57BL6NJ_G0006722
 lincRNA gene Chr5:22529192-22563682 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0005991
 lincRNA gene Chr5:18328863-18363997 (-)
CAST/EiJ MGP_CASTEiJ_G0006431
 lincRNA gene Chr5:20454561-20493071 (-)
CBA/J MGP_CBAJ_G0006487
 lincRNA gene Chr5:22838303-22877191 (-)
DBA/2J MGP_DBA2J_G0006508
 lincRNA gene Chr5:20635238-20670789 (-)
FVB/NJ MGP_FVBNJ_G0006531
 lincRNA gene Chr5:20033484-20067874 (-)
LP/J MGP_LPJ_G0006590
 lincRNA gene Chr5:21429550-21465981 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0006515
 lincRNA gene Chr5:24030748-24066669 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0006728
 lincRNA gene Chr5:20760184-20796254 (-)
PWK/PhJ MGP_PWKPhJ_G0006369
 lincRNA gene Chr5:19718699-19753486 (-)
SPRET/EiJ MGP_SPRETEiJ_G0006280
 lincRNA gene Chr5:20157987-20195840 (-)
WSB/EiJ MGP_WSBEiJ_G0006481
 lincRNA gene Chr5:20858220-20893001 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    16 phenotype references
  • All Mutations and Alleles
    186
  • Chemically induced (other)
    2
  • Gene trapped
    181
  • Radiation induced
    1
  • Spontaneous
    1
  • Targeted
    1
  • Genomic Mutations
    5 involving 5031425E22Rik
  • Find Mice (IMSR)
    3 strains or lines available
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
    706
  • cDNA Data
    7
Sequences &
Gene Models
less
  • All Sequences
    116
  • RefSeq
    3
  • UniProt
    1
Representative SequencesLengthStrain/SpeciesFlank
genomic 269630 NCBI Gene Model | MGI Sequence Detail 52052 C57BL/6J ±  kb
transcript NR_040469 RefSeq | MGI Sequence Detail 2546 C57BL/6  
polypeptide Q3UTW8 UniProt | EBI | MGI Sequence Detail 154 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 9
    cDNA 9

    Microarray probesets 4
Other
Accession IDs
less
MGI:3040684
References
more
  • Summaries
    All 34
    Diseases 1
    Phenotypes 16
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:269071 Wong JC, et al., Functional evidence implicating chromosome 7q22 haploinsufficiency in myelodysplastic syndrome pathogenesis. Elife. 2015 Jul 20;4
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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Send questions and comments to User Support. 		last database update
10/07/2025
MGI 6.24 		The Jackson Laboratory