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4921504A21Rik Gene Detail
Summary
  • Symbol
    4921504A21Rik
  • Name
    RIKEN cDNA 4921504A21 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1918082
    NCBI Gene: 70832
  • Alliance
    genome feature page
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr5:19407366-19431553 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 5, 8.60 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    859 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1918082
 lncRNA gene Chr5:19363531-19432857 (-)
129S1/SvImJ ENSMUSG00200011570
 lncRNA gene Chr5:15057512-15082204 (-)
A/J ENSMUSG00195042029
 lncRNA gene Chr5:14519323-14544342 (-)
AKR/J ENSMUSG00220037791
 lncRNA gene Chr5:14530119-14555102 (-)
BALB/cJ ENSMUSG00180025555
 lncRNA gene Chr5:14371196-14396213 (-)
C3H/HeJ ENSMUSG00175027507
 lncRNA gene Chr5:16322724-16347733 (-)
C57BL/6NJ ENSMUSG00215025119
 lncRNA gene Chr5:14938670-14963683 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0003632
 antisense lncRNA gene Chr5:14301817-14325290 (-)
CAST/EiJ ENSTCUG00005003483
 lncRNA gene Chr5:14640237-14665198 (-)
CBA/J ENSMUSG00210005238
 lncRNA gene Chr5:15362384-15387398 (-)
DBA/2J ENSMUSG00185017669
 lncRNA gene Chr5:16858493-16883784 (-)
FVB/NJ ENSMUSG00205035634
 lncRNA gene Chr5:14075275-14100287 (-)
JF1/MsJ ENSUMUG00000007564
 lncRNA gene Chr5:21485676-21510703 (-)
LP/J ENSMUSG00230026599
 lncRNA gene Chr5:21341963-21366639 (-)
NOD/ShiLtJ ENSMUSG00190005146
 lncRNA gene Chr5:14392954-14417987 (-)
NZO/HlLtJ ENSMUSG00225009788
 lncRNA gene Chr5:26746862-26771869 (-)
PWK/PhJ ENSLUMG00010036698
 lncRNA gene Chr5:14501196-14526778 (-)
SPRET/EiJ ENSMSPG00010031074
 lncRNA gene Chr5:15348516-15370269 (-)
WSB/EiJ ENSIUOG00005032769
 lncRNA gene Chr5:17200318-17225221 (-)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    9 phenotype references
  • All Mutations and Alleles
    4
  • Chemically induced (other)
    2
  • Radiation induced
    1
  • Spontaneous
    1
  • Genomic Mutations
    4 involving 4921504A21Rik
  • Find Mice (IMSR)
    0 strains or lines available
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
    597
  • cDNA Data
    3
Sequences &
Gene Models
less
  • All Sequences
    53
  • RefSeq
    2
Representative SequencesLengthStrain/SpeciesFlank
genomic 70832 NCBI Gene Model | MGI Sequence Detail 24188 C57BL/6J ±  kb
transcript NR_102341 RefSeq | MGI Sequence Detail 2156 C57BL/6  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 3
    cDNA 3
References
more
  • Summaries
    All 17
    Diseases 1
    Phenotypes 9
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:119563 Alt B, et al., Arteries define the position of the thyroid gland during its developmental relocalisation. Development. 2006 Oct;133(19):3797-804
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
09/15/2026
MGI 6.29 		The Jackson Laboratory