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4930578N18Rik Gene Detail
Summary
  • Symbol
    4930578N18Rik
  • Name
    RIKEN cDNA 4930578N18 gene
  • Feature Type
    lncRNA gene
  • IDs
    MGI:1925465
    NCBI Gene: 78215
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:75919501-75952974 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 16, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    967 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1925465
lncRNA gene Chr16:75919438-75952982 (+)
129S1/SvImJ ENSMUSG00200015845
lncRNA gene Chr16:72798042-72831518 (+)
A/J ENSMUSG00195023279
lncRNA gene Chr16:72570762-72595241 (+)
AKR/J ENSMUSG00220017789
lncRNA gene Chr16:72756801-72790278 (+)
BALB/cJ ENSMUSG00180002108
lncRNA gene Chr16:72656388-72689865 (+)
C3H/HeJ ENSMUSG00175009352
lncRNA gene Chr16:72929790-72963266 (+)
C57BL/6NJ ENSMUSG00215001708
lncRNA gene Chr16:72766918-72800400 (+)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005007768
lncRNA gene Chr16:72640227-72667160 (+)
CBA/J ENSMUSG00210019843
lncRNA gene Chr16:72884628-72918101 (+)
DBA/2J ENSMUSG00185005313
lncRNA gene Chr16:72805640-72830119 (+)
FVB/NJ ENSMUSG00205014566
lncRNA gene Chr16:72672624-72706099 (+)
JF1/MsJ ENSUMUG00000014639
lncRNA gene Chr16:73007596-73031627 (+)
LP/J ENSMUSG00230020202
lncRNA gene Chr16:75373104-75406580 (+)
NOD/ShiLtJ ENSMUSG00190011702
lncRNA gene Chr16:72810941-72844416 (+)
NZO/HlLtJ ENSMUSG00225029597
lncRNA gene Chr16:78603967-78628439 (+)
PWK/PhJ ENSLUMG00010005397
lncRNA gene Chr16:72655904-72679858 (+)
SPRET/EiJ ENSMSPG00010015578
lncRNA gene Chr16:73500457-73524826 (+)
WSB/EiJ ENSIUOG00005017472
lncRNA gene Chr16:73044351-73068762 (+)



Homology
less
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    14 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
less
  • All Sequences
  • RefSeq
Representative SequencesLengthStrain/SpeciesFlank
genomic 78215 NCBI Gene Model | MGI Sequence Detail 33474 C57BL/6J ±  kb
transcript NR_040575 RefSeq | MGI Sequence Detail 511 ZRU/MplStud  
For the selected sequence
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2
References
more
  • Summaries
    All 22
    Diseases 1
    Phenotypes 14
  • Earliest
    J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
  • Latest
    J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

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
09/01/2026
MGI 6.24
The Jackson Laboratory