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Gm48978 Gene Detail
Summary
  • Symbol
    Gm48978
  • Name
    predicted gene, 48978
  • Feature Type
    unclassified gene
  • IDs
    MGI:6118322
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr16:94018880-94023871 bp, - strand
    From Ensembl 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
    54 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_6118322
unclassified gene Chr16:94018880-94023871 (-)
129S1/SvImJ ENSMUSG00200038277
unclassified gene Chr16:90956667-90961658 (-)
A/J ENSMUSG00195029864
unclassified gene Chr16:90708124-90713115 (-)
AKR/J ENSMUSG00220016328
unclassified gene Chr16:90953444-90958435 (-)
BALB/cJ ENSMUSG00180016034
unclassified gene Chr16:90782101-90787092 (-)
C3H/HeJ ENSMUSG00175017446
unclassified gene Chr16:91119219-91124210 (-)
C57BL/6NJ ENSMUSG00215033450
unclassified gene Chr16:90910739-90915730 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005021127
unclassified gene Chr16:90507588-90512625 (-)
CBA/J ENSMUSG00210042679
unclassified gene Chr16:91026779-91031770 (-)
DBA/2J ENSMUSG00185035430
unclassified gene Chr16:90966142-90971133 (-)
FVB/NJ ENSMUSG00205027352
unclassified gene Chr16:90745740-90750731 (-)
JF1/MsJ ENSUMUG00000045826
unclassified gene Chr16:91112851-91117848 (-)
LP/J ENSMUSG00230028379
unclassified gene Chr16:93503264-93508255 (-)
NOD/ShiLtJ ENSMUSG00190027392
unclassified gene Chr16:90934701-90939692 (-)
NZO/HlLtJ ENSMUSG00225031693
unclassified gene Chr16:96612510-96617501 (-)
PWK/PhJ ENSLUMG00010014409
unclassified gene Chr16:90752945-90758159 (-)
SPRET/EiJ ENSMSPG00010021035
unclassified gene Chr16:91876704-91883716 (-)
WSB/EiJ ENSIUOG00005021870
unclassified gene Chr16:90872766-90877757 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotype references
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
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000115044 Ensembl Gene Model | MGI Sequence Detail 4992 C57BL/6J ±  kb
For the selected sequence
References
more
  • Summaries
    All 3
    Phenotypes 2
  • Earliest
    J:343786 Lana-Elola E, et al., Congenital heart defects in Down syndrome are caused by increased dosage of DYRK1A. bioRxiv. 2023;
  • Latest
    J:345472 Lana-Elola E, et al., Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Sci Transl Med. 2024 Jan 24;16(731):eadd6883

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
09/08/2026
MGI 6.24
The Jackson Laboratory