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Gm54765 Gene Detail
Summary
  • Symbol
    Gm54765
  • Name
    predicted gene, 54765
Location &
Maps
more
  • Sequence Map
    Chr18:49714763-49714916 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 18, Syntenic
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    115 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_6846007
snRNA gene Chr18:49714763-49714916 (-)
129S1/SvImJ ENSMUSG00200031223
snRNA gene Chr18:46747857-46748010 (-)
A/J ENSMUSG00195025224
snRNA gene Chr18:46897794-46897947 (-)
AKR/J ENSMUSG00220021677
snRNA gene Chr18:46843181-46843334 (-)
BALB/cJ ENSMUSG00180007921
snRNA gene Chr18:47418000-47418153 (-)
C3H/HeJ ENSMUSG00175011136
snRNA gene Chr18:47016657-47016810 (-)
C57BL/6NJ ENSMUSG00215008476
snRNA gene Chr18:46444867-46445020 (-)
CAROLI/EiJ no annotation
CAST/EiJ ENSTCUG00005013857
snRNA gene Chr18:46320176-46320329 (-)
CBA/J ENSMUSG00210022507
snRNA gene Chr18:46975696-46975849 (-)
DBA/2J ENSMUSG00185028317
snRNA gene Chr18:46876633-46876786 (-)
FVB/NJ ENSMUSG00205015070
snRNA gene Chr18:46352763-46352916 (-)
JF1/MsJ ENSUMUG00000028246
snRNA gene Chr18:46869790-46869943 (-)
LP/J ENSMUSG00230029731
snRNA gene Chr18:48924449-48924602 (-)
NOD/ShiLtJ ENSMUSG00190029828
snRNA gene Chr18:46661066-46661219 (-)
NZO/HlLtJ ENSMUSG00225027796
snRNA gene Chr18:48827157-48827310 (-)
PWK/PhJ ENSLUMG00010022426
snRNA gene Chr18:46987435-46987588 (-)
SPRET/EiJ ENSMSPG00010013675
snRNA gene Chr18:47261696-47261849 (-)
WSB/EiJ ENSIUOG00005009836
snRNA gene Chr18:46577052-46577205 (-)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
Sequences &
Gene Models
less
  • All Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00002075161 Ensembl Gene Model | MGI Sequence Detail 154 C57BL/6J ±  kb
transcript ENSMUST00020182895 Ensembl | MGI Sequence Detail 154 Not Applicable  
For the selected sequence
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67

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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last database update
09/15/2026
MGI 6.29
The Jackson Laboratory