Gm18453 Pseudogene Detail

Summary

• Symbol
  Gm18453
• Name
  predicted gene, 18453

• Feature Type
  pseudogene
• IDs
  MGI:5010638
  NCBI Gene: 100417211
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr7:58598682-58599307 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, 33.91 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  140 from dbSNP Build 142
• Strain Annotations
  18

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5010638	pseudogene	Chr7:58598682-58599307 (-)
129S1/SvImJ	ENSMUSG00200009387	pseudogene	Chr7:46076944-46077569 (-)
A/J	ENSMUSG00195011097	pseudogene	Chr7:50293058-50293683 (-)
AKR/J	ENSMUSG00220011405	pseudogene	Chr7:44521386-44522011 (-)
BALB/cJ	ENSMUSG00180011163	pseudogene	Chr7:47112063-47112688 (-)
C3H/HeJ	ENSMUSG00175003447	pseudogene	Chr7:47589200-47589825 (-)
C57BL/6NJ	ENSMUSG00215002085	pseudogene	Chr7:46934960-46935585 (-)
CAROLI/EiJ	no annotation
CAST/EiJ	ENSTCUG00005012104	pseudogene	Chr7:50402420-50403045 (-)
CBA/J	ENSMUSG00210017484	pseudogene	Chr7:47955909-47956534 (-)
DBA/2J	ENSMUSG00185006574	pseudogene	Chr7:51878672-51879297 (-)
FVB/NJ	ENSMUSG00205001406	pseudogene	Chr7:47640985-47641610 (-)
JF1/MsJ	ENSUMUG00000013948	pseudogene	Chr7:56609295-56609920 (-)
LP/J	ENSMUSG00230006390	pseudogene	Chr7:57394214-57394839 (-)
NOD/ShiLtJ	ENSMUSG00190003721	pseudogene	Chr7:47989080-47989705 (-)
NZO/HlLtJ	ENSMUSG00225010982	pseudogene	Chr7:55612700-55613325 (-)
PWK/PhJ	ENSLUMG00010002514	pseudogene	Chr7:46536649-46537274 (-)
SPRET/EiJ	ENSMSPG00010001505	pseudogene	Chr7:46596976-46597601 (-)
WSB/EiJ	ENSIUOG00005005624	pseudogene	Chr7:48224141-48224766 (-)

Homology

• Gene Tree
  Gm18453
  

Human Diseases

• References
  5 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  35 phenotype references
  

• All Mutations and Alleles
  4
• Radiation induced
  1
• Targeted
  2
• Transgenic
  1
• Genomic Mutations
  4 involving Gm18453
• Find Mice (IMSR)
  0 strains or lines available

Expression

• Assay Results
  597

Tissue x Stage Matrix

• Other Mouse Links
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  22
• RefSeq
  1

• Ensembl
  ENSMUSG00000109252 (Evidence)
• NCBI Gene
  100417211

Representative Sequences			Length	Strain/Species
genomic	100417211	NCBI Gene Model | MGI Sequence Detail	626	C57BL/6J

References

• Summaries
  All 38

  Diseases 5

  Phenotypes 35
• Earliest
  J:56614 Gabriel JM, et al., A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9258-63
• Latest
  J:390137 Otani Y, et al., Restoration of axon initial segment plasticity via chemogenetic activation rescues autism-related behaviors. Cell Death Dis. 2026 May 19;17(1)