Gm18127 Pseudogene Detail

Summary

• Symbol
  Gm18127
• Name
  predicted gene, 18127

• Feature Type
  pseudogene
• IDs
  MGI:5010312
  NCBI Gene: 100416464
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr7:57549697-57550395 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, 33.61 cM
• Mapping Data
  1 experiment

Strain
Comparison

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

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5010312	pseudogene	Chr7:57549697-57550435 (-)
129S1/SvImJ	ENSMUSG00200009726	pseudogene	Chr7:45059961-45060685 (-)
A/J	ENSMUSG00195011191	pseudogene	Chr7:49211021-49211745 (-)
AKR/J	ENSMUSG00220011377	pseudogene	Chr7:43506717-43507441 (-)
BALB/cJ	ENSMUSG00180010887	pseudogene	Chr7:46086531-46087255 (-)
C3H/HeJ	ENSMUSG00175003658	pseudogene	Chr7:46560267-46560991 (-)
C57BL/6NJ	ENSMUSG00215002028	pseudogene	Chr7:45882981-45883705 (-)
CAROLI/EiJ	no annotation
CAST/EiJ	ENSTCUG00005023437	pseudogene	Chr7:49370267-49370982 (-)
CBA/J	ENSMUSG00210017548	pseudogene	Chr7:46941807-46942531 (-)
DBA/2J	ENSMUSG00185006735	pseudogene	Chr7:50853142-50853866 (-)
FVB/NJ	ENSMUSG00205001421	pseudogene	Chr7:46609458-46610182 (-)
JF1/MsJ	ENSUMUG00000014946	pseudogene	Chr7:55615757-55616481 (-)
LP/J	ENSMUSG00230006351	pseudogene	Chr7:56380146-56380870 (-)
NOD/ShiLtJ	ENSMUSG00190003732	pseudogene	Chr7:46976058-46976782 (-)
NZO/HlLtJ	ENSMUSG00225010914	pseudogene	Chr7:54562261-54562985 (-)
PWK/PhJ	ENSLUMG00010002409	pseudogene	Chr7:45527602-45528324 (-)
SPRET/EiJ	ENSMSPG00010001546	pseudogene	Chr7:45567964-45568685 (-)
WSB/EiJ	ENSIUOG00005005836	pseudogene	Chr7:47199850-47200574 (-)

Homology

• Gene Tree
  Gm18127
  

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 Gm18127
• 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
  ENSMUSG00000109339 (Evidence)
• NCBI Gene
  100416464

Representative Sequences			Length	Strain/Species
genomic	100416464	NCBI Gene Model | MGI Sequence Detail	699	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)