Gm18119 Pseudogene Detail

Summary

• Symbol
  Gm18119
• Name
  predicted gene, 18119

• Feature Type
  pseudogene
• IDs
  MGI:5010304
  NCBI Gene: 100416456
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr10:77488581-77489193 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 10, 39.72 cM
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  183 from dbSNP Build 142
• Strain Annotations
  24

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5010304	pseudogene	Chr10:77488578-77489193 (-)
129S1/SvImJ	ENSMUSG00200050102	pseudogene	Chr10:74166419-74167034 (-)
A/J	ENSMUSG00195050057	pseudogene	Chr10:74503146-74503761 (-)
AKR/J	ENSMUSG00220049027	pseudogene	Chr10:74162731-74163346 (-)
BALB/cJ	ENSMUSG00180052951	pseudogene	Chr10:74517531-74518146 (-)
C3H/HeJ	ENSMUSG00175052519	pseudogene	Chr10:74388678-74389293 (-)
C57BL/6NJ	ENSMUSG00215053564	pseudogene	Chr10:74126419-74127034 (-)
CAROLI/EiJ	no annotation
CAST/EiJ	ENSTCUG00005051952	pseudogene	Chr10:74031108-74031722 (-)
CBA/J	ENSMUSG00210049885	pseudogene	Chr10:74244854-74245469 (-)
DBA/2J	ENSMUSG00185053329	pseudogene	Chr10:74587164-74587779 (-)
FVB/NJ	ENSMUSG00205051514	pseudogene	Chr10:74279162-74279777 (-)
JF1/MsJ	ENSUMUG00000055677	pseudogene	Chr10:75754153-75754767 (-)
LP/J	ENSMUSG00230051158	pseudogene	Chr10:76356660-76357275 (-)
NOD/ShiLtJ	ENSMUSG00190052611	pseudogene	Chr10:74564635-74565250 (-)
NZO/HlLtJ	ENSMUSG00225047950	pseudogene	Chr10:80653440-80654055 (-)
PWK/PhJ	ENSLUMG00010044288	pseudogene	ChrX:136900224-136900838 (+)
PWK/PhJ	ENSLUMG00010052698	pseudogene	Chr10:74143417-74144031 (-)
PWK/PhJ	ENSLUMG00010036234	pseudogene	Chr2:66778856-66779470 (+)
SPRET/EiJ	ENSMSPG00010018846	pseudogene	Chr16:556343-556957 (-)
SPRET/EiJ	ENSMSPG00010047562	pseudogene	Chr7:36313577-36314191 (+)
SPRET/EiJ	ENSMSPG00010012306	pseudogene	Chr18:2917420-2918034 (-)
SPRET/EiJ	ENSMSPG00010048474	pseudogene	Chr10:75947667-75948281 (-)
SPRET/EiJ	ENSMSPG00010046243	pseudogene	Chr5:28944115-28944729 (-)
WSB/EiJ	ENSIUOG00005051510	pseudogene	Chr10:74174594-74175209 (-)

Homology

• Gene Tree
  Gm18119
  

Human Diseases

• References
  2 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  33 phenotype references
  

• All Mutations and Alleles
  5
• Chemically induced (other)
  1
• Endonuclease-mediated
  1
• Targeted
  3
• Genomic Mutations
  5 involving Gm18119
• 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
  28
• RefSeq
  1

• Ensembl
  ENSMUSG00000112007 (Evidence)
• NCBI Gene
  100416456

Representative Sequences			Length	Strain/Species
genomic	100416456	NCBI Gene Model | MGI Sequence Detail	613	C57BL/6J

References

• Summaries
  All 36

  Diseases 2

  Phenotypes 33
• Earliest
  J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
• Latest
  J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;