Gm29719 Gene Detail

Summary

• Symbol
  Gm29719
• Name
  predicted gene, 29719

• Feature Type
  lncRNA gene
  BioType Conflict
  
• IDs
  MGI:5588878
  NCBI Gene: 101055731
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr17:6407088-6462231 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 17, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  60 from dbSNP Build 142
• Strain Annotations
  12

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5588878	lncRNA gene	Chr17:6407088-6462231 (-)
129S1/SvImJ	no annotation
A/J	no annotation
AKR/J	ENSMUSG00220029247	pseudogene	Chr17:3536067-3577939 (+)
BALB/cJ	ENSMUSG00180026669	pseudogene	Chr17:3194321-3234991 (+)
C3H/HeJ	no annotation
C57BL/6NJ	no annotation
CAROLI/EiJ	no annotation
CAST/EiJ	no annotation
CBA/J	ENSMUSG00210040642	pseudogene	Chr17:3213331-3255280 (+)
DBA/2J	ENSMUSG00185023742	pseudogene	Chr17:3705761-3746953 (+)
FVB/NJ	no annotation
JF1/MsJ	no annotation
LP/J	ENSMUSG00230035319	pseudogene	Chr17:4671366-4712557 (-)
LP/J	ENSMUSG00230035637	pseudogene	Chr17:4836950-4878141 (-)
NOD/ShiLtJ	ENSMUSG00190040918	pseudogene	Chr17:3289254-3332224 (-)
NZO/HlLtJ	ENSMUSG00225029262	pseudogene	Chr17:6805052-6845983 (-)
NZO/HlLtJ	ENSMUSG00225029173	pseudogene	Chr17:6975597-7016788 (-)
PWK/PhJ	no annotation
SPRET/EiJ	ENSMSPG00010038058	pseudogene	Chr17:3288201-3329504 (+)
WSB/EiJ	ENSIUOG00005014757	pseudogene	Chr17:3397389-3438848 (+)

Human Diseases

• References
  6 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  372 phenotype references
  

• All Mutations and Alleles
  1
• Radiation induced
  1
• Genomic Mutations
  1 involving Gm29719
• Find Mice (IMSR)
  0 strains or lines available

Expression

• cDNA Data
  1

• Other Mouse Links
  GEO
  Expression Atlas

Sequences &
Gene Models

• All Sequences
  19
• RefSeq
  1

• Ensembl
  ENSMUSG00000116719 (Evidence), ENSMUSG00000116992 (Evidence)
• NCBI Gene
  101055731

Representative Sequences			Length	Strain/Species
genomic	101055731	NCBI Gene Model | MGI Sequence Detail	55144	C57BL/6J
transcript	NR_163600	RefSeq | MGI Sequence Detail	1812	ZRU/MplStud

Molecular
Reagents

• All nucleic 1

  cDNA 1

References

• Summaries
  All 376

  Diseases 6

  Phenotypes 372
• Earliest
  J:30229 Davisson MT, et al., Segmental trisomy as a mouse model for Down syndrome. Prog Clin Biol Res. 1993;384:117-33
• Latest
  J:391449 Thibodeau J, et al., Loss of cystathionine-beta-synthase contributes to elevated OXPHOS, a vulnerability in Ara-C-resistant Myeloid Leukemia in Down syndrome. Biochem Pharmacol. 2026 Feb 13;247:117815