Gm26288 Gene Detail

Summary

• Symbol
  Gm26288
• Name
  predicted gene, 26288

• Feature Type
  snoRNA gene
• IDs
  MGI:5456065
  NCBI Gene: 115485618
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  Chr7:57797844-57797975 bp, - strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

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

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5456065	snoRNA gene	Chr7:57797844-57797975 (-)
129S1/SvImJ	ENSMUSG00200008927	snoRNA gene	Chr7:45280734-45280865 (-)
A/J	ENSMUSG00195011177	snoRNA gene	Chr7:49490848-49490979 (-)
AKR/J	ENSMUSG00220011329	snoRNA gene	Chr7:43727516-43727647 (-)
BALB/cJ	ENSMUSG00180010829	snoRNA gene	Chr7:46307238-46307369 (-)
C3H/HeJ	ENSMUSG00175003711	snoRNA gene	Chr7:46781039-46781170 (-)
C57BL/6NJ	ENSMUSG00215002190	snoRNA gene	Chr7:46132566-46132697 (-)
CAROLI/EiJ	no annotation
CAST/EiJ	ENSTCUG00005023648	snoRNA gene	Chr7:49593843-49593974 (-)
CBA/J	ENSMUSG00210017475	snoRNA gene	Chr7:47162576-47162707 (-)
DBA/2J	ENSMUSG00185006098	snoRNA gene	Chr7:51073873-51074004 (-)
FVB/NJ	ENSMUSG00205001651	snoRNA gene	Chr7:46854833-46854964 (-)
JF1/MsJ	ENSUMUG00000015400	snoRNA gene	Chr7:55838557-55838688 (-)
LP/J	ENSMUSG00230006405	snoRNA gene	Chr7:56600899-56601030 (-)
NOD/ShiLtJ	ENSMUSG00190003745	snoRNA gene	Chr7:47196817-47196948 (-)
NZO/HlLtJ	ENSMUSG00225011022	snoRNA gene	Chr7:54810376-54810507 (-)
PWK/PhJ	ENSLUMG00010002380	snoRNA gene	Chr7:45752663-45752794 (-)
SPRET/EiJ	ENSMSPG00010001612	snoRNA gene	Chr7:45811930-45812061 (-)
WSB/EiJ	ENSIUOG00005005869	snoRNA gene	Chr7:47425044-47425175 (-)

Homology

• Gene Tree
  Gm26288
  

Human Diseases

• References
  5 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  29 phenotype references
  

• All Mutations and Alleles
  3
• Targeted
  2
• Transgenic
  1
• Genomic Mutations
  3 involving Gm26288
• Find Mice (IMSR)
  0 strains or lines available

Gene Ontology
(GO)
Classifications

• All GO Annotations
  2
• GO References
  1

Sequences &
Gene Models

• All Sequences
  22
• RefSeq
  1

• Ensembl
  ENSMUSG00000119548 (Evidence)
• NCBI Gene
  115485618

Representative Sequences			Length	Strain/Species
genomic	115485618	NCBI Gene Model | MGI Sequence Detail	132	C57BL/6J
transcript	XR_004934689	RefSeq | MGI Sequence Detail	132	C57BL/6J

References

• Summaries
  All 33

  Diseases 5

  Gene Ontology 1

  Phenotypes 29
• 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)