Gm25868 Gene Detail

Summary

• Symbol
  Gm25868
• Name
  predicted gene, 25868

• Feature Type
  snoRNA gene
  BioType Conflict
  
• IDs
  MGI:5455645
  NCBI Gene: 115486117
• Alliance
  genome feature page

Location &
Maps

• Sequence Map
  ChrX:134066597-134066710 bp, + strand

  From NCBI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

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

Strain
Comparison

• SNPs within 2kb
  3 from dbSNP Build 142
• Strain Annotations
  16

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_5455645	snoRNA gene	ChrX:134066597-134066710 (+)
129S1/SvImJ	ENSMUSG00200048097	snoRNA gene	ChrX:113141865-113141978 (+)
A/J	ENSMUSG00195049076	snoRNA gene	ChrX:116981075-116981188 (+)
A/J	ENSMUSG00195049109	snoRNA gene	ChrX:117260713-117260826 (-)
AKR/J	no annotation
BALB/cJ	ENSMUSG00180039813	snoRNA gene	ChrX:113385765-113385878 (+)
C3H/HeJ	ENSMUSG00175035689	snoRNA gene	ChrX:117294025-117294138 (+)
C57BL/6NJ	ENSMUSG00215045169	snoRNA gene	ChrX:113769197-113769310 (+)
CAROLI/EiJ	no annotation
CAST/EiJ	no annotation
CBA/J	no annotation
DBA/2J	ENSMUSG00185030161	snoRNA gene	ChrX:128119467-128119580 (+)
DBA/2J	ENSMUSG00185031461	snoRNA gene	ChrX:128399116-128399229 (-)
FVB/NJ	no annotation
JF1/MsJ	ENSUMUG00000030663	snoRNA gene	ChrX:147409851-147409964 (+)
LP/J	ENSMUSG00230040967	snoRNA gene	ChrX:134808006-134808119 (+)
NOD/ShiLtJ	ENSMUSG00190041798	snoRNA gene	ChrX:113618924-113619037 (+)
NZO/HlLtJ	ENSMUSG00225037324	snoRNA gene	ChrX:139455355-139455468 (+)
NZO/HlLtJ	ENSMUSG00225037330	snoRNA gene	ChrX:139684744-139684857 (-)
PWK/PhJ	ENSLUMG00010044407	snoRNA gene	ChrX:112095984-112096097 (+)
SPRET/EiJ	no annotation
WSB/EiJ	ENSIUOG00005037904	snoRNA gene	ChrX:114322375-114322488 (+)

Homology

• Gene Tree
  Gm25868
  

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  2 phenotype references
  

• All Mutations and Alleles
  1
• Targeted
  1
• Genomic Mutations
  1 involving Gm25868
• Find Mice (IMSR)
  0 strains or lines available

Sequences &
Gene Models

• All Sequences
  19

• Ensembl
  ENSMUSG00000119932 (Evidence)
• NCBI Gene
  115486117

Representative Sequences			Length	Strain/Species
genomic	115486117	NCBI Gene Model | MGI Sequence Detail	114	C57BL/6J

References

• Summaries
  All 5

  Diseases 1

  Phenotypes 2
• Earliest
  J:199138 Zhou J, et al., A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice. Biol Reprod. 2013 Jun;88(6):159
• Latest
  J:210663 Zhou J, et al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet. 2014 Jul 15;23(14):3823-9