Gm55369 Gene Detail

Summary

• Symbol
  Gm55369
• Name
  predicted gene, 55369

• Feature Type
  snRNA gene
• IDs
  MGI:6847209
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr16:18173480-18173627 bp, + strand

  From Ensembl annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 16, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

• Strain Annotations
  1

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_6847209	snRNA gene	Chr16:18173480-18173627 (+)
129S1/SvImJ	no annotation
A/J	no annotation
AKR/J	no annotation
BALB/cJ	no annotation
C3H/HeJ	no annotation
C57BL/6NJ	no annotation
CAROLI/EiJ	no annotation
CAST/EiJ	no annotation
CBA/J	no annotation
DBA/2J	no annotation
FVB/NJ	no annotation
LP/J	no annotation
NOD/ShiLtJ	no annotation
NZO/HlLtJ	no annotation
PWK/PhJ	no annotation
SPRET/EiJ	no annotation
WSB/EiJ	no annotation

Homology

• Gene Tree
  Gm55369
  

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype reference
  

• All Mutations and Alleles
  2
• Endonuclease-mediated
  2
• Genomic Mutations
  2 involving Gm55369
• Find Mice (IMSR)
  0 strains or lines available

Sequences &
Gene Models

• All Sequences
  3

• Ensembl
  ENSMUSG00002075609 (Evidence)

Representative Sequences			Length	Strain/Species
genomic	ENSMUSG00002075609	Ensembl Gene Model | MGI Sequence Detail	148	C57BL/6J
transcript	ENSMUST00020182738	Ensembl | MGI Sequence Detail	148	Not Applicable

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:304974 Saito R, et al., Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders. Mol Brain. 2021 Apr 12;14(1):68