Rr358651 Other Genome Feature Detail

Summary

• Symbol
  Rr358651
• Name
  regulatory region 358651

• Feature Type
  CTCF binding site
• IDs
  MGI:7246873

Location &
Maps

• Sequence Map
  Chr19:4818601-4818800 bp, . strand

  From Ensembl Reg annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 19, Syntenic
• Mapping Data
  1 experiment

Strain
Comparison

• SNPs within 2kb
  95 from dbSNP Build 142

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Endonuclease-mediated
  1
• Genomic Mutations
  1 involving Rr358651
• Find Mice (IMSR)
  0 strains or lines available

Sequences &
Gene Models

• All Sequences
  1

Representative Sequences			Length	Strain/Species
genomic	ENSMUSR00000820202	Ensembl | MGI Sequence Detail	200	Not Applicable

Other Database
Links

Ensembl Regulatory Feature

ENSMUSR00000820202

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:340400 Tsai YY, et al., Activation of TrkB signaling mitigates cerebellar anomalies caused by Rbm4-Bdnf deficiency. Commun Biol. 2023 Sep 5;6(1):910