Phl1 QTL Detail

Summary

• Symbol
  Phl1
• Name
  progressive hearing loss 1

• Feature Type
  QTL
• IDs
  MGI:3046339
  NCBI Gene: 100035570

Location &
Maps

• Sequence Map
  Chr17:7875843-29487423 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 17, 4.76 cM (cM position of peak correlated region/marker)
• Mapping Data
  1 experiment

Human Diseases

• Diseases
  1 with Phl1 mouse models

Human Disease

Mouse Models

autosomal recessive nonsyndromic deafness 38

IDs

autosomal recessive nonsyndromic deafness 38      

DOID:0110496
ICD10CM:H90.3
OMIM:608219

View 2 models

Mouse Models

Human Disease Modeled: autosomal recessive nonsyndromic deafness 38

Allelic Composition	Genetic Background	Reference	Phenotypes
Phl1101/H/Phl1101/H	involves: 101/H * MAI/Pas	J:111682	View
Phl1101/H/Phl1101/H	involves: 101/H * MBT/Pas	J:111682	View

Click on a disease name to see all genes associated with that disease.

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype from 3 alleles in 2 genetic backgrounds
  1 phenotype from multigenic genotypes
  1 phenotype reference
  

• All Mutations and Alleles
  3
• QTL
  3
• Incidental Mutations
  APF
• Find Mice (IMSR)
  0 strains or lines available

Sequences &
Gene Models

• NCBI Gene
  100035570

References

• Summaries
  All 2

  Diseases 1

  Phenotypes 1
• Earliest
  J:111682 Mashimo T, et al., Two quantitative trait loci affecting progressive hearing loss in 101/H mice. Mamm Genome. 2006 Aug;17(8):841-50