Fnld Gene Detail

Summary

• Symbol
  Fnld
• Name
  faint-lined

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:1309996
  NCBI Gene: 14271
• Alliance
  gene page

Location &
Maps

• Sequence Map
  ChrX:36059304-47772849 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome X, Syntenic
• Mapping Data
  2 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Radiation induced
  1
• Find Mice (IMSR)
  0 strains or lines available

Females heterozygous for this X-linked mutation show subtle striping and are smaller than normal siblings. Hemizygous males and some heterozygous females die as embryos.

Sequences &
Gene Models

• NCBI Gene
  14271

References

• Summaries
  All 3

  Phenotypes 1
• Earliest
  J:52809 Gormally E, et al., Faint lined (Fnl): a novel X-linked coat mutant in the mouse. Genet Res. 1998 Dec;72(3):211-6