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Fnld Gene Detail
Summary
  • Symbol
    Fnld
  • Name
    faint-lined
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:1309996
    NCBI Gene: 14271
Location & Maps
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  • Genetic Map
    Chromosome X, Syntenic
  • Mapping Data
    2 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    4 phenotypes from 1 allele in 1 genetic background
    1 phenotype reference
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
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.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Sequences &
Gene Models
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References
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  • Summaries
    All 3
    Gene Ontology 1
    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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory