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Renf1 QTL Detail
Summary
  • Symbol
    Renf1
  • Name
    renal failure 1
  • Feature Type
    QTL
  • IDs
    MGI:2181044
    NCBI Gene: 246740
Location &
Maps
more
  • Sequence Map
    Chr9:52123178-99910428 bp
  • From MGI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 9, cM position of peak correlated region/marker: Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype 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
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Sequences &
Gene Models
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References
more
  • Summaries
    All 3
    Phenotypes 1
  • Earliest
    J:74499 Andrews KL, et al., Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome. Am J Pathol. 2002 Feb;160(2):721-30
  • Latest
    J:96632 Zheng Z, et al., A Mendelian locus on chromosome 16 determines susceptibility to doxorubicin nephropathy in the mouse. Proc Natl Acad Sci U S A. 2005 Feb 15;102(7):2502-7

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/26/2019
MGI 6.14
The Jackson Laboratory