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Sagg Gene Detail
Summary
  • Symbol
    Sagg
  • Name
    saggy
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:1861992
    NCBI Gene: 103917
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr1:40301577-45913558 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 1, Syntenic
  • Mapping Data
    2 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    2 phenotype references
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.
Mice heterozygous for an ENU-induced mutation exhibit loose skin.
Sequences &
Gene Models
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References
more
  • Summaries
    All 3
    Phenotypes 2
  • Earliest
    J:63816 Nolan PM, et al., A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat Genet. 2000 Aug;25(4):440-3
  • Latest
    J:105704 Christner PJ, et al., Collagen dysregulation in the dermis of the sagg/+ mouse: a loose skin model. J Invest Dermatol. 2006 Mar;126(3):595-602

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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Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory