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Sig Gene Detail
Summary
  • Symbol
    Sig
  • Name
    sightless
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98305
    NCBI Gene: 109565
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr6:4464884-8778488 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 6, Syntenic
  • Mapping Data
    10 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    16 phenotypes from 1 allele in 2 genetic backgrounds
    3 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.
Mutations in this gene result in hydrocephaly, open eye lids at birth and sometimes foot anomalies. The homozygous condition is lethal.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-14412
References
more
  • Summaries
    All 16
    Phenotypes 3
  • Earliest
    J:5021 Batchelor AL, et al., A comparison of the mutagenic effectiveness of chronic neutron- and gamma-irradiation of mouse spermatogonia. Mutat Res. 1966 Jun;3(3):218-29
  • Latest
    J:32894 Primo-Parmo SL, et al., The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family. Genomics. 1996 May 1;33(3):498-507

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
04/30/2024
MGI 6.23
The Jackson Laboratory