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Del(7)Tyrc-3H Complex/Cluster/Region Detail
Summary
  • Symbol
    Del(7)Tyrc-3H
  • Name
    deletion, Chr 7, albino 3 Harwell
  • Feature Type
    complex/cluster/region
  • IDs
    MGI:4431232
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 7, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    8 phenotypes from 1 allele in 1 genetic background
    12 phenotypes from multigenic genotypes
    18 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 of Del(7)Tyr comprise a deletion of at least Tyr resulting in albinism and perinatal lethality.
References
more
  • Summaries
    All 18
    Phenotypes 18
  • Earliest
    J:5063 Erickson RP, et al., Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse. Proc Natl Acad Sci U S A. 1968 Feb;59(2):437-44
  • Latest
    J:68210 Wines ME, et al., Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis. Genomics. 2001 Feb 15;72(1):88-98
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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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory