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T(7;19)145H Cytogenetic Marker Detail
Summary
  • Symbol
    T(7;19)145H
  • Name
    reciprocal translocation, Chr 7 and 19, Harwell 145
  • Synonyms
    T145H
  • Feature Type
    reciprocal chromosomal translocation
  • IDs
    MGI:103980
    NCBI Gene: 21271
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 19, cytoband D1
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    7 phenotypes from 1 allele in 1 genetic background
    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.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-25302
References
more
  • Summaries
    All 6
    Phenotypes 3
  • Earliest
    J:34742 Lyon MF, et al., Autosomal translocations causing male sterility and viable aneuploidy in the mouse. Cytogenetics. 1966;5:335-54
  • Latest
    J:182572 Fellmann N, et al., Pituitary-gonadal axis in sterile male mice heterozygous for autosomal reciprocal translocation T145H. J Reprod Fertil. 1982 Nov;66(2):723-8
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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory