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Del(7Herc2-Mkrn3)13FRdni
Cytogenetic Marker Detail
 Symbol
Name
ID
Del(7Herc2-Mkrn3)13FRdni
deletion, Chr 7, R D Nicholls13F
MGI:3769761
Synonyms Del13FRdni, TgPWS/AS(del)
Feature Type chromosomal deletion
Genetic Map
Chromosome 7
Syntenic
Sequence Map
Chr7:56050155-62420139 bp
From MGI annotation of GRCm38

  6369985 bp   ±  kb flank

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Mouse Genome Browser
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Transgenic(1)
Human Diseases Modeled Using Mouse Del(7Herc2-Mkrn3)13FRdni (1)    Alleles Annotated to Human Diseases(1)   
Polymorphisms SNPs within 2kb(56736 from dbSNP Build 137)    SNPs within 2kb including multiple locations(58448)
References (Earliest) J:56614 Gabriel JM, et al., A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9258-63
(Latest) J:198496 Resnick JL, et al., Recommendations for the investigation of animal models of Prader-Willi syndrome. Mamm Genome. 2013 Jun;24(5-6):165-78
All references(8)
Disease annotation references (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/09/2014
MGI 5.19
The Jackson Laboratory