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Del(7Slx1b-Sept1)4Aam
Cytogenetic Marker Detail
Symbol

Name
ID
Del(7Slx1b-Sept1)4Aam
deletion, Chr 7, Alea A Mills 4
MGI:5291501
Feature Type
chromosomal deletion
Genetic Map
Chromosome 7
Syntenic
Sequence Map
Chr7:126689468-127218498 bp
From MGI annotation of GRCm38

  529031 bp   ±  kb flank

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Mouse Genome Browser
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Targeted(1)
 
Mice with this deletion exhibit decreased body size, hyperactivity, and stereotypic behavior.
 
Human Diseases Modeled in Mice Using Del(7Slx1b-Sept1)4Aam (1)    Mutations Annotated to Human Diseases (1)   
Polymorphisms
SNPs within 2kb(2337 from dbSNP Build 137)    SNPs within 2kb including multiple locations(2353)
References
(Earliest) J:176335 Horev G, et al., Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism. Proc Natl Acad Sci U S A. 2011 Oct 3;
(Latest) J:219859 Pucilowska J, et al., The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway. J Neurosci. 2015 Feb 18;35(7):3190-200
All references(6)
Disease annotation references (4)

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
07/21/2015
MGI 5.22
The Jackson Laboratory