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Del(13)1N
Spontaneous Allele Detail
Nomenclature
Symbol: Del(13)1N
Name: Deletion, Chr 13, NIH 1
MGI ID: MGI:6514360
Gene: Del(13)1N  Location: unknown  Genetic Position: Chr13, Syntenic
Mutation
origin
Strain of Origin:  C57BL/6N
Mutation
description
Allele Type:    Spontaneous (Modified regulatory region)
Mutation:    Deletion
 
Mutation detailsThis multigenic deletion, present in C57BL/6NJ and C57BL/6NTac but not C57BL/6J inbred strains, is approximately 1 Mb in size and spans from Chr13:65.66Mb-66.67Mb which includes several lincRNA and pseudogenes along with Zfp998 and Zfp997, with the distal breakpoint falling between Zfp997 and Zfp640. (J:282526)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Del(13)1N Mutation:  1 strain or line available
References
Original:  J:282526 Treger RS, et al., The Lupus Susceptibility Locus Sgp3 Encodes the Suppressor of Endogenous Retrovirus Expression SNERV. Immunity. 2019 Feb 19;50(2):334-347.e9
All:  1 reference(s)

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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last database update
10/05/2021
MGI 6.17
The Jackson Laboratory