MN7 Probe Detail MGI Mouse MGI:17998

MN7 Probe Detail

Name

MN7
Sequence Type

genomic
ID

MGI:17998
Note

MN7 was isolated from a microdissected region of PWS/AS.

Species

human

Herc2

HECT and RLD domain containing E3 ubiquitin protein ligase 2

J:11587 Chaillet JR, et al., Genomics. 1991 Nov;11(3):773-6

Endonuclease	Gene	Allele	Fragments	Strains
ScrF1	Herc2	a	1.0kb	AKR/J
ScrF1	Herc2	d	0.8kb	DBA/2J

J:4101 Nicholls RD, et al., Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4

Endonuclease	Gene	Allele	Fragments	Strains
TaqI	Herc2	m	2.5kb	M. m. musculus
TaqI	Herc2	s	2.7kb	M. spretus

J:11587 Chaillet JR, et al., The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7. Genomics. 1991 Nov;11(3):773-6

J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4

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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