DN10 Probe Detail MGI Mouse MGI:10882

DN10 Probe Detail

Name

DN10
Sequence Type

cDNA
ID

MGI:10882
Insert Size

3.2kb

Species

human
Age

embryonic
Tissue

brain

Oca2

oculocutaneous albinism II

J:14250 Nicholls RD, Mouse News Lett. 1989;84:87-88

Endonuclease	Gene	Allele	Fragments	Strains
MspI	Oca2	a	not given	AKR, C3H/HeJ
		b	not given	C57BL/6J, C57L/J
		c	not given	SJL/J
		d	not given	DBA/2J

J:3600 Rinchik EM, et al., Nature. 1993 Jan 7;361(6407):72-6

Endonuclease	Gene	Allele	Fragments	Strains
BamHI	Oca2	r	6.0,3.3kb	129/Rl-Oca2^p Tyr^c-ch
BamHI	Oca2	s	7.7,3.6kb	M. spretus

J:14250 Nicholls RD, A cDNA from proximal human Chromosome 15q maps near Mtv-1 on mouse Chromosome 7. Mouse News Lett. 1989;84:87-88

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:3600 Rinchik EM, et al., A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism. Nature. 1993 Jan 7;361(6407):72-6

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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