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Symbol
Name
ID
Chromosome
Snrpn
small nuclear ribonucleoprotein N
MGI:98347
7
17 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
7 J:44483 Brady KP, et al., Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Res. 1997 Nov;7(11):1085-93
CROSS Cross Type: Backcross
7 J:29904 Johnson DK, et al., Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. Genetics. 1995 Dec;141(4):1563-71
CROSS Cross Type: Backcross
Mapping Panel: Copeland-Jenkins
7 J:3623 Leff SE, et al., Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat Genet. 1992 Dec;2(4):259-64
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
7 J:43448 MacDonald HR, et al., The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet. 1997 Oct;6(11):1873-8
CROSS Cross Type: Backcross
Mapping Panel: Copeland-Jenkins
7 J:16903 Martin JF, et al., A Mef2 gene that generates a muscle-specific isoform via alternative mRNA splicing. Mol Cell Biol. 1994 Mar;14(3):1647-56
CROSS Cross Type: Backcross
Mapping Panel: Copeland-Jenkins
7 J:17403 Wymore RS, et al., Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p1. Genomics. 1994 Mar 15;20(2):191-202
HYBRID 7 J:3623 Leff SE, et al., Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat Genet. 1992 Dec;2(4):259-64
TEXT 7 J:99883 Buettner VL, et al., Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus. Mamm Genome. 2005 Apr;16(4):219-27
TEXT 7 J:41347 Cattanach BM, et al., A candidate model for Angelman syndrome in the mouse. Mamm Genome. 1997 Jul;8(7):472-8
TEXT 7 J:69578 Chamberlain SJ, et al., The prader-willi syndrome imprinting center activates the paternally expressed murine ube3a antisense transcript but represses paternal ube3a. Genomics. 2001 May 1;73(3):316-22
TEXT 7 J:72512 Choi JD, et al., Microarray expression profiling of tissues from mice with uniparental duplications of Chromosomes 7 and 11 to identify imprinted genes. Mamm Genome. 2001 Oct;12(10):758-64
TEXT 7 J:38906 Dhar MS, et al., A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7. Mamm Genome. 1997 Feb;8(2):143-5
TEXT 7 J:29904 Johnson DK, et al., Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus. Genetics. 1995 Dec;141(4):1563-71
TEXT-Physical Mapping 7 J:69426 Gray TA, et al., An imprinted, mammalian bicistronic transcript encodes two independent proteins. Proc Natl Acad Sci U S A. 1999 May 11;96(10):5616-21
TEXT-Physical Mapping 7 J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-QTL 7 J:24238 Warden CH, et al., Identification of four chromosomal loci determining obesity in a multifactorial mouse model. J Clin Invest. 1995 Apr;95(4):1545-52
TEXT-Radiation Hybrid 7 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory