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argininosuccinate lyase
8 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:68983 Durkin ME, et al., Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams-Beuren Syndrome. Genomics. 2001 Apr 1;73(1):20-7
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:52002 Paperna T, et al., Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion. Genomics. 1998 Dec 15;54(3):453-9
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:58545 Perez Jurado LA, et al., TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog. Cytogenet Cell Genet. 1999;86(3-4):277-84
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:40407 Sutton VR, et al., Regional localization of the mouse argininosuccinate lyase gene to chromosome 5. Mamm Genome. 1997;8(11):871
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:65086 Valero MC, et al., Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the williams-beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s) [In Process Citation]. Genomics. 2000 Oct 1;69(1):1-13
CROSS Cross Type: Backcross
Mapping Panel: JAX (BSS)
5 J:49924 Wang YK, et al., Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome. Genomics. 1999 Apr 15;57(2):235-48
TEXT-Physical Mapping 5 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 5 J:93200 Suto J, et al., Further mapping and characterization of Naq1, a quantitative trait locus responsible for maternal inferior nurturing ability in RR mice. J Vet Med Sci. 2004 Sep;66(9):1033-8

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MGI 6.13
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