|
Symbol Name ID Chromosome |
Asl
argininosuccinate lyase MGI:88084 5 |
| 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 |
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 04/23/2024 MGI 6.23 |
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