Mapping Data Summary

• Symbol: Gtf2ird1
• Name: general transcription factor II I repeat domain-containing 1
• ID: MGI:1861942
• Chromosome: 5

11 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	13	J:36920 Kingsmore SF, et al., Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13. J Investig Med. 1996 Oct;44(8):454-61
CROSS	Cross Type: Backcross	13	J:37823 Tchernev VT, et al., Genetic mapping of 20 novel expressed sequence tags from midgestation mouse embryos suggests chromosomal clustering. Genomics. 1997 Feb 15;40(1):170-4
TEXT		13	J:37823 Tchernev VT, et al., Genetic mapping of 20 novel expressed sequence tags from midgestation mouse embryos suggests chromosomal clustering. Genomics. 1997 Feb 15;40(1):170-4
TEXT-Genetic Cross		13	J:36920 Kingsmore SF, et al., Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13. J Investig Med. 1996 Oct;44(8):454-61
TEXT-Physical Mapping		5	J:73830 DeSilva U, et al., Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. Genome Res. 2002 Jan;12(1):3-15
TEXT-Physical Mapping		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
TEXT-Physical Mapping		13	J:35910 Kingsmore SF, et al., Physical mapping of the beige critical region on mouse chromosome 13. Mamm Genome. 1996 Oct;7(10):773-5
TEXT-Physical Mapping		5	J:72400 Mouse Genome Sequence and Mouse Genome Informatics Scientific Curators, Mouse Genome Sequence Project Annotation. 2001;
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-Physical Mapping		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
TEXT-Radiation Hybrid		5	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;