Mapping Data Summary

• Symbol: Stx1a
• Name: syntaxin 1A (brain)
• ID: MGI:109355
• Chromosome: 5

6 mapping experiments

Experiment Type	Details	Chromosome	Reference
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
TEXT-Physical Mapping		5	J:61965 de Luis O, et al., WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog. Eur J Hum Genet. 2000 Mar;8(3):215-22
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:72400 Mouse Genome Sequence and Mouse Genome Informatics Scientific Curators, Mouse Genome Sequence Project Annotation. 2001;
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;