Mapping Data Summary

• Symbol: Tbx1
• Name: T-box 1
• ID: MGI:98493
• Chromosome: 16

15 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:46649 Aho S, et al., cDNA cloning, mRNA expression, and chromosomal mapping of human and mouse periplakin genes. (Errata: Genomics 1998;51:481). Genomics. 1998 Mar 1;48(2):242-7
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:30494 Fitzgibbon J, et al., Localisation of the gene encoding diacylglycerol kinase 3 (DAGK3) to human chromosome 3q27-28 and mouse chromosome 16. Curr Eye Res. 1995 Nov;14(11):1041-3
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:37738 Kalcheva I, et al., The gene encoding beta-galactoside alpha2,6-sialyltransferase maps to mouse chromosome 16. Mamm Genome. 1997 Aug;8(8):619-20
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:43897 Rhim H, et al., Localization of a neural crest transcription factor, Slug, to mouse chromosome 16 and human chromosome 8. Mamm Genome. 1997;8(11):872-3
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:38907 Saba-el-Leil MK, et al., Chromosomal localization of the mouse genes encoding the ERK1 and ERK2 isoforms of MAP kinases. Mamm Genome. 1997 Feb;8(2):141-2
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	16	J:50106 Yang A, et al., p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell. 1998 Sep;2(3):305-16
TEXT		16	J:110101 Paylor R, et al., Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34
TEXT-Genetic Cross		16	J:18978 Bollag RJ, et al., An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus. Nat Genet. 1994 Jul;7(3):383-9
TEXT-Genetic Cross		16	J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7;
TEXT-Physical Mapping		16	J:60871 Lund J, et al., Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Genomics. 2000 Feb 1;63(3):374-83
TEXT-Physical Mapping		16	J:54501 Lund J, et al., Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2. Mamm Genome. 1999 May;10(5):438-43
TEXT-Physical Mapping		16	J:45079 Puech A, et al., Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14608-13
TEXT-Physical Mapping		16	J:64380 Puech A, et al., Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10090-5
TEXT-Physical Mapping		16	J:49844 Sutherland HF, et al., Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse. Genomics. 1998 Aug 15;52(1):37-43
TEXT-QTL		16	J:109795 Kenney-Hunt JP, et al., Quantitative trait loci for body size components in mice. Mamm Genome. 2006 Jun;17(6):526-37