Mapping Data Summary

• Symbol: Phex
• Name: phosphate regulating endopeptidase homolog, X-linked
• ID: MGI:107489
• Chromosome: X

29 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	X	J:6296 Berning AK, et al., Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice. J Immunol. 1980 Apr;124(4):1875-7
CROSS	Cross Type: Backcross	X	J:6296 Berning AK, et al., Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice. J Immunol. 1980 Apr;124(4):1875-7
CROSS	Cross Type: Backcross	X	J:63696 Blair HJ, et al., Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome. Mamm Genome. 2000 Aug;11(8):710-2
CROSS	Cross Type: Backcross	X	J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31
CROSS	Cross Type: Backcross	X	J:7361 Bulfield G, et al., X chromosome-linked muscular dystrophy (mdx) in the mouse. Proc Natl Acad Sci U S A. 1984 Feb;81(4):1189-92
CROSS	Cross Type: Backcross	X	J:14012 Cattanach BM, Close linkage between Li and Hyp. Mouse News Lett. 1985;73:17
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:50115 Ehrmann IE, et al., Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution. Hum Mol Genet. 1998 Oct;7(11):1725-37
CROSS	Cross Type: Backcross	X	J:5749 Eicher EM, et al., Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4667-71
CROSS	Cross Type: Backcross	X	J:11583 Kay G, et al., Determination of a molecular map position for Hyp using a new interspecific backcross produced by in vitro fertilization. Genomics. 1991 Nov;11(3):651-7
CROSS	Cross Type: Backcross	X	J:615 Kay GF, et al., A candidate spermatogenesis gene on the mouse Y chromosome is homologous to ubiquitin-activating enzyme E1. Nature. 1991 Dec 12;354(6353):486-9
CROSS	Cross Type: Backcross	X	J:8335 Lyon MF, et al., The Gy mutation: another cause of X-linked hypophosphatemia in mouse. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4899-903
CROSS	Cross Type: Backcross	X	J:8335 Lyon MF, et al., The Gy mutation: another cause of X-linked hypophosphatemia in mouse. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4899-903
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31
TEXT		X	J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31
TEXT		X	J:46360 Lorenz B, et al., Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene. Hum Mol Genet. 1998 Mar;7(3):541-7
TEXT		X	J:85297 Sabbagh Y, et al., The X chromosome deletion in HYP mice extends into the intergenic region but does not include the SAT gene downstream from Phex. Cytogenet Genome Res. 2002;99(1-4):344-9
TEXT		X	J:38621 Strom TM, et al., Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia. Hum Mol Genet. 1997 Feb;6(2):165-71
TEXT-Genetic Cross		X	J:79953 Carpinelli MR, et al., An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets. Am J Pathol. 2002 Nov;161(5):1925-33
TEXT-Physical Mapping		X	J:46360 Lorenz B, et al., Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene. Hum Mol Genet. 1998 Mar;7(3):541-7
TEXT-Radiation Hybrid		X	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;