A novel Phex mutation with defective glycosylation causes hypophosphatemia and rickets in mice.Xiong X., Qi X., Ge X., Gu P., Zhao J., Zhao Q., Gao X.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCJ Biomed Sci 15:47-59 (2008)Cited in1Mapped to5
Molecular cloning of a second human stanniocalcin homologue (STC2).Ishiabshi K., Miyamoto K., Taketani Y., Morita K., Takeda E., Sasaki S., Imai M.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCBiochem. Biophys. Res. Commun. 250:252-258 (1998)Cited in1Mapped to8
Characterization of genes encoding translation initiation factor eIF- 2gamma in mouse and human: sex chromosome localization, escape from X- inactivation and evolution.Ehrmann I.E., Ellis P.S., Mazeyrat S., Duthie S., Brockdorff N., Mattei M.-G., Gavin M.A., Affara N.A., Brown G.M.[...], Scott D.M.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 7:1725-1737 (1998)Cited in6Mapped to50
Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse.Meyer R.A. Jr., Henley C.M., Meyer M.H., Morgan P.L., McDonald A.G., Mills C., Price D.K.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCGenomics 48:289-295 (1998)Mapped to8
An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome.Blair H.J., Uwechue I.C., Barsh G.S., Rowe P.S., Boyd Y.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 48:128-131 (1998)Mapped to17
Mouse mutants carrying deletions that remove the genes mutated in Coffin- Lowry syndrome and lactic acidosis.Blair H.J., Gormally E., Uwechue I.C., Boyd Y.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum Mol Genet 7:549-555 (1998)Mapped to15
Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene.Lorenz B., Francis F., Gempel K., Boeddrich A., Josten M., Schmahl W., Schmidt J., Lehrach H., Meitinger T., Strom T.M.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 7:541-547 (1998)Cited in1Mapped to7
Positional cloning of the PEX gene: new insights into the pathophysiology of X-linked hypophosphatemic rickets.Econs M.J., Francis F.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCAm J Physiol 273:F489-98 (1997)Mapped to5
Skeletal casein kinase activity defect in the HYP mouse.Rifas L., Cheng S., Halstead L.R., Gupta A., Hruska K.A., Avioli L.V.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCCalcif Tissue Int 61:256-259 (1997)Mapped to5
Mammalian membrane metallopeptidases: NEP, ECE, KELL, and PEX.Turner A.J., Tanzawa K.View abstractCategoriesFunction, SequencesSourceMGI: 107489PubMedEurope PMCFASEB J 11:355-364 (1997)Mapped to11
Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice.Beck L., Soumounou Y., Martel J., Krishnamurthy G., Gauthier C., Goodyer C.G., Tenenhouse H.S.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCJ. Clin. Invest. 99:1200-1209 (1997)Cited in2Mapped to4
Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.Strom T.M., Francis F., Lorenz B., Boeddrich A., Econs M.J., Lehrach H., Meitinger T.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 6:165-171 (1997)Cited in2Mapped to6
Fine genetic mapping of the Hyp mutation on mouse chromosome X.Du L., Desbarats M., Cornibert S., Malo D., Ecarot B.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 32:177-183 (1996)Mapped to18
cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone.Du L., Desbarats M., Viel J., Glorieux F.H., Cawthorn C., Ecarot B.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 36:22-28 (1996)Cited in1Mapped to4
Increased renal 25-hydroxyvitamin D3-24-hydroxylase messenger ribonucleic acid and immunoreactive protein in phosphate-deprived Hyp mice: a mechanism for accelerated 1,25-dihydroxyvitamin D3 catabolism in X-linked hypophosphatemic rickets.Roy S., Martel J., Ma S., Tenenhouse H.S.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCEndocrinology 134:1761-1767 (1994)Mapped to5
Renal Na(+)-phosphate cotransport in murine X-linked hypophosphatemic rickets. Molecular characterization.Tenenhouse H.S., Werner A., Biber J., Ma S., Martel J., Roy S., Murer H.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCJ Clin Invest 93:671-676 (1994)Mapped to5
Molecular cloning, functional expression, tissue distribution, and in situ hybridization of the renal sodium phosphate (Na+/P(i)) transporter in the control and hypophosphatemic mouse.Collins J.F., Ghishan F.K.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCFASEB J. 8:862-869 (1994)Cited in11Mapped to7
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus.Econs M.J., Rowe P.S., Francis F., Barker D.F., Speer M.C., Norman M., Fain P.R., Weissenbach J., Read A., Davis K.E.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCJ Clin Endocrinol Metab 79:1351-1354 (1994)Mapped to5
Effect of P(i) restriction on renal Na(+)-P(i) cotransporter mRNA and immunoreactive protein in X-linked Hyp mice.Tenenhouse H.S., Martel J., Biber J., Murer H.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCAm J Physiol 268:F1062-9 (1995)Mapped to5
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets.The HYP consortiumFrancis F., Hennig S., Korn B., Reinhardt R., de Jong P., Poustka A., Lehrach H., Rowe P.S.N., Goulding J.N.[...], Meitinger T.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCNat. Genet. 11:130-136 (1995)Cited in1Mapped to5
Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice.Berning A.K., Eicher E.M., Paul W.E., Scher I.View abstractCategoriesFunction, Sequences, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCJ Immunol 124:1875-1877 (1980)Mapped to15
X chromosome-linked muscular dystrophy (mdx) in the mouse.Bulfield G., Siller W.G., Wight P.A., Moore K.J.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCProc Natl Acad Sci U S A 81:1189-1192 (1984)Mapped to41
Abnormal bone formation induced by implantation of osteosarcoma-derived bone-inducing substance in the X-linked hypophosphatemic mouse.Yoshikawa H., Masuhara K., Takaoka K., Ono K., Tanaka H., Seino Y.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCBone 6:235-239 (1985)Mapped to5
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.Lyon M.F., Scriver C.R., Baker L.R., Tenenhouse H.S., Kronick J., Mandla S.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCProc Natl Acad Sci U S A 83:4899-4903 (1986)Mapped to5
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse.Boneh A., Reade T.M., Scriver C.R., Rishikof E.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCAm J Med Genet 27:997-1003 (1987)Mapped to5