Mapping Data Summary

• Symbol: Bmp6
• Name: bone morphogenetic protein 6
• ID: MGI:88182
• Chromosome: 13

15 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	13	J:23148 Avraham KB, et al., Murine chromosomal location of eight members of the hepatocyte nuclear factor 3/fork head winged helix family of transcription factors. Genomics. 1995 Jan 20;25(2):388-93
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:44997 Dai G, et al., Prolactin-like protein-A gene structure and chromosomal mapping. Mamm Genome. 1999 Jan;10(1):78-80
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:59222 Dai G, et al., Three novel paralogs of the rodent prolactin gene family. J Endocrinol. 2000;166(1):63-75
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:46755 Dai GL, et al., A new member of the mouse prolactin (PRL)-like protein-C subfamily, PRL-like protein-C alpha: Structure and expression. Endocrinology. 1998;139(12):5157-5163
CROSS	Cross Type: Backcross	13	J:10440 Dickinson ME, et al., Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci. Genomics. 1990 Mar;6(3):505-20
CROSS	Cross Type: Backcross Mapping Panel: Copeland-Jenkins	13	J:10440 Dickinson ME, et al., Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci. Genomics. 1990 Mar;6(3):505-20
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:50869 Ko MSH, et al., Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome. Hum Mol Genet. 1998 Nov;7(12):1967-78
CROSS	Cross Type: Unspecified	13	J:38300 Perou CM, et al., Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 1997 Jan 15;39(2):136-46
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:39061 Zhang ZX, et al., The methionine synthase (Mtr) gene maps to proximal mouse chromosome 13. Mamm Genome. 1997 Oct;8(10):787-8
TEXT-Genetic Cross		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Physical Mapping		11	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		13	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-QTL		13	J:75819 Shimizu M, et al., Chromosome 13 locus, Pbd2, regulates bone density in mice. J Bone Miner Res. 2001 Nov;16(11):1972-82
TEXT-QTL-Candidate Genes		13	J:77538 Shimizu M, et al., A congenic mouse and candidate gene at the Chromosome 13 locus regulating bone density. Mamm Genome. 2002 Jul;13(7):335-40
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;