Mapping Data Summary

• Symbol: Ncf1
• Name: neutrophil cytosolic factor 1
• ID: MGI:97283
• Chromosome: 5

14 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: Kozak Skive (C58/J or NFS/N)	5	J:56499 Hahm S, et al., Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance. Neuron. 1999 Jul;23(3):537-48
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58 + FvSpr	5	J:56499 Hahm S, et al., Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance. Neuron. 1999 Jul;23(3):537-48
CROSS	Cross Type: Backcross	5	J:17309 Jackson SH, et al., Cloning and functional expression of the mouse homologue of p47phox. Immunogenetics. 1994;39(4):272-5
CROSS	Cross Type: Backcross Mapping Panel: Kozak Skive	5	J:17309 Jackson SH, et al., Cloning and functional expression of the mouse homologue of p47phox. Immunogenetics. 1994;39(4):272-5
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58+FvSpr+Skive	5	J:17309 Jackson SH, et al., Cloning and functional expression of the mouse homologue of p47phox. Immunogenetics. 1994;39(4):272-5
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58+FvSpr+Skive	5	J:46806 Shekels LL, et al., Cloning and characterization of mouse intestinal MUC3 mucin: 3' sequence contains epidermal-growth-factor-like domains. Biochem J. 1998 Mar 15;330(Pt 3):1301-8
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: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:55324 DeSilva U, et al., Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Res. 1999 May;9(5):428-36
TEXT-Physical Mapping		5	J:55324 DeSilva U, et al., Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Res. 1999 May;9(5):428-36
TEXT-Physical Mapping		5	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		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-QTL		5	J:90100 Hernandez-Valladares M, et al., Confirmation and dissection of QTL controlling resistance to malaria in mice. Mamm Genome. 2004 May;15(5):390-8
TEXT-Radiation Hybrid		5	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;