Mapping Details

GENETIC MAPPING PANELS

Chr	Location	Mapped As	Panel	Mapped By	Scoring
12	32.0 cM	z9891	Boston MGH Cross (MGH)	Fishman, Mark C.	Data
12	659.0 cR	z9891	Goodfellow T51 (T51)	Geisler, Robert	Data
Note: Physical map location as displayed in the genome browsers is more precise than linkage map location. Note: Physical map location should be used whenever possible.

MAPPING FROM PUBLICATIONS

Marker	Type	Chr	Distance	Publication / Person	Comments
z10806	SSLP	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
z15261	SSLP	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
fb57a07	EST	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
raraa	GENE	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
fc05c04	EST	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
z4373	SSLP	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
w24	Feature	12	3.5 cM	Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
fb04b08	EST	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.
z23536	SSLP	12		Pietsch et al., 2006	Pietsch et al. (2006, Development 133(3):395-406) mapped lessenw24 to LG24 using bulk segregant analysis.

OTHER MAPPING INFORMATION

Primer Sets:

Strain	Bandsize	Restriction Enzyme	Annealing Temperature [C]
AB	0,194,188		60.0
Forward Primer	GCATGGTTGAATGCATTTGA
Reverse Primer	ATGCTGTTGTGCTCTGCATC
IND	244,0,236		60.0
Forward Primer	GCATGGTTGAATGCATTTGA
Reverse Primer	ATGCTGTTGTGCTCTGCATC
EKW	194,188,206		60.0
Forward Primer	GCATGGTTGAATGCATTTGA
Reverse Primer	ATGCTGTTGTGCTCTGCATC
TU	206,182,194,176		60.0
Forward Primer	GCATGGTTGAATGCATTTGA
Reverse Primer	ATGCTGTTGTGCTCTGCATC