Mapping Details

GENETIC MAPPING PANELS

Chr	Location	Mapped As	Panel	Mapped By	Scoring
19	53.1 cM	z22532	Boston MGH Cross (MGH)	Fishman, Mark C.	Data
19	286.78 cR	Z22532	Loeb/NIH/5000/4000 (LN54)	Dawid, Igor B.	Data
19	3070.0 cR	z22532	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
hey1	GENE	19		Nambiar et al., 2007	b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and  ... b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and 1.6 cM north of Z22532 (17 recombinants out of 1004).
z9059	SSLP	19		Nambiar et al., 2007	b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and  ... b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and 1.6 cM north of Z22532 (17 recombinants out of 1004).
csnk2b	GENE	19		Nambiar et al., 2007	b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and  ... b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and 1.6 cM north of Z22532 (17 recombinants out of 1004).
hdac1	GENE	19		Nambiar et al., 2007	b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and  ... b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and 1.6 cM north of Z22532 (17 recombinants out of 1004).
b382	Feature	19	1.6 cM	Nambiar et al., 2007	b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and  ... b382 was mapped to LG19 0.6cM south of Z9059 (6 recombinants out of 1004) and 1.6 cM north of Z22532 (17 recombinants out of 1004).

OTHER MAPPING INFORMATION

Primer Sets:

Strain	Bandsize	Restriction Enzyme	Annealing Temperature [C]
AB	0,237		60.0
Forward Primer	GCTGGGAATAAAGGACACCA
Reverse Primer	CAGGTGCTGTTTTCAAGCAA
IND	283,0,243		60.0
Forward Primer	GCTGGGAATAAAGGACACCA
Reverse Primer	CAGGTGCTGTTTTCAAGCAA
TU	237,0,293		60.0
Forward Primer	GCTGGGAATAAAGGACACCA
Reverse Primer	CAGGTGCTGTTTTCAAGCAA
EKW	279,311,237		60.0
Forward Primer	GCTGGGAATAAAGGACACCA
Reverse Primer	CAGGTGCTGTTTTCAAGCAA