ZFIN ID: ZDB-SSLP-980528-1412

Mapping Details

SSLP: z10567
PHYSICAL MAP AND BROWSER No data available
PHYSICAL MAPPING No data available

GENETIC MAPPING PANELS
Chr Location Mapped As Panel Mapped By Scoring
21 38.1 cM z10567 Boston MGH Cross (MGH) Fishman, Mark C. Data
21 73.0 cM z10567 Heat Shock (HS) Woods, Ian G. Data
Note: Physical map location as displayed in the genome browsers is more precise than linkage map location.
Physical map location should be used whenever possible.
MAPPING FROM PUBLICATIONS
Marker Type Chr Distance Publication / Person Comments
z21106 SSLP 21 Keegan et al., 2002 Keegan et al. (2002, Dev 129:1623-1632) mapped the pan locus using half-tetrad and bulk segregant analysis to a small (< 1 cM) region on linkage group 21 between SSLP markers Z21106 and Z10567.
z21106 SSLP 21 Keegan et al., 2002 Keegan et al. (2002) used half-tetrad analysis and bulk segregant analysis to map the pandora (pan) locus to a <1 cM interval between the SSLP markers z21106 and z10567 on linkage group 21.
supt6h GENE 21 Keegan et al., 2002 Keegan et al. (2002, Dev 129:1623-1632) mapped the pan locus using half-tetrad and bulk segregant analysis to a small (< 1 cM) region on linkage group 21 between SSLP markers Z21106 and Z10567.
m313 Feature 21 Keegan et al., 2002 Keegan et al. (2002) used half-tetrad analysis and bulk segregant analysis to map the pandora (pan) locus to a <1 cM interval between the SSLP markers z21106 and z10567 on linkage group 21.

OTHER MAPPING INFORMATION
Chr 21 Keegan et al., 2002 Keegan et al. (2002, Dev 129:1623-1632) mapped the pan locus using half-tetrad and bulk  ...
Chr 21 Keegan et al., 2002 Keegan et al. (2002) used half-tetrad analysis and  ...
Primer Sets:
Strain Bandsize Restriction Enzyme Annealing Temperature [C]
AB 0,248,228 60.0
Forward Primer TCGGCCATACCGTATGTTTT
Reverse Primer TACCGTTAGCCCACCTGAAC
IND 242,0,218 60.0
Forward Primer TCGGCCATACCGTATGTTTT
Reverse Primer TACCGTTAGCCCACCTGAAC
EKW 24,212,0,234 60.0
Forward Primer TCGGCCATACCGTATGTTTT
Reverse Primer TACCGTTAGCCCACCTGAAC
TU 0,238 60.0
Forward Primer TCGGCCATACCGTATGTTTT
Reverse Primer TACCGTTAGCCCACCTGAAC