Chromosome V Linkage data

Mitotic map

a. Heterozygosity in T1(V;VI) disomics; reference 338
b. Mitotic recombination in T1(V;VI) homozygotes, using sB (VI) as selective marker. Shaded circles represent alternative centromere positions; reference 338

Meiotic map

First markers are ordered from conventional left to right along each chromosome. Note that for this chromosome only, the genomic sequence has been taken into account where conflicting orders are suggested by the linkage data. The second marker is one indicated by the cross to be to the right of the first marker (except where the map distance is given in square brackets [ ]: see below). Second markers are listed in order of increasing recombination value from the first marker, with the exception of unorientated linkages, which are placed first.
Where the map distance is given in square brackets [ ] the orientation of the linkage has not been determined.
"50%" linkage implies that markers were meiotically unlinked, but orientation has been determined by linkage to other markers.
">50%" implies that markers were meiotically unlinked, but orientation has been ascertained by mitotic recombination.
Linkage given as "?" indicates marker position ascertained relative to neighbouring markers, but distance not estimated.
^a map distance likely to be distorted by heterozygosity for chromosome aberration.

Meiotically unmapped markers located on V only by haploidisation or hybridization:
acuO, aloD, aromB, asuD, camD, comA, comB, csuA, fanA, glrC, hetA,C, hygC, imaB, nimB,C,J, nsdB, pacG, pcaE,F,G, riboC, sgpB, suEpro, suDveA, tpsA, tutD.