Variation Information: hc49

Namehc49 View on WormBase
Species C. elegans
Genetic positionIII:10.57 +/- 0.000 cM
Genomic positionIII: 11508403..11508403
Protein changeY66D12A.20 Substitution

Strains carrying this variation

Strain Genotype Species Description
BA1013 spe-6(hc49) vab-7(e1562)/qC1 [dpy-19(e1259) glp-1(q339)] III; spe-27(it132) IV. C. elegans Male/hermaphrodite line. Maintain at 15C to insure maintenance of male/hermaphrodite line.
BA1061 dpy-18(e364) spe-6(hc49) ale-1(mc14)/qC1 [dpy-19(e1259) glp-1(q339)] III. C. elegans Heterozygotes are WT and segregate WT, Sterile Dpys (Dpy is temperature sensitive), and dead eggs. ale-1 is a recessive embryonic lethal.
BA606 spe-6(hc49) unc-25(e156) III; eDp6 (III;f). C. elegans Animals with the Duplication are WT. Animals without the Duplication are Unc and Sterile.
BA609 spe-6(hc49) vab-7(e1562) III; eDp6 (III;f). C. elegans Animals with the Duplications are WT. Animals which have lost the Duplication are Sterile and have an abnormal tail.
ML456 ale-1(mc14)/spe-6(hc49) unc-25(e156) III. C. elegans Heterozygotes are WT and segregate WT, embryonic lethals (embryos fail to elongate) and Sterile Uncs. mc14 identified as a mutation that leads to abnormal lin-26 expression.