Gene Information: ham-2

Nameham-2 View on WormBase
Species C. elegans
Genetic positionX:-7.30 +/- 0.022 cM
Genomic positionX: 4554685..4559408

Strains carrying this gene

Strain Genotype Description
MT3149 ham-2(n1332) X. Egl. HSNs are migration defective and defective in serotonin expression. See also WBPaper00003422.
VC1680 +/szT1 [lon-2(e678)] I; ham-2(gk780)/szT1 X. C07A12.1. Apparent homozygous lethal deletion chromosome balanced by lon-2-marked translocation. Heterozygotes are WT, and segregate WT, Lon-2 males, arrested szT1 aneuploids, and gk780 homozygotes (arrest stage/phenotype undetermined). Pick WT and check for correct segregation of progeny to maintain. External left primer: GTGATTATGGGGTCGAATGG. External right primer: TGGAAAGATGGGGCAATTAG. Internal left primer: GGGAGCGAGAGAGAGACAAA. Internal right primer: GCTCCAGTGGGAAATTGAAA. Internal WT amplicon: 2317 bp. Deletion size: 1294 bp. Deletion left flank: AATGCATTGTCCAATCGCTGCTATGTATGC. Deletion right flank: AGAGCCAAAATGACCAACATTATTGACAGT. Attribution: This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807