WormBase Tree Display for Variation: WBVar00248909
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WBVar00248909 | Evidence | Person_evidence | WBPerson625 | ||
---|---|---|---|---|---|
Name | Public_name | sy97 | |||
Other_name | ZK1067.1a.1:c.3803-1G>T | ||||
ZK1067.1b.1:c.3620-1G>T | |||||
ZK1067.1c.1:c.3818-1G>T | |||||
ZK1067.1d.1:c.3839-1G>T | |||||
HGVSg | CHROMOSOME_II:g.9206768G>T | ||||
Sequence_details | SMap | S_parent | Sequence | ZK1067 | |
Flanking_sequences | ttttcacccaacgcattaaaaaagttacttttaaaataataaattttca | agctatccccatcaaatggcgattactacaaccaaccaaacactccttca | |||
Mapping_target | ZK1067 | ||||
Type_of_mutation | Substitution | a | t | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00022495 | ||||
WBStrain00030810 | |||||
WBStrain00030821 | |||||
Laboratory | PS | ||||
Author | Aroian R | ||||
Sternberg P | |||||
Person | WBPerson625 | ||||
Status | Live | ||||
Affects | Gene | WBGene00002299 | |||
Transcript | ZK1067.1d.1 | VEP_consequence | splice_acceptor_variant | ||
VEP_impact | HIGH | ||||
HGVSc | ZK1067.1d.1:c.3839-1G>T | ||||
Intron_number | 19/20 | ||||
ZK1067.1b.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | ZK1067.1b.1:c.3620-1G>T | ||||
Intron_number | 15/15 | ||||
ZK1067.1c.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | ZK1067.1c.1:c.3818-1G>T | ||||
Intron_number | 17/18 | ||||
ZK1067.1a.1 | VEP_consequence | splice_acceptor_variant | |||
VEP_impact | HIGH | ||||
HGVSc | ZK1067.1a.1:c.3803-1G>T | ||||
Intron_number | 18/19 | ||||
Interactor | WBInteraction000000671 | ||||
WBInteraction000500653 | |||||
WBInteraction000504224 | |||||
WBInteraction000524138 | |||||
WBInteraction000524142 | |||||
WBInteraction000538578 | |||||
Isolation | Mutagen | EMS | |||
Forward_genetics | standard phenotypic screen | ||||
Genetics | Interpolated_map_position | II | 1.09465 | ||
Description | Phenotype (13) | ||||
Reference (27) | |||||
Remark | Isolated in 1987 as a suppressor of the lin-15(n309) multivulva phenotype | Person_evidence | WBPerson26 | ||
alt_det = affects splide acceptor and causes a missolice two nt 3'; thus a frameshift that replaces C-terminal 56 amino acids with 23 novel amino acids mut_det = ag --> aa at splice acceptor of exon 18 | |||||
Method | Substitution_allele |