Ace View of T04A8.7 | |
T04A8.7 Details | |
Description | T04A8.7 is orthologous to human GLUCOSIDASE, ACID BETA (GBA; OMIM:606463), which when mutated leads to Gaucher disease. |
GO Terms | alpha-amylase activity (GO:0004556) ; carbohydrate metabolism (GO:0005975) ; hydrolase activity, hydrolyzing O-glycosyl compounds (GO:0004553) |
Location | III:4694923..4698370 |
RNAi Phenotypes | |
External Links | |
Associated RNAi Experiments | |
Experiments with Non-Wild Phenotypes | |
TH:300d4 | |
PF:GL1_1G5 | Aberrant AB or P1 spindle orientation ; Ectopic cleavage furrows ; Emb ; Excessive blebbing ; P0 spindle positioning defect ; Polar body reabsorbed ; Pronuclei meet more centrally ; Reversed asynchrony |
Cenix:341-h7 | Pace of P-Lineage abnormal ; WT_postembryonic_morphology |
TH:341h7 | |
Simmer:T04A8.7 | Gro |
JA:T04A8.7 | Bmd ; Emb ; Gro |
Cenix:300-d4 | Cortical Dynamics abnormal ; Sterile F0/Fertility Problems |
Gene Plot of T04A8.7 | |