Ace View of T22F3.3 | |||||
T22F3.3 Details | |||||
Description | T22F3.3 is orthologous to the human gene MUSCLE GLYCOGEN PHOSPHORYLASE (PYGM; OMIM:232600), which when mutated leads to McArdle disease. | ||||
Homology Group (KOG) | Glycogen phosphorylase |
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GO Terms | phosphorylase activity (GO:0004645) ; pyridoxal phosphate binding (GO:0030170) ; carbohydrate metabolism (GO:0005975) | ||||
Location | V:3578472..3585259 | ||||
RNAi Phenotypes |
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External Links | |||||
Associated RNAi Experiments | |||||
Wild Type RNAi Experiments | |||||
JA:F40C5.d | WT | ||||
JA:F40C5.a | WT | ||||
JA:F40C5.h | WT | ||||
JA:F40C5.e | WT | ||||
JA:T22F3.3 | WT | ||||
JA:F40C5.b | WT | ||||
JA:F40C5.c | WT | ||||
Experiments with Non-Wild Phenotypes | |||||
Cenix:76-f1 | Emb ; WT_postembryonic_morphology | ||||
PF:GL1_1H6 | Cytokinesis defect ; Emb ; EMS fails to extend anteriorly ; Large cytoplasmic granules ; Multiple nuclei in 1, 2, or 4-cell embryos ; Slow cell cycle | ||||
Gene Plot of T22F3.3 | |||||