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Gene/ORF T22F3.3 Ace View of T22F3.3
T22F3.3 Details Help
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
GO Terms  phosphorylase activity (GO:0004645) ; pyridoxal phosphate binding (GO:0030170) ; carbohydrate metabolism (GO:0005975)
Location   V:3578472..3585259
RNAi Phenotypes
Early_embryo Slow cell cycle ; Cytokinesis defect ; Large cytoplasmic granules ; EMS fails to extend anteriorly ; Multiple nuclei in 1, 2, or 4-cell embryos
Postembryonic WT_postembryonic_morphology
External Links  wormbase.org NCBI.org NBrowse
Associated RNAi Experiments View Details
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 Browse using GBrowse
Gene Map