about
P688
Functional cloning and mutational analysis of the human cDNA for phosphoacetylglucosamine mutase: identification of the amino acid residues essential for the catalysisAutosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteïne in Phosphoglucomutase 3
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Phosphoglucomutase 3
@en
type
label
Phosphoglucomutase 3
@en
altLabel
N-acetylglucosamine-phosphate mutase 1
@en
N-acetylglucosamine-phosphate mutase
@en
PGM 3
@en
PGM3
@en
Phosphoglucomutase-3
@en
acetylglucosamine phosphomutase
@en
phosphoacetylglucosamine mutase
@en
prefLabel
Phosphoglucomutase 3
@en
P361
P527
P637
P680
P681
P682
P705
P352
P279
P31
P352
P361
P527
P637
NP_001186846
NP_001186847
NP_001186848
NP_001354215
NP_001354216
XP_016866424
XP_016866426
P680
P682
P702
P703
P705
ENSP00000283977
ENSP00000421154
ENSP00000421565
ENSP00000422362
ENSP00000423389
ENSP00000423769
ENSP00000424865
ENSP00000424874
ENSP00000425558
ENSP00000425809