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GNE R266W [cytosol]
Stable Identifier
R-HSA-4088372
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
cytosol
Synonyms
Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, GLCNE_HUMAN
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of glycosylation (Homo sapiens)
Diseases associated with glycosylation precursor biosynthesis (Homo sapiens)
Defective GNE causes sialuria, NK and IBM2 (Homo sapiens)
Defective GNE does not hydrolyse UDP-GlcNAc (Homo sapiens)
GNE mutants [cytosol] (Homo sapiens)
GNE R266W [cytosol] (Homo sapiens)
Defective GNE does not phosphorylate ManNAc to ManNAc-6-P (Homo sapiens)
GNE mutants [cytosol] (Homo sapiens)
GNE R266W [cytosol] (Homo sapiens)
External Reference Information
External Reference
UniProt:Q9Y223 GNE
Gene Names
GNE, GLCNE, IBM2
Chain
chain:1-722
Reference Genes
BioGPS Gene:10020 GNE
COSMIC (genes):GNE GNE
CTD Gene:10020 GNE
dbSNP Gene:10020 GNE
ENSEMBL:ENSG00000159921 GNE
HGNC:23657 GNE
KEGG:hsa:10020 GNE
Monarch:10020 GNE
NCBI Gene:10020 GNE
OMIM:603824 GNE
UCSC:Q9Y223 GNE
Reference Transcript
RefSeq:NM_005476.5 GNE
RefSeq:NM_001190383.1 GNE
RefSeq:NM_001128227.2 GNE
RefSeq:NM_001190384.1 GNE
RefSeq:NM_001190388.1 GNE
RefSeq:XM_017014167.1 GNE
Participates
as a member of
GNE mutants [cytosol] (Homo sapiens)
Other forms of this molecule
GNE [cytosol]
GNE C303V [cytosol]
GNE M171V [cytosol]
GNE A631V [cytosol]
GNE R266Q [cytosol]
GNE R263L [cytosol]
GNE M712T [cytosol]
GNE V572L [cytosol]
Modified Residues
Name
L-arginine 266 replaced with L-tryptophan
Coordinate
266
PsiMod
L-tryptophan residue [MOD:00027]
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
L-arginine removal [MOD:01632]
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name
Identifier
Synonyms
sialuria
DOID:3659
Cross References
RefSeq
NP_001177317.1
,
NP_001177313.1
,
NP_001177312.1
,
NP_001121699.1
,
XP_016869656.1
,
NP_005467.1
OpenTargets
ENSG00000159921
ENSEMBL
ENSP00000494141
,
ENST00000396594
,
ENST00000539208
,
ENST00000447283
,
ENST00000642385
,
ENSG00000159921
,
ENSP00000379839
,
ENSP00000414760
,
ENSP00000445117
HPA
ENSG00000159921-GNE
GeneCards
GNE
PRO
Q9Y223
Pharos - Targets
Q9Y223
Orphanet
GNE
HMDB Protein
HMDBP00332
PDB
3EO3
,
2YHW
,
2YHY
,
4ZHT
,
2YI1
Interactors (4)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:Q7Z3S9 NOTCH2NLA
3
NOTCH2NLA [extracellular region]
(R-HSA-9908935)
NOTCH2NLA(1-?) [extracellular region]
(R-HSA-9911493)
NOTCH2NLA(?-236) [extracellular region]
(R-HSA-9911490)
0.666
4
UniProt:P12814 ACTN1
3
ACTN1 [platelet alpha granule lumen]
(R-HSA-349724)
ACTN1 [extracellular region]
(R-HSA-349722)
ACTN1 [cytosol]
(R-HSA-354096)
0.591
3
UniProt:Q969Y2 GTPBP3
1
GTPBP3 [mitochondrial matrix]
(R-HSA-6787414)
0.556
3
UniProt:O43597 SPRY2
8
p-Y55-SPRY2 [cytosol]
(R-HSA-182950)
SPRY2 [plasma membrane]
(R-HSA-182924)
SPRY2 [cytosol]
(R-HSA-182949)
p-S112,S115-SPRY2 [cytosol]
(R-HSA-1295619)
p-Y55,Y227-SPRY2 [plasma membrane]
(R-HSA-934555)
p-S112,S121-SPRY2 [plasma membrane]
(R-HSA-934595)
p-S110,S120-SPRY2 [cytosol]
(R-HSA-1295590)
p-Y55,Y227-SPRY2 [plasma membrane]
(R-HSA-1295629)
0.556
3
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