Gene Name |
syntaxin 11 |
phenylalanyl-tRNA synthetase 2, mitochondrial |
Image |
No pdb structure |
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Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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- Obesity (early onset extreme) ( 23563609)
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Protein-Protein Interactions |
62 interactors:
AES
APP
BLOC1S6
BYSL
C1orf109
CARD9
CCBE1
CCDC184
CCDC33
CCNK
CDCA7L
CTBP2
CWF19L2
EIF1AD
FAM110A
FAM161A
FAM74A4
FAM90A1
FARS2
FHL5
GOLGA8EP
GOLGA8F
HAUS1
IKBKG
IKZF3
KAT5
KCTD9
KDM1A
KLC3
KXD1
LENG1
LONRF1
MBIP
MEOX2
MFAP1
MID2
NDC80
PPP1R18
PRKAB2
PRPF31
PSMA3
PSMC3
RUNX1T1
SH2D4A
SLC38A2
SMARCE1
SNAP23
SNAP25
SNX3
STXBP1
SUV39H1
TAF6L
TBK1
TCF4
TNFRSF21
USHBP1
VAMP2
VPS52
WDYHV1
ZCCHC10
ZNF417
ZNF587
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23 interactors:
ADAMTSL4
AGTRAP
APPL1
CALCOCO2
CMTM5
HMBOX1
IKZF3
KRT13
KRT31
KRT40
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP10-9
MID2
MKRN3
NOTCH2NL
RCBTB2
STX11
TADA2A
TFCP2
TRIM27
TRIM54
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Entrez ID |
8676 |
10667 |
HPRD ID |
09231 |
09946 |
Ensembl ID |
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ENSG00000145982
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Uniprot IDs |
O75558
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O95363
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PDB IDs |
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3CMQ
3HFV
3TEG
3TUP
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
autosomal
characterised
defect
done
dysregulation
familial
families
fhl
haemophagocytic
harbour
harbouring
killer
leukaemia
lymphohistiocytosis
milder
mutational
myelogenous
nonsense
perforin
periods
prf1
psychomotor
recessive
retardation
segregation
syntaxin
uncommon
undertaken
unrelated
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Tagcloud (Difference) ? |
autosomal
characterised
defect
done
dysregulation
familial
families
fhl
haemophagocytic
harbour
harbouring
killer
leukaemia
lymphohistiocytosis
milder
mutational
myelogenous
nonsense
perforin
periods
prf1
psychomotor
recessive
retardation
segregation
syntaxin
uncommon
undertaken
unrelated
|
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Tagcloud (Intersection) ? |
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