BPGM |
EHD2 |
||
---|---|---|---|
Gene Name | 2,3-bisphosphoglycerate mutase | EH-domain containing 2 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 9 interactors: AKT1 ATF6 ATP4B CEL EGR2 EHD2 GAPDH GRB2 NEK3 | 13 interactors: AP1M1 AP1M2 AP2M1 BPGM DDX56 EHBP1 PICALM PICK1 RBSN SLC2A4 SPATA24 TAGLN2 TBC1D23 | |
Entrez ID | 669 | 30846 | |
HPRD ID | 01961 | 10434 | |
Ensembl ID | ENSG00000172331 | ENSG00000024422 | |
Uniprot IDs | P07738 | Q9NZN4 | |
PDB IDs | 1T8P 2A9J 2F90 2H4X 2H4Z 2H52 2HHJ 3NFY | ||
Enriched GO Terms of Interacting Partners? |
|
|
|
Tagcloud ? | biphosphoglycerate
congenital
csf3r
epo
epor
erythrocytosis
erythropoietin
exhibit
gelsolin
germline
haemoglobin
hereditary
inheritance
inherited
mendelian
mpl
mutase
mutational
myeloproliferative
neutrophilia
oxygen
pedigrees
sensing
syndromes
thpo
thrombocytosis
thrombopoietin
uncovered
v617f
|
acted
adapter
converts
cytoplasm
cytoskeleton
deprived
deregulated
direction
e2
enrichment
fhl2
homer3
hydroxytamoxifen
mcf
modulator
oestrogen
oht
organelle
overlap
pf
rationale
remarkable
remodelling
reorganisation
reprogrammed
rhof
transcriptome
uncovered
unexpectedly
|
|
Tagcloud (Difference) ? | biphosphoglycerate
congenital
csf3r
epo
epor
erythrocytosis
erythropoietin
exhibit
gelsolin
germline
haemoglobin
hereditary
inheritance
inherited
mendelian
mpl
mutase
mutational
myeloproliferative
neutrophilia
oxygen
pedigrees
sensing
syndromes
thpo
thrombocytosis
thrombopoietin
v617f
|
acted
adapter
converts
cytoplasm
cytoskeleton
deprived
deregulated
direction
e2
enrichment
fhl2
homer3
hydroxytamoxifen
mcf
modulator
oestrogen
oht
organelle
overlap
pf
rationale
remarkable
remodelling
reorganisation
reprogrammed
rhof
transcriptome
unexpectedly
|
|
Tagcloud (Intersection) ? | uncovered
|