OCA2 |
ATP13A2 |
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Gene Name | oculocutaneous albinism II | ATPase type 13A2 | |
Image | No pdb structure | No pdb structure | |
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS |
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|
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Protein-Protein Interactions | 1 interactors: ATP13A2 | 36 interactors: ACKR3 ATP5G2 CCKBR CMTM6 COL1A1 CXCR4 CYGB DCAF7 EMC7 F2R FAM111B FAM192A FAM8A1 FKBP8 FUNDC2 GPR21 HIPK1 ICAM2 LMAN2 LRP6 MEX3B MYCBP2 NPY1R NRXN1 OCA2 OSTC PCDHB10 PCMTD2 PDIA6 SEC61B SPCS2 TSPAN14 UBE2J2 VAMP2 WDR5B WDR83OS | |
Entrez ID | 4948 | 23400 | |
HPRD ID | 01945 | 13677 | |
Ensembl ID | ENSG00000104044 | ENSG00000159363 | |
Uniprot IDs | Q04671 | Q9NQ11 | |
PDB IDs | |||
Enriched GO Terms of Interacting Partners? |
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||
Tagcloud ? | albinism
bloc
colocalize
confocal
constituents
disrupt
disrupted
encoded
hair
hypopigmentation
lamp2
localizations
matp
melanogenic
melanosomal
melanosomes
misrouting
oca4
oculocutaneous
organelles
pigmentation
severely
slc45a2
sorting
subcellular
trafficking
transporters
tyrosinase
|
ataxin
atxn3
b12
cag
cgg
chediak
coexist
cytopathies
fmr1
fragile
gaucher
gba
glucocerebrosidase
hereditary
higashi
idiopathic
joseph
kufor
levodopa
lyst
machado
park2
parkin
parkinsonism
pn
polg1
premutation
rakeb
tremor
|
|
Tagcloud (Difference) ? | albinism
bloc
colocalize
confocal
constituents
disrupt
disrupted
encoded
hair
hypopigmentation
lamp2
localizations
matp
melanogenic
melanosomal
melanosomes
misrouting
oca4
oculocutaneous
organelles
pigmentation
severely
slc45a2
sorting
subcellular
trafficking
transporters
tyrosinase
|
ataxin
atxn3
b12
cag
cgg
chediak
coexist
cytopathies
fmr1
fragile
gaucher
gba
glucocerebrosidase
hereditary
higashi
idiopathic
joseph
kufor
levodopa
lyst
machado
park2
parkin
parkinsonism
pn
polg1
premutation
rakeb
tremor
|
|
Tagcloud (Intersection) ? |