GGA2 |
SPG21 |
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Gene Name | golgi-associated, gamma adaptin ear containing, ARF binding protein 2 | spastic paraplegia 21 (autosomal recessive, Mast syndrome) | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 30 interactors: AFTPH APP ARF1 ARF3 ATXN1 BACE1 BACE2 CA8 CCDC91 CLINT1 CLTC GGA1 GGA3 HGS HTT IGF2R LRP3 M6PR PIN1 RAB5A RABEP1 RABGEF1 RNF11 SORL1 SORT1 SPG21 STAB1 SYNRG TRIM23 VPS18 | 37 interactors: AGTRAP AKIRIN2 ARL6IP1 ATPAF2 CCDC102B CCDC33 CD4 CMTM5 CRYAA CTPS2 CUTC DTX2 DTX3L EFHC2 FAM114A1 GGA2 GSK3A IKZF3 INCA1 KRT15 MID2 MTMR9 PRPS1 RABAC1 REEP6 RTN4 S100B SPRED2 TCF12 TCF4 TFG TRAF1 TRAF2 TRIM23 TRIM54 TRIM9 ZNF263 | |
Entrez ID | 23062 | 51324 | |
HPRD ID | 09347 | 10492 | |
Ensembl ID | ENSG00000103365 | ENSG00000090487 | |
Uniprot IDs | Q9UJY4 | Q9NZD8 | |
PDB IDs | 1MHQ | ||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | addressed
adulthood
allele
attributable
byg
c57bl
c57bl6
disrupted
ear
establishes
gga1
gga3
ggas
harbors
homozygous
hypomorphic
insertional
knockout
lethality
mutagenesis
neonatal
ola129sv
placement
redundancy
ribosylation
runted
survive
tigm
true
|
||
Tagcloud (Difference) ? | addressed
adulthood
allele
attributable
byg
c57bl
c57bl6
disrupted
ear
establishes
gga1
gga3
ggas
harbors
homozygous
hypomorphic
insertional
knockout
lethality
mutagenesis
neonatal
ola129sv
placement
redundancy
ribosylation
runted
survive
tigm
true
|
||
Tagcloud (Intersection) ? |