Description |
receptor accessory protein 2 |
solute carrier family 25 member 46 |
Image |
No pdb structure |
No pdb structure |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
- Amyotrophic lateral sclerosis (C9orf72 mutation interaction) ( 22959728)
- Autism spectrum disorder or schizophrenia ( 28540026)
- Bipolar disorder ( 31043756)
- Bipolar I disorder ( 31043756)
- Cerebrospinal AB1-42 levels in Alzheimer's disease dementia ( 29274321)
- Schizophrenia ( 25056061)
|
|
Interacting Genes |
24 interacting genes:
BNIP3
C2CD2L
CMTM5
CYP4F2
CYP4F22
ITGAM
MS4A1
MUL1
NAT8
ORMDL3
RABAC1
SCD
SFT2D2
SLC25A46
TMBIM6
TMEM120B
TMEM208
TMEM239
TMEM31
TMEM42
TMEM60
TMX2
TTPA
YIF1A
|
16 interacting genes:
AQP6
FHL3
FUNDC1
HSD17B11
HSD17B13
LEPROTL1
MFSD14B
ODF4
REEP2
REEP4
SLC10A1
SLC10A6
SLC66A2
SLC7A8
SPCS1
VMA21
|
Entrez ID |
51308 |
91137 |
HPRD ID |
16655 |
14283 |
Ensembl ID |
ENSG00000132563
|
ENSG00000164209
|
Uniprot IDs |
A8K3D2
Q9BRK0
|
B4DY98
Q96AG3
|
PDB IDs |
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|