| Gene Name | fragile X mental retardation, autosomal homolog 1 | |
| Image | ||
| Gene Ontology Annotations | Cellular Component | |
| Molecular Function | ||
| Biological Process | ||
| Pathways | ||
| Drugs | ||
| Diseases | ||
| GWAS |
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| Protein-protein Interactions | 11 interactors: C14orf1 CRMP1 CSNK2A1 CYFIP2 FMR1 FXR2 GBP2 KIAA1377 LRIF1 LUC7L2 PRSS23 | |
| Entrez ID | 8087 | |
| HPRD ID | 02892 | |
| Ensembl ID | ENSG00000114416 | |
| Uniprot IDs | B4DXZ6 E9PFF5 P51114 | |
| PDB IDs | 2CPQ 3KUF 3O8V | |
| Enriched GO Terms of Interacting Partners? | ||
| Tagcloud ? | address
adhesion
arm
comprised
coprecipitated
cytoplasm
cytoplasmic
desmoplakin
desmosomes
destabilized
g3bp
gain
mrnas
outside
pabpc1
particles
pkp1
pkp2
pkp3
plakophilins
posttranscriptional
regulators
repeat
ribonucleoprotein
rnase
serve
stabilized
unaffected
upf1
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