FANCL |
EIF4ENIF1 |
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Gene Name | Fanconi anemia, complementation group L | eukaryotic translation initiation factor 4E nuclear import factor 1 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 24 interactors: ACVR1 BMPR1B C17orf70 CCDC36 CHCHD3 DOCK8 EIF4ENIF1 FANCB FANCD2 FANCI GGN GRN HES1 IKZF3 KIFC3 LZTS2 PCNA RBM45 RIMBP3 SSX2IP TFCP2 TGFBR1 UBE2T UBE2W | 19 interactors: ATXN1 CDK6 DDX6 DEF6 DTX2 EFHC1 EIF3E EIF4E EIF4E2 FANCL FDPS HNRNPF KRT19 MGAT5B OIP5 SMAD3 SPAG5 TTC19 TXLNA | |
Entrez ID | 55120 | 56478 | |
HPRD ID | 06997 | 10456 | |
Ensembl ID | ENSG00000115392 | ENSG00000184708 | |
Uniprot IDs | B5MC31 B5MCZ6 Q9NW38 | Q9NRA8 | |
PDB IDs | 3ZQS | ||
Enriched GO Terms of Interacting Partners? |
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|
|
Tagcloud ? | 2p16
2q24
4p15
agencies
assisting
epilepsies
epilepsy
ethnically
filtering
generalised
governmental
grouping
harbouring
heritability
ie
implicating
imputation
league
lumping
pcdh7
phenotyped
philanthropic
pleiotropically
protocadherin
scn1a
splitting
standardised
unclassified
vrk2
|
||
Tagcloud (Difference) ? | 2p16
2q24
4p15
agencies
assisting
epilepsies
epilepsy
ethnically
filtering
generalised
governmental
grouping
harbouring
heritability
ie
implicating
imputation
league
lumping
pcdh7
phenotyped
philanthropic
pleiotropically
protocadherin
scn1a
splitting
standardised
unclassified
vrk2
|
||
Tagcloud (Intersection) ? |