Gene Name |
Fanconi anemia, complementation group L |
chromosome 17 open reading frame 70 |
Image |
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No pdb structure |
Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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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
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4 interactors:
APP
FANCB
FANCL
MDFI
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Entrez ID |
55120 |
80233 |
HPRD ID |
06997 |
07982 |
Ensembl ID |
ENSG00000115392
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ENSG00000185504
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Uniprot IDs |
B5MC31
B5MCZ6
Q9NW38
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A4ZI32
Q0VG06
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PDB IDs |
3ZQS
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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
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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
|
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Tagcloud (Intersection) ? |
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