Gene Name |
coiled-coil-helix-coiled-coil-helix domain containing 3 |
Fanconi anemia, complementation group L |
Image |
No pdb structure |
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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 |
22 interactors:
BLZF1
CALCOCO2
CCDC33
CCDC85B
FANCL
GMCL1P1
GOLGA2
KRT40
KRTAP4-12
LZTS2
NOTCH2NL
NUDT3
PDE4DIP
RAB3IP
RPGRIP1
SAMM50
SPAG5
SPERT
SSX2IP
TRAF1
TRIM27
USHBP1
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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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Entrez ID |
54927 |
55120 |
HPRD ID |
13044 |
06997 |
Ensembl ID |
ENSG00000106554
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ENSG00000115392
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Uniprot IDs |
A4D1N4
G3V1K1
Q9NX63
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B5MC31
B5MCZ6
Q9NW38
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PDB IDs |
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3ZQS
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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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) ? |
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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) ? |
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