DOCK8 |
FANCL |
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---|---|---|---|
Gene Name | dedicator of cytokinesis 8 | Fanconi anemia, complementation group L | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 25 interactors: BYSL CARHSP1 CDC42 CHMP2A DGCR6 EXOSC5 FAM124A FAM161A FANCL FBXL12 HBZ KRT40 LRCH1 LRCH3 MED30 MEOX2 MRPL38 MTG1 RAC1 RHOJ RHOQ RTP5 SMAD2 ZFC3H1 ZNF581 | 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 | |
Entrez ID | 81704 | 55120 | |
HPRD ID | 10920 | 06997 | |
Ensembl ID | ENSG00000107099 | ENSG00000115392 | |
Uniprot IDs | E2J6M5 E2J6M6 Q8NF50 | B5MC31 B5MCZ6 Q9NW38 | |
PDB IDs | 3ZQS | ||
Enriched GO Terms of Interacting Partners? |
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|
|
Tagcloud ? | akr1c4
anomalies
apparently
array
balanced
bases
cdon
cgh
chrna7
confirming
dd
diagnoses
gata3
id
indistinguishable
inherited
intellectual
karyotype
karyotyping
mb
mca
nr2f2
overlooked
prenatal
pws
rearrangements
spanning
tier
tp63
|
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) ? | akr1c4
anomalies
apparently
array
balanced
bases
cdon
cgh
chrna7
confirming
dd
diagnoses
gata3
id
indistinguishable
inherited
intellectual
karyotype
karyotyping
mb
mca
nr2f2
overlooked
prenatal
pws
rearrangements
spanning
tier
tp63
|
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) ? |