Gene Name |
coiled-coil domain containing 101 |
transcriptional adaptor 3 |
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 |
- Inflammatory bowel disease (early onset) ( 19915574)
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Protein-Protein Interactions |
12 interactors:
CCDC102B
CCDC158
CLHC1
HIST3H3
KRT13
KRT15
LNX1
MED4
NDC80
RINT1
TADA3
TCF4
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27 interactors:
ADPGK
ANKRD12
AR
CCDC101
CCNC
EIF3J
EP300
ESR1
FAM107B
HEXIM2
HIST3H3
HSPA8
ING5
KDM1A
MAGEH1
NR1I2
PIAS4
RARA
RFX1
RXRA
SAP18
TADA2A
TP53
TXNRD2
USP5
XRCC6
ZNF7
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Entrez ID |
112869 |
10474 |
HPRD ID |
13996 |
04252 |
Ensembl ID |
ENSG00000176476
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ENSG00000171148
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Uniprot IDs |
Q96ES7
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A8K899
O75528
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PDB IDs |
3LX7
3ME9
3MEA
3MET
3MEU
3MEV
3MEW
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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3p
anomalies
arm
camk1
congenital
creld1
define
deleted
deletion
deletions
features
give
handicap
interstitial
involve
kb
lengths
mb
mtmr14
overlap
presents
prove
respect
rise
seizures
srgap3
syndrome
terminus
typical
|
Tagcloud (Difference) ? |
|
3p
anomalies
arm
camk1
congenital
creld1
define
deleted
deletion
deletions
features
give
handicap
interstitial
involve
kb
lengths
mb
mtmr14
overlap
presents
prove
respect
rise
seizures
srgap3
syndrome
terminus
typical
|
Tagcloud (Intersection) ? |
|