ZCCHC10 |
THAP1 |
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Gene Name | zinc finger, CCHC domain containing 10 | THAP domain containing, apoptosis associated protein 1 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 50 interactors: ARGLU1 BEND7 CEP63 CEP70 COIL CTNNBL1 DAB1 DACH1 DHX8 DPPA2 DZIP3 EEF1A1 EPB41 FAM9B FRA10AC1 IK KCTD6 KPNA3 LNX1 LUC7L2 NUDT14 PCBP1 PIN1 PPIG PRPF3 PRPF38A PRPF40A PRR13 PSME3 PTPN3 RBM39 SART1 SDCBP SDCBP2 SF3B2 SF3B4 SFMBT1 SIAH1 SLU7 SNIP1 SNRPD2 STAC3 STX11 TCEB3B TFCP2 THAP1 TP53 U2AF1 ZBTB14 ZBTB8A | 58 interactors: ACOT7 AKAP17A AKAP9 AP2B1 ARL6IP4 BAG5 BMS1P5 BYSL C11orf57 C1orf35 C7orf50 CHD2 CSNK2A1 DCAF8 DVL2 FAM124A FAM133A FXR2 GPATCH2L HNRNPLL KLF12 KRTAP10-7 LASP1 MORF4L1 MORF4L2 MRPL11 NKAP NUP62 PAWR PHF1 PID1 POLR2L POLR2M PPIG PRKAA1 PRR20A QKI RALYL RBM39 RIPPLY1 RP9P RPS25 SAP30BP SERF2 SLU7 STRBP TCEA2 TPM3 TRAF5 TRIM26 TTLL10 TXN2 U2AF2 WDYHV1 YES1 ZCCHC10 ZNF385C ZNF408 | |
Entrez ID | 54819 | 55145 | |
HPRD ID | 15699 | 15496 | |
Ensembl ID | ENSG00000155329 | ENSG00000131931 | |
Uniprot IDs | D6R9G7 G3XAM1 Q8TBK6 | Q9NVV9 | |
PDB IDs | 2JTG 2KO0 2L1G | ||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | adcy3
angptl2
annotated
beadchip
bmi
boston
boys
c18orf8
corrected
correction
cpg
dok2
epigenomic
fdr
generational
humanmethylation27
illumina
infant
lends
maternal
mother
offspring
plac1
prepregnancy
prr16
sapcd2
separately
stated
wnt16
|
assembled
childhood
compatible
confirms
contiguous
definite
deletions
distinctive
dystonia
dyt1
eighty
gch1
imprinted
ireland
laxity
maternally
microcephaly
myoclonus
nineteen
nkx2
phenotypically
probable
probands
progressing
sequenced
sgce
stature
uk
upper
|
|
Tagcloud (Difference) ? | adcy3
angptl2
annotated
beadchip
bmi
boston
boys
c18orf8
corrected
correction
cpg
dok2
epigenomic
fdr
generational
humanmethylation27
illumina
infant
lends
maternal
mother
offspring
plac1
prepregnancy
prr16
sapcd2
separately
stated
wnt16
|
assembled
childhood
compatible
confirms
contiguous
definite
deletions
distinctive
dystonia
dyt1
eighty
gch1
imprinted
ireland
laxity
maternally
microcephaly
myoclonus
nineteen
nkx2
phenotypically
probable
probands
progressing
sequenced
sgce
stature
uk
upper
|
|
Tagcloud (Intersection) ? |