Gene Name |
THAP domain containing, apoptosis associated protein 1 |
retinitis pigmentosa 9 pseudogene |
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 |
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
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5 interactors:
PRR13
RBM39
SDCBP
SREK1IP1
THAP1
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Entrez ID |
55145 |
441212 |
HPRD ID |
15496 |
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Ensembl ID |
ENSG00000131931
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ENSG00000205763
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Uniprot IDs |
Q9NVV9
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PDB IDs |
2JTG
2KO0
2L1G
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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
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Tagcloud (Difference) ? |
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
|
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Tagcloud (Intersection) ? |
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