Description |
coiled-coil domain containing 136 |
ubiquitin specific peptidase 2 |
Image |
No pdb structure |
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GO 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 |
- Reading disability or specific language impairment (pleiotropy) ( 25065397)
- Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) ( 25065397)
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Interacting Genes |
64 interacting genes:
ABT1
AQP1
ATP5PO
ATXN1
BARD1
BLOC1S6
BYSL
C1orf216
CBX8
CCDC146
CCHCR1
CDC5L
CDK2AP1
CEP57L1
COIL
CWF19L2
DISC1
ENKD1
FAM107A
FAM161A
GFI1B
HAUS1
HDAC4
HGS
HMG20A
HMG20B
JMY
KANSL1
KAT5
KIFC3
LENG1
MAGEB4
MOS
NDN
NEBL
PDLIM5
PKN2
PPP1R18
PRPF31
PSMD9
RAB33A
SHFL
SMARCE1
TBRG1
TCEA2
TNNT1
TXLNA
UBQLN4
USP2
WT1
ZBTB38
ZC2HC1C
ZNF20
ZNF230
ZNF250
ZNF408
ZNF417
ZNF490
ZNF564
ZNF572
ZNF581
ZNF587
ZNF688
ZSCAN26
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81 interacting genes:
APP
AURKA
BAP1
BEGAIN
BEND5
BRCA1
CBLC
CCDC136
CCDC57
CCDC85B
CCND1
CRY1
CTNNB1
DTX3
ENPP1
ERBB2
GOLGA2
H2AC20
HOMER3
HOOK1
HOOK2
IHO1
IKBKG
IL1RL2
KIFC3
KRT15
KRT40
LHX4
LMNA
LNX2
LONRF1
LRSAM1
LZTS2
MALT1
MAP3K2
MDM2
MNAT1
MTUS2
MYC
NDEL1
NEFL
NFKB2
NOTCH1
ORC3
ORC5
PALB2
PCGF6
PCNA
PEX5
PIK3R3
PLA2G2A
PNMA1
RAD18
RBCK1
RNF125
RNF126
RNF144B
RNF166
SNCA
TRAF2
TRAF6
TRAIP
TRIM21
TRIM23
TRIM27
TRIM34
TRIM35
TRIM39
TRIM46
TRIM5
TRIM54
TRIM63
TRIM74
TRIM8
TRIM9
UBE2S
UBOX5
USP21
VCAM1
VPS52
ZAP70
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Entrez ID |
64753 |
9099 |
HPRD ID |
10887 |
05287 |
Ensembl ID |
ENSG00000128596
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ENSG00000036672
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Uniprot IDs |
A0A024R758
Q96JN2
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O75604
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PDB IDs |
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2HD5
2IBI
3NHE
3V6C
3V6E
5XU8
5XVE
6DGF
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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Tagcloud (Difference) ? |
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Tagcloud (Intersection) ? |
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