| Description |
coiled-coil domain containing 136 |
zinc finger protein 688 |
| Image |
No pdb structure |
No pdb structure |
| 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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70 interacting genes:
ABI2
BEND5
BLZF1
CADPS
CALCOCO2
CARD9
CBY2
CCDC136
CCDC33
CCDC57
CEP44
CEP70
CEP72
CRX
EHMT2
FBXO7
FCHO1
FHL5
GMPPA
GOLGA2
GPRASP2
HMBOX1
HNRNPK
HOMEZ
IHO1
KHDRBS2
KHDRBS3
KIFC3
KRT13
KRT15
KRT31
KRT40
KRTAP10-3
KRTAP10-9
KRTAP12-2
KRTAP4-2
LDOC1
MAGED1
MDFI
MEOX2
MID2
MIPOL1
MKRN3
NOTCH2NLA
PCBD1
PLSCR1
PNMA1
PNMA2
PSMA3
PSTPIP1
REL
RFX6
RINT1
RPGRIP1
SPAG5
SSX2IP
TADA2A
TCF12
TCF4
TMCC2
TNS2
TRAF1
TRAF2
TRAF4
TRIM23
TRIM27
TRIP6
USHBP1
WWP2
ZC4H2
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| Entrez ID |
64753 |
146542 |
| HPRD ID |
10887 |
14070 |
| Ensembl ID |
ENSG00000128596
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ENSG00000229809
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| Uniprot IDs |
A0A024R758
Q96JN2
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A0A024QZB6
A0A0S2Z633
P0C7X2
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| PDB IDs |
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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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