| Description |
coiled-coil domain containing 136 |
zinc finger protein 417 |
| 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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68 interacting genes:
ADAMTSL4
BEGAIN
BEND5
CARD9
CCDC136
CCDC57
CCDC85B
CCNDBP1
CEP44
CEP70
CEP72
CSRNP1
EFS
FHL2
FHL3
FSD2
GOLGA2
HMBOX1
IKZF1
KLC3
KRT15
KRT38
KRT40
KRTAP10-1
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP4-12
KRTAP4-2
KRTAP5-9
KXD1
LURAP1
LZTS2
MDFI
MEOX2
MID2
MTUS2
NDEL1
NINL
NOTCH2NLA
PHC2
PLSCR1
PNMA2
PRPF31
REL
RPGRIP1
RUNDC3A
SPRY2
SSX2IP
STX11
TCF4
TFIP11
TMCC2
TNS2
TRAF1
TRIM27
TRIM36
TRIM37
TRIM41
TRIM54
TSGA10
ZBTB1
ZBTB10
ZBTB43
ZBTB8A
ZNF587
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| Entrez ID |
64753 |
147687 |
| HPRD ID |
10887 |
18341 |
| Ensembl ID |
ENSG00000128596
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ENSG00000173480
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| Uniprot IDs |
A0A024R758
Q96JN2
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M0R230
Q8TAU3
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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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