Description |
bystin like |
coiled-coil domain containing 136 |
Image |
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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 |
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- 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 |
67 interacting genes:
AIMP2
APP
BEND7
C1orf94
CCDC102B
CCDC136
CCDC33
CDC23
CDCA7L
CEP44
CEP57L1
CEP70
COIL
DDX17
DOCK8
DVL2
EMD
EPS8
FAM9B
FXR2
GMCL1
GOLGA2
HMBOX1
IKZF1
KRT31
KRT40
KRT8
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP4-2
L3MBTL3
LMNA
LONRF1
LTV1
LZTS2
MID1
MID2
MIPOL1
MRFAP1L1
MTUS2
NECAB2
OLIG3
PDE4DIP
PHC2
PNMA1
PNMA2
RALYL
SMN2
SSX2IP
STX11
TEKT1
THAP1
TLE5
TNIP1
TRAF4
TRIM27
TRIM37
TRIM54
TRIP6
TRO
TROAP
UBE2H
VPS37B
ZBTB14
ZBTB8A
ZFP64
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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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Entrez ID |
705 |
64753 |
HPRD ID |
04848 |
10887 |
Ensembl ID |
ENSG00000112578
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ENSG00000128596
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Uniprot IDs |
Q13895
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A0A024R758
Q96JN2
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PDB IDs |
6G18
6G4S
6G4W
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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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