Description |
coiled-coil domain containing 136 |
FAM161 centrosomal protein A |
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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66 interacting genes:
BEND3
BEND5
BRCA1
CADPS
CALCOCO1
CALCOCO2
CARD9
CBY2
CCDC102B
CCDC136
CCDC33
CCDC57
CCNDBP1
CDR2
CEP44
CEP57L1
CEP63
CEP70
DHX32
DOCK8
DVL2
EHMT2
FAM9B
FSD2
GOLGA2
HMBOX1
IKZF1
KASH5
KIAA0753
KRTAP10-3
KRTAP10-7
KRTAP10-9
KRTAP5-9
LMNA
LZTS2
MCM6
MDFI
MID2
MIPOL1
MTUS2
NECAB2
NINL
NUTM1
PDE4DIP
PHC2
PNMA2
PPFIA1
PPM1F
RINT1
RUNDC3A
SSX2IP
STX11
SYCE1
TFIP11
TMCC2
TNIP1
TRAF1
TRIM15
TRIM37
TRIM54
TSGA10
TXLNB
ZBTB1
ZBTB14
ZBTB43
ZBTB8A
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Entrez ID |
64753 |
84140 |
HPRD ID |
10887 |
18996 |
Ensembl ID |
ENSG00000128596
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ENSG00000170264
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Uniprot IDs |
A0A024R758
Q96JN2
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Q3B820
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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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