Description |
coilin |
coiled-coil domain containing 136 |
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 |
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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 |
70 interacting genes:
ACTN1
ACTN2
ACTN4
APP
ARMCX1
ATXN1
ATXN1L
BYSL
C1QBP
CCDC136
CCDC159
CCNE1
CDC23
CDK2
CEP70
CEP76
CSNK2B
CYB5R2
DHX16
DNAJA3
DRG1
ELOA2
FGF12
FHL5
FXR2
GCC1
KALRN
KAZN
KLC2
KLC4
KLHL42
KLHL8
KPNA3
LNX1
MAD1L1
MFAP1
MYO5B
NIF3L1
NOLC1
NTAQ1
NUDT18
PDE4D
PDLIM5
PIAS4
PICK1
PLEKHG4
POLR2L
PREPL
PRMT1
PRMT8
PSMA1
PSME3
PTS
SART3
SCYL1
SMN1
SNRPB
SNRPF
SNX6
TAF9
TCAF1
TFCP2
TGS1
TSPYL2
WDR34
XRCC5
XRCC6
ZBTB25
ZCCHC10
ZNF277
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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 |
8161 |
64753 |
HPRD ID |
02605 |
10887 |
Ensembl ID |
ENSG00000121058
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ENSG00000128596
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Uniprot IDs |
P38432
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A0A024R758
Q96JN2
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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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