Description |
kinesin family member C3 |
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 |
93 interacting genes:
ABI2
ANXA13
APP
ARNT2
ATF2
BCL6
C1orf109
CBX8
CBY2
CCDC102B
CCDC136
CCDC28A
CCDC33
CDK18
CDR2
CEP55
CEP57L1
CLIP4
COG7
CREB5
CYTH4
DCTN2
DCX
DEUP1
DTNBP1
ESRRG
FAM124A
FANCL
FBXO7
FCHSD2
GMCL1
GOLGA2
GORASP2
HAUS1
HSBP1
ICA1L
ITGB3BP
KANSL1
KDM1A
KRT15
KRT19
KRT31
KRT40
KRT5
KRT6A
KRT6B
KRT6C
LENG1
LIN37
LZTS2
MCM7
MED4
MFAP1
MID2
MOS
NDEL1
NECAB2
NEDD4
NEDD4L
NEFL
NUP62
PHC2
PRKAA2
PSMB1
RAD51D
RSPH14
SCEL
SIAH1
SMARCE1
SNAP29
SOX30
SOX5
SVIL
SYCE1
TCEANC
TLE5
TNIP1
TPM3
TRAF2
TRIM23
TRIM27
TRIM41
TRIM54
TSG101
TSR2
USP2
ZBTB8A
ZGPAT
ZNF180
ZNF20
ZNF572
ZNF655
ZNF688
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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 |
3801 |
64753 |
HPRD ID |
05171 |
10887 |
Ensembl ID |
ENSG00000140859
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ENSG00000128596
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Uniprot IDs |
B7Z5U4
B7Z808
B7Z896
F5H3M2
Q9BVG8
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A0A024R758
Q96JN2
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PDB IDs |
5WDE
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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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