Description |
HAUS augmin like complex subunit 1 |
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 |
68 interacting genes:
AK8
ARFIP2
BLOC1S6
C3orf62
CAGE1
CBY2
CCDC114
CCDC136
CCDC57
CCHCR1
CDR2
CEP170P1
CEP44
CEP55
CEP57L1
CEP63
CEP70
DCTN2
DMD
DTNBP1
FGFR1OP2
GOLGA2
HOOK2
IFIT3
IFT20
INCA1
KDM1A
KIFC3
KRT15
KRT18
KRT19
KRT31
KRT38
KRT40
KXD1
LDOC1
LURAP1
MAD1L1
MAGEA6
MCM10
MCM3
MED4
MED7
MIPOL1
MTUS2
NDC80
NECAB2
NINL
NUP54
NUP62
PDE4DIP
PIBF1
SPAG5
STX11
SYCE1
SYCE3
TFIP11
TFPT
TRAF1
TRIM23
TRIM27
TRIM54
TRIM69
TSG101
USHBP1
VPS52
WASHC3
ZNF471
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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 |
115106 |
64753 |
HPRD ID |
16385 |
10887 |
Ensembl ID |
ENSG00000152240
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ENSG00000128596
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Uniprot IDs |
Q96CS2
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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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