Description |
coiled-coil domain containing 136 |
cell division cycle 5 like |
Image |
No pdb structure |
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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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69 interacting genes:
AKAP6
AKAP9
BCAS2
BICRAL
CALM1
CCDC136
CDK2
CDKN1A
CDKN2A
CDT1
CTNNBL1
DISC1
DIXDC1
DST
EMID1
ERG
EXOC1
EXOC7
GOLGA2
GOLGA8EP
GOLGA8F
GRB14
GSE1
HNRNPM
HOOK1
KALRN
KANSL1
KDM1A
KIF3C
KIF5B
KRT18
LMO2
MACF1
MCM10
MCM3
MCM4
MCM5
MELK
MYT1L
ORC1
ORC2
ORC5
PCBD2
PDE4DIP
PLRG1
PPFIA2
PPP1CA
PPP1R13B
PPP1R8
PRPF3
RPA1
RPA2
RPA3
SFR1
SH3BP5
SMARCD1
SPTBN1
SYNE1
TRAF3IP1
TRAK1
TRIO
TTF2
WWC1
YWHAG
YWHAQ
YWHAZ
ZNF35
ZNF451
ZSCAN1
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Entrez ID |
64753 |
988 |
HPRD ID |
10887 |
04184 |
Ensembl ID |
ENSG00000128596
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ENSG00000096401
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Uniprot IDs |
A0A024R758
Q96JN2
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Q99459
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PDB IDs |
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2DIM
2DIN
5MQF
5XJC
5YZG
5Z56
5Z57
5Z58
6FF4
6FF7
6ICZ
6ID0
6ID1
6QDV
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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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