| Description |
chromosome 1 open reading frame 216 |
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 |
28 interacting genes:
AMOT
CCDC114
CCDC136
CCDC158
CCDC197
CDR2
CEP170P1
GGA1
KRT13
KRT15
KRT31
KRT38
KRT40
MED4
MTUS2
MYRIP
NMI
NRBF2
NUP62
PSMC6
RALBP1
TLE5
TPM1
TPM3
TRAF1
TRIM54
USHBP1
ZDHHC17
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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 |
127703 |
64753 |
| HPRD ID |
08798 |
10887 |
| Ensembl ID |
ENSG00000142686
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ENSG00000128596
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| Uniprot IDs |
Q8TAB5
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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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