| Description |
chromosome 21 open reading frame 58 |
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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- Electrocardiogram morphology (amplitude at temporal datapoints) ( 32916098)
- Hypertrophic cardiomyopathy ( 33495596)
- Hypertrophic cardiomyopathy (MTAG) ( 33495596)
- 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 |
14 interacting genes:
CCDC125
CCDC136
GRB2
KLHL20
KRT27
KRT35
KRT37
MKRN3
MTUS2
PNMA1
POLR1C
SPTA1
TRIB3
USHBP1
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138 interacting genes:
ABT1
AQP1
ASB7
ATP5PO
ATXN1
BARD1
BLOC1S6
BYSL
C1orf216
C21orf58
CARD9
CBX8
CCDC120
CCDC13
CCDC146
CCDC185
CCDC187
CCDC6
CCHCR1
CDC5L
CDK2AP1
CEP57
CEP57L1
CEP95
COIL
CWF19L2
DDX6
DISC1
DTNB
DYNC1I2
ENKD1
FAM107A
FAM161A
FAM161B
FAM50B
FLYWCH1
GFI1B
HAUS1
HDAC4
HGS
HMG20A
HMG20B
HOXB5
ISCU
JAKMIP2
JMY
JRK
KANSL1
KAT5
KIF5B
KIFC3
LCA5L
LENG1
MAGEB4
MBD1
MBD3L2
MCRS1
MOS
NDC80
NDN
NEBL
NEK6
NME7
NOP53
ODAD3
PDLIM5
PIBF1
PKN1
PKN2
POGZ
PPP1R18
PRPF18
PRPF3
PRPF31
PRR35
PSMA1
PSMC5
PSMD9
RAB33A
RAB33B
RALBP1
RASAL3
RASSF8
SCNM1
SDHAF1
SHFL
SMARCA2
SMARCE1
SYT6
TBRG1
TCEA2
THAP7
TNNT1
TRAF3IP3
TSGA10
TSGA10IP
TSPYL1
TXLNA
UBQLN4
UBTFL1
USP2
WT1
ZBTB24
ZBTB38
ZBTB47
ZC2HC1C
ZFP1
ZFYVE26
ZNF124
ZNF20
ZNF223
ZNF230
ZNF250
ZNF264
ZNF329
ZNF35
ZNF408
ZNF417
ZNF440
ZNF490
ZNF497
ZNF564
ZNF572
ZNF580
ZNF581
ZNF587
ZNF599
ZNF648
ZNF669
ZNF670
ZNF688
ZNF696
ZNF774
ZNF777
ZNF785
ZNF835
ZNF837
ZSCAN26
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| Entrez ID |
54058 |
64753 |
| HPRD ID |
10755 |
10887 |
| Ensembl ID |
ENSG00000160298
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ENSG00000128596
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| Uniprot IDs |
P58505
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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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