Description |
troponin T1, slow skeletal type |
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 |
61 interacting genes:
ARMC8
BLOC1S2
BMPR1B
CCDC136
CCDC85B
CHD3
DDX5
EEF1G
FAF1
FXR2
FYN
HAP1
HMGXB4
HSP90AB1
IMMT
KAT5
KRT40
LARP1
LDOC1
MARS1
MORF4L1
NACAD
NAGK
NFE2L2
NINL
NSG2
OSBP2
OSM
PI4KA
PLEKHF1
PNMA1
PPFIA1
PRKG1
PSMC5
SEC31A
SERPINA4
SH3GL3
SMAD1
SMAD2
SMURF1
SNW1
TBPL1
TFIP11
TGFBR1
TMEM98
TNNC1
TNNI1
TNNI2
TNNI3
TPM1
TPM3
TRA2A
TRIM63
UBE2D1
VIM
WDCP
ZC3H15
ZKSCAN5
ZMYND19
ZNF250
ZNF768
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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 |
7138 |
64753 |
HPRD ID |
01841 |
10887 |
Ensembl ID |
ENSG00000105048
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ENSG00000128596
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Uniprot IDs |
P13805
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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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