Description |
coiled-coil domain containing 136 |
necdin, MAGE family member |
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 |
- Reading disability or specific language impairment (pleiotropy) ( 25065397)
- Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) ( 25065397)
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- Depressive symptoms (SSRI exposure interaction) ( 25649181)
- Plasma anti-thyroid peroxidase levels ( 29678681)
- Serum metabolite concentrations in chronic kidney disease ( 29545352)
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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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47 interacting genes:
APBB1IP
ARSL
BLOC1S6
CALCOCO2
CCDC136
CDR2
DTNBP1
E2F1
E2F4
EEF1AKMT1
EGFR
EID1
EPAS1
FAM131C
FSD2
FXR2
GKAP1
GOLGA2
HIF1A
HNRNPU
IFFO1
IL1A
IL32
IRS4
LAX1
LPXN
MIER2
MKRN2
MPP6
MYG1
NEFL
NGFR
NUBP1
NUCB1
NUCB2
P4HA3
PJA1
PPARGC1A
PPFIA1
SERTAD3
SIRT1
SSX2IP
TFIP11
TP53
U2AF1
ZBTB1
ZBTB7B
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Entrez ID |
64753 |
4692 |
HPRD ID |
10887 |
03667 |
Ensembl ID |
ENSG00000128596
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ENSG00000182636
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Uniprot IDs |
A0A024R758
Q96JN2
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Q99608
X5D982
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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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