Description |
MAGE family member A6 |
actinin alpha 3 |
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 |
- Serum alkaline phosphatase levels ( 33339817)
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- Bipolar disorder ( 21926972)
- Frontotemporal dementia with GRN mutation ( 29724592)
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Interacting Genes |
75 interacting genes:
ACOT7
ACTN3
AKAP6
AKAP9
ANKRD26P1
APOA4
ARFIP1
ATP6V1G1
ATPAF2
BCL7B
BET1
BFSP2
BOLA3
C1orf216
CAMTA2
CBFA2T2
CCDC146
CCDC185
CCDC187
CCDC24
COL4A6
CTF1
DLGAP3
DLGAP4
DNTTIP1
ELMOD3
EXOC5
FAM214A
FRMPD1
GADD45GIP1
GCSH
GFOD1
HAUS1
HLA-DRB4
HNRNPM
IQUB
KIF27
KLHL38
LCORL
LIN37
LIN52
LSM2
MCM7
MCRS1
MED21
MID2
MIPOL1
MORN3
MSGN1
NCK2
NOSTRIN
PCBD2
PDE4D
RASSF10
RASSF4
RCOR3
REX1BD
RPL37A
RUSC1
S100A14
S100A9
SH2D4A
SMARCD1
SNAP47
SNX4
SON
STAMBPL1
STX5
TRIM26
TRIM28
TSPYL6
TULP3
TXNDC9
XRCC4
ZNF76
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64 interacting genes:
ABI3
ACTN1
ACTN2
ACTN4
ADORA2A
ASB9
ATP23
BBS1
BRCA1
C1orf94
C20orf85
C2CD6
CADPS
CTAG1A
CTAG1B
CTDSP1
CXCL5
DDAH2
DUX1
DUX4L9
DYNC1I2
ECM1
FAM90A1
GLIS2
HGS
HOXD12
HSF2BP
IVD
KCTD6
KRT6C
LHX3
LINC01554
LNX1
MAGEA6
MICALL2
MYOT
MYOZ1
MYPN
NDUFAB1
NEBL
NKAPD1
NRAP
ODF3B
PCCB
PKP2
PLEKHG2
POU6F2
PPP1R18
PTK6
REL
RNF111
RTP5
SNAI1
SOHLH1
SUMO1P1
SYNPO2L
TRAF1
TRAF2
TRIM29
TTN
USP2
XPO1
ZNF343
ZNF426
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Entrez ID |
4105 |
89 |
HPRD ID |
02168 |
02148 |
Ensembl ID |
ENSG00000197172
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ENSG00000248746
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Uniprot IDs |
P43360
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A0A087WSZ2
B4DZQ2
Q08043
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PDB IDs |
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1TJT
1WKU
3LUE
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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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