| Description |
coiled-coil domain containing 24 |
MAGE family member A6 |
| 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 |
- Autism spectrum disorder or schizophrenia ( 28540026)
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- Serum alkaline phosphatase levels ( 33339817)
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| Interacting Genes |
39 interacting genes:
ADRA2C
AKAP8L
ANTKMT
ARMH1
CDC23
DISC1
DYNLT4
FAM166B
FNTB
GATA1
HPDL
HYI
IKZF3
KLF17
KRT33B
KRT34
KRTAP13-2
KRTAP15-1
KRTAP19-1
KRTAP19-6
KRTAP19-7
KRTAP6-1
KRTAP6-3
LRP2BP
MAGEA6
NDUFAB1
NDUFB7
OIP5
REN
RNF31
TCEAL8
TRIM42
TRIP6
TTC23
TTC23L
USHBP1
USP54
WWOX
ZMYND12
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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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| Entrez ID |
149473 |
4105 |
| HPRD ID |
14636 |
02168 |
| Ensembl ID |
ENSG00000159214
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ENSG00000197172
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| Uniprot IDs |
Q8N4L8
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P43360
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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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