| Description |
zinc finger MYND-type containing 12 |
coiled-coil domain containing 24 |
| 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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- Autism spectrum disorder or schizophrenia ( 28540026)
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| Interacting Genes |
81 interacting genes:
ABI2
ARHGAP8
ARMC8
ARNTL
C1orf109
C1orf50
CCDC116
CCDC24
CHCHD2
CWF19L2
DMRT3
EVX2
FAM214B
FAM222B
FAM50B
FAM90A1
GPKOW
GSTZ1
HAPLN2
HDAC4
HOXB5
HOXC9
HR
HSF4
ILF2
INCA1
KANK2
LENG1
LMO2
LMO4
MAD2L2
MNS1
MOAP1
MSGN1
MSRB3
NAB2
NUDT22
ONECUT3
PATL1
PICK1
POM121
POU6F2
PPP1R18
PPP1R32
PRKAA2
PRR35
PRR5-ARHGAP8
PRR5L
PSMB8
QARS1
RIPPLY1
RUSC1
SAMD11
SAXO1
SCNM1
SDCBP
SEC14L4
SH2D4A
SHC3
SMARCD1
SMG9
SOHLH1
SPG21
STRA8
TEKT4
TEKT5
TEPSIN
TFAP2D
THOC1
THRSP
TLE5
TSEN54
TSSK3
TTC29
TXN2
TYMP
UNC5CL
VEZF1
VPS37C
ZNF148
ZNF414
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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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| Entrez ID |
84217 |
149473 |
| HPRD ID |
15740 |
14636 |
| Ensembl ID |
ENSG00000066185
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ENSG00000159214
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| Uniprot IDs |
B4DX70
Q9H0C1
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Q8N4L8
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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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