Description |
SET and MYND domain containing 1 |
RUN and SH3 domain containing 1 |
Image |
No pdb structure |
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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 |
- Night sleep phenotypes ( 27126917)
- Retinal detachment or retinal break ( 31816047)
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- Body fat distribution (leg fat ratio) ( 30664634)
- Body fat distribution (trunk fat ratio) ( 30664634)
- Brain morphology (min-P) ( 32665545)
- Brain morphology (MOSTest) ( 32665545)
- Cortical surface area (min-P) ( 32665545)
- Cortical surface area (MOSTest) ( 32665545)
- Cortical thickness (min-P) ( 32665545)
- Cortical thickness (MOSTest) ( 32665545)
- Crohn's disease ( 28067908)
- Inflammatory bowel disease ( 28067908)
- Subcortical volume (min-P) ( 32665545)
- Subcortical volume (MOSTest) ( 32665545)
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Interacting Genes |
44 interacting genes:
ARID5A
BACH2
BHLHE40
C11orf1
C11orf16
C11orf53
CCDC113
CCDC33
DISC1
DVL1
FAM166A
FAM204A
FAM83A
FAM86C1P
H3-5
HDAC2
HDAC3
HDHD3
HMG20A
HOMEZ
KIF16B
KRT35
LENG8
MDFI
MEOX2
MYH7B
NACA
NEFL
OGDHL
PATZ1
POU6F2
PRR22
RBM4B
RSPH6A
RUSC1
SNX11
SPAG8
TBRG1
TTC33
USP54
UTP14A
WDR77
ZBTB3
ZBTB44
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92 interacting genes:
ABHD11
ABHD5
ABI2
AKAP8L
ANKS1A
APP
ATP6V0D2
BPIFA1
C1orf109
CCDC120
CCDC57
CCHCR1
CCNC
CDKN2B
CMTM6
CREM
CRYBA2
CTAG1A
CTAG1B
DMRT3
DOK6
DTX2
DVL2
EXOC8
EXOSC8
FAM9B
FNDC3B
GCM2
HMG20A
HNRNPF
INSC
KCTD9
KRTAP19-1
KRTAP19-5
KRTAP6-2
KRTAP8-1
LIMS3
LIMS4
LMO2
MAGEA3
MAGEA6
MAGED1
MED25
MEIS2
MISP
MOAP1
MORN3
MYOZ3
N4BP3
NICN1
NTAQ1
NTRK1
NUDT22
OIP5
P4HA3
PFDN5
PIK3R3
PLA2G6
PM20D2
PNMA1
POLR1C
PRDM14
PRR35
RBPMS
SMARCB1
SMYD1
SOHLH1
SPAG8
STUB1
SUOX
TBC1D25
TCHP
TEKT4
TENT5B
TLE5
TRAPPC6A
TRIM55
TRIM63
TRIM73
TSSK3
TTC19
TTC7B
UFSP1
VGLL3
WWOX
WWP2
ZIC1
ZMYND12
ZNF34
ZNF620
ZNF765
ZNF77
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Entrez ID |
150572 |
23623 |
HPRD ID |
06025 |
10206 |
Ensembl ID |
ENSG00000115593
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ENSG00000160753
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Uniprot IDs |
E9PHG3
Q5HYE8
Q8NB12
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B4DQB8
Q9BVN2
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PDB IDs |
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4GIW
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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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