Gene Name |
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 |
BEN domain containing 7 |
Image |
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No pdb structure |
Gene Ontology 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, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) ( 23453885)
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Protein-Protein Interactions |
26 interactors:
ACTL6A
ACTL6B
AR
ARID1B
BEND7
BRCA1
CEBPA
DPF3
ESR1
HIST1H3A
KHDRBS1
MDM2
MDM4
MECP2
MYB
MYC
NR0B2
NR3C1
NR4A2
PHB
PITX1
PRMT5
PRPF6
SDCBP
SIN3B
SS18
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28 interactors:
BYSL
C11orf57
CDCA7L
CEP44
CHD2
CIB3
DDX6
EAF1
EAF2
EIF1AD
EMD
FAM133A
LYAR
MFAP1
MORF4L1
MORF4L2
NIF3L1
PIM1
PLEKHF2
PPIG
PPP1R37
PSMF1
RAB29
SDCBP2
SMARCA2
U2AF2
USP20
ZCCHC10
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Entrez ID |
6595 |
222389 |
HPRD ID |
02483 |
12570 |
Ensembl ID |
ENSG00000080503
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ENSG00000165626
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Uniprot IDs |
P51531
Q56A76
Q8N9Q1
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Q8N7W2
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PDB IDs |
2DAT
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
abnormality
arid1a
coinactivation
copyright
fish
frame
harboring
heterozygous
infancy
insights
malignancies
missense
monoploid
mrts
pbrm1
protected
remodeling
reserved
rhabdoid
rights
screened
sense
snf
subunits
swi
trisomy
truncating
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Tagcloud (Difference) ? |
abnormality
arid1a
coinactivation
copyright
fish
frame
harboring
heterozygous
infancy
insights
malignancies
missense
monoploid
mrts
pbrm1
protected
remodeling
reserved
rhabdoid
rights
screened
sense
snf
subunits
swi
trisomy
truncating
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Tagcloud (Intersection) ? |
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