Gene Name |
extracellular matrix protein 1 |
arginine-glutamic acid dipeptide (RE) repeats |
Image |
No pdb structure |
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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 |
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- Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) ( 23453885)
- Bone mineral density ( 22504420)
- Vertical cup-disc ratio ( 20548946)
- Vitiligo ( 20410501)
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Protein-Protein Interactions |
8 interactors:
ATN1
BNIP3L
CPTP
FBLN1
HSPG2
IRAK3
RERE
SRPK1
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20 interactors:
ALG13
ATN1
CBFA2T2
ECM1
EFEMP1
EFEMP2
EHMT2
HIST2H3C
KAT6A
KRTAP4-12
LZTR1
NR2E1
PLSCR1
PRRC2A
PRRC2B
PSMA3
RBFOX2
TRIM22
TRIP6
ZMYND8
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Entrez ID |
1893 |
473 |
HPRD ID |
03727 |
05566 |
Ensembl ID |
ENSG00000143369
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ENSG00000142599
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Uniprot IDs |
Q16610
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B1AKN3
Q9P2R6
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PDB IDs |
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2YQK
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
aberration
additionally
asn
condition
contrary
defect
defective
derived
extracellular
glycan
glycosylated
glycosylation
lipoid
lp
matrix
mutants
mutated
negatively
origin
proteinosis
putative
rare
residues
secretion
sites
spectrometry
suppresses
variety
wide
|
antagonism
caudal
downregulating
e8
ectopic
embryos
exiting
extending
fgf
fgf8
fused
h3k27me3
lacz
mesoderm
neuroectoderm
polycomb
prc2
ra
raldh2
rarb
rare
rares
repress
represses
repressive
somite
somites
trunk
vertebrate
|
Tagcloud (Difference) ? |
aberration
additionally
asn
condition
contrary
defect
defective
derived
extracellular
glycan
glycosylated
glycosylation
lipoid
lp
matrix
mutants
mutated
negatively
origin
proteinosis
putative
residues
secretion
sites
spectrometry
suppresses
variety
wide
|
antagonism
caudal
downregulating
e8
ectopic
embryos
exiting
extending
fgf
fgf8
fused
h3k27me3
lacz
mesoderm
neuroectoderm
polycomb
prc2
ra
raldh2
rarb
rares
repress
represses
repressive
somite
somites
trunk
vertebrate
|
Tagcloud (Intersection) ? |
rare
|