Gene Name |
arginine-glutamic acid dipeptide (RE) repeats |
extracellular matrix protein 1 |
Image |
|
No pdb structure |
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
- 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)
|
|
Protein-Protein Interactions |
20 interactors:
ALG13
ATN1
CBFA2T2
ECM1
EFEMP1
EFEMP2
EHMT2
HIST2H3C
KAT6A
KRTAP4-12
LZTR1
NR2E1
PLSCR1
PRRC2A
PRRC2B
PSMA3
RBFOX2
TRIM22
TRIP6
ZMYND8
|
8 interactors:
ATN1
BNIP3L
CPTP
FBLN1
HSPG2
IRAK3
RERE
SRPK1
|
Entrez ID |
473 |
1893 |
HPRD ID |
05566 |
03727 |
Ensembl ID |
ENSG00000142599
|
ENSG00000143369
|
Uniprot IDs |
B1AKN3
Q9P2R6
|
Q16610
|
PDB IDs |
2YQK
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
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
|
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
|
Tagcloud (Difference) ? |
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
|
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
|
Tagcloud (Intersection) ? |
rare
|