about
P688
Self-assembly and supramolecular organization of EMILINDiagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue DiseaseEMILIN, a component of the elastic fiber and a new member of the C1q/tumor necrosis factor superfamily of proteinsThe solution structure of EMILIN1 globular C1q domain reveals a disordered insertion necessary for interaction with the alpha4beta1 integrin
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Elastin microfibril interfacer 1
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Elastin microfibril interfacer 1
@en
Elastin microfibril interfacer 1
@nl
type
label
Elastin microfibril interfacer 1
@en
Elastin microfibril interfacer 1
@nl
altLabel
EMILIN-1
@en
EMILIN1
@en
elastin microfibril interface-located protein 1
@en
prefLabel
Elastin microfibril interfacer 1
@en
Elastin microfibril interfacer 1
@nl
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ENSP00000369677
ENSP00000411201