About: Thrombospondin type laminin G domain and EAR repeats

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About: Thrombospondin type laminin G domain and EAR repeats Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

mammalian protein found in Homo sapiens

Attributes	Values
rdf:type	Item
description	protein (id) protèin (ace) proteinë (sq) mammalian protein found in Homo sapiens (en) menselijk eiwit (nl) protéine humaine (fr) білок людини (uk) humanes Protein (de) بروتين بشري (ar)
rdfs:label	Thrombospondin type laminin G domain and EAR repeats (en) Thrombospondin type laminin G domain and EAR repeats (nl)
skos:prefLabel	Thrombospondin type laminin G domain and EAR repeats (en) Thrombospondin type laminin G domain and EAR repeats (nl)
name	Thrombospondin type laminin G domain and EAR repeats (en) Thrombospondin type laminin G domain and EAR repeats (nl)
instance of	wds:Q21122900-75C02786-EB97-4777-8A6B-AEF1D86ADB67
part of	wds:Q21122900-30B1A82D-FCA0-4C49-90EC-D7CAD6072915 wds:Q21122900-381435AA-59A2-442C-AE60-0203A294EE94 wds:Q21122900-8892CA70-99CA-441D-AFFF-29047E43BEDC wds:Q21122900-9B9F6FE9-6939-4BDB-BAA8-E93EA41F6C28
instance of	protein
part of	Concanavalin A-like lectin/glucanase domain superfamily Laminin G domain, protein family EAR domain, protein family Leucine-rich glioma-inactivated , EPTP repeat, protein family
has part(s)	wds:Q21122900-17DCA289-1AB7-4049-8044-C9D6086AEE0B wds:Q21122900-5ADC9F69-1E63-42C8-8BDA-C99A908259A8 wds:Q21122900-76A74ED6-D271-416B-A6C5-20CF5ECE7373
has part(s)	Laminin G domain EAR Leucine-rich glioma-inactivated , EPTP repeat
found in taxon	wds:Q21122900-4CC9D8CC-20EB-49EC-8F90-7659AFAF81E3
found in taxon	Homo sapiens
molecular function	wds:Q21122900-EF033B3B-7505-419C-B136-670C1D2DCF9F
molecular function	molecular function
cell component	wds:Q21122900-0243120D-8BBE-4CFC-AAC1-B53219A83889 wds:Q21122900-5F07384E-D803-466D-89E4-F630F26C08A0 wds:Q21122900-A12AC7FC-A10D-4E8E-A457-AE691E55F30C wds:Q21122900-F36E3650-9542-48B8-AA95-BA3D378298CD wds:Q21122900-FD914F6A-6FF4-4159-942E-E2FEC63AA96D
cell component	extracellular region ciliary membrane cell surface cell projection stereocilium
skos:altLabel	TSPEAR (en) thrombospondin-type laminin G domain and EAR repeat-containing protein (en) thrombospondin-type laminin G domain and EAR repeats-containing protein (en)
UniProt protein ID	wds:Q21122900-031DFD2D-9CF6-4AEF-9A59-DFFC81CE0B92
RefSeq protein ID	wds:Q21122900-C7D4D080-BAFF-4C2D-9F42-7D8F991033D1 wds:Q21122900-E6B04993-7A86-42F1-B000-6C8BD040B467
biological process	wds:Q21122900-458C21BC-35D8-4BFF-AD5F-9D88FCA0820C wds:Q21122900-CFB1D8AA-809B-4831-9377-E274C948D09E wds:Q21122900-D0CDD642-1706-4976-9879-A5CECC847FFF
encoded by	wds:Q21122900-1E80C534-02E7-4DE6-AB90-30F6FFD42DC9
Ensembl protein ID	wds:Q21122900-2E4235A2-3893-4D06-848E-FB972FD1A51C wds:Q21122900-6E8DFE7F-6071-42C0-931B-3B46AE9A81BC
UniProt protein ID	uniprot:uniprot/Q8WU66
RefSeq protein ID	uniprot:refseq/NP_001258966 uniprot:refseq/NP_659428
UniProt protein ID	Q8WU66
RefSeq protein ID	NP_001258966 NP_659428
biological process	tooth mineralization sensory perception of sound regulation of Notch signaling pathway
encoded by	TSPEAR
Ensembl protein ID	ENSP00000321987 ENSP00000496535
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q21122900
is main subject of	Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.
is main subject of	wds:Q24337513-F188003A-2E78-4981-B420-F01DD1F86474 wds:Q36162463-C94C3E7F-E1A2-4569-AFC3-C66D4C134279
is encodes of	TSPEAR
is encodes of	wds:Q18040904-FCE488C1-AB76-4C1F-A57F-B752B631932D

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