Entity Details

Primary name TLL1
Entity type gene
Source Source Link

Details

PrimaryID7092
RefseqGeneNG_016278
SymbolTLL1
Nametolloid like 1
Chromosome4
Location4q32.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-02-20
ModificationDate2021-06-13

Ontological Relatives

UniProt IDsTLL1_HUMAN

GO terms

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GOName
GO:0001501 skeletal system development
GO:0004222 metalloendopeptidase activity
GO:0005509 calcium ion binding
GO:0005576 extracellular region
GO:0008270 zinc ion binding
GO:0022617 extracellular matrix disassembly
GO:0030154 cell differentiation
GO:0030199 collagen fibril organization

Diseases

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Disease IDSourceNameDescription
613087 OMIMAtrial septal defect 6 (ASD6)A congenital heart malformation characterized by incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria. The disease is caused by variants affecting the gene represented in this entry.

Interactions

7 interactions

InteractorPartnerSourcesPublicationsLink
TLL1APPBioGRID21832049 details
TLL1CHRDHPRD10479448 details
TLL1BMP1BioGRID, IntAct28514442 details
TLL1C1RIntAct29209066 details
TLL1C1SIntAct29209066 details
TLL1KRT17BioGRID29859926 details
TLL1HNRNPLBioGRID28611215 details