TLL1 Products

Description

TLL1 encodes an astacin-like zinc-dependent metalloprotease and is a subfamily member of the metzincin family. A similar protein in mice is required during heart development and specifically processes procollagen C-propeptides and chordin at similar cleavage sites. [provided by RefSeq]

Bioinformatics

Entrez	7092 Human
Uniprot	AAH16922 Human AAH16922.1 Human NP_036596 Human NP_036596.3 Human
Product By Gene ID	7092
Alternate Names	EC 3.4.24.19 EC 3.4.24 ASD6 TLLEC 3.4.24.- tolloid-like protein 1 tolloid-like 1

Diseases related to TLL1

Discover more about diseases related to TLL1.

Congenital Heart Defects
Atrial Septal Defects
Fetal Stress
Stenosis
Neuroblastoma
Heart Septal Defects
Limb Deformities, Congenital
Aneurysm
Regurgitation
Neuromuscular Diseases
Hypoxia
Single Gene Defect
Dysplasia
Fibrosis
Malignant Neoplasms
Ventricular Septal Defects
Retinal Diseases
Congenital Absence
Charcot-marie-tooth Disease
4q Partial Monosomy Syndrome

Pathways for TLL1

View related products by pathway and learn more about each of the pathways below.

Gastrulation
Heart Development
Endoderm Formation
Cell Activation
Cell Development
T Cell Activation
Proteolysis
Neurogenesis
Ovulation
Methylation
Tissue Development
Flight
Heteroduplex Formation
Myoblast Differentiation
Secretion

PTMs for TLL1

Learn more about PTMs related to TLL1.

Cleavage
Demethylation
Phosphorylation
Methylation

Bioinformatics Tool for TLL1

Discover related pathways, diseases and genes to TLL1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.