CDB15:0000040 AGRN — MUSK

Experimentally validated in Mixed species; Orthology-inferred in Human, Mouse, Rat, Frog, Zebrafish, Chicken, Macaque, Pig, Dog, Cow, Chimp, Horse, Marmoset, Sheep

Title

Journal:; Year Published:

Abstract

Agrin acts via a MuSK receptor complex.

Cell, 1996; PubMed, Homo sapiens AGRN — Gallus gallus MUSK
ABSTRACT: Formation of th neuromuscular junction depends upon reciprocal inductive interactions between the developing nerve and muscle, resulting in the precise juxtaposition of a differentiated nerve terminal with a highly specialized patch on the muscle membrane, termed the motor endplate. Agrin is a nerve-derived factor that can induced molecular reorganizations at the motor endplate, but the mechanism of action of agrin remains poorly understood. MuSK is a receptor tyrosine kinase localized to the motor endplate, seemingly well positioned to receive a key nerve-derived signal. Mice lacking either agrin or MuSK have recently been generated and exhibit similarly profound defects in their neuromuscular junctions. Here we demonstrate that agrin acts via a receptor complex that includes MuSK as well as a myotube-specific accessory component.
Basic Information on AGRN
Ligand Name: agrin
Other Symbols: AGRIN
Ligand Location: secreted based on hpa, perplexity, uniprot, cell membrane based on hpa, uniprot
HGNC Gene Symbol Report: AGRN
GeneCards: AGRN
HGNC Gene Group: Proteoglycans
Interactions with other Receptors for AGRN
Basic Information on MUSK
Receptor Name: muscle associated receptor tyrosine kinase
Other Symbols: N/A
Receptor Location: cell membrane based on perplexity, uniprot
HGNC Gene Symbol Report: MUSK
GeneCards: MUSK
Interactions with other Ligands for MUSK