PGLYRP1 Polyclonal Antibody, 20ul Buffer Solutions but alternatively spliced transcripts may

but alternatively spliced transcripts may produce soluble proteins

Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy

In the mouse

a disease characterized by increased growth at the prenatal stage

PGLYRP1 Polyclonal Antibody, 20ul Buffer Solutions but alternatively spliced transcripts mayPGLYRP1 (Peptidoglycan Recognition Protein 1) is a Protein Coding gene. Among its related pathways are TNF Signaling (sino). GO annotations related to this gene include peptidoglycan binding and N acetylmuramoyl L alanine amidase activity. An important paralog of this gene is PGLYRP4.