MUC19

Description		mucin 19, oligomeric
Image		No pdb structure
GO Annotations	Cellular Component	Extracellular Region Golgi Lumen Plasma Membrane
	Molecular Function
	Biological Process	Stimulatory C-type Lectin Receptor Signaling Pathway O-glycan Processing
Pathways		Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC) Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) Defective GALNT12 causes colorectal cancer 1 (CRCS1) Dectin-2 family O-linked glycosylation of mucins Termination of O-glycan biosynthesis
Drugs
Diseases
GWAS		Chromium levels ( 26025379) Crohn's disease ( 18587394 28067908 21102463) Daytime sleep phenotypes ( 27126917) Inflammatory bowel disease ( 28067908 23128233) Parent of origin effect on receptive language ability (paternal) ( 32635940)
Novel Interacting Genes		1 novel interacting genes: ANO6
Interacting Genes
Entrez ID		283463
HPRD ID		11377
Ensembl ID		ENSG00000205592
Uniprot IDs		Q7Z5P9
PDB IDs
Enriched GO Terms of Interacting Partners?
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