##gff-version 3
Q8BWP8	UniProtKB	Chain	1	415	.	.	.	ID=PRO_0000080556;Note=Beta-1%2C4-glucuronyltransferase 1	
Q8BWP8	UniProtKB	Topological domain	1	8	.	.	.	Note=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q8BWP8	UniProtKB	Transmembrane	9	36	.	.	.	Note=Helical%3B Signal-anchor for type II membrane protein;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q8BWP8	UniProtKB	Topological domain	37	415	.	.	.	Note=Lumenal;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q8BWP8	UniProtKB	Binding site	227	227	.	.	.	Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:O43505	
Q8BWP8	UniProtKB	Binding site	229	229	.	.	.	Ontology_term=ECO:0000250;evidence=ECO:0000250|UniProtKB:O43505	
Q8BWP8	UniProtKB	Glycosylation	204	204	.	.	.	Note=N-linked (GlcNAc...) asparagine;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q8BWP8	UniProtKB	Glycosylation	300	300	.	.	.	Note=N-linked (GlcNAc...) asparagine;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q8BWP8	UniProtKB	Alternative sequence	353	379	.	.	.	ID=VSP_014004;Note=In isoform 2. ACELHVAGFNFEVLNEGFLVHKGFKEA->VLKRERACRTKTGGVSGVKWPLVERRQ;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:16141072;Dbxref=PMID:16141072	
Q8BWP8	UniProtKB	Alternative sequence	380	415	.	.	.	ID=VSP_014005;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:16141072;Dbxref=PMID:16141072	
Q8BWP8	UniProtKB	Mutagenesis	155	155	.	.	.	Note=Mild muscular dystrophy phenotype of variable penetrance due to defects in axon guidance. Mislocalization to the endoplasmic reticulum. M->T;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:23217742;Dbxref=PMID:23217742	
Q8BWP8	UniProtKB	Sequence conflict	175	176	.	.	.	Note=EF->RV;Ontology_term=ECO:0000305;evidence=ECO:0000305