RXYLT1, ribitol xylosyltransferase 1, 10329

N. diseases: 55; N. variants: 13
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514544
rs397514544
Entrez Id: 10329;104169670
Gene Symbol: RXYLT1;RXYLT1-AS1
RXYLT1;RXYLT1-AS1
CUI: C3554381
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 		0.700 GeneticVariation UNIPROT TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement. 27212206 2016
dbSNP: rs397514544
rs397514544
Entrez Id: 10329;104169670
Gene Symbol: RXYLT1;RXYLT1-AS1
RXYLT1;RXYLT1-AS1
CUI: C3554381
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 		0.700 GeneticVariation UNIPROT The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan. 27733679 2016
dbSNP: rs397514544
rs397514544
Entrez Id: 10329;104169670
Gene Symbol: RXYLT1;RXYLT1-AS1
RXYLT1;RXYLT1-AS1
CUI: C3554381
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 		0.700 GeneticVariation UNIPROT The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition. 27130732 2016
dbSNP: rs397514544
rs397514544
Entrez Id: 10329;104169670
Gene Symbol: RXYLT1;RXYLT1-AS1
RXYLT1;RXYLT1-AS1
CUI: C3554381
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 		0.700 GeneticVariation UNIPROT Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry. 23519211 2013
dbSNP: rs397514544
rs397514544
Entrez Id: 10329;104169670
Gene Symbol: RXYLT1;RXYLT1-AS1
RXYLT1;RXYLT1-AS1
CUI: C3554381
Disease:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 		0.700 GeneticVariation UNIPROT Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly. 23217329 2012