DiseaseInfo Viewer : HIX0013973

Transcripts	HIT000011778 HIT000028122 HIT000089183 HIT000094243 HIT000099485 HIT000246380 HIT000252135 HIT000494623
UCSC Genome browser	chr17:48423393-48442593
G-integra	chr17:48423393-48442593
Map position	17q21.33
Symbol	XYLT2
OMIM	608125 Protein title: XYLOSYLTRANSFERASE 2
Disease name	{Pseudoxanthoma elasticum, modifier of severity of} (264800)
MutationView	608125 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0013973

The number of co-localized H-Inv loci was computed by converting each cytogenetic band into a physical range on the chromosome, with additional 1000000 bp added on each side.

	Symbol	OMIM phenotype	Entrez Gene	GenAtlas	Cytogenetic band (Link to the latest human genome on UCSC Genome Browser)	Number-of co-localized H-Inv loci (Click for list)	Description	Source
1	ASRT6	611403	100188840	-	17q21	568	Asthma-related traits, susceptibility to, 6	OMIM
2	AUTS6	609378	554314	34949	17q21	568	Autism, susceptibility to, 6	OMIM
3	AUTS7	610676	100188816	-	17q21	568	Autism, susceptibility to, 7	OMIM
4	WT4	601363	8151	7639	17q12-q21	721	Wilms tumor-4	OMIM
5	GPSC	221820	8156	-	17q21-q22	692	gliosis, familial progressive subcortical	OMIM
6	HPC9	610997	100188826	-	17q21-q22	692	Prostate cancer, hereditary, 9	OMIM
7	MYP5	608474	404682	-	17q21-q22	692	myopia 5 (high grade, autosomal dominant)	OMIM
8	GLC1J	-	-	33730	17q12-q252	1230	glaucoma,primary open angle chronic adult onset,characterized by cupping of the optic nerve head,visual field loss and elevated intraocular pressure,in a series of North American mainly caucasians	GenAtlas
9	EXT4	-	-	27604	17q	1603	exostoses,multiple,4	GenAtlas
10	HYT1	603918	117191	28547	17q	1603	Hypertension, essential, susceptibility to, 1	OMIM
11	PSORS2	602723	5722	4873	17q	1603	psoriasis susceptibility 2	OMIM

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This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.

$Revision: 1.58.2.9.2.46 $