DiseaseInfo Viewer : HIX0012845

Transcripts	HIT000002673 HIT000024003 HIT000056188 HIT000094567 HIT000098201 HIT000246379 HIT000248572
UCSC Genome browser	chr16:17196181-17564738
G-integra	chr16:17196181-17564738
Map position	16p12.3
Symbol	XYLT1
OMIM	608124 Protein title: XYLOSYLTRANSFERASE 1
Disease name	{Pseudoxanthoma elasticum, modifier of severity of} (264800)
MutationView	608124 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0012845

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	MAFD4	611247	100126593	-	16p12	254	Major affective disorder 4	OMIM
2	RP22	602594	6114	28961	16p123-p121	254	retinitis pigmentosa 22 (autosomal recessive)	OMIM
3	ADHD1	608903	450087	-	16p13	507	Attention deficit-hyperactivity disorder, susceptibility to, 1	OMIM
4	BMIQ5	608558	449016	-	16p13	507	body mass index QTL 5	OMIM
5	CHDS1	607339	338334	34352	16pter-p13	507	Coronary heart disease, susceptibility to, 1	OMIM
6	CHDS1	607339	338334	34664	16pter-p13	507	Coronary heart disease, susceptibility to, 1	OMIM
7	EIM	605021	54119	33688	16p13	507	Infantile myoclonic epilepsy	OMIM
8	EIM	605021	54119	34536	16p13	507	Infantile myoclonic epilepsy	OMIM
9	EPRPDC	608105	574044	31529	16p12-p112	474	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp	OMIM
10	IHPS2	610260	780923	35374	16p13-p12	742	Pyloric stenosis, infantile hypertrophic, 2	OMIM
11	MHAC	605013	53341	33694	16p133-p121	742	microhydranencephaly	OMIM
12	IBD8	606668	170595	34095	16p	962	inflammatory bowel disease 8	OMIM
13	BFIC2	605751	81865	-	16p12-q12	645	Benign familial infantile convulsions-2	OMIM
14	ICCA	602066	3387	27338	16p12-q12	645	infantile convulsions and paroxysmal choreoathetosis	OMIM
15	MRT10	611096	100101425	-	16p12-q12	645	Mental retardation, autosomal recessive, 10	OMIM

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

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