DiseaseInfo Viewer : HIX0001257

Transcripts	HIT000000181 HIT000008216 HIT000044995 HIT000063356 HIT000096657 HIT000332414 HIT000340424 HIT000389370 HIT000389371 HIT000488531 HIT000502214 HIT000502223
UCSC Genome browser	chr1:162327308-162356608
G-integra	chr1:162327308-162356608
Map position	1q23.3
Symbol	CAPON
OMIM	605551 Protein title: NITRIC OXIDE SYNTHASE 1 (NEURONAL) ADAPTOR PROTEIN
Disease name	QT interval, modifier of (610141)
MutationView	605551 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0001257

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	QTV	610141	100379215	-	1q233	197	QT interval, variation in	OMIM
2	BDET	605913	85504	-	1q23	363	Bleeding disorder, east Texas type	OMIM
3	LFS3	609266	553989	35395	1q23	363	Li-Fraumeni syndrome 3	OMIM
4	BMND2	605833	338027	33719	1q21-q23	897	Bone mineral density variation 2	OMIM
5	DFNA49	608372	317664	34585	1q21-q23	897	deafness, autosomal dominant 49	OMIM
6	DFNA7	601412	1689	7591	1q21-q23	897	deafness, autosomal dominant 7	OMIM
7	CORD8	605549	54109	33832	1q12-q24	1086	cone rod dystrophy 8	OMIM
8	ARCODS	602483	100381211	-	1p211-q233	1315	Ariculocondylar syndrome	OMIM

---

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

$Revision: 1.58.2.9.2.46 $