DiseaseInfo Viewer : HIX0199788

Transcripts	HIT000000610 HIT000051268 HIT000052174 HIT000081651 HIT000384911 HIT000422586 HIT000489622
UCSC Genome browser	chr1:109512836-109584850
G-integra	chr1:109512836-109584850
Map position	1p13.3
Symbol	WDR47
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0199788

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	CYMP	118943	643160	-	1p133	171	chymosin pseudogene	OMIM
2	VUR	193000	54113	33673	1p13	306	Vesicoureteral reflux	OMIM
3	RP32	609913	641433	35269	1p212-p133	254	retinitis pigmentosa 32 (autosomal recessive)	OMIM
4	MRT4	611107	100009675	-	1p213-p133	345	mental retardation, non-syndromic, autosomal recessive, 4	OMIM
5	WS2B	600193	7488	5128	1p21-p133	345	Waardenburg syndrome, type 2B	OMIM
6	DFNB32	608653	113877	34142	1p221-p133	402	deafness, autosomal recessive 32	OMIM
7	DFNB32	608653	113877	35312	1p221-p133	402	deafness, autosomal recessive 32	OMIM
8	SCA19	607346	140452	34273	1p21-q21	1112	spinocerebellar ataxia 19	OMIM
9	SCA19	607346	140452	34745	1p21-q21	1112	spinocerebellar ataxia 19	OMIM
10	ARCODS	602483	100381211	-	1p211-q233	1315	Ariculocondylar syndrome	OMIM
11	ANON	606788	171514	34131	1p	2813	Anorexia nervosa, susceptibility to	OMIM
12	ANON	606788	171514	34132	1p	2813	Anorexia nervosa, susceptibility to	OMIM
13	PARK10	606852	170534	34395	1p	2813	Parkinson disease 10	OMIM
14	PSORS7	605606	65245	33842	1p	2813	psoriasis susceptibility 7	OMIM
15	SCZD12	608543	619488	-	1p	2813	schizophrenia 12	OMIM

---

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

$Revision: 1.58.2.9.2.46 $