DiseaseInfo Viewer : HIX0028498

Transcripts	HIT000059328 HIT000066939 HIT000094605 HIT000384878 HIT000386040
UCSC Genome browser	chr1:101003693-101007583
G-integra	chr1:101003693-101007583
Map position	1p21.2
Symbol	GPR88
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0028498

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	RP32	609913	641433	35269	1p212-p133	254	retinitis pigmentosa 32 (autosomal recessive)	OMIM
2	STQTL7	609822	100037265	-	1p21	193	stature quantitative trait locus 7	OMIM
3	MRT4	611107	100009675	-	1p213-p133	345	mental retardation, non-syndromic, autosomal recessive, 4	OMIM
4	WS2B	600193	7488	5128	1p21-p133	345	Waardenburg syndrome, type 2B	OMIM
5	DFNB32	608653	113877	34142	1p221-p133	402	deafness, autosomal recessive 32	OMIM
6	DFNB32	608653	113877	35312	1p221-p133	402	deafness, autosomal recessive 32	OMIM
7	SPG29	609727	619379	-	1p311-p211	524	spastic paraplegia 29 (autosomal dominant)	OMIM
8	AVSD1	606215	7446	10895	1p31-p21	661	atrioventricular septal defect 1	OMIM
9	SCA19	607346	140452	34273	1p21-q21	1112	spinocerebellar ataxia 19	OMIM
10	SCA19	607346	140452	34745	1p21-q21	1112	spinocerebellar ataxia 19	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

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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 $