DiseaseInfo Viewer : HIX0001060

Transcripts	HIT000000178 HIT000002674 HIT000054346 HIT000054622 HIT000057810 HIT000059210 HIT000097055 HIT000245498 HIT000259711 HIT000280364 HIT000284758 HIT000298518 HIT000328539 HIT000494415 HIT000494931 HIT000497125
UCSC Genome browser	chr1:151375200-151431941
G-integra	chr1:151375200-151431941
Map position	1q21.3
Symbol	POGZ
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0001060

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	HRM2	139450	100379199	-	1q213	352	Hair, curly	OMIM
2	AD13	611152	100188837	-	1q21	561	Alzheimer disease-13	OMIM
3	MCKD1	174000	4169	29073	1q21	561	medullary cystic kidney disease 1 (autosomal dominant)	OMIM
4	PTCPRN	605642	79052	34082	1q21	561	Papillary thyroid carcinoma with papillary renal neoplasia	OMIM
5	ASPG3	608781	449015	35464	1q21-q22	628	Asperger syndrome, susceptibility to, 3	OMIM
6	SPRR2C	182269	6702	-	1q21-q22	628	small proline-rich protein 2C (pseudogene)	OMIM
7	BMND2	605833	338027	33719	1q21-q23	897	Bone mineral density variation 2	OMIM
8	DFNA49	608372	317664	34585	1q21-q23	897	deafness, autosomal dominant 49	OMIM
9	DFNA7	601412	1689	7591	1q21-q23	897	deafness, autosomal dominant 7	OMIM
10	PSORS4	603935	10547	-	1cen-q21	561	psoriasis susceptibility 4	OMIM
11	CORD8	605549	54109	33832	1q12-q24	1086	cone rod dystrophy 8	OMIM
12	SCA19	607346	140452	34273	1p21-q21	1112	spinocerebellar ataxia 19	OMIM
13	SCA19	607346	140452	34745	1p21-q21	1112	spinocerebellar ataxia 19	OMIM
14	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 $