DiseaseInfo Viewer : HIX0199902

Transcripts	HIT000019173 HIT000021095 HIT000087408 HIT000264343
UCSC Genome browser	chr1:19923467-19956315
G-integra	chr1:19923467-19956315
Map position	1p36.13
Symbol	LOC440574
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0199902

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	ANIB3	609122	497657	34822	1p3613-p343	816	aneurysm, intracranial berry 3	OMIM
2	ALPQTL2	612367	100196914	-	1p36	976	Alkaline phosphatase, plasma level of, QTL 2	OMIM
3	BMND3	606928	246259	29078	1p36	976	Bone mineral density variability 3	OMIM
4	BMND3	606928	246259	29079	1p36	976	Bone mineral density variability 3	OMIM
5	BMND3	606928	246259	29080	1p36	976	Bone mineral density variability 3	OMIM
6	CCV	115665	7792	6072	1p36	976	cataract, congenital, Volkmann type	OMIM
7	CMM	155600	1243	123	1p36	976	cutaneous malignant melanoma/dysplastic nevus	OMIM
8	CTPP	116600	10306	10888	1pter-p361	976	Cataract, posterior polar	OMIM
9	CTPP	116600	10306	34568	1pter-p361	976	Cataract, posterior polar	OMIM
10	DYT13	607671	93983	34130	1p36	976	dystonia 13, torsion	OMIM
11	GLC3B	600975	2728	7589	1p36	976	glaucoma 3, primary infantile, B	OMIM
12	IBD7	605225	57042	33908	1p36	976	inflammatory bowel disease 7	OMIM
13	LCA9	608553	619483	34461	1p36	976	Leber congenital amaurosis 9	OMIM
14	MS4	612596	100271696	-	1p36	976	Multiple sclerosis, susceptiblity to, 4	OMIM
15	MYP14	610320	100359407	-	1p36	976	myopia 14	OMIM
16	SCASI	607317	260415	34534	1p36	976	spinocerebellar ataxia with saccadic intrusions	OMIM
17	DYX8	608995	406874	34708	1p36-p34	1516	dyslexia susceptibility 8	OMIM
18	DYT13	-	93983	34130	1p3132-p3613	1459	primarytorsion dystomia 13 with prominent cranial - cervical and upper limb involvement	GenAtlas
19	ANON	606788	171514	34131	1p	2813	Anorexia nervosa, susceptibility to	OMIM
20	ANON	606788	171514	34132	1p	2813	Anorexia nervosa, susceptibility to	OMIM
21	PARK10	606852	170534	34395	1p	2813	Parkinson disease 10	OMIM
22	PSORS7	605606	65245	33842	1p	2813	psoriasis susceptibility 7	OMIM
23	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 $