DiseaseInfo Viewer : HIX0015175

Transcripts	HIT000000012 HIT000009213 HIT000078412 HIT000436183 HIT000440717
UCSC Genome browser	chr19:42788817-42799949
G-integra	chr19:42788817-42799949
Map position	19q13.2
Symbol	CIC
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0015175

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	TEC	227050	100124696	34762	19q132	266	transient erythroblastopenia of childhood	OMIM
2	MRT11	611097	100101426	-	19q132-q133	664	Mental retardation, autosomal recessive, 11	OMIM
3	E11S	129150	1878	-	19q131-q133	952	ECHO virus (serotypes 4, 6, 11, 19) sensitivity	OMIM
4	CFM1	603855	10167	-	19q132-q134	1071	cystic fibrosis modifier 1	OMIM
5	GLC1K	-	-	33731	19q12-q133	984	glaucoma,primary open angle chronic adult onset,characterized by cupping of the optic nerve head,visual field loss and elevated intraocular pressure,in a series of North American mainly caucasians	GenAtlas
6	AAVS1	102699	17	-	19q13	1359	adeno-associated virus integration site 1	OMIM
7	ANIB2	608542	449013	34632	19q13	1359	aneurysm, intracranial berry 2	OMIM
8	EA7	611907	100188859	-	19q13	1359	Episodic ataxia, type 7	OMIM
9	HHC3	600740	9151	30885	19q13	1359	hypocalciuric hypercalcemia 3 (Oklahoma type)	OMIM
10	LOC619404	609376	619404	-	19q13	1359	cataract, congenital nuclear, autosomal recessive	OMIM
11	MCPH2	604317	4181	32645	19q13	1359	microcephaly, primary autosomal recessive 2	OMIM
12	OFC3	600757	4965	8534	19q13	1359	orofacial cleft 3	OMIM
13	SPG12	604805	23675	33757	19q13	1359	spastic paraplegia 12 (autosomal dominant)	OMIM
14	BFIC	601764	8181	35527	19q	1391	benign familial infantile convulsions	OMIM
15	CILD2	606763	56162	33744	19q	1391	ciliary dyskinesia, primary 2	OMIM
16	HPCQTL19	607592	347747	34340	19q	1391	Prostate cancer aggressiveness quantitative trait locus on chromosome 19	OMIM
17	SLI2	606712	171014	35234	19q	1391	Specific language impairment QTL, 2	OMIM
18	CXB3S	120050	1526	-	19pter-q13	2509	coxsackie virus B3 sensitivity	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 $