DiseaseInfo Viewer : HIX0019730

Transcripts	HIT000002480 HIT000004046 HIT000008647 HIT000037231 HIT000086642 HIT000261494 HIT000423817 HIT000427820 HIT000491027
UCSC Genome browser	chr15:75192328-75199462
G-integra	chr15:75192328-75199462
Map position	15q24.1
Symbol	C15orf17
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0019730

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	ENFL2	603204	50971	30514	15q24	211	Epilepsy, nocturnal frontal lobe, type 2	OMIM
2	MRSPR	-	-	29114	15q24	211	mental retardation with spasticity and retinitis pigmentosa	GenAtlas
3	MRST	602685	8126	-	15q24	211	Mental retardation, severe, with spasticity and tapetoretinal	OMIM
4	DFNB48	609439	404086	34941	15q23-q251	348	deafness, autosomal recessive 48	OMIM
5	CILD8	612274	100190786	-	15q24-q25	407	Ciliary dyskinesia, primary, 8	OMIM
6	GLC1N	611274	777645	-	15q22-q24	715	glaucoma 1, open angle, N (juvenile-onset)	OMIM
7	LOC619540	148600	619540	34601	15q22-q24	715	keratosis palmoplantaris papulosa	OMIM
8	SCAR5	606937	246180	35528	15q24-q26	1045	spinocerebellar ataxia, autosomal recessive 5	OMIM
9	GLM1	607248	338030	-	15q23-q263	1125	Glioma, familial, 1	OMIM
10	CDAN3	105600	981	2781	15q21-q25	1292	congenital dyserythropoietic anemia, type III	OMIM
11	HCVS	122460	3063	35297	15q11-qter	2424	human coronavirus sensitivity	OMIM
12	HYT2	604329	50986	-	15q	2424	Hypertension, essential, susceptibility to, 2	OMIM
13	LCS1	214900	84565	33814	15q	2424	lymphedema-cholestasis syndrome 1	OMIM
14	NEM6	609273	619401	34933	15q	2424	nemaline myopathy 6	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 $