DiseaseInfo Viewer : HIX0012187

Transcripts	HIT000030754 HIT000032853 HIT000099548_03 HIT000276740 HIT000278706 HIT000279063 HIT000284233 HIT000297212 HIT000331145 HIT000430564_04 HIT000488626_02 HIT000490400 HIT000499665 HIT000499737 HIT000499932
UCSC Genome browser	chr15:43985084-43991872
G-integra	chr15:43985084-43991872
Map position	15q15.3
Symbol	-
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0012187

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	FRTS	134600	65211	33868	15q153	91	Fanconi renotubular syndrome	OMIM
2	SCZD10	605419	63944	27610	15q15	189	schizophrenia disorder 10 (periodic catatonia)	OMIM
3	ALS5	602099	255	28971	15q151-q211	222	amyotrophic lateral sclerosis 5	OMIM
4	MCPH4	604321	23701	32731	15q15-q21	548	microcephaly, primary autosomal recessive 4	OMIM
5	MOPCB2	605738	80771	33920	15q12-q15	466	Microphthalmia, colobomatous, 2	OMIM
6	CRAC1	601228	338377	31703	15q13-q21	739	colorectal adenoma and carcinoma 1	OMIM
7	HCVS	122460	3063	35297	15q11-qter	2424	human coronavirus sensitivity	OMIM
8	HYT2	604329	50986	-	15q	2424	Hypertension, essential, susceptibility to, 2	OMIM
9	LCS1	214900	84565	33814	15q	2424	lymphedema-cholestasis syndrome 1	OMIM
10	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 $