DiseaseInfo Viewer : HIX0036688

Transcripts	HIT000000058 HIT000064740 HIT000067454 HIT000329267 HIT000343518 HIT000425265 HIT000429891 HIT000436052 HIT000501630 HIT000503124
UCSC Genome browser	chr12:57345217-57400297
G-integra	chr12:57345217-57400297
Map position	12q13.3
Symbol	RODH-4
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0036688

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	APOF	107760	319	-	12q133	147	apolipoprotein F	OMIM
2	AREI	607936	378889	34935	12q13	456	Exfoliative ichthyosis, autosomal recessive	OMIM
3	HPV18I2	167960	3261	-	12q13	456	human papillomavirus (type 18) integration site 2	OMIM
4	CMT2G	608591	431712	34653	12q12-q133	501	Charcot-Marie-Tooth disease, axonal, type 2G	OMIM
5	PPKB	600231	8084	7862	12q11-q13	501	palmoplantar keratoderma, Bothnia type	OMIM
6	SPG26	609195	550623	34876	12p111-q14	598	spastic paraplegia 26	OMIM
7	STQTL3	606257	282549	-	12p112-q14	668	stature quantitative trait locus 3	OMIM
8	ENUR2	600808	2032	25421	12q13-q21	720	enuresis, nocturnal 2	OMIM
9	RLS	102300	192142	34065	12q12-q21	765	Restless legs syndrome, susceptibility to	OMIM
10	RLS	102300	192142	34675	12q12-q21	765	Restless legs syndrome, susceptibility to	OMIM
11	CNA1	121400	1255	35220	12q	1469	cornea plana 1 (autosomal dominant)	OMIM
12	CODA	611543	100188845	-	12q	1469	Cavitary optic disc anomalies	OMIM
13	IBD2	601458	3378	7615	12p132-q241	1511	inflammatory bowel disease 2	OMIM
14	TELM	609113	550641	35207	12	2213	telomere length, mean leukocyte	OMIM
15	TELM	609113	550641	35208	12	2213	telomere length, mean leukocyte	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 $