DiseaseInfo Viewer : HIX0018470

Transcripts	HIT000038917 HIT000300147 HIT000323781 HIT000497077
UCSC Genome browser	chr9:93976098-94124206
G-integra	chr9:93976098-94124206
Map position	9q22.31
Symbol	AUH
OMIM	600529 Protein title: AU-SPECIFIC RNA-BINDING PROTEIN
Disease name	3-methylglutaconic aciduria, type I (250950)
MutationView	600529 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0018470

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	GLC1J	608695	574078	34690	9q22	341	glaucoma 1, open angle, J (juvenile-onset)	OMIM
2	STQTL8	610114	100037266	35280	9q22	341	stature quantitative trait locus 8	OMIM
3	HPLH1	267700	27259	30882	9q213-q22	578	hemophagocytic lymphohistiocytosis 1	OMIM
4	ALSFTD	105550	60497	34685	9q21-q22	771	Amyotrophic lateral sclerosis with frontotemporal dementia	OMIM
5	EPOLM	611631	100144434	-	9q21-q22	771	epilepsy, occipitotemporal lobe, and migraine with aura	OMIM
6	CMD1B	600884	1218	19094	9q13-q22	819	cardiomyopathy, dilated 1B (autosomal dominant)	OMIM
7	CTPL1	605749	81863	35085	9q13-q22	819	cataract, pulverulent (autosomal recessive, early-onset)	OMIM
8	HCHGQ2	609320	100381205	34875	9q	1739	Hematocrit/hemoglobin quantitative trait locus 2	OMIM
9	SPG19	607152	140907	34669	9q	1739	spastic paraplegia 19 (autosomal dominant)	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 $