DiseaseInfo Viewer : HIX0022762

Transcripts	HIT000025533 HIT000036509 HIT000038416 HIT000041270 HIT000268311 HIT000279243 HIT000300418
UCSC Genome browser	chr8:145159305-145162515
G-integra	chr8:145159305-145162515
Map position	8q24.3
Symbol	MAF1
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0022762

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	BMND10	612113	100188883	-	8q24	464	Bone mineral density QTL 10	OMIM
2	BSZQTL3	610649	100188815	-	8q24	464	Bone size quantitative trait locus 3	OMIM
3	CRCS2	611469	100188841	-	8q24	464	Colorectal cancer, susceptibility to, 2	OMIM
4	ECA1	600131	50966	27525	8q24	464	epilepsy, childhood absence 1	OMIM
5	FCMTE1	601068	50968	35086	8q24	464	familial cortical myoclonic tremor with epilepsy 1	OMIM
6	HPC10	611100	100188834	-	8q24	464	Prostate cancer, hereditary, 10	OMIM
7	HPV18I1	167959	3260	-	8q24	464	human papilloma virus (type 18) integration site 1	OMIM
8	HT	140300	140805	33723	8q23-q24	510	Hashimoto thyroiditis	OMIM
9	HT	140300	140805	33724	8q23-q24	510	Hashimoto thyroiditis	OMIM
10	MGS	611376	100126595	-	8q23-q24	510	Mungen syndrome	OMIM
11	CCAL1	600668	882	18973	8q	1063	chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)	OMIM
12	FHQTL	606789	171515	-	8q	1063	Fetal hemoglobin QTL on chromosome 8	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 $