DiseaseInfo Viewer : HIX0202090

Transcripts	HIT000048069 HIT000061459 HIT000096773 HIT000429315
UCSC Genome browser	chr14:105639276-105647660
G-integra	chr14:105639276-105647660
Map position	14q32.33
Symbol	NUDT14
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0202090

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	IGHR	144120	8117	-	14q3233	212	immunoglobulin heavy chain regulator	OMIM
2	CHDS4	608318	387585	-	14q32	551	Coronary heart disease, susceptibility to, 4	OMIM
3	CKBE	123270	1156	35326	14q32	551	creatine kinase, ectopic expression	OMIM
4	GEVQ1	608875	474334	-	14q32	551	gene expression, variation in, quantitative trait locus	OMIM
5	HFM	164210	170474	34074	14q32	551	Hemifacial microsomia	OMIM
6	IV	270100	8114	-	14q32	551	inversus situs, viscerum	OMIM
7	MCOP	251600	8113	29115	14q32	551	microphthalmia, autosomal recessive	OMIM
8	CTAA1	115650	1483	70	14q24-qter	974	cataract, anterior polar 1	OMIM
9	IBGC1	213600	23706	32135	14q	1654	idiopathic basal ganglia calcification 1	OMIM
10	MNG1	138800	4333	27579	14q	1654	multinodular goitre 1	OMIM
11	SPG32	611252	724107	-	14q	1654	spastic paraplegia 32 (autosomal recessive)	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 $