DiseaseInfo Viewer : HIX0032796

Transcripts	HIT000078325 HIT000251227 HIT000251228 HIT000251229 HIT000340063 HIT000558386
UCSC Genome browser	chr6:39282474-39290364
G-integra	chr6:39282474-39290364
Map position	6p21.2
Symbol	KCNK16
OMIM	NA
Disease name	NA
MutationView	-

Orphan diseases co-localized with HIX0032796

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	LAP	150270	7939	16299	6p213-p212	814	Laryngeal adductor paralysis	OMIM
2	DFNA21	607017	192644	34496	6p21	995	deafness, autosomal dominant 21	OMIM
3	DFNA31	608645	347737	34607	6p21	995	deafness, autosomal dominant 31	OMIM
4	EJM3	608816	449018	35381	6p21	995	Epilepsy, juvenile myoclonic 3	OMIM
5	LATD	601086	207115	35493	6p21	995	Laterality defects, autosomal dominant	OMIM
6	RLS6	611185	100302512	-	6p21	995	Restless legs syndrome, susceptibility to, 6	OMIM
7	UAQTL4	612671	100272225	-	6p21	995	Uric acid concentration, serum, QTL4	OMIM
8	DFNB66	610212	606719	35140	6p223-p212	1189	deafness, autosomal recessive 66	OMIM
9	OTSC3	608244	170532	34225	6p223-p212	1189	otosclerosis 3	OMIM
10	SCAR3	271250	85502	34058	6p23-p21	1396	spinocerebellar ataxia, autosomal recessive 3	OMIM
11	CSCI	122550	7944	-	6p	1829	Corticosterone side-chain isomerase	OMIM
12	IBD3	604519	30829	19355	6p	1829	inflammatory bowel disease 3	OMIM
13	PUJO	143400	7945	16637	6p	1829	pelviureteric junction obstruction	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 $