DiseaseInfo Viewer : HIX0078239

Transcripts	HIT000072994 HIT000101347_03 HIT000101453 HIT000101522_03 HIT000101532 HIT000101787 HIT000192301 HIT000192396 HIT000193110 HIT000193351 HIT000194436 HIT000195468 HIT000196569 HIT000217520 HIT000217542 HIT000217945_03 HIT000217982 HIT000218617 HIT000218618 HIT000218948 : (show all transcripts) HIT000219438_02 HIT000244451_03 HIT000300929_03 HIT000320927_03 HIT000322690 HIT000323377_02 HIT000323951_03 HIT000324402 HIT000324463 HIT000428211 HIT000429452 HIT000432777 HIT000446283_03 HIT000495309 HIT000495632 HIT000495907
UCSC Genome browser	chr6:31236526-31325406
G-integra	chr6:31236526-31325406
Map position	6p21.33

Symbol	HLA-B
OMIM	142830 Protein title: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, B
Disease name	{Abacavir hypersensitivity, susceptibility to} {Spondyloarthropathy, susceptibility to, 1} (106300) {Stevens-Johnson syndrome, carbamazepine-induced, susceptibility to} (608579)
MutationView	142830 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0078239

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	LNCR4	612593	100271693	-	6p2133	257	Lung cancer susceptibility 4	OMIM
2	ASD1	108800	431	16741	6p213	719	atrial septal defect 1	OMIM
3	AZON	606766	338331	-	6p213	719	Azoospremia, nonobstructive	OMIM
4	IGAD1	137100	10986	31267	6p213	719	immunoglobulin A (IgA) deficiency susceptibility 1	OMIM
5	ISCW	146850	7928	-	6p213	719	Immune suppression to streptococcal antigen	OMIM
6	MYAS1	607085	246750	-	6p213	719	Myasthenia gravis with thymus hyperplasia	OMIM
7	NKS1	272370	4819	-	6p213	719	natural killer cell susceptibility 1	OMIM
8	PDB1	167250	5131	16252	6p213	719	Paget disease of bone 1	OMIM
9	RWS	179450	7937	-	6p213	719	Ragweed sensitivity	OMIM
10	WG	608710	474168	-	6p213	719	Wegener granulomatosis	OMIM
11	WM1	153600	100188787	-	6p213	719	Macroglobulinemia, Waldenstrom, susceptibility to, 1	OMIM
12	ZNF204P	603282	7754	-	6p213	719	zinc finger protein 204 (pseudogene)	OMIM
13	LAP	150270	7939	16299	6p213-p212	814	Laryngeal adductor paralysis	OMIM
14	ALPQTL3	612368	100196915	-	6p22	523	Alkaline phosphatase, plasma level of, QTL3	OMIM
15	DFNA21	607017	192644	34496	6p21	995	deafness, autosomal dominant 21	OMIM
16	DFNA31	608645	347737	34607	6p21	995	deafness, autosomal dominant 31	OMIM
17	EJM3	608816	449018	35381	6p21	995	Epilepsy, juvenile myoclonic 3	OMIM
18	LATD	601086	207115	35493	6p21	995	Laterality defects, autosomal dominant	OMIM
19	RLS6	611185	100302512	-	6p21	995	Restless legs syndrome, susceptibility to, 6	OMIM
20	UAQTL4	612671	100272225	-	6p21	995	Uric acid concentration, serum, QTL4	OMIM
21	SCZD3	600511	6365	15929	6p24-p22	656	schizophrenia disorder 3	OMIM
22	DFNB66	610212	606719	35140	6p223-p212	1189	deafness, autosomal recessive 66	OMIM
23	OTSC3	608244	170532	34225	6p223-p212	1189	otosclerosis 3	OMIM
24	SCAR3	271250	85502	34058	6p23-p21	1396	spinocerebellar ataxia, autosomal recessive 3	OMIM
25	CSCI	122550	7944	-	6p	1829	Corticosterone side-chain isomerase	OMIM
26	IBD3	604519	30829	19355	6p	1829	inflammatory bowel disease 3	OMIM
27	PUJO	143400	7945	16637	6p	1829	pelviureteric junction obstruction	OMIM

This database and viewer were originally developed by Dr. Boris Lenhard at Karolinska Institute.

$Revision: 1.58.2.9.2.46 $


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