DiseaseInfo Viewer : HIX0027959

Transcripts	HIT000046294 HIT000050082 HIT000081356 HIT000081357 HIT000081358 HIT000081362 HIT000081367 HIT000081368 HIT000081369 HIT000081373 HIT000081374 HIT000081375 HIT000081390 HIT000081391 HIT000081392 HIT000081398 HIT000081399 HIT000081400 HIT000099434 HIT000193127 : (show all transcripts) HIT000193128 HIT000193129 HIT000193130 HIT000193131 HIT000193821 HIT000193902 HIT000193903_05 HIT000193904 HIT000194598 HIT000194599 HIT000194727 HIT000195620 HIT000195900 HIT000217531 HIT000221378 HIT000265198 HIT000320864 HIT000329563 HIT000432841
UCSC Genome browser	chr6:32595956-32614839
G-integra	chr6:32595956-32614839
Map position	6p21.32

Symbol	HLA-DQA1
OMIM	146880 Protein title: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DQ ALPHA-1
Disease name	{Celiac disease, susceptibility to} (212750)
MutationView	146880 (JRE version 1.4.0 or later is required.)

Orphan diseases co-localized with HIX0027959

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	CMAH	603209	8418	-	6p2132	495	cytidine monophosphate-N-acetylneuraminic acid hydroxylase (CMP-N-acetylneuraminate monooxygenase) pseudogene	OMIM
2	LNCR4	612593	100271693	-	6p2133	257	Lung cancer susceptibility 4	OMIM
3	ASD1	108800	431	16741	6p213	719	atrial septal defect 1	OMIM
4	AZON	606766	338331	-	6p213	719	Azoospremia, nonobstructive	OMIM
5	IGAD1	137100	10986	31267	6p213	719	immunoglobulin A (IgA) deficiency susceptibility 1	OMIM
6	ISCW	146850	7928	-	6p213	719	Immune suppression to streptococcal antigen	OMIM
7	MYAS1	607085	246750	-	6p213	719	Myasthenia gravis with thymus hyperplasia	OMIM
8	NKS1	272370	4819	-	6p213	719	natural killer cell susceptibility 1	OMIM
9	PDB1	167250	5131	16252	6p213	719	Paget disease of bone 1	OMIM
10	RWS	179450	7937	-	6p213	719	Ragweed sensitivity	OMIM
11	WG	608710	474168	-	6p213	719	Wegener granulomatosis	OMIM
12	WM1	153600	100188787	-	6p213	719	Macroglobulinemia, Waldenstrom, susceptibility to, 1	OMIM
13	ZNF204P	603282	7754	-	6p213	719	zinc finger protein 204 (pseudogene)	OMIM
14	LAP	150270	7939	16299	6p213-p212	814	Laryngeal adductor paralysis	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	DFNB66	610212	606719	35140	6p223-p212	1189	deafness, autosomal recessive 66	OMIM
22	OTSC3	608244	170532	34225	6p223-p212	1189	otosclerosis 3	OMIM
23	SCAR3	271250	85502	34058	6p23-p21	1396	spinocerebellar ataxia, autosomal recessive 3	OMIM
24	CSCI	122550	7944	-	6p	1829	Corticosterone side-chain isomerase	OMIM
25	IBD3	604519	30829	19355	6p	1829	inflammatory bowel disease 3	OMIM
26	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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