H-InvDB x AHG DB
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H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0078236

TranscriptsHIT000041505
HIT000191055_04
HIT000191059_03
HIT000195653_04
HIT000195931_04
HIT000495814
UCSC Genome browserchr6:32407647-32412822
G-integrachr6:32407647-32412822
Map position6p21.32

SymbolHLA-DRA
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0078236

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.

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