H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0032795

TranscriptsHIT000077838
HIT000078238
HIT000338614
UCSC Genome browserchr6:27292540-27293742
G-integrachr6:27292540-27293742
Map position6p22.1

SymbolFKSG83
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0032795

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 ALPQTL3 612368 100196915 - 6p22 523 Alkaline phosphatase, plasma level of, QTL3 OMIM
2 SCZD3 600511 6365 15929 6p24-p22 656 schizophrenia disorder 3 OMIM
3 DFNB66 610212 606719 35140 6p223-p212 1189 deafness, autosomal recessive 66 OMIM
4 OTSC3 608244 170532 34225 6p223-p212 1189 otosclerosis 3 OMIM
5 SCAR3 271250 85502 34058 6p23-p21 1396 spinocerebellar ataxia, autosomal recessive 3 OMIM
6 CSCI 122550 7944 - 6p 1829 Corticosterone side-chain isomerase OMIM
7 IBD3 604519 30829 19355 6p 1829 inflammatory bowel disease 3 OMIM
8 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 $