H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0029412

TranscriptsHIT000270693
UCSC Genome browserchr1:246057870-246059667
G-integrachr1:246057870-246059667
Map position1q44

Symbol-
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0029412

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 DFNB45 612433 449483 - 1q43-q44 285 deafness, autosomal recessive 45 OMIM

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

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