H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0001372

TranscriptsHIT000000192
HIT000053040
HIT000053684
HIT000422786
HIT000487740
UCSC Genome browserchr1:178994939-179045702
G-integrachr1:178994939-179045702
Map position1q25.2

SymbolFAM20B
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0001372

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 AD14 611154 100188754 - 1q25 326 Alzheimer disease 14 OMIM
2 PDLA 608526 406237 34635 1q25 326 Periodontitis, localized aggressive OMIM
3 SPG23 270750 353293 35118 1q24-q32 1065 spastic paraplegia 23 (autosomal recessive) OMIM

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

$Revision: 1.58.2.9.2.46 $