H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0199963

TranscriptsHIT000034742
HIT000034991
HIT000081196
HIT000301574
UCSC Genome browserchr1:43849588-43855483
G-integrachr1:43849588-43855483
Map position1p34.2

SymbolMED8
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0199963

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 MRT12 611090 100101420 - 1p34-p33 467 Mental retardation, autosomal recessive, 12 OMIM
2 DYX8 608995 406874 34708 1p36-p34 1516 dyslexia susceptibility 8 OMIM
3 DYT13 - 93983 34130 1p3132-p3613 1459 primarytorsion dystomia 13 with prominent cranial - cervical and upper limb involvement GenAtlas
4 ANON 606788 171514 34131 1p 2813 Anorexia nervosa, susceptibility to OMIM
5 ANON 606788 171514 34132 1p 2813 Anorexia nervosa, susceptibility to OMIM
6 PARK10 606852 170534 34395 1p 2813 Parkinson disease 10 OMIM
7 PSORS7 605606 65245 33842 1p 2813 psoriasis susceptibility 7 OMIM
8 SCZD12 608543 619488 - 1p 2813 schizophrenia 12 OMIM

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

$Revision: 1.58.2.9.2.46 $