H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0000670

TranscriptsHIT000009200
HIT000037499
HIT000052346
HIT000262365
HIT000267680
HIT000322413
HIT000427923
HIT000432477
HIT000435517
HIT000500867
HIT000503283
UCSC Genome browserchr1:65613232-65693177
G-integrachr1:65613232-65693177
Map position1p31.3

SymbolAK3
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0000670

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 AIR 601676 7808 - 1p31 332 Acute insulin response (2) OMIM
2 ASRT4 610906 100188823 - 1p31 332 Asthma-related traits, susceptibility to, 4 OMIM
3 CSE 601042 1433 7937 1p31 332 choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity) OMIM
4 DSAP3 612293 100190982 - 1p313-p311 332 Porokeratosis, disseminated superficial actinic, 3 OMIM
5 PAOD1 606787 171513 34120 1p31 332 Peripheral arterial occlusive disease 1 OMIM
6 AVSD1 606215 7446 10895 1p31-p21 661 atrioventricular septal defect 1 OMIM
7 DYT13 - 93983 34130 1p3132-p3613 1459 primarytorsion dystomia 13 with prominent cranial - cervical and upper limb involvement GenAtlas
8 ANON 606788 171514 34131 1p 2813 Anorexia nervosa, susceptibility to OMIM
9 ANON 606788 171514 34132 1p 2813 Anorexia nervosa, susceptibility to OMIM
10 PARK10 606852 170534 34395 1p 2813 Parkinson disease 10 OMIM
11 PSORS7 605606 65245 33842 1p 2813 psoriasis susceptibility 7 OMIM
12 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 $