H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0012315

TranscriptsHIT000000026
HIT000056301
HIT000056791
HIT000056793
HIT000061887
HIT000065694
HIT000066789
HIT000079120
HIT000450890
HIT000489194
UCSC Genome browserchr15:62939510-63136830
G-integrachr15:62939510-63136830
Map position15q22.2

SymbolTLN2
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0012315

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 USH1H 612632 100271837 - 15q22-q23 549 Usher syndrome 1H (autosomal recessive) OMIM
2 GLC1N 611274 777645 - 15q22-q24 715 glaucoma 1, open angle, N (juvenile-onset) OMIM
3 LOC619540 148600 619540 34601 15q22-q24 715 keratosis palmoplantaris papulosa OMIM
4 CCPSO 605728 80770 34110 15q21-q22 841 Cataract, central pouch-like, with sutural opacities OMIM
5 CDAN3 105600 981 2781 15q21-q25 1292 congenital dyserythropoietic anemia, type III OMIM
6 HCVS 122460 3063 35297 15q11-qter 2424 human coronavirus sensitivity OMIM
7 HYT2 604329 50986 - 15q 2424 Hypertension, essential, susceptibility to, 2 OMIM
8 LCS1 214900 84565 33814 15q 2424 lymphedema-cholestasis syndrome 1 OMIM
9 NEM6 609273 619401 34933 15q 2424 nemaline myopathy 6 OMIM

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

$Revision: 1.58.2.9.2.46 $