H-InvDB x AHG DB
DiseaseInfo Viewer
H-InvDB_8.3 released on March 26, 2013.
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DiseaseInfo Viewer : HIX0012114

TranscriptsHIT000017881
HIT000387939
HIT000388112
UCSC Genome browserchr15:38988799-38992239
G-integrachr15:38988799-38992239
Map position15q14

SymbolFLJ35695
OMIMNA
Disease nameNA
MutationView-

Orphan diseases co-localized with HIX0012114

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 ECT 117100 100379198 30900 15q14 144 Centrotemporal epilepsy OMIM
2 EJM2 604827 50715 7447 15q14 144 epilepsy, juvenile myoclonic 2 OMIM
3 CILD4 608646 408257 34658 15q131-q151 318 Ciliary dyskinesia, primary, 4 OMIM
4 MOPCB2 605738 80771 33920 15q12-q15 466 Microphthalmia, colobomatous, 2 OMIM
5 CRAC1 601228 338377 31703 15q13-q21 739 colorectal adenoma and carcinoma 1 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 $