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. 2009 May 27;1:131–144. doi: 10.1093/gbe/evp013

Table 3.

Candidate Disease Genes (Ka/Ks ≤0.30, maxExp ≥11.75, hetExp ≥0.32, and duplicate sequence similarity ≤50%)

Ensembl ID HGNC Name Description
ENSG00000179776 CDH5 Cadherin 5, type 2 (vascular endothelium)
ENSG00000154734 ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif
ENSG00000099308 MAST3 Microtubule-associated serine/threonine kinase 3
ENSG00000172232 AZU1 Azurocidin 1
ENSG00000124006 OBSL1 Obscurin-like 1
ENSG00000039560 RAI14 Retinoic acid-induced 14
ENSG00000145555 MYO10 Myosin X
ENSG00000169347 GP2 Glycoprotein 2 (zymogen granule membrane)
ENSG00000176956 LY6H Lymphocyte antigen 6 complex, locus H
ENSG00000169509 CRCT1 Cysteine-rich C-terminal 1

NOTE.—Those genes are not included in the list of hOMIM disease genes (Blekhman et al. 2008).