We use the RWRH (random walk with restart on heterogeneous network) algorithm1 to analyze the relationship between lncRNA and OMIM in MATLAB. The upper subnetwork is coding-lncRNA gene co-expression network, and the lower network is OMIM similarity network. OMIM similarity matrix is from Disimweb2 and gene-OMIM relationship is from InterMine3.
1. Li, Y. & Patra, J. C. Genome-wide inferring gene-phenotype relationship by walking on the heterogeneous network. Bioinformatics 26, 1219-1224, doi:10.1093/bioinformatics/btq108 (2010).
2. Caniza, H., Romero, A. E. & Paccanaro, A. A network medicine approach to quantify distance between hereditary disease modules on the interactome. Sci Rep 5, 17658, doi:10.1038/srep17658 (2015).
3. Smith, R. N. et al. InterMine: a flexible data warehouse system for the integration and analysis of heterogeneous biological data. Bioinformatics 28, 3163-3165, doi:10.1093/bioinformatics/bts577 (2012).
ZFLNC lncRNA | OMIM | Phenotype |
---|---|---|
ZFLNCG08399 | 180105 | Retinitis pigmentosa 10 |
ZFLNCG04674 | 228000 | Farber lipogranulomatosis |
ZFLNCG01897 | 613810 | Retinitis pigmentosa 43 |
ZFLNCG12039 | 609532 | Hepatitic C virus, susceptibility to |
ZFLNCG06936 | 610093 | Microphthalmia, isolated 2 |
ZFLNCG11358 | 312300 | Androgen insensitivity, partial, with or without breast cancer |
ZFLNCG09934 | 228000 | Farber lipogranulomatosis |
ZFLNCG05701 | 614195 | Craniofacial anomalies and anterior segment dysgenesis syndrome |
ZFLNCG00825 | 300915 | Microphthalmia, syndromic 13 |
ZFLNCG05213 | 156610 | Symmetric circumferential skin creases, congenital, 1 |
ZFLNCG08214 | 615517 | Hemochromatosis, type 5 |
ZFLNCG09823 | 600072 | Insomnia, fatal familial |
ZFLNCG07882 | 608232 | Leukemia, chronic myeloid, somatic |
ZFLNCG07316 | 610743 | Spinocerebellar ataxia, autosomal recessive 8 |
ZFLNCG00713 | 609532 | Hepatitic C virus, susceptibility to |
ZFLNCG04391 | 112410 | Hypertension and brachydactyly syndrome |
ZFLNCG06936 | 610092 | Microphthalmia with coloboma 3 |
ZFLNCG10483 | 601536 | Bosley-Salih-Alorainy syndrome |
ZFLNCG08626 | 601419 | Myopathy, myofibrillar, 1 |
ZFLNCG08615 | 131750 | Epidermolysis bullosa dystrophica, AD |
ZFLNCG06123 | 601088 | Ayme-Gripp syndrome |
ZFLNCG11173 | 613310 | Exudative vitreoretinopathy 5 |
ZFLNCG02289 | 611664 | Skin/hair/eye pigmentation 7, blond/brown hair |
ZFLNCG03687 | 611724 | Skin/hair/eye pigmentation, variation in, 8 |
ZFLNCG12788 | 302350 | Nance-Horan syndrome |