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 |
---|---|---|
ZFLNCG02254 | 613120 | Brugada syndrome 7 |
ZFLNCG06562 | 154780 | Marshall syndrome |
ZFLNCG06743 | 300004 | Proud syndrome |
ZFLNCG04920 | 609622 | Short QT syndrome 3 |
ZFLNCG02407 | 614284 | Stickler syndrome, type V |
ZFLNCG05515 | 147250 | Single median maxillary central incisor |
ZFLNCG01488 | 602723 | Psoriasis 2 |
ZFLNCG06833 | 613582 | Retinitis pigmentosa 57 |
ZFLNCG07931 | 602481 | Migraine, familial hemiplegic, 2 |
ZFLNCG03410 | 191830 | Renal agenesis |
ZFLNCG11409 | 609622 | Short QT syndrome 3 |
ZFLNCG06932 | 277300 | Spondylocostal dysostosis 1, autosomal recessive |
ZFLNCG05515 | 605355 | Nemaline myopathy 5, Amish type |
ZFLNCG06743 | 300215 | Lissencephaly, X-linked 2 |
ZFLNCG10279 | 184840 | Stickler syndrome, type III |
ZFLNCG01741 | 601003 | Brody myopathy |
ZFLNCG13186 | 145680 | Dystransthyretinemic hyperthyroxinemia |
ZFLNCG03375 | 613388 | Fanconi renotubular syndrome 2 |
ZFLNCG00762 | 148820 | Waardenburg syndrome, type 3 |
ZFLNCG13058 | 181500 | Schizophrenia, susceptibility to |
ZFLNCG03775 | 608747 | Growth retardation with deafness and mental retardation due to IGF1 deficiency |
ZFLNCG04372 | 148190 | Keratitis |
ZFLNCG06961 | 607932 | Microphthalmia, syndromic 6 |
ZFLNCG01693 | 166210 | Osteogenesis imperfecta, type II |
ZFLNCG01693 | 130060 | Ehlers-Danlos syndrome, type VIIB |