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Fusion gene ID: 31300 |
FusionGeneSummary for RLF_MFSD2A |
Fusion gene summary |
Fusion gene information | Fusion gene name: RLF_MFSD2A | Fusion gene ID: 31300 | Hgene | Tgene | Gene symbol | RLF | MFSD2A | Gene ID | 6018 | 84879 |
Gene name | rearranged L-myc fusion | major facilitator superfamily domain containing 2A | |
Synonyms | ZN-15L|ZNF292L | MCPH15|MFSD2|NLS1 | |
Cytomap | 1p34.2 | 1p34.2 | |
Type of gene | protein-coding | protein-coding | |
Description | zinc finger protein RlfZn-15 relatedrearranged L-myc fusion gene proteinrearranged L-myc fusion sequencezn-15-related protein | sodium-dependent lysophosphatidylcholine symporter 1major facilitator superfamily domain-containing protein 2Asodium-dependent LPC symporter 1 | |
Modification date | 20180519 | 20180329 | |
UniProtAcc | Q13129 | Q8NA29 | |
Ensembl transtripts involved in fusion gene | ENST00000372771, | ENST00000372811, ENST00000420632, ENST00000372809, ENST00000480630, | |
Fusion gene scores | * DoF score | 11 X 6 X 6=396 | 6 X 6 X 3=108 |
# samples | 11 | 7 | |
** MAII score | log2(11/396*10)=-1.84799690655495 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(7/108*10)=-0.625604485218502 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: RLF [Title/Abstract] AND MFSD2A [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | Tumor suppressor gene involved fusion gene, in-frame but not retained their domain. Tumor suppressor gene involved fusion gene, retained protein feature but frameshift. DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | RLF | GO:0015074 | DNA integration | 1851085 |
Hgene | RLF | GO:0051276 | chromosome organization | 1649386 |
Tgene | MFSD2A | GO:0051977 | lysophospholipid transport | 24828044 |
Fusion gene information from three resources (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | OV | TCGA-24-1557-01A | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40424373 | + |
TCGA | LD | OV | TCGA-24-1557-01A | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40422759 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
In-frame | ENST00000372771 | ENST00000372811 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40424373 | + |
5CDS-intron | ENST00000372771 | ENST00000420632 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40424373 | + |
5CDS-intron | ENST00000372771 | ENST00000372809 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40424373 | + |
5CDS-intron | ENST00000372771 | ENST00000480630 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40424373 | + |
In-frame | ENST00000372771 | ENST00000372811 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40422759 | + |
5CDS-intron | ENST00000372771 | ENST00000420632 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40422759 | + |
5CDS-intron | ENST00000372771 | ENST00000372809 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40422759 | + |
5CDS-intron | ENST00000372771 | ENST00000480630 | RLF | chr1 | 40627308 | + | MFSD2A | chr1 | 40422759 | + |
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FusionProtFeatures for RLF_MFSD2A |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
RLF | MFSD2A |
May be involved in transcriptional regulation. | Sodium-dependent lysophosphatidylcholine (LPC)symporter, which plays an essential role for blood-brain barrierformation and function (By similarity). Specifically expressed inendothelium of the blood-brain barrier of micro-vessels andtransports LPC into the brain (By similarity). Transport of LPC isessential because it constitutes the major mechanism by whichdocosahexaenoic acid (DHA), an omega-3 fatty acid that isessential for normal brain growth and cognitive function, entersthe brain (PubMed:26005868). Transports LPC carrying long-chainfatty acids such LPC oleate and LPC palmitate with a minimum acylchain length of 14 carbons (By similarity). Does not transportdocosahexaenoic acid in unesterified fatty acid (By similarity).Specifically required for blood-brain barrier formation andfunction, probably by mediating lipid transport (By similarity).Not required for central nervous system vascular morphogenesis (Bysimilarity). Acts as a transporter for tunicamycin, an inhibitorof asparagine-linked glycosylation (PubMed:21677192). In placenta,acts as a receptor for ERVFRD-1/syncytin-2 and is required fortrophoblast fusion (PubMed:18988732, PubMed:23177091).{ECO:0000250|UniProtKB:Q9DA75, ECO:0000269|PubMed:18988732,ECO:0000269|PubMed:21677192, ECO:0000269|PubMed:23177091,ECO:0000269|PubMed:26005868}. |
Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at . * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 35_38 | 31 | 544 | Compositional bias | Note=Poly-Lys |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 35_38 | 31 | 531 | Compositional bias | Note=Poly-Lys |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 35_38 | -48 | 544 | Compositional bias | Note=Poly-Lys |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 102_128 | 31 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 150_160 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 182_256 | 31 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 278_310 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 332_344 | 31 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 366_370 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 392_393 | 31 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 415_437 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 459_480 | 31 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 502_543 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 68_80 | 31 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 102_128 | 31 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 150_160 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 182_256 | 31 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 278_310 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 332_344 | 31 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 366_370 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 392_393 | 31 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 415_437 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 459_480 | 31 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 502_543 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 68_80 | 31 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 102_128 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 150_160 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 182_256 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 1_46 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 278_310 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 332_344 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 366_370 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 392_393 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 415_437 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 459_480 | -48 | 544 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 502_543 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 68_80 | -48 | 544 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 102_128 | 76 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 150_160 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 182_256 | 76 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 278_310 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 332_344 | 76 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 366_370 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 392_393 | 76 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 415_437 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 459_480 | 76 | 531 | Topological domain | Extracellular |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 502_543 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 129_149 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 161_181 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 257_277 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 311_331 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 345_365 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 371_391 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 394_414 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 438_458 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 47_67 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 481_501 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 81_101 | 31 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 129_149 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 161_181 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 257_277 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 311_331 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 345_365 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 371_391 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 394_414 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 438_458 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 47_67 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 481_501 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 81_101 | 31 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 129_149 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 161_181 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 257_277 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 311_331 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 345_365 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 371_391 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 394_414 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 438_458 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 47_67 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 481_501 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372809 | + | 0 | 14 | 81_101 | -48 | 544 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 129_149 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 161_181 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 257_277 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 311_331 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 345_365 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 371_391 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 394_414 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 438_458 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 481_501 | 76 | 531 | Transmembrane | Helical |
Tgene | >MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 81_101 | 76 | 531 | Transmembrane | Helical |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1127_1152 | 79 | 1915 | Zinc finger | C2H2-type 8 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1172_1195 | 79 | 1915 | Zinc finger | C2H2-type 9 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1310_1335 | 79 | 1915 | Zinc finger | C2H2-type 10 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1362_1387 | 79 | 1915 | Zinc finger | C2H2-type 11 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1407_1432 | 79 | 1915 | Zinc finger | C2H2-type 12 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1444_1469 | 79 | 1915 | Zinc finger | C2H2-type 13 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 1549_1574 | 79 | 1915 | Zinc finger | C2H2-type 14 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 582_604 | 79 | 1915 | Zinc finger | C2H2-type 1 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 671_696 | 79 | 1915 | Zinc finger | C2H2-type 2 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 714_736 | 79 | 1915 | Zinc finger | C2H2-type 3 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 742_766 | 79 | 1915 | Zinc finger | C2H2-type 4 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 771_795 | 79 | 1915 | Zinc finger | C2H2-type 5 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 801_825 | 79 | 1915 | Zinc finger | C2H2-type 6 |
Hgene | >RLF | chr1:40627308 | chr1:40422759 | ENST00000372771 | + | 1 | 8 | 954_979 | 79 | 1915 | Zinc finger | C2H2-type 7 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1127_1152 | 79 | 1915 | Zinc finger | C2H2-type 8 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1172_1195 | 79 | 1915 | Zinc finger | C2H2-type 9 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1310_1335 | 79 | 1915 | Zinc finger | C2H2-type 10 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1362_1387 | 79 | 1915 | Zinc finger | C2H2-type 11 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1407_1432 | 79 | 1915 | Zinc finger | C2H2-type 12 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1444_1469 | 79 | 1915 | Zinc finger | C2H2-type 13 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 1549_1574 | 79 | 1915 | Zinc finger | C2H2-type 14 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 582_604 | 79 | 1915 | Zinc finger | C2H2-type 1 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 671_696 | 79 | 1915 | Zinc finger | C2H2-type 2 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 714_736 | 79 | 1915 | Zinc finger | C2H2-type 3 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 742_766 | 79 | 1915 | Zinc finger | C2H2-type 4 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 771_795 | 79 | 1915 | Zinc finger | C2H2-type 5 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 801_825 | 79 | 1915 | Zinc finger | C2H2-type 6 |
Hgene | >RLF | chr1:40627308 | chr1:40424373 | ENST00000372771 | + | 1 | 8 | 954_979 | 79 | 1915 | Zinc finger | C2H2-type 7 |
Tgene | MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 35_38 | 76 | 531 | Compositional bias | Note=Poly-Lys |
Tgene | MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372809 | + | 0 | 14 | 1_46 | 31 | 544 | Topological domain | Extracellular |
Tgene | MFSD2A | chr1:40627308 | chr1:40422759 | ENST00000372811 | + | 0 | 14 | 1_46 | 31 | 531 | Topological domain | Extracellular |
Tgene | MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 1_46 | 76 | 531 | Topological domain | Extracellular |
Tgene | MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 68_80 | 76 | 531 | Topological domain | Cytoplasmic |
Tgene | MFSD2A | chr1:40627308 | chr1:40424373 | ENST00000372811 | + | 1 | 14 | 47_67 | 76 | 531 | Transmembrane | Helical |
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FusionGeneSequence for RLF_MFSD2A |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40424373_+_534aa MADGKGDAAAVAGAGAEAPAVAGAGDGVETESMVRGHRPVSPAPGASGLRPCLWQLETELREQEVSEVSSLNYCRSFCQVGPFSASIILF VGRAWDAITDPLVGLCISKSPWTCLGRLMPWIIFSTPLAVIAYFLIWFVPDFPHGQTYWYLLFYCLFETMVTCFHVPYSALTMFISTEQT ERDSATAYRMTVEVLGTVLGTAIQGQIVGQADTPCFQDLNSSTVASQSANHTHGTTSHRETQKAYLLAAGVIVCIYIICAVILILGVREQ REPYEAQQSEPIAYFRGLRLVMSHGPYIKLITGFLFTSLAFMLVEGNFVLFCTYTLGFRNEFQNLLLAIMLSATLTIPIWQWFLTRFGKK TAVYVGISSAVPFLILVALMESNLIITYAVAVAAGISVAAAFLLPWSMLPDVIDDFHLKQPHFHGTEPIFFSFYVFFTKFASGVSLGIST >In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40422759_+_579aa MADGKGDAAAVAGAGAEAPAVAGAGDGVETESMVRGHRPVSPAPGASGLRPCLWQLETELREQEVSEVSSLNYCRSFCQKEPKKKKQQLS VCNKLCYALGGAPYQVTGCALGFFLQIYLLDVAQVGPFSASIILFVGRAWDAITDPLVGLCISKSPWTCLGRLMPWIIFSTPLAVIAYFL IWFVPDFPHGQTYWYLLFYCLFETMVTCFHVPYSALTMFISTEQTERDSATAYRMTVEVLGTVLGTAIQGQIVGQADTPCFQDLNSSTVA SQSANHTHGTTSHRETQKAYLLAAGVIVCIYIICAVILILGVREQREPYEAQQSEPIAYFRGLRLVMSHGPYIKLITGFLFTSLAFMLVE GNFVLFCTYTLGFRNEFQNLLLAIMLSATLTIPIWQWFLTRFGKKTAVYVGISSAVPFLILVALMESNLIITYAVAVAAGISVAAAFLLP WSMLPDVIDDFHLKQPHFHGTEPIFFSFYVFFTKFASGVSLGISTLSLDFAGYQTRGCSQPERVKFTLNMLVTMAPIVLILLGLLLFKMY |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40424373_+_1602nt ATGGCGGACGGAAAGGGAGACGCCGCCGCTGTCGCCGGGGCTGGGGCTGAGGCTCCGGCGGTAGCGGGAGCCGGAGATGGAGTCGAGACT GAGTCCATGGTTCGGGGTCATCGCCCCGTATCTCCAGCGCCGGGAGCCTCGGGACTGCGGCCGTGTCTGTGGCAGCTGGAGACAGAGCTG AGGGAGCAAGAGGTGTCGGAGGTCTCATCTTTGAACTACTGCCGGAGCTTCTGCCAGGTGGGCCCTTTCTCTGCCTCCATCATCCTGTTT GTGGGCCGAGCCTGGGATGCCATCACAGACCCCCTGGTGGGCCTCTGCATCAGCAAATCCCCCTGGACCTGCCTGGGTCGCCTTATGCCC TGGATCATCTTCTCCACGCCCCTGGCCGTCATTGCCTACTTCCTCATCTGGTTCGTGCCCGACTTCCCACACGGCCAGACCTATTGGTAC CTGCTTTTCTATTGCCTCTTTGAAACAATGGTCACGTGTTTCCATGTTCCCTACTCGGCTCTCACCATGTTCATCAGCACCGAGCAGACT GAGCGGGATTCTGCCACCGCCTATCGGATGACTGTGGAAGTGCTGGGCACAGTGCTGGGCACGGCGATCCAGGGACAAATCGTGGGCCAA GCAGACACGCCTTGTTTCCAGGACCTCAATAGCTCTACAGTAGCTTCACAAAGTGCCAACCATACACATGGCACCACCTCACACAGGGAA ACGCAAAAGGCATACCTGCTGGCAGCGGGGGTCATTGTCTGTATCTATATAATCTGTGCTGTCATCCTGATCCTGGGCGTGCGGGAGCAG AGAGAACCCTATGAAGCCCAGCAGTCTGAGCCAATCGCCTACTTCCGGGGCCTACGGCTGGTCATGAGCCACGGCCCATACATCAAACTT ATTACTGGCTTCCTCTTCACCTCCTTGGCTTTCATGCTGGTGGAGGGGAACTTTGTCTTGTTTTGCACCTACACCTTGGGCTTCCGCAAT GAATTCCAGAATCTACTCCTGGCCATCATGCTCTCGGCCACTTTAACCATTCCCATCTGGCAGTGGTTCTTGACCCGGTTTGGCAAGAAG ACAGCTGTATATGTTGGGATCTCATCAGCAGTGCCATTTCTCATCTTGGTGGCCCTCATGGAGAGTAACCTCATCATTACATATGCGGTA GCTGTGGCAGCTGGCATCAGTGTGGCAGCTGCCTTCTTACTACCCTGGTCCATGCTGCCTGATGTCATTGACGACTTCCATCTGAAGCAG CCCCACTTCCATGGAACCGAGCCCATCTTCTTCTCCTTCTATGTCTTCTTCACCAAGTTTGCCTCTGGAGTGTCACTGGGCATTTCTACC CTCAGTCTGGACTTTGCAGGGTACCAGACCCGTGGCTGCTCGCAGCCGGAACGTGTCAAGTTTACACTGAACATGCTCGTGACCATGGCT CCCATAGTTCTCATCCTGCTGGGCCTGCTGCTCTTCAAAATGTACCCCATTGATGAGGAGAGGCGGCGGCAGAATAAGAAGGCCCTGCAG >In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40422759_+_1737nt ATGGCGGACGGAAAGGGAGACGCCGCCGCTGTCGCCGGGGCTGGGGCTGAGGCTCCGGCGGTAGCGGGAGCCGGAGATGGAGTCGAGACT GAGTCCATGGTTCGGGGTCATCGCCCCGTATCTCCAGCGCCGGGAGCCTCGGGACTGCGGCCGTGTCTGTGGCAGCTGGAGACAGAGCTG AGGGAGCAAGAGGTGTCGGAGGTCTCATCTTTGAACTACTGCCGGAGCTTCTGCCAGAAAGAACCGAAAAAGAAGAAACAACAGTTGTCT GTTTGCAACAAGCTTTGCTATGCACTTGGGGGAGCCCCCTACCAGGTGACGGGCTGTGCCCTGGGTTTCTTCCTTCAGATCTACCTATTG GATGTGGCTCAGGTGGGCCCTTTCTCTGCCTCCATCATCCTGTTTGTGGGCCGAGCCTGGGATGCCATCACAGACCCCCTGGTGGGCCTC TGCATCAGCAAATCCCCCTGGACCTGCCTGGGTCGCCTTATGCCCTGGATCATCTTCTCCACGCCCCTGGCCGTCATTGCCTACTTCCTC ATCTGGTTCGTGCCCGACTTCCCACACGGCCAGACCTATTGGTACCTGCTTTTCTATTGCCTCTTTGAAACAATGGTCACGTGTTTCCAT GTTCCCTACTCGGCTCTCACCATGTTCATCAGCACCGAGCAGACTGAGCGGGATTCTGCCACCGCCTATCGGATGACTGTGGAAGTGCTG GGCACAGTGCTGGGCACGGCGATCCAGGGACAAATCGTGGGCCAAGCAGACACGCCTTGTTTCCAGGACCTCAATAGCTCTACAGTAGCT TCACAAAGTGCCAACCATACACATGGCACCACCTCACACAGGGAAACGCAAAAGGCATACCTGCTGGCAGCGGGGGTCATTGTCTGTATC TATATAATCTGTGCTGTCATCCTGATCCTGGGCGTGCGGGAGCAGAGAGAACCCTATGAAGCCCAGCAGTCTGAGCCAATCGCCTACTTC CGGGGCCTACGGCTGGTCATGAGCCACGGCCCATACATCAAACTTATTACTGGCTTCCTCTTCACCTCCTTGGCTTTCATGCTGGTGGAG GGGAACTTTGTCTTGTTTTGCACCTACACCTTGGGCTTCCGCAATGAATTCCAGAATCTACTCCTGGCCATCATGCTCTCGGCCACTTTA ACCATTCCCATCTGGCAGTGGTTCTTGACCCGGTTTGGCAAGAAGACAGCTGTATATGTTGGGATCTCATCAGCAGTGCCATTTCTCATC TTGGTGGCCCTCATGGAGAGTAACCTCATCATTACATATGCGGTAGCTGTGGCAGCTGGCATCAGTGTGGCAGCTGCCTTCTTACTACCC TGGTCCATGCTGCCTGATGTCATTGACGACTTCCATCTGAAGCAGCCCCACTTCCATGGAACCGAGCCCATCTTCTTCTCCTTCTATGTC TTCTTCACCAAGTTTGCCTCTGGAGTGTCACTGGGCATTTCTACCCTCAGTCTGGACTTTGCAGGGTACCAGACCCGTGGCTGCTCGCAG CCGGAACGTGTCAAGTTTACACTGAACATGCTCGTGACCATGGCTCCCATAGTTCTCATCCTGCTGGGCCTGCTGCTCTTCAAAATGTAC CCCATTGATGAGGAGAGGCGGCGGCAGAATAAGAAGGCCCTGCAGGCACTGAGGGACGAGGCCAGCAGCTCTGGCTGCTCAGAAACAGAC |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40424373_+_2027nt GCCTACGCGCTGGTGGGCCGTGGGAAGATGGCGGACGGAAAGGGAGACGCCGCCGCTGTCGCCGGGGCTGGGGCTGAGGCTCCGGCGGTA GCGGGAGCCGGAGATGGAGTCGAGACTGAGTCCATGGTTCGGGGTCATCGCCCCGTATCTCCAGCGCCGGGAGCCTCGGGACTGCGGCCG TGTCTGTGGCAGCTGGAGACAGAGCTGAGGGAGCAAGAGGTGTCGGAGGTCTCATCTTTGAACTACTGCCGGAGCTTCTGCCAGGTGGGC CCTTTCTCTGCCTCCATCATCCTGTTTGTGGGCCGAGCCTGGGATGCCATCACAGACCCCCTGGTGGGCCTCTGCATCAGCAAATCCCCC TGGACCTGCCTGGGTCGCCTTATGCCCTGGATCATCTTCTCCACGCCCCTGGCCGTCATTGCCTACTTCCTCATCTGGTTCGTGCCCGAC TTCCCACACGGCCAGACCTATTGGTACCTGCTTTTCTATTGCCTCTTTGAAACAATGGTCACGTGTTTCCATGTTCCCTACTCGGCTCTC ACCATGTTCATCAGCACCGAGCAGACTGAGCGGGATTCTGCCACCGCCTATCGGATGACTGTGGAAGTGCTGGGCACAGTGCTGGGCACG GCGATCCAGGGACAAATCGTGGGCCAAGCAGACACGCCTTGTTTCCAGGACCTCAATAGCTCTACAGTAGCTTCACAAAGTGCCAACCAT ACACATGGCACCACCTCACACAGGGAAACGCAAAAGGCATACCTGCTGGCAGCGGGGGTCATTGTCTGTATCTATATAATCTGTGCTGTC ATCCTGATCCTGGGCGTGCGGGAGCAGAGAGAACCCTATGAAGCCCAGCAGTCTGAGCCAATCGCCTACTTCCGGGGCCTACGGCTGGTC ATGAGCCACGGCCCATACATCAAACTTATTACTGGCTTCCTCTTCACCTCCTTGGCTTTCATGCTGGTGGAGGGGAACTTTGTCTTGTTT TGCACCTACACCTTGGGCTTCCGCAATGAATTCCAGAATCTACTCCTGGCCATCATGCTCTCGGCCACTTTAACCATTCCCATCTGGCAG TGGTTCTTGACCCGGTTTGGCAAGAAGACAGCTGTATATGTTGGGATCTCATCAGCAGTGCCATTTCTCATCTTGGTGGCCCTCATGGAG AGTAACCTCATCATTACATATGCGGTAGCTGTGGCAGCTGGCATCAGTGTGGCAGCTGCCTTCTTACTACCCTGGTCCATGCTGCCTGAT GTCATTGACGACTTCCATCTGAAGCAGCCCCACTTCCATGGAACCGAGCCCATCTTCTTCTCCTTCTATGTCTTCTTCACCAAGTTTGCC TCTGGAGTGTCACTGGGCATTTCTACCCTCAGTCTGGACTTTGCAGGGTACCAGACCCGTGGCTGCTCGCAGCCGGAACGTGTCAAGTTT ACACTGAACATGCTCGTGACCATGGCTCCCATAGTTCTCATCCTGCTGGGCCTGCTGCTCTTCAAAATGTACCCCATTGATGAGGAGAGG CGGCGGCAGAATAAGAAGGCCCTGCAGGCACTGAGGGACGAGGCCAGCAGCTCTGGCTGCTCAGAAACAGACTCCACAGAGCTGGCTAGC ATCCTCTAGGGCCCGCCACGTTGCCCGAAGCCACCATGCAGAAGGCCACAGAAGGGATCAGGACCTGTCTGCCGGCTTGCTGAGCAGCTG GACTGCAGGTGCTAGGAAGGGAACTGAAGACTCAAGGAGGTGGCCCAGGACACTTGCTGTGCTCACTGTGGGGCCGGCTGCTCTGTGGCC TCCTGCCTCCCCTCTGCCTGCCTGTGGGGCCAAGCCCTGGGGCTGCCACTGTGAATATGCCAAGGACTGATCGGGCCTAGCCCGGAACAC TAATGTAGAAACCTTTTTTTTTACAGAGCCTAATTAATAACTTAATGACTGTGTACATAGCAATGTGTGTGTATGTATATGTCTGTGAGC >In-frame_RLF_ENST00000372771_chr1_40627308_+_MFSD2A_ENST00000372811_chr1_40422759_+_2162nt GCCTACGCGCTGGTGGGCCGTGGGAAGATGGCGGACGGAAAGGGAGACGCCGCCGCTGTCGCCGGGGCTGGGGCTGAGGCTCCGGCGGTA GCGGGAGCCGGAGATGGAGTCGAGACTGAGTCCATGGTTCGGGGTCATCGCCCCGTATCTCCAGCGCCGGGAGCCTCGGGACTGCGGCCG TGTCTGTGGCAGCTGGAGACAGAGCTGAGGGAGCAAGAGGTGTCGGAGGTCTCATCTTTGAACTACTGCCGGAGCTTCTGCCAGAAAGAA CCGAAAAAGAAGAAACAACAGTTGTCTGTTTGCAACAAGCTTTGCTATGCACTTGGGGGAGCCCCCTACCAGGTGACGGGCTGTGCCCTG GGTTTCTTCCTTCAGATCTACCTATTGGATGTGGCTCAGGTGGGCCCTTTCTCTGCCTCCATCATCCTGTTTGTGGGCCGAGCCTGGGAT GCCATCACAGACCCCCTGGTGGGCCTCTGCATCAGCAAATCCCCCTGGACCTGCCTGGGTCGCCTTATGCCCTGGATCATCTTCTCCACG CCCCTGGCCGTCATTGCCTACTTCCTCATCTGGTTCGTGCCCGACTTCCCACACGGCCAGACCTATTGGTACCTGCTTTTCTATTGCCTC TTTGAAACAATGGTCACGTGTTTCCATGTTCCCTACTCGGCTCTCACCATGTTCATCAGCACCGAGCAGACTGAGCGGGATTCTGCCACC GCCTATCGGATGACTGTGGAAGTGCTGGGCACAGTGCTGGGCACGGCGATCCAGGGACAAATCGTGGGCCAAGCAGACACGCCTTGTTTC CAGGACCTCAATAGCTCTACAGTAGCTTCACAAAGTGCCAACCATACACATGGCACCACCTCACACAGGGAAACGCAAAAGGCATACCTG CTGGCAGCGGGGGTCATTGTCTGTATCTATATAATCTGTGCTGTCATCCTGATCCTGGGCGTGCGGGAGCAGAGAGAACCCTATGAAGCC CAGCAGTCTGAGCCAATCGCCTACTTCCGGGGCCTACGGCTGGTCATGAGCCACGGCCCATACATCAAACTTATTACTGGCTTCCTCTTC ACCTCCTTGGCTTTCATGCTGGTGGAGGGGAACTTTGTCTTGTTTTGCACCTACACCTTGGGCTTCCGCAATGAATTCCAGAATCTACTC CTGGCCATCATGCTCTCGGCCACTTTAACCATTCCCATCTGGCAGTGGTTCTTGACCCGGTTTGGCAAGAAGACAGCTGTATATGTTGGG ATCTCATCAGCAGTGCCATTTCTCATCTTGGTGGCCCTCATGGAGAGTAACCTCATCATTACATATGCGGTAGCTGTGGCAGCTGGCATC AGTGTGGCAGCTGCCTTCTTACTACCCTGGTCCATGCTGCCTGATGTCATTGACGACTTCCATCTGAAGCAGCCCCACTTCCATGGAACC GAGCCCATCTTCTTCTCCTTCTATGTCTTCTTCACCAAGTTTGCCTCTGGAGTGTCACTGGGCATTTCTACCCTCAGTCTGGACTTTGCA GGGTACCAGACCCGTGGCTGCTCGCAGCCGGAACGTGTCAAGTTTACACTGAACATGCTCGTGACCATGGCTCCCATAGTTCTCATCCTG CTGGGCCTGCTGCTCTTCAAAATGTACCCCATTGATGAGGAGAGGCGGCGGCAGAATAAGAAGGCCCTGCAGGCACTGAGGGACGAGGCC AGCAGCTCTGGCTGCTCAGAAACAGACTCCACAGAGCTGGCTAGCATCCTCTAGGGCCCGCCACGTTGCCCGAAGCCACCATGCAGAAGG CCACAGAAGGGATCAGGACCTGTCTGCCGGCTTGCTGAGCAGCTGGACTGCAGGTGCTAGGAAGGGAACTGAAGACTCAAGGAGGTGGCC CAGGACACTTGCTGTGCTCACTGTGGGGCCGGCTGCTCTGTGGCCTCCTGCCTCCCCTCTGCCTGCCTGTGGGGCCAAGCCCTGGGGCTG CCACTGTGAATATGCCAAGGACTGATCGGGCCTAGCCCGGAACACTAATGTAGAAACCTTTTTTTTTACAGAGCCTAATTAATAACTTAA TGACTGTGTACATAGCAATGTGTGTGTATGTATATGTCTGTGAGCTATTAATGTTATTAATTTTCATAAAAGCTGGAAAGCAGCTGCCTG |
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FusionGenePPI for RLF_MFSD2A |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in . |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
RLF | CNKSR2, RIT1, RIT2, GCH1, ALB, PRPF40A, KRAS, HIST1H2BG, HIST1H3A, CLK1, TRIM11 | MFSD2A |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for RLF_MFSD2A |
Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for RLF_MFSD2A |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | MFSD2A | C0025958 | Microcephaly | 2 | CTD_human |
Tgene | MFSD2A | C4225310 | MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE | 2 | UNIPROT |
Tgene | MFSD2A | C0037822 | Speech Disorders | 1 | CTD_human |
Tgene | MFSD2A | C3714756 | Intellectual Disability | 1 | CTD_human |