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Fusion gene ID: 39861 |
FusionGeneSummary for TSPAN5_PKD2 |
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Fusion gene information | Fusion gene name: TSPAN5_PKD2 | Fusion gene ID: 39861 | Hgene | Tgene | Gene symbol | TSPAN5 | PKD2 | Gene ID | 10098 | 25865 |
Gene name | tetraspanin 5 | protein kinase D2 | |
Synonyms | NET-4|NET4|TM4SF9|TSPAN-5 | HSPC187|PKD2|nPKC-D2 | |
Cytomap | 4q23 | 19q13.32 | |
Type of gene | protein-coding | protein-coding | |
Description | tetraspanin-5tetraspan NET-4tetraspan TM4SFtransmembrane 4 superfamily member 9transmembrane 4 superfamily, member 8 | serine/threonine-protein kinase D2 | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | P62079 | Q13563 | |
Ensembl transtripts involved in fusion gene | ENST00000305798, ENST00000505184, ENST00000509168, | ENST00000237596, ENST00000508588, ENST00000511337, ENST00000502363, | |
Fusion gene scores | * DoF score | 4 X 2 X 4=32 | 2 X 2 X 2=8 |
# samples | 4 | 2 | |
** MAII score | log2(4/32*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(2/8*10)=1.32192809488736 | |
Context | PubMed: TSPAN5 [Title/Abstract] AND PKD2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | PKD2 | GO:0006468 | protein phosphorylation | 22228765 |
Tgene | PKD2 | GO:0018105 | peptidyl-serine phosphorylation | 18440775 |
Tgene | PKD2 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 17077180 |
Tgene | PKD2 | GO:0046777 | protein autophosphorylation | 17077180 |
Tgene | PKD2 | GO:0050852 | T cell receptor signaling pathway | 17077180 |
![]() (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 | BRCA | TCGA-E9-A243-01A | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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 | ENST00000305798 | ENST00000237596 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
5CDS-5UTR | ENST00000305798 | ENST00000508588 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
5CDS-intron | ENST00000305798 | ENST00000511337 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
5CDS-intron | ENST00000305798 | ENST00000502363 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-3CDS | ENST00000505184 | ENST00000237596 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-5UTR | ENST00000505184 | ENST00000508588 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-intron | ENST00000505184 | ENST00000511337 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-intron | ENST00000505184 | ENST00000502363 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-3CDS | ENST00000509168 | ENST00000237596 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-5UTR | ENST00000509168 | ENST00000508588 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-intron | ENST00000509168 | ENST00000511337 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
intron-intron | ENST00000509168 | ENST00000502363 | TSPAN5 | chr4 | 99579297 | - | PKD2 | chr4 | 88973143 | + |
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FusionProtFeatures for TSPAN5_PKD2 |
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Hgene | Tgene |
TSPAN5 | PKD2 |
Regulates ADAM10 maturation and trafficking to the cellsurface. Promotes ADAM10-mediated cleavage of CD44.{ECO:0000269|PubMed:26686862}. | Functions as a cation channel involved in fluid-flowmechanosensation by the primary cilium in renal epithelium(PubMed:18695040). Functions as outward-rectifying K(+) channel,but is also permeable to Ca(2+), and to a much lesser degree alsoto Na(+) (PubMed:11854751, PubMed:15692563, PubMed:27071085,PubMed:27991905). May contribute to the release of Ca(2+) storesfrom the endoplasmic reticulum (PubMed:11854751, PubMed:20881056).Together with TRPV4, forms mechano- and thermosensitive channelsin cilium (PubMed:18695040). PKD1 and PKD2 may function through acommon signaling pathway that is necessary to maintain the normal,differentiated state of renal tubule cells. Acts as a regulator ofcilium length, together with PKD1. The dynamic control of ciliumlength is essential in the regulation of mechanotransductivesignaling. The cilium length response creates a negative feedbackloop whereby fluid shear-mediated deflection of the primarycilium, which decreases intracellular cAMP, leads to ciliumshortening and thus decreases flow-induced signaling. Alsoinvolved in left-right axis specification via its role in sensingnodal flow; forms a complex with PKD1L1 in cilia to facilitateflow detection in left-right patterning. Detection of asymmetricnodal flow gives rise to a Ca(2+) signal that is required fornormal, asymmetric expression of genes involved in thespecification of body left-right laterality (By similarity).{ECO:0000250|UniProtKB:O35245, ECO:0000269|PubMed:11854751,ECO:0000269|PubMed:15692563, ECO:0000269|PubMed:16551655,ECO:0000269|PubMed:18695040, ECO:0000269|PubMed:20881056,ECO:0000269|PubMed:27991905, ECO:0000305}. |
![]() * 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 |
Hgene | TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 1_17 | 27 | 269 | Topological domain | Cytoplasmic |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 763_774 | 516 | 969 | Calcium binding | Ontology_term=ECO:0000244,ECO:0000255,ECO:0000269,ECO:0000269 |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 833_872 | 516 | 969 | Coiled coil | Ontology_term=ECO:0000269,ECO:0000305 |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 750_785 | 516 | 969 | Domain | EF-hand |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 632_646 | 516 | 969 | Intramembrane | Pore-forming |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 641_643 | 516 | 969 | Motif | Selectivity filter |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 803_822 | 516 | 969 | Region | Linker |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 527_552 | 516 | 969 | Topological domain | Extracellular |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 574_597 | 516 | 969 | Topological domain | Cytoplasmic |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 620_631 | 516 | 969 | Topological domain | Extracellular |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 647_654 | 516 | 969 | Topological domain | Extracellular |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 676_968 | 516 | 969 | Topological domain | Cytoplasmic |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 553_573 | 516 | 969 | Transmembrane | Helical%3B Name%3DS4 |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 598_619 | 516 | 969 | Transmembrane | Helical%3B Name%3D5 |
Tgene | >PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 655_675 | 516 | 969 | Transmembrane | Helical%3B Name%3DS6 |
- 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 | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 114_232 | 27 | 269 | Topological domain | Extracellular |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 254_268 | 27 | 269 | Topological domain | Cytoplasmic |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 39_61 | 27 | 269 | Topological domain | Extracellular |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 83_92 | 27 | 269 | Topological domain | Cytoplasmic |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 18_38 | 27 | 269 | Transmembrane | Helical |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 233_253 | 27 | 269 | Transmembrane | Helical |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 62_82 | 27 | 269 | Transmembrane | Helical |
Hgene | >TSPAN5 | chr4:99579297 | chr4:88973143 | ENST00000305798 | - | 1 | 8 | 93_113 | 27 | 269 | Transmembrane | Helical |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 153_157 | 516 | 969 | Compositional bias | Note=Poly-Arg |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 95_107 | 516 | 969 | Compositional bias | Note=Poly-Glu |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 1_219 | 516 | 969 | Topological domain | Cytoplasmic |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 242_468 | 516 | 969 | Topological domain | Extracellular |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 490_505 | 516 | 969 | Topological domain | Cytoplasmic |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 220_241 | 516 | 969 | Transmembrane | Helical%3B Name%3DS1 |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 469_489 | 516 | 969 | Transmembrane | Helical%3B Name%3DS2 |
Tgene | PKD2 | chr4:99579297 | chr4:88973143 | ENST00000237596 | + | 5 | 15 | 506_526 | 516 | 969 | Transmembrane | Helical%3B Name%3DS3 |
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FusionGeneSequence for TSPAN5_PKD2 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_TSPAN5_ENST00000305798_chr4_99579297_-_PKD2_ENST00000237596_chr4_88973143_+_480aa MSGKHYKGPEVSCCIKYFIFGFNVIFWLSVVAIGINIYRTSNVEVLLQFLEDQNTFPNFEHLAYWQIQFNNIAAVTVFFVWIKLFKFINF NRTMSQLSTTMSRCAKDLFGFAIMFFIIFLAYAQLAYLVFGTQVDDFSTFQECIFTQFRIILGDINFAEIEEANRVLGPIYFTTFVFFMF FILLNMFLAIINDTYSEVKSDLAQQKAEMELSDLIRKGYHKALVKLKLKKNTVDDISESLRQGGGKLNFDELRQDLKGKGHTDAEIEAIF TKYDQDGDQELTEHEHQQMRDDLEKEREDLDLDHSSLPRPMSSRSFPRSLDDSEEDDDEDSGHSSRRRGSISSGVSYEEFQVLVRRVDRM EHSIGSIVSKIDAVIVKLEIMERAKLKRREVLGRLLDGVAEDERLGRDSEIHREQMERLVREELERWESDDAASQISHGLGTPVGLNGQP |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_TSPAN5_ENST00000305798_chr4_99579297_-_PKD2_ENST00000237596_chr4_88973143_+_1440nt ATGTCCGGGAAGCACTACAAGGGTCCTGAAGTCAGTTGTTGCATCAAATACTTCATATTTGGCTTCAATGTCATATTTTGGCTGTCAGTG GTAGCTATAGGAATTAACATATACAGAACATCAAATGTGGAGGTGCTACTACAGTTTCTGGAAGATCAAAATACTTTCCCCAACTTTGAG CATCTGGCATATTGGCAGATACAGTTCAACAATATAGCTGCTGTCACAGTATTTTTTGTCTGGATTAAGCTCTTCAAATTCATCAATTTT AACAGGACCATGAGCCAGCTCTCGACAACCATGTCTCGATGTGCCAAAGACCTGTTTGGCTTTGCTATTATGTTCTTCATTATTTTCCTA GCGTATGCTCAGTTGGCATACCTTGTCTTTGGCACTCAGGTCGATGACTTCAGTACTTTCCAAGAGTGTATCTTCACTCAATTCCGTATC ATTTTGGGCGATATCAACTTTGCAGAGATTGAGGAAGCTAATCGAGTTTTGGGACCAATTTATTTCACTACATTTGTGTTCTTTATGTTC TTCATTCTTTTGAATATGTTTTTGGCTATCATCAATGATACTTACTCTGAAGTGAAATCTGACTTGGCACAGCAGAAAGCTGAAATGGAA CTCTCAGATCTTATCAGAAAGGGCTACCATAAAGCTTTGGTCAAACTAAAACTGAAAAAAAATACCGTGGATGACATTTCAGAGAGTCTG CGGCAAGGAGGAGGCAAGTTAAACTTTGACGAACTTCGACAAGATCTCAAAGGGAAGGGCCATACTGATGCAGAGATTGAGGCAATATTC ACAAAGTACGACCAAGATGGAGACCAAGAACTGACCGAACATGAACATCAGCAGATGAGAGACGACTTGGAGAAAGAGAGGGAGGACCTG GATTTGGATCACAGTTCTTTACCACGTCCCATGAGCAGCCGAAGTTTCCCTCGAAGCCTGGATGACTCTGAGGAGGATGACGATGAAGAT AGCGGACATAGCTCCAGAAGGAGGGGAAGCATTTCTAGTGGCGTTTCTTACGAAGAGTTTCAAGTCCTGGTGAGACGAGTGGACCGGATG GAGCATTCCATCGGCAGCATAGTGTCCAAGATTGACGCCGTGATCGTGAAGCTAGAGATTATGGAGCGAGCCAAACTGAAGAGGAGGGAG GTGCTGGGAAGGCTGTTGGATGGGGTGGCCGAGGATGAAAGGCTGGGTCGTGACAGTGAAATCCATAGGGAACAGATGGAACGGCTAGTA CGTGAAGAGTTGGAACGCTGGGAATCCGATGATGCAGCTTCCCAGATCAGTCATGGTTTAGGCACGCCAGTGGGACTAAATGGTCAACCT CGCCCCAGAAGCTCCCGCCCATCTTCCTCCCAATCTACAGAAGGCATGGAAGGTGCAGGTGGAAATGGGAGTTCTAATGTCCACGTATGA |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_TSPAN5_ENST00000305798_chr4_99579297_-_PKD2_ENST00000237596_chr4_88973143_+_3926nt GCGAACGGGCGGGCGAGCAAGCGAGCGGCGTCTCCACCAGCATCTGCCGCGGCCGCCTTTGCCCGAAGCCCGGGGACGAACCGACGGACC GACCGCCTGGCGCACGGACGCGGGCGCTCGCTTTGTGTTCGGGGCTAGCGTCGGCGAGGCTTGAGCTTGCAGCGCGCGGCTTCCCTGCTT TCTCGCGGCCACCCCGGCTCCGGCGGCCTCGGCGCGCGAGGGGCTGGAGGTGCGGGAGCCGCTCTCCGCCGGTCGGTCCCCGCGCGGCTG AGCCCAGGCCGCCAGCGCCGCGGCCCCGTGCGGTGTCCCTGAGCTCCTGCTCCCCGCCGGGCTGCTCCGAGCAACGGTGCTTCGGAGCTC CAAACTCGGGCTGCCGGGGCAAGTGTCTTCATGAACCCAGAGGATGTCCGGGAAGCACTACAAGGGTCCTGAAGTCAGTTGTTGCATCAA ATACTTCATATTTGGCTTCAATGTCATATTTTGGCTGTCAGTGGTAGCTATAGGAATTAACATATACAGAACATCAAATGTGGAGGTGCT ACTACAGTTTCTGGAAGATCAAAATACTTTCCCCAACTTTGAGCATCTGGCATATTGGCAGATACAGTTCAACAATATAGCTGCTGTCAC AGTATTTTTTGTCTGGATTAAGCTCTTCAAATTCATCAATTTTAACAGGACCATGAGCCAGCTCTCGACAACCATGTCTCGATGTGCCAA AGACCTGTTTGGCTTTGCTATTATGTTCTTCATTATTTTCCTAGCGTATGCTCAGTTGGCATACCTTGTCTTTGGCACTCAGGTCGATGA CTTCAGTACTTTCCAAGAGTGTATCTTCACTCAATTCCGTATCATTTTGGGCGATATCAACTTTGCAGAGATTGAGGAAGCTAATCGAGT TTTGGGACCAATTTATTTCACTACATTTGTGTTCTTTATGTTCTTCATTCTTTTGAATATGTTTTTGGCTATCATCAATGATACTTACTC TGAAGTGAAATCTGACTTGGCACAGCAGAAAGCTGAAATGGAACTCTCAGATCTTATCAGAAAGGGCTACCATAAAGCTTTGGTCAAACT AAAACTGAAAAAAAATACCGTGGATGACATTTCAGAGAGTCTGCGGCAAGGAGGAGGCAAGTTAAACTTTGACGAACTTCGACAAGATCT CAAAGGGAAGGGCCATACTGATGCAGAGATTGAGGCAATATTCACAAAGTACGACCAAGATGGAGACCAAGAACTGACCGAACATGAACA TCAGCAGATGAGAGACGACTTGGAGAAAGAGAGGGAGGACCTGGATTTGGATCACAGTTCTTTACCACGTCCCATGAGCAGCCGAAGTTT CCCTCGAAGCCTGGATGACTCTGAGGAGGATGACGATGAAGATAGCGGACATAGCTCCAGAAGGAGGGGAAGCATTTCTAGTGGCGTTTC TTACGAAGAGTTTCAAGTCCTGGTGAGACGAGTGGACCGGATGGAGCATTCCATCGGCAGCATAGTGTCCAAGATTGACGCCGTGATCGT GAAGCTAGAGATTATGGAGCGAGCCAAACTGAAGAGGAGGGAGGTGCTGGGAAGGCTGTTGGATGGGGTGGCCGAGGATGAAAGGCTGGG TCGTGACAGTGAAATCCATAGGGAACAGATGGAACGGCTAGTACGTGAAGAGTTGGAACGCTGGGAATCCGATGATGCAGCTTCCCAGAT CAGTCATGGTTTAGGCACGCCAGTGGGACTAAATGGTCAACCTCGCCCCAGAAGCTCCCGCCCATCTTCCTCCCAATCTACAGAAGGCAT GGAAGGTGCAGGTGGAAATGGGAGTTCTAATGTCCACGTATGATATGTGTGTTTCAGTATGTGTGTTTCTAATAAGTGAGGAAGTGGCTG TCCTGAATTGCTGTAACAAGCACACTATTTATATGCCCTGACCACCATAGGATGCTAGTCTTTGTGACCGATTGCTAATCTTCTGCACTT TAATTTATTTTATATAAACTTTACCCATGGTTCAAAGATTTTTTTTTCTTTTTCTCATATAAGAAATCTAGGTGTAAATATTGAGTACAG AAAAAAAATCTTCATGATGTGTATTGAGCGGTACGCCCAGTTGCCACCATGACTGAGTCTTCTCAGTTGACAATGAAGTAGCCTTTTAAA GCTAGAAAACTGTCAAAGGGCTTCTGAGTTTCATTTCCAGTCACAAAAATCAGTATTGTTATTTTTTTCCAAGAGTGTGAAGGAAAATGG GGCATTCCTTTCCACTCTGGCATAGTTCATGAGCTTAATACATAGCTTTCTTTTAAGAAAGGAGCCTTTTTTTTCAACTAGCTTCCTGGG GTAAACTTTTCTAAAAGATAAAATGGAAAGGAACTCCAAACTATGATAGAATCTGTGTGAATGGTTAAGATGAATGTTAAATACTATGCT TTTTTGTAAGTTGATCGTATCTGATGTCTGTGGGACTAACTGTATCACTTAATTTTTACCTTATTTTGGCTCTAATTTGAATAAGCTGAG TAAAACCACCAAAGATCAGTTATAGGATAAAATGGCATCTCTAACCATAACACAGGAGAATTGGAAGGAGCCCTAAGTTGTCACTCAGTT TAATTTCTTTTAATGGTTAGTTTAGCCTAAAGATTTATCTGCATATTCTTTTTCCCATGTGGCTCTACTCATTTGCAACTGAATTTAATG TTATAACTCATCTAGTGAGACCAACTTACTAAATTTTTAGTATGCACTGAAAGTTTTTATCCAACAATTATGTTCATTTTAAGCAAAATT TTAAGAAAGTTTTGAAATTCATAAAGCATTTGGTTTTAAACTATTTTAAGAATATAGTACTCGGTCAGGTATGACGGCTCACGCCTGTAA TCCCAGCACTTTGGGAGGCCGAAACAGGCGAATCACTTGAGCCCAGGAGTTCAAGACCAACATGGGCAATGTGGCGAAACTCCATCTCTA CAAAAAATGCAAAAATAAAAAATATAGTACTCAAGTATTCTTGATCCTGTGTTTCAAAACTAGAATTTGTAATGCAAATGGAGCTCAGTC TAATAAAAAAGAGGTTTTGGTATTAAAAGTTCATACATTAGACAGTATCAGCCAAAATTTGAGTTAGCAACACTGTTTTCTTTACGAGAG GGTCTCACCCAAATTTATGGGGAGAAATCTATTTCTCAAAAAAAAAAATCTTCTTTTACAGAAATGTTGAGTAAGGTGACATTTTGAGCG CTAATAAGCAAAAGAGCATGCAGTGCTGTTGAATAACCCTCACTTGGAGAACCAAGAGAATCCTGTCGTTTAATGCTATATTTTAATTTC ACAAGTTGTTCATTTAACTGGTAGAATGTCAGTCCAATCTCCAATGAGAACATGAGCAAATAGACCTTTCCAGGTTGAAAGTGAAACATA CTGGGTTTCTGTAAGTTTTTCCTCATGGCTTCATCTCTATCTTTACTTTCTCTTGAATATGCTACACAAAGTTCTTTATTACTACATACT AAAGTTTGCATTCCAGGGATATTGACTGTACATATTTATGTATATGTACCATGTTGTTACATGTAAACAAACTTCAATTTGAAGTGCAGC TATTATGTGGTATCCATGTGTATCGACCATGTGCCATATATCAATTATGGTCACTAGAAAGTCTCTTTATGATACTTTTTATTGTACTGT TTTTCATTTCACTTGCAAAATTTTGCAGAATTCCTCCTTTCTACCCATAAATTACATATATTTTTCTTCTTTAGTCATGGAGAACTCCCC CCCTCATCTCTTCCCTATTATCTTTCCCTGTGTACTGGTATTATTAAAAAGACATTACATACGCAAGTCTTTCTCGACAATCAAGAATGT |
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FusionGenePPI for TSPAN5_PKD2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
TSPAN5 | APP, ADAM10, TMEM248, VKORC1L1, TMEM87A, ALG8, GDPD1, THAP11, AGPAT4, AGPAT3, SLC27A2, SPCS2, KLHL2, TMEM186, SOAT1, ATP2B3, RDH11, RFT1, GHDC, SLC7A2, TMUB1, SEC62, EFNB1, BSCL2, SC5D, GPR89A, LCLAT1, CD47, SNX25, ZDHHC9, LEMD2, ZDHHC6, IMMP1L, ALG11, NAT8L, TMEM192, RDH12, TMEM43, TMEM206, FTSJ2, NDC1, DAGLB, PSEN2, DNAJC19, TVP23C, WDR41, RDH14, B4GALT1, RER1, FAM210B, FAM134C, SPCS1, PIEZO1, SCAMP2, PRAF2, CYB5R3, NAT14, GP1BB, BRI3BP, ZDHHC21, SLC38A2, FAM213A, TRIM25 | PKD2 | PKD1, PKD2, TRPC1, TNNI3, CANX, GOLGA2, ATP1A1, MAGEA8, PLSCR1, KRT40, KRTAP10-8, KRTAP10-3, FAM3D, CEP170, ALG5, GLRA2, BCAS4, PICK1, SRPR, TMEM248, PKD2L2, PTGIR, CRYL1, CHRND, EXOC3, TPTE2, TMPRSS12, COG6, CNGA3, CD300E, GCC2, LMNA |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for TSPAN5_PKD2 |
![]() (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 TSPAN5_PKD2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | PKD2 | C2751306 | Polycystic kidney disease, type 2 | 6 | UNIPROT |
Tgene | PKD2 | C0085413 | Polycystic Kidney, Autosomal Dominant | 4 | CTD_human |
Tgene | PKD2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Tgene | PKD2 | C0035309 | Retinal Diseases | 1 | CTD_human |
Tgene | PKD2 | C0042373 | Vascular Diseases | 1 | CTD_human |
Tgene | PKD2 | C0524851 | Neurodegenerative Disorders | 1 | CTD_human |