![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 29296 |
FusionGeneSummary for PTEN_KCNMB4 |
![]() |
Fusion gene information | Fusion gene name: PTEN_KCNMB4 | Fusion gene ID: 29296 | Hgene | Tgene | Gene symbol | PTEN | KCNMB4 | Gene ID | 5728 | 27345 |
Gene name | phosphatase and tensin homolog | potassium calcium-activated channel subfamily M regulatory beta subunit 4 | |
Synonyms | 10q23del|BZS|CWS1|DEC|GLM2|MHAM|MMAC1|PTEN1|PTENbeta|TEP1 | - | |
Cytomap | 10q23.31 | 12q15 | |
Type of gene | protein-coding | protein-coding | |
Description | phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTENMMAC1 phosphatase and tensin homolog deleted on chromosome 10mitochondrial PTENalphamitochondrial phosphatase and tensin protein alphamutated in multip | calcium-activated potassium channel subunit beta-4BK channel beta subunit 4BK channel subunit beta-4BKbeta4MaxiK channel beta-subunit 4big potassium channel beta subunit 4calcium-activated potassium channel, subfamily M subunit beta-4charybdotoxin | |
Modification date | 20180527 | 20180523 | |
UniProtAcc | P60484 | Q86W47 | |
Ensembl transtripts involved in fusion gene | ENST00000371953, ENST00000472832, | ENST00000258111, | |
Fusion gene scores | * DoF score | 16 X 8 X 9=1152 | 10 X 4 X 6=240 |
# samples | 15 | 10 | |
** MAII score | log2(15/1152*10)=-2.94110631094643 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(10/240*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: PTEN [Title/Abstract] AND KCNMB4 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | Oncogene involved fusion gene, in-frame and retained their domain. Tumor suppressor 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) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | PTEN | GO:0001933 | negative regulation of protein phosphorylation | 20123964 |
Hgene | PTEN | GO:0006470 | protein dephosphorylation | 9256433 |
Hgene | PTEN | GO:0008285 | negative regulation of cell proliferation | 19057511 |
Hgene | PTEN | GO:0031658 | negative regulation of cyclin-dependent protein serine/threonine kinase activity involved in G1/S transition of mitotic cell cycle | 21241890 |
Hgene | PTEN | GO:0046855 | inositol phosphate dephosphorylation | 9593664 |
Hgene | PTEN | GO:0046856 | phosphatidylinositol dephosphorylation | 9593664|9811831 |
Hgene | PTEN | GO:0050821 | protein stabilization | 20123964 |
Hgene | PTEN | GO:0060070 | canonical Wnt signaling pathway | 20123964 |
Hgene | PTEN | GO:1904668 | positive regulation of ubiquitin protein ligase activity | 21241890 |
Hgene | PTEN | GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 21241890 |
Hgene | PTEN | GO:2000134 | negative regulation of G1/S transition of mitotic cell cycle | 21241890 |
Tgene | KCNMB4 | GO:0001508 | action potential | 10692449 |
Tgene | KCNMB4 | GO:0005513 | detection of calcium ion | 10692449 |
Tgene | KCNMB4 | GO:0006813 | potassium ion transport | 10692449 |
Tgene | KCNMB4 | GO:0019228 | neuronal action potential | 10692449 |
![]() (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 | LD | PRAD | TCGA-J4-A83I-01A | PTEN | chr10 | 89720875 | + | KCNMB4 | chr12 | 70793989 | + |
* 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 | ENST00000371953 | ENST00000258111 | PTEN | chr10 | 89720875 | + | KCNMB4 | chr12 | 70793989 | + |
3UTR-3CDS | ENST00000472832 | ENST00000258111 | PTEN | chr10 | 89720875 | + | KCNMB4 | chr12 | 70793989 | + |
Top |
FusionProtFeatures for PTEN_KCNMB4 |
![]() |
Hgene | Tgene |
PTEN | KCNMB4 |
Tumor suppressor. Acts as a dual-specificity proteinphosphatase, dephosphorylating tyrosine-, serine- and threonine-phosphorylated proteins. Also acts as a lipid phosphatase,removing the phosphate in the D3 position of the inositol ringfrom phosphatidylinositol 3,4,5-trisphosphate,phosphatidylinositol 3,4-diphosphate, phosphatidylinositol 3-phosphate and inositol 1,3,4,5-tetrakisphosphate with order ofsubstrate preference in vitro PtdIns(3,4,5)P3 > PtdIns(3,4)P2 >PtdIns3P > Ins(1,3,4,5)P4 (PubMed:26504226). The lipid phosphataseactivity is critical for its tumor suppressor function.Antagonizes the PI3K-AKT/PKB signaling pathway bydephosphorylating phosphoinositides and thereby modulating cellcycle progression and cell survival. The unphosphorylated formcooperates with AIP1 to suppress AKT1 activation. Dephosphorylatestyrosine-phosphorylated focal adhesion kinase and inhibits cellmigration and integrin-mediated cell spreading and focal adhesionformation. Plays a role as a key modulator of the AKT-mTORsignaling pathway controlling the tempo of the process of newbornneurons integration during adult neurogenesis, including correctneuron positioning, dendritic development and synapse formation.May be a negative regulator of insulin signaling and glucosemetabolism in adipose tissue. The nuclear monoubiquitinated formpossesses greater apoptotic potential, whereas the cytoplasmicnonubiquitinated form induces less tumor suppressive ability. Inmotile cells, suppresses the formation of lateral pseudopods andthereby promotes cell polarization and directed movement.{ECO:0000269|PubMed:26504226}. Isoform alpha: Functional kinase, like isoform 1 itantagonizes the PI3K-AKT/PKB signaling pathway. Plays a role inmitochondrial energetic metabolism by promoting COX activity andATP production, via collaboration with isoform 1 in increasingprotein levels of PINK1. | Regulatory subunit of the calcium activated potassiumKCNMA1 (maxiK) channel. Modulates the calcium sensitivity andgating kinetics of KCNMA1, thereby contributing to KCNMA1 channeldiversity. Decreases the gating kinetics and calcium sensitivityof the KCNMA1 channel, but with fast deactivation kinetics. Maydecrease KCNMA1 channel openings at low calcium concentrations butincreases channel openings at high calcium concentrations. MakesKCNMA1 channel resistant to 100 nM charybdotoxin (CTX) toxinconcentrations. {ECO:0000269|PubMed:10692449,ECO:0000269|PubMed:10792058, ECO:0000269|PubMed:10828459}. |
![]() * 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 | PTEN | chr10:89720875 | chr12:70793989 | ENST00000371953 | + | 8 | 9 | 14_185 | 342 | 404 | Domain | Phosphatase tensin-type |
Tgene | >KCNMB4 | chr10:89720875 | chr12:70793989 | ENST00000258111 | + | 0 | 3 | 189_210 | 112 | 211 | Topological domain | Cytoplasmic |
Tgene | >KCNMB4 | chr10:89720875 | chr12:70793989 | ENST00000258111 | + | 0 | 3 | 168_188 | 112 | 211 | Transmembrane | Helical%3B Name%3D2 |
- 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 | >PTEN | chr10:89720875 | chr12:70793989 | ENST00000371953 | + | 8 | 9 | 190_350 | 342 | 404 | Domain | C2 tensin-type |
Hgene | >PTEN | chr10:89720875 | chr12:70793989 | ENST00000371953 | + | 8 | 9 | 401_403 | 342 | 404 | Region | Note=PDZ domain-binding |
Tgene | KCNMB4 | chr10:89720875 | chr12:70793989 | ENST00000258111 | + | 0 | 3 | 1_19 | 112 | 211 | Topological domain | Cytoplasmic |
Tgene | KCNMB4 | chr10:89720875 | chr12:70793989 | ENST00000258111 | + | 0 | 3 | 41_167 | 112 | 211 | Topological domain | Extracellular |
Tgene | KCNMB4 | chr10:89720875 | chr12:70793989 | ENST00000258111 | + | 0 | 3 | 20_40 | 112 | 211 | Transmembrane | Helical%3B Name%3D1 |
Top |
FusionGeneSequence for PTEN_KCNMB4 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_PTEN_ENST00000371953_chr10_89720875_+_KCNMB4_ENST00000258111_chr12_70793989_+_441aa MTAIIKEIVSRNKRRYQEDGFDLDLTYIYPNIIAMGFPAERLEGVYRNNIDDVVRFLDSKHKNHYKIYNLCAERHYDTAKFNCRVAQYPF EDHNPPQLELIKPFCEDLDQWLSEDDNHVAAIHCKAGKGRTGVMICAYLLHRGKFLKAQEALDFYGEVRTRDKKGVTIPSQRRYVYYYSY LLKNHLDYRPVALLFHKMMFETIPMFSGGTCNPQFVVCQLKVKIYSSNSGPTRREDKFMYFEFPQPLPVCGDIKVEFFHKQNKMLKKDKM FHFWVNTFFIPGPEETSEKVENGSLCDQEIDSICSIERADNDKEYLVLTLTKNDLDKANKDKANRYFSPNFKCSYIPPCKRENQKNLESV |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_PTEN_ENST00000371953_chr10_89720875_+_KCNMB4_ENST00000258111_chr12_70793989_+_1323nt ATGACAGCCATCATCAAAGAGATCGTTAGCAGAAACAAAAGGAGATATCAAGAGGATGGATTCGACTTAGACTTGACCTATATTTATCCA AACATTATTGCTATGGGATTTCCTGCAGAAAGACTTGAAGGCGTATACAGGAACAATATTGATGATGTAGTAAGGTTTTTGGATTCAAAG CATAAAAACCATTACAAGATATACAATCTTTGTGCTGAAAGACATTATGACACCGCCAAATTTAATTGCAGAGTTGCACAATATCCTTTT GAAGACCATAACCCACCACAGCTAGAACTTATCAAACCCTTTTGTGAAGATCTTGACCAATGGCTAAGTGAAGATGACAATCATGTTGCA GCAATTCACTGTAAAGCTGGAAAGGGACGAACTGGTGTAATGATATGTGCATATTTATTACATCGGGGCAAATTTTTAAAGGCACAAGAG GCCCTAGATTTCTATGGGGAAGTAAGGACCAGAGACAAAAAGGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTATTATAGCTAC CTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACT TGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAGGTGAAGATATATTCCTCCAATTCAGGACCCACACGACGGGAAGACAAGTTCATGTAC TTTGAGTTCCCTCAGCCGTTACCTGTGTGTGGTGATATCAAAGTAGAGTTCTTCCACAAACAGAACAAGATGCTAAAAAAGGACAAAATG TTTCACTTTTGGGTAAATACATTCTTCATACCAGGACCAGAGGAAACCTCAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATC GATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAA GACAAAGCCAACCGATACTTTTCTCCAAATTTTAAGTGCTCCTATATCCCTCCCTGTAAGAGAGAAAATCAGAAGAATTTGGAAAGTGTC ATGAATTGGCAACAGTACTGGAAAGATGAGATTGGTTCCCAGCCATTTACTTGCTATTTTAATCAACATCAAAGACCAGATGATGTGCTT CTGCATCGCACTCATGATGAGATTGTCCTCCTGCATTGCTTCCTCTGGCCCCTGGTGACATTTGTGGTGGGCGTTCTCATTGTGGTCCTG |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_PTEN_ENST00000371953_chr10_89720875_+_KCNMB4_ENST00000258111_chr12_70793989_+_6319nt GGTAACCTCAGACTCGAGTCAGTGACACTGCTCAACGCACCCATCTCAGCTTTCATCATCAGTCCTCCACCCCCGCCCCACAACAGCCTA CCCTGCCTCCGGCTGGGTTTCTGGGCAGAGGCCGAGGCTTAGCTCGTTATCCTCGCCTCGCGTTGCTGCAAAAGCCGCAGCAAGTGCAGC TGCAGGCTGGCGGCTGGGAACCGGCCCGAGCAAGCCCCAGGCAGCTACACTGGGCATGCTCAGTAGAGCCTGCGGCTTGGGGACTCTGCG CTCGCACCCAGAGCTACCGCTCTGCCCCCTCCTACCGCCCCCTGCCCTGCCCTGCCCTCCCCTCGCCCGGCGCGGTCCCGTCCGCCTCTC GCTCGCCTCCCGCCTCCCCTCGGTCTTCCGAGGCGCCCGGGCTCCCGGCGCGGCGGCGGAGGGGGCGGGCAGGCCGGCGGGCGGTGATGT GGCGGGACTCTTTATGCGCTGCGGCAGGATACGCGCTCGGCGCTGGGACGCGACTGCGCTCAGTTCTCTCCTCTCGGAAGCTGCAGCCAT GATGGAAGTTTGAGAGTTGAGCCGCTGTGAGGCGAGGCCGGGCTCAGGCGAGGGAGATGAGAGACGGCGGCGGCCGCGGCCCGGAGCCCC TCTCAGCGCCTGTGAGCAGCCGCGGGGGCAGCGCCCTCGGGGAGCCGGCCGGCCTGCGGCGGCGGCAGCGGCGGCGTTTCTCGCCTCCTC TTCGTCTTTTCTAACCGTGCAGCCTCTTCCTCGGCTTCTCCTGAAAGGGAAGGTGGAAGCCGTGGGCTCGGGCGGGAGCCGGCTGAGGCG CGGCGGCGGCGGCGGCACCTCCCGCTCCTGGAGCGGGGGGGAGAAGCGGCGGCGGCGGCGGCCGCGGCGGCTGCAGCTCCAGGGAGGGGG TCTGAGTCGCCTGTCACCATTTCCAGGGCTGGGAACGCCGGAGAGTTGGTCTCTCCCCTTCTACTGCCTCCAACACGGCGGCGGCGGCGG CTGGCACATCCAGGGACCCGGGCCGGTTTTAAACCTCCCGTGCGCCGCCGCCGCACCCCCCGTGGCCCGGGCTCCGGAGGCCGCCGGCGG AGGCAGCCGTTCGGAGGATTATTCGTCTTCTCCCCATTCCGCTGCCGCCGCTGCCAGGCCTCTGGCTGCTGAGGAGAAGCAGGCCCAGTC GCTGCAACCATCCAGCAGCCGCCGCAGCAGCCATTACCCGGCTGCGGTCCAGAGCCAAGCGGCGGCAGAGCGAGGGGCATCAGCTACCGC CAAGTCCAGAGCCATTTCCATCCTGCAGAAGAAGCCCCGCCACCAGCAGCTTCTGCCATCTCTCTCCTCCTTTTTCTTCAGCCACAGGCT CCCAGACATGACAGCCATCATCAAAGAGATCGTTAGCAGAAACAAAAGGAGATATCAAGAGGATGGATTCGACTTAGACTTGACCTATAT TTATCCAAACATTATTGCTATGGGATTTCCTGCAGAAAGACTTGAAGGCGTATACAGGAACAATATTGATGATGTAGTAAGGTTTTTGGA TTCAAAGCATAAAAACCATTACAAGATATACAATCTTTGTGCTGAAAGACATTATGACACCGCCAAATTTAATTGCAGAGTTGCACAATA TCCTTTTGAAGACCATAACCCACCACAGCTAGAACTTATCAAACCCTTTTGTGAAGATCTTGACCAATGGCTAAGTGAAGATGACAATCA TGTTGCAGCAATTCACTGTAAAGCTGGAAAGGGACGAACTGGTGTAATGATATGTGCATATTTATTACATCGGGGCAAATTTTTAAAGGC ACAAGAGGCCCTAGATTTCTATGGGGAAGTAAGGACCAGAGACAAAAAGGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTATTA TAGCTACCTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGG CGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAGGTGAAGATATATTCCTCCAATTCAGGACCCACACGACGGGAAGACAAGTT CATGTACTTTGAGTTCCCTCAGCCGTTACCTGTGTGTGGTGATATCAAAGTAGAGTTCTTCCACAAACAGAACAAGATGCTAAAAAAGGA CAAAATGTTTCACTTTTGGGTAAATACATTCTTCATACCAGGACCAGAGGAAACCTCAGAAAAAGTAGAAAATGGAAGTCTATGTGATCA AGAAATCGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGC AAATAAAGACAAAGCCAACCGATACTTTTCTCCAAATTTTAAGTGCTCCTATATCCCTCCCTGTAAGAGAGAAAATCAGAAGAATTTGGA AAGTGTCATGAATTGGCAACAGTACTGGAAAGATGAGATTGGTTCCCAGCCATTTACTTGCTATTTTAATCAACATCAAAGACCAGATGA TGTGCTTCTGCATCGCACTCATGATGAGATTGTCCTCCTGCATTGCTTCCTCTGGCCCCTGGTGACATTTGTGGTGGGCGTTCTCATTGT GGTCCTGACCATCTGTGCCAAGAGCTTGGCGGTCAAGGCGGAAGCCATGAAGAAGCGCAAGTTCTCTTAAAGGGGAAGGAGGCTTGTAGA AAGCAAAGTACAGAAGCTGTACTCATCGGCACGCGTCCACCTGCGGAACCTGTGTTTCCTGGCGCAGGAGATGGACAGGGCCACGACAGG GCTCTGAGAGGCTCATCCCTCAGTGGCAACAGAAACAGGCACAACTGGAAGACTTGGAACCTCAAAGCTTGTATTCCATCTGCTGTAGCA ATGGCTAAAGGGTCAAGATCTTAGCTGTATGGAGTAACTATTTCAGAAAACCCTATAAGAAGTTCATTTTCTTTCAAAAGTAACAGTATA TTATTTGTACAGTGTAGTATACAAACCATTATGATTTATGCTACTTAAAAATATTAAAATAGAGTGGTCTGTGTTATTTTCTATTTCCTT TTTTATGCTTAGAACACCAGGGTTTAAAAAAAAAAAAAAGGTGAGGACATCTGGGTCTCATTTGCTTCTGCTAGGTTAAACTTTTACTTG ACAACAAGGATTCCTGCTGAAGTCTGAACCTTACTGTGTAACCCTCAGTTTCCACTATTAAAGAGTATCTTTTGACGTCTGCTTGGAAAA TGAATAGTATACTGGTAACTCAGTCTCCAGTCACCTCTGTGTCTCTTAAGCAAGAGATTCTAAAAGATTGGGAAAACATATCCTCCAACA CCTGCCTTTGCCTAACCATTATTTTTCACCAGATTACTTCTTAAGAGAGGGAGGTGATTCTGAAGAAGGCTTCTATCTCAAAAAGCACTG GGCTTCCTTATTCATCTGTTCTTGTTGTTTTTGACGGAGTTAAAAAAGTTTGTGTGCAATACAATATACATGATGTGAAGGACACTCTTC AGCTTAGTGAAACGCTGTTTTCATTTTTTTTTTTTTTTGTAGGTCAGAAAAAAACAACAAAATCAGTTCAAGCATTTTTTTTTCTTTGTC CTTGCCTTGATGTTATGAGTATTAAAACCAGGAGGATTGCTGCCATTGTGCAGTTTGCTTAGACAAACCTGGAGATGCAACCCAGCTCAC ATCATTGCTACTGATGAGCTTTCTGTGCCTTTATCAAAAGTTGATTGAGAAGACCATATTTCTTTGTATCTTTTTATAAACTCAAATTCC AAGTATCAAATCGCAGGTCTCAGTGAACATCAAACCTATTTACTACATAGAATCAAACCTTTGTTTAGGTGAGATGTACATCGTTAGTGG AGGAAAAACTGACAACCTAATTTCATTTGTTTTCTTCTGATACTCTTCAGACATGCCTCTATTAGAATAAAGGTAAACTGGAATTTAAAG ACAAGTTCCCCTCAGTTATTTCCATGGAGCTGTAATATGTATATATGGAGTGATGGTTTCCTGACCTTTAGTCCACATACCAATGTTTTC TTTTTTCTTTTTTTTTTTTTTTTTTGAGATGGTGTCTCACTCTGTTGCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAGTCT CCACCTCCTGGGTTCAAGTCATTCCTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGCACCACCACGCCTGGCTAATTTTTTT GTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCTGCCCACTTCACCTCCCAAAGT GCTGGGATTACAGGCCAATGTTTTCTTAATCTTAGAATGTGAATAACTGAAAATCATAGTCTGTGGAAAGGTGTTGAATTGAGTATAATC TTCTTCTGTTTATTTTTGTGTTTTGTTTTTTAACAGATGGGTATCTTGCTATGTTGCCCAGGATGGAGTGCAGTAGCTATTCACAGGTAT GATCATAGCACACTGCAGCCTCAAGCTCCTGGGCTCAAGCGATCCCCCTCCCTCAGCCTCCCAAGTATCTGGGGTTACTGGTGTGCACCA CCGTGCTTGGCTCCAATAATTTTTTTTCTAATTCAAAAGTTACAGTTTCACTGTGAAAAAGGCCTTGAACACACTATTTATGACATCTTT TGAGGCAGCTCCAGTGCCTTGACTTCAATCCCAGTTTCCGGTTGCAGCATCCTTGTTGTCTTAGCAACACAGTGAACTATTCTGAAGCAT AGAGTAACACGAAACTGGGAGTCCGAGAAATAATCATCTCTGCATCACATTATGGGAGACGAAGTCTGCTTTATCCATTTTATCTTTATT CAGTTGTCTATGATTAATTGATTACAGAGTAGTAGATTAGAATAGTGCATGGATATACATTTGTGTTGAAAAAAGGGGAAGTTGATATAT ATCAATCTTAGTTTTCATTTATCAGTTTGATATTCATGCATTTACACTAAACGCTTCCATTTATCCCGAAAAAGTATATGCAACTGTATT CTGTAGGTTGATTTTTGGAAAAGGGGAGAAGCACACTGAATTCATAAGGTCACATGTAGTCTTAAGGTCTTACTTGCTTACAGCCAATTA AATTTGAAGCACCTTATTTATACTTGTTAAAGGTAAAACCCAAAAGAACAAGCAGAGGACATTTTAAGGTCATAAAAGGTAAATAAGCTT ACCTTCTTAATGTTTTCATTCTCTTTTTGTATAAATCAGAAAATGATCTAAACTGCTGTAACAAAGAGACCCCAAAATATGATGGCTCAT GTAAGATAATTTATTTTTTTCTCACATAGCAATCCAGAAGTGGCTTCATTTCACAAGGTATTCAAGGGATATAGGAGTCATCTACCTTGT TAGTTCTCTTAATACCCAAGGGTATTGTTCTTTCCATGGTCAAAGCTGGCTCAAGACTTCCTAGCCTGTGAAAAAAGAAGAAGGTGGAGC AAGCCATTTCCTTTTTAGGAAATTACAGCCATCACTTCTGCCCACCGTCCATTCATGAATACTTACTATATAGCTATACCTAGCTTCAAG AAAGCCTGGGACGTGTCTCTAACTAGATGGACATGTGCCCTACTAAAACTCCAGGGAAAGGGTTCTATTACTAAAGCTAAAAAGAGGGGA ATGAATACTAGAGTTAAAGACAAAAATGATAGCAGCCAATGGCCCATGCCGTGATAATCTGCTGAGCAGGCATGATGGAGATCCCTTGCC CAGCAGAAAGTGTTCCTTGGTGAAATCATGAATCTGCTATCTAGGAGAAACTCCCTTGTCCATTGTCTTCTGTGGCCACTAGTTTGACCT CTAGGAAAGTCTTGCTCGTCAGCTTCTGTGGCCCCGTCTGAAACTTTTGAGGGACATCGCAGCTTTTGCAGCCCCTGCTTGCTGGTGCAG ACTTTTAGACCTAGATTGCCTTAGAGACTGAAAAATATACGCTTTTATAGGCCGGGGTTTTAGTTCATTTGACTGTAATAAAGACGTCAA TGCCGTTTTTAATGTTTGACTGCTGACATCTTTCAAGACTCACCTTTCCCTTCTCCCTTATGCTGCACATCTGGGCAAGCTGATGGAAGC ATGGGTGCCTCCTCCTTTGGCCCCAGCAGGAAGTTCAAATCACGCAAGCCCTGGCATGCATGCAGGAAGCTTCACCCCAGCCTCACACTC TAAGACGGATAAAAGCCAAACCAATTAAGCCGTTTCTCGACCCTCCTGGGAGCCTGCCCTATCTCCCTGGAAAGTCTCAGTATGTGAGTA |
Top |
FusionGenePPI for PTEN_KCNMB4 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
PTEN | AR, ESR1, UBE2L3, UBE2I, TP53, CSNK2A1, CSNK2A2, UTP14A, ANG, CHGB, COPS6, HBA1, PTK2, MVP, MAGI3, CAV1, PXN, NEDD4, NDFIP1, NDFIP2, XIAP, CASP8, CCNE2, IRS4, PPP2R4, WNT4, QRFPR, ARHGAP26, G3BP2, CENPC, DBF4B, GPR113, INHBE, GFRA2, SMTN, KRT14, AMHR2, PTK2B, CRKL, MAP2K6, PKN2, PDGFRA, PINK1, P3H4, PTPN14, TCEB3C, BAP1, WWP2, MED12, ZNF787, FBN2, TTBK2, RPL14, EEF1A2, FRK, AKT1, PPP3CA, EGR1, SLC9A3R1, STUB1, ELAVL1, PPP1CA, SHARPIN, BMI1, KAT2B, PARK7, CDC27, ANAPC4, ANAPC5, ANAPC7, FZR1, NCOA3, FBXW7, LATS1, CBL, EPHB1, USP7, USP8, USP10, USP13, USP39, USP4, UBC, CDH1, CTNNB1, WWP1, TNKS, TNKS2, RNF146, TXNDC11, CFB, YME1L1, SUV39H1, HES5, GPER1, MXD1, TTC31, EME2, OPRL1, OSBP2, RFTN1, PBX3, FBXL6, PIGN, POLM, TUBA1A, UBAP2L, TRIM8, CDC42EP5, ST8SIA6, ENO2, BLOC1S1, HES6, IFIH1, CYB5R3, PSMB2, SLC36A1, THBD, CARS2, NOTCH1, PPAP2B, UBE2D1, HEATR6, LLGL2, SLC25A6, KIAA0196, PKMYT1, HAGHL, RASSF2, SOCS1, TRIM24, ACACA, PC, PCCA, PCCB, MCCC2, MCCC1, HSPA8, DBT, HSP90AA1, HSPA1A, TUBA3C, HSPA1L, TUBB2A, AMOT, ETS1, HSPA6, STIP1, TUBB4B, ACACB, HSP90AB1, HSPA2, BCKDHA, TUBA1C, HNRNPU, PPP1R10, TUBB3, BEX1, CXCL1, IL24, OSGIN1, POLDIP2, PELO, RPS2, RPL10A, RPLP0, SSR4, ANXA2, FASN, AKAP12, DBN1, PRDX1, DSP, NME1, HSD17B1, UTRN, SPTAN1, RPS9, RPL38, GNAI1, GNAI2, MPRIP, RPS15A, GSTM2, SKP1, EEF2, GNB4, RPL27, SSFA2, DNAJA1, SPTBN1, LIMA1, RPL22L1, RPLP2, RPL27A, FLNB, MYO1D, TUBB, PLEC, MTHFD2, LDHB, RPS17, SDC1, RPS25, CFL1, RCC2, MYOF, RPS6, GPC1, RPL7, TUBA1B, ATP5C1, JUP, ARF4, PPL, RPL13A, RPL23, NCF1, RPS20, GPC4, RPS27, TUFM, HIST1H2AB, S100A8, MYH10, HSPD1, ATP5A1, KBTBD4, PKM, RPS4X, SLC25A5, DCAF11, S100A9, RPL12, LGALS1, MYO1B, RPS3, SDC4, RPS13, MYL12A, CALM1, SLC25A3, RPL31, SNTB2, MYO1C, SETX, RPL13, RPS26, RPS27A, C16orf13, YES1, DDB1, SDCBP, TXN, PDGFRB, OTUD3, PBK, NGB, BCAR1, SPOP, PLK1, CHEK1, BRD4, VHL, MTOR, NF1, ADA, MET, KDM6A, CDK4, CDKN2A, BRAF, PTEN, PIK3R2, PLEKHA1, PTPN13, DLG1, INS, AATK, ERBB3, PTK7, DLC1, RHOA, EIF2AK2, EGFR, ITPR3, MCRS1 | KCNMB4 |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
RelatedDrugs for PTEN_KCNMB4 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | KCNMB4 | Q86W47 | DB01110 | Miconazole | Calcium-activated potassium channel subunit beta-4 | small molecule | approved|investigational|vet_approved |
Top |
RelatedDiseases for PTEN_KCNMB4 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | PTEN | C0018553 | Hamartoma Syndrome, Multiple | 29 | CTD_human;ORPHANET;UNIPROT |
Hgene | PTEN | C0033578 | Prostatic Neoplasms | 11 | CTD_human |
Hgene | PTEN | C0265326 | Bannayan-Riley-Ruvalcaba Syndrome | 6 | ORPHANET;UNIPROT |
Hgene | PTEN | C0376634 | Craniofacial Abnormalities | 6 | CTD_human |
Hgene | PTEN | C3714756 | Intellectual Disability | 5 | CTD_human;HPO |
Hgene | PTEN | C0004352 | Autistic Disorder | 4 | CTD_human;HPO |
Hgene | PTEN | C0014170 | Endometrial Neoplasms | 4 | CTD_human |
Hgene | PTEN | C1458155 | Mammary Neoplasms | 4 | CTD_human;HPO |
Hgene | PTEN | C0008073 | Developmental Disabilities | 3 | CTD_human |
Hgene | PTEN | C0025202 | melanoma | 3 | CTD_human;HPO |
Hgene | PTEN | C0085261 | Proteus Syndrome | 3 | CTD_human;ORPHANET |
Hgene | PTEN | C0376358 | Malignant neoplasm of prostate | 3 | UNIPROT |
Hgene | PTEN | C0282612 | Prostatic Intraepithelial Neoplasias | 2 | CTD_human |
Hgene | PTEN | C1168401 | Squamous cell carcinoma of the head and neck | 2 | CTD_human;ORPHANET;UNIPROT |
Hgene | PTEN | C1854416 | MACROCEPHALY/AUTISM SYNDROME | 2 | CTD_human;ORPHANET;UNIPROT |
Hgene | PTEN | C0001418 | Adenocarcinoma | 1 | CTD_human |
Hgene | PTEN | C0003081 | Anisometropia | 1 | CTD_human |
Hgene | PTEN | C0004096 | Asthma | 1 | CTD_human |
Hgene | PTEN | C0007134 | Renal Cell Carcinoma | 1 | CTD_human |
Hgene | PTEN | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
Hgene | PTEN | C0014173 | Endometrial Hyperplasia | 1 | CTD_human |
Hgene | PTEN | C0015695 | Fatty Liver | 1 | CTD_human |
Hgene | PTEN | C0017638 | Glioma | 1 | CTD_human |
Hgene | PTEN | C0018916 | Hemangioma | 1 | CTD_human;HPO |
Hgene | PTEN | C0020538 | Hypertensive disease | 1 | CTD_human |
Hgene | PTEN | C0020564 | Hypertrophy | 1 | CTD_human |
Hgene | PTEN | C0021655 | Insulin Resistance | 1 | CTD_human |
Hgene | PTEN | C0023014 | Language Development Disorders | 1 | CTD_human |
Hgene | PTEN | C0023418 | leukemia | 1 | CTD_human |
Hgene | PTEN | C0023798 | Lipoma | 1 | CTD_human;HPO |
Hgene | PTEN | C0023801 | Lipomatosis | 1 | CTD_human |
Hgene | PTEN | C0023976 | Long QT Syndrome | 1 | CTD_human |
Hgene | PTEN | C0024121 | Lung Neoplasms | 1 | CTD_human |
Hgene | PTEN | C0024299 | Lymphoma | 1 | CTD_human |
Hgene | PTEN | C0025286 | Meningioma | 1 | CTD_human;HPO |
Hgene | PTEN | C0026613 | Motor Skills Disorders | 1 | CTD_human |
Hgene | PTEN | C0027055 | Myocardial Reperfusion Injury | 1 | CTD_human |
Hgene | PTEN | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Hgene | PTEN | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Hgene | PTEN | C0030297 | Pancreatic Neoplasm | 1 | CTD_human |
Hgene | PTEN | C0035126 | Reperfusion Injury | 1 | CTD_human |
Hgene | PTEN | C0036920 | Sezary Syndrome | 1 | CTD_human |
Hgene | PTEN | C0037274 | Dermatologic disorders | 1 | CTD_human |
Hgene | PTEN | C0149925 | Small cell carcinoma of lung | 1 | CTD_human |
Hgene | PTEN | C0152427 | Polydactyly | 1 | CTD_human |
Hgene | PTEN | C0175704 | LEOPARD Syndrome | 1 | CTD_human |
Hgene | PTEN | C0206669 | Hepatocellular Adenoma | 1 | CTD_human |
Hgene | PTEN | C0206698 | Cholangiocarcinoma | 1 | CTD_human |
Hgene | PTEN | C0476089 | Endometrial Carcinoma | 1 | HPO;UNIPROT |
Hgene | PTEN | C0919267 | ovarian neoplasm | 1 | CTD_human;HPO |
Hgene | PTEN | C1848599 | VACTERL Association With Hydrocephalus | 1 | CTD_human |
Hgene | PTEN | C2239176 | Liver carcinoma | 1 | CTD_human |
Hgene | PTEN | C2751642 | GLIOMA SUSCEPTIBILITY 2 | 1 | UNIPROT |
Hgene | PTEN | C2931822 | Nasopharyngeal carcinoma | 1 | CTD_human |