![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 19057 |
FusionGeneSummary for KLHL7_TMEM106B |
![]() |
Fusion gene information | Fusion gene name: KLHL7_TMEM106B | Fusion gene ID: 19057 | Hgene | Tgene | Gene symbol | KLHL7 | TMEM106B | Gene ID | 55975 | 54664 |
Gene name | kelch like family member 7 | transmembrane protein 106B | |
Synonyms | CISS3|KLHL6|SBBI26 | HLD16 | |
Cytomap | 7p15.3 | 7p21.3 | |
Type of gene | protein-coding | protein-coding | |
Description | kelch-like protein 7kelch-like 6kelch-like 7kelch/BTB | transmembrane protein 106B | |
Modification date | 20180522 | 20180523 | |
UniProtAcc | Q8IXQ5 | Q9NUM4 | |
Ensembl transtripts involved in fusion gene | ENST00000322231, ENST00000339077, ENST00000539124, ENST00000542558, ENST00000409689, ENST00000545443, ENST00000479288, ENST00000322275, ENST00000410047, ENST00000545771, | ENST00000396668, ENST00000396667, ENST00000453686, | |
Fusion gene scores | * DoF score | 5 X 5 X 3=75 | 2 X 2 X 2=8 |
# samples | 5 | 2 | |
** MAII score | log2(5/75*10)=-0.584962500721156 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(2/8*10)=1.32192809488736 | |
Context | PubMed: KLHL7 [Title/Abstract] AND TMEM106B [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) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | KLHL7 | GO:0016567 | protein ubiquitination | 21828050 |
![]() (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 | GBM | TCGA-14-0736-02A | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
* 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 |
5CDS-5UTR | ENST00000322231 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000322231 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000322231 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000339077 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000339077 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000339077 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000539124 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000539124 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000539124 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000542558 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000542558 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000542558 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000409689 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000409689 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000409689 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000545443 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-5UTR | ENST00000545443 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
5CDS-3UTR | ENST00000545443 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000479288 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000479288 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-3UTR | ENST00000479288 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000322275 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000322275 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-3UTR | ENST00000322275 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000410047 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000410047 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-3UTR | ENST00000410047 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000545771 | ENST00000396668 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-5UTR | ENST00000545771 | ENST00000396667 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
intron-3UTR | ENST00000545771 | ENST00000453686 | KLHL7 | chr7 | 23191828 | + | TMEM106B | chr7 | 12254435 | + |
Top |
FusionProtFeatures for KLHL7_TMEM106B |
![]() |
Hgene | Tgene |
KLHL7 | TMEM106B |
Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3ubiquitin ligase complex. The BCR(KLHL7) complex acts by mediatingubiquitination and subsequent degradation of substrate proteins.Probably mediates 'Lys-48'-linked ubiquitination.{ECO:0000269|PubMed:21828050}. | Involved in dendrite morphogenesis and maintenance byregulating lysosomal trafficking via its interaction with MAP6.May act by inhibiting retrograde transport of lysosomes alongdendrites. Required for dendrite branching.{ECO:0000269|PubMed:23136129, ECO:0000269|PubMed:24357581}. |
![]() * 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 |
- 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 |
Top |
FusionGeneSequence for KLHL7_TMEM106B |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
Top |
FusionGenePPI for KLHL7_TMEM106B |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
KLHL7 | CUL3, RBX1, KLHL7, UBC, MOV10, NXF1, NUP50, C9orf41, NR2C2, YWHAZ, CKAP5, NUP153, FERMT3, BOD1L1, MSRB3, KLHL6, ARIH1, SDC2, STAT5A, CEP44, GLI3 | TMEM106B | BTNL8, CHMP2B |
![]() |
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 KLHL7_TMEM106B |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Top |
RelatedDiseases for KLHL7_TMEM106B |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | KLHL7 | C2751986 | RETINITIS PIGMENTOSA 42 | 1 | CTD_human;UNIPROT |
Tgene | TMEM106B | C0751072 | Frontotemporal Lobar Degeneration | 1 | CTD_human |