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Fusion gene ID: 24694 |
FusionGeneSummary for NPHP1_DDR2 |
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Fusion gene information | Fusion gene name: NPHP1_DDR2 | Fusion gene ID: 24694 | Hgene | Tgene | Gene symbol | NPHP1 | DDR2 | Gene ID | 4867 | 4921 |
Gene name | nephrocystin 1 | discoidin domain receptor tyrosine kinase 2 | |
Synonyms | JBTS4|NPH1|SLSN1 | MIG20a|NTRKR3|TKT|TYRO10 | |
Cytomap | 2q13 | 1q23.3 | |
Type of gene | protein-coding | protein-coding | |
Description | nephrocystin-1juvenile nephronophthisis 1 proteinnephronophthisis 1 (juvenile) | discoidin domain-containing receptor 2CD167 antigen-like family member Bcell migration-inducing protein 20discoidin domain receptor 2discoidin domain receptor family, member 2discoidin domain-containing receptor tyrosine kinase 2hydroxyaryl-protein | |
Modification date | 20180519 | 20180523 | |
UniProtAcc | O15259 | Q16832 | |
Ensembl transtripts involved in fusion gene | ENST00000316534, ENST00000445609, ENST00000393272, ENST00000355301, ENST00000417665, ENST00000418527, | ENST00000367922, ENST00000367921, | |
Fusion gene scores | * DoF score | 3 X 3 X 2=18 | 7 X 5 X 5=175 |
# samples | 3 | 7 | |
** MAII score | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(7/175*10)=-1.32192809488736 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: NPHP1 [Title/Abstract] AND DDR2 [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 | DDR2 | GO:0018108 | peptidyl-tyrosine phosphorylation | 20004161 |
Tgene | DDR2 | GO:0038063 | collagen-activated tyrosine kinase receptor signaling pathway | 16186108 |
Tgene | DDR2 | GO:0046777 | protein autophosphorylation | 16186108 |
![]() (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 | BRCA | TCGA-C8-A12U-01A | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
* 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-3UTR | ENST00000316534 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000316534 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-3UTR | ENST00000445609 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000445609 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-3UTR | ENST00000393272 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000393272 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-3UTR | ENST00000355301 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000355301 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-3UTR | ENST00000417665 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000417665 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-3UTR | ENST00000418527 | ENST00000367922 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
5CDS-intron | ENST00000418527 | ENST00000367921 | NPHP1 | chr2 | 110958998 | - | DDR2 | chr1 | 162753587 | + |
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FusionProtFeatures for NPHP1_DDR2 |
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Hgene | Tgene |
NPHP1 | DDR2 |
Together with BCAR1 it may play a role in the control ofepithelial cell polarity. Involved in the organization of apicaljunctions in kidney cells together with NPHP4 and RPGRIP1L/NPHP8(By similarity). Does not seem to be strictly required forciliogenesis (By similarity). Seems to help to recruit PTK2B/PYK2to cell matrix adhesions, thereby initiating phosphorylation ofPTK2B/PYK2 and PTK2B/PYK2-dependent signaling. May play a role inthe regulation of intraflagellar transport (IFT) during ciliaassembly. Required for normal retina development. In connectingphotoreceptor cilia influences the movement of some IFT proteinssuch as IFT88 and WDR19. Involved in spermatogenesis (Bysimilarity). {ECO:0000250}. | Tyrosine kinase that functions as cell surface receptorfor fibrillar collagen and regulates cell differentiation,remodeling of the extracellular matrix, cell migration and cellproliferation. Required for normal bone development. Regulatesosteoblast differentiation and chondrocyte maturation via asignaling pathway that involves MAP kinases and leads to theactivation of the transcription factor RUNX2. Regulates remodelingof the extracellular matrix by up-regulation of the collagenasesMMP1, MMP2 and MMP13, and thereby facilitates cell migration andtumor cell invasion. Promotes fibroblast migration andproliferation, and thereby contributes to cutaneous wound healing.{ECO:0000269|PubMed:16186104, ECO:0000269|PubMed:16186108,ECO:0000269|PubMed:17665456, ECO:0000269|PubMed:18201965,ECO:0000269|PubMed:20004161, ECO:0000269|PubMed:20564243,ECO:0000269|PubMed:20734453, ECO:0000269|PubMed:9659899}. |
![]() * 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 |
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FusionGeneSequence for NPHP1_DDR2 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for NPHP1_DDR2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
NPHP1 | INVS, TUBB, NPHP3, NPHP1, FLNA, FLNB, BCAR1, NPHP4, PTK2B, TNS1, KHDRBS1, TNK2, ARHGAP32, UBQLN4, ADAM15, MED28, CEP164, CEP128, AGK, ATP2B1, BAIAP2L1, BCAS3, TMEM256, CACYBP, CBL, CEP170, CHTOP, CLTC, COPA, DBT, DNM2, DNMBP, DYNC1H1, ECD, FCHO2, FKBP4, GARS, GPATCH1, HK1, HSDL2, HYOU1, IDH3B, IQGAP1, KDELR2, MOB4, NARS, NDUFS3, NDUFV1, NNT, NUDCD3, PDRG1, PHACTR4, PIH1D1, POLR2E, PRRC2A, PSMD14, PSMD7, RAB35, RAB3GAP1, RAB6A, RPAP3, RPGRIP1L, SEC23IP, SEC63, SH3D19, SNX9, SRSF2, TM9SF3, TMEM237, TNRC6B, TTLL12, UNC45A, UQCRC1, URI1, USP22, UXT, WDR41, WDR92, XPO7, BAG2, FLII, WDR83, KCNA5, DNAJC7, RPGR | DDR2 | SHC1, SRC, ELAVL1, HSP90AA1, CBLB, CDH1, CDH2, NTRK1, CHORDC1, GOLT1B |
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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 NPHP1_DDR2 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | DDR2 | Q16832 | DB08896 | Regorafenib | Discoidin domain-containing receptor 2 | small molecule | approved |
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RelatedDiseases for NPHP1_DDR2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | NPHP1 | C0022658 | Kidney Diseases | 1 | CTD_human;HPO |
Hgene | NPHP1 | C1855681 | Nephronophthisis, familial juvenile | 1 | CTD_human;ORPHANET;UNIPROT |
Tgene | DDR2 | C1849011 | SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE | 2 | CTD_human;ORPHANET;UNIPROT |
Tgene | DDR2 | C0152013 | Adenocarcinoma of lung (disorder) | 1 | CTD_human |