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![]() | Fusion Gene Summary |
![]() | Fusion Gene ORF analysis |
![]() | Fusion Genomic Features |
![]() | Fusion Protein Features |
![]() | Fusion Gene Sequence |
![]() | Fusion Gene PPI analysis |
![]() | Related Drugs |
![]() | Related Diseases |
Fusion gene:ARHGDIA-SQSTM1 (FusionGDB2 ID:HG396TG8878) |
Fusion Gene Summary for ARHGDIA-SQSTM1 |
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Fusion gene information | Fusion gene name: ARHGDIA-SQSTM1 | Fusion gene ID: hg396tg8878 | Hgene | Tgene | Gene symbol | ARHGDIA | SQSTM1 | Gene ID | 396 | 8878 |
Gene name | Rho GDP dissociation inhibitor alpha | sequestosome 1 | |
Synonyms | GDIA1|HEL-S-47e|NPHS8|RHOGDI|RHOGDI-1 | A170|DMRV|FTDALS3|NADGP|OSIL|PDB3|ZIP3|p60|p62|p62B | |
Cytomap | ('ARHGDIA')('SQSTM1') 17q25.3 | 5q35.3 | |
Type of gene | protein-coding | protein-coding | |
Description | rho GDP-dissociation inhibitor 1GDP-dissociation inhibitor, aplysia RAS-related 1Rho GDP dissociation inhibitor (GDI) alphaepididymis secretory sperm binding protein Li 47e | sequestosome-1EBI3-associated protein of 60 kDaEBI3-associated protein p60EBIAPautophagy receptor p62oxidative stress induced likephosphotyrosine independent ligand for the Lck SH2 domain p62phosphotyrosine-independent ligand for the Lck SH2 domain | |
Modification date | 20200327 | 20200327 | |
UniProtAcc | . | Q13501 | |
Ensembl transtripts involved in fusion gene | ENST00000269321, ENST00000582520, ENST00000400721, ENST00000541078, ENST00000580685, ENST00000581876, ENST00000584461, | ||
Fusion gene scores | * DoF score | 7 X 4 X 4=112 | 33 X 21 X 17=11781 |
# samples | 7 | 38 | |
** MAII score | log2(7/112*10)=-0.678071905112638 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(38/11781*10)=-4.95431877505661 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ARHGDIA [Title/Abstract] AND SQSTM1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ARHGDIA(79825598)-SQSTM1(179250858), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | ARHGDIA-SQSTM1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. ARHGDIA-SQSTM1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. ARHGDIA-SQSTM1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. ARHGDIA-SQSTM1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. |
* 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 | SQSTM1 | GO:0006914 | autophagy | 20452972 |
Tgene | SQSTM1 | GO:0007032 | endosome organization | 27368102 |
Tgene | SQSTM1 | GO:0031397 | negative regulation of protein ubiquitination | 20452972 |
Tgene | SQSTM1 | GO:0061635 | regulation of protein complex stability | 25127057 |
Tgene | SQSTM1 | GO:1905719 | protein localization to perinuclear region of cytoplasm | 27368102 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | HNSC | TCGA-CR-7398-01A | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
ChimerDB4 | SKCM | TCGA-EB-A1NK-01A | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
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Fusion Gene ORF analysis for ARHGDIA-SQSTM1 |
![]() * 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-intron | ENST00000269321 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000269321 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000269321 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000269321 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000269321 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000582520 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000582520 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000582520 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000582520 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
5CDS-intron | ENST00000582520 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
In-frame | ENST00000269321 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
In-frame | ENST00000582520 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-3CDS | ENST00000400721 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-3CDS | ENST00000541078 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-3CDS | ENST00000580685 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-3CDS | ENST00000581876 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-3CDS | ENST00000584461 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000400721 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000400721 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000400721 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000400721 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000400721 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000541078 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000541078 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000541078 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000541078 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000541078 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000580685 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000580685 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000580685 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000580685 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000580685 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000581876 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000581876 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000581876 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000581876 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000581876 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000584461 | ENST00000360718 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000584461 | ENST00000389805 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000584461 | ENST00000402874 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000584461 | ENST00000506690 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
intron-intron | ENST00000584461 | ENST00000510187 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000582520 | ARHGDIA | chr17 | 79825598 | - | ENST00000376929 | SQSTM1 | chr5 | 179250858 | + | 2749 | 245 | 304 | 1266 | 320 |
ENST00000269321 | ARHGDIA | chr17 | 79825598 | - | ENST00000376929 | SQSTM1 | chr5 | 179250858 | + | 4410 | 1906 | 1965 | 2927 | 320 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000582520 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + | 0.022531757 | 0.97746825 |
ENST00000269321 | ENST00000376929 | ARHGDIA | chr17 | 79825598 | - | SQSTM1 | chr5 | 179250858 | + | 0.037863262 | 0.9621368 |
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Fusion Genomic Features for ARHGDIA-SQSTM1 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
ARHGDIA | chr17 | 79825596 | - | SQSTM1 | chr5 | 179250857 | + | 1.69E-06 | 0.99999833 |
ARHGDIA | chr17 | 79825596 | - | SQSTM1 | chr5 | 179250857 | + | 1.69E-06 | 0.99999833 |
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Fusion Protein Features for ARHGDIA-SQSTM1 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr17:79825598/chr5:179250858) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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Hgene | Tgene |
. | SQSTM1 |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Autophagy receptor required for selective macroautophagy (aggrephagy). Functions as a bridge between polyubiquitinated cargo and autophagosomes. Interacts directly with both the cargo to become degraded and an autophagy modifier of the MAP1 LC3 family (PubMed:16286508, PubMed:20168092, PubMed:24128730, PubMed:28404643, PubMed:22622177). Along with WDFY3, involved in the formation and autophagic degradation of cytoplasmic ubiquitin-containing inclusions (p62 bodies, ALIS/aggresome-like induced structures). Along with WDFY3, required to recruit ubiquitinated proteins to PML bodies in the nucleus (PubMed:24128730, PubMed:20168092). May regulate the activation of NFKB1 by TNF-alpha, nerve growth factor (NGF) and interleukin-1. May play a role in titin/TTN downstream signaling in muscle cells. May regulate signaling cascades through ubiquitination. Adapter that mediates the interaction between TRAF6 and CYLD (By similarity). May be involved in cell differentiation, apoptosis, immune response and regulation of K(+) channels. Involved in endosome organization by retaining vesicles in the perinuclear cloud: following ubiquitination by RNF26, attracts specific vesicle-associated adapters, forming a molecular bridge that restrains cognate vesicles in the perinuclear region and organizes the endosomal pathway for efficient cargo transport (PubMed:27368102). Promotes relocalization of 'Lys-63'-linked ubiquitinated STING1 to autophagosomes (PubMed:29496741). Acts as an activator of the NFE2L2/NRF2 pathway via interaction with KEAP1: interaction inactivates the BCR(KEAP1) complex, promoting nuclear accumulation of NFE2L2/NRF2 and subsequent expression of cytoprotective genes (PubMed:20452972, PubMed:28380357, PubMed:33393215). {ECO:0000250|UniProtKB:O08623, ECO:0000250|UniProtKB:Q64337, ECO:0000269|PubMed:10356400, ECO:0000269|PubMed:10747026, ECO:0000269|PubMed:11244088, ECO:0000269|PubMed:12471037, ECO:0000269|PubMed:15340068, ECO:0000269|PubMed:15802564, ECO:0000269|PubMed:15911346, ECO:0000269|PubMed:15953362, ECO:0000269|PubMed:16079148, ECO:0000269|PubMed:16286508, ECO:0000269|PubMed:19931284, ECO:0000269|PubMed:20168092, ECO:0000269|PubMed:20452972, ECO:0000269|PubMed:22622177, ECO:0000269|PubMed:24128730, ECO:0000269|PubMed:27368102, ECO:0000269|PubMed:28380357, ECO:0000269|PubMed:28404643, ECO:0000269|PubMed:29496741, ECO:0000269|PubMed:33393215}. |
![]() * 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 | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 272_294 | 16 | 357.0 | Compositional bias | Note=Ser-rich | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 272_294 | 16 | 357.0 | Compositional bias | Note=Ser-rich | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 272_294 | 100 | 441.0 | Compositional bias | Note=Ser-rich | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 272_294 | 16 | 357.0 | Compositional bias | Note=Ser-rich | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 389_434 | 16 | 357.0 | Domain | UBA | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 389_434 | 16 | 357.0 | Domain | UBA | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 389_434 | 100 | 441.0 | Domain | UBA | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 389_434 | 16 | 357.0 | Domain | UBA | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 228_233 | 16 | 357.0 | Motif | Note=TRAF6-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 336_341 | 16 | 357.0 | Motif | Note=LIR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 228_233 | 16 | 357.0 | Motif | Note=TRAF6-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 336_341 | 16 | 357.0 | Motif | Note=LIR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 228_233 | 100 | 441.0 | Motif | Note=TRAF6-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 336_341 | 100 | 441.0 | Motif | Note=LIR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 228_233 | 16 | 357.0 | Motif | Note=TRAF6-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 336_341 | 16 | 357.0 | Motif | Note=LIR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 170_220 | 16 | 357.0 | Region | Note=LIM protein-binding (LB) | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 321_342 | 16 | 357.0 | Region | MAP1LC3B-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 170_220 | 16 | 357.0 | Region | Note=LIM protein-binding (LB) | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 321_342 | 16 | 357.0 | Region | MAP1LC3B-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 170_220 | 100 | 441.0 | Region | Note=LIM protein-binding (LB) | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 321_342 | 100 | 441.0 | Region | MAP1LC3B-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 170_220 | 16 | 357.0 | Region | Note=LIM protein-binding (LB) | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 321_342 | 16 | 357.0 | Region | MAP1LC3B-binding | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 122_167 | 16 | 357.0 | Zinc finger | ZZ-type | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 122_167 | 16 | 357.0 | Zinc finger | ZZ-type | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 122_167 | 100 | 441.0 | Zinc finger | ZZ-type | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 122_167 | 16 | 357.0 | Zinc finger | ZZ-type |
- 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 |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 3_102 | 16 | 357.0 | Domain | PB1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 3_102 | 16 | 357.0 | Domain | PB1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 3_102 | 100 | 441.0 | Domain | PB1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 3_102 | 16 | 357.0 | Domain | PB1 |
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Fusion Gene Sequence for ARHGDIA-SQSTM1 |
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>6165_6165_1_ARHGDIA-SQSTM1_ARHGDIA_chr17_79825598_ENST00000269321_SQSTM1_chr5_179250858_ENST00000376929_length(transcript)=4410nt_BP=1906nt GAGCGGAAGTCTCGTGACCCCGGAAGTGACAGGCAGGGCGGGCGGGGCGGCCGACGACGTTCGTCATTTAGTGCGGGAGGGATCCTGAAC CGCGCGGCCGAACCCTCCGGTGTCCCGACCCAGGCTAAGCTTGAGCATGGCTGAGCAGGAGCCCACAGCCGAGCAGCTGGCCCAGATTGC AGCGGAGAACGAGGAGGATGAGCACTCGGTCAACTACAAGCCCCCGGCCCAGAAGAGCATCCAGGAGATCCAGGAGCTGGACAAGGACGA CGAGAGCCTGCGAAAGTACAAGGAGGCCCTGCTGGGCCGCGTGGCCGTTTCCGCAGACCCCAACGTCCCCAACGTCGTGGTGACTGGCCT GACCCTGGTGTGCAGCTCGGCCCCGGGCCCCCTGGAGCTGGACCTGACGGGCGACCTGGAGAGCTTCAAGAAGCAGTCGTTTGTGCTGAA GGAGGGTGTGGAGTACCGGATAAAAATCTCTTTCCGGGTTAACCGAGAGATAGTGTCCGGCATGAAGTACATCCAGCATACGTACAGGAA AGGCGTCAAGATTGACAAGACTGACTACATGGTAGGCAGCTATGGGCCCCGGGCCGAGGAGTACGAGTTCCTGACCCCCGTGGAGGAGGC ACCCAAGGGTATGCTGGCCCGGGGCAGCTACAGCATCAAGTCCCGCTTCACAGACGACGACAAGACCGACCACCTGTCCTGGGAGTGGAA TCTCACCATCAAGAAGGACTGGAAGGACTGAGCCCAGCCAGAGGCGGGCAGGGCAGACTGACGGACGGACGACGGACAGGCGGATGTGTC CCCCCCAGCCCCTCCCCTCCCCATACCAAAGTGCTGACAGGCCCTCCGTGCCCCTCCCACCCTGGTCCGCCTCCCTGGCCTGGCTCAACC GAGTGCCTCCGACCCCCCTCCTCAGCCCTCCCCCACCCACAGGCCCAGCCTCCTCGGTCTCCTGTCTCGTTGCTGCTTCTGCCTGTGCTG TGGGGGAGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTTCTGTGCCCCCCAGGTTCTATCTCCCCGTCACACCCGAGGCCTGGCTTCAGG AGGGAGCGGAGCAGCCATTCTCCAGGCCCCGTGGTTGCCCCTGGACGTGTGCGTCTGCTGCTCCGGGGTGGAGCTGGGGTGTGGGATGCA CGGCCTCGTGGGGGCCGGGCCGTCCTCCAGCCCCGCTGCTCCCTGGCCAGCCCCCTTGTCGCTGTCGGTCCCGTCTAACCATGATGCCTT AACATGTGGAGTGTACCGTGGGGCCTCACTAGCCTCTAACTCCCTGTGTCTGCATGAGCATGTGGCCTCCCCGTCCCTTCCCCGGTGGCG AACCCAGTGACCCAGGGACACGTGGGGTGTGCTGCTGCTGCTCCCCAGCCCACCAGTGCCTGGCCAGCCTGCCCCCTTCCCTGGACAGGG CTGTGGAGATGGCTCCGGCGGCTTGGGGAAAGCCAAATTGCCAAAACTCAAGTCACCTCAGTACCATCCAGGAGGCTGGGTATTGTCCTG CCTCTGCCTTTTCTGTCTCAGCGGGCAGTGCCCAGAGCCCACACCCCCCCAAGAGCCCTCGATGGACAGCCTCACTCACCCCACCTGGGC CCAGCCAGGAGCCCCGCCTGGCCATCAGTATTTATTGCCTCCGTCCGTGCCGTCCCTGGGCCACTGGCCTGGCGCCTGTTCCCCCAGGCT CTCAGTGCCACCACCCCCGGCAGGCCTTCCCTGACCCAGCCAGGAACAAACAAGGGACCAAGTGCACACATTGCTGAGAGCCGTCTCCTG TGCCTCCCCCGCCCCATCCCCGGTCTTCGTGTTGTGTCTGCCAGGCTCAGGCAGAGGCGCCTGTCCCTGCTTCTTTTCTGACCGGGAAAT AAATGCCCCTGAAGGAAGAAAAAAGAGTGCCGGCGGGACCACCGCCCACCGTGTGCTCAGGAGGCGCCCCGCAACATGGTGCACCCCAAT GTGATCTGCGATGGCTGCAATGGGCCTGTGGTAGGAACCCGCTACAAGTGCAGCGTCTGCCCAGACTACGACTTGTGTAGCGTCTGCGAG GGAAAGGGCTTGCACCGGGGGCACACCAAGCTCGCATTCCCCAGCCCCTTCGGGCACCTGTCTGAGGGCTTCTCGCACAGCCGCTGGCTC CGGAAGGTGAAACACGGACACTTCGGGTGGCCAGGATGGGAAATGGGTCCACCAGGAAACTGGAGCCCACGTCCTCCTCGTGCAGGGGAG GCCCGCCCTGGCCCCACGGCAGAATCAGCTTCTGGTCCATCGGAGGATCCGAGTGTGAATTTCCTGAAGAACGTTGGGGAGAGTGTGGCA GCTGCCCTTAGCCCTCTGGGCATTGAAGTTGATATCGATGTGGAGCACGGAGGGAAAAGAAGCCGCCTGACCCCCGTCTCTCCAGAGAGT TCCAGCACAGAGGAGAAGAGCAGCTCACAGCCAAGCAGCTGCTGCTCTGACCCCAGCAAGCCGGGTGGGAATGTTGAGGGCGCCACGCAG TCTCTGGCGGAGCAGATGAGGAAGATCGCCTTGGAGTCCGAGGGGCGCCCTGAGGAACAGATGGAGTCGGATAACTGTTCAGGAGGAGAT GATGACTGGACCCATCTGTCTTCAAAAGAAGTGGACCCGTCTACAGGTGAACTCCAGTCCCTACAGATGCCAGAATCCGAAGGGCCAAGC TCTCTGGACCCCTCCCAGGAGGGACCCACAGGGCTGAAGGAAGCTGCCTTGTACCCACATCTCCCGCCAGAGGCTGACCCGCGGCTGATT GAGTCCCTCTCCCAGATGCTGTCCATGGGCTTCTCTGATGAAGGCGGCTGGCTCACCAGGCTCCTGCAGACCAAGAACTATGACATCGGA GCGGCTCTGGACACCATCCAGTATTCAAAGCATCCCCCGCCGTTGTGACCACTTTTGCCCACCTCTTCTGCGTGCCCCTCTTCTGTCTCA TAGTTGTGTTAAGCTTGCGTAGAATTGCAGGTCTCTGTACGGGCCAGTTTCTCTGCCTTCTTCCAGGATCAGGGGTTAGGGTGCAAGAAG CCATTTAGGGCAGCAAAACAAGTGACATGAAGGGAGGGTCCCTGTGTGTGTGTGTGCTGATGTTTCCTGGGTGCCCTGGCTCCTTGCAGC AGGGCTGGGCCTGCGAGACCCAAGGCTCACTGCAGCGCGCTCCTGACCCCTCCCTGCAGGGGCTACGTTAGCAGCCCAGCACATAGCTTG CCTAATGGCTTTCACTTTCTCTTTTGTTTTAAATGACTCATAGGTCCCTGACATTTAGTTGATTATTTTCTGCTACAGACCTGGTACACT CTGATTTTAGATAAAGTAAGCCTAGGTGTTGTCAGCAGGCAGGCTGGGGAGGCCAGTGTTGTGGGCTTCCTGCTGGGACTGAGAAGGCTC ACGAAGGGCATCCGCAATGTTGGTTTCACTGAGAGCTGCCTCCTGGTCTCTTCACCACTGTAGTTCTCTCATTTCCAAACCATCAGCTGC TTTTAAAATAAGATCTCTTTGTAGCCATCCTGTTAAATTTGTAAACAATCTAATTAAATGGCATCAGCACTTTAACCAATGACGTTTGCA TAGAGAGAAATGATTGACAGTAAGTTTATTGTTAATGGTTCTTACAGAGTATCTTTAAAAGTGCCTTAGGGGAACCCTGTCCCTCCTAAC AAGTGTATCTCGATTAATAACCTGCCAGTCCCAGATCACACATCATCATCGAAGTCTTCCCCAGTTATAAAGAGGTCACATAGTCGTGTG GGTCGAGGATTCTGTGCCTCCAGGACCAGGGGCCCACCCTCTGCCCAGGGAGTCCTTGCGTCCCATGAGGTCTTCCCGCAAGGCCTCTCA GACCCAGATGTGACGGGGTGTGTGGCCCGAGGAAGCTGGACAGCGGCAGTGGGCCTGCTGAGGCCTTCTCTTGAGGCCTGTGCTCTGGGG GTCCCTTGCTTAGCCTGTGCTGGACCAGCTGGCCTGGGGTCCCTCTGAAGAGACCTTGGCTGCTCACTGTCCACATGTGAACTTTTTCTA GGTGGCAGGACAAATTGCGCCCATTTAGAGGATGTGGCTGTAACCTGCTGGATGGGACTCCATAGCTCCTTCCCAGGACCCCTCAGCTCC CCGGCACTGCAGTCTGCAGAGTTCTCCTGGAGGCAGGGGCTGCTGCCTTGTTTCACCTTCCATGTCAGGCCAGCCTGTCCCTGAAAGAGA AGATGGCCATGCCCTCCATGTGTAAGAACAATGCCAGGGCCCAGGAGGACCGCCTGCCCTGCCTGGGCCTTGGCTGGGCCTCTGGTTCTG ACACTTTCTGCTGGAAGCTGTCAGGCTGGGACAGGCTTTGATTTTGAGGGTTAGCAAGACAAAGCAAATAAATGCCTTCCACCTCACCGC >6165_6165_1_ARHGDIA-SQSTM1_ARHGDIA_chr17_79825598_ENST00000269321_SQSTM1_chr5_179250858_ENST00000376929_length(amino acids)=320AA_BP= MVHPNVICDGCNGPVVGTRYKCSVCPDYDLCSVCEGKGLHRGHTKLAFPSPFGHLSEGFSHSRWLRKVKHGHFGWPGWEMGPPGNWSPRP PRAGEARPGPTAESASGPSEDPSVNFLKNVGESVAAALSPLGIEVDIDVEHGGKRSRLTPVSPESSSTEEKSSSQPSSCCSDPSKPGGNV EGATQSLAEQMRKIALESEGRPEEQMESDNCSGGDDDWTHLSSKEVDPSTGELQSLQMPESEGPSSLDPSQEGPTGLKEAALYPHLPPEA DPRLIESLSQMLSMGFSDEGGWLTRLLQTKNYDIGAALDTIQYSKHPPPL -------------------------------------------------------------- >6165_6165_2_ARHGDIA-SQSTM1_ARHGDIA_chr17_79825598_ENST00000582520_SQSTM1_chr5_179250858_ENST00000376929_length(transcript)=2749nt_BP=245nt AGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTTCTGTGCCCCCCAGGCTCTCAGTGCCACCACCCCCGGCAGGCCTTCCCTGACCCAGCC AGGAACAAACAAGGGACCAAGTGCACACATTGCTGAGAGCCGTCTCCTGTGCCTCCCCCGCCCCATCCCCGGTCTTCGTGTTGTGTCTGC CAGGCTCAGGCAGAGGCGCCTGTCCCTGCTTCTTTTCTGACCGGGAAATAAATGCCCCTGAAGGAAGAAAAAAGAGTGCCGGCGGGACCA CCGCCCACCGTGTGCTCAGGAGGCGCCCCGCAACATGGTGCACCCCAATGTGATCTGCGATGGCTGCAATGGGCCTGTGGTAGGAACCCG CTACAAGTGCAGCGTCTGCCCAGACTACGACTTGTGTAGCGTCTGCGAGGGAAAGGGCTTGCACCGGGGGCACACCAAGCTCGCATTCCC CAGCCCCTTCGGGCACCTGTCTGAGGGCTTCTCGCACAGCCGCTGGCTCCGGAAGGTGAAACACGGACACTTCGGGTGGCCAGGATGGGA AATGGGTCCACCAGGAAACTGGAGCCCACGTCCTCCTCGTGCAGGGGAGGCCCGCCCTGGCCCCACGGCAGAATCAGCTTCTGGTCCATC GGAGGATCCGAGTGTGAATTTCCTGAAGAACGTTGGGGAGAGTGTGGCAGCTGCCCTTAGCCCTCTGGGCATTGAAGTTGATATCGATGT GGAGCACGGAGGGAAAAGAAGCCGCCTGACCCCCGTCTCTCCAGAGAGTTCCAGCACAGAGGAGAAGAGCAGCTCACAGCCAAGCAGCTG CTGCTCTGACCCCAGCAAGCCGGGTGGGAATGTTGAGGGCGCCACGCAGTCTCTGGCGGAGCAGATGAGGAAGATCGCCTTGGAGTCCGA GGGGCGCCCTGAGGAACAGATGGAGTCGGATAACTGTTCAGGAGGAGATGATGACTGGACCCATCTGTCTTCAAAAGAAGTGGACCCGTC TACAGGTGAACTCCAGTCCCTACAGATGCCAGAATCCGAAGGGCCAAGCTCTCTGGACCCCTCCCAGGAGGGACCCACAGGGCTGAAGGA AGCTGCCTTGTACCCACATCTCCCGCCAGAGGCTGACCCGCGGCTGATTGAGTCCCTCTCCCAGATGCTGTCCATGGGCTTCTCTGATGA AGGCGGCTGGCTCACCAGGCTCCTGCAGACCAAGAACTATGACATCGGAGCGGCTCTGGACACCATCCAGTATTCAAAGCATCCCCCGCC GTTGTGACCACTTTTGCCCACCTCTTCTGCGTGCCCCTCTTCTGTCTCATAGTTGTGTTAAGCTTGCGTAGAATTGCAGGTCTCTGTACG GGCCAGTTTCTCTGCCTTCTTCCAGGATCAGGGGTTAGGGTGCAAGAAGCCATTTAGGGCAGCAAAACAAGTGACATGAAGGGAGGGTCC CTGTGTGTGTGTGTGCTGATGTTTCCTGGGTGCCCTGGCTCCTTGCAGCAGGGCTGGGCCTGCGAGACCCAAGGCTCACTGCAGCGCGCT CCTGACCCCTCCCTGCAGGGGCTACGTTAGCAGCCCAGCACATAGCTTGCCTAATGGCTTTCACTTTCTCTTTTGTTTTAAATGACTCAT AGGTCCCTGACATTTAGTTGATTATTTTCTGCTACAGACCTGGTACACTCTGATTTTAGATAAAGTAAGCCTAGGTGTTGTCAGCAGGCA GGCTGGGGAGGCCAGTGTTGTGGGCTTCCTGCTGGGACTGAGAAGGCTCACGAAGGGCATCCGCAATGTTGGTTTCACTGAGAGCTGCCT CCTGGTCTCTTCACCACTGTAGTTCTCTCATTTCCAAACCATCAGCTGCTTTTAAAATAAGATCTCTTTGTAGCCATCCTGTTAAATTTG TAAACAATCTAATTAAATGGCATCAGCACTTTAACCAATGACGTTTGCATAGAGAGAAATGATTGACAGTAAGTTTATTGTTAATGGTTC TTACAGAGTATCTTTAAAAGTGCCTTAGGGGAACCCTGTCCCTCCTAACAAGTGTATCTCGATTAATAACCTGCCAGTCCCAGATCACAC ATCATCATCGAAGTCTTCCCCAGTTATAAAGAGGTCACATAGTCGTGTGGGTCGAGGATTCTGTGCCTCCAGGACCAGGGGCCCACCCTC TGCCCAGGGAGTCCTTGCGTCCCATGAGGTCTTCCCGCAAGGCCTCTCAGACCCAGATGTGACGGGGTGTGTGGCCCGAGGAAGCTGGAC AGCGGCAGTGGGCCTGCTGAGGCCTTCTCTTGAGGCCTGTGCTCTGGGGGTCCCTTGCTTAGCCTGTGCTGGACCAGCTGGCCTGGGGTC CCTCTGAAGAGACCTTGGCTGCTCACTGTCCACATGTGAACTTTTTCTAGGTGGCAGGACAAATTGCGCCCATTTAGAGGATGTGGCTGT AACCTGCTGGATGGGACTCCATAGCTCCTTCCCAGGACCCCTCAGCTCCCCGGCACTGCAGTCTGCAGAGTTCTCCTGGAGGCAGGGGCT GCTGCCTTGTTTCACCTTCCATGTCAGGCCAGCCTGTCCCTGAAAGAGAAGATGGCCATGCCCTCCATGTGTAAGAACAATGCCAGGGCC CAGGAGGACCGCCTGCCCTGCCTGGGCCTTGGCTGGGCCTCTGGTTCTGACACTTTCTGCTGGAAGCTGTCAGGCTGGGACAGGCTTTGA TTTTGAGGGTTAGCAAGACAAAGCAAATAAATGCCTTCCACCTCACCGC >6165_6165_2_ARHGDIA-SQSTM1_ARHGDIA_chr17_79825598_ENST00000582520_SQSTM1_chr5_179250858_ENST00000376929_length(amino acids)=320AA_BP= MVHPNVICDGCNGPVVGTRYKCSVCPDYDLCSVCEGKGLHRGHTKLAFPSPFGHLSEGFSHSRWLRKVKHGHFGWPGWEMGPPGNWSPRP PRAGEARPGPTAESASGPSEDPSVNFLKNVGESVAAALSPLGIEVDIDVEHGGKRSRLTPVSPESSSTEEKSSSQPSSCCSDPSKPGGNV EGATQSLAEQMRKIALESEGRPEEQMESDNCSGGDDDWTHLSSKEVDPSTGELQSLQMPESEGPSSLDPSQEGPTGLKEAALYPHLPPEA DPRLIESLSQMLSMGFSDEGGWLTRLLQTKNYDIGAALDTIQYSKHPPPL -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for ARHGDIA-SQSTM1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 122_224 | 16.333333333333332 | 357.0 | GABRR3 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 122_224 | 16.333333333333332 | 357.0 | GABRR3 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 122_224 | 100.33333333333333 | 441.0 | GABRR3 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 122_224 | 16.333333333333332 | 357.0 | GABRR3 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 347_352 | 16.333333333333332 | 357.0 | KEAP1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 347_352 | 16.333333333333332 | 357.0 | KEAP1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 347_352 | 100.33333333333333 | 441.0 | KEAP1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 347_352 | 16.333333333333332 | 357.0 | KEAP1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 269_440 | 16.333333333333332 | 357.0 | NTRK1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 269_440 | 16.333333333333332 | 357.0 | NTRK1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 269_440 | 100.33333333333333 | 441.0 | NTRK1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 269_440 | 16.333333333333332 | 357.0 | NTRK1 | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 50_80 | 16.333333333333332 | 357.0 | PAWR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 50_80 | 16.333333333333332 | 357.0 | PAWR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 50_80 | 16.333333333333332 | 357.0 | PAWR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 43_107 | 16.333333333333332 | 357.0 | PRKCZ and dimerization | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 43_107 | 16.333333333333332 | 357.0 | PRKCZ and dimerization | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 43_107 | 16.333333333333332 | 357.0 | PRKCZ and dimerization |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000360718 | 0 | 7 | 2_50 | 16.333333333333332 | 357.0 | LCK | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000376929 | 2 | 9 | 2_50 | 16.333333333333332 | 357.0 | LCK | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 2_50 | 100.33333333333333 | 441.0 | LCK | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000402874 | 1 | 8 | 2_50 | 16.333333333333332 | 357.0 | LCK | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 50_80 | 100.33333333333333 | 441.0 | PAWR | |
Tgene | SQSTM1 | chr17:79825598 | chr5:179250858 | ENST00000389805 | 1 | 8 | 43_107 | 100.33333333333333 | 441.0 | PRKCZ and dimerization |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for ARHGDIA-SQSTM1 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for ARHGDIA-SQSTM1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ARHGDIA | C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
Hgene | ARHGDIA | C0019693 | HIV Infections | 1 | CTD_human |
Hgene | ARHGDIA | C0022548 | Keloid | 1 | CTD_human |
Hgene | ARHGDIA | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Hgene | ARHGDIA | C0678222 | Breast Carcinoma | 1 | CTD_human |
Hgene | ARHGDIA | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
Hgene | ARHGDIA | C1458155 | Mammary Neoplasms | 1 | CTD_human |
Hgene | ARHGDIA | C1868672 | NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE | 1 | ORPHANET |
Hgene | ARHGDIA | C3808874 | ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2 | 1 | GENOMICS_ENGLAND |
Hgene | ARHGDIA | C4505456 | HIV Coinfection | 1 | CTD_human |
Hgene | ARHGDIA | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |
Tgene | C4085252 | PAGET DISEASE OF BONE 3 | 9 | GENOMICS_ENGLAND;UNIPROT | |
Tgene | C0002736 | Amyotrophic Lateral Sclerosis | 5 | CTD_human;ORPHANET | |
Tgene | C4225326 | FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3 | 4 | CTD_human;UNIPROT | |
Tgene | C0029463 | Osteosarcoma | 2 | GENOMICS_ENGLAND | |
Tgene | C0221054 | Welander Distal Myopathy | 1 | ORPHANET | |
Tgene | C0242383 | Age related macular degeneration | 1 | CTD_human | |
Tgene | C0393554 | Amyotrophic Lateral Sclerosis With Dementia | 1 | CTD_human | |
Tgene | C0543859 | Amyotrophic Lateral Sclerosis, Guam Form | 1 | CTD_human | |
Tgene | C1853926 | NONAKA MYOPATHY | 1 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C2931290 | Welander distal myopathy, Swedish type | 1 | ORPHANET | |
Tgene | C3888102 | Frontotemporal Dementia With Motor Neuron Disease | 1 | ORPHANET | |
Tgene | C4011788 | Behavioral variant of frontotemporal dementia | 1 | ORPHANET |