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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:ATRX-OGT (FusionGDB2 ID:HG546TG8473) |
Fusion Gene Summary for ATRX-OGT |
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Fusion gene information | Fusion gene name: ATRX-OGT | Fusion gene ID: hg546tg8473 | Hgene | Tgene | Gene symbol | ATRX | OGT | Gene ID | 546 | 8473 |
Gene name | ATRX chromatin remodeler | O-linked N-acetylglucosamine (GlcNAc) transferase | |
Synonyms | JMS|MRX52|RAD54|RAD54L|XH2|XNP|ZNF-HX | HINCUT-1|HRNT1|MRX106|O-GLCNAC|OGT1 | |
Cytomap | ('ATRX')('OGT') Xq21.1 | Xq13.1 | |
Type of gene | protein-coding | protein-coding | |
Description | transcriptional regulator ATRXATP-dependent helicase ATRXX-linked helicase IIX-linked nuclear proteinalpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae) | UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunitO-GlcNAc transferase p110 subunitO-GlcNAc transferase subunit p110O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminy | |
Modification date | 20200313 | 20200327 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000373341, ENST00000373344, ENST00000395603, ENST00000480283, | ||
Fusion gene scores | * DoF score | 17 X 13 X 9=1989 | 7 X 7 X 5=245 |
# samples | 23 | 8 | |
** MAII score | log2(23/1989*10)=-3.11233750988937 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/245*10)=-1.61470984411521 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ATRX [Title/Abstract] AND OGT [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ATRX(76972607)-OGT(70775803), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | ATRX-OGT 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. ATRX-OGT 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. ATRX-OGT 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. ATRX-OGT 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. ATRX-OGT seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. ATRX-OGT seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF. ATRX-OGT seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF. ATRX-OGT seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted 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 |
Hgene | ATRX | GO:0006334 | nucleosome assembly | 20651253 |
Hgene | ATRX | GO:0006338 | chromatin remodeling | 20651253 |
Tgene | OGT | GO:0006110 | regulation of glycolytic process | 22923583 |
Tgene | OGT | GO:0006493 | protein O-linked glycosylation | 21240259|21285374|22923583|23222540|23352454|24474760 |
Tgene | OGT | GO:0006915 | apoptotic process | 20824293 |
Tgene | OGT | GO:0032868 | response to insulin | 18288188 |
Tgene | OGT | GO:0035020 | regulation of Rac protein signal transduction | 18288188 |
Tgene | OGT | GO:0043981 | histone H4-K5 acetylation | 20018852 |
Tgene | OGT | GO:0043982 | histone H4-K8 acetylation | 20018852 |
Tgene | OGT | GO:0043984 | histone H4-K16 acetylation | 20018852 |
Tgene | OGT | GO:0045862 | positive regulation of proteolysis | 21285374 |
Tgene | OGT | GO:0045944 | positive regulation of transcription by RNA polymerase II | 23222540|23353889 |
Tgene | OGT | GO:0046626 | regulation of insulin receptor signaling pathway | 18288188 |
Tgene | OGT | GO:0048015 | phosphatidylinositol-mediated signaling | 18288188 |
![]() * 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 | LGG | TCGA-HT-7695 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
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Fusion Gene ORF analysis for ATRX-OGT |
![]() * 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 | ENST00000373341 | ENST00000498566 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
5CDS-intron | ENST00000373344 | ENST00000498566 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
5CDS-intron | ENST00000395603 | ENST00000498566 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
5UTR-3CDS | ENST00000480283 | ENST00000373701 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
5UTR-3CDS | ENST00000480283 | ENST00000373719 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
5UTR-intron | ENST00000480283 | ENST00000498566 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
Frame-shift | ENST00000373344 | ENST00000373701 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
Frame-shift | ENST00000373344 | ENST00000373719 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
Frame-shift | ENST00000395603 | ENST00000373701 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
Frame-shift | ENST00000395603 | ENST00000373719 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
In-frame | ENST00000373341 | ENST00000373701 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
In-frame | ENST00000373341 | ENST00000373719 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + |
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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) |
ENST00000373341 | ATRX | chrX | 76972607 | - | ENST00000373719 | OGT | chrX | 70775803 | + | 4433 | 113 | 152 | 2329 | 725 |
ENST00000373341 | ATRX | chrX | 76972607 | - | ENST00000373701 | OGT | chrX | 70775803 | + | 2352 | 113 | 152 | 2329 | 725 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000373341 | ENST00000373719 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + | 0.000679143 | 0.99932086 |
ENST00000373341 | ENST00000373701 | ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + | 0.004088301 | 0.9959117 |
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Fusion Genomic Features for ATRX-OGT |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + | 5.32E-10 | 1 |
ATRX | chrX | 76972607 | - | OGT | chrX | 70775803 | + | 5.32E-10 | 1 |
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Fusion Protein Features for ATRX-OGT |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chrX:76972607/chrX:70775803) - 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 |
. | . |
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: 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}. |
![]() * 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 | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 487_503 | 298 | 1037.0 | Motif | Nuclear localization signal | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 487_503 | 308 | 1047.0 | Motif | Nuclear localization signal | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 906_908 | 298 | 1037.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 911_914 | 298 | 1037.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 930_932 | 298 | 1037.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 906_908 | 308 | 1047.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 911_914 | 308 | 1047.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 930_932 | 308 | 1047.0 | Nucleotide binding | UDP | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 991_1010 | 298 | 1037.0 | Region | Note=Required for phosphatidylinositol 3%2C4%2C5-triphosphate binding | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 991_1010 | 308 | 1047.0 | Region | Note=Required for phosphatidylinositol 3%2C4%2C5-triphosphate binding | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 327_360 | 298 | 1037.0 | Repeat | Note=TPR 9 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 361_394 | 298 | 1037.0 | Repeat | Note=TPR 10 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 395_428 | 298 | 1037.0 | Repeat | Note=TPR 11 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 429_462 | 298 | 1037.0 | Repeat | Note=TPR 12 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 463_473 | 298 | 1037.0 | Repeat | Note=TPR 13%3B truncated | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 327_360 | 308 | 1047.0 | Repeat | Note=TPR 9 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 361_394 | 308 | 1047.0 | Repeat | Note=TPR 10 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 395_428 | 308 | 1047.0 | Repeat | Note=TPR 11 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 429_462 | 308 | 1047.0 | Repeat | Note=TPR 12 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 463_473 | 308 | 1047.0 | Repeat | Note=TPR 13%3B truncated |
- 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 | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1151_1156 | 44 | 2493.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1166_1169 | 44 | 2493.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1202_1206 | 44 | 2493.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1259_1266 | 44 | 2493.0 | Compositional bias | Note=Poly-Asp |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1443_1466 | 44 | 2493.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1499_1502 | 44 | 2493.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1929_1939 | 44 | 2493.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1941_1948 | 44 | 2493.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 2222_2225 | 44 | 2493.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 2262_2265 | 44 | 2493.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 2420_2425 | 44 | 2493.0 | Compositional bias | Note=Poly-Gln |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 745_750 | 44 | 2493.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1151_1156 | 44 | 2455.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1166_1169 | 44 | 2455.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1202_1206 | 44 | 2455.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1259_1266 | 44 | 2455.0 | Compositional bias | Note=Poly-Asp |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1443_1466 | 44 | 2455.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1499_1502 | 44 | 2455.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1929_1939 | 44 | 2455.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1941_1948 | 44 | 2455.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 2222_2225 | 44 | 2455.0 | Compositional bias | Note=Poly-Lys |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 2262_2265 | 44 | 2455.0 | Compositional bias | Note=Poly-Glu |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 2420_2425 | 44 | 2455.0 | Compositional bias | Note=Poly-Gln |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 745_750 | 44 | 2455.0 | Compositional bias | Note=Poly-Ser |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1581_1768 | 44 | 2493.0 | Domain | Helicase ATP-binding |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 159_296 | 44 | 2493.0 | Domain | ADD |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 2025_2205 | 44 | 2493.0 | Domain | Helicase C-terminal |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1581_1768 | 44 | 2455.0 | Domain | Helicase ATP-binding |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 159_296 | 44 | 2455.0 | Domain | ADD |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 2025_2205 | 44 | 2455.0 | Domain | Helicase C-terminal |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1719_1722 | 44 | 2493.0 | Motif | Note=DEGH box |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 581_594 | 44 | 2493.0 | Motif | Note=PxVxL motif |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1719_1722 | 44 | 2455.0 | Motif | Note=DEGH box |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 581_594 | 44 | 2455.0 | Motif | Note=PxVxL motif |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1594_1601 | 44 | 2493.0 | Nucleotide binding | ATP |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1594_1601 | 44 | 2455.0 | Nucleotide binding | ATP |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 170_206 | 44 | 2493.0 | Zinc finger | GATA-type%3B atypical |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 217_272 | 44 | 2493.0 | Zinc finger | PHD-type%3B atypical |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 170_206 | 44 | 2455.0 | Zinc finger | GATA-type%3B atypical |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 217_272 | 44 | 2455.0 | Zinc finger | PHD-type%3B atypical |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 123_156 | 298 | 1037.0 | Repeat | Note=TPR 3 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 157_190 | 298 | 1037.0 | Repeat | Note=TPR 4 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 191_224 | 298 | 1037.0 | Repeat | Note=TPR 5 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 21_54 | 298 | 1037.0 | Repeat | Note=TPR 1 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 225_258 | 298 | 1037.0 | Repeat | Note=TPR 6 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 259_292 | 298 | 1037.0 | Repeat | Note=TPR 7 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 293_326 | 298 | 1037.0 | Repeat | Note=TPR 8 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373701 | 6 | 22 | 89_122 | 298 | 1037.0 | Repeat | Note=TPR 2 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 123_156 | 308 | 1047.0 | Repeat | Note=TPR 3 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 157_190 | 308 | 1047.0 | Repeat | Note=TPR 4 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 191_224 | 308 | 1047.0 | Repeat | Note=TPR 5 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 21_54 | 308 | 1047.0 | Repeat | Note=TPR 1 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 225_258 | 308 | 1047.0 | Repeat | Note=TPR 6 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 259_292 | 308 | 1047.0 | Repeat | Note=TPR 7 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 293_326 | 308 | 1047.0 | Repeat | Note=TPR 8 | |
Tgene | OGT | chrX:76972607 | chrX:70775803 | ENST00000373719 | 6 | 22 | 89_122 | 308 | 1047.0 | Repeat | Note=TPR 2 |
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Fusion Gene Sequence for ATRX-OGT |
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>8357_8357_1_ATRX-OGT_ATRX_chrX_76972607_ENST00000373341_OGT_chrX_70775803_ENST00000373701_length(transcript)=2352nt_BP=113nt TGAAAGCAAGTTGAATACATTGGTGCAGAAGCTTCATGACTTCCTTGCACACTCATCAGAAGAATCTGAAGAAACAAGTTCTCCTCCACG ACTTGCAATGAATCAAAACACAGGTTGCTGAAGCAGAAGATTGTTATAATACAGCTCTCCGTCTGTGTCCCACCCATGCAGACTCTCTGA ATAACCTAGCCAATATCAAACGAGAACAGGGAAACATTGAAGAGGCAGTTCGCTTGTATCGTAAAGCATTAGAAGTCTTCCCAGAGTTTG CTGCTGCCCATTCAAATTTAGCAAGTGTACTGCAGCAGCAGGGAAAACTGCAGGAAGCTCTGATGCATTATAAGGAGGCTATTCGAATCA GTCCTACCTTTGCTGATGCCTACTCTAATATGGGAAACACTCTAAAGGAGATGCAGGATGTTCAGGGAGCCTTGCAGTGTTATACGCGTG CCATCCAAATTAATCCTGCATTTGCAGATGCACATAGCAATCTGGCTTCCATTCATAAGGATTCAGGGAATATTCCAGAAGCCATAGCTT CTTACCGCACGGCTCTGAAACTTAAGCCTGATTTTCCTGATGCTTATTGTAACTTGGCTCATTGCCTGCAGATTGTCTGTGATTGGACAG ACTATGATGAGCGAATGAAGAAGTTGGTCAGTATTGTGGCTGACCAGTTAGAGAAGAATAGGTTGCCTTCTGTGCATCCTCATCATAGTA TGCTATATCCTCTTTCTCATGGCTTCAGGAAGGCTATTGCTGAGAGGCACGGCAACCTGTGCTTAGATAAGATTAATGTTCTTCATAAAC CACCATATGAACATCCAAAAGACTTGAAGCTCAGTGATGGTCGGCTGCGTGTAGGATATGTGAGTTCCGACTTTGGGAATCATCCTACTT CTCACCTTATGCAGTCTATTCCAGGCATGCACAATCCTGATAAATTTGAGGTGTTCTGTTATGCCCTGAGCCCAGACGATGGCACAAACT TCCGAGTGAAGGTGATGGCAGAAGCCAATCATTTCATTGATCTTTCTCAGATTCCATGCAATGGAAAAGCAGCTGATCGCATCCATCAGG ATGGAATTCATATCCTTGTAAATATGAATGGCTATACTAAGGGCGCTCGAAATGAGCTTTTTGCTCTCAGGCCAGCTCCTATTCAGGCAA TGTGGCTGGGATACCCTGGGACGAGTGGTGCGCTTTTCATGGATTATATTATCACTGATCAGGAAACTTCGCCAGCTGAAGTTGCTGAGC AGTATTCCGAGAAATTGGCTTATATGCCCCACACTTTTTTTATTGGTGATCATGCTAATATGTTCCCTCACCTGAAGAAAAAAGCAGTCA TCGATTTTAAGTCCAATGGGCACATTTATGACAATCGGATAGTTCTGAATGGCATCGACCTCAAAGCATTTCTTGATAGTCTACCAGATG TGAAAATTGTCAAGATGAAGTGTCCTGATGGAGGAGACAATGCAGATAGCAGTAACACAGCTCTTAATATGCCTGTTATTCCTATGAATA CTATTGCAGAAGCAGTTATTGAAATGATTAACCGAGGACAGATTCAAATAACAATTAATGGATTCAGTATTAGCAATGGACTGGCAACTA CTCAGATCAACAATAAGGCTGCAACTGGAGAGGAGGTTCCCCGTACCATTATTGTAACCACCCGTTCTCAGTACGGGTTACCAGAAGATG CCATCGTATACTGTAACTTTAATCAGTTGTATAAAATTGACCCTTCTACTTTGCAGATGTGGGCAAACATTCTGAAGCGTGTTCCCAATA GTGTACTCTGGCTGTTGCGTTTTCCAGCAGTAGGAGAACCTAATATTCAACAGTATGCACAAAACATGGGCCTGCCCCAGAACCGTATCA TTTTTTCACCTGTTGCTCCTAAAGAGGAACACGTCAGGAGAGGCCAGCTGGCTGATGTCTGCTTGGACACTCCACTCTGTAATGGGCACA CCACAGGGATGGATGTCCTCTGGGCAGGGACCCCCATGGTGACTATGCCAGGAGAGACTCTTGCTTCTCGAGTTGCAGCATCCCAGCTCA CTTGCTTAGGTTGTCTTGAGCTTATTGCTAAAAACAGACAAGAATATGAAGACATAGCTGTGAAGCTGGGAACTGATCTAGAATACCTGA AGAAAGTTCGTGGCAAAGTCTGGAAGCAAAGAATATCTAGCCCTCTGTTCAACACCAAACAATACACAATGGAACTAGAGCGGCTCTATC TACAGATGTGGGAGCATTATGCAGCTGGCAACAAACCTGACCACATGATTAAGCCTGTTGAAGTCACTGAGTCAGCATAAATAAAGACTG >8357_8357_1_ATRX-OGT_ATRX_chrX_76972607_ENST00000373341_OGT_chrX_70775803_ENST00000373701_length(amino acids)=725AA_BP= MCPTHADSLNNLANIKREQGNIEEAVRLYRKALEVFPEFAAAHSNLASVLQQQGKLQEALMHYKEAIRISPTFADAYSNMGNTLKEMQDV QGALQCYTRAIQINPAFADAHSNLASIHKDSGNIPEAIASYRTALKLKPDFPDAYCNLAHCLQIVCDWTDYDERMKKLVSIVADQLEKNR LPSVHPHHSMLYPLSHGFRKAIAERHGNLCLDKINVLHKPPYEHPKDLKLSDGRLRVGYVSSDFGNHPTSHLMQSIPGMHNPDKFEVFCY ALSPDDGTNFRVKVMAEANHFIDLSQIPCNGKAADRIHQDGIHILVNMNGYTKGARNELFALRPAPIQAMWLGYPGTSGALFMDYIITDQ ETSPAEVAEQYSEKLAYMPHTFFIGDHANMFPHLKKKAVIDFKSNGHIYDNRIVLNGIDLKAFLDSLPDVKIVKMKCPDGGDNADSSNTA LNMPVIPMNTIAEAVIEMINRGQIQITINGFSISNGLATTQINNKAATGEEVPRTIIVTTRSQYGLPEDAIVYCNFNQLYKIDPSTLQMW ANILKRVPNSVLWLLRFPAVGEPNIQQYAQNMGLPQNRIIFSPVAPKEEHVRRGQLADVCLDTPLCNGHTTGMDVLWAGTPMVTMPGETL ASRVAASQLTCLGCLELIAKNRQEYEDIAVKLGTDLEYLKKVRGKVWKQRISSPLFNTKQYTMELERLYLQMWEHYAAGNKPDHMIKPVE -------------------------------------------------------------- >8357_8357_2_ATRX-OGT_ATRX_chrX_76972607_ENST00000373341_OGT_chrX_70775803_ENST00000373719_length(transcript)=4433nt_BP=113nt TGAAAGCAAGTTGAATACATTGGTGCAGAAGCTTCATGACTTCCTTGCACACTCATCAGAAGAATCTGAAGAAACAAGTTCTCCTCCACG ACTTGCAATGAATCAAAACACAGGTTGCTGAAGCAGAAGATTGTTATAATACAGCTCTCCGTCTGTGTCCCACCCATGCAGACTCTCTGA ATAACCTAGCCAATATCAAACGAGAACAGGGAAACATTGAAGAGGCAGTTCGCTTGTATCGTAAAGCATTAGAAGTCTTCCCAGAGTTTG CTGCTGCCCATTCAAATTTAGCAAGTGTACTGCAGCAGCAGGGAAAACTGCAGGAAGCTCTGATGCATTATAAGGAGGCTATTCGAATCA GTCCTACCTTTGCTGATGCCTACTCTAATATGGGAAACACTCTAAAGGAGATGCAGGATGTTCAGGGAGCCTTGCAGTGTTATACGCGTG CCATCCAAATTAATCCTGCATTTGCAGATGCACATAGCAATCTGGCTTCCATTCATAAGGATTCAGGGAATATTCCAGAAGCCATAGCTT CTTACCGCACGGCTCTGAAACTTAAGCCTGATTTTCCTGATGCTTATTGTAACTTGGCTCATTGCCTGCAGATTGTCTGTGATTGGACAG ACTATGATGAGCGAATGAAGAAGTTGGTCAGTATTGTGGCTGACCAGTTAGAGAAGAATAGGTTGCCTTCTGTGCATCCTCATCATAGTA TGCTATATCCTCTTTCTCATGGCTTCAGGAAGGCTATTGCTGAGAGGCACGGCAACCTGTGCTTAGATAAGATTAATGTTCTTCATAAAC CACCATATGAACATCCAAAAGACTTGAAGCTCAGTGATGGTCGGCTGCGTGTAGGATATGTGAGTTCCGACTTTGGGAATCATCCTACTT CTCACCTTATGCAGTCTATTCCAGGCATGCACAATCCTGATAAATTTGAGGTGTTCTGTTATGCCCTGAGCCCAGACGATGGCACAAACT TCCGAGTGAAGGTGATGGCAGAAGCCAATCATTTCATTGATCTTTCTCAGATTCCATGCAATGGAAAAGCAGCTGATCGCATCCATCAGG ATGGAATTCATATCCTTGTAAATATGAATGGCTATACTAAGGGCGCTCGAAATGAGCTTTTTGCTCTCAGGCCAGCTCCTATTCAGGCAA TGTGGCTGGGATACCCTGGGACGAGTGGTGCGCTTTTCATGGATTATATTATCACTGATCAGGAAACTTCGCCAGCTGAAGTTGCTGAGC AGTATTCCGAGAAATTGGCTTATATGCCCCACACTTTTTTTATTGGTGATCATGCTAATATGTTCCCTCACCTGAAGAAAAAAGCAGTCA TCGATTTTAAGTCCAATGGGCACATTTATGACAATCGGATAGTTCTGAATGGCATCGACCTCAAAGCATTTCTTGATAGTCTACCAGATG TGAAAATTGTCAAGATGAAGTGTCCTGATGGAGGAGACAATGCAGATAGCAGTAACACAGCTCTTAATATGCCTGTTATTCCTATGAATA CTATTGCAGAAGCAGTTATTGAAATGATTAACCGAGGACAGATTCAAATAACAATTAATGGATTCAGTATTAGCAATGGACTGGCAACTA CTCAGATCAACAATAAGGCTGCAACTGGAGAGGAGGTTCCCCGTACCATTATTGTAACCACCCGTTCTCAGTACGGGTTACCAGAAGATG CCATCGTATACTGTAACTTTAATCAGTTGTATAAAATTGACCCTTCTACTTTGCAGATGTGGGCAAACATTCTGAAGCGTGTTCCCAATA GTGTACTCTGGCTGTTGCGTTTTCCAGCAGTAGGAGAACCTAATATTCAACAGTATGCACAAAACATGGGCCTGCCCCAGAACCGTATCA TTTTTTCACCTGTTGCTCCTAAAGAGGAACACGTCAGGAGAGGCCAGCTGGCTGATGTCTGCTTGGACACTCCACTCTGTAATGGGCACA CCACAGGGATGGATGTCCTCTGGGCAGGGACCCCCATGGTGACTATGCCAGGAGAGACTCTTGCTTCTCGAGTTGCAGCATCCCAGCTCA CTTGCTTAGGTTGTCTTGAGCTTATTGCTAAAAACAGACAAGAATATGAAGACATAGCTGTGAAGCTGGGAACTGATCTAGAATACCTGA AGAAAGTTCGTGGCAAAGTCTGGAAGCAAAGAATATCTAGCCCTCTGTTCAACACCAAACAATACACAATGGAACTAGAGCGGCTCTATC TACAGATGTGGGAGCATTATGCAGCTGGCAACAAACCTGACCACATGATTAAGCCTGTTGAAGTCACTGAGTCAGCATAAATAAAGACTG CACAGGAGAATTACCCCTATACCTGAGCCTCAACCTTCTGGGGGAAAGGGAACTAGATAACATACTTCTTACTTGTCTGTACAGTACCTT GTTGCAGATGGGTGATATATAATGGTAATAGAATAGCACAGCCAGACTTGCTTCCTGCATGGTAGGGAGAGACACAAAAGATGGGAAACT GCTTTTCCACAAGGAATCTCCGTAGAATTTTGCGGCGACCAGATGGTGCATAGGTCTGGAAGGTCTGATCTCCCTTGGTCTTCCATGGGA TGGTTAGTGTGGAGGGGAGATATAGATTGTCCGGCCGCTTTGTGATTCCATGGATTGATTCAGTCTTCTGGATTTTTTTTTCTTTATATT TTGGGTACTGGAGCTTTTAAAAATGTTTGGTTTCAGGTATTTTTATTCATGTGAAGTGTATATGATTCTCTTGAGATAAGGTTTTAAGCT AAAATGTTACTCCCTGTTTTAGTTTCTGAACTCTGACAGATTGACAGGGACTTTGCTGGTGTAGTCTTTTTATAGGTTTTATAAACCACT TGAGCCTATATCAGTCGTTTTAGTGTCTGACCTAATATTTGGAGCTATCAGTGCTTTGTTGATTTAGATGATGACTCAAGATTTTTTCTG GTCCATTTCCCATTTCCTTTTCTTCCCTGACCCCCATACCCTCACCCTTAAAATTCTCCTGTAACTCAACTAACAAAATCAAGCCTGATT CAAAACATCCTAGGGTGTTTTAAACACACCATCTGGTGCCAAATGAAGATTTTTAGGAGTGATTACTAATTATCAAGGGCACAGTTGTGG TACTGTCATTGATAATAATATAGTTTTTTTTTTTTTCCTAATTTTGACCTGTTTCACCAGTGTTTTACCCTTGACTGCCCCTTCTATGCT GCTTCCAAAAGTGATAGTGTGTGTAAGATTTTTACCTTCCTTTCTAAAGTTTTTTTTTTTTTTTTTTAAGTGAGTCCTGTTCTTCCTATT TCTTTCAGCAGAAATGAAATCCCAGGTAAGTATAAGTATTCAAGTATTTGATCAGTAAGTCACAGTTATCTCCAGTGCATTAAATAACCT TCATCAAGAAATAGGTTATAGGTAAAATCTCTGAAGGATCATCTATGTATTCAAGTAATTATTTTTTAGATAATAACTGTCTTCTGGACT TGGTCTTGAAGTCTGTACAGATTCAGCCTCAGTAGTAGCGAACTGCACTGCTGTTTGGTTTGGAGTACAAATTAGACTTATAGTCCTCCT GGAACTTGAGTTATTAAAATCATAGGAATAAAATTATGGGATCTCAACAAAGGGTCGAGGGTTTGAGGCTTAAACAAGCCAACATATGAA TATATGTTTTGTCTCGCTATACTGCACTTACGCTATCCAGTTGCAGGTAATTTTTTGTCTGCTAGTAGTGTTCTAGATTATGTCTTTCCA AAGCGCTGAGGCTGTGCACCTATTCTGTAGTTGCAGCTGATGCCTGAATGTATCCTAGCTGACAAATTATTGATTAATAAGAACTTGAAT TTCTGGAAGATTCTTACTGTTAACCAAATTTTGAGCAAGGAGTCTCAAAGGTAATTCTGAACCAGAATTACATGTTAATGAACAGTGTAC CTTTTAACAGTGTAAATCACGGAATATCCGTGAAGGGATTTCTTAATTTATTTTTTACCGGTTGATTGAAATATCAGTTAAAGGTTGCCA GCATGGTTGCAGATAAACTGATGTTTGAAATTCGCTGAAATACTTAATGTGGAATAGGATAATATACTTCCAATGCCCTCAAGGCTGTGA CCTTACAGCCATTTTACATAGCACATCATTCCTCCTATAGGGATGAACTTTTTCCTGGCACGAAAAGTAGCCGCTCTGGTTGAAGCTTTG CTTATTGTAACAGGCTTTTATTTCCAGGTAATATGTCTTGGAAGACTTAATTCTGATTAGAGATATAGATATTACTGGAAACTAATTGTT TTTTTTCTATTGTACTCTGCTTTATCAAAGAAGTAAAACATTTAAATCGTACTACAGAAATTAAGATGTTGTCTTGCGATCCTTAATAAA >8357_8357_2_ATRX-OGT_ATRX_chrX_76972607_ENST00000373341_OGT_chrX_70775803_ENST00000373719_length(amino acids)=725AA_BP= MCPTHADSLNNLANIKREQGNIEEAVRLYRKALEVFPEFAAAHSNLASVLQQQGKLQEALMHYKEAIRISPTFADAYSNMGNTLKEMQDV QGALQCYTRAIQINPAFADAHSNLASIHKDSGNIPEAIASYRTALKLKPDFPDAYCNLAHCLQIVCDWTDYDERMKKLVSIVADQLEKNR LPSVHPHHSMLYPLSHGFRKAIAERHGNLCLDKINVLHKPPYEHPKDLKLSDGRLRVGYVSSDFGNHPTSHLMQSIPGMHNPDKFEVFCY ALSPDDGTNFRVKVMAEANHFIDLSQIPCNGKAADRIHQDGIHILVNMNGYTKGARNELFALRPAPIQAMWLGYPGTSGALFMDYIITDQ ETSPAEVAEQYSEKLAYMPHTFFIGDHANMFPHLKKKAVIDFKSNGHIYDNRIVLNGIDLKAFLDSLPDVKIVKMKCPDGGDNADSSNTA LNMPVIPMNTIAEAVIEMINRGQIQITINGFSISNGLATTQINNKAATGEEVPRTIIVTTRSQYGLPEDAIVYCNFNQLYKIDPSTLQMW ANILKRVPNSVLWLLRFPAVGEPNIQQYAQNMGLPQNRIIFSPVAPKEEHVRRGQLADVCLDTPLCNGHTTGMDVLWAGTPMVTMPGETL ASRVAASQLTCLGCLELIAKNRQEYEDIAVKLGTDLEYLKKVRGKVWKQRISSPLFNTKQYTMELERLYLQMWEHYAAGNKPDHMIKPVE -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for ATRX-OGT |
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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 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 1189_1326 | 44.333333333333336 | 2493.0 | DAXX |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 1189_1326 | 44.333333333333336 | 2455.0 | DAXX |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000373344 | - | 2 | 35 | 2010_2280 | 44.333333333333336 | 2493.0 | MECP2 |
Hgene | ATRX | chrX:76972607 | chrX:70775803 | ENST00000395603 | - | 2 | 34 | 2010_2280 | 44.333333333333336 | 2455.0 | MECP2 |
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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 ATRX-OGT |
![]() (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 ATRX-OGT |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ATRX | C0796003 | Juberg-Marsidi syndrome | 17 | CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Hgene | ATRX | C1845055 | ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED | 16 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | ATRX | C0017638 | Glioma | 2 | CTD_human |
Hgene | ATRX | C0027819 | Neuroblastoma | 2 | CTD_human |
Hgene | ATRX | C0259783 | mixed gliomas | 2 | CTD_human |
Hgene | ATRX | C0555198 | Malignant Glioma | 2 | CTD_human |
Hgene | ATRX | C0010417 | Cryptorchidism | 1 | CTD_human |
Hgene | ATRX | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
Hgene | ATRX | C0018273 | Growth Disorders | 1 | CTD_human |
Hgene | ATRX | C0030297 | Pancreatic Neoplasm | 1 | CTD_human |
Hgene | ATRX | C0030846 | Penile Diseases | 1 | CTD_human |
Hgene | ATRX | C0039978 | Thoracic Diseases | 1 | CTD_human |
Hgene | ATRX | C0206754 | Neuroendocrine Tumors | 1 | CTD_human |
Hgene | ATRX | C0346647 | Malignant neoplasm of pancreas | 1 | CTD_human |
Hgene | ATRX | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
Hgene | ATRX | C0431663 | Bilateral Cryptorchidism | 1 | CTD_human |
Hgene | ATRX | C0431664 | Unilateral Cryptorchidism | 1 | CTD_human |
Hgene | ATRX | C0585216 | Alpha-Thalassemia Myelodysplasia Syndrome | 1 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
Hgene | ATRX | C0796159 | Mental retardation Smith Fineman Myers type | 1 | ORPHANET |
Hgene | ATRX | C1136249 | Mental Retardation, X-Linked | 1 | CTD_human |
Hgene | ATRX | C1563730 | Abdominal Cryptorchidism | 1 | CTD_human |
Hgene | ATRX | C1563731 | Inguinal Cryptorchidism | 1 | CTD_human |
Hgene | ATRX | C2713368 | Hematopoetic Myelodysplasia | 1 | CTD_human |
Hgene | ATRX | C3463824 | MYELODYSPLASTIC SYNDROME | 1 | CTD_human |
Tgene | C4478379 | MENTAL RETARDATION, X-LINKED 106 | 3 | GENOMICS_ENGLAND;UNIPROT |