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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:DPM1-CDKN2A (FusionGDB2 ID:HG8813TG1029) |
Fusion Gene Summary for DPM1-CDKN2A |
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Fusion gene information | Fusion gene name: DPM1-CDKN2A | Fusion gene ID: hg8813tg1029 | Hgene | Tgene | Gene symbol | DPM1 | CDKN2A | Gene ID | 8813 | 1029 |
Gene name | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | cyclin dependent kinase inhibitor 2A | |
Synonyms | CDGIE|MPDS | ARF|CDK4I|CDKN2|CMM2|INK4|INK4A|MLM|MTS-1|MTS1|P14|P14ARF|P16|P16-INK4A|P16INK4|P16INK4A|P19|P19ARF|TP16 | |
Cytomap | ('DPM1')('CDKN2A') 20q13.13 | 9p21.3 | |
Type of gene | protein-coding | protein-coding | |
Description | dolichol-phosphate mannosyltransferase subunit 1DPM synthase complex, catalytic subunitDPM synthase subunit 1MPD synthase subunit 1dolichol monophosphate mannose synthasedolichol-phosphate mannose synthase subunit 1dolichyl-phosphate beta-D-mannosyl | cyclin-dependent kinase inhibitor 2ACDK4 inhibitor p16-INK4alternative reading framecell cycle negative regulator betacyclin-dependent kinase 4 inhibitor Acyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4)multiple tumor suppressor 1 | |
Modification date | 20200313 | 20200329 | |
UniProtAcc | O60762 | . | |
Ensembl transtripts involved in fusion gene | ENST00000371582, ENST00000371583, ENST00000371588, ENST00000466152, | ||
Fusion gene scores | * DoF score | 11 X 8 X 6=528 | 13 X 5 X 10=650 |
# samples | 13 | 16 | |
** MAII score | log2(13/528*10)=-2.02202630633 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(16/650*10)=-2.02236781302845 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: DPM1 [Title/Abstract] AND CDKN2A [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | DPM1(49574900)-CDKN2A(21968241), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. |
* 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 | DPM1 | GO:0006506 | GPI anchor biosynthetic process | 9535917|9724629|10835346 |
Hgene | DPM1 | GO:0019348 | dolichol metabolic process | 9535917|9724629 |
Hgene | DPM1 | GO:0035268 | protein mannosylation | 9535917 |
Hgene | DPM1 | GO:0035269 | protein O-linked mannosylation | 9535917 |
Tgene | CDKN2A | GO:0000082 | G1/S transition of mitotic cell cycle | 10208428 |
Tgene | CDKN2A | GO:0007050 | cell cycle arrest | 15149599 |
Tgene | CDKN2A | GO:0008285 | negative regulation of cell proliferation | 15149599 |
Tgene | CDKN2A | GO:0030308 | negative regulation of cell growth | 10208428 |
Tgene | CDKN2A | GO:0032088 | negative regulation of NF-kappaB transcription factor activity | 10353611 |
Tgene | CDKN2A | GO:0042326 | negative regulation of phosphorylation | 8259215|10208428 |
Tgene | CDKN2A | GO:0045736 | negative regulation of cyclin-dependent protein serine/threonine kinase activity | 7739547|8259215 |
![]() * 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 | STAD | TCGA-CD-8525-01A | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
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Fusion Gene ORF analysis for DPM1-CDKN2A |
![]() * 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 | ENST00000371582 | ENST00000304494 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000361570 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000494262 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000498124 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000498628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000530628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000578845 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000579122 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371582 | ENST00000579755 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000304494 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000361570 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000494262 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000498124 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000498628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000530628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000578845 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000579122 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371583 | ENST00000579755 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000304494 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000361570 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000494262 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000498124 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000498628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000530628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000578845 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000579122 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-3UTR | ENST00000371588 | ENST00000579755 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371582 | ENST00000446177 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371582 | ENST00000470819 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371582 | ENST00000479692 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371582 | ENST00000497750 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371583 | ENST00000446177 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371583 | ENST00000470819 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371583 | ENST00000479692 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371583 | ENST00000497750 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371588 | ENST00000446177 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371588 | ENST00000470819 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371588 | ENST00000479692 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5CDS-intron | ENST00000371588 | ENST00000497750 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000304494 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000361570 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000494262 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000498124 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000498628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000530628 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000578845 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000579122 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-3UTR | ENST00000466152 | ENST00000579755 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-intron | ENST00000466152 | ENST00000446177 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-intron | ENST00000466152 | ENST00000470819 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-intron | ENST00000466152 | ENST00000479692 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
5UTR-intron | ENST00000466152 | ENST00000497750 | DPM1 | chr20 | 49574900 | - | CDKN2A | chr9 | 21968241 | - |
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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) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for DPM1-CDKN2A |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for DPM1-CDKN2A |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:49574900/:21968241) - 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 |
DPM1 | . |
FUNCTION: Transfers mannose from GDP-mannose to dolichol monophosphate to form dolichol phosphate mannose (Dol-P-Man) which is the mannosyl donor in pathways leading to N-glycosylation, glycosyl phosphatidylinositol membrane anchoring, and O-mannosylation of proteins; catalytic subunit of the dolichol-phosphate mannose (DPM) synthase complex. | 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 |
- 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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Fusion Gene Sequence for DPM1-CDKN2A |
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Fusion Gene PPI Analysis for DPM1-CDKN2A |
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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 |
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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 DPM1-CDKN2A |
![]() (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 DPM1-CDKN2A |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | DPM1 | C1837396 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie | 5 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | DPM1 | C4317224 | Congenital disorder of glycosylation type 1q | 1 | GENOMICS_ENGLAND |
Tgene | C1835044 | MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 | 13 | CTD_human;GENOMICS_ENGLAND;UNIPROT | |
Tgene | C1838547 | MELANOMA-PANCREATIC CANCER SYNDROME | 10 | CLINGEN;CTD_human | |
Tgene | C0024121 | Lung Neoplasms | 4 | CTD_human;UNIPROT | |
Tgene | C0242379 | Malignant neoplasm of lung | 4 | CTD_human | |
Tgene | C0011570 | Mental Depression | 3 | PSYGENET | |
Tgene | C0011581 | Depressive disorder | 3 | PSYGENET | |
Tgene | C0023903 | Liver neoplasms | 3 | CTD_human | |
Tgene | C0345904 | Malignant neoplasm of liver | 3 | CTD_human | |
Tgene | C0345967 | Malignant mesothelioma | 3 | CTD_human | |
Tgene | C1168401 | Squamous cell carcinoma of the head and neck | 3 | CTD_human | |
Tgene | C0005684 | Malignant neoplasm of urinary bladder | 2 | CTD_human | |
Tgene | C0005695 | Bladder Neoplasm | 2 | CTD_human;UNIPROT | |
Tgene | C0006118 | Brain Neoplasms | 2 | CTD_human | |
Tgene | C0006826 | Malignant Neoplasms | 2 | CGI;CTD_human | |
Tgene | C0007131 | Non-Small Cell Lung Carcinoma | 2 | CTD_human;UNIPROT | |
Tgene | C0017638 | Glioma | 2 | CGI;CTD_human | |
Tgene | C0023452 | Childhood Acute Lymphoblastic Leukemia | 2 | CTD_human;GENOMICS_ENGLAND | |
Tgene | C0025202 | melanoma | 2 | CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT | |
Tgene | C0027651 | Neoplasms | 2 | CTD_human | |
Tgene | C0030297 | Pancreatic Neoplasm | 2 | CGI;CTD_human;UNIPROT | |
Tgene | C0040715 | Chromosomal translocation | 2 | CTD_human | |
Tgene | C0041696 | Unipolar Depression | 2 | PSYGENET | |
Tgene | C0085390 | Li-Fraumeni Syndrome | 2 | ORPHANET | |
Tgene | C0086692 | Benign Neoplasm | 2 | CTD_human | |
Tgene | C0153633 | Malignant neoplasm of brain | 2 | CTD_human | |
Tgene | C0259783 | mixed gliomas | 2 | CTD_human | |
Tgene | C0346647 | Malignant neoplasm of pancreas | 2 | CGI;CTD_human | |
Tgene | C0496899 | Benign neoplasm of brain, unspecified | 2 | CTD_human | |
Tgene | C0555198 | Malignant Glioma | 2 | CTD_human | |
Tgene | C0750974 | Brain Tumor, Primary | 2 | CTD_human | |
Tgene | C0750977 | Recurrent Brain Neoplasm | 2 | CTD_human | |
Tgene | C0750979 | Primary malignant neoplasm of brain | 2 | CTD_human | |
Tgene | C1269683 | Major Depressive Disorder | 2 | PSYGENET | |
Tgene | C1527390 | Neoplasms, Intracranial | 2 | CTD_human | |
Tgene | C2239176 | Liver carcinoma | 2 | CTD_human | |
Tgene | C0001418 | Adenocarcinoma | 1 | CTD_human | |
Tgene | C0001624 | Adrenal Gland Neoplasms | 1 | CTD_human | |
Tgene | C0005940 | Bone Diseases | 1 | CTD_human | |
Tgene | C0006142 | Malignant neoplasm of breast | 1 | CTD_human | |
Tgene | C0006413 | Burkitt Lymphoma | 1 | ORPHANET | |
Tgene | C0007137 | Squamous cell carcinoma | 1 | CTD_human;UNIPROT | |
Tgene | C0008628 | Chromosome Deletion | 1 | CTD_human | |
Tgene | C0014859 | Esophageal Neoplasms | 1 | CTD_human;UNIPROT | |
Tgene | C0016325 | Fluoride Poisoning | 1 | CTD_human | |
Tgene | C0017601 | Glaucoma | 1 | CTD_human | |
Tgene | C0022783 | Vulvar Lichen Sclerosus | 1 | CTD_human | |
Tgene | C0023449 | Acute lymphocytic leukemia | 1 | GENOMICS_ENGLAND | |
Tgene | C0023453 | L2 Acute Lymphoblastic Leukemia | 1 | CTD_human | |
Tgene | C0024232 | Lymphatic Metastasis | 1 | CTD_human | |
Tgene | C0024299 | Lymphoma | 1 | CTD_human | |
Tgene | C0024623 | Malignant neoplasm of stomach | 1 | CTD_human | |
Tgene | C0025500 | Mesothelioma | 1 | CTD_human | |
Tgene | C0026640 | Mouth Neoplasms | 1 | CTD_human | |
Tgene | C0026764 | Multiple Myeloma | 1 | CTD_human | |
Tgene | C0027626 | Neoplasm Invasiveness | 1 | CTD_human | |
Tgene | C0027819 | Neuroblastoma | 1 | CTD_human | |
Tgene | C0032927 | Precancerous Conditions | 1 | CTD_human | |
Tgene | C0036920 | Sezary Syndrome | 1 | CTD_human | |
Tgene | C0038356 | Stomach Neoplasms | 1 | CTD_human | |
Tgene | C0040100 | Thymoma | 1 | CTD_human | |
Tgene | C0041107 | Trisomy | 1 | CTD_human | |
Tgene | C0042065 | Genitourinary Neoplasms | 1 | CTD_human | |
Tgene | C0079744 | Diffuse Large B-Cell Lymphoma | 1 | CTD_human | |
Tgene | C0079773 | Lymphoma, T-Cell, Cutaneous | 1 | CTD_human | |
Tgene | C0151779 | Cutaneous Melanoma | 1 | CGI;CTD_human | |
Tgene | C0153381 | Malignant neoplasm of mouth | 1 | CTD_human | |
Tgene | C0205641 | Adenocarcinoma, Basal Cell | 1 | CTD_human | |
Tgene | C0205642 | Adenocarcinoma, Oxyphilic | 1 | CTD_human | |
Tgene | C0205643 | Carcinoma, Cribriform | 1 | CTD_human | |
Tgene | C0205644 | Carcinoma, Granular Cell | 1 | CTD_human | |
Tgene | C0205645 | Adenocarcinoma, Tubular | 1 | CTD_human | |
Tgene | C0205969 | Thymic Carcinoma | 1 | CTD_human | |
Tgene | C0206686 | Adrenocortical carcinoma | 1 | CTD_human | |
Tgene | C0206727 | Nerve Sheath Tumors | 1 | CTD_human | |
Tgene | C0279626 | Squamous cell carcinoma of esophagus | 1 | CTD_human | |
Tgene | C0279628 | Adenocarcinoma Of Esophagus | 1 | CTD_human | |
Tgene | C0282313 | Condition, Preneoplastic | 1 | CTD_human | |
Tgene | C0376407 | Granulomatous Slack Skin | 1 | CTD_human | |
Tgene | C0546837 | Malignant neoplasm of esophagus | 1 | CTD_human | |
Tgene | C0596263 | Carcinogenesis | 1 | CTD_human | |
Tgene | C0677866 | Brain Stem Neoplasms | 1 | CTD_human | |
Tgene | C0678222 | Breast Carcinoma | 1 | CTD_human | |
Tgene | C0750887 | Adrenal Cancer | 1 | CTD_human | |
Tgene | C0751569 | Genitourinary Cancer | 1 | CTD_human | |
Tgene | C0751606 | Adult Acute Lymphocytic Leukemia | 1 | GENOMICS_ENGLAND | |
Tgene | C0751689 | Peripheral Nerve Sheath Neoplasm | 1 | CTD_human | |
Tgene | C0751691 | Perineurioma | 1 | CTD_human | |
Tgene | C0751886 | Brain Stem Neoplasms, Primary | 1 | CTD_human | |
Tgene | C0751887 | Medullary Neoplasms | 1 | CTD_human | |
Tgene | C0751888 | Mesencephalic Neoplasms | 1 | CTD_human | |
Tgene | C0751889 | Pontine Tumors | 1 | CTD_human | |
Tgene | C0887833 | Carcinoma, Pancreatic Ductal | 1 | CTD_human | |
Tgene | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human | |
Tgene | C1292769 | Precursor B-cell lymphoblastic leukemia | 1 | ORPHANET | |
Tgene | C1297882 | Partial Trisomy | 1 | CTD_human | |
Tgene | C1449861 | Micronuclei, Chromosome-Defective | 1 | CTD_human | |
Tgene | C1449862 | Micronuclei, Genotoxicant-Induced | 1 | CTD_human | |
Tgene | C1458155 | Mammary Neoplasms | 1 | CTD_human | |
Tgene | C1708349 | Hereditary Diffuse Gastric Cancer | 1 | CTD_human | |
Tgene | C1835042 | Melanoma astrocytoma syndrome | 1 | CTD_human;ORPHANET | |
Tgene | C1961099 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 1 | ORPHANET | |
Tgene | C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | 1 | CTD_human | |
Tgene | C2314896 | Familial Atypical Mole Melanoma Syndrome | 1 | ORPHANET | |
Tgene | C2930745 | Partial Monosomy | 1 | CTD_human | |
Tgene | C2931038 | Pancreatic carcinoma, familial | 1 | ORPHANET | |
Tgene | C2931822 | Nasopharyngeal carcinoma | 1 | CTD_human | |
Tgene | C4283859 | Cutaneous Malignant Melanoma 2 | 1 | GENOMICS_ENGLAND | |
Tgene | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human | |
Tgene | C4721453 | Peripheral Nervous System Diseases | 1 | CTD_human |