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Fusion Protein:NF1-CCDC47 |
Fusion Gene and Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: NF1-CCDC47 | FusionPDB ID: 58675 | FusionGDB2.0 ID: 58675 | Hgene | Tgene | Gene symbol | NF1 | CCDC47 | Gene ID | 4763 | 57003 |
| Gene name | neurofibromin 1 | coiled-coil domain containing 47 | |
| Synonyms | NFNS|VRNF|WSS | GK001|MSTP041|THNS | |
| Cytomap | 17q11.2 | 17q23.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | neurofibrominneurofibromatosis 1neurofibromatosis-related protein NF-1truncated neurofibromin 1 | coiled-coil domain-containing protein 47Calumin | |
| Modification date | 20200322 | 20200313 | |
| UniProtAcc | P21359 Main function of 5'-partner protein: FUNCTION: Stimulates the GTPase activity of Ras. NF1 shows greater affinity for Ras GAP, but lower specific activity. May be a regulator of Ras activity. {ECO:0000269|PubMed:2121371, ECO:0000269|PubMed:8417346}. | Q96A33 Main function of 5'-partner protein: FUNCTION: Component of the PAT complex, an endoplasmic reticulum (ER)-resident membrane multiprotein complex that facilitates multi-pass membrane proteins insertion into membranes (PubMed:32814900). The PAT complex acts as an intramembrane chaperone by directly interacting with nascent transmembrane domains (TMDs), releasing its substrates upon correct folding, and is needed for optimal biogenesis of multi-pass membrane proteins (PubMed:32814900). WDR83OS/Asterix is the substrate-interacting subunit of the PAT complex, whereas CCDC47 is required to maintain the stability of WDR83OS/Asterix (PubMed:32814900). The PAT complex favors the binding to TMDs with exposed hydrophilic amino acids within the lipid bilayer and provides a membrane-embedded partially hydrophilic environment in which the first transmembrane domain binds (PubMed:32814900). Component of a ribosome-associated ER translocon complex involved in multi-pass membrane protein transport into the ER membrane and biogenesis (PubMed:32820719). Involved in the regulation of calcium ion homeostasis in the ER (PubMed:30401460). Required for proper protein degradation via the ERAD (ER-associated degradation) pathway (PubMed:25009997). Has an essential role in the maintenance of ER organization during embryogenesis (By similarity). {ECO:0000250|UniProtKB:Q9D024, ECO:0000269|PubMed:25009997, ECO:0000269|PubMed:30401460, ECO:0000269|PubMed:32814900, ECO:0000269|PubMed:32820719}. | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000358273, ENST00000356175, ENST00000417592, ENST00000431387, ENST00000444181, ENST00000581113, | ENST00000582252, ENST00000403162, ENST00000225726, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 47 X 26 X 21=25662 | 8 X 7 X 5=280 |
| # samples | 69 | 8 | |
| ** MAII score | log2(69/25662*10)=-5.21689344093196 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/280*10)=-1.8073549220576 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Fusion gene context | PubMed: NF1 [Title/Abstract] AND CCDC47 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Fusion neoantigen context | PubMed: NF1 [Title/Abstract] AND CCDC47 [Title/Abstract] AND neoantigen [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | NF1(29580018)-CCDC47(61824321), # samples:2 | ||
| Anticipated loss of major functional domain due to fusion event. | NF1-CCDC47 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. NF1-CCDC47 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. NF1-CCDC47 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. NF1-CCDC47 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. NF1-CCDC47 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. NF1-CCDC47 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF. NF1-CCDC47 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) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Hgene | NF1 | GO:0043547 | positive regulation of GTPase activity | 2121371 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr17:29580018/chr17:61824321) - 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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| Retention analysis results of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features, are available here. |
| Fusion gene breakpoints across NF1 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across CCDC47 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Amino Acid Sequences |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000358273 | NF1 | chr17 | 29580018 | + | ENST00000225726 | CCDC47 | chr17 | 61824321 | - | 6268 | 4556 | 254 | 4636 | 1460 |
| DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
| ENST00000358273 | ENST00000225726 | NF1 | chr17 | 29580018 | + | CCDC47 | chr17 | 61824321 | - | 0.000278003 | 0.99972194 |
| Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones. |
Get the fusion protein sequences from here. |
| Fusion protein sequence information is available in the fasta format. >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP |
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Fusion Protein Breakpoint Sequences for NF1-CCDC47 |
| +/-13 AA sequence from the breakpoints of the fusion protein sequences. |
| Hgene | Hchr | Hbp | Tgene | Tchr | Tbp | Length(fusion protein) | BP in fusion protein | Peptide |
| NF1 | chr17 | 29580018 | CCDC47 | chr17 | 61824321 | 4556 | 1434 | KATVKEKKENKKSEAALRREQKKLEK |
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Potential FusionNeoAntigen Information of NF1-CCDC47 in HLA I |
| Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific. |
| NF1-CCDC47_29580018_61824321.msa |
| Potential FusionNeoAntigen Information * We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5) |
| Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA I | FusionNeoAntigen peptide | Binding score | Immunogenic score | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B45:01 | KENKKSEAA | 0.9907 | 0.8534 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B50:02 | KENKKSEAA | 0.9639 | 0.7063 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B41:01 | KENKKSEAA | 0.5766 | 0.89 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B50:01 | KENKKSEAA | 0.1923 | 0.7214 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B39:13 | KENKKSEAAL | 0.8533 | 0.8682 | 7 | 17 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B41:01 | KKENKKSEAA | 0.5733 | 0.8636 | 6 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B45:01 | KKENKKSEAA | 0.506 | 0.8248 | 6 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B40:06 | KENKKSEAA | 0.9971 | 0.559 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B14:03 | ENKKSEAAL | 0.6559 | 0.6948 | 8 | 17 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B39:08 | KENKKSEAAL | 0.9297 | 0.8682 | 7 | 17 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B08:12 | ENKKSEAAL | 0.8174 | 0.5217 | 8 | 17 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B41:03 | KENKKSEAA | 0.5453 | 0.5635 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B50:05 | KENKKSEAA | 0.1923 | 0.7214 | 7 | 16 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | HLA-B50:04 | KENKKSEAA | 0.1923 | 0.7214 | 7 | 16 |
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Potential FusionNeoAntigen Information of NF1-CCDC47 in HLA II |
| Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific. |
| NF1-CCDC47_29580018_61824321.msa |
| Potential FusionNeoAntigen Information * We used NetMHCIIpan v4.1 (%rank<0.5). |
| Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA II | FusionNeoAntigen peptide | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | DRB1-1381 | KSEAALRREQKKLEK | 11 | 26 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | DRB1-1389 | KSEAALRREQKKLEK | 11 | 26 |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 | DRB1-1394 | KSEAALRREQKKLEK | 11 | 26 |
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Fusion breakpoint peptide structures of NF1-CCDC47 |
| 3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens * The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA. |
| File name | BPseq | Hgene | Tgene | Hchr | Hbp | Tchr | Tbp | AAlen |
| 4332 | KKENKKSEAALRRE | NF1 | CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 4556 |
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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NF1-CCDC47 |
| Virtual screening between 25 HLAs (from PDB) and FusionNeoAntigens * We used Glide to predict the interaction between HLAs and neoantigens. |
| HLA allele | PDB ID | File name | BPseq | Docking score | Glide score |
| HLA-B14:02 | 3BVN | 4332 | KKENKKSEAALRRE | -7.15543 | -7.26883 |
| HLA-B14:02 | 3BVN | 4332 | KKENKKSEAALRRE | -4.77435 | -5.80965 |
| HLA-B52:01 | 3W39 | 4332 | KKENKKSEAALRRE | -6.80875 | -6.92215 |
| HLA-B52:01 | 3W39 | 4332 | KKENKKSEAALRRE | -4.20386 | -5.23916 |
| HLA-A11:01 | 4UQ2 | 4332 | KKENKKSEAALRRE | -7.5194 | -8.5547 |
| HLA-A11:01 | 4UQ2 | 4332 | KKENKKSEAALRRE | -6.9601 | -7.0735 |
| HLA-A24:02 | 5HGA | 4332 | KKENKKSEAALRRE | -7.52403 | -7.63743 |
| HLA-A24:02 | 5HGA | 4332 | KKENKKSEAALRRE | -5.82433 | -6.85963 |
| HLA-B27:05 | 6PYJ | 4332 | KKENKKSEAALRRE | -3.28285 | -4.31815 |
| HLA-B44:05 | 3DX8 | 4332 | KKENKKSEAALRRE | -5.91172 | -6.94702 |
| HLA-B44:05 | 3DX8 | 4332 | KKENKKSEAALRRE | -4.24346 | -4.35686 |
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Vaccine Design for the FusionNeoAntigens of NF1-CCDC47 |
| mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is. |
| Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide sequence | FusionNeoAntigen RNA sequence |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 6 | 16 | KKENKKSEAA | AAAAAGGAAAACAAAAAATCAGAGGCTGCA |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 7 | 16 | KENKKSEAA | AAGGAAAACAAAAAATCAGAGGCTGCA |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 7 | 17 | KENKKSEAAL | AAGGAAAACAAAAAATCAGAGGCTGCATTG |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 8 | 17 | ENKKSEAAL | GAAAACAAAAAATCAGAGGCTGCATTG |
| mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs. |
| Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide | FusionNEoAntigen RNA sequence |
| NF1-CCDC47 | chr17 | 29580018 | chr17 | 61824321 | 11 | 26 | KSEAALRREQKKLEK | AAATCAGAGGCTGCATTGAGGCGTGAGCAAAAGAAGTTGGAAAAG |
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Information of the samples that have these potential fusion neoantigens of NF1-CCDC47 |
| These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens. |
| Cancer type | Fusion gene | Hchr | Hbp | Henst | Tchr | Tbp | Tenst | Sample |
| HNSC | NF1-CCDC47 | chr17 | 29580018 | ENST00000358273 | chr17 | 61824321 | ENST00000225726 | TCGA-CQ-7069 |
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Potential target of CAR-T therapy development for NF1-CCDC47 |
| Predicted 3D structure. We used RoseTTAFold. |
| Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features * Minus value of BPloci means that the break point is located before the CDS. |
| - In-frame and retained 'Transmembrane'. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| Tgene | CCDC47 | chr17:29580018 | chr17:61824321 | ENST00000582252 | 0 | 12 | 136_155 | 0 | 481.0 | Transmembrane | Helical |
| Subcellular localization prediction of the transmembrane domain retained fusion proteins * We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image. |
| Hgene | Hchr | Hbp | Henst | Tgene | Tchr | Tbp | Tenst | DeepLoc result |
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Related Drugs to NF1-CCDC47 |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to NF1-CCDC47 |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | NF1 | C0027831 | Neurofibromatosis 1 | 44 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Hgene | NF1 | C1708353 | Hereditary Paraganglioma-Pheochromocytoma Syndrome | 10 | CLINGEN |
| Hgene | NF1 | C0349639 | Juvenile Myelomonocytic Leukemia | 7 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
| Hgene | NF1 | C2931482 | Neurofibromatosis-Noonan syndrome | 6 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
| Hgene | NF1 | C0553586 | Cafe-au-lait macules with pulmonary stenosis | 5 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
| Hgene | NF1 | C0162678 | Neurofibromatoses | 3 | CGI;CTD_human;GENOMICS_ENGLAND |
| Hgene | NF1 | C0004114 | Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0023467 | Leukemia, Myelocytic, Acute | 2 | CTD_human |
| Hgene | NF1 | C0025202 | melanoma | 2 | CGI;CTD_human |
| Hgene | NF1 | C0026998 | Acute Myeloid Leukemia, M1 | 2 | CTD_human |
| Hgene | NF1 | C0205768 | Subependymal Giant Cell Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0206727 | Nerve Sheath Tumors | 2 | CTD_human |
| Hgene | NF1 | C0280783 | Juvenile Pilocytic Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0280785 | Diffuse Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0334579 | Anaplastic astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0334580 | Protoplasmic astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0334581 | Gemistocytic astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0334582 | Fibrillary Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0334583 | Pilocytic Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0338070 | Childhood Cerebral Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0547065 | Mixed oligoastrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0750935 | Cerebral Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0750936 | Intracranial Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C0751689 | Peripheral Nerve Sheath Neoplasm | 2 | CTD_human |
| Hgene | NF1 | C0751691 | Perineurioma | 2 | CTD_human |
| Hgene | NF1 | C1704230 | Grade I Astrocytoma | 2 | CTD_human |
| Hgene | NF1 | C1834235 | NEUROFIBROMATOSIS, FAMILIAL SPINAL | 2 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Hgene | NF1 | C1879321 | Acute Myeloid Leukemia (AML-M2) | 2 | CTD_human |
| Hgene | NF1 | C0001430 | Adenoma | 1 | CTD_human |
| Hgene | NF1 | C0004352 | Autistic Disorder | 1 | CTD_human |
| Hgene | NF1 | C0016057 | Fibrosarcoma | 1 | CTD_human |
| Hgene | NF1 | C0017636 | Glioblastoma | 1 | CTD_human |
| Hgene | NF1 | C0017638 | Glioma | 1 | CGI;CTD_human |
| Hgene | NF1 | C0020796 | Profound Mental Retardation | 1 | CTD_human |
| Hgene | NF1 | C0023186 | Learning Disorders | 1 | CTD_human |
| Hgene | NF1 | C0023827 | liposarcoma | 1 | CTD_human |
| Hgene | NF1 | C0025363 | Mental Retardation, Psychosocial | 1 | CTD_human |
| Hgene | NF1 | C0026654 | Moyamoya Disease | 1 | GENOMICS_ENGLAND |
| Hgene | NF1 | C0027809 | Neurilemmoma | 1 | CTD_human |
| Hgene | NF1 | C0027830 | neurofibroma | 1 | CTD_human |
| Hgene | NF1 | C0027962 | Melanocytic nevus | 1 | CTD_human |
| Hgene | NF1 | C0028326 | Noonan Syndrome | 1 | GENOMICS_ENGLAND |
| Hgene | NF1 | C0031511 | Pheochromocytoma | 1 | CTD_human |
| Hgene | NF1 | C0035320 | Retinal Neovascularization | 1 | CTD_human |
| Hgene | NF1 | C0205646 | Adenoma, Basal Cell | 1 | CTD_human |
| Hgene | NF1 | C0205647 | Follicular adenoma | 1 | CTD_human |
| Hgene | NF1 | C0205648 | Adenoma, Microcystic | 1 | CTD_human |
| Hgene | NF1 | C0205649 | Adenoma, Monomorphic | 1 | CTD_human |
| Hgene | NF1 | C0205650 | Papillary adenoma | 1 | CTD_human |
| Hgene | NF1 | C0205651 | Adenoma, Trabecular | 1 | CTD_human |
| Hgene | NF1 | C0205824 | Liposarcoma, Dedifferentiated | 1 | CTD_human |
| Hgene | NF1 | C0205825 | Liposarcoma, Pleomorphic | 1 | CTD_human |
| Hgene | NF1 | C0205944 | Sarcoma, Epithelioid | 1 | CTD_human |
| Hgene | NF1 | C0205945 | Sarcoma, Spindle Cell | 1 | CTD_human |
| Hgene | NF1 | C0259783 | mixed gliomas | 1 | CTD_human |
| Hgene | NF1 | C0334588 | Giant Cell Glioblastoma | 1 | CTD_human |
| Hgene | NF1 | C0555198 | Malignant Glioma | 1 | CTD_human |
| Hgene | NF1 | C0751262 | Adult Learning Disorders | 1 | CTD_human |
| Hgene | NF1 | C0751263 | Learning Disturbance | 1 | CTD_human |
| Hgene | NF1 | C0751265 | Learning Disabilities | 1 | CTD_human |
| Hgene | NF1 | C0751374 | Schwannomatosis, Plexiform | 1 | CTD_human |
| Hgene | NF1 | C0917816 | Mental deficiency | 1 | CTD_human |
| Hgene | NF1 | C0917817 | Neurofibromatosis 3 | 1 | CTD_human |
| Hgene | NF1 | C1257877 | Pheochromocytoma, Extra-Adrenal | 1 | CTD_human |
| Hgene | NF1 | C1261473 | Sarcoma | 1 | CTD_human |
| Hgene | NF1 | C1330966 | Developmental Academic Disorder | 1 | CTD_human |
| Hgene | NF1 | C1370889 | Liposarcoma, well differentiated | 1 | CTD_human |
| Hgene | NF1 | C1621958 | Glioblastoma Multiforme | 1 | CTD_human |
| Hgene | NF1 | C3150928 | NF1 Microdeletion Syndrome | 1 | ORPHANET |
| Hgene | NF1 | C3714756 | Intellectual Disability | 1 | CTD_human |
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