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Fusion gene ID: 26250 |
FusionGeneSummary for PCM1_NRG1 |
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Fusion gene information | Fusion gene name: PCM1_NRG1 | Fusion gene ID: 26250 | Hgene | Tgene | Gene symbol | PCM1 | NRG1 | Gene ID | 5108 | 3084 |
Gene name | pericentriolar material 1 | neuregulin 1 | |
Synonyms | PTC4|RET/PCM-1 | ARIA|GGF|GGF2|HGL|HRG|HRG1|HRGA|MST131|MSTP131|NDF|NRG1-IT2|SMDF | |
Cytomap | 8p22 | 8p12 | |
Type of gene | protein-coding | protein-coding | |
Description | pericentriolar material 1 proteinPCM-1hPCM-1pericentriolar material 1, PCM1 | pro-neuregulin-1, membrane-bound isoformacetylcholine receptor-inducing activityglial growth factor 2heregulin, alpha (45kD, ERBB2 p185-activator)neu differentiation factorpro-NRG1sensory and motor neuron derived factor | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q15154 | Q02297 | |
Ensembl transtripts involved in fusion gene | ENST00000325083, ENST00000519253, ENST00000524226, ENST00000518537, ENST00000518936, ENST00000327578, | ENST00000519301, ENST00000520407, ENST00000523079, ENST00000338921, ENST00000356819, ENST00000287845, ENST00000341377, ENST00000287842, ENST00000521670, ENST00000405005, ENST00000520502, ENST00000539990, ENST00000523681, | |
Fusion gene scores | * DoF score | 8 X 7 X 5=280 | 16 X 6 X 11=1056 |
# samples | 8 | 16 | |
** MAII score | log2(8/280*10)=-1.8073549220576 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(16/1056*10)=-2.72246602447109 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: PCM1 [Title/Abstract] AND NRG1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | NRG1 | GO:0003222 | ventricular trabecula myocardium morphogenesis | 17336907 |
Tgene | NRG1 | GO:0038127 | ERBB signaling pathway | 11389077 |
Tgene | NRG1 | GO:0038129 | ERBB3 signaling pathway | 27353365 |
Tgene | NRG1 | GO:0043497 | regulation of protein heterodimerization activity | 10559227 |
Tgene | NRG1 | GO:0045892 | negative regulation of transcription, DNA-templated | 15073182 |
Tgene | NRG1 | GO:0051048 | negative regulation of secretion | 10559227 |
Tgene | NRG1 | GO:0060379 | cardiac muscle cell myoblast differentiation | 17336907 |
Tgene | NRG1 | GO:0060956 | endocardial cell differentiation | 17336907 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | KIRC | TCGA-B8-5553-01A | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
5UTR-3CDS | ENST00000325083 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000325083 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000325083 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000325083 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000325083 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000325083 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3CDS | ENST00000519253 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000519253 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000519253 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000519253 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000519253 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000519253 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3CDS | ENST00000524226 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000524226 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000524226 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000524226 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000524226 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000524226 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3CDS | ENST00000518537 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000518537 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000518537 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000518537 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-3UTR | ENST00000518537 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
5UTR-intron | ENST00000518537 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-3CDS | ENST00000518936 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-3UTR | ENST00000518936 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-3UTR | ENST00000518936 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-3UTR | ENST00000518936 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-3UTR | ENST00000518936 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
3UTR-intron | ENST00000518936 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-3CDS | ENST00000327578 | ENST00000519301 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000520407 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000523079 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000338921 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000356819 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000287845 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-3UTR | ENST00000327578 | ENST00000341377 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-3UTR | ENST00000327578 | ENST00000287842 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-3UTR | ENST00000327578 | ENST00000521670 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-3UTR | ENST00000327578 | ENST00000405005 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000520502 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000539990 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
intron-intron | ENST00000327578 | ENST00000523681 | PCM1 | chr8 | 17782289 | + | NRG1 | chr8 | 32611890 | + |
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FusionProtFeatures for PCM1_NRG1 |
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Hgene | Tgene |
PCM1 | NRG1 |
![]() * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for PCM1_NRG1 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for PCM1_NRG1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
PCM1 | BBS4, KRT15, ING5, KIAA0368, KRT19, CCDC53, ABI2, EXOC8, EPS8, CEP72, PCNT, HAP1, EWSR1, HNRNPUL1, CLTC, MIB1, FUS, CEP131, PPIB, SIRT7, NEURL4, PAN2, CASK, E2F4, YWHAQ, LATS2, SAV1, CEP250, HAUS2, OBSL1, CCDC8, CSPP1, CCDC183, SLC25A41, SSFA2, RASSF8, RASSF7, IFT81, NTRK1, BTRC, MED4, HERC2, AHI1, CEP162, RPGRIP1L, CC2D2A, CEP128, LCA5, OFD1, CCDC138, CEP170, PIBF1, SSX2IP, WRAP73, HAUS1, HAUS4, KIAA0753, CCDC77, CCNB2, CEP350, CEP95, CSNK1A1, DSP, KIF20A, LUZP1, MCM10, MCRS1, MPRIP, NDC80, SMARCD2, TPGS1, SUPT5H, SSBP1, KIF7, SKA1, TSPYL1, SREK1IP1, CSNK1D, IFT172, CEP55, IFT20, CCDC14, HMMR, CFAP97, IPO5, KCTD12, SNRPE, SPICE1, ABCD3, ACOT9, ATP5L, CAMSAP1, CC2D1A, CCDC66, CEP120, CKAP2, FGFR1OP, HAUS3, HAUS5, HAUS6, HAUS7, HAUS8, IDH3B, IFT57, IFT74, NCKAP5L, RAE1, STAU1, TP53BP2, TTK, TXLNA, TXLNG, TBC1D31, WDR83, XRN1, ZNF280C, ACTR2, ANKRD26, BAIAP2, BICD1, BICD2, BTF3, C11orf49, KNSTRN, C2CD3, CAMSAP2, CCDC112, CCDC18, CCDC22, CCDC85C, CCDC92, CCNB1, CCP110, CDC123, CEP164, CEP192, CEP57L1, CEP63, CEP85, CEP89, CEP97, CKAP2L, CNOT10, COMMD2, COMMD4, CSNK1E, DAPK3, DIAPH3, ERC1, EXOC4, FOPNL, GNAO1, GPATCH1, IBTK, IQCB1, KIAA1328, KIF14, LRRC49, LRRCC1, MAGED1, MAP7D3, MED29, MIS18A, MIS18BP1, MOB4, MPHOSPH9, MYO9A, NAV1, NEDD1, NME7, NOL11, NUF2, ODF2L, ODF2, PCBP3, PKN2, PLK1, KIZ, PPP1R9B, IFT22, RRM2, SCLT1, SDCCAG3, SECISBP2, SMG5, SMG7, SPATA24, SPATS2, SPC24, SRGAP2, STRN4, TANC1, TCHP, TEX9, TNIP1, TRAF3IP1, TTC12, TTF2, TTLL4, TTLL5, CEP104, CEP290, CEP152, CEP135, CNTRL, FBF1, NINL, NIN, POC5, SASS6, RPGRIP1, STIL, CENPJ, CENPE, PPP2CA, PRKAR2B, DYNLL1, MAPRE1, SLAIN2, CEP170P1, PPP2R3C, YWHAE, YWHAZ, MTMR7, C6orf118, BIN3, CCDC172, LPXN, FAM81B, COG5, ING2, CCDC65, LCA5L, CCDC40, DKK3, NECAB2, ATG14, TSC1, RNF168 | NRG1 | LIMK1, ERBB3, ERBB2, EGFR, ERBB4, MBOAT7, LSR, PGAP1, KIAA2013, SREBF2, LEMD3, TMTC3, TMTC4, POMGNT2, SLC38A10, ATP7B, SLC35B2, NDUFA3, ZDHHC17, TMEM39B, DNAAF5, B3GNT2, RHOBTB3, CISD2, POMT1, SPTLC2, SLC25A16, RDH11, MGAT1, HMOX1, KIAA1467, EXTL3, SLC25A23, NETO2, LPHN1, CNTNAP3, HLA-DPB1, UQCRQ, GLMN, DEGS1, TMEM63B, DDX11L8, ABCB10, GYLTL1B, B3GALNT2, TMEM181, INTS7, MYO19, GALNT11, C1GALT1C1, SLC22A18, NEK4, ABCA3, TMEM164, MTCH1, OPA3, HS6ST1, SFXN3, TM2D3, DSE, TMEM205, RNF130, PIGU, CDC5L, LGR4, TUBB3 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for PCM1_NRG1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for PCM1_NRG1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | PCM1 | C0036341 | Schizophrenia | 1 | CTD_human |
Tgene | NRG1 | C0036341 | Schizophrenia | 7 | CTD_human |
Tgene | NRG1 | C0005586 | Bipolar Disorder | 5 | PSYGENET |
Tgene | NRG1 | C0024809 | Marijuana Abuse | 3 | PSYGENET |
Tgene | NRG1 | C0011570 | Mental Depression | 2 | PSYGENET |
Tgene | NRG1 | C0011581 | Depressive disorder | 2 | PSYGENET |
Tgene | NRG1 | C0006870 | Cannabis Dependence | 1 | PSYGENET |
Tgene | NRG1 | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
Tgene | NRG1 | C0011616 | Contact Dermatitis | 1 | CTD_human |
Tgene | NRG1 | C0018801 | Heart failure | 1 | CTD_human |
Tgene | NRG1 | C0019569 | Hirschsprung Disease | 1 | CTD_human |
Tgene | NRG1 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Tgene | NRG1 | C0026650 | Movement Disorders | 1 | CTD_human |
Tgene | NRG1 | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Tgene | NRG1 | C0030193 | Pain | 1 | CTD_human |
Tgene | NRG1 | C0032460 | Polycystic Ovary Syndrome | 1 | CTD_human |
Tgene | NRG1 | C0033937 | Psychoses, Drug | 1 | PSYGENET |
Tgene | NRG1 | C0038358 | Gastric ulcer | 1 | CTD_human |
Tgene | NRG1 | C0236733 | Amphetamine-Related Disorders | 1 | CTD_human |
Tgene | NRG1 | C1458155 | Mammary Neoplasms | 1 | CTD_human |
Tgene | NRG1 | C3495559 | Juvenile arthritis | 1 | CTD_human |