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Fusion gene ID: 23733 |
FusionGeneSummary for NCOR2_FMR1NB |
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Fusion gene information | Fusion gene name: NCOR2_FMR1NB | Fusion gene ID: 23733 | Hgene | Tgene | Gene symbol | NCOR2 | FMR1NB | Gene ID | 9612 | 158521 |
Gene name | nuclear receptor corepressor 2 | FMR1 neighbor | |
Synonyms | CTG26|N-CoR2|SMAP270|SMRT|SMRTE|SMRTE-tau|TNRC14|TRAC|TRAC-1|TRAC1 | CT37|NY-SAR-35|NYSAR35 | |
Cytomap | 12q24.31 | Xq27.3-q28 | |
Type of gene | protein-coding | protein-coding | |
Description | nuclear receptor corepressor 2CTG repeat protein 26T3 receptor-associating factorsilencing mediator for retinoid and thyroid hormone receptorsthyroid-, retinoic-acid-receptor-associated corepressor | fragile X mental retardation 1 neighbor proteincancer/testis antigen 37sarcoma antigen NY-SAR-35 | |
Modification date | 20180527 | 20180519 | |
UniProtAcc | Q9Y618 | Q8N0W7 | |
Ensembl transtripts involved in fusion gene | ENST00000405201, ENST00000404621, ENST00000404121, ENST00000356219, ENST00000397355, ENST00000429285, | ENST00000370467, | |
Fusion gene scores | * DoF score | 18 X 20 X 15=5400 | 1 X 1 X 1=1 |
# samples | 30 | 1 | |
** MAII score | log2(30/5400*10)=-4.16992500144231 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: NCOR2 [Title/Abstract] AND FMR1NB [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 |
![]() (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-B0-4699-01A | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
* 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 |
In-frame | ENST00000405201 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
Frame-shift | ENST00000404621 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
Frame-shift | ENST00000404121 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
Frame-shift | ENST00000356219 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
Frame-shift | ENST00000397355 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
Frame-shift | ENST00000429285 | ENST00000370467 | NCOR2 | chr12 | 124882665 | - | FMR1NB | chrX | 147084721 | + |
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FusionProtFeatures for NCOR2_FMR1NB |
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Hgene | Tgene |
NCOR2 | FMR1NB |
Transcriptional corepressor. Mediates thetranscriptional repression activity of some nuclear receptors bypromoting chromatin condensation, thus preventing access of thebasal transcription. Isoform 1 and isoform 5 have differentaffinities for different nuclear receptors. Involved in theregulation BCL6-dependent of the germinal center (GC) reactions,mainly through the control of the GC B-cells proliferation andsurvival. {ECO:0000269|PubMed:18212045,ECO:0000269|PubMed:23911289}. |
![]() * 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 |
Hgene | NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 174_215 | 625 | 2522 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 522_561 | 625 | 2522 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 494_510 | 625 | 2522 | Compositional bias | Note=Poly-Gln |
Hgene | NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 427_478 | 625 | 2522 | Domain | SANT 1 |
Tgene | >FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 125_184 | 92 | 194 | Domain | Note=P-type |
Tgene | >FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 205_255 | 92 | 194 | Topological domain | Cytoplasmic |
Tgene | >FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 90_183 | 92 | 194 | Topological domain | Extracellular |
Tgene | >FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 184_204 | 92 | 194 | Transmembrane | Helical |
- 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 | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 1392_1397 | 625 | 2522 | Compositional bias | Note=Poly-Pro |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 1850_1854 | 625 | 2522 | Compositional bias | Note=Poly-Gly |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 2487_2490 | 625 | 2522 | Compositional bias | Note=Poly-Pro |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 682_685 | 625 | 2522 | Compositional bias | Note=Poly-Lys |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 778_820 | 625 | 2522 | Compositional bias | Note=Pro-rich |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 995_1003 | 625 | 2522 | Compositional bias | Note=Poly-Pro |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 610_661 | 625 | 2522 | Domain | SANT 2 |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 2147_2151 | 625 | 2522 | Motif | Note=CORNR box of ID1 |
Hgene | >NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 2350_2354 | 625 | 2522 | Motif | Note=CORNR box of ID2 |
Tgene | FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 1_68 | 92 | 194 | Topological domain | Cytoplasmic |
Tgene | FMR1NB | chr12:124882665 | chrX:147084721 | ENST00000370467 | + | 0 | 6 | 69_89 | 92 | 194 | Transmembrane | Helical |
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FusionGeneSequence for NCOR2_FMR1NB |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_NCOR2_ENST00000405201_chr12_124882665_-_FMR1NB_ENST00000370467_chrX_147084721_+_789aa MSGSTQPVAQTWRATEPRYPPHSLSYPVQIARTHTDVGLLEYQHHSRDYASHLSPGSIIQPQRRRPSLLSEFQPGNERSQELHLRPESHS YLPELGKSEMEFIESKRPRLELLPDPLLRPSPLLATGQPAGSEDLTKDRSLTGKLEPVSPPSPPHTDPELELVPPRLSKEELIQNMDRVD REITMVEQQISKLKKKQQQLEEEAAKPPEPEKPVSPPPIESKHRSLVQIIYDENRKKAEAAHRILEGLGPQVELPLYNQPSDTRQYHENI KINQAMRKKLILYFKRRNHARKQWEQKFCQRYDQLMEAWEKKVERIENNPRRRAKESKVREYYEKQFPEIRKQRELQERMQSRVGQRGSG LSMSAARSEHEVSEIIDGLSEQENLEKQMRQLAVIPPMLYDADQQRIKFINMNGLMADPMKVYKDRQVMNMWSEQEKETFREKFMQHPKN FGLIASFLERKTVAECVLYYYLTKKNENYKSLVRRSYRRRGKSQQQQQQQQQQQQQQQQQPMPRSSQEEKDEKEKEKEAEKEEEKPEVEN DKEDLLKEKTDDTSGEDNDEKEAVASKGRKTANSQGRRKGRITRSMANEANSEEAITPQQSAELASMELNESSRWTEEEMETAKKGSSYF VLANGHILPNSENAHGQSLEEDSALEALLNFFFPTTCNLRENQVAKPCNELQDLSESECLRHKCCFSSSGTTSFKCFAPFRDVPKQMMQM |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_NCOR2_ENST00000405201_chr12_124882665_-_FMR1NB_ENST00000370467_chrX_147084721_+_2367nt ATGTCGGGATCCACACAGCCTGTGGCACAGACGTGGAGGGCCACTGAGCCCCGCTACCCGCCCCACAGCCTTTCCTACCCAGTGCAGATC GCCCGGACGCACACGGACGTCGGGCTCCTGGAGTACCAGCACCACTCCCGCGACTATGCCTCCCACCTGTCGCCCGGCTCCATCATCCAG CCCCAGCGGCGGAGGCCCTCCCTGCTGTCTGAGTTCCAGCCCGGGAATGAACGGTCCCAGGAGCTCCACCTGCGGCCAGAGTCCCACTCA TACCTGCCCGAGCTGGGGAAGTCAGAGATGGAGTTCATTGAAAGCAAGCGCCCTCGGCTAGAGCTGCTGCCTGACCCCCTGCTGCGACCG TCACCCCTGCTGGCCACGGGCCAGCCTGCGGGATCTGAAGACCTCACCAAGGACCGTAGCCTGACGGGCAAGCTGGAACCGGTGTCTCCC CCCAGCCCCCCGCACACTGACCCTGAGCTGGAGCTGGTGCCGCCACGGCTGTCCAAGGAGGAGCTGATCCAGAACATGGACCGCGTGGAC CGAGAGATCACCATGGTAGAGCAGCAGATCTCTAAGCTGAAGAAGAAGCAGCAACAGCTGGAGGAGGAGGCTGCCAAGCCGCCCGAGCCT GAGAAGCCCGTGTCACCGCCGCCCATCGAGTCGAAGCACCGCAGCCTGGTGCAGATCATCTACGACGAGAACCGGAAGAAGGCTGAAGCT GCACATCGGATTCTGGAAGGCCTGGGGCCCCAGGTGGAGCTGCCGCTGTACAACCAGCCCTCCGACACCCGGCAGTATCATGAGAACATC AAAATAAACCAGGCGATGCGGAAGAAGCTAATCTTGTACTTCAAGAGGAGGAATCACGCTCGGAAACAATGGGAGCAGAAGTTCTGCCAG CGCTATGACCAGCTCATGGAGGCCTGGGAGAAGAAGGTGGAGCGCATCGAGAACAACCCCCGGCGGCGGGCCAAGGAGAGCAAGGTGCGC GAGTACTACGAGAAGCAGTTCCCTGAGATCCGCAAGCAGCGCGAGCTGCAGGAGCGCATGCAGAGCAGGGTGGGCCAGCGGGGCAGTGGG CTGTCCATGTCGGCCGCCCGCAGCGAGCACGAGGTGTCAGAGATCATCGATGGCCTCTCAGAGCAGGAGAACCTGGAGAAGCAGATGCGC CAGCTGGCCGTGATCCCGCCCATGCTGTACGACGCTGACCAGCAGCGCATCAAGTTCATCAACATGAACGGGCTTATGGCCGACCCCATG AAGGTGTACAAAGACCGCCAGGTCATGAACATGTGGAGTGAGCAGGAGAAGGAGACCTTCCGGGAGAAGTTCATGCAGCATCCCAAGAAC TTTGGCCTGATCGCATCATTCCTGGAGAGGAAGACAGTGGCTGAGTGCGTCCTCTATTACTACCTGACTAAGAAGAATGAGAACTATAAG AGCCTGGTGAGACGGAGCTATCGGCGCCGCGGCAAGAGCCAGCAGCAGCAACAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAG CCCATGCCCCGCAGCAGCCAGGAGGAGAAAGATGAGAAGGAGAAGGAAAAGGAGGCGGAGAAGGAGGAGGAGAAGCCGGAGGTGGAGAAC GACAAGGAAGACCTCCTCAAGGAGAAGACAGACGACACCTCAGGGGAGGACAACGACGAGAAGGAGGCTGTGGCCTCCAAAGGCCGCAAA ACTGCCAACAGCCAGGGAAGACGCAAAGGCCGCATCACCCGCTCAATGGCTAATGAGGCCAACAGCGAGGAGGCCATCACCCCCCAGCAG AGCGCCGAGCTGGCCTCCATGGAGCTGAATGAGAGTTCTCGCTGGACAGAAGAAGAAATGGAAACAGCCAAGAAAGGGTCCTCATATTTT GTGCTTGCAAATGGACATATCCTGCCCAACAGTGAAAATGCTCATGGCCAATCTCTGGAAGAAGATTCCGCATTGGAAGCTTTGCTGAAT TTTTTCTTTCCAACAACTTGCAATCTGAGGGAAAATCAGGTGGCAAAGCCTTGTAATGAGCTGCAAGATCTTAGTGAGAGTGAATGTTTG AGACACAAATGCTGTTTTTCATCATCGGGGACCACGAGCTTCAAATGTTTTGCTCCATTTAGAGATGTGCCTAAACAGATGATGCAAATG TTTGGGCTTGGTGCGATCAGCCTTATCCTGGTATGTCTGCCCATTTATTGCCGCTCTCTTTTCTGGAGGAGCGAACCGGCCGATGATTTA CAAAGGCAGGACAACAGAGTTGTAACGGGTTTGAAGAAACAAAGAAGGAAGCGAAAGAGGAAGTCTGAAATGTTACAGAAAGCAGCAAGA |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_NCOR2_ENST00000405201_chr12_124882665_-_FMR1NB_ENST00000370467_chrX_147084721_+_2547nt CATGTCGGGATCCACACAGCCTGTGGCACAGACGTGGAGGGCCACTGAGCCCCGCTACCCGCCCCACAGCCTTTCCTACCCAGTGCAGAT CGCCCGGACGCACACGGACGTCGGGCTCCTGGAGTACCAGCACCACTCCCGCGACTATGCCTCCCACCTGTCGCCCGGCTCCATCATCCA GCCCCAGCGGCGGAGGCCCTCCCTGCTGTCTGAGTTCCAGCCCGGGAATGAACGGTCCCAGGAGCTCCACCTGCGGCCAGAGTCCCACTC ATACCTGCCCGAGCTGGGGAAGTCAGAGATGGAGTTCATTGAAAGCAAGCGCCCTCGGCTAGAGCTGCTGCCTGACCCCCTGCTGCGACC GTCACCCCTGCTGGCCACGGGCCAGCCTGCGGGATCTGAAGACCTCACCAAGGACCGTAGCCTGACGGGCAAGCTGGAACCGGTGTCTCC CCCCAGCCCCCCGCACACTGACCCTGAGCTGGAGCTGGTGCCGCCACGGCTGTCCAAGGAGGAGCTGATCCAGAACATGGACCGCGTGGA CCGAGAGATCACCATGGTAGAGCAGCAGATCTCTAAGCTGAAGAAGAAGCAGCAACAGCTGGAGGAGGAGGCTGCCAAGCCGCCCGAGCC TGAGAAGCCCGTGTCACCGCCGCCCATCGAGTCGAAGCACCGCAGCCTGGTGCAGATCATCTACGACGAGAACCGGAAGAAGGCTGAAGC TGCACATCGGATTCTGGAAGGCCTGGGGCCCCAGGTGGAGCTGCCGCTGTACAACCAGCCCTCCGACACCCGGCAGTATCATGAGAACAT CAAAATAAACCAGGCGATGCGGAAGAAGCTAATCTTGTACTTCAAGAGGAGGAATCACGCTCGGAAACAATGGGAGCAGAAGTTCTGCCA GCGCTATGACCAGCTCATGGAGGCCTGGGAGAAGAAGGTGGAGCGCATCGAGAACAACCCCCGGCGGCGGGCCAAGGAGAGCAAGGTGCG CGAGTACTACGAGAAGCAGTTCCCTGAGATCCGCAAGCAGCGCGAGCTGCAGGAGCGCATGCAGAGCAGGGTGGGCCAGCGGGGCAGTGG GCTGTCCATGTCGGCCGCCCGCAGCGAGCACGAGGTGTCAGAGATCATCGATGGCCTCTCAGAGCAGGAGAACCTGGAGAAGCAGATGCG CCAGCTGGCCGTGATCCCGCCCATGCTGTACGACGCTGACCAGCAGCGCATCAAGTTCATCAACATGAACGGGCTTATGGCCGACCCCAT GAAGGTGTACAAAGACCGCCAGGTCATGAACATGTGGAGTGAGCAGGAGAAGGAGACCTTCCGGGAGAAGTTCATGCAGCATCCCAAGAA CTTTGGCCTGATCGCATCATTCCTGGAGAGGAAGACAGTGGCTGAGTGCGTCCTCTATTACTACCTGACTAAGAAGAATGAGAACTATAA GAGCCTGGTGAGACGGAGCTATCGGCGCCGCGGCAAGAGCCAGCAGCAGCAACAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA GCCCATGCCCCGCAGCAGCCAGGAGGAGAAAGATGAGAAGGAGAAGGAAAAGGAGGCGGAGAAGGAGGAGGAGAAGCCGGAGGTGGAGAA CGACAAGGAAGACCTCCTCAAGGAGAAGACAGACGACACCTCAGGGGAGGACAACGACGAGAAGGAGGCTGTGGCCTCCAAAGGCCGCAA AACTGCCAACAGCCAGGGAAGACGCAAAGGCCGCATCACCCGCTCAATGGCTAATGAGGCCAACAGCGAGGAGGCCATCACCCCCCAGCA GAGCGCCGAGCTGGCCTCCATGGAGCTGAATGAGAGTTCTCGCTGGACAGAAGAAGAAATGGAAACAGCCAAGAAAGGGTCCTCATATTT TGTGCTTGCAAATGGACATATCCTGCCCAACAGTGAAAATGCTCATGGCCAATCTCTGGAAGAAGATTCCGCATTGGAAGCTTTGCTGAA TTTTTTCTTTCCAACAACTTGCAATCTGAGGGAAAATCAGGTGGCAAAGCCTTGTAATGAGCTGCAAGATCTTAGTGAGAGTGAATGTTT GAGACACAAATGCTGTTTTTCATCATCGGGGACCACGAGCTTCAAATGTTTTGCTCCATTTAGAGATGTGCCTAAACAGATGATGCAAAT GTTTGGGCTTGGTGCGATCAGCCTTATCCTGGTATGTCTGCCCATTTATTGCCGCTCTCTTTTCTGGAGGAGCGAACCGGCCGATGATTT ACAAAGGCAGGACAACAGAGTTGTAACGGGTTTGAAGAAACAAAGAAGGAAGCGAAAGAGGAAGTCTGAAATGTTACAGAAAGCAGCAAG AGGACGTGAGGAACATGGTGACGAGTAGCAAGAGACCAAAGCATTATTTTCCCCTCAAGACAACAGAAACCATTCAGAGCAGAGGGGACT GTCTCAGCCATGCAAACCTCATGGAGCATTTTGGAAAGTTAAAAATTGATTCTTATTTTTGTCATGTTTACTTTCAAACATGAAATAAAA |
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FusionGenePPI for NCOR2_FMR1NB |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
NCOR2 | SPEN, ZBTB16, AR, IKZF1, RUNX1T1, HDAC3, TBL1X, RELA, NFKBIA, HDAC4, HDAC7, SNW1, HDAC1, HDAC10, PML, PPARD, BCL6, NCOR1, SMARCA4, SIN3A, HDAC2, SAP30, HDAC5, RBPJ, POU2F1, RARA, INPP5K, CIR1, JUN, FOS, SRF, NR3C1, PPARA, THRB, VDR, NR4A1, PGR, RXRA, NCOA6, ZBTB7A, NR4A2, EP300, CREBBP, CNOT2, AKT1, CHUK, HIST1H4A, NR1I2, HNF4A, ATXN1, ATXN1L, SF1, SP1, CEBPB, NFE2L2, PPARG, FOXP1, NFKBIB, NFKBIE, NFKB1, SKIL, THRA, ESR1, ESR2, BACH2, NCOA3, GPS2, SUMO1, UBE2I, IRF5, CDKN1A, RARB, RARG, AP2M1, RANBP9, RXRG, NR1H2, TNIP2, CEP63, TNIK, SOX2, E2F4, NRD1, CTBP1, ARNT, AHR, NR1D1, NR1H4, C1D, RUNX1, CBX6, BTRC, E2F1, BCOR, AURKA, HMGA1, KLF5, HSPA5, SEC16A, FBXO22, RGMA, FOXK2, NANOG, POU5F1, ITGAV, EYA2, TBL1Y, ZSCAN5A, LASP1, USP44, TRIM25 | FMR1NB | NOP56, CEBPZ, RRP12, RPL26L1, NRD1, CWC22, CHCHD2P9, PITHD1, BOP1, RPL5, WT1 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
Hgene | NCOR2 | chr12:124882665 | chrX:147084721 | ENST00000356219 | - | 17 | 48 | 254_312 | 625 | 2522 | SIN3A/B |
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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 NCOR2_FMR1NB |
![]() (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 NCOR2_FMR1NB |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | NCOR2 | C0005586 | Bipolar Disorder | 1 | PSYGENET |
Hgene | NCOR2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |