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Fusion gene ID: 1432 |
FusionGeneSummary for ALB_EXOSC9 |
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Fusion gene information | Fusion gene name: ALB_EXOSC9 | Fusion gene ID: 1432 | Hgene | Tgene | Gene symbol | ALB | EXOSC9 | Gene ID | 213 | 5393 |
Gene name | albumin | exosome component 9 | |
Synonyms | HSA|PRO0883|PRO0903|PRO1341 | PM/Scl-75|PMSCL1|RRP45|Rrp45p|p5|p6 | |
Cytomap | 4q13.3 | 4q27 | |
Type of gene | protein-coding | protein-coding | |
Description | serum albumin | exosome complex component RRP45P75 polymyositis-scleroderma overlap syndrome associated autoantigenPMSCL autoantigen, 75kDautoantigen PM/Scl 1exosome complex exonuclease RRP45polymyositis/scleroderma autoantigen 1, 75kDa | |
Modification date | 20180522 | 20180523 | |
UniProtAcc | P02768 | Q06265 | |
Ensembl transtripts involved in fusion gene | ENST00000295897, ENST00000415165, ENST00000503124, ENST00000509063, ENST00000401494, ENST00000505649, | ENST00000243498, ENST00000509980, ENST00000379663, ENST00000512454, | |
Fusion gene scores | * DoF score | 19 X 15 X 3=855 | 2 X 2 X 3=12 |
# samples | 25 | 3 | |
** MAII score | log2(25/855*10)=-1.77399632511117 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(3/12*10)=1.32192809488736 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: ALB [Title/Abstract] AND EXOSC9 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | Tissue-specifically expressed gene involved fusion gene, inframe and retained their domain. |
* 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 | ALB | GO:0009267 | cellular response to starvation | 16245148 |
Hgene | ALB | GO:0019836 | hemolysis by symbiont of host erythrocytes | 16394536 |
Hgene | ALB | GO:0043066 | negative regulation of apoptotic process | 16153637 |
Hgene | ALB | GO:0051659 | maintenance of mitochondrion location | 16153637 |
![]() (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 | KIRP | TCGA-SX-A7SS-01A | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
TCGA | RV | LIHC | TCGA-XR-A8TG-01A | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
* 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 | ENST00000295897 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000295897 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000295897 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000295897 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
In-frame | ENST00000415165 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000415165 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000415165 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000415165 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5UTR-3CDS | ENST00000503124 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5UTR-intron | ENST00000503124 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5UTR-intron | ENST00000503124 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5UTR-intron | ENST00000503124 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
In-frame | ENST00000509063 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000509063 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000509063 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000509063 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
In-frame | ENST00000401494 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000401494 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000401494 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
5CDS-intron | ENST00000401494 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
intron-3CDS | ENST00000505649 | ENST00000243498 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
intron-intron | ENST00000505649 | ENST00000509980 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
intron-intron | ENST00000505649 | ENST00000379663 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
intron-intron | ENST00000505649 | ENST00000512454 | ALB | chr4 | 74270123 | + | EXOSC9 | chr4 | 122737927 | + |
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FusionProtFeatures for ALB_EXOSC9 |
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Hgene | Tgene |
ALB | EXOSC9 |
Non-catalytic component of the RNA exosome complex whichhas 3'->5' exoribonuclease activity and participates in amultitude of cellular RNA processing and degradation events. Inthe nucleus, the RNA exosome complex is involved in propermaturation of stable RNA species such as rRNA, snRNA and snoRNA,in the elimination of RNA processing by-products and non-coding'pervasive' transcripts, such as antisense RNA species andpromoter-upstream transcripts (PROMPTs), and of mRNAs withprocessing defects, thereby limiting or excluding their export tothe cytoplasm. The RNA exosome may be involved in Ig class switchrecombination (CSR) and/or Ig variable region somatichypermutation (SHM) by targeting AICDA deamination activity totranscribed dsDNA substrates. In the cytoplasm, the RNA exosomecomplex is involved in general mRNA turnover and specificallydegrades inherently unstable mRNAs containing AU-rich elements(AREs) within their 3' untranslated regions, and in RNAsurveillance pathways, preventing translation of aberrant mRNAs.It seems to be involved in degradation of histone mRNA. Thecatalytic inactive RNA exosome core complex of 9 subunits (Exo-9)is proposed to play a pivotal role in the binding and presentationof RNA for ribonucleolysis, and to serve as a scaffold for theassociation with catalytic subunits and accessory proteins orcomplexes. EXOSC9 binds to ARE-containing RNAs.{ECO:0000269|PubMed:11782436, ECO:0000269|PubMed:16455498,ECO:0000269|PubMed:16912217, ECO:0000269|PubMed:17545563}. |
![]() * 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 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000295897 | + | 1 | 15 | 19_210 | 26 | 661 | Domain | Albumin 1 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000295897 | + | 1 | 15 | 211_403 | 26 | 661 | Domain | Albumin 2 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000295897 | + | 1 | 15 | 404_601 | 26 | 661 | Domain | Albumin 3 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000509063 | + | 1 | 14 | 19_210 | 26 | 605 | Domain | Albumin 1 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000509063 | + | 1 | 14 | 211_403 | 26 | 605 | Domain | Albumin 2 |
Hgene | >ALB | chr4:74270123 | chr4:122737927 | ENST00000509063 | + | 1 | 14 | 404_601 | 26 | 605 | Domain | Albumin 3 |
Tgene | EXOSC9 | chr4:74270123 | chr4:122737927 | ENST00000243498 | + | 10 | 12 | 1_268 | 411 | 440 | Region | Note=ARE binding |
Tgene | EXOSC9 | chr4:74270123 | chr4:122737927 | ENST00000379663 | + | 11 | 13 | 1_268 | 428 | 457 | Region | Note=ARE binding |
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FusionGeneSequence for ALB_EXOSC9 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_54aa |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_164nt ATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCA |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_306nt AATTATTGGTTAAAGAAGTATATTAGTGCTAATTTCCCTCCGTTTGTCCTAGCTTTTCTCTTCTGTCAACCCCACACGCCTTTGGCACAA TGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCAC CAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTGCCAATTAAAGCTAACAGTTGTATAT >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_258nt CTAGCTTTTCTCTTCTGTCAACCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTT ATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAG >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_241nt TCAACCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTT CGTCGAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTG >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_237nt CCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTC GAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTGCCAA >In-frame_ALB_ENST00000295897_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_306nt AATTATTGGTTAAAGAAGTATATTAGTGCTAATTTCCCTCCGTTTGTCCTAGCTTTTCTCTTCTGTCAACCCCACACGCCTTTGGCACAA TGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCAC CAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTGCCAATTAAAGCTAACAGTTGTATAT >In-frame_ALB_ENST00000415165_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_258nt CTAGCTTTTCTCTTCTGTCAACCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTT ATTCCAGGGGTGTGTTTCGTCGAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAG >In-frame_ALB_ENST00000509063_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_241nt TCAACCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTT CGTCGAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTG >In-frame_ALB_ENST00000401494_chr4_74270123_+_EXOSC9_ENST00000243498_chr4_122737927_+_237nt CCCCACACGCCTTTGGCACAATGAAGTGGGTAACCTTTATTTCCCTTCTTTTTCTCTTTAGCTCGGCTTATTCCAGGGGTGTGTTTCGTC GAGATGCACAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTGCCAA |
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FusionGenePPI for ALB_EXOSC9 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
ALB | LUC7L2, FCGRT, PRB3, AMBP, USP37, UIMC1, DMWD, PSMD4, NR5A2, YWHAG, PSMA3, TK1, IMMT, PFDN1, FBXO25, CRYAB, APP, EEF2K, ADRA1B, APOA1, APOC1, SETX, KCNMA1, PDE4B, CTSL, CDC45, GJC2, CDCP1, DDB1, FGA, FN1, GABBR1, HP, IGHG1, IGHG2, IGKV2-40, KRT10, KRT14, KRT9, KRT1, OR8D2, KLK3, ATM, OR2T6, TLN2, TTR, CACNA1I, ZNF232, PLAG1, RLF, AHSG, APOA4, APOC3, CRB1, EXOC6, SCAF1, GFAP, IGL, TSC22D1, IGKC, ITGB5, KRT6A, SERPING1, TTPAL, F2, AP1M1, AMPD3, APOA2, APOC2, CHKB, F7, C4A, CFB, CFD, CFH, CST3, DCD, ETF1, GSN, IGDCC4, HBA2, HPX, PHC3, ST13, DERL1, FAM71E2, QTRTD1, KIAA0232, ITIH1, KRT13, KRT16, KRT5, KRT6B, OBSL1, CTAGE5, AGA, NCOA3, OR3A2, PPBP, PF4V1, PCDH1, RANBP2, RYR2, SACS, SH3BP5, PLA2G4F, TIAM1, PRSS3, PRSS3P2, ZNF292, AP4E1, APOE, CABLES1, SLC25A13, NLRC4, CLCA2, DGKG, DMD, DICER1, GRAP2, TRAPPC11, SPATA31A7, PDZRN4, PALB2, LDB3, CEP44, ITGA2, JARID2, GCN1L1, CAMTA1, SLC9A8, CNOT1, LAT, MYL4, MYLK3, TTN, NPHS1, SLC1A5, PEG3, CROT, BBC3, RANBP3, SCN5A, SPAST, SLA2, THRAP3, SGOL2, PRSS1, DCC, SORBS3, IQCB1, PAN2, PARK2, FUS, CCDC8, LAMTOR5, CA8, GDPD1, PINX1, ZNF558, RPS6KB2, HNRNPA1, MED4, MED20, SOD1, LRP8, TIMM13, GAR1, FOXA3, FOXJ3, FOXP3, RC3H1, CDC73, CPS1, MAPK6, DDX31, SNX27, HSPA8, UPF3A, CCDC82, ADAMTS18, RALBP1, CYLD | EXOSC9 | UBE2I, CUL3, COPS5, CAND1, CHMP4B, EXOSC4, DIS3, DIS3L, EXOSC3, EXOSC2, EXOSC5, EXOSC10, CSNK2A1, AICDA, MPG, ZDHHC17, OBSL1, SUMO2, EXOSC7, EXOSC8, EXOSC1, EXOSC6, PSMA2, PSMA6, PSMA7, STAG1, STAG2, MPHOSPH6, PSMA5, NTRK1, EEF1G, HP, RBM7, NOP56, TKT, TRIP12, C1D, HBS1L, ZNF106, SLC35E1, KIAA1804, DAB2IP, FAM111B, YBX1, USP37, LUM, RSRC1, SLIT2, LRRC47, NCL, FOXA1 |
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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 ALB_EXOSC9 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | ALB | P02768 | DB00493 | Cefotaxime | Serum albumin | small molecule | approved |
Hgene | ALB | P02768 | DB01045 | Rifampicin | Serum albumin | small molecule | approved |
Hgene | ALB | P02768 | DB03255 | Phenol | Serum albumin | small molecule | approved|experimental |
Hgene | ALB | P02768 | DB00276 | Amsacrine | Serum albumin | small molecule | approved|investigational |
Hgene | ALB | P02768 | DB00545 | Pyridostigmine | Serum albumin | small molecule | approved|investigational |
Hgene | ALB | P02768 | DB06713 | Norelgestromin | Serum albumin | small molecule | approved|investigational |
Hgene | ALB | P02768 | DB11638 | Artenimol | Serum albumin | small molecule | approved|investigational |
Hgene | ALB | P02768 | DB00199 | Erythromycin | Serum albumin | small molecule | approved|investigational|vet_approved |
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RelatedDiseases for ALB_EXOSC9 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ALB | C0033687 | Proteinuria | 9 | CTD_human |
Hgene | ALB | C0017658 | Glomerulonephritis | 8 | CTD_human |
Hgene | ALB | C0022658 | Kidney Diseases | 8 | CTD_human |
Hgene | ALB | C0017665 | Membranous glomerulonephritis | 6 | CTD_human |
Hgene | ALB | C0027697 | Nephritis | 6 | CTD_human |
Hgene | ALB | C0027707 | Nephritis, Interstitial | 4 | CTD_human |
Hgene | ALB | C0038454 | Cerebrovascular accident | 4 | CTD_human |
Hgene | ALB | C0342185 | Hyperthyroxinemia, Familial Dysalbuminemic | 4 | CTD_human;UNIPROT |
Hgene | ALB | C0023893 | Liver Cirrhosis, Experimental | 3 | CTD_human |
Hgene | ALB | C0025290 | Aseptic Meningitis | 3 | CTD_human |
Hgene | ALB | C2609414 | Acute kidney injury | 3 | CTD_human |
Hgene | ALB | C0014544 | Epilepsy | 2 | CTD_human |
Hgene | ALB | C0020649 | Hypotension | 2 | CTD_human;HPO |
Hgene | ALB | C0023890 | Liver Cirrhosis | 2 | CTD_human |
Hgene | ALB | C0027726 | Nephrotic Syndrome | 2 | CTD_human |
Hgene | ALB | C0036830 | Serum Sickness | 2 | CTD_human |
Hgene | ALB | C0162557 | Liver Failure, Acute | 2 | CTD_human |
Hgene | ALB | C4277682 | Chemical and Drug Induced Liver Injury | 2 | CTD_human |
Hgene | ALB | C0002994 | Angioedema | 1 | CTD_human |
Hgene | ALB | C0003460 | Anuria | 1 | CTD_human |
Hgene | ALB | C0004509 | Azoospermia | 1 | CTD_human |
Hgene | ALB | C0006111 | Brain Diseases | 1 | CTD_human |
Hgene | ALB | C0007222 | Cardiovascular Diseases | 1 | CTD_human |
Hgene | ALB | C0007786 | Brain Ischemia | 1 | CTD_human |
Hgene | ALB | C0011581 | Depressive disorder | 1 | CTD_human |
Hgene | ALB | C0011875 | Diabetic Angiopathies | 1 | CTD_human |
Hgene | ALB | C0011881 | Diabetic Nephropathy | 1 | CTD_human |
Hgene | ALB | C0013502 | Echinococcosis | 1 | CTD_human |
Hgene | ALB | C0016059 | Fibrosis | 1 | CTD_human |
Hgene | ALB | C0017662 | Glomerulonephritis, Membranoproliferative | 1 | CTD_human |
Hgene | ALB | C0018799 | Heart Diseases | 1 | CTD_human |
Hgene | ALB | C0018801 | Heart failure | 1 | CTD_human |
Hgene | ALB | C0019061 | Hemolytic-Uremic Syndrome | 1 | CTD_human |
Hgene | ALB | C0019158 | Hepatitis | 1 | CTD_human |
Hgene | ALB | C0019693 | HIV Infections | 1 | CTD_human |
Hgene | ALB | C0019699 | HIV Seropositivity | 1 | CTD_human |
Hgene | ALB | C0020517 | Hypersensitivity | 1 | CTD_human |
Hgene | ALB | C0020522 | Delayed Hypersensitivity | 1 | CTD_human |
Hgene | ALB | C0020538 | Hypertensive disease | 1 | CTD_human |
Hgene | ALB | C0022548 | Keloid | 1 | CTD_human |
Hgene | ALB | C0022661 | Kidney Failure, Chronic | 1 | CTD_human |
Hgene | ALB | C0026848 | Myopathy | 1 | CTD_human |
Hgene | ALB | C0027055 | Myocardial Reperfusion Injury | 1 | CTD_human |
Hgene | ALB | C0027720 | Nephrosis | 1 | CTD_human |
Hgene | ALB | C0028797 | Occupational Diseases | 1 | CTD_human |
Hgene | ALB | C0030193 | Pain | 1 | CTD_human |
Hgene | ALB | C0030286 | Pancreatic Diseases | 1 | CTD_human |
Hgene | ALB | C0030305 | Pancreatitis | 1 | CTD_human |
Hgene | ALB | C0035222 | Respiratory Distress Syndrome, Adult | 1 | CTD_human |
Hgene | ALB | C0035242 | Respiratory Tract Diseases | 1 | CTD_human |
Hgene | ALB | C0035457 | Rhinitis, Allergic, Perennial | 1 | CTD_human |
Hgene | ALB | C0038325 | Stevens-Johnson Syndrome | 1 | CTD_human |
Hgene | ALB | C0038356 | Stomach Neoplasms | 1 | CTD_human |
Hgene | ALB | C0040034 | Thrombocytopenia | 1 | CTD_human |
Hgene | ALB | C0041755 | Adverse reaction to drug | 1 | CTD_human |
Hgene | ALB | C0042109 | Urticaria | 1 | CTD_human |
Hgene | ALB | C0042164 | Uveitis | 1 | CTD_human |
Hgene | ALB | C0152013 | Adenocarcinoma of lung (disorder) | 1 | CTD_human |
Hgene | ALB | C0239981 | Hypoalbuminemia | 1 | CTD_human;HPO |
Hgene | ALB | C0993582 | Arthritis, Experimental | 1 | CTD_human |