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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:ALDH2-HSPA1A (FusionGDB2 ID:HG217TG3303) |
Fusion Gene Summary for ALDH2-HSPA1A |
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Fusion gene information | Fusion gene name: ALDH2-HSPA1A | Fusion gene ID: hg217tg3303 | Hgene | Tgene | Gene symbol | ALDH2 | HSPA1A | Gene ID | 217 | 3303 |
Gene name | aldehyde dehydrogenase 2 family member | heat shock protein family A (Hsp70) member 1A | |
Synonyms | ALDH-E2|ALDHI|ALDM | HEL-S-103|HSP70-1|HSP70-1A|HSP70-2|HSP70.1|HSP70.2|HSP70I|HSP72|HSPA1 | |
Cytomap | ('ALDH2')('HSPA1A') 12q24.12 | 6p21.33 | |
Type of gene | protein-coding | protein-coding | |
Description | aldehyde dehydrogenase, mitochondrialALDH class 2acetaldehyde dehydrogenase 2aldehyde dehydrogenase 2 family (mitochondrial)epididymis secretory sperm binding proteinliver mitochondrial ALDHnucleus-encoded mitochondrial aldehyde dehydrogenase 2 | heat shock 70 kDa protein 1AHSP70-1/HSP70-2HSP70.1/HSP70.2Heat shock 70 kDa protein 1BHeat shock 70 kDa protein 2dnaK-type molecular chaperone HSP70-1epididymis secretory protein Li 103epididymis secretory sperm binding proteinheat shock 70 kDa pr | |
Modification date | 20200313 | 20200327 | |
UniProtAcc | P05091 | . | |
Ensembl transtripts involved in fusion gene | ENST00000261733, ENST00000416293, | ||
Fusion gene scores | * DoF score | 26 X 20 X 11=5720 | 6 X 15 X 4=360 |
# samples | 21 | 11 | |
** MAII score | log2(21/5720*10)=-4.76755391399963 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(11/360*10)=-1.71049338280502 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ALDH2 [Title/Abstract] AND HSPA1A [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ALDH2(112221083)-HSPA1A(31785084), # samples:2 | ||
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 |
Tgene | HSPA1A | GO:0006402 | mRNA catabolic process | 10205060 |
Tgene | HSPA1A | GO:0006986 | response to unfolded protein | 10859165 |
Tgene | HSPA1A | GO:0031396 | regulation of protein ubiquitination | 16809764 |
Tgene | HSPA1A | GO:0031397 | negative regulation of protein ubiquitination | 12150907 |
Tgene | HSPA1A | GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 24613385 |
Tgene | HSPA1A | GO:0033120 | positive regulation of RNA splicing | 20625543 |
Tgene | HSPA1A | GO:0034605 | cellular response to heat | 24061851 |
Tgene | HSPA1A | GO:0042026 | protein refolding | 15603737|21231916 |
Tgene | HSPA1A | GO:0046034 | ATP metabolic process | 23921388 |
Tgene | HSPA1A | GO:0050821 | protein stabilization | 21909508 |
Tgene | HSPA1A | GO:0051131 | chaperone-mediated protein complex assembly | 10811660 |
Tgene | HSPA1A | GO:0090084 | negative regulation of inclusion body assembly | 15603737|21231916 |
Tgene | HSPA1A | GO:0097201 | negative regulation of transcription from RNA polymerase II promoter in response to stress | 9499401 |
Tgene | HSPA1A | GO:1901029 | negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway | 20625543 |
Tgene | HSPA1A | GO:1902236 | negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway | 12150907|20625543 |
Tgene | HSPA1A | GO:1902380 | positive regulation of endoribonuclease activity | 20625543 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * 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 | COAD | TCGA-AA-3510-01A | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
ChimerDB4 | UCEC | TCGA-B5-A11S-01A | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
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Fusion Gene ORF analysis for ALDH2-HSPA1A |
![]() * 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-intron | ENST00000261733 | ENST00000383389 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000400040 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000422919 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000430065 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000433487 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000441618 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000449876 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
5CDS-intron | ENST00000261733 | ENST00000452298 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
In-frame | ENST00000261733 | ENST00000375651 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
In-frame | ENST00000261733 | ENST00000458062 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
In-frame | ENST00000261733 | ENST00000608703 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-3CDS | ENST00000416293 | ENST00000375651 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-3CDS | ENST00000416293 | ENST00000458062 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-3CDS | ENST00000416293 | ENST00000608703 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000383389 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000400040 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000422919 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000430065 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000433487 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000441618 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000449876 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
intron-intron | ENST00000416293 | ENST00000452298 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + |
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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) |
ENST00000261733 | ALDH2 | chr12 | 112221083 | + | ENST00000375651 | HSPA1A | chr6 | 31785084 | + | 932 | 299 | 266 | 673 | 135 |
ENST00000261733 | ALDH2 | chr12 | 112221083 | + | ENST00000458062 | HSPA1A | chr6 | 31785084 | + | 674 | 299 | 266 | 673 | 136 |
ENST00000261733 | ALDH2 | chr12 | 112221083 | + | ENST00000608703 | HSPA1A | chr6 | 31785084 | + | 938 | 299 | 266 | 673 | 135 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000261733 | ENST00000375651 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + | 0.007877686 | 0.99212223 |
ENST00000261733 | ENST00000458062 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + | 0.007414042 | 0.99258596 |
ENST00000261733 | ENST00000608703 | ALDH2 | chr12 | 112221083 | + | HSPA1A | chr6 | 31785084 | + | 0.008096871 | 0.9919031 |
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Fusion Genomic Features for ALDH2-HSPA1A |
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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 ALDH2-HSPA1A |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr12:112221083/chr6:31785084) - 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 |
ALDH2 | . |
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 |
Hgene | ALDH2 | chr12:112221083 | chr6:31785084 | ENST00000261733 | + | 1 | 13 | 262_267 | 0 | 518.0 | Nucleotide binding | NAD |
Hgene | ALDH2 | chr12:112221083 | chr6:31785084 | ENST00000416293 | + | 1 | 12 | 262_267 | 0 | 471.0 | Nucleotide binding | NAD |
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Fusion Gene Sequence for ALDH2-HSPA1A |
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>3874_3874_1_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000375651_length(transcript)=932nt_BP=299nt TCAGTGGCCCTGAGACCCTAGCTCTGCTCTCGGTCCGCTCGCTGTCCGCTAGCCCGCTGCGATGTTGCGCGCTGCCGCCCGCTTCGGGCC CCGCCTGGGCCGCCGCCTCTTGTCAGCCGCCGCCACCCAGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGGTCTTCTGCAACCAGATTTT CATAAACAATGAATGGCACGATGCCGTCAGCAGGAAAACATTCCCCACCGTCAATCCGTCCACTGGAGAGGTCATCTGTCAGGTAGCTGA AGGGGACAAGGGACCGGACCTACCTGGCGATGGTGCAGGAGGCGGAGAAGTACAAAGCGGAGGACGAGGTGCAGCGCGAGAGGGTGTCAG CCAAGAACGCCCTGGAGTCCTACGCCTTCAACATGAAGAGCGCCGTGGAGGATGAGGGGCTCAAGGGCAAGATCAGCGAGGCGGACAAGA AGAAGGTGCTGGACAAGTGTCAAGAGGTCATCTCGTGGCTGGACGCCAACACCTTGGCCGAGAAGGACGAGTTTGAGCACAAGAGGAAGG AGCTGGAGCAGGTGTGTAACCCCATCATCAGCGGACTGTACCAGGGTGCCGGTGGTCCCGGGCCTGGGGGCTTCGGGGCTCAGGGTCCCA AGGGAGGGTCTGGGTCAGGCCCCACCATTGAGGAGGTAGATTAGGGGCCTTTCCAAGATTGCTGTTTTTGTTTTGGAGCTTCAAGACTTT GCATTTCCTAGTATTTCTGTTTGTCAGTTCTCAATTTCCTGTGTTTGCAATGTTGAAATTTTTTGGTGAAGTACTGAACTTGCTTTTTTT CCGGTTTCTACATGCAGAGATGAATTTATACTGCCATCTTACGACTATTTCTTCTTTTTAATACACTTAACTCAGGCCATTTTTTAAGTT >3874_3874_1_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000375651_length(amino acids)=135AA_BP=11 MKGTRDRTYLAMVQEAEKYKAEDEVQRERVSAKNALESYAFNMKSAVEDEGLKGKISEADKKKVLDKCQEVISWLDANTLAEKDEFEHKR -------------------------------------------------------------- >3874_3874_2_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000458062_length(transcript)=674nt_BP=299nt TCAGTGGCCCTGAGACCCTAGCTCTGCTCTCGGTCCGCTCGCTGTCCGCTAGCCCGCTGCGATGTTGCGCGCTGCCGCCCGCTTCGGGCC CCGCCTGGGCCGCCGCCTCTTGTCAGCCGCCGCCACCCAGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGGTCTTCTGCAACCAGATTTT CATAAACAATGAATGGCACGATGCCGTCAGCAGGAAAACATTCCCCACCGTCAATCCGTCCACTGGAGAGGTCATCTGTCAGGTAGCTGA AGGGGACAAGGGACCGGACCTACCTGGCGATGGTGCAGGAGGCGGAGAAGTACAAAGCGGAGGACGAGGTGCAGCGCGAGAGGGTGTCAG CCAAGAACGCCCTGGAGTCCTACGCCTTCAACATGAAGAGCGCCGTGGAGGATGAGGGGCTCAAGGGCAAGATCAGCGAGGCGGACAAGA AGAAGGTGCTGGACAAGTGTCAAGAGGTCATCTCGTGGCTGGACGCCAACACCTTGGCCGAGAAGGACGAGTTTGAGCACAAGAGGAAGG AGCTGGAGCAGGTGTGTAACCCCATCATCAGCGGACTGTACCAGGGTGCCGGTGGTCCCGGGCCTGGGGGCTTCGGGGCTCAGGGTCCCA >3874_3874_2_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000458062_length(amino acids)=136AA_BP=11 MKGTRDRTYLAMVQEAEKYKAEDEVQRERVSAKNALESYAFNMKSAVEDEGLKGKISEADKKKVLDKCQEVISWLDANTLAEKDEFEHKR -------------------------------------------------------------- >3874_3874_3_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000608703_length(transcript)=938nt_BP=299nt TCAGTGGCCCTGAGACCCTAGCTCTGCTCTCGGTCCGCTCGCTGTCCGCTAGCCCGCTGCGATGTTGCGCGCTGCCGCCCGCTTCGGGCC CCGCCTGGGCCGCCGCCTCTTGTCAGCCGCCGCCACCCAGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGGTCTTCTGCAACCAGATTTT CATAAACAATGAATGGCACGATGCCGTCAGCAGGAAAACATTCCCCACCGTCAATCCGTCCACTGGAGAGGTCATCTGTCAGGTAGCTGA AGGGGACAAGGGACCGGACCTACCTGGCGATGGTGCAGGAGGCGGAGAAGTACAAAGCGGAGGACGAGGTGCAGCGCGAGAGGGTGTCAG CCAAGAACGCCCTGGAGTCCTACGCCTTCAACATGAAGAGCGCCGTGGAGGATGAGGGGCTCAAGGGCAAGATCAGCGAGGCGGACAAGA AGAAGGTGCTGGACAAGTGTCAAGAGGTCATCTCGTGGCTGGACGCCAACACCTTGGCCGAGAAGGACGAGTTTGAGCACAAGAGGAAGG AGCTGGAGCAGGTGTGTAACCCCATCATCAGCGGACTGTACCAGGGTGCCGGTGGTCCCGGGCCTGGGGGCTTCGGGGCTCAGGGTCCCA AGGGAGGGTCTGGGTCAGGCCCCACCATTGAGGAGGTAGATTAGGGGCCTTTCCAAGATTGCTGTTTTTGTTTTGGAGCTTCAAGACTTT GCATTTCCTAGTATTTCTGTTTGTCAGTTCTCAATTTCCTGTGTTTGCAATGTTGAAATTTTTTGGTGAAGTACTGAACTTGCTTTTTTT CCGGTTTCTACATGCAGAGATGAATTTATACTGCCATCTTACGACTATTTCTTCTTTTTAATACACTTAACTCAGGCCATTTTTTAAGTT >3874_3874_3_ALDH2-HSPA1A_ALDH2_chr12_112221083_ENST00000261733_HSPA1A_chr6_31785084_ENST00000608703_length(amino acids)=135AA_BP=11 MKGTRDRTYLAMVQEAEKYKAEDEVQRERVSAKNALESYAFNMKSAVEDEGLKGKISEADKKKVLDKCQEVISWLDANTLAEKDEFEHKR -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for ALDH2-HSPA1A |
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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 ALDH2-HSPA1A |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | ALDH2 | P05091 | DB00536 | Guanidine | Inhibitor | Small molecule | Approved |
Hgene | ALDH2 | P05091 | DB00536 | Guanidine | Inhibitor | Small molecule | Approved |
Hgene | ALDH2 | P05091 | DB00822 | Disulfiram | Inhibitor | Small molecule | Approved |
Hgene | ALDH2 | P05091 | DB00822 | Disulfiram | Inhibitor | Small molecule | Approved |
Hgene | ALDH2 | P05091 | DB00157 | NADH | Small molecule | Approved|Nutraceutical | |
Hgene | ALDH2 | P05091 | DB00157 | NADH | Small molecule | Approved|Nutraceutical |
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Related Diseases for ALDH2-HSPA1A |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ALDH2 | C0001973 | Alcoholic Intoxication, Chronic | 7 | CTD_human;PSYGENET |
Hgene | ALDH2 | C0085762 | Alcohol abuse | 7 | CTD_human;PSYGENET |
Hgene | ALDH2 | C0001969 | Alcoholic Intoxication | 5 | PSYGENET |
Hgene | ALDH2 | C0393756 | Hangover from alcohol | 4 | PSYGENET |
Hgene | ALDH2 | C0236664 | Alcohol-Related Disorders | 3 | PSYGENET |
Hgene | ALDH2 | C0001956 | Alcohol Use Disorder | 2 | CTD_human |
Hgene | ALDH2 | C0004096 | Asthma | 2 | CTD_human |
Hgene | ALDH2 | C0005586 | Bipolar Disorder | 2 | PSYGENET |
Hgene | ALDH2 | C0279626 | Squamous cell carcinoma of esophagus | 2 | CTD_human |
Hgene | ALDH2 | C0009402 | Colorectal Carcinoma | 1 | CTD_human |
Hgene | ALDH2 | C0009404 | Colorectal Neoplasms | 1 | CTD_human |
Hgene | ALDH2 | C0014859 | Esophageal Neoplasms | 1 | CTD_human |
Hgene | ALDH2 | C0016382 | Flushing | 1 | CTD_human |
Hgene | ALDH2 | C0016689 | Freckles | 1 | CTD_human |
Hgene | ALDH2 | C0021364 | Male infertility | 1 | CTD_human |
Hgene | ALDH2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Hgene | ALDH2 | C0025209 | Melanosis | 1 | CTD_human |
Hgene | ALDH2 | C0025218 | Chloasma | 1 | CTD_human |
Hgene | ALDH2 | C0028796 | Dermatitis, Occupational | 1 | CTD_human |
Hgene | ALDH2 | C0032927 | Precancerous Conditions | 1 | CTD_human |
Hgene | ALDH2 | C0042373 | Vascular Diseases | 1 | CTD_human |
Hgene | ALDH2 | C0086457 | Industrial Dermatosis | 1 | CTD_human |
Hgene | ALDH2 | C0236970 | Alcohol-Induced Disorders | 1 | CTD_human |
Hgene | ALDH2 | C0242973 | Ventricular Dysfunction | 1 | CTD_human |
Hgene | ALDH2 | C0282313 | Condition, Preneoplastic | 1 | CTD_human |
Hgene | ALDH2 | C0342257 | Complications of Diabetes Mellitus | 1 | CTD_human |
Hgene | ALDH2 | C0349464 | Wernicke-Korsakoff Syndrome | 1 | PSYGENET |
Hgene | ALDH2 | C0400966 | Non-alcoholic Fatty Liver Disease | 1 | CTD_human |
Hgene | ALDH2 | C0520459 | Necrotizing Enterocolitis | 1 | CTD_human |
Hgene | ALDH2 | C0546837 | Malignant neoplasm of esophagus | 1 | CTD_human |
Hgene | ALDH2 | C0848676 | Subfertility, Male | 1 | CTD_human |
Hgene | ALDH2 | C0917731 | Male sterility | 1 | CTD_human |
Hgene | ALDH2 | C2674838 | ALCOHOL SENSITIVITY, ACUTE | 1 | CTD_human |
Hgene | ALDH2 | C3241937 | Nonalcoholic Steatohepatitis | 1 | CTD_human |
Tgene | C0036341 | Schizophrenia | 5 | PSYGENET | |
Tgene | C0041696 | Unipolar Depression | 3 | PSYGENET | |
Tgene | C1269683 | Major Depressive Disorder | 3 | PSYGENET | |
Tgene | C0022660 | Kidney Failure, Acute | 2 | CTD_human | |
Tgene | C1565662 | Acute Kidney Insufficiency | 2 | CTD_human | |
Tgene | C2609414 | Acute kidney injury | 2 | CTD_human | |
Tgene | C0013182 | Drug Allergy | 1 | CTD_human | |
Tgene | C0023895 | Liver diseases | 1 | CTD_human | |
Tgene | C0024517 | Major depression, single episode | 1 | PSYGENET | |
Tgene | C0025202 | melanoma | 1 | CTD_human | |
Tgene | C0027627 | Neoplasm Metastasis | 1 | CTD_human | |
Tgene | C0030567 | Parkinson Disease | 1 | CTD_human | |
Tgene | C0033578 | Prostatic Neoplasms | 1 | CTD_human | |
Tgene | C0035126 | Reperfusion Injury | 1 | CTD_human | |
Tgene | C0036349 | Paranoid Schizophrenia | 1 | PSYGENET | |
Tgene | C0086565 | Liver Dysfunction | 1 | CTD_human | |
Tgene | C0151744 | Myocardial Ischemia | 1 | CTD_human | |
Tgene | C0282507 | Heat Stress Disorders | 1 | CTD_human | |
Tgene | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human | |
Tgene | C0887833 | Carcinoma, Pancreatic Ductal | 1 | CTD_human |