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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:YY1-MAPK1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: YY1-MAPK1
FusionPDB ID: 100252
FusionGDB2.0 ID: 100252
HgeneTgene
Gene symbol

YY1

MAPK1

Gene ID

7528

5594

Gene nameYY1 transcription factormitogen-activated protein kinase 1
SynonymsDELTA|GADEVS|INO80S|NF-E1|UCRBP|YIN-YANG-1ERK|ERK-2|ERK2|ERT1|MAPK2|P42MAPK|PRKM1|PRKM2|p38|p40|p41|p41mapk|p42-MAPK
Cytomap

14q32.2

22q11.22

Type of geneprotein-codingprotein-coding
Descriptiontranscriptional repressor protein YY1INO80 complex subunit SYY-1Yin and Yang 1 proteindelta transcription factormitogen-activated protein kinase 1MAP kinase 1MAP kinase 2MAP kinase isoform p42MAPK 2extracellular signal-regulated kinase 2mitogen-activated protein kinase 2protein tyrosine kinase ERK2
Modification date2020031320200327
UniProtAcc

YY1AP1

Q8NDC0

Ensembl transtripts involved in fusion geneENST idsENST00000262238, ENST00000491588, 
ENST00000215832, ENST00000398822, 
ENST00000544786, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 7 X 7=44115 X 8 X 9=1080
# samples 916
** MAII scorelog2(9/441*10)=-2.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1080*10)=-2.75488750216347
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: YY1 [Title/Abstract] AND MAPK1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)YY1(100728803)-MAPK1(22162135), # samples:1
Anticipated loss of major functional domain due to fusion event.YY1-MAPK1 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.
YY1-MAPK1 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.
YY1-MAPK1 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.
YY1-MAPK1 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.
YY1-MAPK1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
YY1-MAPK1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
YY1-MAPK1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
YY1-MAPK1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
YY1-MAPK1 seems lost the major protein functional domain in Tgene partner, which is a kinase 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneYY1

GO:0000122

negative regulation of transcription by RNA polymerase II

9857059|16260628

HgeneYY1

GO:0032688

negative regulation of interferon-beta production

16260628

TgeneMAPK1

GO:0006468

protein phosphorylation

23184662

TgeneMAPK1

GO:0010800

positive regulation of peptidyl-threonine phosphorylation

16314496

TgeneMAPK1

GO:0018105

peptidyl-serine phosphorylation

15850461

TgeneMAPK1

GO:0034198

cellular response to amino acid starvation

11096076

TgeneMAPK1

GO:0038127

ERBB signaling pathway

15133037

TgeneMAPK1

GO:0051403

stress-activated MAPK cascade

11096076

TgeneMAPK1

GO:0070371

ERK1 and ERK2 cascade

16314496

TgeneMAPK1

GO:0070849

response to epidermal growth factor

18794356


check buttonFusion gene breakpoints across YY1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across MAPK1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-EQ-8122-01AYY1chr14

100728803

+MAPK1chr22

22162135

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000262238YY1chr14100728803+ENST00000398822MAPK1chr2222162135-223011022602065601
ENST00000262238YY1chr14100728803+ENST00000544786MAPK1chr2222162135-193411022601933558

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000262238ENST00000398822YY1chr14100728803+MAPK1chr2222162135-0.0037851610.9962148
ENST00000262238ENST00000544786YY1chr14100728803+MAPK1chr2222162135-0.0044297770.99557024

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>100252_100252_1_YY1-MAPK1_YY1_chr14_100728803_ENST00000262238_MAPK1_chr22_22162135_ENST00000398822_length(amino acids)=601AA_BP=278
MASGDTLYIATDGSEMPAEIVELHEIEVETIPVETIETTVVGEEEEEDDDDEDGGGGDHGGGGGHGHAGHHHHHHHHHHHPPMIALQPLV
TDDPTQVHHHQEVILVQTREEVVGGDDSDGLRAEDGFEDQILIPVPAPAGGDDDYIEQTLVTVAAAGKSGGGGSSSSGGGRVKKGGGKKS
GKKSYLSGGAGAAGGGGADPGNKKWEQKQVQIKTLEGEFSVTMWSSDEKKDIDHETVVEEQIIGENSPPDYSEYMTGKKLPPGGIPGIDL
SDPKQLAEFASSAYDNVNKVRVAIKKISPFEHQTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQMKDVYIVQDLMETDLYKLLKTQ
HLSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDHTGFLTEYVATRWYRAPEIMLNSKGYTKSI
DIWSVGCILAEMLSNRPIFPGKHYLDQLNHILGILGSPSQEDLNCIINLKARNYLLSLPHKNKVPWNRLFPNADSKALDLLDKMLTFNPH

--------------------------------------------------------------

>100252_100252_2_YY1-MAPK1_YY1_chr14_100728803_ENST00000262238_MAPK1_chr22_22162135_ENST00000544786_length(amino acids)=558AA_BP=278
MASGDTLYIATDGSEMPAEIVELHEIEVETIPVETIETTVVGEEEEEDDDDEDGGGGDHGGGGGHGHAGHHHHHHHHHHHPPMIALQPLV
TDDPTQVHHHQEVILVQTREEVVGGDDSDGLRAEDGFEDQILIPVPAPAGGDDDYIEQTLVTVAAAGKSGGGGSSSSGGGRVKKGGGKKS
GKKSYLSGGAGAAGGGGADPGNKKWEQKQVQIKTLEGEFSVTMWSSDEKKDIDHETVVEEQIIGENSPPDYSEYMTGKKLPPGGIPGIDL
SDPKQLAEFASSAYDNVNKVRVAIKKISPFEHQTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQMKDVYIVQDLMETDLYKLLKTQ
HLSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDHTGFLTEYVATRWYRAPEIMLNSKGYTKSI
DIWSVGCILAEMLSNRPIFPGKHYLDQLNHILALDLLDKMLTFNPHKRIEVEQALAHPYLEQYYDPSDEPIAEAPFKFDMELDDLPKEKL

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr14:100728803/chr22:22162135)
- 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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
YY1

YY1AP1

MAPK1

Q8NDC0

796

check buttonRetention 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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25159_170280.6666666666667415.0Compositional biasNote=Gly/Ser-rich
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+2543_53280.6666666666667415.0Compositional biasNote=Asp/Glu-rich (acidic)
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+2554_69280.6666666666667415.0Compositional biasNote=Gly-rich
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+2570_80280.6666666666667415.0Compositional biasNote=Poly-His
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209259_27739.6666666666666643486.3333333333335DNA binding.
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208259_27739.666666666666664361.0DNA binding.
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607259_27739.666666666666664317.0DNA binding.
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209185_18739.6666666666666643486.3333333333335MotifTXY
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209318_32239.6666666666666643486.3333333333335MotifCytoplasmic retention motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209327_33339.6666666666666643486.3333333333335MotifNuclear translocation motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208185_18739.666666666666664361.0MotifTXY
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208318_32239.666666666666664361.0MotifCytoplasmic retention motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208327_33339.666666666666664361.0MotifNuclear translocation motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607185_18739.666666666666664317.0MotifTXY
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607318_32239.666666666666664317.0MotifCytoplasmic retention motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607327_33339.666666666666664317.0MotifNuclear translocation motif
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209105_10839.6666666666666643486.3333333333335RegionNote=Inhibitor-binding
TgeneMAPK1chr14:100728803chr22:22162135ENST0000021583209153_15439.6666666666666643486.3333333333335RegionNote=Inhibitor-binding
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208105_10839.666666666666664361.0RegionNote=Inhibitor-binding
TgeneMAPK1chr14:100728803chr22:22162135ENST0000039882208153_15439.666666666666664361.0RegionNote=Inhibitor-binding
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607105_10839.666666666666664317.0RegionNote=Inhibitor-binding
TgeneMAPK1chr14:100728803chr22:22162135ENST0000054478607153_15439.666666666666664317.0RegionNote=Inhibitor-binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25257_341280.6666666666667415.0RegionNote=Involved in nuclear matrix association
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25295_414280.6666666666667415.0RegionNote=Binding to DNA
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25333_371280.6666666666667415.0RegionNote=Involved in repression of activated transcription
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25371_397280.6666666666667415.0RegionNote=Involved in masking transactivation domain
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25296_320280.6666666666667415.0Zinc fingerC2H2-type 1
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25325_347280.6666666666667415.0Zinc fingerC2H2-type 2
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25353_377280.6666666666667415.0Zinc fingerC2H2-type 3
HgeneYY1chr14:100728803chr22:22162135ENST00000262238+25383_407280.6666666666667415.0Zinc fingerC2H2-type 4
TgeneMAPK1chr14:100728803chr22:22162135ENST00000215832092_939.6666666666666643486.3333333333335Compositional biasNote=Poly-Ala
TgeneMAPK1chr14:100728803chr22:22162135ENST00000398822082_939.666666666666664361.0Compositional biasNote=Poly-Ala
TgeneMAPK1chr14:100728803chr22:22162135ENST00000544786072_939.666666666666664317.0Compositional biasNote=Poly-Ala
TgeneMAPK1chr14:100728803chr22:22162135ENST000002158320925_31339.6666666666666643486.3333333333335DomainProtein kinase
TgeneMAPK1chr14:100728803chr22:22162135ENST000003988220825_31339.666666666666664361.0DomainProtein kinase
TgeneMAPK1chr14:100728803chr22:22162135ENST000005447860725_31339.666666666666664317.0DomainProtein kinase
TgeneMAPK1chr14:100728803chr22:22162135ENST000002158320931_3939.6666666666666643486.3333333333335Nucleotide bindingATP
TgeneMAPK1chr14:100728803chr22:22162135ENST000003988220831_3939.666666666666664361.0Nucleotide bindingATP
TgeneMAPK1chr14:100728803chr22:22162135ENST000005447860731_3939.666666666666664317.0Nucleotide bindingATP


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors
YY1FKBP1A, YAF2, MTA2, NOTCH1, SAP30, HDAC1, HDAC2, HDAC3, KAT2B, EP300, FKBP3, RYBP, SP1, SREBF1, MYC, ATF6, PPIA, CTCF, HDAC4, ATF2, ZNF232, Hoxa11, HOXA11, MAX, CREBBP, HDAC5, TP53, MDM2, CDKN2A, SMAD4, SMAD1, SMAD2, SMAD3, PRMT1, ILF3, HCVgp1, NPM1, TFAP2A, tat, EZH2, INO80, TFCP2, PRKDC, ACTR8, HSPA4, ACTR5, ACTL6A, RUVBL1, RUVBL2, RELB, YY1, JUNB, JUND, RB1, NFE2L2, MECP2, TERF1, TERF2, INO80C, INO80E, NFRKB, TCF3, INO80B, UCHL5, INO80D, MCRS1, TFPT, HSPA5, BCL6, NEDD4, UHRF2, CREB1, ATF7, BAP1, HCFC1, NEDD4L, Nedd4, XRCC6, XRCC5, SMARCAD1, DDX5, DDX3X, SP3, PSMD9, SKP2, ELAVL1, EED, APP, ZNF830, NHP2L1, ZNF638, NCL, WDHD1, ZNF24, ARRB1, RING1, RNF2, PCGF2, LAMC2, GABPB1, GABPA, SLC39A7, CRKL, GRN, NFKB1, RAF1, TESK1, NR1H2, SPRY1, SHFM1, SMURF2, SUZ12, BMI1, TWIST1, PPP1R3B, TMEM150A, TRPV5, CEP164, BAX, Ruvbl2, Ruvbl1, FOXB1, FOXJ2, FOXL1, FOXN1, KMT2E, DNMT3L, AURKA, ID2, F9, TRIM25, AGO2, EGLN3, EFTUD2, RNF4, BCCIP, HIST1H3A, NR2C2, HIST1H4A, Dppa3, ITFG1, GMCL1, CEP76, SF3A2, ZNF85, LHX3, MDFI, FHL2, LHX4, MED20, IL10, TRIM42, ESM1, PLEKHF2, ALOXE3, KRTAP17-1, KRTAP9-8, KRTAP10-8, VWC2, CYSRT1, KRTAP4-5, XAGE1B, XAGE1E, KRTAP9-3, KRTAP12-3, KRTAP5-6, KRTAP2-3, KRTAP2-4, KRTAP10-9, KRTAP1-5, KRTAP12-2, KRTAP1-3, KRTAP10-5, KRTAP4-2, PLEKHA4, LOC102724334, HIST3H3, HIST2H2BF, HIST1H2BM, HIST1H2BH, SMC3, PRC1, BRD1, BRD2, ARHGAP26, ARHGEF15, FASN, MKI67, CIC, BRD4, NSRP1, DDX42, PPP1R10, NUFIP2, PPIL4, CPSF7, MEPCE, CCNT1, PSPC1, CDK9, PRPF4B, CTTN, SP100, CSNK1D, GTF2I, ATXN2L, TAF2, C1orf35, FAM76B, LRPAP1, RPS19, FIP1L1, WDR82, SART1, TOP1, RBM25, PRPF38A, NUDT21, CBX4, PRPF40A, TOX4, RCL1, RPSA, HEXIM1, POP1, PIP4K2A, EIF5A, CCNT2, DDX56, RBM15B, RPL23A, MFAP1, DCAF13, TACO1, METTL17, SNIP1, SF3B4, DDX6, FAM98A, CPSF6, FAM76A, AAMDC, LYAR, CPSF1, GFER, APEX1, CBX3, CD3EAP, CENPA, COIL, PARP1, ZNF330, TRIP12, USP8, CAND1, UBB, HMGB1, RPL35A, BAG2, IFI27L1, ADSSL1, EZH1, SPANXN2, IGFL3, MTSS1L, NIPA2, SEMA4C, RRP8, SPRTN, FBXW7, RCHY1, ELF1, ELF2, ELF4, ELK3, FEV, HNF1B, HNF4A, KLF12, KLF16, KLF8, KLF9, LHX2, MYB, NFIA, NFIX, PAX6, SOX2, TEAD1, MDC1, TAF4, SETD1A, TRIM24, OGT, ZNHIT1, SMARCA5, TAF1, TAF6, WDR5, CBX1, KMT2A, BPTF, CHD3, TFDP1, ZMYM3, TAF9, ARID4B, TAF3, ZMYM4, ARID2, SRCAP, POGZ, PBRM1, KDM1B, KAT2A, KAT5, L3MBTL2, PCGF6, BRD8, EHMT1, DMAP1, BRD7, CXXC1, CHD7, ZMYM2, KMT2B, TRRAP, GTF3C3, SMCHD1, RAD21, YEATS4, RBBP5, MSL1, ASXL2, ASXL1, ASH2L, NOP56, YY2, TADA2A, TADA3, WIZ, HIVEP1, ZNF131, SSBP1, GTF3C1, PWP1, NUMA1, TAF5, VPS72, BRMS1L, ZMYM1, LRIF1, LIN9, RIF1, CDCA2, THOC7, LIN54, MSANTD2, ATF7IP, KANSL1, C11orf30, MGA, C17orf49, ZZZ3, ZNF687, GTF3C2, GATAD1, ZNF592, ZBTB9, INTS12, MBD6, THAP11, CCDC101, DYNLL2, L3MBTL3, ZNF512B, EHMT2, EP400, ZNF512, PHF12, C7orf50, DIDO1, ACTR6, ADNP, ZHX3, ZNF644, KAT8, CSRP2BP, KANSL2, TAF9B, CHD8, FAM60A, MBIP, RBM28, KANSL3, HMGXB4, ZHX1, YEATS2, ZMYND8, MRPS17, HCFC2, CABIN1, ZHX2, MORC2, NFIC,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
YY1all structure
MAPK1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to YY1-MAPK1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to YY1-MAPK1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneYY1C4479652GABRIELE-DE VRIES SYNDROME2GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneYY1C0006826Malignant Neoplasms1CTD_human
HgeneYY1C0007873Uterine Cervical Neoplasm1CTD_human
HgeneYY1C0019693HIV Infections1CTD_human
HgeneYY1C0020796Profound Mental Retardation1CTD_human
HgeneYY1C0025363Mental Retardation, Psychosocial1CTD_human
HgeneYY1C0027651Neoplasms1CTD_human
HgeneYY1C0086692Benign Neoplasm1CTD_human
HgeneYY1C0235874Disease Exacerbation1CTD_human
HgeneYY1C0917816Mental deficiency1CTD_human
HgeneYY1C3714756Intellectual Disability1CTD_human;GENOMICS_ENGLAND
HgeneYY1C4048328cervical cancer1CTD_human
HgeneYY1C4505456HIV Coinfection1CTD_human