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    SUPT3H SPT3 homolog, SAGA and STAGA complex component [ Homo sapiens (human) ]

    Gene ID: 8464, updated on 2-Nov-2024

    Summary

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    Official Symbol
    SUPT3Hprovided by HGNC
    Official Full Name
    SPT3 homolog, SAGA and STAGA complex componentprovided by HGNC
    Primary source
    HGNC:HGNC:11466
    See related
    Ensembl:ENSG00000196284 MIM:602947; AllianceGenome:HGNC:11466
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SPT3; SPT3L
    Summary
    Enables transcription coactivator activity. Involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of SAGA complex and transcription factor TFTC complex. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Ubiquitous expression in testis (RPKM 1.4), ovary (RPKM 1.0) and 24 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See SUPT3H in Genome Data Viewer
    Location:
    6p21.1
    Exon count:
    21
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (44809057..45377934, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (44643948..45212744, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (44776794..45345671, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375075 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:44588544-44589128 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44592119-44592626 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44592627-44593135 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44594661-44595168 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44595169-44595676 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44597530-44598150 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:44598773-44599392 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:44610400-44611599 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:44619143-44619644 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:44619645-44620144 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44634844-44635352 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44636371-44636878 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24641 Neighboring gene uncharacterized LOC124901325 Neighboring gene uncharacterized LOC101929770 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24642 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24643 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44727363-44727954 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr6:44739389-44740008 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:44838634-44839257 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:44846566-44847066 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_91988 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:44897835-44898036 Neighboring gene NUDT19 pseudogene 4 Neighboring gene MPRA-validated peak5818 silencer Neighboring gene MPRA-validated peak5819 silencer Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:45029844-45030504 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:45030505-45031165 Neighboring gene MPRA-validated peak5820 silencer Neighboring gene poly(rC) binding protein 2 pseudogene Neighboring gene RNA binding motif protein 22 pseudogene 4 Neighboring gene MPRA-validated peak5821 silencer Neighboring gene MPRA-validated peak5822 silencer Neighboring gene microRNA 586 Neighboring gene RUNX2 P1 promoter region Neighboring gene MPRA-validated peak5825 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17265 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:45345603-45346146 Neighboring gene uncharacterized LOC124901324 Neighboring gene runt related transcription factor 2 polyalanine expansion region Neighboring gene RUNX family transcription factor 2 Neighboring gene NANOG hESC enhancer GRCh37_chr6:45413685-45414186 Neighboring gene Sharpr-MPRA regulatory region 695 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr6:45487956-45488510 Neighboring gene Sharpr-MPRA regulatory region 12811 Neighboring gene RUNX2 antisense RNA 1

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

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    Related articles in PubMed

    1. Characterization of a human homologue of the Saccharomyces cerevisiae transcription factor spt3 (SUPT3H). Yu J, et al. Genomics, 1998 Oct 1. PMID 9787080
    2. Identification of SUPT3H as a novel 8q24/MYC partner in blastic plasmacytoid dendritic cell neoplasm with t(6;8)(p21;q24) translocation. Nakamura Y, et al. Blood Cancer J, 2015 Apr 10. PMID 25860292, Free PMC Article
    3. Adaptive evolution of loci covarying with the human African Pygmy phenotype. Mendizabal I, et al. Hum Genet, 2012 Aug. PMID 22407027, Free PMC Article
    4. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Holliday EG, et al. Nat Genet, 2012 Oct. PMID 22941190, Free PMC Article
    5. Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity. de Vries PS, et al. Blood, 2015 Jun 18. PMID 25934476

    See all (73) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Here, genotype at an Osteoarthritis (OA) risk locus correlates with differential DNA methylation, with altered gene expression of both a transcriptional regulator (RUNX2), and a chromatin remodelling protein (SUPT3H).
      Title: Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis risk.
    2. significance of the formation PVT1- SUPT3H chimeric gene remains unknown and the overexpression of MYC by ectopic promoter on chromosome 6 may be essential to tumor genesis.
      Title: Identification of SUPT3H as a novel 8q24/MYC partner in blastic plasmacytoid dendritic cell neoplasm with t(6;8)(p21;q24) translocation.
    3. we identified rs41314453 as the main genetic determinant of ADAMTS13 activity, and we present preliminary findings for further associations at the ADAMTS13 and SUPT3H loci.
      Title: Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity.
    4. identified a significant excess of genes with pivotal roles in bone homeostasis, such as PPPT3B and the height associated SUPT3H-RUNX2
      Title: Adaptive evolution of loci covarying with the human African Pygmy phenotype.
    5. Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
      Title: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
    6. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
      Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
    7. Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)
      Title: Identification of 15 loci influencing height in a Korean population.
    8. Clinical trial and genome-wide association study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
      Title: Molecular genetics of successful smoking cessation: convergent genome-wide association study results.
    9. Found evidence of Mendelian Transmission Distortion in the region harboring SUPT3H in one HapMap population.
      Title: Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs.
    10. Observational study of gene-disease association. (HuGE Navigator)
      Title: Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs.
    Submit: New GeneRIF Correction See all GeneRIFs (11)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    EBI GWAS Catalog

    Description
    A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine.
    EBI GWAS Catalog
    Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.
    EBI GWAS Catalog
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
    EBI GWAS Catalog
    Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
    EBI GWAS Catalog
    Hundreds of variants clustered in genomic loci and biological pathways affect human height.
    EBI GWAS Catalog
    Identification of 15 loci influencing height in a Korean population.
    EBI GWAS Catalog
    Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.
    EBI GWAS Catalog
    Many sequence variants affecting diversity of adult human height.
    EBI GWAS Catalog
    Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.
    EBI GWAS Catalog
    Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
    EBI GWAS Catalog
    Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
    EBI GWAS Catalog
    Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Genotypes

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • FLJ35021

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein heterodimerization activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables transcription coactivator activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables transcription coactivator activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in positive regulation of DNA-templated transcription NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in regulation of DNA repair NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in regulation of DNA-templated transcription NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in regulation of RNA splicing NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in regulation of transcription by RNA polymerase II IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in transcription by RNA polymerase II IEA
    Inferred from Electronic Annotation
    more info
    		  
    Component Evidence Code Pubs
    part_of SAGA complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of SAGA complex NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of transcription factor TFTC complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of transcription factor TFTC complex NAS
    Non-traceable Author Statement
    more info
    		 PubMed 

    General protein information

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    Preferred Names
    transcription initiation protein SPT3 homolog
    Names
    SPT3-like protein
    suppressor of Ty 3 homolog

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_001261823.2 → NP_001248752.1  transcription initiation protein SPT3 homolog isoform 3

      See identical proteins and their annotated locations for NP_001248752.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) encodes isoform 3.
      Source sequence(s)
      AK303838, AL360272, DA012115
      UniProtKB/TrEMBL
      B4E1H0
      Conserved Domains (2) summary
      pfam14961
      Location:22 → 80
      BROMI; Broad-minded protein
      cl02176
      Location:123 → 141
      TAF11; TATA Binding Protein (TBP) Associated Factor 11 (TAF11) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex

    2. NM_001350324.2 → NP_001337253.1  transcription initiation protein SPT3 homolog isoform 4

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) encodes isoform 4.
      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272
      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    3. NM_001350325.2 → NP_001337254.1  transcription initiation protein SPT3 homolog isoform 5

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) encodes isoform 5.
      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272
      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 114
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    4. NM_001350326.2 → NP_001337255.1  transcription initiation protein SPT3 homolog isoform 6

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) encodes isoform 6.
      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272, AL499610
      UniProtKB/TrEMBL
      A0A1B0GVT7
      Conserved Domains (1) summary
      cl02174
      Location:14 → 95
      TAF13; The TATA Binding Protein (TBP) Associated Factor 13 (TAF13) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex

    5. NM_001350327.2 → NP_001337256.1  transcription initiation protein SPT3 homolog isoform 7

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7) encodes isoform 7.
      Source sequence(s)
      AL096865, AL161905, AL360272
      UniProtKB/TrEMBL
      A0A1B0GVT7
      Conserved Domains (2) summary
      cl02174
      Location:1 → 30
      TAF13; The TATA Binding Protein (TBP) Associated Factor 13 (TAF13) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex
      pfam14961
      Location:88 → 146
      BROMI; Broad-minded protein

    6. NM_001350329.2 → NP_001337258.1  transcription initiation protein SPT3 homolog isoform 1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (8), as well as variant 1, encodes isoform 1.
      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272
      Consensus CDS
      CCDS34465.1
      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7
      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    7. NM_003599.4 → NP_003590.1  transcription initiation protein SPT3 homolog isoform 1

      See identical proteins and their annotated locations for NP_003590.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1), as well as variant 8, encodes isoform 1.
      Source sequence(s)
      AF073930, AL360272, DA012115
      Consensus CDS
      CCDS34465.1
      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7
      UniProtKB/TrEMBL
      Q5U608
      Related
      ENSP00000360514.1, ENST00000371459.6
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    8. NM_181356.3 → NP_852001.1  transcription initiation protein SPT3 homolog isoform 2

      See identical proteins and their annotated locations for NP_852001.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) represents the longest transcript and encodes the longest isoform (2).
      Source sequence(s)
      AL360272, BC050384, DA012115
      Consensus CDS
      CCDS34466.1
      Related
      ENSP00000360515.1, ENST00000371460.5
      Conserved Domains (3) summary
      pfam02269
      Location:46 → 127
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit
      pfam14961
      Location:185 → 243
      BROMI; Broad-minded protein
      cl02176
      Location:286 → 304
      TAF11; TATA Binding Protein (TBP) Associated Factor 11 (TAF11) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex

    RNA

    1. NR_146632.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272

    2. NR_146633.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272

    3. NR_146634.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272

    4. NR_146635.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL096865, AL138880, AL161905, AL360272

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      44809057..45377934 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_011514953.4 → XP_011513255.1  transcription initiation protein SPT3 homolog isoform X2

      See identical proteins and their annotated locations for XP_011513255.1

      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    2. XM_024446572.2 → XP_024302340.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7
      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    3. XM_011514954.4 → XP_011513256.1  transcription initiation protein SPT3 homolog isoform X2

      See identical proteins and their annotated locations for XP_011513256.1

      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    4. XM_011514952.3 → XP_011513254.1  transcription initiation protein SPT3 homolog isoform X2

      See identical proteins and their annotated locations for XP_011513254.1

      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    5. XM_017011371.2 → XP_016866860.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7
      UniProtKB/TrEMBL
      Q5U608
      Conserved Domains (1) summary
      pfam02269
      Location:24 → 116
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit

    6. XM_047419416.1 → XP_047275372.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7

    7. XM_011514949.4 → XP_011513251.1  transcription initiation protein SPT3 homolog isoform X1

      Conserved Domains (3) summary
      pfam02269
      Location:46 → 127
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit
      pfam14961
      Location:185 → 243
      BROMI; Broad-minded protein
      cl02176
      Location:286 → 304
      TAF11; TATA Binding Protein (TBP) Associated Factor 11 (TAF11) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex

    8. XM_017011370.2 → XP_016866859.1  transcription initiation protein SPT3 homolog isoform X1

      Conserved Domains (3) summary
      pfam02269
      Location:46 → 127
      TFIID-18kDa; Transcription initiation factor IID, 18kD subunit
      pfam14961
      Location:185 → 243
      BROMI; Broad-minded protein
      cl02176
      Location:286 → 304
      TAF11; TATA Binding Protein (TBP) Associated Factor 11 (TAF11) is one of several TAFs that bind TBP and is involved in forming Transcription Factor IID (TFIID) complex

    9. XM_017011374.3 → XP_016866863.1  transcription initiation protein SPT3 homolog isoform X5

      UniProtKB/TrEMBL
      A0A1B0GVT7
      Related
      ENSP00000490652.2, ENST00000637763.2

    10. XM_047419417.1 → XP_047275373.1  transcription initiation protein SPT3 homolog isoform X4

    RNA

    1. XR_007059345.1 RNA Sequence

    2. XR_926319.4 RNA Sequence

    3. XR_001743692.2 RNA Sequence

    4. XR_007059346.1 RNA Sequence

    5. XR_007059347.1 RNA Sequence

    6. XR_926321.1 RNA Sequence

    7. XR_926320.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      44643948..45212744 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054356576.1 → XP_054212551.1  transcription initiation protein SPT3 homolog isoform X2

    2. XM_054356578.1 → XP_054212553.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7

    3. XM_054356577.1 → XP_054212552.1  transcription initiation protein SPT3 homolog isoform X2

    4. XM_054356575.1 → XP_054212550.1  transcription initiation protein SPT3 homolog isoform X2

    5. XM_054356580.1 → XP_054212555.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7

    6. XM_054356579.1 → XP_054212554.1  transcription initiation protein SPT3 homolog isoform X3

      UniProtKB/Swiss-Prot
      A6NKG9, B2R9Q5, O75486, O76066, Q5TAV9, Q86VN7

    7. XM_054356573.1 → XP_054212548.1  transcription initiation protein SPT3 homolog isoform X1

    8. XM_054356574.1 → XP_054212549.1  transcription initiation protein SPT3 homolog isoform X1

    9. XM_054356582.1 → XP_054212557.1  transcription initiation protein SPT3 homolog isoform X5

    10. XM_054356572.1 → XP_054212547.1  transcription initiation protein SPT3 homolog isoform X1

    11. XM_054356581.1 → XP_054212556.1  transcription initiation protein SPT3 homolog isoform X4

    RNA

    1. XR_008487449.1 RNA Sequence

    2. XR_008487447.1 RNA Sequence

    3. XR_008487452.1 RNA Sequence

    4. XR_008487451.1 RNA Sequence

    5. XR_008487453.1 RNA Sequence

    6. XR_008487450.1 RNA Sequence

    7. XR_008487448.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    O75486.3 GenPept UniProtKB/Swiss-Prot:O75486

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