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    SECISBP2 SECIS binding protein 2 [ Homo sapiens (human) ]

    Gene ID: 79048, updated on 2-Nov-2024

    Summary

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    Official Symbol
    SECISBP2provided by HGNC
    Official Full Name
    SECIS binding protein 2provided by HGNC
    Primary source
    HGNC:HGNC:30972
    See related
    Ensembl:ENSG00000187742 MIM:607693; AllianceGenome:HGNC:30972
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SBP2; THMA1
    Summary
    The protein encoded by this gene is one of the essential components of the machinery involved in co-translational insertion of selenocysteine (Sec) into selenoproteins. Sec is encoded by the UGA codon, which normally signals translation termination. The recoding of UGA as Sec codon requires a Sec insertion sequence (SECIS) element; present in the 3' untranslated regions of eukaryotic selenoprotein mRNAs. This protein specifically binds to the SECIS element, which is stimulated by a Sec-specific translation elongation factor. Mutations in this gene have been associated with reduction in enzymatic activity of type II iodothyronine deiodinase (a selenoprotein) and abnormal thyroid hormone metabolism. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]
    Expression
    Ubiquitous expression in testis (RPKM 20.1), thyroid (RPKM 9.1) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See SECISBP2 in Genome Data Viewer
    Location:
    9q22.2
    Exon count:
    22
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (89318500..89367117)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (101482274..101530894)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (91933415..91974578)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376136 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:91896966-91897484 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20005 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20006 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28527 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28528 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28529 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20007 Neighboring gene microRNA 3153 Neighboring gene CDC28 protein kinase regulatory subunit 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:91978812-91979312 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:91979313-91979813 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28530 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20008 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28531 Neighboring gene semaphorin 4D Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_108523 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_108535 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92020317-92021138 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92021139-92021959 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28535 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:92026366-92026868 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:92026869-92027370 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:92027622-92028122 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:92028123-92028623 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28536 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28537 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92040313-92041172 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28538 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28539 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28540 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28541 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28542 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28543 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:92046837-92047618 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92049183-92049964 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92049965-92050746 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92050747-92051528 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92051529-92052310 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92054729-92055306 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:92057617-92058192 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_108605 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92061728-92062338 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92064045-92064893 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20009 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28545 Neighboring gene proliferation-associated 2G4 pseudogene 6 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92080560-92081256 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92081257-92081952 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:92082322-92083285 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28546 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:92086209-92086710 Neighboring gene ubiquitin-conjugating enzyme E2 variant 1-like

    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. Mutations in SECISBP2 result in abnormal thyroid hormone metabolism. Dumitrescu AM, et al. Nat Genet, 2005 Nov. PMID 16228000
    2. Functional characterization of alternatively spliced human SECISBP2 transcript variants. Papp LV, et al. Nucleic Acids Res, 2008 Dec. PMID 19004874, Free PMC Article
    3. Selenium supplementation fails to correct the selenoprotein synthesis defect in subjects with SBP2 gene mutations. Schomburg L, et al. Thyroid, 2009 Mar. PMID 19265499, Free PMC Article
    4. SBP2 binding affinity is a major determinant in differential selenoprotein mRNA translation and sensitivity to nonsense-mediated decay. Squires JE, et al. Mol Cell Biol, 2007 Nov. PMID 17846120, Free PMC Article
    5. SECISBP2 is a novel prognostic predictor that regulates selenoproteins in diffuse large B-cell lymphoma. Taguchi T, et al. Lab Invest, 2021 Feb. PMID 33077808

    See all (68) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Human Genetic Disorders Resulting in Systemic Selenoprotein Deficiency.
      Title: Human Genetic Disorders Resulting in Systemic Selenoprotein Deficiency.
    2. SECISBP2 is a novel prognostic predictor that regulates selenoproteins in diffuse large B-cell lymphoma.
      Title: SECISBP2 is a novel prognostic predictor that regulates selenoproteins in diffuse large B-cell lymphoma.
    3. Selenium-sensitive miR-181a-5p to participate and regulate SBP2 at post-transcriptional level.
      Title: Selenium-sensitive miRNA-181a-5p targeting SBP2 regulates selenoproteins expression in cartilage.
    4. SECISBP2 expression in healthy human palatal mucosa is strongly negatively correlated with serum cotinine levels.
      Title: Whole transcriptome analysis of smoker palatal mucosa identifies multiple downregulated innate immunity genes.
    5. In osteoarthritis pro-inflammatory factors mediate miR-181a-5p expression, and then miR-181a-5p regulates the pivotal selenoproteins GPX1 and GPX4 through its target SBP2, resulting in alterations to the overall activity of GPXs, which are the most important oxidation resistance proteins in cartilage.
      Title: The hsa-miR-181a-5p reduces oxidation resistance by controlling SECISBP2 in osteoarthritis.
    6. functions as a vital factor in selenoprotein translation and regulates the pro-oxidant/antioxidant balance in trophoblasts
      Title: Loss of selenocysteine insertion sequence binding protein 2 suppresses the proliferation, migration/invasion and hormone secretion of human trophoblast cells via the PI3K/Akt and ERK signaling pathway.
    7. SBP2 interacts directly with four proteins of the SMN complex and the methylosome core proteins.
      Title: SECIS-binding protein 2 interacts with the SMN complex and the methylosome for selenoprotein mRNP assembly and translation.
    8. SBP2 makes direct contacts with a discrete region of the human 28S rRNA.
      Title: The SBP2 protein central to selenoprotein synthesis contacts the human ribosome at expansion segment 7L of the 28S rRNA.
    9. The patient showed typical symptoms of SBP2 deficiency, and novel compound heterozygous mutations were identified in SBP2 (p.M515fsX563/p.Q79X).
      Title: Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation.
    10. Selenocysteine insertion sequence (SECIS)-binding protein 2 alters conformational dynamics of residues involved in tRNA accommodation in 80 S ribosomes.
      Title: Selenocysteine insertion sequence (SECIS)-binding protein 2 alters conformational dynamics of residues involved in tRNA accommodation in 80 S ribosomes.
    Submit: New GeneRIF Correction See all GeneRIFs (22)

    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

    Associated conditions

    Description Tests
    Thyroid hormone metabolism, abnormal 1
    MedGen: C5676891 OMIM: 609698 GeneReviews: Not available
    		Compare labs

    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

    • FLJ45753, DKFZp686C09169

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables DNA binding EXP
    Inferred from Experiment
    more info
    		 PubMed 
    enables RNA binding HDA PubMed 
    enables mRNA 3'-UTR binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables mRNA 3'-UTR binding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables ribonucleoprotein complex binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables selenocysteine insertion sequence binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables selenocysteine insertion sequence binding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in RNA catabolic process IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in forebrain neuron development IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in mRNA stabilization IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in selenocysteine incorporation IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in selenocysteine incorporation IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in striatum development IEA
    Inferred from Electronic Annotation
    more info
    		  
    Component Evidence Code Pubs
    is_active_in mitochondrion IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in mitochondrion IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    part_of ribonucleoprotein complex IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  

    General protein information

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    Preferred Names
    selenocysteine insertion sequence-binding protein 2
    Names
    Sec insertion sequence-binding protein 2

    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.

    Genomic

    1. NG_012177.2 RefSeqGene

      Range
      5002..46165
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001282688.2 → NP_001269617.1  selenocysteine insertion sequence-binding protein 2 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate in-frame acceptor splice site in the 5' coding region compared to variant 1. The encoded isoform (2) is 1 aa shorter than isoform 1.
      Source sequence(s)
      AF380995, AK302852, AL160054, BG572344, BX000356
      UniProtKB/TrEMBL
      B4DZC7
      Conserved Domains (1) summary
      pfam01248
      Location:656 → 756
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    2. NM_001282689.2 → NP_001269618.1  selenocysteine insertion sequence-binding protein 2 isoform 3

      See identical proteins and their annotated locations for NP_001269618.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) uses an alternate in-frame acceptor splice site in the 5' coding region, which results in translation initiation from an alternate start codon compared to variant 1. The encoded isoform (3) is shorter, with a distinct N-terminus compared to isoform 1.
      Source sequence(s)
      AK290182, AL929575, BG572344, BP219148
      Consensus CDS
      CCDS65076.1
      UniProtKB/TrEMBL
      B4DR97
      Related
      ENSP00000364959.3, ENST00000339901.8
      Conserved Domains (1) summary
      pfam01248
      Location:584 → 684
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    3. NM_001282690.1 → NP_001269619.1  selenocysteine insertion sequence-binding protein 2 isoform 4

      See identical proteins and their annotated locations for NP_001269619.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) contains an alternate 5' terminal exon, which results in translation initiation from an in-frame downstream start codon compared to variant 1. The encoded isoform (4) has a shorter N-terminus compared to isoform 1
      Source sequence(s)
      AK299161, AL160054, AL929575, BG572344, BX000356
      Consensus CDS
      CCDS65077.1
      UniProtKB/TrEMBL
      B4DR97
      Related
      ENSP00000436650.2, ENST00000534113.6
      Conserved Domains (1) summary
      pfam01248
      Location:589 → 689
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    4. NM_001354696.2 → NP_001341625.1  selenocysteine insertion sequence-binding protein 2 isoform 5

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) uses an alternate in-frame acceptor splice site in the mid-coding region compared to variant 1. The encoded shorter isoform (5) lacks an internal protein segment compared to isoform 1.
      Source sequence(s)
      BC068466, BC099900, BG572344, BP219148
      UniProtKB/TrEMBL
      Q59H19
      Conserved Domains (1) summary
      pfam01248
      Location:618 → 718
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    5. NM_001354697.2 → NP_001341626.1  selenocysteine insertion sequence-binding protein 2 isoform 6

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6) uses an alternate in-frame acceptor splice site in the mid-coding region compared to variant 1. The encoded shorter isoform (6) lacks an internal protein segment compared to isoform 1.
      Source sequence(s)
      BC068466, BG572344, BP219148, KX533480
      UniProtKB/TrEMBL
      Q59H19
      Conserved Domains (1) summary
      pfam01248
      Location:619 → 719
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    6. NM_001354698.2 → NP_001341627.1  selenocysteine insertion sequence-binding protein 2 isoform 7

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7) uses an alternate in-frame acceptor splice site and lacks an in-frame exon in the mid-coding region compared to variant 1. The encoded shorter isoform (7) lacks two internal protein segments compared to isoform 1.
      Source sequence(s)
      BC099900, BG572344, BP219148, KX533480
      UniProtKB/TrEMBL
      Q59H19
      Conserved Domains (1) summary
      pfam01248
      Location:588 → 688
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    7. NM_001354702.2 → NP_001341631.1  selenocysteine insertion sequence-binding protein 2 isoform 8

      Status: REVIEWED

      Description
      Transcript Variant: This variant (8) uses an alternate acceptor splice site in the mid-coding region and initiates translation from an alternate start codon compared to variant 1. The encoded isoform (8) is shorter, with a distinct N-terminus compared to isoform 1.
      Source sequence(s)
      AI127999, BC068466, BG572344, BP219148
      Conserved Domains (1) summary
      pfam01248
      Location:362 → 462
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    8. NM_024077.5 → NP_076982.3  selenocysteine insertion sequence-binding protein 2 isoform 1

      See identical proteins and their annotated locations for NP_076982.3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the predominant transcript, and encodes the longest isoform (1).
      Source sequence(s)
      BC068466, BG572344, BP219148
      Consensus CDS
      CCDS6683.1
      UniProtKB/Swiss-Prot
      F8W892, Q5HYY1, Q7L1Z0, Q8IYC0, Q96T21, Q9H0A1
      UniProtKB/TrEMBL
      B4DZC7
      Related
      ENSP00000364965.3, ENST00000375807.8
      Conserved Domains (1) summary
      pfam01248
      Location:657 → 757
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      89318500..89367117
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047423856.1 → XP_047279812.1  selenocysteine insertion sequence-binding protein 2 isoform X5

      UniProtKB/Swiss-Prot
      F8W892, Q5HYY1, Q7L1Z0, Q8IYC0, Q96T21, Q9H0A1

    2. XM_047423857.1 → XP_047279813.1  selenocysteine insertion sequence-binding protein 2 isoform X5

      UniProtKB/Swiss-Prot
      F8W892, Q5HYY1, Q7L1Z0, Q8IYC0, Q96T21, Q9H0A1

    3. XM_047423859.1 → XP_047279815.1  selenocysteine insertion sequence-binding protein 2 isoform X8

    4. XM_017015122.3 → XP_016870611.1  selenocysteine insertion sequence-binding protein 2 isoform X7

      UniProtKB/TrEMBL
      B4DZC7

    5. XM_024447666.2 → XP_024303434.1  selenocysteine insertion sequence-binding protein 2 isoform X9

      UniProtKB/TrEMBL
      A0A1S5UZH3, Q59H19
      Conserved Domains (1) summary
      pfam01248
      Location:589 → 689
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    6. XM_047423854.1 → XP_047279810.1  selenocysteine insertion sequence-binding protein 2 isoform X1

    7. XM_011519000.3 → XP_011517302.1  selenocysteine insertion sequence-binding protein 2 isoform X1

      See identical proteins and their annotated locations for XP_011517302.1

      UniProtKB/TrEMBL
      B4DR97
      Conserved Domains (1) summary
      pfam01248
      Location:589 → 689
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    8. XM_047423855.1 → XP_047279811.1  selenocysteine insertion sequence-binding protein 2 isoform X3

    9. XM_011519001.2 → XP_011517303.1  selenocysteine insertion sequence-binding protein 2 isoform X2

      UniProtKB/TrEMBL
      B4DR97
      Conserved Domains (1) summary
      pfam01248
      Location:559 → 659
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    10. XM_011519002.2 → XP_011517304.1  selenocysteine insertion sequence-binding protein 2 isoform X3

      UniProtKB/TrEMBL
      B4DR97
      Conserved Domains (1) summary
      pfam01248
      Location:551 → 651
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    11. XM_047423858.1 → XP_047279814.1  selenocysteine insertion sequence-binding protein 2 isoform X6

    12. XM_011519003.2 → XP_011517305.1  selenocysteine insertion sequence-binding protein 2 isoform X4

      UniProtKB/TrEMBL
      B4DR97
      Conserved Domains (1) summary
      pfam01248
      Location:550 → 650
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    13. XM_047423860.1 → XP_047279816.1  selenocysteine insertion sequence-binding protein 2 isoform X10

    14. XM_024447667.2 → XP_024303435.1  selenocysteine insertion sequence-binding protein 2 isoform X11

      UniProtKB/TrEMBL
      B4DR97
      Conserved Domains (1) summary
      pfam01248
      Location:545 → 645
      Ribosomal_L7Ae; Ribosomal protein L7Ae/L30e/S12e/Gadd45 family

    15. XM_047423861.1 → XP_047279817.1  selenocysteine insertion sequence-binding protein 2 isoform X12

    16. XM_047423862.1 → XP_047279818.1  selenocysteine insertion sequence-binding protein 2 isoform X13

    17. XM_047423863.1 → XP_047279819.1  selenocysteine insertion sequence-binding protein 2 isoform X14

      UniProtKB/TrEMBL
      Q9H948

    RNA

    1. XR_007061351.1 RNA Sequence

    2. XR_007061350.1 RNA Sequence

    3. XR_007061352.1 RNA Sequence

    4. XR_007061353.1 RNA Sequence

    5. XR_007061354.1 RNA Sequence

    6. XR_007061347.1 RNA Sequence

    7. XR_929840.2 RNA Sequence

    8. XR_007061346.1 RNA Sequence

    9. XR_007061345.1 RNA Sequence

    10. XR_007061348.1 RNA Sequence

    11. XR_007061349.1 RNA Sequence

    12. XR_007061355.1 RNA Sequence

    13. XR_007061356.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      101482274..101530894
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054363775.1 → XP_054219750.1  selenocysteine insertion sequence-binding protein 2 isoform X5

      UniProtKB/Swiss-Prot
      F8W892, Q5HYY1, Q7L1Z0, Q8IYC0, Q96T21, Q9H0A1

    2. XM_054363776.1 → XP_054219751.1  selenocysteine insertion sequence-binding protein 2 isoform X5

      UniProtKB/Swiss-Prot
      F8W892, Q5HYY1, Q7L1Z0, Q8IYC0, Q96T21, Q9H0A1

    3. XM_054363779.1 → XP_054219754.1  selenocysteine insertion sequence-binding protein 2 isoform X8

    4. XM_054363778.1 → XP_054219753.1  selenocysteine insertion sequence-binding protein 2 isoform X7

    5. XM_054363780.1 → XP_054219755.1  selenocysteine insertion sequence-binding protein 2 isoform X9

      UniProtKB/TrEMBL
      A0A1S5UZH3

    6. XM_054363770.1 → XP_054219745.1  selenocysteine insertion sequence-binding protein 2 isoform X1

    7. XM_054363769.1 → XP_054219744.1  selenocysteine insertion sequence-binding protein 2 isoform X1

    8. XM_054363773.1 → XP_054219748.1  selenocysteine insertion sequence-binding protein 2 isoform X3

    9. XM_054363771.1 → XP_054219746.1  selenocysteine insertion sequence-binding protein 2 isoform X2

    10. XM_054363772.1 → XP_054219747.1  selenocysteine insertion sequence-binding protein 2 isoform X3

    11. XM_054363777.1 → XP_054219752.1  selenocysteine insertion sequence-binding protein 2 isoform X6

    12. XM_054363774.1 → XP_054219749.1  selenocysteine insertion sequence-binding protein 2 isoform X4

    13. XM_054363781.1 → XP_054219756.1  selenocysteine insertion sequence-binding protein 2 isoform X10

    14. XM_054363782.1 → XP_054219757.1  selenocysteine insertion sequence-binding protein 2 isoform X11

    15. XM_054363783.1 → XP_054219758.1  selenocysteine insertion sequence-binding protein 2 isoform X12

    16. XM_054363784.1 → XP_054219759.1  selenocysteine insertion sequence-binding protein 2 isoform X13

    17. XM_054363785.1 → XP_054219760.1  selenocysteine insertion sequence-binding protein 2 isoform X14

      UniProtKB/TrEMBL
      Q9H948

    RNA

    1. XR_008488072.1 RNA Sequence

    2. XR_008488071.1 RNA Sequence

    3. XR_008488073.1 RNA Sequence

    4. XR_008488074.1 RNA Sequence

    5. XR_008488075.1 RNA Sequence

    6. XR_008488068.1 RNA Sequence

    7. XR_008488065.1 RNA Sequence

    8. XR_008488067.1 RNA Sequence

    9. XR_008488066.1 RNA Sequence

    10. XR_008488069.1 RNA Sequence

    11. XR_008488070.1 RNA Sequence

    12. XR_008488076.1 RNA Sequence

    13. XR_008488077.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q96T21.2 GenPept UniProtKB/Swiss-Prot:Q96T21

    Gene LinkOut

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