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    SGO1 shugoshin 1 [ Homo sapiens (human) ]

    Gene ID: 151648, updated on 2-Nov-2024

    Summary

    Official Symbol
    SGO1provided by HGNC
    Official Full Name
    shugoshin 1provided by HGNC
    Primary source
    HGNC:HGNC:25088
    See related
    Ensembl:ENSG00000129810 MIM:609168; AllianceGenome:HGNC:25088
    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
    SGO; CAID; SGOL1; NY-BR-85
    Summary
    The protein encoded by this gene is a member of the shugoshin family of proteins. This protein is thought to protect centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression of this gene leads to the premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest. Evidence suggests that this protein also protects a small subset of cohesin found along the length of the chromosome arms during mitotic prophase. An isoform lacking exon 6 has been shown to play a role in the cohesion of centrioles (PMID: 16582621 and PMID:18331714). Mutations in this gene have been associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by the co-occurrence of Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO) within the first four decades of life (PMID:25282101). Fibroblast cells from CAID patients exhibited both increased cell proliferation and higher rates of senescence. Pseudogenes of this gene have been found on chromosomes 1 and 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]
    Expression
    Broad expression in testis (RPKM 1.6), bone marrow (RPKM 1.4) and 16 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See SGO1 in Genome Data Viewer
    Location:
    3p24.3
    Exon count:
    10
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (20160593..20186886, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (20164579..20190864, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (20202085..20227698, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene CRISPRi-validated cis-regulatory element chr3.1018 Neighboring gene ribosomal protein L39 pseudogene 18 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:20081563-20082533 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19579 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19580 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19581 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19582 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_67745 Neighboring gene lysine acetyltransferase 2B Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19583 Neighboring gene MPRA-validated peak4562 silencer Neighboring gene microRNA 3135a Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14135 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19584 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19585 Neighboring gene SGO1 antisense RNA 1 Neighboring gene RNY4 pseudogene 22 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14136 Neighboring gene RNA, U6 small nuclear 822, pseudogene

    Genomic regions, transcripts, and products

    Expression

    • 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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Chronic atrial and intestinal dysrhythmia
    MedGen: C4015474 OMIM: 616201 GeneReviews: Not available
    Compare labs

    EBI GWAS Catalog

    Description
    Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
    EBI GWAS Catalog
    Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Vpr vpr HIV-1 Vpr interferes with the heterochromatin structure by displacing HP1-alpha and HP1-gamma proteins in interphase, which leads to relocalization of the centromere chromatin proteins Mis12, Sgo1, and CPC after prophase PubMed
    vpr HIV-1 Vpr inhibits Sgo1 expression in spread chromosomes and prometaphase cells PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    General gene information

    Clone Names

    • FLJ14230

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables kinase binding PubMed 
    enables protein binding PubMed 
    Component Evidence Code Pubs
    located_in centrosome PubMed 
    located_in chromosome, centromeric region PubMed 
    located_in condensed chromosome, centromeric region PubMed 
    located_in cytosol  
    located_in cytosol  
    colocalizes_with kinetochore PubMed 
    located_in kinetochore PubMed 
    located_in nucleoplasm  
    located_in spindle pole PubMed 

    General protein information

    Preferred Names
    shugoshin 1
    Names
    serologically defined breast cancer antigen NY-BR-85
    shugoshin 1AB protein
    shugoshin 1CD protein
    shugoshin 1EF protein
    shugoshin 1GH protein
    shugoshin 1KL protein

    NCBI Reference Sequences (RefSeq)

    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_042062.1 RefSeqGene

      Range
      5026..21748
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001012409.4NP_001012409.1  shugoshin 1 isoform 1

      See identical proteins and their annotated locations for NP_001012409.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (A1) differs in the 5' UTR compared to variant 1. Both variants 1 and A1 encode the same isoform (1).
      Source sequence(s)
      AB187577, AB193058, AC099057, AF308299, BC032696, BX494477, BX648516
      Consensus CDS
      CCDS46773.1
      UniProtKB/TrEMBL
      A0A024R2K2, B5BUA4
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    2. NM_001012410.5NP_001012410.1  shugoshin 1 isoform EF

      See identical proteins and their annotated locations for NP_001012410.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1F, PMID:15737064; also known as A2) differs in the 5' UTR and contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1EF which is longer and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1E and Sgo1F encode the same isoform (1EF).
      Source sequence(s)
      AB187578, AB193061, BX494477
      Consensus CDS
      CCDS33716.1
      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Related
      ENSP00000263753.4, ENST00000263753.8
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    3. NM_001012411.4NP_001012411.1  shugoshin 1 isoform 1CD

      See identical proteins and their annotated locations for NP_001012411.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1C, PMID:15737064; also known as B1) differs in its 5' UTR and uses an alternate in-frame splice site in its central coding region compared to variant 1. It encodes isoform 1CD which is shorter and has a distinct internal amino acid, compared to isoform 1. Both variants Sgo1C and Sgo1D encode the same isoform (1CD).
      Source sequence(s)
      AB193058, AC099057, AF308299, BC032696, BX494477, BX648516
      Consensus CDS
      CCDS46774.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000389034.1, ENST00000437051.5
      Conserved Domains (2) summary
      pfam07557
      Location:222244
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    4. NM_001012412.5NP_001012412.1  shugoshin 1 isoform 1GH

      See identical proteins and their annotated locations for NP_001012412.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1H, PMID:15737064, also known as B2) differs in its 5' UTR, uses an alternate in-frame splice site in its central coding region, and contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1GH which is shorter, has a distinct internal amino acid, and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1G and Sgo1H encode the same isoform (1GH).
      Source sequence(s)
      AB187578, AB193063, BX494477
      Consensus CDS
      CCDS46771.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000394625.2, ENST00000419233.6
      Conserved Domains (2) summary
      pfam07557
      Location:222244
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    5. NM_001012413.4NP_001012413.1  shugoshin 1 isoform 1AB

      See identical proteins and their annotated locations for NP_001012413.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1B, PMID:15737064; also known as C1) differs in its 5' UTR and lacks an alternate in-frame exon in its central coding region compared to variant 1. It encodes isoform 1AB which is shorter and has a distinct internal amino acid, compared to isoform 1. Both variants Sgo1A and Sgo1B encode the same isoform (1AB).
      Source sequence(s)
      AB193057, AC099057, AF308299, BC032696, BX494477, BX648516
      Consensus CDS
      CCDS46772.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Conserved Domains (2) summary
      pfam07557
      Location:205227
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    6. NM_001199251.3NP_001186180.1  shugoshin 1 isoform 1

      See identical proteins and their annotated locations for NP_001186180.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript. Both variants 1 and A1 encode the same isoform (1).
      Source sequence(s)
      AB190994, AC099057, AF308299, AK308095, BC032696, BX648516
      Consensus CDS
      CCDS46773.1
      UniProtKB/TrEMBL
      A0A024R2K2, B5BUA4
      Related
      ENSP00000410458.1, ENST00000412997.6
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    7. NM_001199252.3NP_001186181.1  shugoshin 1 isoform EF

      See identical proteins and their annotated locations for NP_001186181.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1E, PMID:15737064) contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1EF which is longer and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1E and Sgo1F encode the same isoform (1EF).
      Source sequence(s)
      AB187578, AB193060, BX494477
      Consensus CDS
      CCDS33716.1
      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Related
      ENSP00000414129.1, ENST00000421451.5
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    8. NM_001199253.3NP_001186182.1  shugoshin 1 isoform 1CD

      See identical proteins and their annotated locations for NP_001186182.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1D, PMID:15737064) uses an alternate in-frame splice site in its central coding region compared to variant 1. It encodes isoform 1CD which is shorter and has a distinct internal amino acid, compared to isoform 1. Both variants Sgo1C and Sgo1D encode the same isoform (1CD).
      Source sequence(s)
      AB193059, AC099057, AF308299, BC032696, BX494477, BX648516
      Consensus CDS
      CCDS46774.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000394613.1, ENST00000417364.1
      Conserved Domains (2) summary
      pfam07557
      Location:222244
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    9. NM_001199254.3NP_001186183.1  shugoshin 1 isoform 1GH

      See identical proteins and their annotated locations for NP_001186183.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1G, PMID:15737064) uses an alternate in-frame splice site in its central coding region and contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1GH which is shorter, has a distinct internal amino acid, and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1G and Sgo1H encode the same isoform (1GH).
      Source sequence(s)
      AB187578, AB193062, BX494477
      Consensus CDS
      CCDS46771.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000414960.1, ENST00000425061.5
      Conserved Domains (2) summary
      pfam07557
      Location:222244
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    10. NM_001199255.3NP_001186184.1  shugoshin 1 isoform 1AB

      See identical proteins and their annotated locations for NP_001186184.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1A, PMID:15737064) lacks an alternate in-frame exon in its central coding region compared to variant 1. It encodes isoform 1AB which is shorter and has a distinct internal amino acid, compared to isoform 1. Both variants Sgo1A and Sgo1B encode the same isoform (1AB).
      Source sequence(s)
      AB193056, AC099057, AF308299, BC032696, BX494477, BX648516
      Consensus CDS
      CCDS46772.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000394957.1, ENST00000442720.5
      Conserved Domains (2) summary
      pfam07557
      Location:205227
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    11. NM_001199256.3NP_001186185.1  shugoshin 1 isoform 1KL

      See identical proteins and their annotated locations for NP_001186185.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1K, PMID:15737064; also known as sSGO1, PMID:18331714) lacks an alternate in-frame exon in its central coding region, and contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1KL which is shorter, has a distinct internal amino acid, and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1K and Sgo1L encode the same isoform (1KL).
      Source sequence(s)
      AB187578, AB193065, BX494477
      Consensus CDS
      CCDS2635.1
      Related
      ENSP00000411200.1, ENST00000452020.5
      Conserved Domains (2) summary
      pfam07557
      Location:205226
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    12. NM_001199257.3NP_001186186.1  shugoshin 1 isoform 1J

      See identical proteins and their annotated locations for NP_001186186.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1J, PMID:15737064) uses an alternate splice site in its 3' coding region, lacks two exons in the 3' coding region, and contains an alternate 3' terminal exon compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1J which is shorter and has a distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AB187578, AB193064, BX494477
      Consensus CDS
      CCDS56243.1
      UniProtKB/Swiss-Prot
      Q5FBB7
      Related
      ENSP00000413070.1, ENST00000443724.5
      Conserved Domains (1) summary
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    13. NM_138484.5NP_612493.1  shugoshin 1 isoform 1KL

      See identical proteins and their annotated locations for NP_612493.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (Sgo1L, PMID:15737064; also known as sSGO1, PMID:18331714 or C2) differs in the 5' UTR, lacks an alternate in-frame exon in its central coding region, and contains an alternate 3' terminal segment compared to variant 1, resulting in a novel 3' coding region and distinct 3' UTR. It encodes isoform 1KL which is shorter, has a distinct internal amino acid, and has a distinct C-terminus, compared to isoform 1. Both variants Sgo1K and Sgo1L encode the same isoform (1KL).
      Source sequence(s)
      AB187578, AB193066, BX494477
      Consensus CDS
      CCDS2635.1
      Related
      ENSP00000306581.2, ENST00000306698.6
      Conserved Domains (2) summary
      pfam07557
      Location:205226
      Shugoshin_C; Shugoshin C terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region

    RNA

    1. NR_131179.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (14) differs in its 5' terminal exon and lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AB193058, AB567657, AC099057, AF308299, BC032696, BX494477, BX648516
    2. NR_131180.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (15) differs in its 5' terminal exon and lacks two alternate internal exons, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AB193058, AB567656, AC099057, AF308299, BC032696, BX494477, BX648516

    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_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      20160593..20186886 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_011533377.3XP_011531679.1  shugoshin 1 isoform X1

      See identical proteins and their annotated locations for XP_011531679.1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    2. XM_047447486.1XP_047303442.1  shugoshin 1 isoform X2

    3. XM_011533373.3XP_011531675.1  shugoshin 1 isoform X1

      See identical proteins and their annotated locations for XP_011531675.1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    4. XM_011533376.3XP_011531678.1  shugoshin 1 isoform X1

      See identical proteins and their annotated locations for XP_011531678.1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    5. XM_047447487.1XP_047303443.1  shugoshin 1 isoform X3

    6. XM_011533375.3XP_011531677.1  shugoshin 1 isoform X1

      See identical proteins and their annotated locations for XP_011531677.1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
      Conserved Domains (2) summary
      pfam07557
      Location:474496
      Shugoshin_C; Shugoshin C-terminus
      pfam07558
      Location:2266
      Shugoshin_N; Shugoshin N-terminal coiled-coil region
    7. XM_047447489.1XP_047303445.1  shugoshin 1 isoform X5

    8. XM_047447490.1XP_047303446.1  shugoshin 1 isoform X5

    9. XM_047447488.1XP_047303444.1  shugoshin 1 isoform X4

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      20164579..20190864 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054345327.1XP_054201302.1  shugoshin 1 isoform X1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
    2. XM_054345326.1XP_054201301.1  shugoshin 1 isoform X1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
    3. XM_054345328.1XP_054201303.1  shugoshin 1 isoform X2

    4. XM_054345324.1XP_054201299.1  shugoshin 1 isoform X1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
    5. XM_054345329.1XP_054201304.1  shugoshin 1 isoform X3

    6. XM_054345325.1XP_054201300.1  shugoshin 1 isoform X1

      UniProtKB/Swiss-Prot
      Q588H5, Q5FBB4, Q5FBB5, Q5FBB6, Q5FBB7, Q5FBB8, Q8N579, Q8WVL0, Q9BVA8, Q9H275
    7. XM_054345331.1XP_054201306.1  shugoshin 1 isoform X5

    8. XM_054345330.1XP_054201305.1  shugoshin 1 isoform X4

    9. XM_054345332.1XP_054201307.1  shugoshin 1 isoform X5

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