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    MSTO1 misato mitochondrial distribution and morphology regulator 1 [ Homo sapiens (human) ]

    Gene ID: 55154, updated on 27-Dec-2024

    Summary

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    Official Symbol
    MSTO1provided by HGNC
    Official Full Name
    misato mitochondrial distribution and morphology regulator 1provided by HGNC
    Primary source
    HGNC:HGNC:29678
    See related
    Ensembl:ENSG00000125459 MIM:617619; AllianceGenome:HGNC:29678
    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
    MST; MMYAT; LST005
    Summary
    Involved in mitochondrion distribution; mitochondrion organization; and positive regulation of mitochondrial fusion. Located in mitochondrial outer membrane. Is active in cytosol. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Ubiquitous expression in testis (RPKM 18.6), fat (RPKM 12.3) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See MSTO1 in Genome Data Viewer
    Location:
    1q22
    Exon count:
    18
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (155563246..155614967)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (154748735..154753532)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (155579961..155584758)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene ASH1 like histone lysine methyltransferase Neighboring gene RNA, U6 small nuclear 1297, pseudogene Neighboring gene POU class 5 homeobox 1 pseudogene 4 Neighboring gene NANOG hESC enhancer GRCh37_chr1:155469805-155470306 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:155484783-155485282 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:155499969-155500470 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1406 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:155515470-155515970 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1817 Neighboring gene Sharpr-MPRA regulatory region 11909 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1407 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:155532613-155533180 Neighboring gene Sharpr-MPRA regulatory region 7926 Neighboring gene uncharacterized LOC101929703 Neighboring gene ASH1L antisense RNA 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:155546798-155546935 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:155556739-155556902 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:155560641-155561220 Neighboring gene Sharpr-MPRA regulatory region 723 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr1:155569297-155569949 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:155569950-155570603 Neighboring gene claudin 6 pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:155578996-155579870 Neighboring gene uncharacterized LOC105371452 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:155579871-155580745 Neighboring gene gon-4 like pseudogene Neighboring gene death associated protein 3 pseudogene 1 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr1:155604951-155605710 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:155605711-155606471 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:155606472-155607231 Neighboring gene gon-4 like pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

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    Related articles in PubMed

    1. Evidence of motor axon or motor neuron damage in a Chinese patient with compound heterozygous MSTO1 variants. Jiao Y, et al. Acta Neurol Belg, 2021 Jun. PMID 33222031
    2. Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy. Gerber S, et al. EMBO Mol Med, 2023 Aug 7. PMID 37431816, Free PMC Article
    3. MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. Donkervoort S, et al. Acta Neuropathol, 2019 Dec. PMID 31463572, Free PMC Article
    4. Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia. Nasca A, et al. Hum Mutat, 2017 Aug. PMID 28544275, Free PMC Article
    5. MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans. Gal A, et al. EMBO Mol Med, 2017 Jul. PMID 28554942, Free PMC Article

    See all (52) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy.
      Title: Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy.
    2. Evidence of motor axon or motor neuron damage in a Chinese patient with compound heterozygous MSTO1 variants.
      Title: Evidence of motor axon or motor neuron damage in a Chinese patient with compound heterozygous MSTO1 variants.
    3. Whole-exome sequencing identifies rare compound heterozygous mutations in the MSTO1 gene associated with cerebellar ataxia and myopathy.
      Title: Whole-exome sequencing identifies rare compound heterozygous mutations in the MSTO1 gene associated with cerebellar ataxia and myopathy.
    4. MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement.
      Title: MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement.
    5. we have described two unrelated patients with biallelic MSTO1 mutations. Our report provides valuable information on the consequences of MSTO1 mutations for human phenotypes.
      Title: Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy.
    6. Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
      Title: Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia.
    7. Thus, an MSTO1 loss-of-function mutation is associated with a human disorder showing mitochondrial involvement. MSTO1 likely has a physiologically relevant role in mitochondrial morphogenesis by supporting mitochondrial fusion.
      Title: MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
    8. These results indicated that human Misato has a role(s) in mitochondrial distribution and morphology and that its unregulated expression leads to cell death.
      Title: Human Misato regulates mitochondrial distribution and morphology.
    Submit: New GeneRIF Correction

    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
    Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
    MedGen: C4540096 OMIM: 617675 GeneReviews: Not available
    		Compare labs

    EBI GWAS Catalog

    Description
    Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
    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)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • FLJ10504, DKFZp686B1757, DKFZp686I01261

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in mitochondrion distribution IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in mitochondrion organization IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in mitochondrion organization IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in positive regulation of mitochondrial fusion IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    Component Evidence Code Pubs
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    is_active_in cytosol IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
    		  
    located_in mitochondrial outer membrane IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in mitochondrion HTP PubMed 
    is_active_in mitochondrion IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  

    General protein information

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    Preferred Names
    protein misato homolog 1
    Names
    misato 1, mitochondrial distribution and morphology regulator
    misato homolog 1

    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_001256532.1 → NP_001243461.1  protein misato homolog 1 isoform b

      See identical proteins and their annotated locations for NP_001243461.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform b), compared to isoform a.
      Source sequence(s)
      AF272833, AK222863, BC002535, DA807092
      UniProtKB/TrEMBL
      A8K3J5
      Conserved Domains (1) summary
      cd06060
      Location:6 → 562
      misato; Misato segment II tubulin-like domain

    2. NM_001256533.1 → NP_001243462.1  protein misato homolog 1 isoform c

      See identical proteins and their annotated locations for NP_001243462.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) uses two alternate in-frame splice sites in the 3' coding region, compared to variant 1. This results in a shorter protein (isoform c), compared to isoform a.
      Source sequence(s)
      AF272833, BC002535, CR749791, DA807092
      UniProtKB/TrEMBL
      A8K3J5
      Conserved Domains (1) summary
      cd06060
      Location:6 → 551
      misato; Misato segment II tubulin-like domain

    3. NM_001350772.1 → NP_001337701.1  protein misato homolog 1 isoform 4

      Status: VALIDATED

      Source sequence(s)
      AF272833, BC002535, CR749791, DA807092
      UniProtKB/TrEMBL
      A8K3J5
      Related
      ENSP00000357325.4, ENST00000368341.8
      Conserved Domains (1) summary
      cd06060
      Location:6 → 552
      misato; Misato segment II tubulin-like domain

    4. NM_001350773.1 → NP_001337702.1  protein misato homolog 1 isoform 5

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BE717044, DA807092
      Conserved Domains (1) summary
      cd06060
      Location:6 → 428
      misato; Misato segment II tubulin-like domain

    5. NM_001350774.1 → NP_001337703.1  protein misato homolog 1 isoform 6

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BE717044, DA807092
      Consensus CDS
      CCDS91070.1
      UniProtKB/TrEMBL
      A0A3B3IUD2
      Related
      ENSP00000498188.1, ENST00000649846.1
      Conserved Domains (1) summary
      cd06060
      Location:6 → 428
      misato; Misato segment II tubulin-like domain

    6. NM_001350775.1 → NP_001337704.1  protein misato homolog 1 isoform 7

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, BX421996, DA807092, H12094
      UniProtKB/TrEMBL
      A8K3J5
      Conserved Domains (1) summary
      cd06060
      Location:6 → 511
      misato; Misato segment II tubulin-like domain

    7. NM_001350776.1 → NP_001337705.1  protein misato homolog 1 isoform 8

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, BF027217, DA070565, DA807092
      UniProtKB/TrEMBL
      B4DLS9
      Conserved Domains (1) summary
      cd06060
      Location:88 → 508
      misato; Misato segment II tubulin-like domain

    8. NM_001350777.1 → NP_001337706.1  protein misato homolog 1 isoform 9

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BX421996, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:11 → 386
      misato; Misato segment II tubulin-like domain

    9. NM_001350778.1 → NP_001337707.1  protein misato homolog 1 isoform 9

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BX421996, DA272145, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:11 → 386
      misato; Misato segment II tubulin-like domain

    10. NM_001350779.1 → NP_001337708.1  protein misato homolog 1 isoform 9

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BX421996, DA379275, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:11 → 386
      misato; Misato segment II tubulin-like domain

    11. NM_001350780.1 → NP_001337709.1  protein misato homolog 1 isoform 10

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, DA070565, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:1 → 385
      misato; Misato segment II tubulin-like domain

    12. NM_001350781.1 → NP_001337710.1  protein misato homolog 1 isoform 10

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, AY334564, BC002535, DA070565, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:1 → 385
      misato; Misato segment II tubulin-like domain

    13. NM_001350782.1 → NP_001337711.1  protein misato homolog 1 isoform 10

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, DA070565, DA272145, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Related
      ENSP00000513434.1, ENST00000697770.1
      Conserved Domains (1) summary
      cd06060
      Location:1 → 385
      misato; Misato segment II tubulin-like domain

    14. NM_001350783.1 → NP_001337712.1  protein misato homolog 1 isoform 11

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, DA070565, DA272145, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:1 → 384
      misato; Misato segment II tubulin-like domain

    15. NM_001350784.1 → NP_001337713.1  protein misato homolog 1 isoform 12

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, DA379275, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:7 → 382
      misato; Misato segment II tubulin-like domain

    16. NM_001350785.1 → NP_001337714.1  protein misato homolog 1 isoform 12

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, AY334564, BC002535, DA272145, DA379275, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:7 → 382
      misato; Misato segment II tubulin-like domain

    17. NM_001350786.1 → NP_001337715.1  protein misato homolog 1 isoform 13

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, BE717044, DA070565, DA272145, DA807092
      Conserved Domains (1) summary
      cl10017
      Location:1 → 250
      Tubulin_FtsZ_Cetz-like; Tubulin protein family of FtsZ and CetZ-like

    18. NM_001350787.1 → NP_001337716.1  protein misato homolog 1 isoform 14

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, CR749791, DA379275, DA807092
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:7 → 371
      misato; Misato segment II tubulin-like domain

    19. NM_001350788.1 → NP_001337717.1  protein misato homolog 1 isoform 15

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, DA070565, DA272145, DA807092, H12094
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cd06060
      Location:1 → 333
      misato; Misato segment II tubulin-like domain

    20. NM_001350789.1 → NP_001337718.1  protein misato homolog 1 isoform 16

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, DA070565, DA272145, DA807092, H12094
      UniProtKB/TrEMBL
      A0A8V8TLP0
      Conserved Domains (1) summary
      cl10017
      Location:7 → 330
      Tubulin_FtsZ_Cetz-like; Tubulin protein family of FtsZ and CetZ-like

    21. NM_018116.4 → NP_060586.2  protein misato homolog 1 isoform a

      See identical proteins and their annotated locations for NP_060586.2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (a).
      Source sequence(s)
      AF272833, AK001366, AK222863, BX537684
      Consensus CDS
      CCDS1114.1
      UniProtKB/Swiss-Prot
      Q53GR8, Q5CZ69, Q5T717, Q68CT6, Q7LBZ8, Q7Z3M7, Q7Z558, Q8TE05, Q9BUK6, Q9NQX2, Q9NVU4
      UniProtKB/TrEMBL
      A8K3J5
      Related
      ENSP00000245564.3, ENST00000245564.8
      Conserved Domains (1) summary
      cd06060
      Location:6 → 563
      misato; Misato segment II tubulin-like domain

    RNA

    1. NR_046292.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) uses two alternate splice sites, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AF272833, AK001366, AK297140, AK309573, AL353807, BC002535, DA807092

    2. NR_046293.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) uses two alternate splice sites, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AF272833, AK001366, AK309573, BC002535, DA807092

    3. NR_046294.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) has multiple differences compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AF272833, AK056128, DA807092
      Related
      ENST00000494995.5

    4. NR_046295.1 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7) lacks an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AF272833, AK001366, BC002535, BX537684, DA807092
      Related
      ENST00000490743.5

    5. NR_146907.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, BC002535, DA807092

    6. NR_146908.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AF272833, AK001366, AL353807, BC002535, BX421996, DA807092

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      155563246..155614967
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047424007.1 → XP_047279963.1  protein misato homolog 1 isoform X1

      UniProtKB/Swiss-Prot
      Q53GR8, Q5CZ69, Q5T717, Q68CT6, Q7LBZ8, Q7Z3M7, Q7Z558, Q8TE05, Q9BUK6, Q9NQX2, Q9NVU4
      UniProtKB/TrEMBL
      A8K3J5

    2. XM_047424008.1 → XP_047279964.1  protein misato homolog 1 isoform X1

      UniProtKB/Swiss-Prot
      Q53GR8, Q5CZ69, Q5T717, Q68CT6, Q7LBZ8, Q7Z3M7, Q7Z558, Q8TE05, Q9BUK6, Q9NQX2, Q9NVU4
      UniProtKB/TrEMBL
      A8K3J5

    3. XM_047424021.1 → XP_047279977.1  protein misato homolog 1 isoform X3

      UniProtKB/TrEMBL
      B4DLS9

    4. XM_047424030.1 → XP_047279986.1  protein misato homolog 1 isoform X4

      UniProtKB/TrEMBL
      B4DLS9

    5. XM_047424011.1 → XP_047279967.1  protein misato homolog 1 isoform X2

      UniProtKB/TrEMBL
      B4DLS9
      Related
      ENST00000483734.5

    6. XM_047424040.1 → XP_047279996.1  protein misato homolog 1 isoform X5

      UniProtKB/TrEMBL
      A0A8V8TLP0

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      154748735..154753532
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054337366.1 → XP_054193341.1  protein misato homolog 1 isoform X3

      UniProtKB/TrEMBL
      B4DLS9

    2. XM_054337372.1 → XP_054193347.1  protein misato homolog 1 isoform X4

      UniProtKB/TrEMBL
      B4DLS9

    3. XM_054337364.1 → XP_054193339.1  protein misato homolog 1 isoform X2

      UniProtKB/TrEMBL
      B4DLS9

    4. XM_054337371.1 → XP_054193346.1  protein misato homolog 1 isoform X15

    5. XM_054337368.1 → XP_054193343.1  protein misato homolog 1 isoform X12

      UniProtKB/TrEMBL
      A8K3J5

    6. XM_054337369.1 → XP_054193344.1  protein misato homolog 1 isoform X13

      UniProtKB/TrEMBL
      A8K3J5

    7. XM_054337370.1 → XP_054193345.1  protein misato homolog 1 isoform X14

      UniProtKB/TrEMBL
      B4DLS9

    8. XM_054337360.1 → XP_054193335.1  protein misato homolog 1 isoform X6

    9. XM_054337361.1 → XP_054193336.1  protein misato homolog 1 isoform X7

    10. XM_054337362.1 → XP_054193337.1  protein misato homolog 1 isoform X8

    11. XM_054337367.1 → XP_054193342.1  protein misato homolog 1 isoform X11

    12. XM_054337363.1 → XP_054193338.1  protein misato homolog 1 isoform X9

      UniProtKB/TrEMBL
      A8K3J5

    13. XM_054337365.1 → XP_054193340.1  protein misato homolog 1 isoform X10

      UniProtKB/TrEMBL
      A8K3J5

    14. XM_054337374.1 → XP_054193349.1  protein misato homolog 1 isoform X16

    15. XM_054337373.1 → XP_054193348.1  protein misato homolog 1 isoform X5

      UniProtKB/TrEMBL
      A0A8V8TLP0
    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9BUK6.1 GenPept UniProtKB/Swiss-Prot:Q9BUK6

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