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    MYO3A myosin IIIA [ Homo sapiens (human) ]

    Gene ID: 53904, updated on 3-Apr-2024

    Summary

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    Official Symbol
    MYO3Aprovided by HGNC
    Official Full Name
    myosin IIIAprovided by HGNC
    Primary source
    HGNC:HGNC:7601
    See related
    Ensembl:ENSG00000095777 MIM:606808; AllianceGenome:HGNC:7601
    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
    DFNA90; DFNB30
    Summary
    The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008]
    Expression
    Biased expression in testis (RPKM 1.4), skin (RPKM 0.2) and 4 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    Location:
    10p12.1
    Exon count:
    43
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (25934229..26212532)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (25959075..26237044)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (26223158..26501461)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376460 Neighboring gene uncharacterized LOC101929073 Neighboring gene NANOG hESC enhancer GRCh37_chr10:26263803-26264349 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr10:26289384-26290583 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr10:26290901-26292100 Neighboring gene NANOG hESC enhancer GRCh37_chr10:26488725-26489248 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr10:26502717-26503284 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:26503285-26503850 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:26503851-26504417 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:26507027-26507655 Neighboring gene glutamate decarboxylase 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3164 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3165 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:26726587-26727116 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3167 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2235 Neighboring gene amyloid beta precursor protein binding family B member 1 interacting protein Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3168 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:26778915-26779063 Neighboring gene RNA, 5S ribosomal pseudogene 307

    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
    • 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. Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism. Gunther LK, et al. Mol Biol Cell, 2022 Jan 1. PMID 34788109, Free PMC Article
    2. Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. Souissi A, et al. J Biomol Struct Dyn, 2022. PMID 34423747
    3. Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss. Bueno AS, et al. Eur J Hum Genet, 2022 Jan. PMID 33953343, Free PMC Article
    4. A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family. Doll J, et al. Mol Genet Genomic Med, 2020 Aug. PMID 32519820, Free PMC Article
    5. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Dantas VGL, et al. Sci Rep, 2018 Jun 7. PMID 29880844, Free PMC Article

    See all (41) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. The dynamics of actin protrusions can be controlled by tip-localized myosin motors.
      Title: The dynamics of actin protrusions can be controlled by tip-localized myosin motors.
    2. Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment.
      Title: Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment.
    3. Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism.
      Title: Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism.
    4. Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss.
      Title: Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss.
    5. Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon.
      Title: Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon.
    6. A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family.
      Title: A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family.
    7. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss.
      Title: Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss.
    8. MYO3A is more efficient than MYO3B at increasing formation and elongation of stable microvilli on the surface of cultured epithelial cells.
      Title: Impact of the Motor and Tail Domains of Class III Myosins on Regulating the Formation and Elongation of Actin Protrusions.
    9. The structures of Myo3 in complex with Espin1 not only elucidate the mechanism of the binding, but also reveal a Myo3-induced release of Espin1 auto-inhibition mechanism.
      Title: Myosin III-mediated cross-linking and stimulation of actin bundling activity of Espin.
    10. Study reports an amino acid substitution in MYO3A motor-head domain disrupting its ATPase activity that can cause autosomal dominant progressive hereditary hearing loss. Also, these results uncovered a novel interaction between MYO3A and PCDH15 shedding new light on the function of myosin IIIA at stereocilia tips.
      Title: MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.
    Submit: New GeneRIF Correction See all GeneRIFs (23)

    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
    Autosomal recessive nonsyndromic hearing loss 30
    MedGen: C1846784 OMIM: 607101 GeneReviews: Genetic Hearing Loss Overview
    		Compare labs
    Deafness, autosomal dominant 90
    MedGen: CN376841 OMIM: 620722 GeneReviews: Not available
    		not available

    EBI GWAS Catalog

    Description
    Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.
    EBI GWAS Catalog
    Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
    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

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ADP binding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables actin binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables calmodulin binding IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables microfilament motor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables microfilament motor activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables microfilament motor activity IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    enables plus-end directed microfilament motor activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables protein kinase activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables protein serine kinase activity IEA
    Inferred from Electronic Annotation
    more info
    		  
    enables protein serine/threonine kinase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    Process Evidence Code Pubs
    involved_in cochlea morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    involved_in peptidyl-serine phosphorylation IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in positive regulation of filopodium assembly IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in protein autophosphorylation IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    involved_in regulation of actin filament length IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in response to stimulus IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in sensory perception of sound IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in sensory perception of sound IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    involved_in sensory perception of sound ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    involved_in visual perception IEA
    Inferred from Electronic Annotation
    more info
    		  
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of filamentous actin IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in filopodium IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    is_active_in filopodium tip IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in filopodium tip IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of myosin complex IEA
    Inferred from Electronic Annotation
    more info
    		  
    is_active_in photoreceptor inner segment IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    is_active_in stereocilium tip IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in stereocilium tip ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  

    General protein information

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    Preferred Names
    myosin-IIIa
    Names
    epididymis secretory sperm binding protein
    NP_001355194.1
    NP_059129.3
    XP_011517800.1
    XP_011517801.1
    XP_011517802.1
    XP_011517804.1
    XP_011517805.1
    XP_011517807.1
    XP_011517808.1
    XP_011517810.1
    XP_011517812.1
    XP_011517813.1
    XP_011517814.1
    XP_011517815.1
    XP_047281311.1
    XP_047281312.1
    XP_047281313.1
    XP_047281314.1
    XP_047281315.1
    XP_047281316.1
    XP_047281317.1
    XP_047281319.1
    XP_054222072.1
    XP_054222073.1
    XP_054222074.1
    XP_054222075.1
    XP_054222076.1
    XP_054222077.1
    XP_054222078.1
    XP_054222079.1
    XP_054222080.1
    XP_054222081.1
    XP_054222082.1
    XP_054222083.1
    XP_054222084.1
    XP_054222085.1
    XP_054222086.1
    XP_054222087.1
    XP_054222088.1
    XP_054222089.1
    XP_054222090.1
    XP_054222091.1

    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.

    Genomic

    1. NG_011635.1 RefSeqGene

      Range
      5157..283460
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_1354

    mRNA and Protein(s)

    1. NM_001368265.1 → NP_001355194.1  myosin-IIIa isoform 2

      Status: REVIEWED

      Source sequence(s)
      AL358612, BC036079
      Consensus CDS
      CCDS91223.1
      UniProtKB/TrEMBL
      Q86VY5
      Related
      ENSP00000365479.1, ENST00000376302.5

    2. NM_017433.5 → NP_059129.3  myosin-IIIa isoform 1

      See identical proteins and their annotated locations for NP_059129.3

      Status: REVIEWED

      Source sequence(s)
      AL162503, AL360217, AL391812, AY101367, CD628204, CD628208, CK903348
      Consensus CDS
      CCDS7148.1
      UniProtKB/Swiss-Prot
      Q4G0X2, Q5VZ28, Q8NEV4, Q8WX17, Q9NYS8
      UniProtKB/TrEMBL
      A0A384MED1
      Related
      ENSP00000495965.1, ENST00000642920.2
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      25934229..26212532
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_011519498.3 → XP_011517800.1  myosin-IIIa isoform X1

      See identical proteins and their annotated locations for XP_011517800.1

      UniProtKB/Swiss-Prot
      Q4G0X2, Q5VZ28, Q8NEV4, Q8WX17, Q9NYS8
      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    2. XM_011519500.3 → XP_011517802.1  myosin-IIIa isoform X1

      See identical proteins and their annotated locations for XP_011517802.1

      UniProtKB/Swiss-Prot
      Q4G0X2, Q5VZ28, Q8NEV4, Q8WX17, Q9NYS8
      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    3. XM_011519503.2 → XP_011517805.1  myosin-IIIa isoform X3

      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    4. XM_011519505.2 → XP_011517807.1  myosin-IIIa isoform X6

      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    5. XM_047425358.1 → XP_047281314.1  myosin-IIIa isoform X8

    6. XM_047425355.1 → XP_047281311.1  myosin-IIIa isoform X4

    7. XM_047425360.1 → XP_047281316.1  myosin-IIIa isoform X10

    8. XM_047425357.1 → XP_047281313.1  myosin-IIIa isoform X5

    9. XM_047425361.1 → XP_047281317.1  myosin-IIIa isoform X11

    10. XM_011519502.1 → XP_011517804.1  myosin-IIIa isoform X2

      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    11. XM_047425359.1 → XP_047281315.1  myosin-IIIa isoform X9

    12. XM_047425363.1 → XP_047281319.1  myosin-IIIa isoform X13

    13. XM_011519506.3 → XP_011517808.1  myosin-IIIa isoform X7

      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    14. XM_011519510.2 → XP_011517812.1  myosin-IIIa isoform X14

      Related
      ENST00000642197.1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    15. XM_011519508.2 → XP_011517810.1  myosin-IIIa isoform X12

      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    16. XM_011519511.3 → XP_011517813.1  myosin-IIIa isoform X15

      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1000
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1007
      MYSc_Myo3; class III myosin, motor domain

    17. XM_047425356.1 → XP_047281312.1  myosin-IIIa isoform X5

    18. XM_011519499.2 → XP_011517801.1  myosin-IIIa isoform X1

      See identical proteins and their annotated locations for XP_011517801.1

      UniProtKB/Swiss-Prot
      Q4G0X2, Q5VZ28, Q8NEV4, Q8WX17, Q9NYS8
      UniProtKB/TrEMBL
      A0A384MED1
      Conserved Domains (4) summary
      cd06638
      Location:2 → 287
      STKc_myosinIIIA_N; N-terminal Catalytic domain of the Serine/Threonine Kinase, Class IIIA myosin
      smart00220
      Location:21 → 287
      S_TKc; Serine/Threonine protein kinases, catalytic domain
      smart00242
      Location:337 → 1053
      MYSc; Myosin. Large ATPases
      cd01379
      Location:352 → 1041
      MYSc_Myo3; class III myosin, motor domain

    19. XM_011519512.2 → XP_011517814.1  myosin-IIIa isoform X16

      Conserved Domains (2) summary
      smart00015
      Location:457 → 477
      IQ; Calmodulin-binding motif
      cl22853
      Location:12 → 417
      Motor_domain; Myosin and Kinesin motor domain

    20. XM_011519513.3 → XP_011517815.1  myosin-IIIa isoform X17

      Conserved Domains (2) summary
      smart00015
      Location:304 → 324
      IQ; Calmodulin-binding motif
      cl22853
      Location:1 → 264
      Motor_domain; Myosin and Kinesin motor domain

    RNA

    1. XR_930494.1 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      25959075..26237044
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054366098.1 → XP_054222073.1  myosin-IIIa isoform X1

    2. XM_054366101.1 → XP_054222076.1  myosin-IIIa isoform X3

    3. XM_054366105.1 → XP_054222080.1  myosin-IIIa isoform X6

    4. XM_054366107.1 → XP_054222082.1  myosin-IIIa isoform X8

    5. XM_054366102.1 → XP_054222077.1  myosin-IIIa isoform X4

    6. XM_054366109.1 → XP_054222084.1  myosin-IIIa isoform X10

    7. XM_054366103.1 → XP_054222078.1  myosin-IIIa isoform X5

    8. XM_054366110.1 → XP_054222085.1  myosin-IIIa isoform X11

    9. XM_054366100.1 → XP_054222075.1  myosin-IIIa isoform X2

    10. XM_054366108.1 → XP_054222083.1  myosin-IIIa isoform X9

    11. XM_054366112.1 → XP_054222087.1  myosin-IIIa isoform X13

    12. XM_054366106.1 → XP_054222081.1  myosin-IIIa isoform X7

    13. XM_054366113.1 → XP_054222088.1  myosin-IIIa isoform X14

    14. XM_054366111.1 → XP_054222086.1  myosin-IIIa isoform X12

    15. XM_054366114.1 → XP_054222089.1  myosin-IIIa isoform X15

    16. XM_054366099.1 → XP_054222074.1  myosin-IIIa isoform X1

    17. XM_054366104.1 → XP_054222079.1  myosin-IIIa isoform X5

    18. XM_054366097.1 → XP_054222072.1  myosin-IIIa isoform X1

    19. XM_054366115.1 → XP_054222090.1  myosin-IIIa isoform X16

    20. XM_054366116.1 → XP_054222091.1  myosin-IIIa isoform X17

    RNA

    1. XR_008488220.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q8NEV4.2 GenPept UniProtKB/Swiss-Prot:Q8NEV4

    Gene LinkOut

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