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MYO3A myosin IIIA [ Homo sapiens (human) ]

Gene ID: 53904, updated on 20-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
Hearing loss, 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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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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