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MYO7A myosin VIIA [ Homo sapiens (human) ]

Gene ID: 4647, updated on 7-Apr-2024

Summary

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Official Symbol
MYO7Aprovided by HGNC
Official Full Name
myosin VIIAprovided by HGNC
Primary source
HGNC:HGNC:7606
See related
Ensembl:ENSG00000137474 MIM:276903; AllianceGenome:HGNC:7606
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
DFNB2; MYU7A; NSRD2; USH1B; DFNA11; MYOVIIA
Summary
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Expression
Broad expression in adrenal (RPKM 8.3), testis (RPKM 6.5) and 17 other tissues See more
Orthologs
mouse all
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Genomic context

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See MYO7A in Genome Data Viewer
Location:
11q13.5
Exon count:
56
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (77128246..77215241)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (77058823..77147851)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (76839292..76926286)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369400 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76777177-76777677 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76797624-76798572 Neighboring gene calpain 5 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76824170-76824764 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76824765-76825360 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76825361-76825954 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76837978-76838700 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76838701-76839424 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76840147-76840870 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76842316-76843037 Neighboring gene olfactory marker protein Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:76851056-76851622 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:76893658-76894158 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76902287-76902788 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:76902789-76903288 Neighboring gene glycerophosphodiester phosphodiesterase domain containing 4 Neighboring gene TOMM20 pseudogene 1

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. Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS. Kim YR, et al. Genes Genomics, 2023 Feb. PMID 36630074
  2. New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family. Lin Q, et al. Int Ophthalmol, 2023 Jun. PMID 36484953
  3. Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss. Xiang Y, et al. J Clin Lab Anal, 2022 Nov. PMID 36164746, Free PMC Article
  4. Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease. Roman-Naranjo P, et al. Hear Res, 2021 Sep 15. PMID 34391192
  5. Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous Mutations. Kabahuma RI, et al. Genes (Basel), 2021 Feb 15. PMID 33671976, Free PMC Article

See all (155) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Expression of two major isoforms of MYO7A in the retina: Considerations for gene therapy of Usher syndrome type 1B.
    Title: Expression of two major isoforms of MYO7A in the retina: Considerations for gene therapy of Usher syndrome type 1B.
  2. Dispersed DNA variants underlie hearing loss in South Florida's minority population.
    Title: Dispersed DNA variants underlie hearing loss in South Florida's minority population.
  3. New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family.
    Title: New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family.
  4. Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS.
    Title: Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS.
  5. Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss.
    Title: Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss.
  6. Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease.
    Title: Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease.
  7. The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes MYO7A and USH2A.
    Title: The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes MYO7A and USH2A.
  8. Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials.
    Title: Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials.
  9. Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.
    Title: Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.
  10. Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene.
    Title: Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene.
Submit: New GeneRIF Correction See all GeneRIFs (95)

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

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables ADP binding IEA
Inferred from Electronic Annotation
more info
  
enables ATP binding IEA
Inferred from Electronic Annotation
more info
  
enables actin filament binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables actin filament binding IDA
Inferred from Direct Assay
more info
 PubMed 
enables calmodulin binding IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables identical protein binding IEA
Inferred from Electronic Annotation
more info
  
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 protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables protein domain specific binding IEA
Inferred from Electronic Annotation
more info
  
enables spectrin binding IDA
Inferred from Direct Assay
more info
 PubMed 
Process Evidence Code Pubs
involved_in actin filament organization IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in actin filament-based movement IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in actin filament-based movement IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in auditory receptor cell stereocilium organization IEA
Inferred from Electronic Annotation
more info
  
involved_in cochlea development IEA
Inferred from Electronic Annotation
more info
  
involved_in endocytosis IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in equilibrioception IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in eye photoreceptor cell development IC
Inferred by Curator
more info
 PubMed 
involved_in intracellular protein transport IEA
Inferred from Electronic Annotation
more info
  
involved_in lysosome organization IDA
Inferred from Direct Assay
more info
 PubMed 
acts_upstream_of_or_within mechanoreceptor differentiation ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in phagolysosome assembly IEA
Inferred from Electronic Annotation
more info
  
involved_in pigment granule transport IEA
Inferred from Electronic Annotation
more info
  
involved_in protein localization ISS
Inferred from Sequence or Structural Similarity
more info
  
involved_in sensory organ development IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in sensory perception of light stimulus IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in sensory perception of sound IBA
Inferred from Biological aspect of Ancestor
more info
  
acts_upstream_of_or_within sensory perception of sound IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in sensory perception of sound IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in visual perception IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
is_active_in actin cytoskeleton IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in apical plasma membrane IEA
Inferred from Electronic Annotation
more info
  
located_in cell cortex IEA
Inferred from Electronic Annotation
more info
  
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in cytoplasm IDA
Inferred from Direct Assay
more info
 PubMed 
located_in cytosol IDA
Inferred from Direct Assay
more info
 PubMed 
located_in lysosomal membrane IDA
Inferred from Direct Assay
more info
 PubMed 
located_in melanosome IEA
Inferred from Electronic Annotation
more info
  
is_active_in membrane IBA
Inferred from Biological aspect of Ancestor
more info
  
is_active_in microvillus IBA
Inferred from Biological aspect of Ancestor
more info
  
part_of myosin VII complex IEA
Inferred from Electronic Annotation
more info
  
located_in photoreceptor connecting cilium IEA
Inferred from Electronic Annotation
more info
  
located_in photoreceptor inner segment IDA
Inferred from Direct Assay
more info
 PubMed 
located_in photoreceptor outer segment IDA
Inferred from Direct Assay
more info
 PubMed 
located_in stereocilium ISS
Inferred from Sequence or Structural Similarity
more info
  
located_in stereocilium base ISS
Inferred from Sequence or Structural Similarity
more info
  
located_in synapse IDA
Inferred from Direct Assay
more info
 PubMed 
located_in upper tip-link density IEA
Inferred from Electronic Annotation
more info
  

General protein information

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Preferred Names
unconventional myosin-VIIa
Names
myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))

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_009086.2 RefSeqGene

    Range
    5001..91996
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_1420

mRNA and Protein(s)

  1. NM_000260.4 → NP_000251.3  unconventional myosin-VIIa isoform 1

    See identical proteins and their annotated locations for NP_000251.3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
    Source sequence(s)
    AP000752, BG108466, U34227, U39226, U55208
    Consensus CDS
    CCDS53683.1
    UniProtKB/Swiss-Prot
    B9A011, F8VUN5, P78427, Q13321, Q13402, Q14785, Q92821, Q92822
    Related
    ENSP00000386331.3, ENST00000409709.9
    Conserved Domains (14) summary
    smart00015
    Location:766 → 787
    IQ; Calmodulin-binding motif
    smart00139
    Location:1763 → 1896
    MyTH4; Domain in Myosin and Kinesin Tails
    smart00242
    Location:60 → 741
    MYSc; Myosin. Large ATPases
    smart00295
    Location:1903 → 2115
    B41; Band 4.1 homologues
    cd13198
    Location:1468 → 1604
    FERM_C1_MyoVII; FERM domain C-lobe, repeat 1, of Myosin VII (MyoVII/Myo7)
    cd13199
    Location:2111 → 2206
    FERM_C2_MyoVII; FERM domain C-lobe, repeat 2, of Myosin VII (MyoVII, Myo7)
    cd14473
    Location:1363 → 1463
    FERM_B-lobe; FERM domain B-lobe
    cd01381
    Location:79 → 729
    MYSc_Myo7; class VII myosin, motor domain
    pfam00373
    Location:2013 → 2115
    FERM_M; FERM central domain
    pfam05672
    Location:866 → 935
    MAP7; MAP7 (E-MAP-115) family
    pfam09379
    Location:1262 → 1301
    FERM_N; FERM N-terminal domain
    pfam15743
    Location:808 → 946
    SPATA1_C; Spermatogenesis-associated C-terminus
    cl17036
    Location:1605 → 1669
    SH3; Src Homology 3 domain superfamily
    cl19107
    Location:866 → 934
    SPFH_like; core domain of the SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily

  2. NM_001127180.2 → NP_001120652.1  unconventional myosin-VIIa isoform 2

    See identical proteins and their annotated locations for NP_001120652.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an in-frame segment in the coding region, compared to variant 1. It encodes isoform 2 which is shorter than isoform 1.
    Source sequence(s)
    AP000752, BG108466, U39226, U55208
    Consensus CDS
    CCDS53684.1
    UniProtKB/Swiss-Prot
    Q13402
    Related
    ENSP00000392185.2, ENST00000458637.6
    Conserved Domains (13) summary
    smart00015
    Location:766 → 787
    IQ; Calmodulin-binding motif
    smart00139
    Location:1725 → 1858
    MyTH4; Domain in Myosin and Kinesin Tails
    smart00242
    Location:60 → 741
    MYSc; Myosin. Large ATPases
    smart00295
    Location:1865 → 2077
    B41; Band 4.1 homologues
    cd13198
    Location:1468 → 1566
    FERM_C1_MyoVII; FERM domain C-lobe, repeat 1, of Myosin VII (MyoVII/Myo7)
    cd13199
    Location:2073 → 2166
    FERM_C2_MyoVII; FERM domain C-lobe, repeat 2, of Myosin VII (MyoVII, Myo7)
    cd14473
    Location:1363 → 1463
    FERM_B-lobe; FERM domain B-lobe
    cd01381
    Location:79 → 729
    MYSc_Myo7; class VII myosin, motor domain
    pfam00373
    Location:1975 → 2077
    FERM_M; FERM central domain
    pfam05672
    Location:866 → 935
    MAP7; MAP7 (E-MAP-115) family
    pfam09379
    Location:1262 → 1301
    FERM_N; FERM N-terminal domain
    cl17036
    Location:1567 → 1631
    SH3; Src Homology 3 domain superfamily
    cl19107
    Location:866 → 934
    SPFH_like; core domain of the SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily

  3. NM_001369365.1 → NP_001356294.1  unconventional myosin-VIIa isoform 4

    Status: REVIEWED

    Source sequence(s)
    AP000752, AP001855, KF511157
    Consensus CDS
    CCDS91543.1
    Related
    ENSP00000386635.2, ENST00000409619.6
    Conserved Domains (11) summary
    smart00015
    Location:755 → 776
    IQ; Calmodulin-binding motif
    smart00139
    Location:1714 → 1847
    MyTH4; Domain in Myosin and Kinesin Tails
    smart00295
    Location:1854 → 2066
    B41; Band 4.1 homologues
    COG3064
    Location:785 → 955
    TolA; Membrane protein involved in colicin uptake [Cell wall/membrane/envelope biogenesis]
    cd13198
    Location:1457 → 1555
    FERM_C1_MyoVII; FERM domain C-lobe, repeat 1, of Myosin VII (MyoVII/Myo7)
    cd13199
    Location:2062 → 2157
    FERM_C2_MyoVII; FERM domain C-lobe, repeat 2, of Myosin VII (MyoVII, Myo7)
    cd01381
    Location:68 → 718
    MYSc_Myo7; class VII myosin, motor domain
    pfam05672
    Location:846 → 923
    MAP7; MAP7 (E-MAP-115) family
    cd17092
    Location:1246 → 1344
    FERM1_F1_Myosin-VII; FERM (Four.1 protein, Ezrin, Radixin, Moesin) domain 1, F1 sub-domain, found in Myosin-VIIa, Myosin-VIIb, and similar proteins
    cd17093
    Location:1852 → 1949
    FERM2_F1_Myosin-VII; FERM (Four.1 protein, Ezrin, Radixin, Moesin) domain 2, F1 sub-domain, found in Myosin-VIIa, Myosin-VIIb, and similar proteins
    cl17036
    Location:1556 → 1620
    SH3; Src Homology 3 domain superfamily

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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    77128246..77215241
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011545044.3 → XP_011543346.1  unconventional myosin-VIIa isoform X5

    Conserved Domains (13) summary
    smart00015
    Location:766 → 787
    IQ; Calmodulin-binding motif
    smart00139
    Location:1763 → 1896
    MyTH4; Domain in Myosin and Kinesin Tails
    smart00242
    Location:60 → 741
    MYSc; Myosin. Large ATPases
    smart00295
    Location:1903 → 2115
    B41; Band 4.1 homologues
    cd13198
    Location:1468 → 1604
    FERM_C1_MyoVII; FERM domain C-lobe, repeat 1, of Myosin VII (MyoVII/Myo7)
    cd14473
    Location:1363 → 1463
    FERM_B-lobe; FERM domain B-lobe
    cd01381
    Location:79 → 729
    MYSc_Myo7; class VII myosin, motor domain
    pfam00373
    Location:2013 → 2115
    FERM_M; FERM central domain
    pfam05672
    Location:866 → 935
    MAP7; MAP7 (E-MAP-115) family
    pfam09379
    Location:1262 → 1301
    FERM_N; FERM N-terminal domain
    pfam15743
    Location:808 → 946
    SPATA1_C; Spermatogenesis-associated C-terminus
    cl17036
    Location:1605 → 1669
    SH3; Src Homology 3 domain superfamily
    cl19107
    Location:866 → 934
    SPFH_like; core domain of the SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily

  2. XM_047426970.1 → XP_047282926.1  unconventional myosin-VIIa isoform X10

  3. XM_047426971.1 → XP_047282927.1  unconventional myosin-VIIa isoform X13

  4. XM_017017780.2 → XP_016873269.1  unconventional myosin-VIIa isoform X4

  5. XM_017017788.2 → XP_016873277.1  unconventional myosin-VIIa isoform X19

  6. XM_017017784.2 → XP_016873273.1  unconventional myosin-VIIa isoform X9

  7. XM_017017786.2 → XP_016873275.1  unconventional myosin-VIIa isoform X12

  8. XM_017017778.2 → XP_016873267.1  unconventional myosin-VIIa isoform X2

  9. XM_017017779.2 → XP_016873268.1  unconventional myosin-VIIa isoform X3

  10. XM_011545046.3 → XP_011543348.2  unconventional myosin-VIIa isoform X1

  11. XM_017017781.2 → XP_016873270.1  unconventional myosin-VIIa isoform X6

  12. XM_017017785.2 → XP_016873274.1  unconventional myosin-VIIa isoform X11

  13. XM_017017782.2 → XP_016873271.1  unconventional myosin-VIIa isoform X7

  14. XM_017017783.2 → XP_016873272.1  unconventional myosin-VIIa isoform X8

  15. XM_047426972.1 → XP_047282928.1  unconventional myosin-VIIa isoform X15

  16. XM_047426974.1 → XP_047282930.1  unconventional myosin-VIIa isoform X17

  17. XM_017017787.2 → XP_016873276.1  unconventional myosin-VIIa isoform X18

  18. XM_047426973.1 → XP_047282929.1  unconventional myosin-VIIa isoform X16

  19. XM_011545050.3 → XP_011543352.1  unconventional myosin-VIIa isoform X14

    Conserved Domains (12) summary
    smart00015
    Location:680 → 701
    IQ; Calmodulin-binding motif
    smart00139
    Location:1675 → 1808
    MyTH4; Domain in Myosin and Kinesin Tails
    smart00242
    Location:10 → 655
    MYSc; Myosin. Large ATPases
    smart00295
    Location:1815 → 2027
    B41; Band 4.1 homologues
    cd13198
    Location:1418 → 1516
    FERM_C1_MyoVII; FERM domain C-lobe, repeat 1, of Myosin VII (MyoVII/Myo7)
    cd14473
    Location:1313 → 1413
    FERM_B-lobe; FERM domain B-lobe
    cd01381
    Location:10 → 643
    MYSc_Myo7; class VII myosin, motor domain
    pfam00373
    Location:1925 → 2027
    FERM_M; FERM central domain
    pfam05672
    Location:780 → 849
    MAP7; MAP7 (E-MAP-115) family
    pfam09379
    Location:1176 → 1215
    FERM_N; FERM N-terminal domain
    cl17036
    Location:1517 → 1581
    SH3; Src Homology 3 domain superfamily
    cl19107
    Location:780 → 848
    SPFH_like; core domain of the SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily

RNA

  1. XR_001747888.2 RNA Sequence

  2. XR_001747889.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    77058823..77147851
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054368856.1 → XP_054224831.1  unconventional myosin-VIIa isoform X5

  2. XM_054368861.1 → XP_054224836.1  unconventional myosin-VIIa isoform X10

  3. XM_054368864.1 → XP_054224839.1  unconventional myosin-VIIa isoform X13

  4. XM_054368869.1 → XP_054224844.1  unconventional myosin-VIIa isoform X31

  5. XM_054368868.1 → XP_054224843.1  unconventional myosin-VIIa isoform X30

  6. XM_054368857.1 → XP_054224832.1  unconventional myosin-VIIa isoform X23

  7. XM_054368853.1 → XP_054224828.1  unconventional myosin-VIIa isoform X20

  8. XM_054368854.1 → XP_054224829.1  unconventional myosin-VIIa isoform X21

  9. XM_054368852.1 → XP_054224827.1  unconventional myosin-VIIa isoform X16

  10. XM_054368862.1 → XP_054224837.1  unconventional myosin-VIIa isoform X27

  11. XM_054368866.1 → XP_054224841.1  unconventional myosin-VIIa isoform X29

  12. XM_054368858.1 → XP_054224833.1  unconventional myosin-VIIa isoform X24

  13. XM_054368859.1 → XP_054224834.1  unconventional myosin-VIIa isoform X25

  14. XM_054368863.1 → XP_054224838.1  unconventional myosin-VIIa isoform X28

  15. XM_054368855.1 → XP_054224830.1  unconventional myosin-VIIa isoform X22

  16. XM_054368860.1 → XP_054224835.1  unconventional myosin-VIIa isoform X26

  17. XM_054368870.1 → XP_054224845.1  unconventional myosin-VIIa isoform X32

  18. XM_054368867.1 → XP_054224842.1  unconventional myosin-VIIa isoform X16

  19. XM_054368865.1 → XP_054224840.1  unconventional myosin-VIIa isoform X14

RNA

  1. XR_008488401.1 RNA Sequence

  2. XR_008488400.1 RNA Sequence

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001127179.2: Suppressed sequence

    Description
    NM_001127179.2: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q13402.2 GenPept UniProtKB/Swiss-Prot:Q13402

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