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MGI:Myo6

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Myo6 ( synonyms: Tlc )
Protein Name(s) myosin VI,
External Links
MGI MGI:104785

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000166

nucleotide binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0547

F

From MGI

GO:0001726

ruffle

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0005515

protein binding

MGI:MGI:3610864
PMID:15975910[1]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0
UniProtKB:P17809

F

From MGI

GO:0005515

protein binding

MGI:MGI:3654775
PMID:16819522[2]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0

F

From MGI

GO:0005515

protein binding

MGI:MGI:3656369
PMID:16467373[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q66T02

F

From MGI

GO:0005524

ATP binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0067

F

From MGI

GO:0005622

intracellular

MGI:MGI:3610864
PMID:15975910[1]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0

C

From MGI

GO:0005623

cell

MGI:MGI:3654775
PMID:16819522[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0005634

nucleus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0005654

nucleoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4430014
PMID:20016102[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0005792

microsome

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0005794

Golgi apparatus

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0005794

Golgi apparatus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0005886

plasma membrane

MGI:MGI:3610864
PMID:15975910[1]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0

C

From MGI

GO:0005902

microvillus

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0006605

protein targeting

MGI:MGI:3610864
PMID:15975910[1]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0

P

From MGI

GO:0006897

endocytosis

MGI:MGI:3527915
PMID:15657400[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0006897

endocytosis

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:3654775
PMID:16819522[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007416

synapse assembly

MGI:MGI:3527915
PMID:15657400[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:1346380
PMID:10525338[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:2150215
PMID:11468689[7]

ISO: Inferred from Sequence Orthology

UniProtKB:Q14784

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:3527915
PMID:15657400[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:3703302
PMID:17329413[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3708361

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:53523
PMID:5980120[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:77423
PMID:7493015[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:77423
PMID:7493015[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3664354
PMID:16962269[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0012506

vesicle membrane

MGI:MGI:3610864
PMID:15975910[1]

IPI: Inferred from Physical Interaction

UniProtKB:Q9Z0G0

C

From MGI

GO:0014047

glutamate secretion

MGI:MGI:3654775
PMID:16819522[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0016023

cytoplasmic membrane-bounded vesicle

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0016358

dendrite development

MGI:MGI:3527915
PMID:15657400[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0016459

myosin complex

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0518

C

From MGI

GO:0016591

DNA-directed RNA polymerase II, holoenzyme

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0030139

endocytic vesicle

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0030330

DNA damage response, signal transduction by p53 class mediator

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

P

From MGI

GO:0030424

axon

MGI:MGI:3654775
PMID:16819522[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0031941

filamentous actin

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0031965

nuclear membrane

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0032587

ruffle membrane

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0042472

inner ear morphogenesis

MGI:MGI:77423
PMID:7493015[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0042491

auditory receptor cell differentiation

MGI:MGI:1346380
PMID:10525338[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0042491

auditory receptor cell differentiation

MGI:MGI:53523
PMID:5980120[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0042491

auditory receptor cell differentiation

MGI:MGI:77423
PMID:7493015[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0042493

response to drug

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

P

From MGI

GO:0043025

neuronal cell body

MGI:MGI:3654775
PMID:16819522[2]

IDA: Inferred from Direct Assay

C

From MGI

GO:0043234

protein complex

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0045177

apical part of cell

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:XP_001061392

C

From MGI

GO:0045202

synapse

MGI:MGI:3527915
PMID:15657400[5]

ISO: Inferred from Sequence Orthology

RefSeq:XP_236444

C

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

P

From MGI

GO:0048167

regulation of synaptic plasticity

MGI:MGI:3654775
PMID:16819522[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0048471

perinuclear region of cytoplasm

MGI:MGI:3527915
PMID:15657400[5]

ISO: Inferred from Sequence Orthology

RefSeq:XP_236444

C

From MGI

GO:0048471

perinuclear region of cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

C

From MGI

GO:0048839

inner ear development

MGI:MGI:1346380
PMID:10525338[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0048839

inner ear development

MGI:MGI:53523
PMID:5980120[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0048839

inner ear development

MGI:MGI:77423
PMID:7493015[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1856555

P

From MGI

GO:0051015

actin filament binding

MGI:MGI:3527915
PMID:15657400[5]

ISO: Inferred from Sequence Orthology

RefSeq:XP_236444

F

From MGI

GO:0051015

actin filament binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

F

From MGI

GO:0051046

regulation of secretion

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9UM54

P

From MGI

GO:0071257

cellular response to electrical stimulus

MGI:MGI:4849309
PMID:21052544[12]

IMP: Inferred from Mutant Phenotype

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 1.4 Reed BC et al. (2005) GLUT1CBP(TIP2/GIPC1) interactions with GLUT1 and myosin VI: evidence supporting an adapter function for GLUT1CBP. Mol Biol Cell 16: 4183-201 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Yano H et al. (2006) BDNF-mediated neurotransmission relies upon a myosin VI motor complex. Nat Neurosci 9: 1009-18 PubMed GONUTS page
  3. Liu M & Horowitz A (2006) A PDZ-binding motif as a critical determinant of Rho guanine exchange factor function and cell phenotype. Mol Biol Cell 17: 1880-7 PubMed GONUTS page
  4. Grimsley-Myers CM et al. (2009) The small GTPase Rac1 regulates auditory hair cell morphogenesis. J Neurosci 29: 15859-69 PubMed GONUTS page
  5. 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Osterweil E et al. (2005) A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis. J Cell Biol 168: 329-38 PubMed GONUTS page
  6. 6.0 6.1 6.2 Self T et al. (1999) Role of myosin VI in the differentiation of cochlear hair cells. Dev Biol 214: 331-41 PubMed GONUTS page
  7. Melchionda S et al. (2001) MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. Am J Hum Genet 69: 635-40 PubMed GONUTS page
  8. Schwander M et al. (2007) A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci 27: 2163-75 PubMed GONUTS page
  9. 9.0 9.1 9.2 Deol MS & Green MC (1966) Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse. Genet Res 8: 339-45 PubMed GONUTS page
  10. 10.0 10.1 10.2 10.3 10.4 Avraham KB et al. (1995) The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nat Genet 11: 369-75 PubMed GONUTS page
  11. Calderon A et al. (2006) Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse. Hear Res 221: 44-58 PubMed GONUTS page
  12. Won J et al. (2011) Mouse model resources for vision research. J Ophthalmol 2011: 391384 PubMed GONUTS page
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