myo3a

Ensembl ID:
ENSDARG00000010186
ZFIN ID:
ZDB-GENE-041026-4
Description:
myosin-IIIa [Source:RefSeq peptide;Acc:NP_991142]
Human Orthologue:
MYO3A
Human Description:
myosin IIIA [Source:HGNC Symbol;Acc:7601]
Mouse Orthologue:
Myo3a
Mouse Description:
myosin IIIA Gene [Source:MGI Symbol;Acc:MGI:2183924]

Alleles

There are 9 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa18647 Nonsense Available for shipment Available now
sa13131 Nonsense Available for shipment Available now
sa16564 Essential Splice Site Available for shipment Available now
sa3278 Nonsense F2 line generated During 2016
sa5701 Nonsense F2 line generated During 2016
sa32475 Nonsense Available for shipment Available now
sa37820 Nonsense Mutation detected in F1 DNA During 2016
sa32474 Nonsense Available for shipment Available now
sa6756 Essential Splice Site Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa18647
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 427 1775 13 39
ENSDART00000136041 Nonsense 427 1775 13 38
ENSDART00000006636 Nonsense 427 1775 13 39
ENSDART00000136041 Nonsense 427 1775 13 38
Genomic Location (Zv9):
Chromosome 24 (position 6298237)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6185529
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAACGAACATCAAACCCYCCACATATATATGCWGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGRTAGAGCATGTTCCTCTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13131
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 427 1775 13 39
ENSDART00000136041 Nonsense 427 1775 13 38
ENSDART00000006636 Nonsense 427 1775 13 39
ENSDART00000136041 Nonsense 427 1775 13 38
Genomic Location (Zv9):
Chromosome 24 (position 6298237)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6185529
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAACGAACATCAAACCCYCCACATATATATGCWGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGGTAGAGCATGTTCCTCTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16564
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Essential Splice Site 437 1775 13 39
ENSDART00000136041 Essential Splice Site 437 1775 13 38
Genomic Location (Zv9):
Chromosome 24 (position 6298206)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6185498
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CWGTGGCAGACATTGCGTAWCAGTCCATGGTGTCCTATAATGCAGATCAG[G/A]TAGAGCATGTTCCTCTGTGAGCTGYTGGAGTGTGTCAGTCATAGTGTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3278
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 483 1775 15 39
ENSDART00000136041 Nonsense 483 1775 15 38
ENSDART00000006636 Nonsense 483 1775 15 39
ENSDART00000136041 Nonsense 483 1775 15 38
Genomic Location (Zv9):
Chromosome 24 (position 6297589)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6184881
KASP Assay ID:
554-3384.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTRGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5701
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 483 1775 15 39
ENSDART00000136041 Nonsense 483 1775 15 38
ENSDART00000006636 Nonsense 483 1775 15 39
ENSDART00000136041 Nonsense 483 1775 15 38
Genomic Location (Zv9):
Chromosome 24 (position 6297589)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6184881
KASP Assay ID:
554-3384.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTRGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32475
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 1057 1775 29 39
ENSDART00000136041 Nonsense 1057 1775 29 38
Genomic Location (Zv9):
Chromosome 24 (position 6263690)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6150982
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTGCCTTTTACCAACCATCTGGCTTTTTCAGGTACTCCATATTAGCATTT[A/T]GAGCTAATGAAGAGCCAGCAATCAGTCCTGAGACGTGTGCGGTTATTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37820
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 1181 1775 32 39
ENSDART00000136041 Nonsense 1181 1775 32 38
Genomic Location (Zv9):
Chromosome 24 (position 6262250)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6149542
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACCCTTTCTCTTTACACAGGGTGCAGAGGATATTTGGCAAGGCAGAATTA[C/A]AAGGAGCTACTAGATGAGAAGAACAAAGCTGCTGCAAAGATCCAGGCCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32474
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Nonsense 1620 1775 34 39
ENSDART00000136041 Nonsense 1620 1775 34 38
Genomic Location (Zv9):
Chromosome 24 (position 6257424)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6144716
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCCTCGCCCATCAGCTTAACCCCAGCAAAAATGGCATGTTTGTGAAAGGA[C/T]AACCCATGAATGGCTACATGGGCTACTACCAGCCACCAGGTAAACAGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6756
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006636 Essential Splice Site 1677 1775 36 39
ENSDART00000136041 Essential Splice Site 1677 1775 36 38
Genomic Location (Zv9):
Chromosome 24 (position 6254333)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 6141625
KASP Assay ID:
554-5364.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTTTACAGAGGTCTGTCCAGGAYGATAAAAGGAGGCCGCGGAAACAAAGG[T/A]AATTCTATTAGCAGAAGTTTTATGCTAGAGANNNNNNNNNNTTCCCCTTTAGAGAAAGAG
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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