MYO9A (2 of 2)

Ensembl ID:
ENSDARG00000073843
Description:
myosin IXA [Source:HGNC Symbol;Acc:7608]
Human Orthologue:
MYO9A
Human Description:
myosin IXA [Source:HGNC Symbol;Acc:7608]
Mouse Orthologue:
Myo9a
Mouse Description:
myosin IXa Gene [Source:MGI Symbol;Acc:MGI:107735]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa4301 Nonsense Mutation detected in F1 DNA During 2014
sa16393 Nonsense Available for shipment Available now
sa24581 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa4301
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 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028997 Nonsense 406 1740 11 33
Genomic Location:
Chromosome 25 (position 534355)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TASTTCTCTCRCAGCTTCCTCTGCGCTTCAATGATGCGCTGGTGCTGCGA[C/T]AGCTCAGGTACACCGGCATGYTGGAGACCGTCAGGATACGACAGTCTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16393
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028997 Nonsense 465 1740 12 33
Genomic Location:
Chromosome 25 (position 532925)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ATGGGCATCCGAGAGTTCCTGCGCAGTGCAGACTTGGAGCCCAGYGGCTA[T/G]CAAGTGGGCCGCAGTATGGTAAGAGACACACTGACCAMCCCTATAATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24581
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028997 Nonsense 1302 1740 25 33
Genomic Location:
Chromosome 25 (position 516842)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTGGAGAAGCTGATCAACTACATCGAGATGCACGGCCTCTACACC[G/T]AGGGCATCTACAGGAAGTCTGGATCCACCAATAAGATCAAAGAGCTGAAG
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/.)

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/uj9hrd58