ZMP
MYO9A (2 of 2)
Ensembl ID:
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39467 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44210 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16393 | Nonsense | Available for shipment | Available now |
sa37972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24581 | Nonsense | Available for shipment | Available now |
sa30171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39467
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Nonsense | 59 | 1740 | 2 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 545467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 504381 |
GRCz11 | 25 | 527278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATATTAAAAGTTGAAGAGGATTTAAGTCTGATGTCTTATGTGATCAG[G/T]AGGAGTATCGATCTGAGGGCATCAACTGGCACATGATCGATTATATTGAT
Long Flanking Sequence:
CCTGTCCATTGGTGTGCTGGACATCTTCGGTTTCGAGGACTACGAGAACAACAGTTTCGAGCAGTTCTGCATCAACTTCGCCAATGAGACGCTGCAGCATTACTTTAACCAGCACGTCTTTAAACTGGAGCAGGTGAAGAATACATGAACAACCGTCACATGACCTTCATTAGTACATATAGACCCTCACTCATGGACATCTGCTCTGAGGAGGACTTGCTGTACAGTGGCAGCATTGCAATAGCAACATACCTGGGGGTTTACAGTAATTATGCTTATTCAGGTTGTAGGAGTGTTAGATTTTTGATGTTTGTGCTTTAGAAAAGTCGGAGTAGTTAATTTCCTATTTATTATTTATTCTATAATTGTCACTTAGTTTAAACTAGTCATCCTCAAACAGCACACTAGGGTGGAGTTTAATAAATAAATGGTAAAATGAAGTTAATAGATGTAATATTAAAAGTTGAAGAGGATTTAAGTCTGATGTCTTATGTGATCAG[G/T]AGGAGTATCGATCTGAGGGCATCAACTGGCACATGATCGATTATATTGATAATACGGCCTGCATCAACCTCATCAGTAAGAAGCCCACAGCACTGCTCCACCTGCTGGACGAGGAGTGCAAGTGAGTTTCTCACCACAGCAGATGAAACACAACAGGCAAAACGCAACAGACAATACTTACCAGACAAAACGCAACAATTCACCAGATGAAATGCAGCAAGCAAAACTCACCTGATATCACGCAGCAAACAAAACTTGCCTAACAAAACTCACCTGACAAAATGCAGCAGACGAATAACATTTTGTGACTGGCAAAACACACCAGACGAAATGCAACAAACAAAACTCACCTAACAAAATGCAACAGACGAAACACCAAAAAAACAAAATGCATCTGATAAAACACACCAGACGAAACACATTTGACAAAACACACCAGATGAAACACATTTGACAAAACACACCAGATGAAACACAATTGACAGAACGCACCAGACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44210
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Essential Splice Site | 325 | 1740 | 8 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 536510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 495524 |
GRCz11 | 25 | 518421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCTGAAGGAGAAACAAGAACTACAAGCCCAAACCCAGCCTCCCTAAG[G/A]TAAACCTCACGACTTGAATGTGTGAAATACTCAGTGTTGGTTGTTTCTTA
Long Flanking Sequence:
CCACATATACCCTATTATTTTAATATTATTTTATAAATCATTTGTAATGAATAACTCCAATTGTTTAATTCATTATAAACATTATTGACCAAGGTAATGTACTCAGTGAAAAATGAAATACTCATTTATGAACACACATACATAATTATGTACACACACATTAATTTCCATTAAAAACAATTTGCATATTTTCTGCATTTTATTTGCTGTTTATGCATGTAATGTATTTCATTTATTCATTTATTAATATTATTGTCTGTCTCAGTAATGGTCGTGGCTGGAGGTCTGAGCGCGTCTCCTCGTTCGCTCATGAAGACGAGGGAATCTTCGTCAACTCCGTCAACAACCGTCTGCTGGAGCGAGCGCAGGGAATCCTCATGTGAGTCTCAGATAAACGAATAAACAAAAGCTTAAAGTCACTCTGTGTTGGACAGTACAGACTAACTCTGTTTTTCTGAAGGAGAAACAAGAACTACAAGCCCAAACCCAGCCTCCCTAAG[G/A]TAAACCTCACGACTTGAATGTGTGAAATACTCAGTGTTGGTTGTTTCTTAAATGTATATGTCTCTCAAATGCAGACAGTAGTCATGATATATACTGTATAATCGTTGTCTGTTTTGGTGTGTGTGCAGCACTTGCTGGATGTGAAGTCTCTGAAGTATCTGAGCAGTCTGACGCTCCACGACCGCATCACTAAATCACTGCTGCATCTGCACAAGAAGAAGAAACCGCCCAGCATCAGCGCACAGTTCAACGTGAGAGAAACACACCTGTTACCTGTCAGACAGCAGTAGACCAATCAGAGCAGAGTATGGACATCAGACCACTCAGAGCAGAGTATGGCCATCCGATCAATTAAAGCAGAGTGTGGCCATCTGACCAATCAGAGCAGAGTAGGGCAATCAGGCCAATCAGAGCAGAGCAGAGAAGAGACATCTGATCAAATAAATTAGAGTGTGGTCATCTGACCAATCAGAGCAGAGTGTCGCCATCTGACCAATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16393
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Nonsense | 465 | 1740 | 12 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 532925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 491939 |
GRCz11 | 25 | 514836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGGCATCCGAGAGTTCCTGCGCAGTGCAGACTTGGAGCCCAGYGGCTA[T/G]CAAGTGGGCCGCAGTATGGTAAGAGACACACTGACCAMCCCTATAATGGT
Long Flanking Sequence:
CATCAGTTATGGATCTGATTCAGTTCAGTAAGTGATCCAAATCACCTTCATAATTAATGGCATTTGCAAAATTCATCATTTATAAATTTGATTTGGTTCATTTTTGATTCAGTTCAGTAACTGTCAGTGTTGTAAACTTAATCATGTATGAATGATTCAGTTCAGTGTCAGTGTTGCAGTTTTCGATTGTAAACCTGATCATTTTTGATTCAGTTCAGGTCAGTGTTGAAAATGTCCTAAATCACTGATCACATTCAATTTAAAGCTCAATCAGCCCTTTTCAGAAATTGACGTTGCCATGTTTTAAAAGAGCTGTTTATACAGTGTGTGTTCGGGAAAAGATTAGTTTAAAGATGATTCACGTCTCTCTGAGTCAGCCGTTGTGTGTTTCTCCAGGATTTTGCTCATCATTTCCACGTTCTGCTGCCGGCTGGATTCAGTGCCAGTCAGATGGGCATCCGAGAGTTCCTGCGCAGTGCAGACTTGGAGCCCAGCGGCTA[T/G]CAAGTGGGCCGCAGTATGGTAAGAGACACACTGACCACCCCTATAATGGTTCATACCATTATGAATGCATAATCACACCAATCAGTCTATTCATTCAACAGTCTGGAACTGGCAGATCTAGAGGACTGATAGACACTGTAAGCTGTAAGCTGGTTGTATCTATATATAGTCTAGAAGTAAAGTCAAATTAGACGCATAGTTTGAACACTTTGACCCAACCACTGAAACCATCCAACTAAAGTCTATACACTAAATGTCCCTCAAAACACTGAACACTTCACCATGTTTCATTAGTAAATTAGAAGTAATTTAAATAAATACATGCTCATACTTGCCTCAACACACCTCCAATGCTGTTTCTAGAAAGCCTGGTATGAGCTTGATTAGCTGGCCCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTTTGCAGGACACCAGCCCTCCAGGACTGAGTTTGGACACCCCTGCTGTTAGAGGACGTGTATTTCAGCTCCAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37972
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Nonsense | 705 | 1740 | 15 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 527889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 486903 |
GRCz11 | 25 | 509800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAACGAGAACTCGAACAAGCCACGTTCAGTTTAGAGCTGCTCAAAGTC[C/T]GATCCGGATCAAACACAGAAGACGCTCAGATCCCTCCGTCCAAACATCAT
Long Flanking Sequence:
ACCCCCCTCTTGTGGATCATTCACGTAGTGTCTCGTAGTGTGAACACCACAGCGATTTAAAGACACAAAATCAAGTCATGTAGCGTGAACGGCACAGCGATCTGCCCATGTTTAAAGTCGTGTAGGTTGAACGTGAGCATTATCTTAATAAATCGTCATAAATTACAAGGATTGTCATGTGTTTTACTGCGTATTGTGTCTGAAATTGGTTCAATATTTTGTAAAGTATTAAAATTGTGCTTTTTTGTTTCTTTTTAAGGTGCCGAATTCTGAGAGAGCAACAATGTAGAGAGCAAAGCAAGCATCCAAGCACTGTGACCAAGAGTTTACACCAAAACACAGAAGAAGCAGAGAAGCTGGAGGAGGTTTGGGAAAAGCAGACCACCGATCCTCCTCCAAAAGCTGTAGACGACAGCACTCTGAAGAGCCGAAACAAAAGAGAAAGCAGGAGGCAACGAGAACTCGAACAAGCCACGTTCAGTTTAGAGCTGCTCAAAGTC[C/T]GATCCGGATCAAACACAGAAGACGCTCAGATCCCTCCGTCCAAACATCATCCTCCTCATCAAGCCTCCACTGATAGCCAAGAAAGCTTTGAGCTCCTTGAAAACGAGGATTCAGCCTCAGCAAAACTTGAACTTTCCAAATCCGAACCAATGGAGGTCAACCAAACAAGTCCGGCTGCATCCTTCAAACCCCATTTCTACATCCCTGATGAAGACGGGAGTCCGATTAATAGTGCGCCACAAACGCCAAACCGTGCCAAGCAGATCCGAGAGAAGAAGGAGTCTGTGGTGGTCATCATCAGCATGCAGAAGGAAAACCCTGTTGACCGGAGCAGTCTGCAAACACTAGAAGCTCAGGACGTCCCGCTCTCCAATGGAGAATCTGCTTCGGATTGTTCAATCATTCCTGAACCTCGAACCAATCATGAGCTGGACACTGGTTCTTCATTTTCGGTTTCCTCCAAACCCCTCCAGCTGGACTTGAGGAGTGCGGCGTCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24581
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Nonsense | 1302 | 1740 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 516842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 475856 |
GRCz11 | 25 | 498753 |
KASP Assay ID:
2261-9208.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTGGAGAAGCTGATCAACTACATCGAGATGCACGGCCTCTACACC[G/T]AGGGCATCTACAGGAAGTCTGGATCCACCAATAAGATCAAAGAGCTGAAG
Long Flanking Sequence:
TTGTTTGTATGTGTGCGCGTGCACATTGTGTTTTGTGTGTGTGTGTACATGTGTTTGTATGTATGTGTGTGTGTGGTGTTGTTGCACATGTTTGTTTTTTATTTGTGTGCACATCATGTTTTTGTGTGTGTGCATTGTGCATGTTTGTTTGTGTGTGCACATTGTGTTTTTGTTTGTGTGCGCACGTGTCCATATATGTGTGTGTTTTGTGTGTGCATCTGTGTTGTGTATGTATGTATGTATGTATGTGCGCATGTTGTGTGTGGTCATGTTTATGTGTGTGTGTGTGTGTGTGTATATATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGCATGCATCCATGTGTGTGTTCTCAGTTTGACCCAGAGCTGTCTTCACGGCAGTTCGGTGTAGAGTTGTCTCGTCTGACGAGTGATGAGCGAAGCGTCCCGCTGGTGGTGGAGAAGCTGATCAACTACATCGAGATGCACGGCCTCTACACC[G/T]AGGGCATCTACAGGAAGTCTGGATCCACCAATAAGATCAAAGAGCTGAAGCAGGGGCTGGACACGGGTGAGCTGCACCACATCACAACACCTAATACACAAACACACTCCATTCAGCACCTGTACACTGGAGAACTGCAGCTTAACTCTGCTCATATAATAATAGTTAAAAGCTATTACTAAACTATTGTTACTAGTTAGTTAAAGTTATTAGTAACTAATAAAGTTGTGGAAACTAATAATTGGATTGTAATGCAAGAATGTGCACATGTGAAGCTGCTTTACTATATTTGGTAACACTTTACAATAAGGTTACATTAGTTAATGCATTTATTTATATGAACAATACATTTATAACAGTTTGTGCTCATGTTACTTCATGAAAATACAGTGTTCATTGTTAGTTGGTGTTGACTCACGGTGCATTAACTAATGTTAACAAGCATGAATGTGGATGTTAATAATGCATTAGTAAATGTTGAACTATGATTATTAAATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30171
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028997 | Nonsense | 1453 | 1740 | 29 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 510323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 469337 |
GRCz11 | 25 | 492234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACTAAATGCCGTTATCTTGCCCTCAGGTGTGTGGAGCTTATCATCTG[T/A]GAGCAGATGAGGAAATATAAAGCCCGACTGAAGGACATCAACACACTGGA
Long Flanking Sequence:
GCACTTTGTGACTCAATAAGTGTGGGGAAGGTGCTATATAAATTAATCATTACTTACTTATATAAACTAAAAATTTAGGAAGAAGTAAATACTGTGAGAAACTGAATTGTGAAAAGTCTGATTTTCAGAGAATTGCAATCTGAGAAAATGGTCAGAATAATGAGGTAAAGCTAAGAACAGAGATCAAATCTGAGGGAAAAAGTCAAAATGATGAGATTTAAGACAAGAATTTTAACAAAATTGGCAGAATTGTGGGGTAAAAACCTTGCAATTACCATTTTTAATAATTACTGCAAACATACACTGAAATAATGGCTCAACTTTAACTCCAACCTTTGACTCCAACTTGTTACACACAAAAGATTGACATTTTTTCAACTTAACTTCTTTAGGTGTAACACGTGTAGTCAATTAATTAACGTTTTAACAGTGTAACTGCCATCTGCATGTGAAACTAAATGCCGTTATCTTGCCCTCAGGTGTGTGGAGCTTATCATCTG[T/A]GAGCAGATGAGGAAATATAAAGCCCGACTGAAGGACATCAACACACTGGAGTTTGCAGAAAACAAAGCCAAGAGTCGCCTGACGCACATCCGCCGCTCCATGGTGAGGGAAATCTACAGGATCTACATAATGCTAATGCACACCCATTTAAACCCCACCTCCATATAAGCCCCGCCCCATCACGACACCTCACTTTCTATGAATTTGGTACATTCCAAAATGTGGTCATGAAATCTAAAAACAACAATTTCAATTAAATCGTGTTGCGATTAACTATGATATTCAGTATTACCGCGATATTAAAGACATAAACTGCAAAAAAAGGTATTTTAATAATAATATTAATAATTCCTTACATTTATATAGTGCTTTTCTGGACACGCAAAGCGGTTTACACATTTTTGATGGGAAACTCCTAATCCATCTTCAGCATTTAACAGGTATAAGAACAAAGAATAGTTACTATGTTAATATTAGTTATTTACTCTATTTAATAAAAG
Associated Phenotype:
Not determined