ZMP
MYO15A (1 of 3)
Ensembl ID:
Description:
myosin XVA [Source:HGNC Symbol;Acc:7594]
Human Orthologue:
MYO15A
Human Description:
myosin XVA [Source:HGNC Symbol;Acc:7594]
Mouse Orthologue:
Myo15
Mouse Description:
myosin XV Gene [Source:MGI Symbol;Acc:MGI:1261811]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13847 | Essential Splice Site | Available for shipment | Available now |
| sa11241 | Essential Splice Site | Available for shipment | Available now |
| sa6043 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40133 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6909 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44570 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20095 | Essential Splice Site | Available for shipment | Available now |
| sa15876 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13847
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 24 | 1558 | 2 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40101666)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39965026 |
| GRCz11 | 3 | 40106884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTTTCAATCCAACATTAAAAAGTTTTGACCTGCTTTTTCTTCCGTTTT[A/G]GCTGAGATATGAGGCCAGGAGAAAGGCAGAAGAGGAGCAGAGGAGAAWAG
Long Flanking Sequence:
AATGTGGACTTTATGATGTGAAAGGTCTCCCTCAGTAGTTTTTATTACTTAATTGCACTTATTATTATTTGTTAGCTGTTCATGAAAGAGGAAATCTACTTCCTGCTGGAGAGTAAGAGGGACAGGGTAAGGCACGTGGCCGCCCTGACTCTTCAGCGTTACACCAGGATGTTTTTTGTGAGAAAACGATATACTGCCTTCCGCATGAAGATCATACGTCTGCAAGCCCACTGCCGAGGCTTTCTTACAAGGTACAGCCTATATCACCTTCCCTCTAAATCATTCCAGGCGCCATATGATTATTGTTAAAATATTAATTGTGCATGTTTCTCCCAGGAAACGCTATGTTAAAATGAGAGTGAGCCTGGTGAAGTTCCGCTCTCTGGTCCATATGTATGTTGATCGCAAGAGATACATTAGGGTAAGAACGATGCTGTTTTAGTGTATCATCAGTTTCAATCCAACATTAAAAAGTTTTGACCTGCTTTTTCTTCCGTTTT[A/G]GCTGAGATATGAGGCCAGGAGAAAGGCAGAAGAGGAGCAGAGGAGAATAGAAATGGTATTTGTTTTCCAAATGAACCACATTGGAATACTTTTATGCTTTCCGTTCAGGGCCAGCAATTAACTTTCCCATTAAGAGACAATATCTGCCCACTAAAATTGATTTCTAGGGGTTTATTTTAAATATATAATTATCTTATTAATTGTACCTGTGTTGTCATTTGTGTCACACACTTTTATTTCAACCATTTTTCCAGTGAATCAGAATACTGTAACTGCTACTAATATAAATACTTTAAAAACAGGAGCACATTACAGGTTAAGGCAGCAGTGTTATGACAGAAATCAATTTGTTGAATATTACTATAGATAATGTAATAATTCATAGATTACATAGCAATGATGCTGTAACGCCTCAAAATGACATTCATTTTCACATTTCACATAATAGCCATAATATATTTTGCTATAATGGGTATTTTGTGCTCCATTATCTTGAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11241
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 41 | 1558 | 2 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40101609)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39964969 |
| GRCz11 | 3 | 40106827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATGAGGCCAGGAGAAAGGCAGAAGAGGAGCAGAGGAGAATAGAAATGG[T/A]ATTTGTTTTCCAAATGAACCACATTGGAATACKTTTATGCTTTCCGTTCA
Long Flanking Sequence:
CTTATTATTATTTGTTAGCTGTTCATGAAAGAGGAAATCTACTTCCTGCTGGAGAGTAAGAGGGACAGGGTAAGGCACGTGGCCGCCCTGACTCTTCAGCGTTACACCAGGATGTTTTTTGTGAGAAAACGATATACTGCCTTCCGCATGAAGATCATACGTCTGCAAGCCCACTGCCGAGGCTTTCTTACAAGGTACAGCCTATATCACCTTCCCTCTAAATCATTCCAGGCGCCATATGATTATTGTTAAAATATTAATTGTGCATGTTTCTCCCAGGAAACGCTATGTTAAAATGAGAGTGAGCCTGGTGAAGTTCCGCTCTCTGGTCCATATGTATGTTGATCGCAAGAGATACATTAGGGTAAGAACGATGCTGTTTTAGTGTATCATCAGTTTCAATCCAACATTAAAAAGTTTTGACCTGCTTTTTCTTCCGTTTTAGCTGAGATATGAGGCCAGGAGAAAGGCAGAAGAGGAGCAGAGGAGAATAGAAATGG[T/A]ATTTGTTTTCCAAATGAACCACATTGGAATACTTTTATGCTTTCCGTTCAGGGCCAGCAATTAACTTTCCCATTAAGAGACAATATCTGCCCACTAAAATTGATTTCTAGGGGTTTATTTTAAATATATAATTATCTTATTAATTGTACCTGTGTTGTCATTTGTGTCACACACTTTTATTTCAACCATTTTTCCAGTGAATCAGAATACTGTAACTGCTACTAATATAAATACTTTAAAAACAGGAGCACATTACAGGTTAAGGCAGCAGTGTTATGACAGAAATCAATTTGTTGAATATTACTATAGATAATGTAATAATTCATAGATTACATAGCAATGATGCTGTAACGCCTCAAAATGACATTCATTTTCACATTTCACATAATAGCCATAATATATTTTGCTATAATGGGTATTTTGTGCTCCATTATCTTGAATTTGGGATTGAATGTCATTTTTGAGCATTTGTTTTGCTCGTTTTTGGCCCCTCTTACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6043
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 |
|---|---|---|---|---|---|
| ENSDART00000110025 | Nonsense | 71 | 1558 | 4 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40100580)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39963940 |
| GRCz11 | 3 | 40105798 |
KASP Assay ID:
554-3956.1 (used for ordering genotyping assays)
KASP Sequence:
TATAGAGTGTAATTCNNNNNNNCTTATTCTTTCACTCTCATCTGTGTTTTAGGTGGT[C/T]GAGAGCTCCATTCTGATTGTTTGGCTTTGGTCCAGGCTCCCACAGTTCAG
Long Flanking Sequence:
CATTTCTAGTATCTCATTTCTACGATTTCATTTCTGTAATCATGTCATTTTTATCTATGCTCAATTGCATCCCTGCTCATGTGTTTTCTTGCTTTGTAGGAGCTGTCAAAACGGGAAGTGGTCAATGTAACTCATCTGGTCATTCCAGCTGAACTCGGAGCCTTGCTTCAAGCAGCAGCTGGTACTGCAGGACAGTTTTCCATCTTTAATGATACACTAATATAAAAATGATAACTACATTAATATTTTAACATGCTAATTTGTAACACATCTATTACAAATTACCTTATTAAAATGATTTCTGAAGGACCGATGAAGACTGGATTAACAATGCTGAAATTTCAGATCTTACATCACAGAAATCATTTATATCTAAAAATAGAAAACAGTTATTTTAAAATGCATTAACAATAAGGTTATCCAAACTTTTGTATTGCTGTACAAACTGTATATAGAGTGTAATTCCTTATTCTTTCACTCTCATCTGTGTTTTAGGTGGT[C/T]GAGAGCTCCATTCTGATTGTTTGGCTTTGGTCCAGGCTCCCACAGTTCAGGTGGAGACACAGCTCACGCTGCCTCTCGACATCAACAACTACACCATCTCCAAATTAGTCCAGATTCACTTCAAAGTAAGAGTAATGTAATCACAAATAGTCCCTCATATGTAGATAATCATGCAATATTGAGTGATATGCTGTTTATGTCTTTTTTGATTACCAAATAGGAGCCAAAGTTTGGAATGTTAACCGCACCTTTGAAGACACCACTGACCCACGTTGATGACGATCTTACTCATGAGGCTCTAGACGTTTTTGTCATGGTACACTGTGTTTTATAGTGTTGAAGATGACACCACTGTCATGTAATATGCATGCAATTAAACGCAAAATGTCTTACAAATTTAAGTTGATTGAACATAAAACAATTAAGTTATCCCACAACAACCCTCAAGAGTTGTGTTAATTCAGCTCTTTATTTAATAAGTAGTTTGAACAAGCAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40134
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Nonsense | 258 | 1558 | 7 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40098022)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39961382 |
| GRCz11 | 3 | 40103240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAAGCCATGCAGAAGTCCCTGTATGGACCAGAGACAGCGAGGACTTA[C/A]CCATTGTCTCTGCTGGAATGGACAGCCAATAGGAAGAAAGCAAACATGGT
Long Flanking Sequence:
TCATATTGCTCGTTAAGTATGCCTTATTCAGCATTATCTCAGCTCTTCTGTCTCTCTATTATCATTACTTCTTTCACTATGTAGATCTTGAGGTTCATGGGTGACCCACATCTGAATGGCGCTCAGGAGAACTTATTCGGAAACTACATCATCCAGAAGGGGCTCACCAACCTCAACCTGCGGGATGAAATCCTATGTCAAATTGCCAACCAGGTTTGGAGAAATCCCAATCCAGATAACTCAGAGAGAGGCTGGCTGCTGCTGTTAGCCTGCCTGAGTGCATTCGCACCATCAGCCAAAGTGGAGAAATACCTTTTGAAGTAAGCAGAACCCCAGTATTTACTCCGAGTGTGTTACGAAACACATTTGATCGTTCATTGCTTTCTGACTTTCAGATTTGTCTCAGACCATGCCTATAATGAATTTAAAGCAGTCGGCCAACACAAGCTCATTCAAGCCATGCAGAAGTCCCTGTATGGACCAGAGACAGCGAGGACTTA[C/A]CCATTGTCTCTGCTGGAATGGACAGCCAATAGGAAGAAAGCAAACATGGTTTTGCAAGTTCACTGTTTTGACGGTGCGTGTCAGTTTCACTCTGTTTGAGTTTCTGTAGCCTTCAGCCAGTGTTTGCCAATTAAATGCCTCAGGGTGGGTTGCTTCAAAAAAGCGAACAAAATATAGCCTGGATTCAGAATGACTCAGATAGTTCACCCCAAAATTAAATTCCATCATCATTTATACACCCTCCAAATTGGTGCCATATTTTGCCTGATTATTACAAAAACATCATGTTTTGGCCCGTATTTAATTTTTGTCCTAAAAATTCTTAATCCTTTATGGGGCATTTTAAAAATACTAATTGTGAAAATCCTTAAGTGTTACTCCAAGCTTATTACAGGACTTTTGAACTTTTCTGATTGTTATCAGCTTCAGTTAAGTTGCCATTTAGAATTATTTGCCTGAATAAGGGATTAATTGCTGAGCTCTTATAGTAATGGTCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40133
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 407 | 1558 | 10 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40088729)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39952089 |
| GRCz11 | 3 | 40093947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATGCTCAGCTCCAGCCTCCCAGATTCAGATGGATATTACAGCCATGG[T/G]CTGCTATTGTTTTAGTTTTTACATTTTTATTTGTAATAAAAAAACTATTT
Long Flanking Sequence:
ATAAATGAAGTAAATAAATATGTAAAAATATTTTTGGGACATTTTTGCCTTTAATATGTTGTATAAGTATTTAGATAGGAAGTAAAGTTAGAGAGAGAAGGGATGGGATTGAGACAAGCCAGGAACTGAACCTGGTACACCCATAGTGTGATGGTGCTCTGTCAGCACACTGATCATGAGGCTATTAACACCAGTATTAGAATTTTGAGGGTAAAAGCCTAAAAAATGCACTTTTTGTTCACTAATTCATCTTTAATTTCTATGTCCCATCAGGGTCAAAACCAAATGGAATGCATTATGGTGGTTTATTATGTGGTAGATCTTGCTTTAGATTCTTGTTTGCCTCACTGTAGTAATCACTAATATTTTACCCTCAATCTGACCTTTCCCAGGGCTCTGTTTGGAAGTGGATTTGACTCTGATGATGACAGCTCACTTCTGCTCCCTCAGACCATGCTCAGCTCCAGCCTCCCAGATTCAGATGGATATTACAGCCATGG[T/G]CTGCTATTGTTTTAGTTTTTACATTTTTATTTGTAATAAAAAAACTATTTTGGTCGTTTTTACACAGCATTAACATATTCTGTACAATAAACTGCATCTTTTTTTTCTCTCTTTAATAACTGAAAAATAGCAGAATCAGACTTTAGTGAAGCACCAACTCAGAAAGGCATGGACCGATATCTAGACAGCTTGTTTGACCCTGTGTTATCTGATGGGAATGGGGTAAGTGTCTCTCGAGTTTTGGGTTGCCTTGTGAAAACAGACATCCATAACACATATATTAAATTGTCTGATTGTGATTATAGATAGAAAGATTTGCGTAGACATACTTAAGGCATAGTGAACATGGTGCTTAACATGAAGTGTAGTGATTATCAATCACACTGAAGTGGTTTATTTGTAATAAAATTGGCTGGGTGTCTGTTTTCATGCTTATTAAGGATAGTTGAAATGTTTCTACAATTAATTATTTATACAATTCATTCTAATTTTCATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6909
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 |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 750 | 1558 | 20 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40076100)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39939460 |
| GRCz11 | 3 | 40081318 |
KASP Assay ID:
554-4949.1 (used for ordering genotyping assays)
KASP Sequence:
CAAAAGACAGCTTCAACCACCCACTGATACTAGACCTACTGTTTAAGCAG[G/A]TTAGTTTTGGTTTTGATTCATTTTTAGCAYCATTCCTCCAGTCTTCAGTG
Long Flanking Sequence:
GTAGCAAATTAATAATAAAAATAAAAGTAGCTCAGCTGTTTGAATTTCTGTCCTCTGTTGAACACAAAAGATATTTTGAAGTATGTTGTAAACCAGTTGTTTAATGCAAAAAAAGAGAAACTCATAAATGGTTTGGAACCTCTTCAGAATAAGCAAATGTTGCGTAAATACAATTTTGCTGTGAAATATTACTTTAATAATAGTCGCTGTGGTGTGTTTTATGACAGTATCTAGAGATCTTCCAGTAGAAGATGAGAATATTCAGACTCAACTGCACAAGAGGAGCAGTGAAGAGCACTACACCTACACCAACGTGCCCTGGAAGATCTACCTGAGGAAAGAGGCCAGTGTCATCAGGGCTCTGATGTGACAATGTGACAATGCGCATTTGATGTAAAATATAGATTTTAAAATAATAATTTTGTGTCGTGTGTTTTTAGGTTTTTTATCCAAAAGACAGCTTCAACCACCCACTGATACTAGACCTACTGTTTAAGCAG[G/A]TTAGTTTTGGTTTTGATTCATTTTTAGCATCATTCCTCCAGTCTTCAGTGTCACACGATCCTTCAAAAATCCATTTAATTTGTTGAGTGTTTAACCACCATTTAATACTGAATACTTCCTAATATTTTTTTTAAAACTTCAATCGTTTTTTTCTGGATTATTTCATGATCATTATTTACAAATATTCTAGTCTTTTGTGTCACTTTTGATAAGATTACTGTGCACTTGCATTTTTTTTCTGACCCCAAAGTTTTAAACAGATGTGAAACTAAACATCGTCTGTTGTTGTTTTTTCTTTTATAAACAATATTAAAATGCATACTTTCTTGTCAGATTGTTCACGATACATTCTCAGAGGCTTGTATTCGCATTACAACAGAAGAAAGGCAGAAGATGAAATCCATTTTTGGTACGATTCATGCCAATTAGTTTTCCGTATGTGATGCTGCATGTGATGTGAACTGTGCTTGTAAAGAGAAAAATTCTCCTGTTGTATCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44570
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 |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 1129 | 1558 | 30 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40064623)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39927983 |
| GRCz11 | 3 | 40069841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTATGAAAGGCCAAGCTGAGCAGGACGTCATCAGCACCATCCTAAGG[G/A]TATGCACCTCTTCAAATATTCCAATATGCCTTCCCATCATGAAATATTAA
Long Flanking Sequence:
TTTAGACTTTTTATATTTTAAATTTATTAAACTATTTAATATATTTTCTATTTTATTTTTTCCCTCACAATTATTCTTTTTTATTGAAATTTGTTATTTAAAAGTATGACAGTGGTTATAATACACATGATTATATTATTGAATTACAACATTATGCTAATTGCATAGATTATTTATTTATTTTAAATAAGAGAAAGTTTGGGAACTTTCTCAAAAGTTTCTTAATTTTTTTATCCACATTCTGCTTGGTTTTTGCTTTGATTATTTAGTCCCCAATTCAAGAGTCCCTGATTGAGTTCACTGATGAAAACCTAAACAAAGTAGCTGCAGAGATTTTTCTTGGTAAGCAGAATGTAAATATATTAACTAATAAATGAAGTGACATAATTATTATCCAATGTGATTTAAATGACTCTTATCCCTCAGCTATAATGAAGTTTATGGGCGACTACCCTATGAAAGGCCAAGCTGAGCAGGACGTCATCAGCACCATCCTAAGG[G/A]TATGCACCTCTTCAAATATTCCAATATGCCTTCCCATCATGAAATATTAAAACAGGGATGTGTGTAATGTCTCCAAAGCAGTGTGATATGAGCTCTGTGTCTGTTTCAGCTGAGTGGCGAGTATGGACTAATGAGGGATGAAGCATACTGCCAAGTGCTCAGACAGATCACTGGAAACACCAGCTCTAAGACGTATGAGCTGCTTTCTTTTTTACATGTACATTTGAATGGTAAAAAAGGCAGACACAGTGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGAAGGTTGCTGGTTTGAGTCCCGGCTAGGTCAGTTGGCATTTCTGTGTGGAGTTTGCTTGTTCTCCCATTGTTGGCATGGGTTTTCTCCAGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCGGCAGGTGAATTGAATAAGCTAAATTGTCCGTAGTGTATGTGTGTGAGTGTGTATGGATGTTGTCCAATATTGGGTCGCAGCTGGAAGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20095
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Essential Splice Site | 1233 | 1558 | 34 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40060536)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39923896 |
| GRCz11 | 3 | 40065754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCACATTTCACCAATCTGTACATAATCATGCATAATGTGTTGTTTTTC[A/G]GGCTGGAAGGAGCTCCAAACGGCAGTTGTTTCTTCTTCCTGGTGGAATTG
Long Flanking Sequence:
CATTTTTGTCCATACTATAAAAATGCATGATGCACGACTGTTCATGCACACTGGGCATTTGCATATTTCATCATTCTGTTCTAATATTTATTCACATTTATTGGTAACACTTTATTTTGATGCTCCATTTGAGTATTAGTAGAATGTCTGCTTAATATCTGTTGATACAGACATTCAACTAACCCCAACCTAACAGTCTACTAATAATCTAATGAGAATTAGCTTGCAAGTAGATGCAATGTAACTTAAATTCAACAAACGGACCATAAAAATAAAGTGTAACTGAAGTAAAGTGTATTTGGTGCTAAAATAGTAACATGAAAGAGTTTATGAAGTGATTTGTTCCGAAAAATTGAGGAACATCAAAACTGTTACATTTGTATTTTGGGATAAAACTTTGTATTTAAAAAAAATTGCTGATGATTTCTGCTGCACCGCTACAATATTTTTTGTCACATTTCACCAATCTGTACATAATCATGCATAATGTGTTGTTTTTC[A/G]GGCTGGAAGGAGCTCCAAACGGCAGTTGTTTCTTCTTCCTGGTGGAATTGAGCGCCACCTAAAGATCAAAACCTGCTCAGTAAGTTGTCTCTATCTTATTTATTGCAGCGTGAATTTTCATAGTTTTCATTTAAAAGGAAAGATTCCATTCTGGGGGGTCACTGTGGCTCAGGGGTTAGCACTGTTGCCTTGCAGCAAGAAGGTTGCTGGTTCGAGTCCCAGTTGGTCCAGCTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCATGTTCACGTGGGTTTCCTCCGGGTGCTTCGGTTCTCCCCACAGTCCAAAGAAATGCGTTATAGGTGAATTAAATAAGCTAAATTGTTCATAGTGTATGTGTGTGAATGAATGTGTATGGGGTTTTCCGAGTAATGGGTTGCGCCTGGAAGGGCATCCGCTGTGTAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCTACCCCAGATTAATAAAGGGACCAAGCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15876
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110025 | Nonsense | 1473 | 1558 | 39 | 41 |
Genomic Location (Zv9):
Chromosome 3 (position 40056697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 39920057 |
| GRCz11 | 3 | 40061915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCGACACCCCCTGTGTACTGGCTGTCAATCAAAACGGTYTGAACTTTT[T/A]GAGCAAAGAGACTCATGTAAGTGTAATCACATTGGCTTYTRGATAAAATA
Long Flanking Sequence:
GTGGTGTTAAAAAACGTTTAGATGTTGAAAACACTTGTATTAATTGTAATTGTTCAGTTGGCACCTGATGGAAAACAGCACCTGGCTACAATCCCCGGCAATCATTTACATGTGAATACCTTTTCTATAAGCTAAGCGTCTCTTGTTCTCTGCCATCAGCCATGAGGTTCAGGAGTATATTCCCACCCAGCTCTCCGGTCTCCAGCGGGCTCAGCAGTGGTTAAACATGGCGACCCAACATATGCAGCAGGTGCAGCCCCTCAGTCCCCATCAGGCCAAAGCACAGTTTCTGGGTGAGGTGTTGACTCAGGAGAACAGTCAGTGTGTAGGCGCACAGTCATTTATTCACAAGGCTGATTGTTGTGCTTGTGTTTCTGTGTCAGGACTCGTGAGTGCTTTTCCTATGTTTGGCTCATCATTCTTCTACATACTGAGCAGCAGCAACAGTGCTGTCGACACCCCCTGTGTACTGGCTGTCAATCAAAACGGTCTGAACTTTT[T/A]GAGCAAAGAGACTCATGTAAGTGTAATCACATTGGCTTCTAGATAAAATAAGGATTATTTGGTTGGAAGTCGTTTAAAGCTCGCGCTACAAATTAATATTCTGTCATGATCTGAAAAACTAAAAAAATAAATAAATAGAATTTTAAATTTCCTTATGCATCTAAACAGCTGCATGACATTTCTCAGTAGTGAGGCTATAATGGTGGTGGGTCTTGACCATTTCAATTGTGGAATAATGCAAAAAGAAAACATATTTACTGAAATTACAGGCATGATGTATAGAATCAAACTGAAGAACTATAGTTGCTAATGATGCATCTTCCCAGTAGGCACTGGACGTCAGATTGATGTTGTACCCCAACGACATGGGGACGTTGCATTTTATTTGGAAATGAAAATCAGGTCAACATCAGAACAGTACTTTCAGACTGACGTCAATGTCCAATATCCAACCTAAAATCAACTAAATAGCAACATCTAATGATGTTACAGCTTGAGGT
Associated Phenotype:
Not determined