ZMP
myo3a
Ensembl ID:
ZFIN ID:
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 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
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 | Not yet available |
sa5701 | Nonsense | F2 line generated | Not yet available |
sa32475 | Nonsense | Available for shipment | Available now |
sa37820 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32474 | Nonsense | Available for shipment | Available now |
sa6756 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18647
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 24 | 6214858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACGAACATCAAACCCYCCACATATATATGCWGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGRTAGAGCATGTTCCTCTGTG
Long Flanking Sequence:
GTAATCAAATGAAAAAAAAAACAAAAAAAAACTAAATAAATCATTCATTCGTTGCTCTTTAATCAGAATGTGTACGTTATACAGTGAAGAAACGACTATTGGGATTTGATAACTTGATTCTATTTCTTTTCTTTTAGCTATTCATTTTAATAAGTTGAACTGTTTGCTAATGTATTTGCTGCTAATGTATACTATTTATTTTTTAATTTGTAAATATTAATAAAACATTACTGACCATTTAACTGTTTATTTACAACGAAACAGCTCTAAATGAGCATCTTTAGTAATTTTGGGATTTTTTAAAGGGGGTCAGGGGAATCCCTTATTATGGTGGGCATATCCCTTATTTTCACATCCCAATGTTGACAGGTATGGAAGTCTTATTATCAAATTAATCAATGCCTAATACTTTTTGTTTTCTTACAGCATACTAAGAGTTATGTTGGCGCCAAACGAACATCAAACCCCCCACATATATATGCAGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGGTAGAGCATGTTCCTCTGTGAGCTGCTGGAGTGTGTCAGTCATAGTGTAAACACTGTACATCTCTGTGTGTAGTGTATTGTCATCAGTGGAGAAAGCGGCGCTGGGAAAACAGAGAGTGCTCACCTGCTAGTCCAACAGCTGACTGTCCTTGGAAAGGTCTGGAGAGCAGACTTATTTGCTTACTGTTTTACATGCTAGATTTCTTTTTTAGTATCTATGAATACATGTTTTTACCATAGTGTAGAATAAACAAATAATGATAATTTATACTTTTATTTGTAGGAATTGCATAGTTTTGATTTTGTTTTTCTCACGGTTGATTATTTTAGATCTCTAATTTATTTTTATCCCCTCAGAATTCACACTTCTGGTATTTTTTTTAGAAGATTGTGAGATGTTAACTGCAAAATTACATCTCAAAATTATAAGAAAGAAATACCAAAGTCACTTAATGAATAATTTATGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13131
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 24 | 6214858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACGAACATCAAACCCYCCACATATATATGCWGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGGTAGAGCATGTTCCTCTGTG
Long Flanking Sequence:
GTAATCAAATGAAAAAAAAAACAAAAAAAAACTAAATAAATCATTCATTCGTTGCTCTTTAATCAGAATGTGTACGTTATACAGTGAAGAAACGACTATTGGGATTTGATAACTTGATTCTATTTCTTTTCTTTTAGCTATTCATTTTAATAAGTTGAACTGTTTGCTAATGTATTTGCTGCTAATGTATACTATTTATTTTTTAATTTGTAAATATTAATAAAACATTACTGACCATTTAACTGTTTATTTACAACGAAACAGCTCTAAATGAGCATCTTTAGTAATTTTGGGATTTTTTAAAGGGGGTCAGGGGAATCCCTTATTATGGTGGGCATATCCCTTATTTTCACATCCCAATGTTGACAGGTATGGAAGTCTTATTATCAAATTAATCAATGCCTAATACTTTTTGTTTTCTTACAGCATACTAAGAGTTATGTTGGCGCCAAACGAACATCAAACCCCCCACATATATATGCAGTGGCAGACATTGCGTA[T/A]CAGTCCATGGTGTCCTATAATGCAGATCAGGTAGAGCATGTTCCTCTGTGAGCTGCTGGAGTGTGTCAGTCATAGTGTAAACACTGTACATCTCTGTGTGTAGTGTATTGTCATCAGTGGAGAAAGCGGCGCTGGGAAAACAGAGAGTGCTCACCTGCTAGTCCAACAGCTGACTGTCCTTGGAAAGGTCTGGAGAGCAGACTTATTTGCTTACTGTTTTACATGCTAGATTTCTTTTTTAGTATCTATGAATACATGTTTTTACCATAGTGTAGAATAAACAAATAATGATAATTTATACTTTTATTTGTAGGAATTGCATAGTTTTGATTTTGTTTTTCTCACGGTTGATTATTTTAGATCTCTAATTTATTTTTATCCCCTCAGAATTCACACTTCTGGTATTTTTTTTAGAAGATTGTGAGATGTTAACTGCAAAATTACATCTCAAAATTATAAGAAAGAAATACCAAAGTCACTTAATGAATAATTTATGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16564
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 > A
Consequence:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 24 | 6214827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWGTGGCAGACATTGCGTAWCAGTCCATGGTGTCCTATAATGCAGATCAG[G/A]TAGAGCATGTTCCTCTGTGAGCTGYTGGAGTGTGTCAGTCATAGTGTAAA
Long Flanking Sequence:
CTAAATAAATCATTCATTCGTTGCTCTTTAATCAGAATGTGTACGTTATACAGTGAAGAAACGACTATTGGGATTTGATAACTTGATTCTATTTCTTTTCTTTTAGCTATTCATTTTAATAAGTTGAACTGTTTGCTAATGTATTTGCTGCTAATGTATACTATTTATTTTTTAATTTGTAAATATTAATAAAACATTACTGACCATTTAACTGTTTATTTACAACGAAACAGCTCTAAATGAGCATCTTTAGTAATTTTGGGATTTTTTAAAGGGGGTCAGGGGAATCCCTTATTATGGTGGGCATATCCCTTATTTTCACATCCCAATGTTGACAGGTATGGAAGTCTTATTATCAAATTAATCAATGCCTAATACTTTTTGTTTTCTTACAGCATACTAAGAGTTATGTTGGCGCCAAACGAACATCAAACCCCCCACATATATATGCAGTGGCAGACATTGCGTATCAGTCCATGGTGTCCTATAATGCAGATCAG[G/A]TAGAGCATGTTCCTCTGTGAGCTGCTGGAGTGTGTCAGTCATAGTGTAAACACTGTACATCTCTGTGTGTAGTGTATTGTCATCAGTGGAGAAAGCGGCGCTGGGAAAACAGAGAGTGCTCACCTGCTAGTCCAACAGCTGACTGTCCTTGGAAAGGTCTGGAGAGCAGACTTATTTGCTTACTGTTTTACATGCTAGATTTCTTTTTTAGTATCTATGAATACATGTTTTTACCATAGTGTAGAATAAACAAATAATGATAATTTATACTTTTATTTGTAGGAATTGCATAGTTTTGATTTTGTTTTTCTCACGGTTGATTATTTTAGATCTCTAATTTATTTTTATCCCCTCAGAATTCACACTTCTGGTATTTTTTTTAGAAGATTGTGAGATGTTAACTGCAAAATTACATCTCAAAATTATAAGAAAGAAATACCAAAGTCACTTAATGAATAATTTATGCAAAAAAATCAGTATATTATGCCTCTTAATGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3278
Status:
F2 line generated
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 24 | 6214210 |
KASP Assay ID:
554-3384.1 (used for ordering genotyping assays)
KASP Sequence:
CCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTRGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTT
Long Flanking Sequence:
TGCTCACCTGCTAGTCCAACAGCTGACTGTCCTTGGAAAGGTCTGGAGAGCAGACTTATTTGCTTACTGTTTTACATGCTAGATTTCTTTTTTAGTATCTATGAATACATGTTTTTACCATAGTGTAGAATAAACAAATAATGATAATTTATACTTTTATTTGTAGGAATTGCATAGTTTTGATTTTGTTTTTCTCACGGTTGATTATTTTAGATCTCTAATTTATTTTTATCCCCTCAGAATTCACACTTCTGGTATTTTTTTTAGAAGATTGTGAGATGTTAACTGCAAAATTACATCTCAAAATTATAAGAAAGAAATACCAAAGTCACTTAATGAATAATTTATGCAAAAAAATCAGTATATTATGCCTCTTAATGGTTTTTAGCTTCTTATTATTATTAAGGAGTAGCCATGTAATAATGCAATGCTTTTTGTTTTCTTTTCAGGCCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTGGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTTGGCAAATATCTGGAGATGAAGTTCACCTGTGGTGGGACAGTAGTGGGAGCTCAGATCTCTGATTATCTGCTGGAGAAGTCTCGAGTCGTCCACCATGCAGTGTAAGTGTGTATGAGTTTATAAAATATATAGTGGGTATTTCTGTTGCCTTAGTTGCTGGTTTGAGCCCTGGCTGGGTCAGTTGGCATTTCTATGTGGAGTTTCAGCCAGATTTCATGAGAAAATGTAAGCATTTTACATTTTGTCAGTTTAGTGGCTAATTCGTATAAAATTGTACAATTTTAAAAAGGAGGCTTGGCACCCAACCCCTAACCCCAACCGTCATTGGGGGATGAGCAAATCGTACTAAGTTGTACAAATTAGATCGTACAGATTCATACGAATTAGCCACTGAATCAAAAGTTACGAATTGCTATGAGATTGTGTTGTGAGTTTGCATGTTCTCGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5701
Status:
F2 line generated
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 24 | 6214210 |
KASP Assay ID:
554-3384.1 (used for ordering genotyping assays)
KASP Sequence:
CCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTRGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTT
Long Flanking Sequence:
TGCTCACCTGCTAGTCCAACAGCTGACTGTCCTTGGAAAGGTCTGGAGAGCAGACTTATTTGCTTACTGTTTTACATGCTAGATTTCTTTTTTAGTATCTATGAATACATGTTTTTACCATAGTGTAGAATAAACAAATAATGATAATTTATACTTTTATTTGTAGGAATTGCATAGTTTTGATTTTGTTTTTCTCACGGTTGATTATTTTAGATCTCTAATTTATTTTTATCCCCTCAGAATTCACACTTCTGGTATTTTTTTTAGAAGATTGTGAGATGTTAACTGCAAAATTACATCTCAAAATTATAAGAAAGAAATACCAAAGTCACTTAATGAATAATTTATGCAAAAAAATCAGTATATTATGCCTCTTAATGGTTTTTAGCTTCTTATTATTATTAAGGAGTAGCCATGTAATAATGCAATGCTTTTTGTTTTCTTTTCAGGCCAACAATCGGACCCTCCAGGAGAAGATTTTGCTGGTTAACAGTCTGGTC[G/T]AGGCATTCGGAAATGCCTGCACTGTGATCAATGATAACTCCAGTCGCTTTGGCAAATATCTGGAGATGAAGTTCACCTGTGGTGGGACAGTAGTGGGAGCTCAGATCTCTGATTATCTGCTGGAGAAGTCTCGAGTCGTCCACCATGCAGTGTAAGTGTGTATGAGTTTATAAAATATATAGTGGGTATTTCTGTTGCCTTAGTTGCTGGTTTGAGCCCTGGCTGGGTCAGTTGGCATTTCTATGTGGAGTTTCAGCCAGATTTCATGAGAAAATGTAAGCATTTTACATTTTGTCAGTTTAGTGGCTAATTCGTATAAAATTGTACAATTTTAAAAAGGAGGCTTGGCACCCAACCCCTAACCCCAACCGTCATTGGGGGATGAGCAAATCGTACTAAGTTGTACAAATTAGATCGTACAGATTCATACGAATTAGCCACTGAATCAAAAGTTACGAATTGCTATGAGATTGTGTTGTGAGTTTGCATGTTCTCGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32475
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 > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 24 | 6180311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCTTTTACCAACCATCTGGCTTTTTCAGGTACTCCATATTAGCATTT[A/T]GAGCTAATGAAGAGCCAGCAATCAGTCCTGAGACGTGTGCGGTTATTTTA
Long Flanking Sequence:
TTAATTCAGTGTCTATGGGAGAAAAGACCAAAAATGGATAAAAATGGTCAAACTACTAGCTCTAGAAACAAGTGTGTTCATGACAATCCATAAAAAGCGTAATAATTTAATAATAAAATATCAGTTTGCAACATCATACAGCACAATGAGCTGTTTTTAACATCTAAAAATGAATGGAAGTGAGAGAGACTTGAAGTCTAGAGCCAAATAGATTCCATTGGCACCTGCTCGTCGTGAAGAATAAGGTCAATACACTATCAATGCCTTTAAAGAAACCTCATGAAATTAAAGATGCCTTCAACCACCATTTTCCAGCTGGTATAAAAACGTTCTTTACGTATGGTCAATTGCATAAAATGGACCACCAATTGCGTTATCCACACTAGCATATTACCAGTGGAAGAAGGATTGCATGCTGGGTGTATAATTGCTGACTTGTTATGTTCATTGTTGCCTTTTACCAACCATCTGGCTTTTTCAGGTACTCCATATTAGCATTT[A/T]GAGCTAATGAAGAGCCAGCAATCAGTCCTGAGACGTGTGCGGTTATTTTAGAGAAGGCCAAACTGGAGAACTGGATTTTGGGCAAGACAAAGGTTTGTAAATCAATGACATTAATAACTCTAGCTGATGCTCAACAAAGCTTGTAACTATGACGGTTATGTGTTCAGGTCTTTCTGAAGTATTATCATGTGGAGCAGCTGAATCTGATGGTCAGGCAGACCACTGACCGGATTGTTCTAGTTCAGGCATATGTACGGGGCTGGATGGCATTCAAGCGATACTGTTTGCTGAAGGAAAAGAGAGAACAAAGCGCTGTGGTGTTACAATCAGGTAATGTTATGTTTGTCTGATATTCCCTTAACTGCCACAGATAACGGAAGGCTTAGGTTTACTCTTCCATACTGCAATTAAATCCTAATCTAATAGTGACAAACTATGTATAATTGGAAAGATCTACGTTTTCTAAATACATATTTTACTGTTGTACTGTTTTTGATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37820
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 |
---|---|---|---|---|---|
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 |
GRCz11 | 24 | 6178871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTTTCTCTTTACACAGGGTGCAGAGGATATTTGGCAAGGCAGAATTA[C/A]AAGGAGCTACTAGATGAGAAGAACAAAGCTGCTGCAAAGATCCAGGCCCA
Long Flanking Sequence:
TAAAATCCATATTTTGTCTAATGTAATAAAATATACATTTATTGTTTTATTATTTTCATATAAACTTAAACCCACATAACTTTTGTTTTATTTGACTTTTTGAACTTTTAGCTGCAATCTGCCTAGTGTCTTTAGACTGTTAGTTAGAGAAGTTAGACAGCTTAAATCCATGCACCAAAGCATTGAAGATTGGAAATCATTGAAGTTAAACATGTAATTTTCATGTCTGTGTTTAAAAAAGAGAGAACCACAGTTAAGGGGATAATACTTTGATTCTTAAAAATTTAATTTCCCTTATAGCATACAGAGGACACAAGGCTCGGAAAAGTATAGCTGATGACAGAAGTAAAGCAAAGTCTGAAATAGTTTTCACCCAACTTCAAGCTTGTAAGTCAAACAACTATAACAGTGTTGTAATAAATGATTTTTCATAGTAAATAATGTACTTAAACCCTTTCTCTTTACACAGGGTGCAGAGGATATTTGGCAAGGCAGAATTA[C/A]AAGGAGCTACTAGATGAGAAGAACAAAGCTGCTGCAAAGATCCAGGCCCATTACAGGGGACAAAAAGAGAGGAAGAGTTTCCAGAGGAAAAAGTGAGAATCATTCTTATTCAAGCTGATTTAGTTTTCTTGCTTGTAGTTTATCTTATAAATACTATTGTTTTAATTGAATCTTATTCTCTTTCAAAAAGCTATTTGGGTTGCTGTGTATTTGATATTTCAGGCAGTGTCCTGAAAATGGCCACTCTTGAGTCTTTAGCTATTTAAAGGGATAGTTTATCCAAAAATGAATCTATCAGTAGTTCTGAACTTTTCTTTCTTCCGTTAAACACCAAACAAGATAATCAAAAGAAACAGATCTATTCAATTTTATTTCCAATTTTAAGTCCTTGTATTGGAATGTTTATACAGTGTCTGGTGAATATATAGGGGAAAGAGTGTTTCTTGCAGGTGGTGCAAAATAAAAATGAAACAAAAGAATACCATGGAAGTCAATGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32474
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:
C > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 24 | 6174045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCGCCCATCAGCTTAACCCCAGCAAAAATGGCATGTTTGTGAAAGGA[C/T]AACCCATGAATGGCTACATGGGCTACTACCAGCCACCAGGTAAACAGCCA
Long Flanking Sequence:
TATAACCAAGGACATTTGATTCTGTTACTAATTGTTGTTTAATTATAGTTAAACGTTTTAAATCATAACAGAGTTGACTATCTCTACCATTTTGTTCTTTAGCTTAAGGTACTGTTAAGGTACCAGATACTACATGGCAATTCTAAAGCTAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACACACAAATAATTAATCTACCATTAGTGTATCCTAAACTCTTTTTACAAATCATAATAACATGCTTCAATGCCTTGCAGAGTTTCCCACCAAAGGAAGTGACATCATTTGGAGCAAGTCATATGCTTTTTCTCACAGTGCTTTCATTTGATGACTGCTGTACTTCTTTGTAACCTGTCTAGGTATCCAAGGCCTCTGAAGACTACCTTTCCCTTCAGAAGAAGTTAAATGAAATCATCCTCGCCCATCAGCTTAACCCCAGCAAAAATGGCATGTTTGTGAAAGGA[C/T]AACCCATGAATGGCTACATGGGCTACTACCAGCCACCAGGTAAACAGCCATATCTCAGTCATTTTAACCATACTCTATTCAAAGTCCTCTTGAAATCAAAATGTTTTTACAAGTTAACATAAGTATGTTAGTCCTAGGGTTCATTCTCACCGAACATGTCCTCCTAAAACAGGTTCTTTTTTCTCAACAAAAAAAATACTTTTTTTGCAGAGATTTAAGGTTTAATTACTGCATTTTAGTGACATTTTAAGCACTAATTTGTGATGGATTAGCGTGCTGGATGGAAATCATTAACACATTTTTGATGCAACAAAAAAACTTCCTATGTTTTTGTCCAACTGCTTATCATACTATTTTTTGTTTCCAAAAAATGTACATTTATTTACAAATGTTCATTTAAACTGTAAGTCATTACTAGAATTTTAGAAATATGAAAAAATACTTATTTTTAAATATTCATTTTTTATTATTCATCATAAAAAAAATAAATTAAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6756
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:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 24 | 6170954 |
KASP Assay ID:
554-5364.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTACAGAGGTCTGTCCAGGAYGATAAAAGGAGGCCGCGGAAACAAAGG[T/A]AATTCTATTAGCAGAAGTTTTATGCTAGAGANNNNNNNNNNTTCCCCTTTAGAGAAAGAG
Long Flanking Sequence:
GGATAATTACAAATACTGAGTCCTTAGGGGTTAAACCACACCACACTTTTTTTCAGATAAGAACAAAGGGGTGAAAGGTCAGCTGGATGTTTTGAGCTGATCTTATTCTTCTATGTAGCAGTCGGGATTCCCTCCAGGGAATTATTTAATGTATTCTCCTTTTCCCACAGGAGATCTATGGACTAGGCATAAATAATACCTAGAATGGGTTCAAATGGGTGAAAAATCACTTGGTATTATTTAAATACTGATTTTCTGTTTTAAACCCACAGCTGACACAAAGCAGTCTCGAACACCACGCCGCGCACAACAACCCAAGACCCTGAACACGCCGGAGGACTCCACATACTACACACTTATTCATGTGAGTCAACATCCCACAATGACACTCACTTTATCTAGAGATTATCTGGGCTTTGGCTTTAATGATTTTTTTTCGCACACTGGGTCTTTTACAGAGGTCTGTCCAGGACGATAAAAGGAGGCCGCGGAAACAAAGG[T/A]AATTCTATTAGCAGAAGTTTTATGCTAGAGATTCCCCTTTAGAGAAAGAGACAAAAGCTATGCTTGGATTTCAATACTTATACTAATACATCATTTATTTGATCAAACTTAAAGGGAAAAACAGCAACATTTTGATGTACCGTTATTGTTTTAACCGTAATACAATTTAAATATCCACTTACTGGCCACTTTATTAGGTACACCTTACCAGTAGTACCGGGTTGGAGCCCCTTTTGCTTTCAGAACTGCCTTAATTCTTTGTGGTATAGATTCAGCAAGGAACTGGAAATAATCCTTAGAGATTTGGGTCTATATTAACATGAAAGCATCACGCAGTTGCTGCGGATTTGTCGGCGGCACATCCATGATGCGAATCTCCCGTTCCACAACATCCCAAAGGTGCTCTATTGGATTGAGATTTATTATATTATCAGACATACTGTGAAAATTTCCCTGCTCTGTTAAACATAATTTGGGAACTATTTAAAAAAAAGGGGGTT
Associated Phenotype:
Not determined