ZMP
myo5ab
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO5A
Human Description:
myosin VA (heavy chain 12, myoxin) [Source:HGNC Symbol;Acc:7602]
Mouse Orthologue:
Myo5a
Mouse Description:
myosin VA Gene [Source:MGI Symbol;Acc:MGI:105976]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32515 | Nonsense | Available for shipment | Available now |
| sa24605 | Essential Splice Site | Available for shipment | Available now |
| sa32514 | Essential Splice Site | Available for shipment | Available now |
| sa44232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9541 | Nonsense | Available for shipment | Available now |
| sa38002 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24604 | Essential Splice Site | Available for shipment | Available now |
| sa44231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa3305 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa32515
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 31 | 1395 | 2 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7913055)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7525579 |
| GRCz11 | 25 | 7649671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCCAGACCCTGCAGAGGTGTGGAGATCAGCAGAGCTCAGCAGAGACTA[C/A]AGACCTGGAGATCCTGTCCTGCATCTACTGCTGGAGGATGAGACGGTGAG
Long Flanking Sequence:
TTTGAACATGTTTACTTGTATGTATTTGGTAAAGCTGAAAGAAAATGAAAAGTTAATTACATGACAGAAATATGAATGTATTGACCTCTGAGAAACTTGATAAAAGTTGAAAGAAAATCAAATATATTATAGAGAGATTTGTCACTTTAAATTTAGGAAATATTTAAGAGTAAAACTAGACAAAATAGATACTGTTTTGTTTTAAAGGTGAATGCATTTATTTAAATATTTAATGCAGTTTTATTAAAGTTAAAAGAAAACAAAACAAAAGAAGCTGCAGTTCAAATGAAACCCATTGAGTTTATTGTTGATTGCTATAGTAAATCAATGAGATATTATATATAATAATCATTATATCAGTTGCATAAATTAGATCATTTTACATCTGTGTTTGAATGCCACTGATATTCAGACTAACTTGATGTTTGTCTGCAGTTGGCCCGAGTCTGGATCCCAGACCCTGCAGAGGTGTGGAGATCAGCAGAGCTCAGCAGAGACTA[C/A]AGACCTGGAGATCCTGTCCTGCATCTACTGCTGGAGGATGAGACGGTGAGACTTTCGCACTCTTTAGCTAGTTTGGCGTCTGATCTGAAGGTTAAGATACAAAAACATGAGCAGAAAAAGGATCTAGACCTAGAACATCTTAAATTGCACCTATTATGCCCCTTGTTTACAAGATGTAAAACAAGTCTCTGATATCCCACAGTGTGTTTGTGATGTTTCAGCTCAAAATTCCTCAGAAATGGTGTTTTAAAACTATTTGAAACTGCCCATTTTACGCTTAGATCCAAATTGTGCCTTTTTGGTGACTGTCACTTTAAATTGAAATATGATAGGCAGAGCTACACATGTCTTTGTGTCAGCACAGTAGCAGATTCAAAACCCTAATGGCAGATGGCTGCTTCTCACTCAGGGCTGTCTATGCTTATGAGGGAGAAACCATAAGCATGGACACTAATGGGCGGGGTTTCTCCCTCTGATGACACGTACAATCGAAGAATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24605
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Essential Splice Site | 279 | 1395 | 7 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7903622)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7466060 |
| GRCz10 | 25 | 7516146 |
| GRCz11 | 25 | 7640238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCTCTGTGCCTGCGCTCATTTACCTGAATTTAAACCTCTAAAGTTAG[G/A]TAAGTGCGCAGTCTACAGTGTGCGTCTTTATTTGACTGATTACAGATGGT
Long Flanking Sequence:
GTGAGTTTCGTCACTGTTTTGGAACACACTAGCTTATCGATATCCTTAAGACTAACATACTGATGCTAAGATTTAAAAAACTTTAATTTGATTTCACATGGACTTTAAACACTTTAATACTACGTGGAAACAATGCATCTTGACTTTTTCATCTGTGCGTAGGCTTTTGGAAATGCCAAGACCACCAGAAATGACAACAGCAGCCGCTTTGGGAAGTACATTGAGATCGGGTTTGACAGGAAACATCACATCATTGGAGCAAACATGAGGACGTACCTTCTGGAGAAATCTAGAGTTGTTTTCCAGGTTAGTTTTTCTCATTGGAAGAGTCTGAATGTCATTAATTTCAGTATCACAAAACATTTATATCCAATACATATAAATTGTGTGGTAATTTCAGTCTTAATCTATGTTGTAGGCAAGTGAGGAGAGAAACTACCACATCTTCTATCAGCTCTGTGCCTGCGCTCATTTACCTGAATTTAAACCTCTAAAGTTAG[G/A]TAAGTGCGCAGTCTACAGTGTGCGTCTTTATTTGACTGATTACAGATGGTGTTGTTGTAGGTTTTGTGTTGCAAGCTGATATTTTGTAGTGGGAACATCTGCTGGCCACTTCTCCTCAGGGTGACTCGTTCTCTTCAGTAACCAGTCTTTCTCTTAAGGTAGCGCTGATGATTTTCCTTACACTAACCAAGGCGGAAGTCCAGTCATCGTGGGAGTGAATGACCTGAAGGAGATGCAGGCCACAAGGAAAGCCTTTTCACTGCTGGGTATGAATCGTTTTAGATTTTCATCTCACTTGTGGGGTTTTGTAATCCAGAGTCCTATTCATGCGTCTCTGTAACTTATTTTTGGAATAATAAAAAGGGGTCACATCATTGATTTTATATTTATTTTTTAAATGTATTTATATTTGCAATATTTAATTCATGTATTTTGCTTTAAAATGTAATTTCTATTCTAAATTGTTGTAAAAATGATATATACATTGTTATAATTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32514
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Essential Splice Site | 315 | 1395 | 8 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7903355)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7465793 |
| GRCz10 | 25 | 7515879 |
| GRCz11 | 25 | 7639971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGACCTGAAGGAGATGCAGGCCACAAGGAAAGCCTTTTCACTGCTGG[G/A]TATGAATCGTTTTAGATTTTCATCTCACTTGTGGGGTTTTGTAATCCAGA
Long Flanking Sequence:
AGGACGTACCTTCTGGAGAAATCTAGAGTTGTTTTCCAGGTTAGTTTTTCTCATTGGAAGAGTCTGAATGTCATTAATTTCAGTATCACAAAACATTTATATCCAATACATATAAATTGTGTGGTAATTTCAGTCTTAATCTATGTTGTAGGCAAGTGAGGAGAGAAACTACCACATCTTCTATCAGCTCTGTGCCTGCGCTCATTTACCTGAATTTAAACCTCTAAAGTTAGGTAAGTGCGCAGTCTACAGTGTGCGTCTTTATTTGACTGATTACAGATGGTGTTGTTGTAGGTTTTGTGTTGCAAGCTGATATTTTGTAGTGGGAACATCTGCTGGCCACTTCTCCTCAGGGTGACTCGTTCTCTTCAGTAACCAGTCTTTCTCTTAAGGTAGCGCTGATGATTTTCCTTACACTAACCAAGGCGGAAGTCCAGTCATCGTGGGAGTGAATGACCTGAAGGAGATGCAGGCCACAAGGAAAGCCTTTTCACTGCTGG[G/A]TATGAATCGTTTTAGATTTTCATCTCACTTGTGGGGTTTTGTAATCCAGAGTCCTATTCATGCGTCTCTGTAACTTATTTTTGGAATAATAAAAAGGGGTCACATCATTGATTTTATATTTATTTTTTAAATGTATTTATATTTGCAATATTTAATTCATGTATTTTGCTTTAAAATGTAATTTCTATTCTAAATTGTTGTAAAAATGATATATACATTGTTATAATTTTTAATAAGAATTAAAAAAATATTAATATAATTTATAAATTATATTAATTTTAATTATTTTATTTATTTTCATTTGCATTTAAACATGTTTGTTCTTTTTTATTTTCTATTGCTTAAATTTCTTCTGTTTTATTTTATAAATTTTTTTCTTCTATTTTTTATTTTATGTAATGCCTTTGGTTTCGTTTTTGTATTGTCATTTTGTTTCATAATATTTATTTATAAATTTATTTGAAGTTAAAAAATTGCCCTTTTTATTTTCTTATTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44232
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 322 | 1395 | 9 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7901797)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7514321 |
| GRCz11 | 25 | 7638413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCACAAACATGCAAGTATCTGCTGATTCCAGGAATTACCGAGGCACAC[C/T]AAATGGGTTTATTCCAAATCCTGTCAGCCATTCTTCATCTGGGGAATGTG
Long Flanking Sequence:
CCATTATCTAAATATGACTTTACTGCCAGTTTCTAATTATTCAGTCACTATTTTATGTAATGCCTATTTAATGTTACATTACTTTATGTAATGCCTTTTGTTTTTTATTTATTTTATTGTCACTGGTTTAAAATTATACCTTTTTATTTTTCCTTTTTAATTGTTTTGTTTTTTCTATTTTTTATTTGAGTTAATTTATTCAGTCTATTAGTATTATTTGATTTGTTATTTATAATATCATAAATACATTTTTTAAATAATTTTTTAAAATAATTTTATTTTAATCTCCTTATTATACAAATACGACTAGACTGGCAGTTTCTGATCATTCAGCACACGCAGAAGTGACTGTGTTTTCATAGTGCATAAAGCTCTTGAATCAGATCATATCAGATCCAATTAAATTCCTCATGATATGAGCCCCTTCACATGCTCTTAGTTTATTCATTCAACCACAAACATGCAAGTATCTGCTGATTCCAGGAATTACCGAGGCACAC[C/T]AAATGGGTTTATTCCAAATCCTGTCAGCCATTCTTCATCTGGGGAATGTGGAAGTGAAAGAGAGAGGATCATCCAGCTGTAGCATCTCTGTAAGCTATCATAAAAATTCAAGAATGAATAATTTCTACTATACTGATTTCACAATACCATTTCATCACACCCAGGATGAAAACGGACACCTAGCCATGTTTTGTGACCTGACTGAAGTGTCAAATGAATCCATGGCTCACTGGTTGTGTCATAAAAAGCTGAAAACGGCCACGGAAACCCTTAATAAACCTGTGACCCGACTGGAAGCTGTGAACGGTCGGGACGCTCTTGCAAAGCACATTTACGCCAAGCTCTTCTCGTGGATCGTCAGCCAGGTCAACAAGGCTTTGAGCACTTCTTCTAAACCGCACTCGTTCATCGGTGTCCTAGACATCTATGGGTGGGTGAGCCTCCTGCTATTTCTTCTTCTTTATACTTTATTTAGTTGTGTGTCGAATTTAATCAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9541
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 393 | 1395 | 10 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7901509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7463947 |
| GRCz10 | 25 | 7514033 |
| GRCz11 | 25 | 7638125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYCATAAAAAGCTGAAAACGGCCACGGAAACCCTWAATAAACCTGTRACC[C/T]GACTGGAAGCTGTGAACGGTCGRGACGCTCTTGCAAAGCACATTTACGCC
Long Flanking Sequence:
CTTATTATACAAATACGACTAGACTGGCAGTTTCTGATCATTCAGCACACGCAGAAGTGACTGTGTTTTCATAGTGCATAAAGCTCTTGAATCAGATCATATCAGATCCAATTAAATTCCTCATGATATGAGCCCCTTCACATGCTCTTAGTTTATTCATTCAACCACAAACATGCAAGTATCTGCTGATTCCAGGAATTACCGAGGCACACCAAATGGGTTTATTCCAAATCCTGTCAGCCATTCTTCATCTGGGGAATGTGGAAGTGAAAGAGAGAGGATCATCCAGCTGTAGCATCTCTGTAAGCTATCATAAAAATTCAAGAATGAATAATTTCTACTATACTGATTTCACAATACCATTTCATCACACCCAGGATGAAAACGGACACCTAGCCATGTTTTGTGACCTGACTGAAGTGTCAAATGAATCCATGGCTCACTGGTTGTGTCATAAAAAGCTGAAAACGGCCACGGAAACCCTTAATAAACCTGTGACC[C/T]GACTGGAAGCTGTGAACGGTCGGGACGCTCTTGCAAAGCACATTTACGCCAAGCTCTTCTCGTGGATCGTCAGCCAGGTCAACAAGGCTTTGAGCACTTCTTCTAAACCGCACTCGTTCATCGGTGTCCTAGACATCTATGGGTGGGTGAGCCTCCTGCTATTTCTTCTTCTTTATACTTTATTTAGTTGTGTGTCGAATTTAATCAGCTTTGTTATTAGGTAGAGGTGGTACGGTGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGCCTCACTGGTTCGAATCCCGGTTGGGCCACTTGGCATTACTGTATGTAGTTTGCATGTTGTCCCTGTGTTAGCCTTGGTTTCCTCCGGTTGCTCCCGTTTTCTCCACAGTCCAAAGACATGCGCTATAGGTGAATTGGGTTAATAAAATTGGCTGTAGTATGAGTGTGTGTGTGAATGTGAGATTGTATGGTTGTTTCCCAGTACTGGGTTGCGGCTGAAAGGGCATCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38002
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 823 | 1395 | 20 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7893955)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7456393 |
| GRCz10 | 25 | 7506479 |
| GRCz11 | 25 | 7630571 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGGGCCACCGTCGTCTTCCAGAAGAACACGCGCATGTGGGCTGCAAGA[C/T]GACAGTACCTGAGGCAGAAAACGGCAGCGGTGCTCATTCAGAGGATACTG
Long Flanking Sequence:
TGGTTTCCTTAATGAGAGTGTCTACAACTAGAAGAAACACAAGCTTGGGACATTTCTTTTTAAGTAGTCCAATGTTACTCTGTTTTCCCTCTGCAGAACAAAGATAAATACCAGTTTGGAAAGACGAAGATCTTCTTTCGGGCTGGTCAGGTGGCTTACTTGGAGAAGCTGAGGGCTGATAAACTGCGTACGGCCTGCATCCACATCCAAAAAACCATCCGCTGCTGGCTCGCCCGAATGAAATACCTACGCATTCGACAAGCGGCCATAACATTGCAGAAATACACTAGAGGACACCAGGCTCGATGGTGGGTCACACTTGTAAAATTTGCAAATTAATGGAGTTGGTTGAAATGAAGTTAATAGAGACTGAAGGTTACTCAGTTACTGGTTGCAGACTAAAGTGTTTTGTGTGCCCTTTGTTTAGCTTGTGTAAGACTCTGAGGAGGACACGGGCCACCGTCGTCTTCCAGAAGAACACGCGCATGTGGGCTGCAAGA[C/T]GACAGTACCTGAGGCAGAAAACGGCAGCGGTGCTCATTCAGAGGATACTGCGTGGATATACGGCTAGACTGGAGTACAAGCGGGTATGAGAGAGCAATTACATTTTTATTGAGTGTATTATATTTTATATTGTGTATTCTGAGTAGATGCCTTGGTGTTATGTTATCTTAGTGGTTGCTAGAATGTTTTATGCACAGTGTTGGGTGTAATTTGTTACAAAGTAACTCCTCGCAGTATTTCAATTGCTTTTCTAATGAAAAAGTAATGTGATGGATTACTTTTCGTTTTTAGGTAATTTACTTTTTATTTTATTAGGTAATTTATTAAAGTTACTTAAAACATACTTACTTACACCCAGGGCCATTTATATCAAATTTGATATTTATCTGCACCATGTTGGTGTTTCGTAACATCTAATTTTTACGAGGTGGGTCATTAGCCCAAAGCTCAATCTCCAACCTGGAGGACCGGGATATACACACATACACTACGGACAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24604
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Essential Splice Site | 930 | 1395 | 21 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7891213)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7453651 |
| GRCz10 | 25 | 7503737 |
| GRCz11 | 25 | 7627829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCATGGAAAACAAGATCATGCAGCTGCAGAGGAAACTAGATGAGCAG[G/A]TCTCCTTTTTTCCATTTTGGAGTTTGTACTGATTTCTAAAGAGGAGTCCG
Long Flanking Sequence:
CCCTGACAAATAAAGGCACTAAGCCGAAGGAAAATGAATGAATAAATGAATGAATTGGTACCTTGAGGTAATTTATCCAACACTGGCTATGCAGTTAGTAGGCCACAGTTTCCAGGATGTTGCCAAGTGGTTGTCAGGTTGTGCTGGATGCTATATGGTTTGCTCTGTGTTTTCAATGTTTAAATCAGGAATGGTGTGTTATGCAAGTAAAACAGTTAATAAATGCTTTATAGAGCTTGTCCTGCGGTTTTCTTCCACAGTTGGTGTGTGAGCACAAGGCTCTACTGATCCAGCGGTGGGTGCGTGGCTTCCTGGCCCGCTGGCGTTATCGGCGCATCAAGCGGGCTGTGGTGTATCTTCAGTGTTGCGTGCGCAGGATGCTGGCCCGCAGAGAGCTCAAGAAACTCAAGATTGAAGCCAGATCGGTCGAACACTACAAGAAGCTCAATTATGGCATGGAAAACAAGATCATGCAGCTGCAGAGGAAACTAGATGAGCAG[G/A]TCTCCTTTTTTCCATTTTGGAGTTTGTACTGATTTCTAAAGAGGAGTCCGGTTAAATAAACAATGTATTTATGCATCTTTCAGCACAAAGAGAACCGAGAGCTTTCAGAGCAAATAGGTGCAATAGAGAGCCACAGTGTCGTTGAGTTGGAGAAGTTGCATGTGCAGCTCAAAACGCTTCAGGAGGCGGAAGAAGAGGCCCGTCATCGGGAAGACCTGGTGACATCATTACAGGAGGAGCTGGATTTGGTTCGCCGGGAGCTGGAGAAGAACAAAGAGGTGAAATTAATTAATGACATTTATTTAGGATATATTTAATTAAAAACTATCAATCTATATAAATGTTTTTCAGATGAACAACCTGAGTCAGTTAGGACATCACAGTTTGGTGTCCACTTCAAATTAAATTTACAAAAGTGATTTTATAACAGTATCTTAAAACTGTAAAATTGAACTAAAATACTGTTTTACTGTATTTTTCAGTGATCTTGGTTAGAGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44231
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 |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 1222 | 1395 | 28 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7885560)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7448099 |
| GRCz11 | 25 | 7622277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCAAAGGTGACGTCCCCTGGAGGTCGGGCATATAATGTGATCCTGGAG[C/T]AGCTCAACTCCACCAATGAGGAGCTGGAGGTGCGGAAGGAGGAAGTGCTC
Long Flanking Sequence:
ATTGGCCTGATTTGGTTACAAAACATTCATCAGTTCATTTATTGGTTTCACTCAATCAAAAGGCTCAAAATATACATTTAATACAAACAAACTAAAACAGTCATTTCTTTCTTAACACCATGCTTGTTTTTTCAGGAGTTGGAAGATTGTCGAAAAACATTAGGGGCTGAAAGAGACTACGAGGCTCTGAAGGTACAAAAACACTTTTATTCACCAAATGAATTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGTTAAATGTATTGGTGTGCATATGTGTGATGATCTGTTCCTTAGCGTCAGGAGCTGGAGTCTGACAATAAGAAGCTGAAGAAAGATCTTCAGGAGCTGCGTCAGTCTCTCAGTAAGGGGACCGGGTCAAAGGTGACGTCCCCTGGAGGTCGGGCATATAATGTGATCCTGGAG[C/T]AGCTCAACTCCACCAATGAGGAGCTGGAGGTGCGGAAGGAGGAAGTGCTCATTTTACGATCTCAACTAGTCAGCCATGAGGCCTTCAAACACAAGGTATTATGCCAAATTTATTTTCCTTTTATAGCCACTGACAATGTTTTATAATTAGAGTAATGGTTAATTAAAAAATGTAAAACTTAATGAAATAAATAAATATTAAGTGGTTTAAAATATACATTAAAAAGTATTTTGTTTTACTTTTAGGAATTAGGAACTGTAGGAGATTCAGGTGATTCGAGCAGGTTCGTCAGTCTTTATATTTCAAAACTTTTTTATTTCAAGTCCACAAATATGCGTTCACTCTTCAACATTCTTGCTTTTTAATAATAGAGTGTCCATTCTTTTCTCTCTCAGATCTCCAACACTGGACCTGACAGAGCTTAATGAGGATGGAGAACTCTGGATGGCTTATGAGAGCCTGAAGGAAACGAACAGGTGAAATTTACTATACAAAGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3305
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058337 | Nonsense | 1241 | 1395 | 28 | 32 |
Genomic Location (Zv9):
Chromosome 25 (position 7885503)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 7448042 |
| GRCz11 | 25 | 7622220 |
KASP Assay ID:
554-3026.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCCACCAATGAGGAGCTGGAGGTGCGGAAGGAGGAAGTGCTCATTTTA[C/T]GATCTCAACTAGTCAGCCATGAGGCCTTCAAACACAAGGTATTATGCCAA
Long Flanking Sequence:
AAAAGGCTCAAAATATACATTTAATACAAACAAACTAAAACAGTCATTTCTTTCTTAACACCATGCTTGTTTTTTCAGGAGTTGGAAGATTGTCGAAAAACATTAGGGGCTGAAAGAGACTACGAGGCTCTGAAGGTACAAAAACACTTTTATTCACCAAATGAATTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGTTAAATGTATTGGTGTGCATATGTGTGATGATCTGTTCCTTAGCGTCAGGAGCTGGAGTCTGACAATAAGAAGCTGAAGAAAGATCTTCAGGAGCTGCGTCAGTCTCTCAGTAAGGGGACCGGGTCAAAGGTGACGTCCCCTGGAGGTCGGGCATATAATGTGATCCTGGAGCAGCTCAACTCCACCAATGAGGAGCTGGAGGTGCGGAAGGAGGAAGTGCTCATTTTA[C/T]GATCTCAACTAGTCAGCCATGAGGCCTTCAAACACAAGGTATTATGCCAAATTTATTTTCCTTTTATAGCCACTGACAATGTTTTATAATTAGAGTAATGGTTAATTAAAAAATGTAAAACTTAATGAAATAAATAAATATTAAGTGGTTTAAAATATACATTAAAAAGTATTTTGTTTTACTTTTAGGAATTAGGAACTGTAGGAGATTCAGGTGATTCGAGCAGGTTCGTCAGTCTTTATATTTCAAAACTTTTTTATTTCAAGTCCACAAATATGCGTTCACTCTTCAACATTCTTGCTTTTTAATAATAGAGTGTCCATTCTTTTCTCTCTCAGATCTCCAACACTGGACCTGACAGAGCTTAATGAGGATGGAGAACTCTGGATGGCTTATGAGAGCCTGAAGGAAACGAACAGGTGAAATTTACTATACAAAGACTTTTTCTCTTATATACCCTATTATACACACACGTACAAAGACCTGCAGAATTATTATTG
Associated Phenotype:
Not determined