ZMP
myo7ab
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO7A
Human Description:
myosin VIIA [Source:HGNC Symbol;Acc:7606]
Mouse Orthologue:
Myo7a
Mouse Description:
myosin VIIA Gene [Source:MGI Symbol;Acc:MGI:104510]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43636 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37294 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11875 | Nonsense | Available for shipment | Available now |
sa32344 | Nonsense | Available for shipment | Available now |
sa23923 | Nonsense | Available for shipment | Available now |
sa37295 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23924 | Nonsense | Available for shipment | Available now |
sa3116 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa43636
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003181 | Splice Site, Nonsense | 95 | 2178 | 3 | 47 |
ENSDART00000148019 | Splice Site, Nonsense | 90 | 2098 | 2 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21190996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22202489 |
GRCz11 | 21 | 22239125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGGATTCTTAGAAATCTCCTGATTCGTTACAATGACAGAGTCATATA[T/A]GTAAGTCTGAACATTTCTCTGTTCAATGTGTCATGTGGAATCCAATAAGG
Long Flanking Sequence:
GCTTTATGTGAAATATATATTCATAAATGTATAATAATCATGCTGTTTTCGTAATTTGATTATAAGACATTTTTACTCGTCTTTTAGGGGGACTATGTCTGGTTGGACCTCAGAACAGACCATGAGTTTGACGTCCCTGTTGGTGCTGTGGTCAAATTTTGTGACTCGGGTCAAATCCAGGTCTTGGATGATGAAGGAAAGGTGGGCTTTTCACTGTTTACTAATCAATAATACAACTGACATGTGCAAAACAAAAACTTAAACTATAGATTCTGCTTAACTATTAATATGAATTAATATGAATATTGAACTTTGTCTTGGTTAATTAACAATATTCTCTTAATATAGGAGCAACAGATCTCTCTTCAGAATGCAACGAACATCAAGCCCATGCACCCAACCTCCATTCACGGGGTGGAGGATATGATCCGCCTAGGGGACCTGAATGAAGCTGGGATTCTTAGAAATCTCCTGATTCGTTACAATGACAGAGTCATATA[T/A]GTAAGTCTGAACATTTCTCTGTTCAATGTGTCATGTGGAATCCAATAAGGCTGCATGAGTTAGATTGGGTTAATCATCCTAATTGTTTAAAAATGTGTGCTTAATATAACATAAAACACCTATTTTACAGAGAACTAATCCAAAAATTGTATTTCTTAACATCACCTGAGATTGACAGTGGCTAATGATTTTAAAATGAATATTCAGGACATTCAAGATTTGCTTGTACAAATGTACAAAATGACTTTTTTGTGGAATTGATTGTGTTAATATTATATTTTTAAGTTTCATTACATTTATTCTTTTAGTCAATATGGTAAAATTTCAAATAAATAAAAACAAACTGGTTTAATCAGTCTAGGCTTCACTTGAAGCGTATTATCAAACTGGCGTGATCAGTCAGGGCTTAAGCATATGATCATACTGGTGTGATCAATCTAGGCTTGTCTGTGAAGTGTAAGATCAAACTGGTGGGATCAGTGTAGGCTTGTCTTAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37294
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003181 | Essential Splice Site | 602 | 2178 | 14 | 47 |
ENSDART00000148019 | Essential Splice Site | 594 | 2098 | 13 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21231258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22242751 |
GRCz11 | 21 | 22279387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCAAAAACAAGTTCATCAAGCAGATCTTCCAAGCTGATGTTGCCATGG[T/C]GATGCCCTTTTCCAATACCCAATCCATATTTGCTCAGCATTAATATGCTC
Long Flanking Sequence:
TGGGGTTTATTACAAAACTTTTGAACTTTTTCGACTAAAAAATAATTTTACTGTAATCAATGTCAATGAAGTTACTATATATGATTCATCTCCAGATAAAGGGTTAATAGATGAAGAACAGGTTAATTAAAAGTGACAGTAAAGACATTTATAAAGTTACAAATCATTACTAGTTCAATTAAGGATTTGTTTCAGGGAGTGGTTTCAGGCAGTTTTTAACCACATTAAAGTTCCATACATTTCAGGGTTTTATTTAAAGGCCATGTCAGCCTACAACAAAGAAATAAAAGCCTGTGAAGACACTGAGCAATCATATTAAATATTACAGCAGTTACAAAAGACATTTTTTTCTATTTTCATGAAAATGTAAAACCTCTTGTTTCATTGTTCAGGTTTCCTGGAGAAGAACCGAGACAGTCTCCACAGTGACATCATCCAACTCGTCCATTCATCCAAAAACAAGTTCATCAAGCAGATCTTCCAAGCTGATGTTGCCATGG[T/C]GATGCCCTTTTCCAATACCCAATCCATATTTGCTCAGCATTAATATGCTCACGACATGCCAGCGTGGCCACAGCTCTCCGAGGGCCAAATGTTGGCCATGCAGGTTTATGGCAGGGTTGCATTTGAAAAGAAAAGACGTGTGCTAGCATAATAGCCTTGAAAGAACACGCTGTGAATGAGAGAAGCGACTGCAACAAATGAGTCTCTAACATGACATTATGAGCACATCTGACTAACCCTGCTGCTGATACTCACTTTTTCTGTGGTAATGTCAGCCCTAATCTCTCTTGGCTGATTCTCAGCACACTTGGCTAACAGCAGTCAATTCTCTGTCTCTCTTTCTGTCCTCCTTCTGTCCTTCATTCCTTTACCTCATGTTTTGGCCTCAGTTTCTGTGTGGCTATATGGAGCCCACTGCAACCCTTCAAAAGGTAATCAATGGTGTGGTTTGTGTCCCTCTCAGACCCCTACCAAACTGCTTTTTCTCAATAGTCCTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11875
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 |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 659 | 2178 | 16 | 47 |
ENSDART00000148019 | Nonsense | 651 | 2098 | 15 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21233715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22245208 |
GRCz11 | 21 | 22281844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCATTCTCTTCTCTGCAGATGTTTGATAGAGGWCTGYGTGTCAGGCAGT[T/A]GCGCTACTCTGGGATGATGGAGACGATCCGCATACGCAGAGCTGGATATC
Long Flanking Sequence:
TCTCTTGAATCAGTTCGGAGCAGTTCTGAGCTGTTAAAAAAATCCATACTCTTCTTTCACCAGTTCCTCACAAAAATATCAATTAATAATAACTTTAAGTGAATTTAAGTAGTTTAAGTGAATTACAAGAGTGTTCCCTGTGAGCTGTTTACATTGATTTTGTGACATAAAAGCCAACTTACATAATAGAACTGAAATACACAAGCATCCTTCCTAGTGAGCAGCAAAAATGGGTTTTGTCTTGTTTATCATTTAAAGAGCCTTAAACCAAGTTTTATTTAGAAATCAAAGTAAAAATTCATTTCTTAACCATACATTTCATTAAAAACCAACCAACAATACGAGGAAACTAGTAGACATGTTAAGATAAAGATATTGTCTGAAGAGAATGTATAATACTGATTATGCTAATGAGAAGAAAAAACTTTAAAGTCAAACTCTGAATCGGCCCTCATTCTCTTCTCTGCAGATGTTTGATAGAGGACTGTGTGTCAGGCAGT[T/A]GCGCTACTCTGGGATGATGGAGACGATCCGCATACGCAGAGCTGGATATCCCATACGCTATACCTTCGCTGAGTTCGTGGACCGCTATCGGGTGCTAATGCCTGGGGTCAAACCAGCCCACAAACAGGCAAGTCCAAAGCTTTACTGTGTTAATGCAGTCAGCAGCCAATGTTTGCTTGACAGCTTTTCTCAAAGCTTATTTCCACGCAGCCGTTTTTAAAATTCCATCTGGTCATGTTATTTGACAAGTGTGAAGTGCATGAAGGGAGCTCAATCTCTGTCTTCTCACAGGAAGATCTGCGAGGGACCTGTCAGCGTATTGTTGTGTCAGTTCTGCTGAGAGACGATGACTGGCAGATCGGAAAGACAAAAATTTTTCTGAAGGTTTTGCTACGAGTCATTGTTTTCTGAAGATTTTGGTGTTCCAGATTTGTAACTAATTGTGTACCCGGTCTGTATTTGGCATAGGATCACCATGACATGCTCCTGGAAATGGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32344
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 |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 827 | 2178 | 20 | 47 |
ENSDART00000148019 | Nonsense | 822 | 2098 | 19 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21234642)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22246135 |
GRCz11 | 21 | 22282771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTATCAGGCGACCAGGATACGTGTCACATTGCTGCAGGCCTGGTGT[C/T]GAGGACTCCTGGTACGGCGTACTTTTTCCAAACGCTTCCATGCGGTTCTG
Long Flanking Sequence:
AGATTTGTAACTAATTGTGTACCCGGTCTGTATTTGGCATAGGATCACCATGACATGCTCCTGGAAATGGAAAGAGATAAAGTGATCACTGACAAGGTCATTCTCATCCAGAAGACTGTGAGAGGAATGAAAGAGAGGTATGAGGAAAAAGAAAGAGTAAAGATGAGGGGACAAAAACAAAAATAAAATCAAAATCTGATGTGTATCTGTCTCTTTTGTTCTCCAGAACTAAATTCCTGAAGGTTAGAAGAGCTGTGATGTTAATCCAGCGCATATGGAGAGGCTACATCACTAGAAAGCACTACGCTGTGGTGAGTTGTGTCGTTTGTGAAACCTGAGCAGGAATAATCTGTTTGGAGGTTTTGTCTGATTGTTATTATGTCTGTTTTTTCCAGATGCGTGTAGGTTTCTTGCGACTTCAGGCCTTGTACAGGTCACGGAAACTGCATCAGGAGTATCAGGCGACCAGGATACGTGTCACATTGCTGCAGGCCTGGTGT[C/T]GAGGACTCCTGGTACGGCGTACTTTTTCCAAACGCTTCCATGCGGTTCTGACAATCCAGGCTTATGCTCGAGGAATGATAGCACGGAGACAGTGCAAGAGACTCAGACTGGAGGTAAATCTTATGTCTGTCCATTCAACAATCCTCCATCCATCGTTTATAATATTCATCTGTCCATCTAAGTATCTAAACATCCATCTGTTTATTCATCCATACATTTGTCCATCTGTCTATTAGTCTGTCAAGTCCATTTATTCATCCATCTATCAATTTATTCATTTTATCCATCCATCAATCATCCGTCCACCCACCATCATACATCTATTGATCTATTTATATATTCATCCATCCATCCACCTATCTGTGTATTCCTCTATCCATCTATGTATTGATCTCTCTCCATTTATCCAACTATTCATTCATTTGTTTGTCCATCCATCTTTCAGTCTGCCTATCAATCTAAACGTCTATCCATCATCTGTTTATCTCTCCATCTATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23923
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 |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 1018 | 2178 | 22 | 47 |
ENSDART00000148019 | Nonsense | 1013 | 2098 | 21 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21237195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22248688 |
GRCz11 | 21 | 22285324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCAAAGTTTGCTGCAACCTACTTCCAGGGAAATGCAACACACATGTA[T/A]GTACGCCGGCCACTGAAACAGCCTCTTTTGTTTCATGAAGATGAAGGAGA
Long Flanking Sequence:
GAGCGTCTGAAAAACCAGATGACGGCGCGCAGGGCTCGGGCTGAGGCAGCCAGGAAGCATCAGGAGCGCCTGGCGCAGCTCGACCGAGAGCAGGAGGAGAGAGAGCTGGCAGAGCGCAACGAGACACGGAGGAAAAAAGAGCTTCTAGAGCAGATGGAGAGAGAAAAAAAGGAGCCAGTAAATGACTCCGACATGGTGGACAAGATGTTCGGATTCCTGGGCAATGCCAATTCCCTTCCCAACCTGGAGGGTGAAGCACCAGAAGGGTTTGAGGTGTGGAGCTTTGTCAATTTCAACCTAAATTGCATTGCTTGGCTTGAATCTTATCTGAGTTTTCTTAATGTTTGGATGTTACAGGATCTAGAGAATGCTCCAAAACAGTTTAAGGAAGTCATTGATGAGCCTCTTCCACTTCCTGACGATGAAGAGGAGGACCTATCGGAGTATAAGTTTGCAAAGTTTGCTGCAACCTACTTCCAGGGAAATGCAACACACATGTA[T/A]GTACGCCGGCCACTGAAACAGCCTCTTTTGTTTCATGAAGATGAAGGAGATCAGCTAGTAAGCATTTATTTATTTATTAGTCATCTCTATGCTTACCTGCTTACTGTAAAATAGGATTAAAAGCTGCATTGACTGTATCATATGTGTTTTTAGGCTGCTCTGGCTGTGTGGATCACTGTGTTGAGGTTTATGGGAGATCTTCCAGAACCCAAATATCATATCAGTATTAGTGATGGCAGTGAGAAGATACCAGTTATGACTAAAATCTATGAGACGTTGGGAAAGAGAACCTACAAAAGGGAGCTGCAGGCCTTGCAGGTGGATGAGGAGGTGAAAATGAGTCTTAAAATTCACATTGTCTAAATGAATAATTTCTACATGTAATACATTTCAGCAATATAAGGTTCCTGTTTATACTTACAGAAACATGAAGTCCACTCCAAAGACACTTATACTCTATCAGTAAGCACTCTTTCAGAACACCCTCAAAGGCCCCAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37295
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 |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 1076 | 2178 | 23 | 47 |
ENSDART00000148019 | Nonsense | 1071 | 2098 | 22 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21237465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22248958 |
GRCz11 | 21 | 22285594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTATTAGTGATGGCAGTGAGAAGATACCAGTTATGACTAAAATCTA[T/A]GAGACGTTGGGAAAGAGAACCTACAAAAGGGAGCTGCAGGCCTTGCAGGT
Long Flanking Sequence:
GAGGTGTGGAGCTTTGTCAATTTCAACCTAAATTGCATTGCTTGGCTTGAATCTTATCTGAGTTTTCTTAATGTTTGGATGTTACAGGATCTAGAGAATGCTCCAAAACAGTTTAAGGAAGTCATTGATGAGCCTCTTCCACTTCCTGACGATGAAGAGGAGGACCTATCGGAGTATAAGTTTGCAAAGTTTGCTGCAACCTACTTCCAGGGAAATGCAACACACATGTATGTACGCCGGCCACTGAAACAGCCTCTTTTGTTTCATGAAGATGAAGGAGATCAGCTAGTAAGCATTTATTTATTTATTAGTCATCTCTATGCTTACCTGCTTACTGTAAAATAGGATTAAAAGCTGCATTGACTGTATCATATGTGTTTTTAGGCTGCTCTGGCTGTGTGGATCACTGTGTTGAGGTTTATGGGAGATCTTCCAGAACCCAAATATCATATCAGTATTAGTGATGGCAGTGAGAAGATACCAGTTATGACTAAAATCTA[T/A]GAGACGTTGGGAAAGAGAACCTACAAAAGGGAGCTGCAGGCCTTGCAGGTGGATGAGGAGGTGAAAATGAGTCTTAAAATTCACATTGTCTAAATGAATAATTTCTACATGTAATACATTTCAGCAATATAAGGTTCCTGTTTATACTTACAGAAACATGAAGTCCACTCCAAAGACACTTATACTCTATCAGTAAGCACTCTTTCAGAACACCCTCAAAGGCCCCAATGGGCCATATGCACAGCTAGTGTTTTTCAGCCAATGGTGAACTTCCAGGGAAAGCTTTATGTGACTATTTTCAATTTCACAAGGTTTCTTTTTACATCTTCTTGTTTTGTCTGAGATCCATTTTATATTGTATATAAATCAGCAGTGAAAATTACAGATTTTTCAAGAAATCAGATCTTAAACTTGACACTTTTGTATAGACCTTTTTCTTAAAAACGCAAAATTACCCATTATGCTTTGCGTGTATGCGCAAGGAGAATGCGAAGAACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23924
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 |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 1600 | 2178 | 34 | 47 |
ENSDART00000148019 | Nonsense | 1594 | 2098 | 33 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21248603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22260096 |
GRCz11 | 21 | 22296732 |
KASP Assay ID:
2261-5562.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATGCTTCGTTCCTGAGATTCTCAAAGGGAGATCTGATCTTTCTGGAT[G/T]AGCACACTGGAGAACAGGTCCTGACTTCAGGCTGGGCTCATGGGGTCAAT
Long Flanking Sequence:
GGAGCAGGTCCTTCTAGACCTTTCTTTCCCAGAGATCACTGCGGTCTCCAGCAGCAGGTGCATTACATTATCCAACCAAACACACTTCATTTGATCTAAGTGCTCACTGTATTATACATTAACTCATTTTCATCCACTTTTAATCAATGTGCTTTCAGAGGTGGAAAACTGCAGGGACAGAGCTTTACCCTGGCCACTATTAAAGGAGATGAGTACACCTTCACATCCAACAACGCTGAAGACATCCGGGATCTGGTTGTGGCTTTTCTAGAGGGCCTGCGTTCCAGGTCAAAGTTTGTGGTGGCAATGATGGACAGCCATTATCCAGGTGAGCTCACAGTTGGGTTTAACTTTAATAACATTGTATTTGATTTGGGCCCCAAAACAATTAGGTTGAGCATAATTAATAAAACATCTAAAAAATGTTTTTGTTTGTTTTTTCAGCTGGGCAAGATGCTTCGTTCCTGAGATTCTCAAAGGGAGATCTGATCTTTCTGGAT[G/T]AGCACACTGGAGAACAGGTCCTGACTTCAGGCTGGGCTCATGGGGTCAATGACCGAACCAAGAAGAGAGGAGACTTTCCTGCGGACAATGTCTATGTGCTGCCCACCATCACCAGGCCACAGTATGATATTGTGGTGAGTGGGCTTTCATCCAATACATTCCTTGTACATTGTCAGAAAACAAAAAAATGGACTTATGTAGGAATTTTCACTTTTTTAATCACCAATTTGTAAACAGCATGTGGGAAACCAAACCTTTTCCAACTTTTAGACTGTTTTGCAGGGAAAATTAAAAAAGAAAACAATGTTTACATATGTGCAACAGGCTGCATTTGGTTTTGGCTCATGAAATGAATATTTAGCTTCTGTTTGTGTTTCTTGCAGTCATTGATCATCATGTCTCCAGACCAGCGTAAGGACTCTGTAAATTTGTCCCAGCAGAATCTGCTGGACAGTGGGGAGAAAGTCCAGCCGTACACTTTAGAGGAGTTCTCCTACGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3116
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003181 | Nonsense | 1888 | 2178 | 40 | 47 |
ENSDART00000148019 | Nonsense | 1882 | 2098 | 39 | 46 |
Genomic Location (Zv9):
Chromosome 21 (position 21255530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22267023 |
GRCz11 | 21 | 22303659 |
KASP Assay ID:
554-2750.1 (used for ordering genotyping assays)
KASP Sequence:
TATTCCTTTTTTRTTTGCAGGCTTTTGAGGTTGAATCCAGTACAAAAGCC[A/T]AAGATTTCTGCCGAAACATCGCCGGCAGGATGATGCTTCATTCCTCTGAA
Long Flanking Sequence:
AAGCAAACAGTACCCCTTTTTTGGCAGCTATTCAATTTTTGGTACCTAGCACAACAGTACTGTACCAAAAAGGTGGAACTAGACTCACTGCTGAATGCTATTGGTTTACAGAGAATCATCACTTGCATGACAAAAAGCCAGGAGAACGACAACAGGACTCACTATTTTTACATAGCTAAAAGACAACACCATAATAATACAATAACAAACCAAACAAAGCTTGTCGTCTTCTTTTGACAAACAGCCACATGCCAAAAGCAAGAACAGGGCCTGCTGTATGTCCTCCTTTGTTGTTTATGAGGTCATTTACATGTAGAAAGCACGAAGCACACCGCTTTCTGACATTCGGACACCAATCCAACCAAGTAAAGGATGCTGTCAGCAGTGGAAACAAAAACCTGTTTAAATAATCAGGTGAAATAATGACGTCTGAAATGTCTGTTTTTTAAATATTCCTTTTTTGTTTGCAGGCTTTTGAGGTTGAATCCAGTACAAAAGCC[A/T]AAGATTTCTGCCGAAACATCGCCGGCAGGATGATGCTTCATTCCTCTGAAGGTTTCAGCTTGTTTGTCAAAATTTCTGACAAGGTGAGTCTACAGAGCTGTCTAGATGAATCGAGGATGTGTGAGTTTATGGCACCATAAATAACTCCTTCAAAAGCCCAACCGCTGAGTGTTACTGCTTTCTCCTCTACTTTTCTCCTCACAGCTGGCAGTTGTTTGTCAGTATATTGTGATATAAATGTCTCATCGTGTTTCAGGTGATCAGTGTGCCAGAAGGAGATTTCTTCTTTGACTTTGTTCGACATCTGACAGACTGGATCAAAAAAGCCAGAGCTGTGAAAGACGGTGATTATGTGTTTTGCTCATTAAAGTATGGTGAAAGAAAGAGCTTAAATGTGCTGCAAGTTAAGAAAACAGATGCAAATAGAAAAACATTAAGAGAGTTTTAACAACACGCACTCACAAATTCATTCAGCACATGCAAATACATGCAAATGAGCT
Associated Phenotype:
Not determined