ZMP
dnah7
Ensembl ID:
ZFIN ID:
Human Orthologue:
DNAH7
Human Description:
dynein, axonemal, heavy chain 7 [Source:HGNC Symbol;Acc:18661]
Mouse Orthologues:
Dnahc3, Dnahc7a, Dnahc7c
Mouse Descriptions:
dynein, axonemal, heavy chain 3 Gene [Source:MGI Symbol;Acc:MGI:2683040]
dynein, axonemal, heavy chain 7A Gene [Source:MGI Symbol;Acc:MGI:2685838]
dynein, axonemal, heavy chain 7C Gene [Source:MGI Symbol;Acc:MGI:3639762]
dynein, axonemal, heavy chain 7A Gene [Source:MGI Symbol;Acc:MGI:2685838]
dynein, axonemal, heavy chain 7C Gene [Source:MGI Symbol;Acc:MGI:3639762]
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34648 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27405 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34647 | Nonsense | Available for shipment | Available now |
sa38742 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7185 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2518 | Nonsense | F2 line generated | Not yet available |
sa41422 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1268 | Nonsense | Available for shipment | Available now |
sa34646 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1875 | Nonsense | Available for shipment | Available now |
sa21492 | Nonsense | Available for shipment | Available now |
sa10194 | Nonsense | Available for shipment | Available now |
sa8862 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11115 | Nonsense | Available for shipment | Available now |
sa8404 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34648
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 135 | 3984 | 5 | 65 |
ENSDART00000137131 | Nonsense | 153 | 4001 | 5 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26086815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25242601 |
GRCz11 | 9 | 25053470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTTTCTTTCAGAGGTACTGTTATTACATCCGCAATGGCATCGGCACA[G/T]AAGATGTGGCAGCCATGGAAGATTCCTGGCTTAAGAATGTTCTTGCTTTA
Long Flanking Sequence:
TTCCAACTGCTTGGCTATAATGCTGAGGTTTCATCTTTGGGTAGAGACTGGATAATATCCGTCTGCAGTGTGACTTCAATCGACCGGCATGTTTGTGTGTGTGTGTTTGTGTGTGTGTGTGTCTGGGTTTCTGTGTCAGAGGGCGGGGCCGCAGGTTTCTCAGGGTTTGCGCGTGCACGTGAATAACTTGGTTTCGTTCGTACGTCATGGCGAAACACCTAATGACTCGGTATCAAGGCGACTCGTTTGAAGCACTATGAGTCGACTCTTTTATAGATGAATCAACCGTTTTAAACAACTTTTATTCTTACAGATTTAAGCCTTAGCTGGATACTTCACTTCACTTAGAGCTGTGTTACACACTACATGGAGGGGAATTTTCAAAATCCCATAATATGGGCTCTTTAAAACTTCTGTATATCCTCATCCAGTATGGACACAAACATTATGACTCTTTCTTTCAGAGGTACTGTTATTACATCCGCAATGGCATCGGCACA[G/T]AAGATGTGGCAGCCATGGAAGATTCCTGGCTTAAGAATGTTCTTGCTTTAGTCCCAGAACATCTGAAGAGTTTGACCAGAACCATTGAGGCTCTTTCAGATGAGATGAGAGAAGACTATCTGCTCAGTATCAAAAAAAATATTGGTACTGTCTCCTGCTATTTGCAGTATAGAAAGATGCAAGATTTTTTTTTGTATGCAATGCCTGTACACAAAATCTGAGGTGAAGGTGCTTGTTGTTCTAACAAAACAAGTTTAACTTTTATTTGAACAAACATTTATTTATTTACTTAATTATAATTTGCTACCATCCCTGTGCTATTAAATGTTTTCCATCCATGACCATCCTTTATTCTCCATGCAGTGGACTTTGTGCTGCAGGACCCGAGAGAAAATAAAGAGCTCAAAGCCAGAGATCTCCCCCCACACAGACAGGAGTGAGTCCTGCTAAATTAATTTTAGTGGTGCTGTTCACACGATTAAAAACAAAATAATAATTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27405
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 463 | 3984 | 12 | 65 |
ENSDART00000137131 | Nonsense | 481 | 4001 | 11 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26083650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25239436 |
GRCz11 | 9 | 25050305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAAGCATGTCCATCTCTATGATAAGTATGCTCCGCTGGTGTCCCAG[C/T]AAGCTGAGGAGGATGTTACTCAGTTTTTGCTGGAGCAGCACTCTTTCCAG
Long Flanking Sequence:
TTGTGCGGTGTGGTTTGATAGCTAAAATATTAAAGGGATTGTATCACGAGGAATCAAATTGTCATTAATCTTTGGAGATCTTTGGAATAATTTCAAACACACTATATGTTTTAGGATTCAAAATGTCCTCCCTAGTGTGCAATTTGTTGTTTAAAAGGACTAATTCTGAAACAGGAGTTAACATATATTTTATACACATATCTATACATAAACTTAGAGCAAATTATGAATGATATTGGCACAGAGAAAGTTTCTTGCTACTGTATAATCTAACAAATCCCAGTGCAGTCTTTACTGTGATCCCTGCCAATTATATTTCATACATGTAATTTTTTGTATTCCAGCCTGGCCCAGAAACACACCATACTCTAAAGCCCATCATCCTACCAGAGATCCTGGAGGCCCAGCAGGAGAAGGTCAGACGGGTAATACGTGCAGAAAGTGCTGAGCCTTTGAAGCATGTCCATCTCTATGATAAGTATGCTCCGCTGGTGTCCCAG[C/T]AAGCTGAGGAGGATGTTACTCAGTTTTTGCTGGAGCAGCACTCTTTCCAGGAGCTGATGATGGAGGTGATCCGCTACCAACAACTGGCTGATGAAATCCAATGCAGCACAGTGAAGGTACATGCAGCTATGTATATTCTACTAGCATTTCCTCACAGAAATATGACAGATTGAGAATATTTAGCATTTTGTTTTTTAGGTGGTGCGTTTGGGTATGTTTGAACTGCACTCCCATGATCTGGTCCGTGCCCTTGTAAAGCGAGCAGAGGGTCTTTTGCAGAAACTGGTAAATCATATGTTGCAGGGTCATCAGGAGTTCAATAACAAGTAAGTCAAAGACAGATTGACAGAAATGTTTTGTCGGTGACATTCTAATAATCTTGCTGATCTTTCTAGATTGTGTGAGGAATATGATACTATAGCAAATAAAGCCCTCAGAAGTCCATCAAACACAGAGGAACTCATGGAACTTAGGGTAACACTGACCGAGTTTTGTTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34647
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 488 | 3984 | 12 | 65 |
ENSDART00000137131 | Nonsense | 506 | 4001 | 11 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26083573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25239359 |
GRCz11 | 9 | 25050228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGGAGCAGCACTCTTTCCAGGAGCTGATGATGGAGGTGATCCGCTA[C/A]CAACAACTGGCTGATGAAATCCAATGCAGCACAGTGAAGGTACATGCAGC
Long Flanking Sequence:
ATCTTTGGAATAATTTCAAACACACTATATGTTTTAGGATTCAAAATGTCCTCCCTAGTGTGCAATTTGTTGTTTAAAAGGACTAATTCTGAAACAGGAGTTAACATATATTTTATACACATATCTATACATAAACTTAGAGCAAATTATGAATGATATTGGCACAGAGAAAGTTTCTTGCTACTGTATAATCTAACAAATCCCAGTGCAGTCTTTACTGTGATCCCTGCCAATTATATTTCATACATGTAATTTTTTGTATTCCAGCCTGGCCCAGAAACACACCATACTCTAAAGCCCATCATCCTACCAGAGATCCTGGAGGCCCAGCAGGAGAAGGTCAGACGGGTAATACGTGCAGAAAGTGCTGAGCCTTTGAAGCATGTCCATCTCTATGATAAGTATGCTCCGCTGGTGTCCCAGCAAGCTGAGGAGGATGTTACTCAGTTTTTGCTGGAGCAGCACTCTTTCCAGGAGCTGATGATGGAGGTGATCCGCTA[C/A]CAACAACTGGCTGATGAAATCCAATGCAGCACAGTGAAGGTACATGCAGCTATGTATATTCTACTAGCATTTCCTCACAGAAATATGACAGATTGAGAATATTTAGCATTTTGTTTTTTAGGTGGTGCGTTTGGGTATGTTTGAACTGCACTCCCATGATCTGGTCCGTGCCCTTGTAAAGCGAGCAGAGGGTCTTTTGCAGAAACTGGTAAATCATATGTTGCAGGGTCATCAGGAGTTCAATAACAAGTAAGTCAAAGACAGATTGACAGAAATGTTTTGTCGGTGACATTCTAATAATCTTGCTGATCTTTCTAGATTGTGTGAGGAATATGATACTATAGCAAATAAAGCCCTCAGAAGTCCATCAAACACAGAGGAACTCATGGAACTTAGGGTAACACTGACCGAGTTTTGTTCAAATGTAATACCTCTGCTTTTTGGTACGGTTGACAAAAAAGATATTGTTAAGTATGTTTTATGTTATTTGTTATTTATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38742
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 762 | 3984 | 17 | 65 |
ENSDART00000137131 | Nonsense | 780 | 4001 | 16 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26080947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25236733 |
GRCz11 | 9 | 25047602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACTCACAGCCGTCAACCCAGACAAAGTGGAAGTTGATGTGGGAAACTA[C/A]AGCCGTGGCCTATACAAACTGGAGAAAACCTTTCAGGACTTGCCCAAACC
Long Flanking Sequence:
TTATATAAATATACATTTCTTACTTACATAGCTGGAAGGTTGATGGAGGAAGTAGAAAGACGTGCATATAAACAGTGATAGTAAGCCCATTTACTGAATAAATTCCTGTCCAGTAGAAGGAAAACCTATTGTTCATGTCATCCTGATGCCAAAGCCTAGTCACAGTGCAGTAAAAATGTAAGTTAAAATCCAGTTTGTCAACTGGATTTGTCAAAGTGTCTTAGAAATTCTCTGAGAAAAGCTGCTCTTTTCAATGCACCTCCAAAAATTAAACTAATGCACTGTCCTATCTTTCAGATCAGAGGCATCAACCAGGAAGAGGAAGCCTTTGACTGGCCTGTCTCTCAGTATCCACAACGCAAAACTGTTCAAGACCAACTGCTCCCTTATCTGCGGCTCTATGAGACGGCAGCTGAGTTTCAGAGCCAGCACCATCAGTGGGTGACGGGCCCACTCACAGCCGTCAACCCAGACAAAGTGGAAGTTGATGTGGGAAACTA[C/A]AGCCGTGGCCTATACAAACTGGAGAAAACCTTTCAGGACTTGCCCAAACCTCTTCAAATTGCCACCTCTGTGAAGGCAGAAGTTGAAGCCTTTAAGGAACACATTCCTATAGTGCAGGTGCCATACAGAGATATCATTCTTTCTTTTTTTGAGGATGTAGGAGAAATCTATTGAATGTTTATCGAGGGTAAAATATACCAGACAGTGCCTTATTCTTATTTCTAGCTGAAAACATTATAGATTAGCCAAATATTTAATAAATAAACATGTAAGAGGCTGAATTCTGCTACTCTTTCTTGGGAATTATGAGAGTACAGACTGCACATTGTCCTGCTCATTAATTACAGAGATGATTTGTTTCGGCAGGTGCTTTGTAACCCCGGTCTGCGCGAGCGCCACTGGGAGGCCATGTCTGCAGTTGTTGGTTTCCCTCTCAAGCCCTCAGAGGAGGATGCCTGTGTGGCCCACTTTCTTCCCCTACATCTGGAAGCTCATCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7185
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Essential Splice Site | 1164 | 3984 | 22 | 65 |
ENSDART00000137131 | Essential Splice Site | 1182 | 4001 | 21 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26061423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25217209 |
GRCz11 | 9 | 25028078 |
KASP Assay ID:
554-5015.1 (used for ordering genotyping assays)
KASP Sequence:
AGGTTTACTGGACAAAGGACATTCATGAAGCCATTGCAAAGGGACCAAAG[G/A]TATGTTAAACTGTTGYATGCTTTCCAGAACATCAAGTTCTTATTCTATAC
Long Flanking Sequence:
AAAATATTTTAAAAGGGTGTTTAAAAAGTCATAAAAAGGTATTGAAATTGCCTTTAGGATTCCTGTATATAGCCTGATATATAAATATCTATAAATTTCTATAAATTTTATTTTTTAAACTGGCTCCTTTGCAAAGTTTCAGTAATATTACTTTTATGGCAAAGAACAAGACCTTTTTAAGGTCTTTAAAGTGAAATAATTCAATGTAAACAAACGAGGCTGAGAAAAATGTTTATTTTGATGTAAATTTCAGATTTCACTTAGAGGTTTTTGCACCTGAACTGTTCATATATAATTTTTGCTATTTTTGAAATGTAAATTGTTGAAACTATGAGTTAAACTATGCTCCTGGCTGACAGGTGATTGGAAAGGCATGTGAAGCATATCTGAATGATCTACGGATCAATTGGGTCAGAGCCTGGCCGGGCCAGACAGTGCTTTGTGTGTCGCAGGTTTACTGGACAAAGGACATTCATGAAGCCATTGCAAAGGGACCAAAG[G/A]TATGTTAAACTGTTGCATGCTTTCCAGAACATCAAGTTCTTATTCTATACTATATATGGCAGTGTTTTGTTGTTCTGTGATTTGCCATTAATGACAATATCTAGGCAATATATGGCGTATAATGTATATACTTTACATTCAGAATCTTAAGCTGTTCTCATTGTCTCTAAAAGAACATACATTGGCAATGTTTTGTTGTTGTTTTTAGTGTTTCTTTTATTATACTGTAGTGAGTAATTGGCTGTGGTTTGACAGTTTTTGCTGAGAGTTAGGGTTCAGGGTTAGTTCATACGAAAATTAATTAATTACTAGTTATTATTTACTCTCCTTCATGTCATTTTGAAACTGAAATGTTTGCCAAATTTTTTTTTTTCACCAATTGCTCACAAGGACATTTTACTTACTATCAGCAACTTTGCAAGTATGTCAACCTATATTACCAACCATAATCGACTCCATCTAACCAGGTAGTTGACCAGGTTTTTAAAGTCAACTGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2518
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 1233 | 3984 | 23 | 65 |
ENSDART00000137131 | Nonsense | 1251 | 4001 | 22 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
ENSDART00000026924 | Nonsense | 1233 | 3984 | 23 | 65 |
ENSDART00000137131 | Nonsense | 1251 | 4001 | 22 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26060548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25216334 |
GRCz11 | 9 | 25027203 |
KASP Assay ID:
554-3256.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGTTGATGATGAGACCAACTTTGAGTGGCTCAGCCAGCTGCGCTACTA[T/A]TGGATTGTAAGCCAGYTTGAKTGTGATTRAAAATGAWATGTGTGTGACCT
Long Flanking Sequence:
ACCAATTGCTCACAAGGACATTTTACTTACTATCAGCAACTTTGCAAGTATGTCAACCTATATTACCAACCATAATCGACTCCATCTAACCAGGTAGTTGACCAGGTTTTTAAAGTCAACTGCATGTCTTAAGTGGACCATAAAGATAAAGTGTTAGTCTGTTTGTAGGAAGCAGGATAATGTGTCGACATTATCTGCTTTATTTTGAATAGGATTTATTTTCAATCAGTGTCTGTCTTACTGCACACTCGTATAGCATCCTATTAAATGACTGAATTGTTATTCTGTTTTCAGGCTCTTCAGGCTTATCTGGAGCAGAACAATACTCAGATAGATGACATTGTCACTCTGGTTCGTGGAAAGCTTTCCAAACAGAACCGAGTGACACTTGGAGCACTGGTGGTGCTAGACGTTCACGCCCGAGATGTATTGGCATCTCTGGTACAGAAGGGTGTTGATGATGAGACCAACTTTGAGTGGCTCAGCCAGCTGCGCTACTA[T/A]TGGATTGTAAGCCAGTTTGATTGTGATTAAAAATGAAATGTGTGTGACCTTGTTTGTTCAAAGTTATTGTTTTGGACAGTCAGAAGATCTGCTTTGATTTGCTTTTTCTCCTCTTGATATGATTATTTGACCCTGTCTGTAAAGGAGAACCAGCTTCATACAAAGATGATCAATGCAGGCTTGGCGTATGGCTACGAGTATCTTGGAAACACACCACGACTGGTGATCACCCCTCTCACTGATCGCTGCTATAGGTCAGGATGATTTACATTATACACAAAGATCAAAAGCAACTACTTTTCTATGTAGCTGCGTTTAGAAGAGGCTCTTCAAACAACCATTTAATTGGATTGTAAGTTTGATTTGTACATTTGATCAAGCCTTGGAGGTCATACAAGGCTTCGTTTAAAAACATTGTACTGACATCAAGCGATCATTCTTTCAATGGTAGTGTGTGTTATCTCTGAAAATAGTTTGAATAATTTGTTTATATTTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41422
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 1276 | 3984 | 25 | 65 |
ENSDART00000137131 | Nonsense | 1294 | 4001 | 24 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26059974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25215760 |
GRCz11 | 9 | 25026629 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGACATTCCTGCAATTTTTGACATGCTTTCTTTTTCAGGACTCTGTTT[G/T]GAGCTTTGCATTTACATCTTGGTGGAGCCCCCGAGGGACCTGCAGGTACA
Long Flanking Sequence:
GGACAGTCAGAAGATCTGCTTTGATTTGCTTTTTCTCCTCTTGATATGATTATTTGACCCTGTCTGTAAAGGAGAACCAGCTTCATACAAAGATGATCAATGCAGGCTTGGCGTATGGCTACGAGTATCTTGGAAACACACCACGACTGGTGATCACCCCTCTCACTGATCGCTGCTATAGGTCAGGATGATTTACATTATACACAAAGATCAAAAGCAACTACTTTTCTATGTAGCTGCGTTTAGAAGAGGCTCTTCAAACAACCATTTAATTGGATTGTAAGTTTGATTTGTACATTTGATCAAGCCTTGGAGGTCATACAAGGCTTCGTTTAAAAACATTGTACTGACATCAAGCGATCATTCTTTCAATGGTAGTGTGTGTTATCTCTGAAAATAGTTTGAATAATTTGTTTATATTTTTAAATTAATTAGATTATTTTTACTGAACACGACATTCCTGCAATTTTTGACATGCTTTCTTTTTCAGGACTCTGTTT[G/T]GAGCTTTGCATTTACATCTTGGTGGAGCCCCCGAGGGACCTGCAGGTACAGGCAAAACCGAGACCACAAAAGATCTGGCTAAAGCCATAGCTAAGCAGTGTGTAGTATTCAACTGCTCTGATGGCCTGGACTACATTGCGCTTGGCAAGTTCTTTAAGGTAAACACTTTTGGAAAGTCTTCAGATTTAGTGCACAAGATTGACACAAGTAAAAAATAAATAAATCCAAATATAAAAATTGAAATCTCAGTGAAATATTGTAACAGGATTTTGGCATTGGCTTAGTGTAAAAGACATGCTGATGGCCATGTTACAGAAAATAACACACATGAGGTCAAACACTATCTGTCCGAAAAAAAAAAAAACTCTCAGGCACTGACTTACACAGTCATCACTGGTTGCTATAGTAATAGATTTAGATCAAAATTGTTGTGGTACTGTTAAAAAATCTAAGTAAAATTAATGTTTTCAAGAGAAAAGTACTTAATAAAGCATAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1268
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 1724 | 3984 | 33 | 65 |
ENSDART00000137131 | Nonsense | 1742 | 4001 | 32 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26040788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25196574 |
GRCz11 | 9 | 25007443 |
KASP Assay ID:
554-1183.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTATGATCTACATGGAGCCTCACATGTTGGGATGGCGTCCTGTGATGT[T/A]GTCCTGGCTCAACACCGTGCCRTCCACTTTGAGCTCCATGCACAAAGACC
Long Flanking Sequence:
TACATCTATATACATCCATCTGTATTTTAACTTATATTCAATATCTAGAAATACAGTTAGGTCCATACATATTTGGACGTTGACACAATTCTAACTGTTTTGGCTCTATACACAAAGACAGTGGATTCGACATGAAACGAGCAAGATGTGGTTTAGCAGCAGACTGTCAGCTTTAATTTGAGGGTATTTACATCCAAAACAAGTGAACGCTGTAGGAATTACAACAGTTTGCAAATGTGCCTCCCACTTGTTAAGGGTCCAAAAGTAATTGGAAAGAATAATAATCATTAATCAAACTTACACCTTTTATTACTTGGTTGAATGAATGAATATTGCTGTTGTGTTGTTAAAAAACGAATGCACCATTGGTGAGAATCTAAAAAATAAATCAGTAAAAATATTCTTGATCAAGCTGGGATTTTTGCTGATTTTTGTGCAGGTGTCTCGGTGTGGTATGATCTACATGGAGCCTCACATGTTGGGATGGCGTCCTGTGATGT[T/A]GTCCTGGCTCAACACCGTGCCGTCCACTTTGAGCTCCATGCACAAAGACCTCATTACTGGCCTCTTCGACCGCATGCTGCCTGCTTGTCTTCAGCTCATCCGCAAAGGCACTAAGGTAACTGTGCTGCAGACAATGAGTTTGGCCTTTCCCACTAAATTAAAAGGCATCTTTAATATCAAAAGCAACAACTGCACACACTGAATTATTAGGTGCCTTTTGTAAAACCTTGGCAAATTATTTTAGTCCCCCGATCTCTCAAGCTAAGCCAGATGTTTTTTTTTACATGGATGAACTAATTGTTGAGGCGTTGGGAGAGAATTTTTTAATGGCAATGAGACATCGGGCCCTATCATACACCTGGCTAATAAGACATGCATTTTTTGCTATTTTCAGACAAGCAAAACCCTAATTTTCACGTTTACGCCACGTTCTTTAAATAGCAAATGGGTGTTCCGATTTAAAAAGATGTGTTAGGCACATTGTTGGTGCATTGCTATTT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa34646
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 1788 | 3984 | 34 | 65 |
ENSDART00000137131 | Nonsense | 1806 | 4001 | 33 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26038231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25194017 |
GRCz11 | 9 | 25004886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGGTGAAATCTCTGATGAATCTGATGGACTGCATGATGGATGAGTTC[G/T]GAGATGAGAGCCAGATGAAGAGGATGGACCAGAGAGATGTCTGCTCCTGG
Long Flanking Sequence:
TCCTTTTTCAATAATTACAGGCTTCTGCAATTAAGGCTTCTTTTATGCTTGCACGCATGCATTGTGCACAGAATGGGATAACGCACTAATTATGTGCTTTCTTTTTTTAAATACCACTTCTCTTGACAGTCCCCTTTTGTCTCTTAGTGCTTACAGTGCACTTTGGTTAATACAGTTTTTGTCAGACAGAGTAGTTCTTTCTTGACAATCATTTAGCTGCTACGTTTCTTTGTTGCCTTGTTTGTCTTTTTGAAACATTAATTTTTTTGTATATCAATTATCAAGTTTTTATGTAATTACCTCGCATCACAGCATGTCTTGTGTGCCTTTAAGATAGTTTTGCCCAGTATGATGGCACACCACCACTCATCTAGCCACAGGTTTGCAGTCCAAACTAATGTAGTGTTTTTTGTGTGGGCATTCAGGAATTATCACCCACATCCAACACGAGCCTGGTGAAATCTCTGATGAATCTGATGGACTGCATGATGGATGAGTTC[G/T]GAGATGAGAGCCAGATGAAGAGGATGGACCAGAGAGATGTCTGCTCCTGGCTTGAGGTTAGGCGATGAAAGGAAATATGAAGGAGATAAAGTGTAAAATGTTGGACACTTCATGCACTCAACGCTTGCAGTTTTCTTTATGTAGCTCAGATTGATCCGCATTTCTGCTGAGTCTGCACTCAAGCTGCTCGCTAGACCAAACAAAACATCCAAGCAACCACGTTTAACTCTCCTAGCAATCATCCACAGCAAATCAGCCTCATTTTGCATAGGCACTACTCGCATTTTTAACTGCAAAAATGTAAAAATCTGCTTGATCTAATTATGATTAATCTCTATATGCCAGAGTTTCAACATGTATTAATTGATTCAATATATCTGACCCATAGAGAGGGTGTAGAAGGTTATAAATACAAATTAGAGATGTCATATACGGGATATAATGTATCTCACATTACCTTTTTTCATTTAGTTGATTTATTGACTGTCACGGATAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1875
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 2267 | 3984 | 41 | 65 |
ENSDART00000137131 | Nonsense | 2285 | 4001 | 40 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26026968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25182754 |
GRCz11 | 9 | 24993623 |
KASP Assay ID:
554-1865.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTCCGYCAAGTGGTGGAGACCCATCTTGAAGAGTACAAYAATATCAGC[A/T]AGGCTCCCATGAATCTTGTACTTTTCCGATTTGCCATTGAGCATGTTTGT
Long Flanking Sequence:
TACCAACCCCAGCTAAATCCCATTACCTTTTCAATCTTCGAGATTTTTCCCGCGTCATTCAGGGTATCTGCTTATCACGGCCAGAAACTGCAGACGACCTTACAGCCATCAAACGGTTATGGGTGCATGAGGTACTGTAACTGCAAACACGGTTTTATAGGCCATATTCTAATAAAAAAGACTAACTGATGATTAAATCTTCTCTTGTGCAGGTCCTGAGAGTGTATTATGACCGTTTAGTTCATCCGGATGATTGTGCATGGATGGTGGGCTTCCTGCAAGAAGTCTCCAAATCTCACCTGAATGAAGATTTCCATCAGCTCTTCAAGCATCTAGACAGCAACTCAGATGGACTTGTAACTGAAGATGATCTTCGCAGCCTCATGTTCTGTGATTTTCATGACCCCAAGGGTGAGGACCGCAACTACCGTGAAGTGGGTGATGCTGAGAAGCTCCGTCAAGTGGTGGAGACCCATCTTGAAGAGTACAATAATATCAGC[A/T]AGGCTCCCATGAATCTTGTACTTTTCCGATTTGCCATTGAGCATGTTTGTCGAATCTCCCGCATTCTCAAGCAGCCCCGTGGTCATGCTCTCCTTGTAGGTGTTGGAGGGAGTGGACGACAGTCATTGACTCGCTTGGCCGCCCACATGGCTGAAGCCGAACTCTTCCAAGTAGAGATCTCCAAGAGTTATGGAGTTTCCGAATGGCGAGACGACCTCAAACTCATCATGCAAAAATCAACATCTGGGGATACTCATGGAGTCTTCCTATTCACAGACACCCAGATTAAGATGGAGTCATTTTTAGAAGATGTGAGTAACTTGTTAAACACTGGTGAAGTTCCCAATCTCTTTGCTGTAGATGAGAAGCAGGAGATTTGTGAGCGCATGCGTGTCTTGGACCGTCAGCGGGATCGTGACAAGCAGACGGATGGCAGCACGCTGGCTCTCTTTAACATGTTTTTAGAGCGCTGTCGCAGTCAGTTGCACGTGGTGCTAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21492
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 2490 | 3984 | 42 | 65 |
ENSDART00000137131 | Nonsense | 2507 | 4001 | 41 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26026163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25181949 |
GRCz11 | 9 | 24992818 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGTTTCCTGGAAGACGTTGAAATGACAAACACTGCTCGTGAAGGCTG[T/A]ATCAGCATGTGCAAGAGCTTCCACACATCCACCATCGATCTCTCTGCACA
Long Flanking Sequence:
AGAAGATGTGAGTAACTTGTTAAACACTGGTGAAGTTCCCAATCTCTTTGCTGTAGATGAGAAGCAGGAGATTTGTGAGCGCATGCGTGTCTTGGACCGTCAGCGGGATCGTGACAAGCAGACGGATGGCAGCACGCTGGCTCTCTTTAACATGTTTTTAGAGCGCTGTCGCAGTCAGTTGCACGTGGTGCTAGCCATGAGTCCTATTGGTGATACCTTCAGAAGCCGCCTGCGACGTTTCCCTGCTCTCATTAACTGCTGCACTATTGACTGGTTTCAGGTTGGTGTTAATGTGAATCATATGCTTTGTTAAATGCTATTTTAATATCATTGATATTCCACTTAATGATACAGGAAACCTTGTTATAATCAAGGAATAAAAGTGTAATCACTGTCAATCATTGTATGTTTCAAAAGAGCTGGCCAGAAGATGCACTGCAGGCTGTGGCCTCTCGTTTCCTGGAAGACGTTGAAATGACAAACACTGCTCGTGAAGGCTG[T/A]ATCAGCATGTGCAAGAGCTTCCACACATCCACCATCGATCTCTCTGCACATTTCCTTTCAGAGCTGCAGCGCTACAACTATGTCACACCAACCTCCTATTTGGAGCTTATCTCTATGTTCAAACACCTACTCCAGCGCAAAAGAACGTAAGTCATTCTTCTGTAACTCTGTAAAGGGCTTTACATCAGAAACATTGACTGGTTTGGTTTGAATAATTGGGTTTTGTCATTTTGCCAAGTGAATTCTTTCTAAAATAAGCATTATTTCTGCCAATAATGATTTCAGGGAAGTCATGAAGCTGAAGAGTCGTTATGAGGTTGGTCTTCAGAAGCTGGAATCGGCTGCCACACAGGTGTCCACAATGCAGGGGGAGCTGGAGGCTCTTCAGCCTCAGCTGCGAGTTGCAACTAAAGAGGTGGAAGAGATGATGGTGGTCATTCAGCATGAGTCTGAAGAGGTGTCCAAGACAGAGAAGGTGGTCCGTGTGGATGAAGCGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10194
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 2557 | 3984 | 43 | 65 |
ENSDART00000137131 | Nonsense | 2574 | 4001 | 42 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26025824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25181610 |
GRCz11 | 9 | 24992479 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCATGAAGCTGAAGAGTCGTTATGAGRTTGGTCTTCAGAAGCTGGAAT[C/A]GGCTGCCACACAGGTGTCCACAATGCAGGGGGAGCTGGAGGCTCTTCAGC
Long Flanking Sequence:
CACTTAATGATACAGGAAACCTTGTTATAATCAAGGAATAAAAGTGTAATCACTGTCAATCATTGTATGTTTCAAAAGAGCTGGCCAGAAGATGCACTGCAGGCTGTGGCCTCTCGTTTCCTGGAAGACGTTGAAATGACAAACACTGCTCGTGAAGGCTGTATCAGCATGTGCAAGAGCTTCCACACATCCACCATCGATCTCTCTGCACATTTCCTTTCAGAGCTGCAGCGCTACAACTATGTCACACCAACCTCCTATTTGGAGCTTATCTCTATGTTCAAACACCTACTCCAGCGCAAAAGAACGTAAGTCATTCTTCTGTAACTCTGTAAAGGGCTTTACATCAGAAACATTGACTGGTTTGGTTTGAATAATTGGGTTTTGTCATTTTGCCAAGTGAATTCTTTCTAAAATAAGCATTATTTCTGCCAATAATGATTTCAGGGAAGTCATGAAGCTGAAGAGTCGTTATGAGGTTGGTCTTCAGAAGCTGGAAT[C/A]GGCTGCCACACAGGTGTCCACAATGCAGGGGGAGCTGGAGGCTCTTCAGCCTCAGCTGCGAGTTGCAACTAAAGAGGTGGAAGAGATGATGGTGGTCATTCAGCATGAGTCTGAAGAGGTGTCCAAGACAGAGAAGGTGGTCCGTGTGGATGAAGCGGAGGCTAATGAGCAGGCCATGGCTGCCAAGGCCATTAAAGATGAATGTGACGCCGATCTGGCGGTTGCTGTGCCCATCCTGGAAGCTGCACTGGCTGCTTTGGACACACTCACCCAACAGGTTTTTTTCTTGCTTTATAAACCACATGAAATGGTTATAACATTAGATAACTCGCAGAATACATTTTTGAGAGATAATTTACAGTGCTTACCCCCTGACCATTGAAGATATAGATGACTTTCTTCTTTATTAAAAATAAATGAAGATTTTTAGCTGAATTTGTGGTCTTTGGTGAGTAGTATAGTTTAAATCAATGGTCAACCTTTTTTAGATAAAAAAGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8862
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Essential Splice Site | 2825 | 3984 | 45 | 65 |
ENSDART00000137131 | Essential Splice Site | 2842 | 4001 | 44 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26023005)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25178791 |
GRCz11 | 9 | 24989660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGACCCTGGAAACCAACAAGAACAAAAAGGCTGACCTTGAGAATCAGG[T/G]ATGCAGAGGAMAGCAGTCACAAAAGAGTCCACACAAGACTCTGTCATCAA
Long Flanking Sequence:
GCCTCTTCGGGGCGAGTCTTTCATAACTAGGAACTAGGAAATATGACAGTTGTTTTCATGTGAGCTGAGCAGCTGTATATAATTAAAGTAAGACATATAAAAAATTATTTGATTTTTTACAAATGAAGCATGAACATACATTGCTTTGCATCTTATAAACACAACCACCCCTTTAATTAATTGGTATTTGTCCCTTAAAGTGTGAGAAATAATGTGAACTTAATTTAGAATTCAGGACATCATCAATTAACTCTGGATCTTATGTGGCTATCCAATAAATAAATTTATGGTGCAAAAATGTATTTTTGTCTTTGACAGAGTGGCAAAGGTAGTGGCCCCCAAAAAAGAAAAGTTGGCACATGCTGAAGAGAAGCTGAAGGTGGCCATGGAGAGCCTCCGGAAGAAACAGGCTGCTTTGAAGGAGGTCCAGGACAAACTGGCAAAACTGCAGGAGACCCTGGAAACCAACAAGAACAAAAAGGCTGACCTTGAGAATCAGG[T/G]ATGCAGAGGACAGCAGTCACAAAAGAGTCCACACAAGACTCTGTCATCAAATTGTTAACTACTGTTCCTGAAAGCTTCTGTTTTACACCACATTCAACTATTTTTTGTTGACATTCTTTGTAACCTCTCCTCCAGCAGAACCCAGCCCTGTTTAAAATGTCCGCTTTTTGATGGATGTTTATTTAGGAATTTAGTTTGTGTTTTTACATCAAGAGGGGTTAAGGGGATGTTTTCCTTTTCTTCCTTGTTTACTTTCCTTCAGATCATTTTTACGTTCAAACTTTGAAGTTGCAAGAGTGAAGCCTTTGTTTTCTAAACCCACACAGAAAACACACAGGGGCACATGCATACGCACACACACCCTGTTCTCATTTGTCTGTGGAGACTGCCTGTCAGTTTAGCGTGTGTTTGGGTAAACCAAGCATCACCAAGGCCCCGCTGCCGTTTTCTGCCCTATTTCACTTCCTTTCATGTTCCCCTCTTCTTTTTTCCCCTCGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11115
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 2859 | 3984 | 46 | 65 |
ENSDART00000137131 | Nonsense | 2876 | 4001 | 45 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 26020996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25176782 |
GRCz11 | 9 | 24987651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTAGGAGGAGAGAARTCCCGCTGGAGTGAGACAGCATTTAACTTAGGT[C/T]AACTCTACAACAACCTTACTGGAGACATTCTCATCTCTGCTGCCATAGTG
Long Flanking Sequence:
CCAACTATGCATAGATCTGCTTTGATGATTTTATGTTCATTTTGTCTCCAGTAGCAGGGTGTTTGTGTCCAGTAGCAGTAGATTCTCAGACAGTATGTCTGTGCATATACTGGCAGCAGCTAGGCATGGAGCTACCACTGATAATCAAAGCAGCAGCAGCAGCATGGCAGATTTGTTCCGCCAAGATCAAATACATCAAAATTGTTTATATTTACATACATACATATATATATATTTTTTTTAACCGTACTAATATCTCCAAGGGTTGTCATGAAAGAATAGATTTATAGACAATAAATGCATTATTATTACCTTTTTAGCAATGAAAGTATGAATTACTTTAAAATCTTACTGAGACCAAACTTTTGAACTGTTAAAAATGTTTTCTTCTTTTTCTATAGGTGGAGATGTGCAGTAAAAAGCTAGAGAGAGCAGAGCAGCTGATTGGTGGGTTAGGAGGAGAGAAGTCCCGCTGGAGTGAGACAGCATTTAACTTAGGT[C/T]AACTCTACAACAACCTTACTGGAGACATTCTCATCTCTGCTGCCATAGTGGCCTACCTGGGCGCTTTTACTTCCAGCTTTAGACAGGTATGCCAACACATACAAAAATGCTCTTCACCCAACAAGCCATCAATAAACATTGTTCATGTCTTTACAGATAATGTTGTCAAAGCATGTACACATGTGCATAACCAAACTGACAATATTTGCTATGCAATGACATAAACCAATTTCACTATTAAAGGTGCAGTATGTAAGTTTGACACCCAGTGCTTGCTATTACACACCTGGTTCAAAACATGCGCAAGTGCAGGTTGCCAGATTAACGACATCAACGGAAGTGTGCCAAACTACTGAGGGCAAAGGCTGATTTAAATCATGATCTAAATAAAAACAACGGCACGCGATAGAAGGAATATTTTTCATATAAAAAATACATTTTTGTTTTAACCAACACCTGAAATTTATATTTTAGAATTTTTTTGCAGCTGAACTACAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8404
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 |
---|---|---|---|---|---|
ENSDART00000026924 | Nonsense | 3854 | 3984 | 63 | 65 |
ENSDART00000137131 | Nonsense | 3871 | 4001 | 62 | 64 |
ENSDART00000141957 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 25990724)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25146510 |
GRCz11 | 9 | 24957379 |
KASP Assay ID:
2260-1876.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTTTTTCACTCAGGCGTTTCTCACTGGAGGCCAGCAGAATTACGCC[C/T]GAAGATACACCATCCCCATTGACCTGCTCAGCTTCGACTTTGAAGTCATG
Long Flanking Sequence:
TTGAATTTGACAGCAACAATTCTGTACATATTAATAATTTCTAGTTGATCAGTTCATAGTCCAGACTTCTATTCAGTTGTTTTCCAGTGAGTCTTTGGGATACTGCGCAATCATAAATAAAGAAGATGAAACAGAAAGCATTCTAGAGTACATTGTGAGCCAGGGGAAAATCACATGAAATGCAACTGACTCTCACATTCAGCAAACTCTGATTACATCACAGCTTCTGCAAAAGACTGGTATTGTAAATATAATATACAAGTGTCTTTCCGTTGAATGAAAGAAGTGCTTAGAGCCTGTTACATTCCAAAATTATTTTTGGCCTTCAAGTTATGCCCTTAGAATGAGTTGTACATGTTTCTTGATTTTAAGCATTAAAAATAGTTTCATCTGTGTCATTGACCCAGGACTGGTACATGGACGGCATGCCTGCAGTGTTCTGGATGTCCGGTTTCTTTTTCACTCAGGCGTTTCTCACTGGAGGCCAGCAGAATTACGCC[C/T]GAAGATACACCATCCCCATTGACCTGCTCAGCTTCGACTTTGAAGTCATGGAGGACAAAGAATATAAAAACCCACCAGAGGATGGTGAGAAAGACAAAGAAATAAAGTACTGACAGGCATGAAATGTAAAATATATAAGAGGGAAATGGGTAACAAGTGACAAAAGGAAAGAGAGAGGCAGAGTTTCATTAACCCCTCGCCGTGTCTGAGTGCCATCAATCAGAGTCAACATTACAGTGCTCTGACATCAGACCCCTGCTGCTCTTTCATCAGTACATGATGAGCATCTCTCAGAGAAAAACCATCTCTCTGAGTCCCATCACACACCGCATGAGGCTGTTTATGTGTGCGCTTGACTTTAACAGAGAGTTTGTTGTGTCTACTCTATTTTTAAAGTTAAGTCAGTGTGTATAAAATGAAAGGCGATGTTTATTGTGCAAGGGTGTAAAGTGCTTCATTTTTAAAGTATTGTTTTGAGGAATTTGTACAGAGTGCTCATT
Associated Phenotype:
Not determined