ZMP
inadl
Ensembl ID:
ZFIN ID:
Description:
InaD-like [Source:RefSeq peptide;Acc:NP_001120657]
Human Orthologue:
INADL
Human Description:
InaD-like (Drosophila) [Source:HGNC Symbol;Acc:28881]
Mouse Orthologue:
Inadl
Mouse Description:
InaD-like (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1277960]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24137 | Nonsense | Available for shipment | Available now |
sa6702 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37482 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa648 | Nonsense | F2 line generated | Not yet available |
sa24136 | Nonsense | Available for shipment | Available now |
sa32397 | Essential Splice Site, Missense | Available for shipment | Available now |
sa5970 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43805 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24135 | Essential Splice Site | Available for shipment | Available now |
sa43804 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24137
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 111 | 1180 | 3 | 41 |
ENSDART00000132829 | Nonsense | 115 | 1831 | 4 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16971854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16723612 |
GRCz11 | 22 | 16749882 |
KASP Assay ID:
2261-6669.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATG
Long Flanking Sequence:
AAAAGCACAATTAGGCCATTATTAATAAAATTAGTTGTAGTATTAATTGAAGTAGTGTTGTAATTTTGTCTTTTTGTTTTATATATTTAAAACCAATTTGTGATTTGTGTTGGTTTGGGTTTTTTTTATTTTTTTTTTAGTTGAAGCTGTTTGTTTTGTAGCTTGTCTTTTTTATTATTTATTTAACCATTTTTATTATTTTCCATTATTATTATTTGTTCTTTTTAATGTTAGAATTTATTTAAATCCATATTTATTGCAAGTAATATAAAGAGCTCCAGGTTTAAGTTTTGCTTGTAGTCATCGATGGATTTTTCTACATGTCTTTTAAAAATGTCTTTGTCTTCTTCTATCTGCAGTTGAACAGTTTGCCTCCGGACACATGCAGCGAGTTCAGTTTCTCCAGGAAGGGTCAGCTGATCGTCAGTGCCAGTCGGCCGTCCAGTAGTCTGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATGTCAGCTTTTATTTCACAAATGCAGTTTCTACCATGCTTTGGCCTAGTTTGCATTAGTTAAGTCATTCTACAGGAATTACTTCCTTCGATAAAATACCTAAAAAATGTCTTTGCAAAAACCTTAAAGTCTTTGCAGCCATTAACCACTTTTAGCTACCTTTAGTCACACTTAACTGCACCACTCTTATTGCTGGTCTTGACTTGTGGTGCTCTTCAAGTTATGCTTGCGTCTCCATATTATACCGGCAATGTCCTTTCCTTCTGATATTGTTGAACCATGTATAATTTCCCTTCGTTGCCTTGGACAACAGAACACTTGACTGAGTTCATTGGTTAAATTGTCCTGGTTCTTCTTTCATACTTGTATTGAGCCTTGTTCTTACTGTAGCTCCCTTCAGCAACAAACGAGCAAGAGTCTTTTTTTTTTTTTTTACTGACTGGTTTATTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6702
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 248 | 1180 | 9 | 41 |
ENSDART00000132829 | Nonsense | 234 | 1831 | 7 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16959657)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16711415 |
GRCz11 | 22 | 16737685 |
KASP Assay ID:
554-4601.1 (used for ordering genotyping assays)
KASP Sequence:
GACAAGTCAAGGGATTGAAARCGGTCCCCSGTGTGTGTCTTTTGCAGGAT[C/T]AGTGGGGACACGTGGAGGAGATCGAGCTGGTGAATGATGGATCCGGTCTG
Long Flanking Sequence:
CGGGATGAGCACTAGTGTAAAGCTTTGTTTCGAAAGAGCGACAAGGCGAACGACAGAGGAGGGGTTTCATTAGATAGTGAGAAAATTGCAGAGGTAGTCACCCGGCAGATAACGGCCAGGTAATAAGAGAACAGAAATGTACTGATTGTGGGTCATTTATATGAGCCCAAGGAGACTTGGGCGATTAGAAAGTGTGGCTGACGTGAGATCACAAAGACTCTCGTGGGCTTTCCTGACCCGGACATTGATCAGCCGCTGCAGGATCACACCGTTAACTTGTTCATTAGCATTCCCTGGCCTATTACCACTCCGTAGTCACAGGTCTTGGGTCGTCAATCGCTCCCTATTTGGACAATCAAAGGTGATTGAATGGATCTTTATTCTTTAAGTAGACAGTTTTGTGGCTCAAAGTAAAATATAGCTGACACTCGCTGACCTCTAAATGTACAAGACAAGTCAAGGGATTGAAAGCGGTCCCCGGTGTGTGTCTTTTGCAGGAT[C/T]AGTGGGGACACGTGGAGGAGATCGAGCTGGTGAATGATGGATCCGGTCTGGGATTTGGGATTGTCGGTGGAAAGACGACAGGGATGGTGGTCAGAACCGTGGTGCCAGGCAGCGTTGCAGATAAGGTTTGTGTTTGCATAATTTTACTGAACTATTAATGATGTTAATTTTAGAACCAAATTTCAGATGTTGAAAAAATACTTTTGAAGGTGTTCTCCCTAGGAAATTTTGCATTTCTTGCAATAATATTGAATTCCTTTGCAAAATATTCACAAATGTGTGTGCATTTTGCCATTTTAAAGCCGGTTTTGTAATTACTAGTAAATTTCCATACTTGTGAATGGGGTAGCGTTTACTACGTTGTACACTGATAAGCTATGCAAAATTGCATGTATAATCAAGCTATTGTGAGACCAAAGATAAGCATTCTGTGATTTAATGACAGCTGTGAAAGCAGTTAAATCTTCTCTTTATTAAGCGACTGCTATATGGATTTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37482
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 516 | 1180 | 17 | 41 |
ENSDART00000132829 | None | None | 1831 | None | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16945552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16697310 |
GRCz11 | 22 | 16723580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGTGGTTTTGCTAAATTTCACCCGTCAATTTTATAGATAACAACCCT[G/T]GAAGTGCCATTAAAATTTATTTTGTGTCACGTAAAAGTTGACAAGCCCTG
Long Flanking Sequence:
GCTTAGCAGGCTTTGTTTCAGTCATGTTAGCCGGCAGATATAAATATGCAGATAGGCGAACTGGAAGCGGAAGAGCAGGCCTTGGCTGAAGCCGAAGCAGCCCGGAGCTCTGGTTACATTCTGCCCTAATTAATCCGGACAAGACCCGGTACCTGCCAAACTCCGAAATAAAGCGTTCTGTTGCGCTGGGCCAATACATGCCCGGGATAACAATGATTGGTTGTCAGGGACTCATTTCCCAAAGCTGGAATAGCAGCACGTGTAAAATGATAGCCGCCCTCAAGTCAAAACACACAGCGCTTTAATCATGCTTTCACCTCCCGACTCCTTTTTCCCTGCGGTCTTAAGAAATTACATTGCCATGTGAGCGTGTAGATGTTGAAATCTTTTTCTTCATGGATAATGCTCGGCTGTTTTGGTACATTGACGTGACATTCGATAAGCGCAAACTTGAGTGGTTTTGCTAAATTTCACCCGTCAATTTTATAGATAACAACCCT[G/T]GAAGTGCCATTAAAATTTATTTTGTGTCACGTAAAAGTTGACAAGCCCTGAAAACAGATGTGTTTCAGCCCATTATTATAAGAACGTGGATCAAAGTTGCATTTTTTCTTTCCCCAAGTTCTGTCATTGGACAGTAAATAAGTCAAGTTTGGTGAAAGAAAATCATGGTTAGGGGTTACAATTAGTAGCTCATTGGAAACATACACAATAGTGATTAATTTTCCACTGCACTATGCCTTTATATTCTATACTGTAGACCATTTTTGTTAAGAGACAAGACTTTTGTCTAAGCAAAGTCAGACATTACTGTCCTAATAAAATAATTAAAAATCAGGGCATCATCATATTTATTTATTTTTTGTAAATAAGCATAATCTAGAGGCTTTTTATCTTTTATAAGCCACATCTGTTTTCAAATGATCAACCAGAAGTCAAGTTTTTATTTTTTGTTCCTAAAACTTGGATAGGTGACAAGACTTTTGTCATGATTTCTTTTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa648
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 543 | 1180 | 18 | 41 |
ENSDART00000132829 | Nonsense | 526 | 1831 | 13 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16942443)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16694201 |
GRCz11 | 22 | 16720471 |
KASP Assay ID:
554-0556.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAAGAGCCGGCCTCGCTGACGGAGATGGAGCTTCGCGCTAAATGGGAG[C/T]AGGCTCTTGGTCCACATTACGATGTTATGGTAAGCAAAAACGAAGAGGAA
Long Flanking Sequence:
CTCACTGTCTCACCAAAAACCCCACCATATTCTGTTAAGTTATAGCTTAGGTTACAGAAAAAAACTTCTTTTACTATCCAGATCCCATTTTGTCTAAAACCCCCTCTATACTCACTCCATATCATAGTTAAGGGTCAAAAGTGCCCATAAAAGCTGTTCCACCCATTTATTTGCCTCCATTGCCCTTTGGGCTTCCAGCCGATACTGTTCCCAGGCGTCCCGTTGTCGTTTTCTGCAGGATCACTACTGACTCCTCTCTCAACTCTTGCCCTCAGCTCACTCTCAGCCCTCTGATTATATTCATCCGTCAGCTTGACATCAATCCCATGCTAGTATGCGGCACCTGACATTAATGTCATACGTTTCCACTCACTCTGTCATGGACAGTGGGCACCCAAATGGCGGTAATTGACTTTAAACGCTGCTCTCATTATTGTGTGTGTGTTGTAGTGCAAGAGCCGGCCTCGCTGACGGAGATGGAGCTTCGCGCTAAATGGGAG[C/T]AGGCTCTTGGTCCACATTACGATGTTATGGTAAGCAAAAACGAAGAGGAAGTAATGTTAACAGATGCTAAGTGCGGCTCTCAATTAAACATGAAGCAAACTGCACATCAGCAAGAACAGCCAGCACTTACGCATACTGTGATAAGAGATGTTCGATCGACCAGCTAAATCTGGCTGTAGATTGCCTCAGTTGACTCCTGTTGAATTTGGGTTCATGTGCTGACACTTTGTTGTTTGGGTTTATTTACCATAATAGGAGTGTAATGACCCCGTTCAGGTCACAACTGTGATTGAGATAAATATAAATAAATTATATAGTAAATAAAACAATTAAGATACTTTTTTTTTTTGTTTTTTTTGTTTTGTAGATTGTACAGCTTGACCCGGTCATAGAAGATGATATTGAGCTGCAGAAGTACTCCAAGGTAACATGGAAACAGCTGTCACAATTCATGATTCATTCATTCGTTCATTCATCTCCGTAGTAGGGCTGGGTAATCC
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:
sa24136
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 648 | 1180 | 21 | 41 |
ENSDART00000132829 | Nonsense | 631 | 1831 | 16 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16940425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16692183 |
GRCz11 | 22 | 16718453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCAC
Long Flanking Sequence:
CTTTCAATATAACCAATATTCTTATGTACTCCTTTTGGCCTCATTTGATGCTTAAAAGCCTAATGATGCATGATGATGATGATGATGATGATGATGATGTGTGTGTGTGTGTATGGGAAAGGGTTATGTGATGACCATGGCTTCCCCTTGATTTGGGCAGATGGCACAGTGCCGCCCCCACTCACCATAGCAGCTCCAGGCTTGACCGCTCCTGGAAATGCCAATCAAAAATGGTCATTAGATGCCACAGAGACTATGGAATATAGTTACTTGCCTAATAAGCACTAAATGCGCATGTCCAAAATGTGCAAAAAAATAGGTGGATGGAAATGTAGCTATTGAGAAAATCCATATTCTGAGTTTTTGCATAATTTTCTATCAAACAATTCTGAATTTTAATTTTGCAGGTGAATGGTGTGCAGCTGTATGGGAAGTCTAGACGAGAGTCTGTAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCACTCATCCAGCTTACAGGAGCAGGTAACCGAGGAGTAATGAGTAAAAGCTGGCTTCGGCAAGTATTGGCTGATACTTTAAAGAGTACTACAAAACAATACATTCTCATTTAGTAATTATTCCACAGATTGAGCATAACCTCTCCATGTTGGCCAGAGATACAAGTCTACGCGACAGCATTAGGGAAGAGTTTCAGGTTTGTTCATGTTTTCTAATATAAAATTACTATTATATTGACAGTTATAGTGTTTATGATGGTGTTGCTTCAGGTTTTAAGTCAAACATATTTTTATTTTTTACTTCAATATGTTCAATTAAATGAAATGTAACATGACATAGATTTGTCCTATATGTGTGTTCACTGTTGGTTAACAAGAAAGTCGTCACTTCCTGATTAACTGGTGGCAAATTTTGAGATATTAAGCTTCAAAGTTTTTGCATTTCATAGCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32397
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036467 | Essential Splice Site | 650 | 1180 | 22 | 41 |
ENSDART00000132829 | Missense | 684 | 1831 | 18 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16939032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16690790 |
GRCz11 | 22 | 16717060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCT
Long Flanking Sequence:
TCAATATTTTTTTATGTGCTTACCAAAAATGTGCATAAAAATAGGTTGATAGAAACGTAGCTAGTGAAATCAAAGTAATGTCTGTATTTCCACTTAAAGAAGCGACCACTTTCGACAGCAGCTATTTCAGCTCATGCTTATTAACTGACGTTTCAGTGGAAGACGTGATTTAAAAGAAGTATTTTTTTCCTTCTAAAAACTATCATTGTAATGTACAGTAAGTAACGCAATTACTTGACGCAATTAACTTGACTTAAGTGACTGTAATCGAATTACACAAATTTAAAATGTAATTCGTTACATTACTGCATTCCTCAGAAATGTAATTAGAATACAGTAATGGGTTACTGTGAAACGCCTTACTCCCAACTGTGTCTGATTGATTGATTAAGTGACCCCATCATAATAGACCCATTTTTGGGCCACAACCCACCAATTTAGAGCCACTCCTTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCTGAGAAAGAGCAGATGGACCAGGAGAATGATGATGACGACGAAGAGGAAGAGGAGGAGGATGAAGGAGAACTAGCTCTATGGTCTCCAAATGTGCAAGTGTTAGAACTAGAGAAAGCAGAGCGAGGTCTTGGCTTCAGTATACTAGACTATCAGGTAGGCAGTAATTTTTTTGCACTTTATATGCATCATTAAATTACTAAATGTATGCAGTAAAGCAATTTAGAAAAAGTCTTTAAGGAATACAGCTTTATTGCAAAAAAAAAAACTATAAATAGACAAAATAACAAACTTCAGAGCATAAACATAAGATTTGTTCTAAACGTCATCATTAAACTACGTTTACTGTAAAAAGTCAAGACAAGGAATCTGTTCACACATAATCTAGCTGAGGGGAAGGGGACCAGACTCAGTTAATCCCCATTGACTTTCCCAAAGTGCGATCACAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5970
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 698 | 1180 | 22 | 41 |
ENSDART00000132829 | Nonsense | 732 | 1831 | 18 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16938888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16690646 |
GRCz11 | 22 | 16716916 |
KASP Assay ID:
554-3668.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAAGAGGANNNNNNGGAGGATGAAGGAGAACTAGCWCTATGGTCTCCAAATGTG[C/T]AAGTGTTAGAACTAGAGAAAKCAGAGCGAGGTCTTGGCTTCAGTATACTA
Long Flanking Sequence:
CTGACGTTTCAGTGGAAGACGTGATTTAAAAGAAGTATTTTTTTCCTTCTAAAAACTATCATTGTAATGTACAGTAAGTAACGCAATTACTTGACGCAATTAACTTGACTTAAGTGACTGTAATCGAATTACACAAATTTAAAATGTAATTCGTTACATTACTGCATTCCTCAGAAATGTAATTAGAATACAGTAATGGGTTACTGTGAAACGCCTTACTCCCAACTGTGTCTGATTGATTGATTAAGTGACCCCATCATAATAGACCCATTTTTGGGCCACAACCCACCAATTTAGAGCCACTCCTTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCAGTAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCTGAGAAAGAGCAGATGGACCAGGAGAATGATGATGACGACGAAGAGGAAGAGGAGGAGGATGAAGGAGAACTAGCTCTATGGTCTCCAAATGTG[C/T]AAGTGTTAGAACTAGAGAAAGCAGAGCGAGGTCTTGGCTTCAGTATACTAGACTATCAGGTAGGCAGTAATTTTTTTGCACTTTATATGCATCATTAAATTACTAAATGTATGCAGTAAAGCAATTTAGAAAAAGTCTTTAAGGAATACAGCTTTATTGCAAAAAAAAAAACTATAAATAGACAAAATAACAAACTTCAGAGCATAAACATAAGATTTGTTCTAAACGTCATCATTAAACTACGTTTACTGTAAAAAGTCAAGACAAGGAATCTGTTCACACATAATCTAGCTGAGGGGAAGGGGACCAGACTCAGTTAATCCCCATTGACTTTCCCAAAGTGCGATCACAGGAAATGCGCATTGATGTCCCAAGTTGTTGAACATCGAACAAAAGAATGCAATGAAACCTTTCCGACTAGGGCCGCCGCTGTTTATCTGGCTCGGTGCCAACCGTCAAACCCTTTGCTCTGCTCACTTAGTACAAAAAGCTGCTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43805
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Nonsense | 934 | 1180 | 32 | 41 |
ENSDART00000132829 | Nonsense | 930 | 1831 | 21 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16923962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16675720 |
GRCz11 | 22 | 16701990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATA[T/A]CTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTA
Long Flanking Sequence:
GACAATTTTAACATTTGTTCAAGGACAAAAGATGAAAAAATTCTAGTGCATTTGCAGTAATACTACTCAATGGACACTGTCAAATTTTGCAGCTACAGGGATAGTTTACCCAAAAATGCAGATTCTGCCCTCAATTACTCACCTTTGTGCCATTGCTTCTTCTGAAAAACACAACCTTAAATGTTTAGCTGAAAGCTCCTTTCCATATAATAATGGTAGAATTAATCTATGCTAAAATGCTAATCATACAAAGTGAAGCTAAGTCACTTTCTTTGTTTATAGGACTTTGTAAACGGCTCCATTTTATCTGACGACCTGGATGAGGAGCCAGAGCTGATCCTGGACGCAGAGCCGCGCTACGCCTCTCCCCTCACCACTGTTGACCTCCAGCCTGACGTAGAGAAAGAGATGGCTGTGGATGAGGAGGAGGAAGATGTAGACGTGAATGTCATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATA[T/A]CTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTACCATCTCAACACAGAGCCTGATTTACAAGAACAGGTGAAACTCCAATGATTTGACGGCTTTCCTAAAGTAATGTATACAGTTTTACAACTGTTGTGTTTCTGCTGTGGTTTGCAAAGGTGGACGACGATCTTTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCGGTAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTGAGTTTGTCAATTAAGAAGACTACACTTCCCCGCCATTGGGTTTTTACAGCAACACAAATTTCTGGTGTGTTATGGTAAGGAAAAACCCTAATGCATGGCAAGAACAGAACGCTAATCCATTGGTTCATATGAGCTGTCAATCACTCTGTTCCGATGACAGGGTGCCACAGCCGCAAAAATATAAAGGTCTGGATCTGAGAGAATAACAATAACACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24135
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 |
---|---|---|---|---|---|
ENSDART00000036467 | Essential Splice Site | 977 | 1180 | 33 | 41 |
ENSDART00000132829 | Essential Splice Site | 979 | 1831 | 22 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16923730)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16675488 |
GRCz11 | 22 | 16701758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTG
Long Flanking Sequence:
TAAAATGCTAATCATACAAAGTGAAGCTAAGTCACTTTCTTTGTTTATAGGACTTTGTAAACGGCTCCATTTTATCTGACGACCTGGATGAGGAGCCAGAGCTGATCCTGGACGCAGAGCCGCGCTACGCCTCTCCCCTCACCACTGTTGACCTCCAGCCTGACGTAGAGAAAGAGATGGCTGTGGATGAGGAGGAGGAAGATGTAGACGTGAATGTCATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATATCTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTACCATCTCAACACAGAGCCTGATTTACAAGAACAGGTGAAACTCCAATGATTTGACGGCTTTCCTAAAGTAATGTATACAGTTTTACAACTGTTGTGTTTCTGCTGTGGTTTGCAAAGGTGGACGACGATCTTTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTGAGTTTGTCAATTAAGAAGACTACACTTCCCCGCCATTGGGTTTTTACAGCAACACAAATTTCTGGTGTGTTATGGTAAGGAAAAACCCTAATGCATGGCAAGAACAGAACGCTAATCCATTGGTTCATATGAGCTGTCAATCACTCTGTTCCGATGACAGGGTGCCACAGCCGCAAAAATATAAAGGTCTGGATCTGAGAGAATAACAATAACACTGACAGATTTAGTTTAAGAAACCAGCTAGAGTTACAATTATGACACATCTGATTAGTGATCATGTGCTGAATGTCAGTCCAGCATTTACACTTTTCGAAGAGTGGATAAAAGACTTCCCGCGTTTAAAGTCCGCTATGAATAAAGCATTCACTGTAAAGCCAGTAGGGCGGAGTTTTCAGGTAAGTGTTTGCCTCATCTACACATTTTAAGCACAGGATGTTCTAACGTTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43804
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 |
---|---|---|---|---|---|
ENSDART00000036467 | None | None | 1180 | None | 41 |
ENSDART00000132829 | Essential Splice Site | 1209 | 1831 | 29 | 45 |
ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16906054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16657812 |
GRCz11 | 22 | 16684082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCAGGAGGAGGAGCATGAGCAGGAGGAGGAGGATGAGCAGGATACAG[G/A]TGAGAGACTGCTGGTCATTACACACTTGCTGTGTTTGGAGTCAAACTGAC
Long Flanking Sequence:
CACTTTGGAGGGCATCTGCTGCGTAAAACATATGCTGGACAAGTTGGCGGTTCATTCCGCTGTTGTGATTCCAGATTATTAAAGGGACTTAGCCGAAAAGAAAATGAATGAATGATCGCATATATAACTTTGTTTTTGTTCCAGTCACATACATTTAATGTTTAAATATCTATTACATATATGGTACTGCTTATATTATTTCACCATCTGTACACCAAAATAAGTAGTGAATGTGCGTGTCCGTGCATGGGGCTGTGTTGGTGTAGTAATGTGGGCTGGTGTGGCTACAGTGCCAGGGCTGATTTTTAGTCCCAGTCCGCCCCTGTTTGCATGTGTCCTGTGGCATTGTTCTCACTCTCGGTTTCTTTGGTTTTGTGCAAAGCAGAAAGCAGGACAGGGTGCTGCTCCTCCACCCATGCGTCTCCCCCCACCCTACAGACCCCCTAGTCAAGTTCAGGAGGAGGAGCATGAGCAGGAGGAGGAGGATGAGCAGGATACAG[G/A]TGAGAGACTGCTGGTCATTACACACTTGCTGTGTTTGGAGTCAAACTGACATTCTGTTGAGCATATTATGATTTTTTATATGCCTGAATAATTTACATGTGTTTGAGTGTATATGTTTGTTTGTGTTTACACATTTGTTGTGTTGTGTTGGTATTGGTGGTTTACAAGGACTCTCCATAGCCGTTAAATATTTTTATACTGTAAAAATCGTTTTATTCAACCGCTATCTCTAAAACCCAACCACCTCAAAGGAAACCTGTGGCAAATTTTGAATGTGAAAAGAGCCTCTTAAGTATAATTTTTAAGCATTTAGATTTACAAAACACAAGGTTTGTCCTCATAAACCACCTCAATTTTGTAATACCTAGAGCATACCCATGTGATTATACAAATTTCTGTTTTAAACAGTACACACACACACACTCTACCATTGTTCTAAAGTTTTTAGAATTTTTGAAAAATTTTATTTAATTTTTTTGTTTAAAGAGTACTTTTCTGCT
Associated Phenotype:
Not determined