ZMP
si:ch211-12m10.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate odz, odd Oz/ten-m homolog 2 (Drosophila) (ODZ2) [Source:UniProtK
Human Orthologue:
ODZ2
Human Description:
odz, odd Oz/ten-m homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:29943]
Mouse Orthologue:
Odz2
Mouse Description:
odd Oz/ten-m homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1345184]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45742 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12677 | Nonsense | Available for shipment | Available now |
sa14272 | Nonsense | Available for shipment | Available now |
sa15048 | Nonsense | Available for shipment | Available now |
sa13815 | Nonsense | Available for shipment | Available now |
sa37350 | Nonsense | Available for shipment | Available now |
sa10500 | Nonsense | Available for shipment | Available now |
sa9107 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23981 | Nonsense | Available for shipment | Available now |
sa23982 | Nonsense | Available for shipment | Available now |
sa43678 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45742
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040740 | Essential Splice Site | 65 | 1473 | 2 | 9 |
ENSDART00000135591 | Essential Splice Site | 1107 | 2515 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30753098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31953022 |
GRCz11 | 21 | 31986280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTCATGCATGAGTATTGAGTTTTTATTCACTGTCGGCTCTTTCTTGC[A/G]GGAGTCGCACTGGATAAGAACGGCCTGATGTACTTTGTGGATGCTACAAT
Long Flanking Sequence:
AAAAGTATACGTATCACCCAATCCCACCCCTAAACTCAGCTGTCATTGGTGGAAGAGCAAATTGTACTAAATTGTAGGAATGAGATTATACGAGTTCATACAAATAAGACACTGAATTAAAACGTTACGAATTGTCGTTGGTTTTCCATCGATGGATTAATTCCTCAGATTGACAACTTCAGCACAAAGATTCTTTACACTCCTAGATTTTTCTTCCTTCTCAAAAAATAAAAATAAGCATTATTTGATGTGAGTGGGTGAACCGGCTGTCACTTCTTATTATATGAACCATATATAGCCTCTTCACTGGTTTAAAAAGAAAATTAGCATGATTATTCAACTGTTTTGATCCTCCTTTATAATTATTACATTTAAACTGTCCTTCCTCTTGCGACCAGGTGAATGTTTTCTACATTTTTGGAATACTATTTTAAAATATCTTATATAAGTTCTGTCATGCATGAGTATTGAGTTTTTATTCACTGTCGGCTCTTTCTTGC[A/G]GGAGTCGCACTGGATAAGAACGGCCTGATGTACTTTGTGGATGCTACAATGATACGCAAAGTGGATCAGAATGGCATTATCTCCACTCTGATAAAGACCAATGACCTGACTGCAGTCAGACCTCTCAGCTGTGACTCCAGCATGGACGTCAGCCAGGTTATTATTTCCTTCCTCAACTCTCTCGCACTTCTACTTAAGCTCCTGGTCCATAAAAGATGCTCCAGCCTGCTGAAATAAGAACTGATGTTGAAATCAGGGCTATTGTGCATATCTCAAATCCATTATATTCTTAGGCCATAGTATTTAGCATCCGCATCATTAGGTCAAAATTAATATGGAGCTTTATTATCCATTTGTTTTGGTTAGTAATGCAGCTAAGACAGGGAAAATATTGCATTTGCGTACAAACCCTTTAACTAACATTGTTTTGTTTTAAGTTTATTAAATTTCAATGGAAGAAATTGTGTATAAGAGCATTTTAAGTTTAAAAGAGCGGGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12677
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 179 | 1473 | 3 | 9 |
ENSDART00000135591 | Nonsense | 1221 | 2515 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30757398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31957322 |
GRCz11 | 21 | 31990580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTYCCTGGCATTGATTACTCRCTCAGCAAACTTGCAATCCATTCTGCGT[T/A]GGAGAGCGCCACAGCTATCGCCATCTCCCACACAGGTGTGCTMTACATTG
Long Flanking Sequence:
CATAGTTTACCTAACTTCCTTAAACACACCTGCCTGGAAGTTTCTAGTATACCTTGAAAGAGCTTGATTAGCCGGTTCAGGTGTGTTTACTTGGGGTTGGAACTAAACTTTGTAGGACACCGGCTCTCAAGGACTGAGTTTGGACACCCTTGGGTTACATGTTTGTGTCCGTAGGAAATCTGTGGTTTCAAGGGGTATTTTTGAGACTACACTGTAGTTTTAAAAAGAAGATGCTCAGCAATGGTCTTGATAAATGGATTTACACAAAACCAAAGCTAGACAAAGCTAAAAATATATACTTTTAATGTTTTAGGTACGTCTGGAGTGGCCCACAGACCTGGCCATCAACCCAATGGACAACTCTCTGTATGTGCTGGAGAACAACGTCATCCTGCGCATCTCCGAGAACCACCAGGTCAGCATTATTGCGGGACGGCCCATGCACTGCCAGGTTCCTGGCATTGATTACTCGCTCAGCAAACTTGCAATCCATTCTGCGT[T/A]GGAGAGCGCCACAGCTATCGCCATCTCCCACACAGGTGTGCTCTACATTGCTGAGACAGATGAGAAGCGGATCAACCGCATCCGGCAGGTTAGCACCAGTGGCGAGATCTCCCTTGTAGCTGGTGCCACTTCCGAATGCGACTGCAAGAATGATGTCAACTGCAACTGCTTTTCAGGAGATGAAGGCTATGCTGCTGACGCCTTTCTCAATTGTCCCACTTCACTGGCCGTGTCACCTGATGGCACCCTGTACATCGCTGACCTCAACAATATCCGTGTCCGTTCAGTCCGAGGAAACCGTCCCAATGCCACAGCAAGTGGACAATATGAAGTGGGTTCATCTCTGGAACAGGAACTGTATGTTTTTAGTGCTGACGGCCTTCACAGGCAAACGATTAGCCTCATTACAGGCTTGCCCCTGTATAACTTTACCTATGGGTTGGACGGGGAGTTGGCGGCTGTTACCGATGCCTCTAACAACACACTTCGGGTGCGGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14272
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 648 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 1690 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30768490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31968414 |
GRCz11 | 21 | 32001672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTACTYGTTTTGTTTACGTNNNNNNTTTCTCTTNNNNNNNNNNTCTCYCTCTGCAGTCCATGGTGT[T/A]GCTGCTYCAGCAAAGTCAAAAGCARTACGTCTTTGATTTTGATACAGCAG
Long Flanking Sequence:
CATATTTGTACAACCTGAGAAGCAATGATATTATAAAGCATCCAGTGTGCAGCTAACTTTAACAAGAGTTTAAGATTGGAGCTTATAACTTGAAATAACCTTAAATGTTTTCCTGCAGGTCCACAGCAGAAACCTTCTGTCCATTGACTATGACCGCAACACCAGAACCGAGAAGATCTACGATGACCACCGAAAGTTCACTCTGCGCATTATCTATGATGCCCAGGGCCGACCAGCCACCTGGCTGCCTAGCAGCAGCTTAGCCCTGGTCAATGTGTCTTACTCACCCACTGGTCGACTAGTGGGCTTGCAGAGGGGCAGCATGAGTGAGAAGAGCGAGTTTGACACTTTTGGACGGATCCTGTCAAGAACCTTTGTTGATGGCAAAATCTGGAGCTTCAGTTACGTGGACAAAGTGAGTTGAATTACTTTCCACCAATATTTATGAGTGTACTTGTTTTGTTTACGTTTTCTCTTTCTCTCTCTGCAGTCCATGGTGT[T/A]GCTGCTCCAGCAAAGTCAAAAGCAGTACGTCTTTGATTTTGATACAGCAGGCCGACTCACAGCGGTCACAATGCCCAGCATGGCTCGACACACAATGGCCACCCATGTGTCTGTCGGGTACATTCGCAACACCTACAACCCCCCTGAAAGCAATGCCACTGTCATCCATGATTTTAGCGTGGATGGACGTCCATGTGCAATGTTCTACCTTGGAACGGGACGACGTGTACTCTACAAGTACGGGAAGCTGGGAAAACTCTCTGAGGTGTTGTATGATGCCACTGCAGTCACCTTTGGCTATGATGAGACAACAGGAGTCCTCAAAATGGTCAACCTGCAGAGTGGAGGCTTCTCCTGCACCATTCGCTATCGCAAACTGGGTCCTCTAGTGGACAAGCAGATGTACCGCTTCTCTGAAGAAGGAATGGTCAACGCTCGCTTCGACTACACCTATCATGACAACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15048
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 890 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 1932 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969139 |
GRCz11 | 21 | 32002397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTTCGCTCATTGATGTATTGGAKGACAGTGCAGTATGACAGCATGGGA[A/T]GAGTTATCAAAYGTGAGTTAAAGATTGGTCCCTATGCCAATACYACACAG
Long Flanking Sequence:
GTGTACTCTACAAGTACGGGAAGCTGGGAAAACTCTCTGAGGTGTTGTATGATGCCACTGCAGTCACCTTTGGCTATGATGAGACAACAGGAGTCCTCAAAATGGTCAACCTGCAGAGTGGAGGCTTCTCCTGCACCATTCGCTATCGCAAACTGGGTCCTCTAGTGGACAAGCAGATGTACCGCTTCTCTGAAGAAGGAATGGTCAACGCTCGCTTCGACTACACCTATCATGACAACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAGAAACCCCACTTCCTGTGGATCTATACCGCTATGATGAGATCTCCGGCAAGGTTGAACACTTTGGCAAGTTTGGCATCATATACTATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGA[A/T]GAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13815
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 954 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 1996 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969333 |
GRCz11 | 21 | 32002591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTYCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATA[T/A]GATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTAWCAACTCGA
Long Flanking Sequence:
GAAGGAATGGTCAACGCTCGCTTCGACTACACCTATCATGACAACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAGAAACCCCACTTCCTGTGGATCTATACCGCTATGATGAGATCTCCGGCAAGGTTGAACACTTTGGCAAGTTTGGCATCATATACTATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATA[T/A]GATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37350
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 957 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 1999 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969340 |
GRCz11 | 21 | 32002598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTT[C/T]GAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGAC
Long Flanking Sequence:
TGGTCAACGCTCGCTTCGACTACACCTATCATGACAACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAGAAACCCCACTTCCTGTGGATCTATACCGCTATGATGAGATCTCCGGCAAGGTTGAACACTTTGGCAAGTTTGGCATCATATACTATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTT[C/T]GAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10500
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 968 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2010 | 2515 | 23 | 25 |
ENSDART00000040740 | Nonsense | 968 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2010 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969375 |
GRCz11 | 21 | 32002633 |
KASP Assay ID:
2261-5824.1 (used for ordering genotyping assays)
KASP Sequence:
CTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTA[T/A]CAACTCGATGARGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGA
Long Flanking Sequence:
AACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAGAAACCCCACTTCCTGTGGATCTATACCGCTATGATGAGATCTCCGGCAAGGTTGAACACTTTGGCAAGTTTGGCATCATATACTATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTA[T/A]CAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9107
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 968 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2010 | 2515 | 23 | 25 |
ENSDART00000040740 | Nonsense | 968 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2010 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969375 |
GRCz11 | 21 | 32002633 |
KASP Assay ID:
2261-5824.1 (used for ordering genotyping assays)
KASP Sequence:
CTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTA[T/A]CAACTCGATGARGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGA
Long Flanking Sequence:
AACAGCTTCAGGGTGGCTAGCATAAAGCCGGTAATAGGAGAAACCCCACTTCCTGTGGATCTATACCGCTATGATGAGATCTCCGGCAAGGTTGAACACTTTGGCAAGTTTGGCATCATATACTATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTA[T/A]CAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23981
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 1009 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2051 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969498 |
GRCz11 | 21 | 32002756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTA[C/A]GATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCA
Long Flanking Sequence:
TATGACATCAACCAAATCATCACCACAGCGGTGATGACGCTCAGTAAGCACTTTGATGCACATGGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTA[C/A]GATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCCCAGAGAGACTATGATGTCCTGGCAGGAAGATGGATTGCACCTGACCATACGCTGTGGTCGAAAATAGGCAAAGAGCCAGCTCCATTCAATCTGTATATGTTCAAGAACAACAATCCACTCAGTGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23982
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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 1030 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2072 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969561 |
GRCz11 | 21 | 32002819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTA[T/A]GCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAG
Long Flanking Sequence:
GGTCGCATCAAGGAAGTGCAATATGAGATCTTTCGCTCATTGATGTATTGGATGACAGTGCAGTATGACAGCATGGGAAGAGTTATCAAACGTGAGTTAAAGATTGGTCCCTATGCCAATACTACACAGTACCGCTATGAATATGATGGTGATGGACAACTTGTGGGGGTCAAAGTTGATGACTGGTCTACATGGCGCTACAGTTATGACCTGAACGGCAATCTCCATTTGCTCAACCCGGGTAACAGTGCCCGTTTGCTGCCACTACGATATGATCTTCGAGACCGAATTACGAGGTTGGGTGACATGCAGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTA[T/A]GCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCCCAGAGAGACTATGATGTCCTGGCAGGAAGATGGATTGCACCTGACCATACGCTGTGGTCGAAAATAGGCAAAGAGCCAGCTCCATTCAATCTGTATATGTTCAAGAACAACAATCCACTCAGTGATATGATTGACGTAAAAAACTATGTGACAGGTGAGAGGGTGATAAAACCTATGAGCTTCAGCTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43678
Status:
Mutation detected in F1 DNA
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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 |
---|---|---|---|---|---|
ENSDART00000040740 | Nonsense | 1134 | 1473 | 7 | 9 |
ENSDART00000135591 | Nonsense | 2176 | 2515 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 30769947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31969871 |
GRCz11 | 21 | 32003129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCC[C/T]AGAGAGACTATGATGTCCTGGCAGGAAGATGGATTGCACCTGACCATACG
Long Flanking Sequence:
AGTATCAACTCGATGAGGACGGTGTGCTCATGCAGAGGGGCTCGGATGTATTTGAGTACAACTCTAAGGGTCTTCTTGAGCGAGCCTACAGCCGCACAGCAGGAGGTTGGAGTGTCCGTTACCGTTACGATGGCCTTGGTCGCAGAGTCTCCCGCAGAACAAGTGAAGGCGAGCATCAGCAGTACTTCTATGCAGACTTGAACTATCCCACTCGGGTCACCCATGTGTACAACCACACGAGAGCTGAAATCACCTCCTTCTATTATGACCTACAGGGTCATCTGTTCGCTATGGAGGTCAGCGGTGGAGAGGAATATTACATCGCCTCTGACAATGTAGGCACTCCACTTGCCATCTTCAGCAGTAACGGGCAGATGGTCAAGCAGATGCAGTACACAGCGTACGGAGAGATCTACCATGATTCTAACCCGGATTTCCAGCTCATATTGGGCTTCCATGGAGGGCTTTATGATTCTCTCACAAAGCTGGTGCATTTTGCC[C/T]AGAGAGACTATGATGTCCTGGCAGGAAGATGGATTGCACCTGACCATACGCTGTGGTCGAAAATAGGCAAAGAGCCAGCTCCATTCAATCTGTATATGTTCAAGAACAACAATCCACTCAGTGATATGATTGACGTAAAAAACTATGTGACAGGTGAGAGGGTGATAAAACCTATGAGCTTCAGCTTTTGTGTAAATGATGCACAGTGCTTCCTATGACAACTTGTAAAAGGAAGTTTTTTTCTTTTTTTTTTTCTTGCAGATGTGAAGAGTTGGCTGGTTATGTTCGGCTTTCAACTCAGCAATATCATACCAGGGTTTCCAAGGCATTCACTTTATTTTGTCAACCCTCCTTATGAGATATTTGCCAGTCAGGACTCTGATAATGCTCAGGTGAGTTTGATTTGGTGCCTCTTTAACAACAAAAATCACATGTCAACACTGACACAGTGCTCCCCACTAAATAAGTAAAAACCTAAAAATGGAACAATAAAAACGTGT
Associated Phenotype:
Not determined