ZMP
si:dkey-237h12.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
ODZ3
Human Description:
odz, odd Oz/ten-m homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:29944]
Mouse Orthologue:
Odz3
Mouse Description:
odd Oz/ten-m homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1345183]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8543 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24965 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa5872 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15467 | Nonsense | Available for shipment | Available now |
| sa22527 | Essential Splice Site | Available for shipment | Available now |
| sa22526 | Nonsense | Available for shipment | Available now |
| sa42428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22525 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8543
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125345 | Essential Splice Site | 362 | 2467 | 6 | 26 |
| ENSDART00000136233 | Essential Splice Site | 360 | 2446 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38108910)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36302003 |
| GRCz11 | 14 | 36642317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGATCCTGCATATGTAACCCTGGCTTCAGAGGTGACAACTGCGACCAAG[G/T]TAACTGGACARTTTTCAGTAGCTATGCAAAGAAACTCCAACACATGTAGC
Long Flanking Sequence:
AACACTATAATTGTAGTTACTGGGAAAAAAAATAAATTAAAACGCATATATTCAACAGCAAGACCATAACTCTTATACTGTTTTTAATTTGCATGTTAACTTTAAAATAAAACAACTGTGTCCAGAAAGGATGACTTCCATTACTAGATTATAATAATGAGAATCTAATGAGAATCATGATTGAGATTAATGAAATTGCACAACTCAAATTGTCCTGGGTATGTTTCTTGTGTGTGTGAGATTCTCTCATCCGTGATCTACTTTCATCCATCTAGCTTTAATCATTTTTTTCCTCTCACTATTAGCGGCGTGTCCAGTGCTGTGCAGCGGGAATGGTCAATACAACGGCGGTCGCTGTCAGTGTTACAGCGGTTGGAAAGGGATCGAATGTGATGTGCCCAGCGGTCAGTGTATGGATGCTCAGTGTGGGGGTCATGGCCTGTGTGTTTCAGGATCCTGCATATGTAACCCTGGCTTCAGAGGTGACAACTGCGACCAAG[G/T]TAACTGGACAATTTTCAGTAGCTATGCAAAGAAACTCCAACACATGTAGCTCATTGTGGTGAAGGAGGGCGCTTTTTCAACACCAGCGCGCAGCTAATTACATGGATGAGTGTGCTGACTTAAAGACTGGTTTTTGTTGTGATAAATTAGCCACACCATTTAGCAGCATCCACTGACTGAAATGGATTCTACATATGGGATCGAGATAAGGCAGACAGCCAAGAAAATACCCCTTGTGTGCACACAAAATATTTCCTGTCTTGTGATTCTTCTCCTCCCGCTGTCTCTGGGTAAAACCAATTGAGTCTATCGATCCACATTCAATAGGCTTGGGAATGAACTCTTTAGATGTCTATGTTCGGGTCACTTGACCAATGTTATAATTGTCATTGGACTGAATAAGTAACCTTGAGGTCGGGAAGAGAAAGAATGACCCAGTGAAAGAGAGACTTGCCGAATAGATTTTTAAAAGCATGTTTTTCTATTCTACTCGTATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24965
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 |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 459 | 2467 | 8 | 26 |
| ENSDART00000136233 | Nonsense | 457 | 2446 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38095178)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36315735 |
| GRCz11 | 14 | 36656049 |
KASP Assay ID:
554-7356.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGGAGGTGTGTGTCGGTGTGCGGACGGCTGGTCGGGGGCCGGGTGT[G/T]AACAGGAGGACTGTCAGGCTCACTGTGGGGAGCATGGTGTGTGTCGAAAG
Long Flanking Sequence:
ACCTGACCCAGCTAGGGCTCGATACAGTGACTTTCTTGCTGTGGGGCTATCGTGCTACCCACTGTGCCACCGTGCTGCCCTTGAGTCTACAGAACAAATCAACGTTATCAATAGCTTGCCTAATTACCCTATCCTGCTTAGTTAACCTAATTAACCGAGTTAAGCCTTTAAATGCCTCTTTAAGCTGTATTGAAATGTCTTGAAAAATATCTAGTAAAATATTATTTACTGTCATCATGGCAAATATAAAATAAATCAGTTATTAGAAATGAGTTAAACAGAAATTGGGGGAAAAACAAACAGGGGGGGCTAATAATTTTGATTTCATCTGTATAGATAGATAATAATATGATTGTTGAACAGACTTCATTCACTACATGCGTGTATTATTAAACTCTGTGTTGTCTGTTTCAGAAGTGTGTGCGGCGGACTGCAGTCCTCACGGCGTGTGTGTTGGAGGTGTGTGTCGGTGTGCGGACGGCTGGTCGGGGGCCGGGTGT[G/T]AACAGGAGGACTGTCAGGCTCACTGTGGGGAGCATGGTGTGTGTCGAAAGGGGAAGTGTGAGTGTCACCAAGGTTGGACGGGAGAAAACTGCAATATCGGTGAGTTCACCCTGTTGTCAACCTTGTATTTTGTTTGTTTAGCTTCAAAAAATATAACCTGTTCCAGACTCCTGCAGTCAAAACTTGAGAAAATATCACAAATAAAATGTTTTGCAGGGCTGTTACAAAGGTCAAGAAAATGCCTAGGTTTCTGTAATGGATGTACAATACTGTTCCAAAGTTTGGGGTCATTGCAATGTCATTATCTGTTTTGAAACAACTAATAATTTTTCACACAGCAAAAGCTGTAAAGATATTACAAAATAATAAATGTATTCAAGATGCATAAATATGAATAAATACATATTAAAATTATTTTGCTGAAGACTGGAAAAATTATGCTGAATTCATTTTTTTGATATCATAAATTACAATTTAAAATATAATAAAACAGAAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5872
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 887 | 2467 | 16 | 26 |
| ENSDART00000136233 | Nonsense | 876 | 2446 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38051039)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36359874 |
| GRCz11 | 14 | 36700188 |
KASP Assay ID:
554-3831.1 (used for ordering genotyping assays)
KASP Sequence:
AATGCTGTTTTTCCCCTCTTCTACTCCCTCTGGTGTACAGGGATCCTGTA[T/G]AAAGGGAACGGTGAGAATGTGTTCCTCTCTCAGCTTCCTCCCATCATMAG
Long Flanking Sequence:
GGCTAAGCAAAATTTTCTGTAGAGTATGTGTGTATATGAGAATGTATGGGTGTTTCCTAGTGATGGGTTAAAGCTGGAAGGGCATCCGTGGCGTAAAACATATGCTGGATAAGTTGGCGGTTTATTCAACTGTGGCGACCCCTGATTAATAAAGGGACTAAGCCGAAAAGAATTCCACCAAATATTGACTTTAGCTTTTCGTAATTCAAAGCATTTGTATTGTGTGGTTTAAAAAAAAATAGATAATAATAATATATATATATATATATACACACACACACACACATACACACATTGTCATAAGTAGTTTACGGAATAAAAAAATTGCACAACTGTATATTGTGATGTCAGAAATTCTTAACATTTCTTTGTCTGTCTGTGTAAAACAAAACAAGTTAACCACTCGTAAAATAGCTTTTTTTGTATCTATTTTTTTTCTACAAAATAATAAATGCTGTTTTTCCCCTCTTCTACTCCCTCTGGTGTACAGGGATCCTGTA[T/G]AAAGGGAACGGTGAGAATGTGTTCCTCTCTCAGCTTCCTCCCATCATCAGCACTGTAATGGGGAACGGCAGACGCAGAAGCATCTCCTGTCCGAGCTGTAATGGCCAGGCGGAGGGAAACAAACTGCTGGCCCCTGTTGCTCTGGCATGGGGCATTGATGGCAGTCTGTATGTTGGCGACTTTAATTACATTCGACGCATCTATCCGTCAGGCAATGTCACCAGTGTCATGGAGCTCAGGTGAGCACAGCGAAAACACAACTTCAACATCAGCATAGCATACCTTACGTGACAAATCACAGGATCCTGTCAGGCAGCATCTACAAACAATTTAATAGTATTACTATTTTTTTTCTTTCTTCGCAAAACAGTCAGTTCTCACAAAAAGCAGGCCTTCAGATTTTGCATAATAGCAGGAACAATTCTCACAGCAGGTGATTTGAAGTAATTGTTTTGAAAGTTATTGTTGAAGGCTGTGGATTTGGCAGCAGTGCTTTGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15467
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 |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 1739 | 2467 | 24 | 26 |
| ENSDART00000136233 | Nonsense | 1718 | 2446 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38034255)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36376658 |
| GRCz11 | 14 | 36716972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAAGCTCTCGGAGGTTCTGTATGACAGCACTCGTGTCAGCTTCACCTA[T/A]GATGAGACAGCAGGTGTGCTGAAGACAGTCAATCTGCAGAGCGAGGGCTT
Long Flanking Sequence:
TGCTTAAATGGCATTAAGATAAAATATTGCAGCTTTTTTGTAGTTTTCACTGGGGACTTTTTGTCCTCAAGGTCCTAGGAGGAACTATTTTTGTTCCTTTAGCCAAACTCAAAGTTGAGCTTTGTGCTTAAATAAAAAATAAAAAAGCTATAAGGATGCACAAGGTTAATGTTTGTTTTCTTTCTGTTCTAGTCCACTGTCCTGATACTGGCGAGTCAGCGGCAGTACGTCTTTGAATATGACCCTCAGGGAGGCCTTTCTGCAGTCACCATGCCCAGTGTTGCCCGCTACACCATGGAGACCATCCGCTCTGTGTCTTACTACCGCAACCTTTACCATATGCCAGAAAGCAATGCCTCTGTCGCTGTAGATTACACTGAGGACGGCCGACTCCTGAGAGTGGCACAGCTGGGCACAGGTCGGAGGGTCTTGTACCGTTACCGGTGGCACAACAAGCTCTCGGAGGTTCTGTATGACAGCACTCGTGTCAGCTTCACCTA[T/A]GATGAGACAGCAGGTGTGCTGAAGACAGTCAATCTGCAGAGCGAGGGCTTCATATGCACCATTAGATACAGGCAGCTCGGCCCACTGGTAGACCGGCAGATTTACCGCTTCAGTGAAGATGGGATGGTCAATGCTCGATTCGACTACGCTTATGACAGTAGTCTGCGTGTGACAAGTGTTCAGGGGGTCATCAATGAGACCCCACTGCCCATTGATCTCTACCAGTATGATGACATCTCAGGCAAGGTGGAGCAATTTGGCAAATTTGGCGTCATTTATTACGACATCAACCAGATCATCTCCACCTCCGTCATGACTTACACCAAACACTTTGACGGGCACAGTCGAGTCCGAGAGATTCAGTATGAACTGTTCCGTTCTTTGCTCTTCTGGATTACAGTTCAGTATGACGATATGGGCCGAGTCACCAAGCGGGAGATGAAGATCGGTCCATTCGCCAACGCCACCAAGTATAGCTATGAATATGATGTGGACGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22527
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125345 | Essential Splice Site | 2174 | 2467 | 24 | 26 |
| ENSDART00000136233 | Essential Splice Site | 2153 | 2446 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38032950)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36377963 |
| GRCz11 | 14 | 36718277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACAACCCAATAAGTAAAGTGCAGAAAGTTGGGGACTACTTAACAGG[T/C]ACTCCATGGATTCACTGCATCTTCAAATAACTACTGGAAGTAATCTATAT
Long Flanking Sequence:
AAGTCCACCGTGGGGCAACATCTGCAGTTCTTCTATGCAGACCTGAGCTATCCAAGTAGGATAACACATGTCTACAACCACTCCAGCTCACAGATCACCTCTCTATATTACGATCTGCAAGGGCACTTGTTTGCGATGGAGATCAGCAATGGAGCAGAGTTCTACATAGCTTGTGATAACACAGGAACACCACTGGCAGTGTTTGGCAGTGATGGCATTCTTCTGAAACAGGTTCATTATACGGCCTACGGCGAGGTCTACTCTGACTCTAATCCTGACATTCAGTTGGTGATTGGATTTCACGGTGGACTTTATGACCCTTTAACAAGACTGCTTCATTTTGGGGTGCGTGATTATGACATAATGGCAGGTCGCTGGACTGCACCTGATTTCATGCTGTGGGAGAATCTCAGTAAGAACCCGGGCCCTTTCAACCTTTATATGTTCCGAAACAACAACCCAATAAGTAAAGTGCAGAAAGTTGGGGACTACTTAACAGG[T/C]ACTCCATGGATTCACTGCATCTTCAAATAACTACTGGAAGTAATCTATATCTGCTGTACATTCCACAGTGCACATTATGACTGATTTATTAATATTTCTACAGATGTGAACAGCTGGCTGGTCACATTTGGGTTCCATCTACATAACAGTATTCCTGGTTTCCCAATTCCTGTTTCTGAGATGACTCAAGTATCTTACGAACTGGCCAAAAGTCAAGTGTGGGATGATCTAACAGTAAGTTTGTTTTTTAATAATTCTTCATATAATAGTTTTAGTTTTTTATTATGTAACAATCAGATTATTATTATTATTATTATTATTATTATTATTATTGTTATTATTAACTGTATAAATAATAAACACAAGTGTCTCATGAACTGTCCAAAAGTCAAGTGTGAAATGACCTGTCAGTAACTGAGCTAGCCTAATATCTTTACATAACAAGTTTAGGAATTTGTTTGGGGATTATATTACAATGTTTTATATTAGATAATATTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22526
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 2256 | 2467 | 26 | 26 |
| ENSDART00000136233 | Nonsense | 2235 | 2446 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38030940)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36379973 |
| GRCz11 | 14 | 36720287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGGTGGAGTTCGGCCACAGCCACTGTTCCTCCAAACCCTGGCTGTG[G/A]TTTGCCTTGAGCGATTCGCTGATAGGTCGTGGGATCATGCTGGCACTTTA
Long Flanking Sequence:
GCCCCAACTTCAGACACACCCTCTGTCAAGCGTTGACGCTGAAGCCCTGTGTGAATTGGGCATTAAGGGTACATTTTGAAGCCCTTTCCTTTCAAGGGCCACGGGCAAGGGGTCCAAAAATAAAATTGGGATTGGGCCTAAATCTTTCCCCGAAAAAAGGAAATTTTTGTTATTATTATTTATATAAATTATTATATTTAATTATATTATAATAAATAAATGACATATCATATACATATAAATTTTATTGTTATGTAATCTATAATTTTGCTTTAAGAAATTTCCATTTTACTTCAATCTTCCAGCATCTCTTTTGAAAAATGTGTTAAGCACATAGAACAAGAGGTGGTTTCCCTAAAATGTCAATCTCATCTTCTCTTGTAGCCCAGCTTCGCAGTCCAACAGCATGTCATCCGGCAAGCGAAAGCATTTTTACGGTTTGGTGATCTGCCTCAGGTGGAGTTCGGCCACAGCCACTGTTCCTCCAAACCCTGGCTGTG[G/A]TTTGCCTTGAGCGATTCGCTGATAGGTCGTGGGATCATGCTGGCACTTTACAAGGGCATCGTGATAACCCGTGCTCTAAGCCTGGCTAATGAGGATTGCGTCAAGGTTGCCAACATCCTCAACGGCGCCCTTTACTTGAAAGACTTGCACTTTATTGTGGACGGAAGAGACACACACTTTTTTGTTAAAATGAACTCTCCTGAAGCAGATCTAGCGGCGCTGCGGCTCACCAGTGGACGGAAAGAGCTAGAGAACGCAGTGAATGTGACCGTTTCACAGTCTACAGCTGTGCTCGGAGGCCGAACACGGCGATTTGCGGATGTGGAGTTTCAGCGTGGGTCACTAACCTTACATGTGCGTTATGGGGCATCGCTAGATGAAGAGCGGGTGCGTGTTTTAGAGCTCGCCCGGCAGAGGGCACTCGCCATTTCATGGACACGTGAACAGCAACGAGTTCGAAATGGAGAGGAGGGATCCAGACTCTGGACTGAAGGGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42428
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 |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 2262 | 2467 | 26 | 26 |
| ENSDART00000136233 | Nonsense | 2241 | 2446 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38030923)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36379990 |
| GRCz11 | 14 | 36720304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAGCCACTGTTCCTCCAAACCCTGGCTGTGGTTTGCCTTGAGCGATT[C/A]GCTGATAGGTCGTGGGATCATGCTGGCACTTTACAAGGGCATCGTGATAA
Long Flanking Sequence:
ACCCTCTGTCAAGCGTTGACGCTGAAGCCCTGTGTGAATTGGGCATTAAGGGTACATTTTGAAGCCCTTTCCTTTCAAGGGCCACGGGCAAGGGGTCCAAAAATAAAATTGGGATTGGGCCTAAATCTTTCCCCGAAAAAAGGAAATTTTTGTTATTATTATTTATATAAATTATTATATTTAATTATATTATAATAAATAAATGACATATCATATACATATAAATTTTATTGTTATGTAATCTATAATTTTGCTTTAAGAAATTTCCATTTTACTTCAATCTTCCAGCATCTCTTTTGAAAAATGTGTTAAGCACATAGAACAAGAGGTGGTTTCCCTAAAATGTCAATCTCATCTTCTCTTGTAGCCCAGCTTCGCAGTCCAACAGCATGTCATCCGGCAAGCGAAAGCATTTTTACGGTTTGGTGATCTGCCTCAGGTGGAGTTCGGCCACAGCCACTGTTCCTCCAAACCCTGGCTGTGGTTTGCCTTGAGCGATT[C/A]GCTGATAGGTCGTGGGATCATGCTGGCACTTTACAAGGGCATCGTGATAACCCGTGCTCTAAGCCTGGCTAATGAGGATTGCGTCAAGGTTGCCAACATCCTCAACGGCGCCCTTTACTTGAAAGACTTGCACTTTATTGTGGACGGAAGAGACACACACTTTTTTGTTAAAATGAACTCTCCTGAAGCAGATCTAGCGGCGCTGCGGCTCACCAGTGGACGGAAAGAGCTAGAGAACGCAGTGAATGTGACCGTTTCACAGTCTACAGCTGTGCTCGGAGGCCGAACACGGCGATTTGCGGATGTGGAGTTTCAGCGTGGGTCACTAACCTTACATGTGCGTTATGGGGCATCGCTAGATGAAGAGCGGGTGCGTGTTTTAGAGCTCGCCCGGCAGAGGGCACTCGCCATTTCATGGACACGTGAACAGCAACGAGTTCGAAATGGAGAGGAGGGATCCAGACTCTGGACTGAAGGGGAAAAAAGGCAGCTTCTTACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22525
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 |
|---|---|---|---|---|---|
| ENSDART00000125345 | Nonsense | 2431 | 2467 | 26 | 26 |
| ENSDART00000136233 | Nonsense | 2410 | 2446 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 38030417)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 36380496 |
| GRCz11 | 14 | 36720810 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCAGACTCTGGACTGAAGGGGAAAAAAGGCAGCTTCTTACCAGTGGA[C/T]GAGTTCAAGGCTATGATGGATACTACGTGCTGTCGGTAGAGCAGTATCCT
Long Flanking Sequence:
TAGGTCGTGGGATCATGCTGGCACTTTACAAGGGCATCGTGATAACCCGTGCTCTAAGCCTGGCTAATGAGGATTGCGTCAAGGTTGCCAACATCCTCAACGGCGCCCTTTACTTGAAAGACTTGCACTTTATTGTGGACGGAAGAGACACACACTTTTTTGTTAAAATGAACTCTCCTGAAGCAGATCTAGCGGCGCTGCGGCTCACCAGTGGACGGAAAGAGCTAGAGAACGCAGTGAATGTGACCGTTTCACAGTCTACAGCTGTGCTCGGAGGCCGAACACGGCGATTTGCGGATGTGGAGTTTCAGCGTGGGTCACTAACCTTACATGTGCGTTATGGGGCATCGCTAGATGAAGAGCGGGTGCGTGTTTTAGAGCTCGCCCGGCAGAGGGCACTCGCCATTTCATGGACACGTGAACAGCAACGAGTTCGAAATGGAGAGGAGGGATCCAGACTCTGGACTGAAGGGGAAAAAAGGCAGCTTCTTACCAGTGGA[C/T]GAGTTCAAGGCTATGATGGATACTACGTGCTGTCGGTAGAGCAGTATCCTGAACTAGCAGACAGCGTCAACAACATGCAGTTTCTACGACAAAACGAGATCGGCAAGAGGTAGTGAACAGACTACCATTAATCAAGGTTTTACCAAGCGGTTCATGTCCTGAGGCCGATATTTTATATGATGTACCCAAAAACAACTAAGCCTCAACCAATGAGTTGTCAGCACCATGACTAGCTCAGCCTGTCACCTTAATTCCAAAATGTGAAAATACAAAGCTTTAAAGCAAACTATCTTCACTATAATAAAGCCATAAAAGCAGATTAGTGGAAAATAATATGAAAATGAAAAACCTCAGATTAAAGGGTCGTCAATTGAAGGCGATTTTCATGTGCAGGTTGTCAGTTAAGCCGGTTCTACCAGAAAGACCAGGGAGATAAATGTGATATTGAGTTACTTTTATTTGATGAGAGTATTATCTGACAAAGTATTATTTAATAAAAC
Associated Phenotype:
Not determined