ZMP
si:dkey-27i16.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
PCDH20
Human Description:
protocadherin 20 [Source:HGNC Symbol;Acc:14257]
Mouse Orthologue:
Pcdh20
Mouse Description:
protocadherin 20 Gene [Source:MGI Symbol;Acc:MGI:2443376]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11477 | Nonsense | Available for shipment | Available now |
sa22452 | Nonsense | Available for shipment | Available now |
sa24956 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13628 | Nonsense | Available for shipment | Available now |
sa31977 | Nonsense | Available for shipment | Available now |
sa35668 | Nonsense | Available for shipment | Available now |
sa13218 | Nonsense | Available for shipment | Available now |
sa42371 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35669 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11477
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 77 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18470209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14264662 |
GRCz11 | 14 | 14570225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAACAGGGGATCTGTTCACTAAAGAWCGCCYTGATAGAGAAACTTTGTG[T/A]CCATCACATCAGGATGGAGAATGTACTTTTTTAAATACTGCAGTCGTGAG
Long Flanking Sequence:
CATTTGGGAAGTATTTAAAAAAAGAAAAAAAAAATTGTTCAGTTAAATTTTGTCCCCTGTTCATAGAAAACATGCAGACATTTGCAAGCTTGGTTTAGATTATTCTAAAGTTACATTTCTGAGTGCTGGAACATGTAAGACTACATTTCAGCATGAGTAACAACACATGGGAGAAAAAAAAAACTCTGACTTGGTGGTTAAGGATTACACGCTTAACTCCTGAGTCTGGTTAAACTTTCATTTGGAAAGAAGGATGTCTGCCAGTAGTAAGTCTCTTCTCTTGTTTTGTAGTGGGTGCTTCTCTTGGCATGTGCTGGGCAAATCCATAGCCTTGCACTGCGTTTCAGCGTCCTGGAGGAGCAAGAAGCAGGCCTTAAAATTGGAACACTAAGTACAAACTACTCAGCTCCATACCGGCTTCTCAATGAAAGATACATCAGGGTGGATGAGATAACAGGGGATCTGTTCACTAAAGATCGCCTTGATAGAGAAACTTTGTG[T/A]CCATCACATCAGGATGGAGAATGTACTTTTTTAAATACTGCAGTCGTGAGCCCTCATTTGGACGTAGTTCCAATGGTAATTGTTGTGAATGATATTAATGACAATGCTCCTGTTTTCGAAAGGAATGAAATTCCTCTACGCATACCTGAAGATACGTCCATTGGGACTACTTTCCTGCTGGATGACCAAGCCCAGGATAAGGACACTGCAAATAATGGCTTGATACATTATCATTTAGAGGGATCTAATGGATTTTTTGGCATCAGACAAGAGGATTATGGACTCGAGCTCATAGTACAAAAGGAACTAGACCGAGAAACTCAGGATAACTACTTCTTAGTTCTTGTAGCAGTAGACAGAGGTTCAATGCCACTCAGCGCTACTGCTAATCTCAGTGTAACTGTAACCGATGTTGATGACAACTGCCCAGAATTTGATGATGATAGCCCCATCAAAGCCATTGTGCCAGGATTAGGAATCAAGGGCACTGCGGTGGCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22452
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 117 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18470327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14264780 |
GRCz11 | 14 | 14570343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAATGGTAATTGTTGTGAATGATATTAATGACAATGCTCCTGTTTTC[G/T]AAAGGAATGAAATTCCTCTACGCATACCTGAAGATACGTCCATTGGGACT
Long Flanking Sequence:
CTGAGTGCTGGAACATGTAAGACTACATTTCAGCATGAGTAACAACACATGGGAGAAAAAAAAAACTCTGACTTGGTGGTTAAGGATTACACGCTTAACTCCTGAGTCTGGTTAAACTTTCATTTGGAAAGAAGGATGTCTGCCAGTAGTAAGTCTCTTCTCTTGTTTTGTAGTGGGTGCTTCTCTTGGCATGTGCTGGGCAAATCCATAGCCTTGCACTGCGTTTCAGCGTCCTGGAGGAGCAAGAAGCAGGCCTTAAAATTGGAACACTAAGTACAAACTACTCAGCTCCATACCGGCTTCTCAATGAAAGATACATCAGGGTGGATGAGATAACAGGGGATCTGTTCACTAAAGATCGCCTTGATAGAGAAACTTTGTGTCCATCACATCAGGATGGAGAATGTACTTTTTTAAATACTGCAGTCGTGAGCCCTCATTTGGACGTAGTTCCAATGGTAATTGTTGTGAATGATATTAATGACAATGCTCCTGTTTTC[G/T]AAAGGAATGAAATTCCTCTACGCATACCTGAAGATACGTCCATTGGGACTACTTTCCTGCTGGATGACCAAGCCCAGGATAAGGACACTGCAAATAATGGCTTGATACATTATCATTTAGAGGGATCTAATGGATTTTTTGGCATCAGACAAGAGGATTATGGACTCGAGCTCATAGTACAAAAGGAACTAGACCGAGAAACTCAGGATAACTACTTCTTAGTTCTTGTAGCAGTAGACAGAGGTTCAATGCCACTCAGCGCTACTGCTAATCTCAGTGTAACTGTAACCGATGTTGATGACAACTGCCCAGAATTTGATGATGATAGCCCCATCAAAGCCATTGTGCCAGGATTAGGAATCAAGGGCACTGCGGTGGCTCAGCTTAAAGCAACAGACAAAGACCTGGGCCAAAATGCCCAGATCACATTTTCCTTCAGCCGTCAGATCTCAGACAGAGCCAAAACACTCTTTTACATGGACAGACACACAGGCCTGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24956
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 154 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18470440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14264893 |
GRCz11 | 14 | 14570456 |
KASP Assay ID:
554-7496.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGACCAAGCCCAGGATAAGGACACTGCAAATAATGGCTTGATACATTA[T/A]CATTTAGAGGGATCTAATGGATTTTTTGGCATCAGACAAGAGGATTATGG
Long Flanking Sequence:
AAACTTTCATTTGGAAAGAAGGATGTCTGCCAGTAGTAAGTCTCTTCTCTTGTTTTGTAGTGGGTGCTTCTCTTGGCATGTGCTGGGCAAATCCATAGCCTTGCACTGCGTTTCAGCGTCCTGGAGGAGCAAGAAGCAGGCCTTAAAATTGGAACACTAAGTACAAACTACTCAGCTCCATACCGGCTTCTCAATGAAAGATACATCAGGGTGGATGAGATAACAGGGGATCTGTTCACTAAAGATCGCCTTGATAGAGAAACTTTGTGTCCATCACATCAGGATGGAGAATGTACTTTTTTAAATACTGCAGTCGTGAGCCCTCATTTGGACGTAGTTCCAATGGTAATTGTTGTGAATGATATTAATGACAATGCTCCTGTTTTCGAAAGGAATGAAATTCCTCTACGCATACCTGAAGATACGTCCATTGGGACTACTTTCCTGCTGGATGACCAAGCCCAGGATAAGGACACTGCAAATAATGGCTTGATACATTA[T/A]CATTTAGAGGGATCTAATGGATTTTTTGGCATCAGACAAGAGGATTATGGACTCGAGCTCATAGTACAAAAGGAACTAGACCGAGAAACTCAGGATAACTACTTCTTAGTTCTTGTAGCAGTAGACAGAGGTTCAATGCCACTCAGCGCTACTGCTAATCTCAGTGTAACTGTAACCGATGTTGATGACAACTGCCCAGAATTTGATGATGATAGCCCCATCAAAGCCATTGTGCCAGGATTAGGAATCAAGGGCACTGCGGTGGCTCAGCTTAAAGCAACAGACAAAGACCTGGGCCAAAATGCCCAGATCACATTTTCCTTCAGCCGTCAGATCTCAGACAGAGCCAAAACACTCTTTTACATGGACAGACACACAGGCCTGATCAGCTTAGCAGTTGATGTGCACACTGACAGTCCTGAGGAGCACATGCTGAAAGTTTTTGCGAATGGTCCACTTTGCCCCCCTGCACAAGCTCAAGTAACTGTATACATTCAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13628
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 386 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18471136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14265589 |
GRCz11 | 14 | 14571152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAGAAACAGACAGCATGCCATTTTCTTTGAAACAGCAAGCAGGCAGCTA[T/A]TTGCTTTCAACATCAAAAGCTCTAGAWTTTGAGCTGTGCGGCGAGTACGA
Long Flanking Sequence:
CCAGAATTTGATGATGATAGCCCCATCAAAGCCATTGTGCCAGGATTAGGAATCAAGGGCACTGCGGTGGCTCAGCTTAAAGCAACAGACAAAGACCTGGGCCAAAATGCCCAGATCACATTTTCCTTCAGCCGTCAGATCTCAGACAGAGCCAAAACACTCTTTTACATGGACAGACACACAGGCCTGATCAGCTTAGCAGTTGATGTGCACACTGACAGTCCTGAGGAGCACATGCTGAAAGTTTTTGCGAATGGTCCACTTTGCCCCCCTGCACAAGCTCAAGTAACTGTATACATTCAGCCCATGGTGAGCTCTGAGCCGACCATAAAGATCAGGTTTGTCACAGAGCATAAAAACCAAGTAATCATGTTACAAGAGAACGAACCCCCCACCGTCTTGGCCCTCTTGGAGTTGGAAGACACCTCTAGTGATAAAGGTACTCTGTCCTTAGAAACAGACAGCATGCCATTTTCTTTGAAACAGCAAGCAGGCAGCTA[T/A]TTGCTTTCAACATCAAAAGCTCTAGATTTTGAGCTGTGCGGCGAGTACGATGTTACAGTTGTTATTTCTGATCCTCATGGCGCACGCCTACATGGAAGGGAAGTGATCAAAGTGGTGGTTCAAGATCTGAATGATAATGCCCCAAAGTTTGAACAAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCTGGAGAGTTTCTGCTGAAGGTACAGGCTACTGATGCAGATAGCCATCAGTTTGGCAAAGTAGAGTATAGGATTACAAACGGGAGTCCTTTCAGAATTCAGGAAGAGACAGGTGTGATATTGGTCACAGAGCCTTTAGATAGAGAACAGCAGGGGACATACATCCTGACTGTTCTTGCCCAGGACGGCGGCGATCCTTCTCAGGAGGCCTTTGCTATTGTGTTTGTAAATGTACTGGATATGAACGACAATCCACCAGCCTTTCCAACCCCTCATTTCTATTTTTTTGTGTCTGAGAGCCTTCCGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31977
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 438 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18471290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14265743 |
GRCz11 | 14 | 14571306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCAAAGTGGTGGTTCAAGATCTGAATGATAATGCCCCAAAGTTTGAA[C/T]AAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCTGGAGAGTTT
Long Flanking Sequence:
AAACACTCTTTTACATGGACAGACACACAGGCCTGATCAGCTTAGCAGTTGATGTGCACACTGACAGTCCTGAGGAGCACATGCTGAAAGTTTTTGCGAATGGTCCACTTTGCCCCCCTGCACAAGCTCAAGTAACTGTATACATTCAGCCCATGGTGAGCTCTGAGCCGACCATAAAGATCAGGTTTGTCACAGAGCATAAAAACCAAGTAATCATGTTACAAGAGAACGAACCCCCCACCGTCTTGGCCCTCTTGGAGTTGGAAGACACCTCTAGTGATAAAGGTACTCTGTCCTTAGAAACAGACAGCATGCCATTTTCTTTGAAACAGCAAGCAGGCAGCTATTTGCTTTCAACATCAAAAGCTCTAGATTTTGAGCTGTGCGGCGAGTACGATGTTACAGTTGTTATTTCTGATCCTCATGGCGCACGCCTACATGGAAGGGAAGTGATCAAAGTGGTGGTTCAAGATCTGAATGATAATGCCCCAAAGTTTGAA[C/T]AAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCTGGAGAGTTTCTGCTGAAGGTACAGGCTACTGATGCAGATAGCCATCAGTTTGGCAAAGTAGAGTATAGGATTACAAACGGGAGTCCTTTCAGAATTCAGGAAGAGACAGGTGTGATATTGGTCACAGAGCCTTTAGATAGAGAACAGCAGGGGACATACATCCTGACTGTTCTTGCCCAGGACGGCGGCGATCCTTCTCAGGAGGCCTTTGCTATTGTGTTTGTAAATGTACTGGATATGAACGACAATCCACCAGCCTTTCCAACCCCTCATTTCTATTTTTTTGTGTCTGAGAGCCTTCCGCATCTTTCTCAAGTCGGTAAAGTCACAGTAAGTGATGCTGATGACGGAGACAATGGAAGAATAGTGGATTTGCGTATATTAAATGACAAGGCCCCTTTCGTCATAGACATGTCACAAGGGATGCTCCGCAGTACTGGTGAAGTCGACCGTGAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35668
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 452 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18471332)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14265785 |
GRCz11 | 14 | 14571348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTGAACAAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCT[G/T]GAGAGTTTCTGCTGAAGGTACAGGCTACTGATGCAGATAGCCATCAGTTT
Long Flanking Sequence:
TAGCAGTTGATGTGCACACTGACAGTCCTGAGGAGCACATGCTGAAAGTTTTTGCGAATGGTCCACTTTGCCCCCCTGCACAAGCTCAAGTAACTGTATACATTCAGCCCATGGTGAGCTCTGAGCCGACCATAAAGATCAGGTTTGTCACAGAGCATAAAAACCAAGTAATCATGTTACAAGAGAACGAACCCCCCACCGTCTTGGCCCTCTTGGAGTTGGAAGACACCTCTAGTGATAAAGGTACTCTGTCCTTAGAAACAGACAGCATGCCATTTTCTTTGAAACAGCAAGCAGGCAGCTATTTGCTTTCAACATCAAAAGCTCTAGATTTTGAGCTGTGCGGCGAGTACGATGTTACAGTTGTTATTTCTGATCCTCATGGCGCACGCCTACATGGAAGGGAAGTGATCAAAGTGGTGGTTCAAGATCTGAATGATAATGCCCCAAAGTTTGAACAAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCT[G/T]GAGAGTTTCTGCTGAAGGTACAGGCTACTGATGCAGATAGCCATCAGTTTGGCAAAGTAGAGTATAGGATTACAAACGGGAGTCCTTTCAGAATTCAGGAAGAGACAGGTGTGATATTGGTCACAGAGCCTTTAGATAGAGAACAGCAGGGGACATACATCCTGACTGTTCTTGCCCAGGACGGCGGCGATCCTTCTCAGGAGGCCTTTGCTATTGTGTTTGTAAATGTACTGGATATGAACGACAATCCACCAGCCTTTCCAACCCCTCATTTCTATTTTTTTGTGTCTGAGAGCCTTCCGCATCTTTCTCAAGTCGGTAAAGTCACAGTAAGTGATGCTGATGACGGAGACAATGGAAGAATAGTGGATTTGCGTATATTAAATGACAAGGCCCCTTTCGTCATAGACATGTCACAAGGGATGCTCCGCAGTACTGGTGAAGTCGACCGTGAGAAGCAAGATCGCTATGAGCTTTTGGTTGTCGCTGTAGATGGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13218
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 459 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18471353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14265806 |
GRCz11 | 14 | 14571369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACAGACATCAAGGAGAACAACAAGCCTGGAGAGTTTCTGCTGAAGGTA[C/T]AGGCTACTGATGCAGATAGCCATCAGTTTGGCAAAGTAGAGTATAGGATT
Long Flanking Sequence:
ACAGTCCTGAGGAGCACATGCTGAAAGTTTTTGCGAATGGTCCACTTTGCCCCCCTGCACAAGCTCAAGTAACTGTATACATTCAGCCCATGGTGAGCTCTGAGCCGACCATAAAGATCAGGTTTGTCACAGAGCATAAAAACCAAGTAATCATGTTACAAGAGAACGAACCCCCCACCGTCTTGGCCCTCTTGGAGTTGGAAGACACCTCTAGTGATAAAGGTACTCTGTCCTTAGAAACAGACAGCATGCCATTTTCTTTGAAACAGCAAGCAGGCAGCTATTTGCTTTCAACATCAAAAGCTCTAGATTTTGAGCTGTGCGGCGAGTACGATGTTACAGTTGTTATTTCTGATCCTCATGGCGCACGCCTACATGGAAGGGAAGTGATCAAAGTGGTGGTTCAAGATCTGAATGATAATGCCCCAAAGTTTGAACAAACACGTTACGAAACAGACATCAAGGAGAACAACAAGCCTGGAGAGTTTCTGCTGAAGGTA[C/T]AGGCTACTGATGCAGATAGCCATCAGTTTGGCAAAGTAGAGTATAGGATTACAAACGGGAGTCCTTTCAGAATTCAGGAAGAGACAGGTGTGATATTGGTCACAGAGCCTTTAGATAGAGAACAGCAGGGGACATACATCCTGACTGTTCTTGCCCAGGACGGCGGCGATCCTTCTCAGGAGGCCTTTGCTATTGTGTTTGTAAATGTACTGGATATGAACGACAATCCACCAGCCTTTCCAACCCCTCATTTCTATTTTTTTGTGTCTGAGAGCCTTCCGCATCTTTCTCAAGTCGGTAAAGTCACAGTAAGTGATGCTGATGACGGAGACAATGGAAGAATAGTGGATTTGCGTATATTAAATGACAAGGCCCCTTTCGTCATAGACATGTCACAAGGGATGCTCCGCAGTACTGGTGAAGTCGACCGTGAGAAGCAAGATCGCTATGAGCTTTTGGTTGTCGCTGTAGATGGTGGCAGTCCAGTCCTCTCCACTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42371
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 674 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18471999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14266452 |
GRCz11 | 14 | 14572015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCCAGGCAGGAAGCATGATAACAAAGATCTACGCCATTGACGAGGACT[C/A]AGGAATGAATTCAGATATCACATATCAAATTATTGCAAGTGAACCAGCTC
Long Flanking Sequence:
TGTTCTTGCCCAGGACGGCGGCGATCCTTCTCAGGAGGCCTTTGCTATTGTGTTTGTAAATGTACTGGATATGAACGACAATCCACCAGCCTTTCCAACCCCTCATTTCTATTTTTTTGTGTCTGAGAGCCTTCCGCATCTTTCTCAAGTCGGTAAAGTCACAGTAAGTGATGCTGATGACGGAGACAATGGAAGAATAGTGGATTTGCGTATATTAAATGACAAGGCCCCTTTCGTCATAGACATGTCACAAGGGATGCTCCGCAGTACTGGTGAAGTCGACCGTGAGAAGCAAGATCGCTATGAGCTTTTGGTTGTCGCTGTAGATGGTGGCAGTCCAGTCCTCTCCACTACTGTGAAAATGACTGTTTTTGTTGAGGATATCAATGATAATCAACCACAGGTCCTTCTTCCTAGCAGCAACCTGTCCTGTCTGACCATATCTCCAGCTACCCAGGCAGGAAGCATGATAACAAAGATCTACGCCATTGACGAGGACT[C/A]AGGAATGAATTCAGATATCACATATCAAATTATTGCAAGTGAACCAGCTCTCCAAAGCCCCTTTCAGATTGACCAGCACTCAGGAAACATCACCCTTGTCCAGCATCTGCGCGGTGAAGACTACGGCATGCACCACCTTTTCATAGTTGTTCGTGATGGAGGAAAACCAGACCCGCTGCAGACCACCATATGGGTTAATTTACTGGTCAATGAAACTTTGGAAAAATGTCACGTTAATGCTGTCCCAGAATACTCTCCTCAGACATTGCCTACTTCAATGCCGCTTTCTGTCAGAGGCTCCAGATGTGAATCAAATTCCTGGCTCATTTTTCTTTGTGGCCTGGGCCTGATGGTCATGTCGGTTTTTATTCTTCTAGTGTCTGTAGTGGTATTTCTAAAACACAAAAAGACGAGAAGAAAAATGGAAAAAAAGGATGTATGGGAAAGTAAAAATATCTGTGAACTGAAACCTTTAAACTAATGCAAAGGCCTTACAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35669
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 |
---|---|---|---|---|---|
ENSDART00000080527 | Nonsense | 734 | 833 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 18472178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14266631 |
GRCz11 | 14 | 14572194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACCACCTTTTCATAGTTGTTCGTGATGGAGGAAAACCAGACCCGCTG[C/T]AGACCACCATATGGGTTAATTTACTGGTCAATGAAACTTTGGAAAAATGT
Long Flanking Sequence:
ACGGAGACAATGGAAGAATAGTGGATTTGCGTATATTAAATGACAAGGCCCCTTTCGTCATAGACATGTCACAAGGGATGCTCCGCAGTACTGGTGAAGTCGACCGTGAGAAGCAAGATCGCTATGAGCTTTTGGTTGTCGCTGTAGATGGTGGCAGTCCAGTCCTCTCCACTACTGTGAAAATGACTGTTTTTGTTGAGGATATCAATGATAATCAACCACAGGTCCTTCTTCCTAGCAGCAACCTGTCCTGTCTGACCATATCTCCAGCTACCCAGGCAGGAAGCATGATAACAAAGATCTACGCCATTGACGAGGACTCAGGAATGAATTCAGATATCACATATCAAATTATTGCAAGTGAACCAGCTCTCCAAAGCCCCTTTCAGATTGACCAGCACTCAGGAAACATCACCCTTGTCCAGCATCTGCGCGGTGAAGACTACGGCATGCACCACCTTTTCATAGTTGTTCGTGATGGAGGAAAACCAGACCCGCTG[C/T]AGACCACCATATGGGTTAATTTACTGGTCAATGAAACTTTGGAAAAATGTCACGTTAATGCTGTCCCAGAATACTCTCCTCAGACATTGCCTACTTCAATGCCGCTTTCTGTCAGAGGCTCCAGATGTGAATCAAATTCCTGGCTCATTTTTCTTTGTGGCCTGGGCCTGATGGTCATGTCGGTTTTTATTCTTCTAGTGTCTGTAGTGGTATTTCTAAAACACAAAAAGACGAGAAGAAAAATGGAAAAAAAGGATGTATGGGAAAGTAAAAATATCTGTGAACTGAAACCTTTAAACTAATGCAAAGGCCTTACAGATATACTGATTAAATATTTTTGCAAGTATGGCAAGAGTGAAAATATATGTATATATTTCTTTCTTTGAAATAATATTCTTTGGCTAGTATTATAATAGGTCCATAATATATTGCTGTAGTACTGCTATGATCTACTGTCAAGTCTATTAGTGCTTTTGCCAAGAATATGAGTCTTAACTTAA
Associated Phenotype:
Not determined