Busch Lab

ZMP

trio

Ensembl ID:
ENSDARG00000000370
ZFIN ID:
ZDB-GENE-030616-399
Description:
Novel protein similar to human triple functional domain protein TRIO (PTPRF interacting) [Source:Uni
Human Orthologue:
TRIO
Human Description:
triple functional domain (PTPRF interacting) [Source:HGNC Symbol;Acc:12303]
Mouse Orthologue:
Trio
Mouse Description:
triple functional domain (PTPRF interacting) Gene [Source:MGI Symbol;Acc:MGI:1927230]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa22758 Nonsense Available for shipment Available now
sa42663 Nonsense Mutation detected in F1 DNA Not yet available
sa39081 Nonsense Mutation detected in F1 DNA Not yet available
sa31000 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17346 Nonsense Available for shipment Available now
sa10735 Essential Splice Site Available for shipment Available now
sa28584 Nonsense Mutation detected in F1 DNA Not yet available
sa36045 Nonsense Available for shipment Available now
sa22757 Essential Splice Site Available for shipment Available now
sa12241 Essential Splice Site Available for shipment Available now
sa6408 Nonsense Mutation detected in F1 DNA Not yet available
sa42662 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22758
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Nonsense 363 2996 6 59
Genomic Location (Zv9):
Chromosome 16 (position 10215353)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8998599
GRCz11 16 8890935
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTCGGATTATGTCAGTGGGGAACAGGCTGCTGGAGTCAGGTCACTA[T/A]GCGACCCAGCAGATTCAGCAGATCTCAGGTCAGCTGGAGCAAGAGTGGAA
Long Flanking Sequence:
GATTCGATCTCCTTATCGGAAATCGGACCCGATCACACGGTTTCAGACTCGATCGGAATCAGACGTTACCTCCAGATCAGGACTCTAATCGTGCTATCTATTTTTATATTAGATTTTTTTTTTAGCACTAAAATCCAAAAGTGAAGAATTTGTTATTTATTACTTGATTGTTCAAGCTACCTCACAGAACTGTTCTGTTTATTAACAGAGTTGTTGAATGTTAAAATAAGGTGAATTAAATAAAAAAAATAAGGAACATCCTGGATCTGTTTCTTCACTCTTTTTTTAAATTATTGTTTTCATGTATTATAGATGTCTCAGATCGGGTTTCAGGATTGGTAGATTCTCAAAATCAAATGATTCCGACTCGAGGGCAAAAAAACCTGATCGAGACATCCCTAGTAAATACATACCTTTGTTTTTGGTGTCTTGCAGAATGTGTACGTGAACATCAGTCGGATTATGTCAGTGGGGAACAGGCTGCTGGAGTCAGGTCACTA[T/A]GCGACCCAGCAGATTCAGCAGATCTCAGGTCAGCTGGAGCAAGAGTGGAAAGCATTCGCCGCTGCACTGGACGAGAGAAGTACACTGTTGGAAATGTCTGCCAACTTCCACCAGAAAACTGACCAGGTGAGGCTCATGTGTTACCATATCTTCTGATACACTGGATGAACAAACAAACAAATGGATAATGTCTTTCAAATGATTAATTATGAGAGTTATGAGATAAAAATCTATAAAATTAAAGCTGTGGTGAAAAGATAAGAGATAAATTCTCAGGTTGATTTACTGGATGTTTTAGGTATGGTTTTGAGTAAAATTATATTTATTCTATATAGGTGTGATAATAGCTTTCAAATTAGAAATAATTGTGTTAATTTGACTTGTTTCTATGGTTTATAAGGACACAAATTTGTGTAATGACATGGGTATTGCCTAGTTCAGGGGTGCTCAACCCTGTTCCTGGAGATCTACTTTCCTGTAGATTTCAGTTGCTACCCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42663
Status:
Mutation detected in F1 DNA
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
ENSDART00000000382 Nonsense 499 2996 8 59
Genomic Location (Zv9):
Chromosome 16 (position 10210502)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8993748
GRCz11 16 8886084
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCATCACGTTCTGGATATCATTCATGAGGTTCTGCATCACCAGAGG[C/T]AGTTGGAGAACATCTGGCAACACCGCAAACTCCGTCTCCACCAACGGCTG
Long Flanking Sequence:
TTTTGGCAAATAAAATCACGATTCACATTTTAGCCAGAATCGTGCAGCCCTAATATGGTGTCATGACTTTGCATTAAAAACACTTCATTATAATGGTAGTCAATGAGGCAAGAACGGCCACCAATATAATGAAAGGGTTGCAAATTTGAGTGTAATGTTGAGTTTTCTTTCAAAGCATTTTCCCAAAATATATGTCAAAATAAGATTTCACAGAGAGAATTGTGGCCAATTTAAAACATCCCTGCAGCCTGCATCATGTATCCTTTTATGGTATATATTTTAGTTATTTAATCAAAGTAGGAATTTCGTCTTCAAAACATATCTTGATGTGTGTGTTATGTGTTTATCCTCAGGTAAGTCAGGATGGCAAAGCCCTGCTAGATAAGCTCCAGCGCCCTTTGACCCCGGGCAGTGCTGATTCGCTGACTTCCTCGGCTAACTACTCCAAGGCTGTTCATCACGTTCTGGATATCATTCATGAGGTTCTGCATCACCAGAGG[C/T]AGTTGGAGAACATCTGGCAACACCGCAAACTCCGTCTCCACCAACGGCTGCAGCTTTGCGTCTTCCAACAGGACGTTCAGCAGGTCAGACAATTTTTAAAATGGGTGGGATGTTCACAAAATTGATGATTGGTTTGTATTATGGTTCTCTGGTCAAGGTTTTTGGTTTGATTCAGTTTACATTGGAAACAAAAACACACTTAAAGGGCCATGAAACCTCTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGAGTGTCGGAGGAACTAAAGTGGGGGGGTGGTGGAGTGTCTACTTGGGCACGTGCGAGTTTCAGAGTCAAAATACAGACACAGGAAAAAGTGAAGGTGTTTAACCTACATGGACATCTGTAGTTGAATTATTTGCCAAATTATTAAATGTTGGACTTTAACTGCAGTTTGGCTCTTTCATTCAGGGAATTCATTCATGTCCCTCGCGACAAACAAGATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39081
Status:
Mutation detected in F1 DNA
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
ENSDART00000000382 Nonsense 742 2996 12 59
Genomic Location (Zv9):
Chromosome 16 (position 10194421)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8977667
GRCz11 16 8870003
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAACGCAAGATCAAACTCGAACTTTTCCTCCAGCTCAGGATCTTTGAA[C/T]GAGATGCGATTGACGTAAGTCTACACTCCACCACACGGCTCAGTTGTCAT
Long Flanking Sequence:
CTAAGTTTTGAATAAAATTTGAAATGGCAAAAAATGACTTTAAAAAATGTAAAAGTTTTTTTTGTAGTGTACCATTTTCCAATTGTCATTTCAGACAGTCACCAGATGATTTAATATTAAATAGCATGAAATCAGACTTTTATGTTGATTTCCACCAATGATACTTGGCTTATTTTTTCACTGATTTTAGAACCTAGAGCTGCAGCAACTACTATAACCTAAAAACACACACTCAAATCACTGACCTGCAGAAGCTAATTAAACTACAGAAAGAATAGACTTCAACTCCTGTAGATGTTATCTCTGATATGTTCTCTCGTATCCTCTTCTGTGACTCCAGAGACTCCGCAATCTCTAGCAATAAGACTCCTCATAACAGCTCGATGGCACACATCGAGAGTGTCCTGCAGCAGCTGGATGAGGCTCAGGCTCAGATGGAGGAGCTGTTTCAGGAACGCAAGATCAAACTCGAACTTTTCCTCCAGCTCAGGATCTTTGAA[C/T]GAGATGCGATTGACGTAAGTCTACACTCCACCACACGGCTCAGTTGTCATTCCCAAATCACAAACCACTGATTTTGTTGTAAACAGTGAGTTTTTGCACTCAAGACAAATAGTTCAATATAGATCCTCTGCCCCTCGTCAATCTGAGAGATTCAATTTAATCAACTTTAGTTAACACTTTAGTTTAGGTCATAATCCATGCTATTAACTACTGGCTTATTACCATTAAGATATGAACTGTTCATTAGTAGTTATAAAGTATGATCTTATTCTGTATCCCTAATGCTACCCAAAACTTAAACCCAACTTCTTCCTTACTAACTATTAATAAACAGCTAATTATTAGTTTATTAAGCTAGTAGGGTTAGTTAATGGTCTGTTAATACCATAAATTATAACTTAAGCCAGGGGTGTCCAAACTCGGTCCTGGAGGGCTGGTGTCCTGCATAGTTAACTCCAACTTCCTCCAACACACCTGCCTAGAAGTCGAGTATACCTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31000
Status:
Mutation detected in F1 DNA
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
ENSDART00000000382 Essential Splice Site 1304 2996 25 59
Genomic Location (Zv9):
Chromosome 16 (position 10150306)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8933552
GRCz11 16 8831997
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTATTTAACATCCATTGTTTCCTTACTGTTGCTTTCCTCTCTTTCTCA[G/T]CATTTTCCTTAAAGAACTGGAAAAATATGAGCAGCTTCCAGAGGATGTGG
Long Flanking Sequence:
TGACCGTTACACTTTTCCCCATTCAAAACTATACAAGTGACACGTCTTGTGTATTCTATAGTCCTTGACTAAAGTTGAGGTTGTCCTTTTTTCTGACGTACATCTACTTGATATGGTTTCTGAAGTATAAAAAATGTATGGCGGTGCTTGATTTTCTTATTTTGGAGCCGGTTGGATCATTGGAAGATGGGCTTTGCTAACAAAACAAAAAAAAATACACATTGGGAATTTGCACCGAAATGTTTTTTATTTATTAATAGCATTAGTTTGTTATCAGAATTGTAACTGCAAGTGTGTTTGTGTGTTTTAGACTTATCTTTGGGAGATGAGCAGTGGCGTGGAGGAGATTCCCCCAGGGATTGTCAACAAAGAGCACATCATTTTTGGCAACATGCAAGATCTATACGAGTTCCATCACAAGTCAGTGAAGTTAATGTAAATAATAATTTCATTTATTTAACATCCATTGTTTCCTTACTGTTGCTTTCCTCTCTTTCTCA[G/T]CATTTTCCTTAAAGAACTGGAAAAATATGAGCAGCTTCCAGAGGATGTGGGTCACTGTTTTGTCACATGGGTGAGTGTGTCAGTGTGCTGGAGATAATCTGATCACGAAGCGCGCTGGCGTTATGTTGATATTAAATCAGATCCTTAGCACATATATCTGGGTTACTGCACTTACAGTGTACATACACCGTTTTATAAAAGTTATATATTATTTACATATGATATCACTTAATGAGTCCTTTATTTCAAAACTGAGAGATTAAACATAAATATTTATAAATGCTACTTAAAATAACTAATGAACAATAATATTCTCAGGATTCTTAGATGATAAAGAGTTTTTTTCAAAATGTCATTTTTAAGTAGTGTAACCTGTGATAATTATTTTTTTTTTAAAAAGTAACTTGAGCACCAAATCAGCATTGCTGGTTTGTGAAGGATCAGGCGAGCTCTGATATTGAAAATTTAGCTTAGGCATAATAATGCAATATTGTAATCGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17346
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Nonsense 1932 2996 41 59
Genomic Location (Zv9):
Chromosome 16 (position 10101636)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8884882
GRCz11 16 8783327
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGATTTTCAGCTACGTCCTGCTGGAACTGGTGGAAACAGAAAGAGACTA[T/A]GTGAGAGACCTTGGTGCAGTCGTGGAGGTGGGCTCATATTCACTTCTTTT
Long Flanking Sequence:
AAAACATAAGTAGGGTGAAACTAATTCAACAAACGGACAAAAGCACACTGTTTGAAAAAAAGCACACTGTTATACACTTACCGGCCCCTTTATTAGGTACACCTGTCCAACTGCTCGATAACGCAAATTTCTAATCAGCCAATCAATGGCAGCAAGTCAATGCATTTAGGCATGCAGACATGGTCAAGATGAGTTCAAACTGAGCATCAGAATAGGGACAAAAGGTGATTTAAGTGACTTTGAACGTGGCTGGTCTGATGATTTCTGAAACTGCTGATCCAGTGGGATTTTCATGCACAGCCATCTCTAGGGTTTACAAAGAATGGTAACATTGCGCATATTTAGTTATATTTCTTAATGATAAATTTGTACAAATACTGAATGTAATGGATTGTTTCAACCAGCCATCTTGGTTTGCTTGCTGTGTGAATATGAATATCTTTTCTCTCTTTGATTTTCAGCTACGTCCTGCTGGAACTGGTGGAAACAGAAAGAGACTA[T/A]GTGAGAGACCTTGGTGCAGTCGTGGAGGTGGGCTCATATTCACTTCTTTTAACAAATACAGCAGTGAGATCACTATGGCGACCACATGCAACCGCATACATTCATTCAACTACTCGTAATTGGCAGATGCTGTCAGGGTTGAGTTCTGGTTGTTCAATAGCCTGTCTATCTAAGGAGATCTGTCTACTGCGGTTTTGTGAACCGATCACGTGATCTTATTTGACTCTTTAAAAGTAACCCTGTGAATCTCATCAGCTGGCACAGGAAATGAAAATGGTGATGTGCCATACGTTCAGTATGGTGGCTCAGTAAAATAGCGTTTTGTATGTCGCTGTCACTATTGTAACCATGCACACGTGCACCTGCAGGGCTACATGAGCAGGATGAAGGAGGAGGGTGTACCCGATGACATGAAGGGCAAGGATAAGATTGTCTTTGGGAACATTCACCAGATATTCGACTGGCATAAAGAGTATGTGTCACCTCAGAAGCAATATCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10735
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Essential Splice Site 1999 2996 43 59
Genomic Location (Zv9):
Chromosome 16 (position 10101017)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8884263
GRCz11 16 8782708
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGTGCTTGGAGGACCCCGATAGACTYGCACCCCTSTTTGTCAGACAG[G/A]TAGGGAATGAATCATTGTGCCATTTCACTCTYACTAAKATAAATTCSCTT
Long Flanking Sequence:
ATTGGCAGATGCTGTCAGGGTTGAGTTCTGGTTGTTCAATAGCCTGTCTATCTAAGGAGATCTGTCTACTGCGGTTTTGTGAACCGATCACGTGATCTTATTTGACTCTTTAAAAGTAACCCTGTGAATCTCATCAGCTGGCACAGGAAATGAAAATGGTGATGTGCCATACGTTCAGTATGGTGGCTCAGTAAAATAGCGTTTTGTATGTCGCTGTCACTATTGTAACCATGCACACGTGCACCTGCAGGGCTACATGAGCAGGATGAAGGAGGAGGGTGTACCCGATGACATGAAGGGCAAGGATAAGATTGTCTTTGGGAACATTCACCAGATATTCGACTGGCATAAAGAGTATGTGTCACCTCAGAAGCAATATCAACTTGCCCTACTTTCATTTCCTAACATGAATTATTTAAACCCTGTCTAGTTTCTTTCTTGCTGAGCTGGAGAAGTGCTTGGAGGACCCCGATAGACTCGCACCCCTGTTTGTCAGACAG[G/A]TAGGGAATGAATCATTGTGCCATTTCACTCTTACTAAGATAAATTCGCTTTATCAGACTAATATTGATGAGCTAAACAAACAGACCAACCTAAACAAAATTGGTTTAACCAGTGGTGCTGCTTCTTGAAAAAAAGCACACTGTTATACACTTACCGGCCCCTTTATTAGGTACACCTGTCCAACTGCTCGATAACGCAAATTTCTAATCAGCCAATCAATGGCAGCAAGTCAATGCATTTAGGCATGCAGACATGGTCAAGATGAGTTCAAACTGAGCATCAGAATAGGGGACTTTGAACGTGGAATGGTTTTTGGTGCCAGACAGGCTGGTCTGAGGATTTCTGAAACTGCTGATCCAGTGAGATTTTCATGCACAGCCATCTTAAGGGTTTACAGAGAATGGTCCAAAAAAGAGAAAACATCCAGTGACCGGAACTTCTGTGGCCGCAGATGCCATGTTGATGCCAGAGGTCAGAGGAGAATGGCCAGATTGGTTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28584
Status:
Mutation detected in F1 DNA
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
ENSDART00000000382 Nonsense 2011 2996 44 59
Genomic Location (Zv9):
Chromosome 16 (position 10098388)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8881634
GRCz11 16 8780079
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTACTTGGTTACAGGAACGTAGACTACACATGTACATCGTGTACTGC[C/T]AAAACAAGCCCAAATCTGAGCACATTGTTTCGGAGTACATAGACACGTAT
Long Flanking Sequence:
TATACTGTATCTATGAGTATGAGTATTACTAAAAAAAATCTTAGAAGCCTTTTAACCTTTCCATGGTTTTGGAAAAAGAAATTGACTCTGATTGGACAAGGAAAAATGAGCTACTTTTTATTCCTTTTGAGTGGGTGGGGCTGGACCTGGCAACCCTATGTGTCATACAGTATTTCTAATGCAGTTCTCTTTAGAATATGAACCCCAAGTGTTTTAAATATGATTATTTTTCTACCATATACCATCAATTCAATTCATTAACCCACTAGAGTCATACAGATTGCTTTTATTATGGATGGACTATAACAGTGTTCAATGATGGAACAATAAAGTTGCACCACAGCTGTTGTTATTGTTGCATAATCTATTTTAGCACAGCTAGAAAGATGTATTGATCAATCAATATGAGGTGTTTACATGATGACTGAGTCATAATGTTCTGTAAATGAAACTGTACTTGGTTACAGGAACGTAGACTACACATGTACATCGTGTACTGC[C/T]AAAACAAGCCCAAATCTGAGCACATTGTTTCGGAGTACATAGACACGTATTTTGAGGTAAGACTCCAGTCACTGCCTACATCCTTCTTGACATTTAACCATGAGTCATGAAAACTGAGACAGACTCATAACCACACTCACATCTCATCTTTTTGTTTTTGCTTGTAATTTCATCAGGATTTAAAGCAGAGGTTGGGCCACAGGCTACAGATCACAGATCTACTGATTAAACCAGTGCAGCGGATCATGAAATACCAGCTTCTGCTAAAGGTCGGATATGGAAATTACTAGGGGTGTAACGATACACTCAGCTCACGATACGATGTGTATCACGATATAATGTTCACGATTTGATATGTATCACGATATTTTGAATAAAAATTGAAAATTAAACTGAAATGCAAATTTTACCAAGTAAATTATTTTTTATGTATTTCTTTTGTTTCAACTTGTTAAACTGAACCTTCTTTAAGAAAATAAATTAAACAGGCCTGTCACTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36045
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Nonsense 2134 2996 48 59
Genomic Location (Zv9):
Chromosome 16 (position 10091096)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8874342
GRCz11 16 8772787
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCATGGTCTCAGATCAGGATGGTGGTCTTCTTTCTCGCTTGAAGGAG[A/T]GACGCATCTTCCTCTTCGAGCAGATAGTTATCTTCAGCGAGCCTCTGGAT
Long Flanking Sequence:
GTGGCAAAATCATGACGTGTGCTACAGGTGAATGGCTGGAGAAATGTTCATAAAGCTGGAGTGTCCACCAGACTCACTAGAGGGCACTCCAGCTTTATGAACGTTAGTCCTGATGACTGTATGATGTAACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATTATATATGTTATGTCAAAATAGACGTTTAATTTGGATGCGATTAATTGCAATTAGTCTTTGCCCAGCATTAATCTGACCAAAGTTTGCTATTCCTAGTCATTTACCCATAGGCATCCTAAAACAATCACAGAAAAGAACTTGTGTTTGTGTGTTTTTGCTTTTAATCTAAGCATTCTAGTGATCTCTGTGCTATGTTTGTTCAGGGTAAAATTGTAGCCCAGGGTCGACTGCTTCTTCAGGATACCTTCATGGTCTCAGATCAGGATGGTGGTCTTCTTTCTCGCTTGAAGGAG[A/T]GACGCATCTTCCTCTTCGAGCAGATAGTTATCTTCAGCGAGCCTCTGGATAAAAAGAAGGGATTTTCTATGCCAGGCTACCTTTTTAAGAACAGCATAAAGGTATGTAGGTATAACCACTGCTGTAAAAAAAAAACACTGTGGCACAACATAGACCTTATAAATCCATGTCACTCTTTTCCTGCAGGTCAGTTGGCTGGGTCTAGAGGAAAGTCCTGACAATGACCCTTGTAAGTTTATTTTGACCTCAAGGTCATCGGCTGGCAGTTTAGAGCATTACGTCCTCCATTCCTCCAACCGGGTGGTTTGCCAGACCTGGATCCACCAGATCAGCAGCATCCTGGAGAACCAGAGAAACTTCCTTAATGGTATTATTCAGACAGTGTCCTTTAAACTAATCGTCATAAATATTTTTAATGATTATTAACTTTTGTAGCTTTGCTACATTCATTCAAGATGATTTGTTTGATGATTTACATGTTTTAACCAACCAGAGTTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22757
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Essential Splice Site 2228 2996 49 59
ENSDART00000000382 Essential Splice Site 2228 2996 49 59
Genomic Location (Zv9):
Chromosome 16 (position 10090727)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8873973
GRCz11 16 8772418
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCACCAGATCAGCAGCATCCTGGAGAACCAGAGAAACTTCCTTAATGG[T/C]ATTATTCAGACAGTGTCCTTTAAACTAATCGTCATAAATATTTTTAATGA
Long Flanking Sequence:
AATCTAAGCATTCTAGTGATCTCTGTGCTATGTTTGTTCAGGGTAAAATTGTAGCCCAGGGTCGACTGCTTCTTCAGGATACCTTCATGGTCTCAGATCAGGATGGTGGTCTTCTTTCTCGCTTGAAGGAGAGACGCATCTTCCTCTTCGAGCAGATAGTTATCTTCAGCGAGCCTCTGGATAAAAAGAAGGGATTTTCTATGCCAGGCTACCTTTTTAAGAACAGCATAAAGGTATGTAGGTATAACCACTGCTGTAAAAAAAAAACACTGTGGCACAACATAGACCTTATAAATCCATGTCACTCTTTTCCTGCAGGTCAGTTGGCTGGGTCTAGAGGAAAGTCCTGACAATGACCCTTGTAAGTTTATTTTGACCTCAAGGTCATCGGCTGGCAGTTTAGAGCATTACGTCCTCCATTCCTCCAACCGGGTGGTTTGCCAGACCTGGATCCACCAGATCAGCAGCATCCTGGAGAACCAGAGAAACTTCCTTAATGG[T/C]ATTATTCAGACAGTGTCCTTTAAACTAATCGTCATAAATATTTTTAATGATTATTAACTTTTGTAGCTTTGCTACATTCATTCAAGATGATTTGTTTGATGATTTACATGTTTTAACCAACCAGAGTTAGGTGTAATTAGTTACAAAGTAACTAACTACTGTAATTAAATTACTTTTCTGCTAAAAAGTAAACTATGGGATTCATTTGAACTTATCATGTACTTGCATTAAATGCATGTAAATAAATGTAACATTAGTGTATAAAGCAGAGGAAATATTTTTTGTTTTACAATATGTTTTGTCAAATAATTGTATTTTTAAGTAAAGAAGATTGAATTCATCTCTGATGATTATACATGACTAAATAAGTAAAGAAATTACAAAATATAAGGTATAGATTCAAAGAAGCAAAGTACATGTGTGTATTTATATACTAGGGATGTCAAAATGAATTGATTCATAGATGCACTGTGATGCAGACACAAACAATTCGGTATCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12241
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000382 Essential Splice Site 2228 2996 49 59
ENSDART00000000382 Essential Splice Site 2228 2996 49 59
Genomic Location (Zv9):
Chromosome 16 (position 10090727)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8873973
GRCz11 16 8772418
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCACCAGATCAGCAGCATCCTGGAGAACCAGAGAAACTTCCTTAATGG[T/A]ATTATTCAGACAGTGTCCTTTAAACTAATCRTCATAAATATTTTTAATRA
Long Flanking Sequence:
AATCTAAGCATTCTAGTGATCTCTGTGCTATGTTTGTTCAGGGTAAAATTGTAGCCCAGGGTCGACTGCTTCTTCAGGATACCTTCATGGTCTCAGATCAGGATGGTGGTCTTCTTTCTCGCTTGAAGGAGAGACGCATCTTCCTCTTCGAGCAGATAGTTATCTTCAGCGAGCCTCTGGATAAAAAGAAGGGATTTTCTATGCCAGGCTACCTTTTTAAGAACAGCATAAAGGTATGTAGGTATAACCACTGCTGTAAAAAAAAAACACTGTGGCACAACATAGACCTTATAAATCCATGTCACTCTTTTCCTGCAGGTCAGTTGGCTGGGTCTAGAGGAAAGTCCTGACAATGACCCTTGTAAGTTTATTTTGACCTCAAGGTCATCGGCTGGCAGTTTAGAGCATTACGTCCTCCATTCCTCCAACCGGGTGGTTTGCCAGACCTGGATCCACCAGATCAGCAGCATCCTGGAGAACCAGAGAAACTTCCTTAATGG[T/A]ATTATTCAGACAGTGTCCTTTAAACTAATCGTCATAAATATTTTTAATGATTATTAACTTTTGTAGCTTTGCTACATTCATTCAAGATGATTTGTTTGATGATTTACATGTTTTAACCAACCAGAGTTAGGTGTAATTAGTTACAAAGTAACTAACTACTGTAATTAAATTACTTTTCTGCTAAAAAGTAAACTATGGGATTCATTTGAACTTATCATGTACTTGCATTAAATGCATGTAAATAAATGTAACATTAGTGTATAAAGCAGAGGAAATATTTTTTGTTTTACAATATGTTTTGTCAAATAATTGTATTTTTAAGTAAAGAAGATTGAATTCATCTCTGATGATTATACATGACTAAATAAGTAAAGAAATTACAAAATATAAGGTATAGATTCAAAGAAGCAAAGTACATGTGTGTATTTATATACTAGGGATGTCAAAATGAATTGATTCATAGATGCACTGTGATGCAGACACAAACAATTCGGTATCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6408
Status:
Mutation detected in F1 DNA
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
ENSDART00000000382 Nonsense 2456 2996 51 59
Genomic Location (Zv9):
Chromosome 16 (position 10087119)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8870365
GRCz11 16 8768810
KASP Assay ID:
554-5284.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTGCTGTCAGAGTGAAAGCAGCAGCAGCAGCAGTGTGTCYACCATGT[T/A]GGTGACCCAGGACTACGTGGCTCTAAAGGAGGATGAGATCAGCGTATATC
Long Flanking Sequence:
CAAAGGTAAAATGCATGGACCTAAAAGTCAAACAACGATTTAAGTTTCTGTTAACCTACAGCACCTTAAGGGGAAATCCCACTAGAGGCAATTTTCAGTAATAAAAGGCAAGGAGTCATTCATTTTAAATAGAAGTAGGCTATCAGAGACAAAGTGATCAATAGACACGGTGAATAAATGCTCTAGCAAATATGAGTAGGGGTATAGACATCGAAACTCACACCATCCACCTCATGATACACTTAGTACAGCATCTAGATAACATCAAGCTCTTAATATGAACAACTCGTAGGAGGATCTTGTAAACTAAAATGACTTTGCTTTGTAAATAAACTTTCCTAGAACTGCTCTCACTTGCATCATTCTTGCTCTCTGGCATGTCCAGCTCACTAAATGTCTTGAAAATACTTCAAAATAACATCACGCTATTATGCTAATACTGTGTGTATGTTTCTGCTGTCAGAGTGAAAGCAGCAGCAGCAGCAGTGTGTCCACCATGT[T/A]GGTGACCCAGGACTACGTGGCTCTAAAGGAGGATGAGATCAGCGTATATCAAGGAGAAGTTGTGCAGATATTGGCGTCTAACCAGCAGAACATGTTTCTAGTATTCCGTGCCGCCACAGAACAAGGCCCAGCAGCTGAGGGCTGGATCCCCGGCTACGTTCTGGGTCACACCTCCATCATCATTCCCGACTACCCTGATGGAACCCTCAAGTGAGGATTGGATATTAATTGTTATATGTTATAAAGACTGTTATTTTATATTATTTGTTATAAATCTGACTCTTCAGTCAGATTTAAAGTGAAGACACACCATAAGTCTTTATAACTGGGTAAATTATGTTAACCAGTACTCATGTATCATGGCTGTAGCAGGCACAATGAAAATATGCTGCACATGGAAATAGTACCCAGTTAGCTAACTAGGTAAATTGTTAACCAGTACTTTCTTAGGTAAATACATTGTACAGTAAGTGCCAGATATGACTATGTTACTATTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42662
Status:
Mutation detected in F1 DNA
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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
ENSDART00000000382 Essential Splice Site 2769 2996 57 59
Genomic Location (Zv9):
Chromosome 16 (position 10080463)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 8863709
GRCz11 16 8762154
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGGACACCTACGAGACCCCAGCCAGCTATGTTCTCATCCTGGAGAT[G/T]TACGTGTAATGTATAGTCTTCACACAATTGACTCTAGAACTGTTACATGG
Long Flanking Sequence:
TCATCAGCCTACCTCAGAGTGCTCGGTCAGCTGACTTTATCAATCTGTTTATTAATCTTTTACTTTTTAGTTTTCTCCACGTTTGATAATTGAGTCTGTGACGTTGTTATTTTGTACATAGGCACATCCTGTGACGGAATTCTCTGGAAGGATAACTTTGAGTCTCTCTACACTGAAGTTATGGAGCTTGGGAGGTACTGTACAAATTAACTGCTGAATTAAAACACAACCTTCTTCTATGCAAACTACTGTACTTATGTTTTATAATAGCTAAAAATATGTTTGATGTTCCTCTTTAGAGGCAGGTTTGCCGTCACTAAGTGGTGTGAGCAGAGAGGAAGCAGGCGATCTGTGGCCGCAAAGCTCGTCAACAAGAAGCTAATGCGTCGAGAGCAGGTGGTTCAGGAGCTGGGGGTTTTACAGTGTCTTCAGCACCCTCACCTAGTGGGCTTGCTGGACACCTACGAGACCCCAGCCAGCTATGTTCTCATCCTGGAGAT[G/T]TACGTGTAATGTATAGTCTTCACACAATTGACTCTAGAACTGTTACATGGAACAAAATGACCAATTGCTGTTTTACACAGTATGTCTGATAATATTTTTTCTTCTTTAGAAAGTTGTATTTGATTTATTTTGGCTAGAATAAAATCAGTTTTTAATTTCTTATAAATCATTTTAAGGTCAATATTGTTAGCCACTTTAAGCTAGATTTTTTTCAATAGTCTACAGAACAAACCATCGTTACACAATAACTTGCCTTATTACCCTATTCTGCCCAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTTAGGGATGCCACAGTTCTCAATATAATATTGAACCGTACAGTACGACCTCCATGGTTCAATACGCGCTTGTGAATTGCGGTTTTCTCGGTTTTGCGTTTAAATAATTTATGTGCGTTTTATATCTCCCCGAATTGACTGTGTGTGCCTGTAAGTCCATGATCTGAGATAAGGAAACTCC
Associated Phenotype:
Not determined