Busch Lab

ZMP

tprb

Ensembl ID:
ENSDARG00000016630
ZFIN ID:
ZDB-GENE-030131-6410
Description:
nucleoprotein TPR [Source:RefSeq peptide;Acc:NP_001025294]
Human Orthologue:
TPR
Human Description:
translocated promoter region (to activated MET oncogene) [Source:HGNC Symbol;Acc:12017]
Mouse Orthologue:
Tpr
Mouse Description:
translocated promoter region Gene [Source:MGI Symbol;Acc:MGI:1922066]

Alleles

There are 15 alleles of this gene:

Allele Name Consequence Status Availability
sa37090 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39290 Nonsense Mutation detected in F1 DNA Not yet available
sa29399 Nonsense Mutation detected in F1 DNA Not yet available
sa37089 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa37088 Essential Splice Site Available for shipment Available now
sa23754 Nonsense Available for shipment Available now
sa43486 Nonsense Mutation detected in F1 DNA Not yet available
sa14064 Essential Splice Site Available for shipment Available now
sa18388 Nonsense Available for shipment Available now
sa45709 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23753 Nonsense Available for shipment Available now
sa32305 Nonsense Available for shipment Available now
sa23752 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa37090
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Essential Splice Site 86 2352 2 50
ENSDART00000109614 Essential Splice Site 86 2316 2 52
Genomic Location (Zv9):
Chromosome 20 (position 34094027)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34166540
GRCz11 20 34069419
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCAGACTCAAGAACATCAGATCCTGAAAGAGGAGCACTATAAATTGGG[T/C]AAGTAGGTGTCAATCAAATGTCTATATTGTATTGTATTTAGAATTTGAAT
Long Flanking Sequence:
GTGTTGCAGCAGATACTTGAGCGGTCGGAGATATCGAAACTCCAAAAAACAGTTTTGACTAAATTAGAGAAGTACATTTCTGAGCAGCAATGTGAAGTTGATGACCTCAAGGCACAACAGGAGCAATTTCGTGTGGATAGCGGTAAGGCTATGCTATTTTAGTCAATGTAAACAGTTCATAGTCACGAACGAGGCCTGGGTCTGGTTATCTTGAGGTAATTTGTATGATGTTGTTTACGTTAATTCTTGGACGTGTTGTTCTGCAAACTATAACTAGTAAACAATTGTTACAATTAAATTCATAATCTAAATAATTTTTTTCTGTCCACATTGTTACCGTGCACTTGTTTGCAGGCATGTTAATGTGTTTTGGTATTTTACTTTTTTAACATAGAACAACAGTATTTTGACATCGAGAAAAAGTTCGCAGAGAGTCAGGCTCAGTTTGTGTCCCAGACTCAAGAACATCAGATCCTGAAAGAGGAGCACTATAAATTGGG[T/C]AAGTAGGTGTCAATCAAATGTCTATATTGTATTGTATTTAGAATTTGAATGTTATGCTTAATTGTATTTGCTCTTTTCGATTACAGAGGATGAGCTGAAATGTTTAAGAGAGAACAATAAGGAGCAAGCAGCTTCATACGCCAAACTAGAATCTAAACAGGTAAAATTTTACATGACAGTTTGCTAGAGGAGAAGATCTCAGTGTCTTCTTGAGGTGTGTGATGAGACTAGAAAGACTGTGCCTTGTTTGCAGAATGACCTTTCCAAAGCCAAAGATGAGCTCGAAGCAGAAAAAAGAGAGCTGGTCCGTACACTGGAAAGAAGATCTCAGGAGATGGAACACCAAAGCGGTATTTAAGTATTATTTAAGAAACTTTTTTTATTGTAATGTTGCACTGTAATACTGAAAGGGCAGATTTTGTTTGGACGTCTTGTTTACATACACTAAAATGTTTACACAGATTTATGTTTTGATTTTGAATCAAGTTCGGAATTTGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39290
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
ENSDART00000017941 Nonsense 151 2352 5 50
ENSDART00000109614 Nonsense 152 2316 5 52
Genomic Location (Zv9):
Chromosome 20 (position 34092927)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34165440
GRCz11 20 34068319
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATTATTATTATTGTTGTTTTACAGAGGACCTTAAGCGTCTTAATGAT[C/T]GATTGGTGGAAGTCAGTGCAGAAAAAATGCAGCTTCAGCTCAAACTGGAG
Long Flanking Sequence:
AATTAGATTGTTTATTAAAGTTACAAGATAAAGATATTAACTATCATTATTTATAAAATTATGATCATTATATTTTACATTTGATTGTTTCATTTCTGTACTTGGATACTGTTAGGCTTCCCAGAAAACCTTAAAGCACTGTTTATTTATTTGTTTTTCCTTGTAATTAATTATTATTTATGCAAATCCACTGCAAAGAATCATCTCAATCAATCTAAATAATGAAATCTTTCCAAATAGAGCTATTCATATCATCTGCTGAGACTATATTCATACAATATATGCTGCGAAACAACATATTGCAATGTCAGATCTTTCCAATATCGTGCAGCCCTACTTGTTATCAAAAACAGAATGAAATTAAATTAAATGCAATGTAAAATAACTATTACTATTTTAAAAATCCTGCGTAAGCATATTTCAAAAGAATGGCCTTTATTTATTTATTTTTTAATTATTATTATTGTTGTTTTACAGAGGACCTTAAGCGTCTTAATGAT[C/T]GATTGGTGGAAGTCAGTGCAGAAAAAATGCAGCTTCAGCTCAAACTGGAGGAGTCAGAAACCTCTGAAGTTTCAATCAAGGTAAAAAAAAAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACGTATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTTACGTATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTATATATGTGTGTATATATATATATTTATATATGTATGTATATATATATATTAAGGGTGTAACTTTATGCGTATTCGTATTGAATCGTTCGGTACGCATTGCAAACCGAACGATTCAGACTAAGATCTAAAAAGATATAAGACAATACGTTCAAAAAAGCCAGCAATGCTTGCCCCGCCCTCAAGCTCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29399
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
ENSDART00000017941 Nonsense 161 2352 5 50
ENSDART00000109614 Nonsense 162 2316 5 52
Genomic Location (Zv9):
Chromosome 20 (position 34092897)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34165410
GRCz11 20 34068289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTAAGCGTCTTAATGATCGATTGGTGGAAGTCAGTGCAGAAAAAATG[C/T]AGCTTCAGCTCAAACTGGAGGAGTCAGAAACCTCTGAAGTTTCAATCAAG
Long Flanking Sequence:
AAGATATTAACTATCATTATTTATAAAATTATGATCATTATATTTTACATTTGATTGTTTCATTTCTGTACTTGGATACTGTTAGGCTTCCCAGAAAACCTTAAAGCACTGTTTATTTATTTGTTTTTCCTTGTAATTAATTATTATTTATGCAAATCCACTGCAAAGAATCATCTCAATCAATCTAAATAATGAAATCTTTCCAAATAGAGCTATTCATATCATCTGCTGAGACTATATTCATACAATATATGCTGCGAAACAACATATTGCAATGTCAGATCTTTCCAATATCGTGCAGCCCTACTTGTTATCAAAAACAGAATGAAATTAAATTAAATGCAATGTAAAATAACTATTACTATTTTAAAAATCCTGCGTAAGCATATTTCAAAAGAATGGCCTTTATTTATTTATTTTTTAATTATTATTATTGTTGTTTTACAGAGGACCTTAAGCGTCTTAATGATCGATTGGTGGAAGTCAGTGCAGAAAAAATG[C/T]AGCTTCAGCTCAAACTGGAGGAGTCAGAAACCTCTGAAGTTTCAATCAAGGTAAAAAAAAAAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACGTATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTTACGTATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTATATATGTGTGTATATATATATATTTATATATGTATGTATATATATATATTAAGGGTGTAACTTTATGCGTATTCGTATTGAATCGTTCGGTACGCATTGCAAACCGAACGATTCAGACTAAGATCTAAAAAGATATAAGACAATACGTTCAAAAAAGCCAGCAATGCTTGCCCCGCCCTCAAGCTCTCCTTATTGACCCACTGCAGTAGAATAGAATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37089
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
ENSDART00000017941 Essential Splice Site 465 2352 12 50
ENSDART00000109614 Essential Splice Site 466 2316 13 52
Genomic Location (Zv9):
Chromosome 20 (position 34088500)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34161013
GRCz11 20 34063892
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACG[G/T]TGAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTT
Long Flanking Sequence:
GTTTGCTTTTTACTGTTTTTTTATGTTTATTTCTGCAACTTTGACTAGTGGTTTTTGATATAAAATGTATACAAGTTTTTCATTTGCCACTCCAGGAGCTGCTTCAATTCTTACAGAAGAGCAGGTGACCATAATGTCCCCCACTGCTGCTGCAGTTGCCAAAATGATCAAACCAGGCATGAAACTCACAGAGGTGATAACCTTACTTCTGATCAGTTATACCAGTCTAAGGTTCATTTTCATAAATCATTTTTATGAGGTAAAGTAAGCTAATGCACATTTTCCAATTTTTTTTTTTGTAGATCTATACCGCATACGTTGAGACCCAAGAGCATTTACAGCGTGAAAAACTCGAGAACAAGCGACTGCACAAGTACCTGGATGACATTGTGCAGGAAATGGAAGCAAAGGCTCCTATACTGAAAAGACAGAGAGAAGAGTACGAGCGCATGCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACG[G/T]TGAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTTTATATTTATAAAACCAAATCTACAATTGTGTATTTTTTGGTACTTTTCAGGAGGTACATCGCTTGCAAAAAGAATCGGATGAAAGCAACAAGCGTGCATCAGTTTTGGAAAGAGATAACCAGAGGTTTGAGGTTCAGCTGGCTGACATGGCTCAACAGGTGAGGCCTGGAGGCACAACTTTGCGATCAGTGTTTCATGCCAGAGCAAAAAAAAAAAAAAAAAGATCTAAGTTACAATAATTTTAACATTGTAATCTCAGGTGCGAGTTCTTCTCGTTGAGCTGGAGGAAGCACGTGGTAACCATGTTATGCGGGAGGATGATGATGTGGGTTCGGCAGATGTGAGCAGCACATCGGAGGTTATTTCTCAGCACCTGGTCACTTTCCGTAGCGTTGAAGAGCTGCAGCAGCAGAACCAGCGACTCCTAGTGGCGCTCAGAGACCTTAGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37088
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
ENSDART00000017941 Essential Splice Site 465 2352 12 50
ENSDART00000109614 Essential Splice Site 466 2316 13 52
Genomic Location (Zv9):
Chromosome 20 (position 34088499)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34161012
GRCz11 20 34063891
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACGG[T/C]GAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTTT
Long Flanking Sequence:
TTTGCTTTTTACTGTTTTTTTATGTTTATTTCTGCAACTTTGACTAGTGGTTTTTGATATAAAATGTATACAAGTTTTTCATTTGCCACTCCAGGAGCTGCTTCAATTCTTACAGAAGAGCAGGTGACCATAATGTCCCCCACTGCTGCTGCAGTTGCCAAAATGATCAAACCAGGCATGAAACTCACAGAGGTGATAACCTTACTTCTGATCAGTTATACCAGTCTAAGGTTCATTTTCATAAATCATTTTTATGAGGTAAAGTAAGCTAATGCACATTTTCCAATTTTTTTTTTTGTAGATCTATACCGCATACGTTGAGACCCAAGAGCATTTACAGCGTGAAAAACTCGAGAACAAGCGACTGCACAAGTACCTGGATGACATTGTGCAGGAAATGGAAGCAAAGGCTCCTATACTGAAAAGACAGAGAGAAGAGTACGAGCGCATGCAGAAATCAGTTTCCAGTCTCTCTGCTAAATTAGAGCAAGCTGTCACGG[T/C]GAGAATTGAAAAGTTTTATTACATGTCACATTACCAGATGATTACTTTTTATATTTATAAAACCAAATCTACAATTGTGTATTTTTTGGTACTTTTCAGGAGGTACATCGCTTGCAAAAAGAATCGGATGAAAGCAACAAGCGTGCATCAGTTTTGGAAAGAGATAACCAGAGGTTTGAGGTTCAGCTGGCTGACATGGCTCAACAGGTGAGGCCTGGAGGCACAACTTTGCGATCAGTGTTTCATGCCAGAGCAAAAAAAAAAAAAAAAAGATCTAAGTTACAATAATTTTAACATTGTAATCTCAGGTGCGAGTTCTTCTCGTTGAGCTGGAGGAAGCACGTGGTAACCATGTTATGCGGGAGGATGATGATGTGGGTTCGGCAGATGTGAGCAGCACATCGGAGGTTATTTCTCAGCACCTGGTCACTTTCCGTAGCGTTGAAGAGCTGCAGCAGCAGAACCAGCGACTCCTAGTGGCGCTCAGAGACCTTAGTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23754
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Nonsense 1033 2352 23 50
ENSDART00000109614 Nonsense 1034 2316 24 52
Genomic Location (Zv9):
Chromosome 20 (position 34085235)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34157748
GRCz11 20 34060627
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACAGAACTTGCTGGAAGAGAAAAACAAAGCTGTTGCTGCTGTAGAG[C/T]AAGAGGTAGTGAATTTACACCTTGGATCACTACATTTTACCTGTTTAAAA
Long Flanking Sequence:
GCAGGGCAGTGAGAGGGACATGGAGGTTCTGCGTGCCCAGATAAGGCAGACTGAGAACAGAATTGAAGAACTGACAGAGCGACTTAAAAACACTACTGCCAGTATGGAGCAATACAAGGCTATGAGTCTTAGCCTGGAGGAGTCTCTAGATAAGGAGAAGCAGGTAGTTAGACATTTTCATTTATTCATTTTTTTTTTCTTCGGCTTAGTCCTTTTATTCGGTGTATATGAATATCACATCAAATCACAGTGCTTGGCTATTAAAGGCTGGCTTAGAGTACATTTTTATACTACAATTCATTGGCACTTTTGTTTGATTTTTAGAATTTTGTTTGTTTGTTTCCCATTTCTAGGTAACTGAGCAAGTTCGTTCATCTGTAGAAAACCAAGTGGAGGCAGCTCAGGAGCAGTATAAACGGCTAGAGCAGAAACTGCTGGAAATGGACAAGGAGAAACAGAACTTGCTGGAAGAGAAAAACAAAGCTGTTGCTGCTGTAGAG[C/T]AAGAGGTAGTGAATTTACACCTTGGATCACTACATTTTACCTGTTTAAAAAAAGGCCTGTTTTTTTATTAATGGCTGTCCTGTGCAAAACGATAATCATTTTAAGGACCTCTTAAAGTGACTGTTCACTGAAAATTCTGCCATAATAGTCACATTTGACTTGTTCTAATACACTTAGAATTTTTATGTTCTGCCAAATTATGTATATTTTAAAAACTGTTGGAAGCCTGTAACCACTGAATACCATAGTAAAGAAAACAAATACTATAGAAGTCAACTGTTACAGGTTTCCAACATTTTTCAAAATATATTTTTTTTAGTTTTTAGCAACTGCTTTGTAGCAAGACATGGATAAGTGAAGGATGGCAGAATTTCATCTTTAAGTGAACTTTAAGATTACATTAGCCATGTTTCCATTCAAAGATGAGATTTAAATTCATGCACAAAACTGGATTATCACATTAAAGACTTTCAAATAAAGCAGCTTTTCAATCCAATGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43486
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Nonsense 1357 2352 29 50
ENSDART00000109614 Nonsense 1349 2316 30 52
Genomic Location (Zv9):
Chromosome 20 (position 34081072)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34153585
GRCz11 20 34056464
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTTAGCACCTGGTGAGCCAGCAAAAAGACACTGACCCGGAAGAGTA[C/A]AAGCGTCTGCACTCTGAGCGGGAAGCACATCTTAAACGCATCCAGCAACT
Long Flanking Sequence:
AAGTGATCCACCCAAAAATGAAAACTCTCTCCTGTTTTAATCCTTATTGAGTTTTTTTTTTATTCTGTTGAACACTAAAAAGGATGATTTGAGATTTGTTGGAAACCTGTAACCATTGATTTCCAACAAATTATGAGTAGTCGTGAGTAAATAAATGACAGAATTTTCATTTTGGGGTGAACTATCTATTTAAAAATGAATGGCAAAAGTTAGAACTACTGTTTTTGTTCACAGATACGTAAACTAGAGTCCGACATCATGCCGGTGCAGGAGTCCAATTCAGAGCTGAGTGAGAAGAGTGGCATGCTTCAGGCAGAGAAGAAACTTCTGGAAGAAGACATCAAACGCTGGAAAGCTCGCACTCAGGTCAGAAGCTTTCATGTATCTTCAAGTGATTTCTGCAGAAAATATTTTTCATAGACATTAACTGTCTTGATTATGCATTCTCATGGTGTTTAGCACCTGGTGAGCCAGCAAAAAGACACTGACCCGGAAGAGTA[C/A]AAGCGTCTGCACTCTGAGCGGGAAGCACATCTTAAACGCATCCAGCAACTTGTTGAAGAAACCGGCCGACTAAAAGCTGATGCTGCCAGGTTAAAACAGCTCTCTTCACAGGATTCACCAAAGCCTTGTTTTTCGTTTTTGTGTATTGATAAATGACTTGTTCTCTACAGGAGCAGTGGCTCTTTGACTACTCTGCAGTCTCAAGTGCAGAACCTAAGGGAGAACCTCGGAAAGGTGATGGTGGAGAGGGACAACCTGAAGAAAGACCAGGAGGCCAAAATACTGGACATCCAGGAGAAAATAAAAACCATCACACAAGTTAAAAAAATTGGTCGTCGGTATAAAACACAATATGAGGAGCTCAAGGTTGAATATGAAAAGGTGTGAAGTCAAGGCTTATGATTAGGAGCATGCAAGTATGTGTTTGGTGTGGAAGTCTGTGTTAATTGTGGTCTTTGTGTAGTTGGTAGCAGCGGCGGCATCTGCACCAGCCCAGGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14064
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
ENSDART00000017941 Essential Splice Site 1573 2352 32 50
ENSDART00000109614 Essential Splice Site 1565 2316 33 52
Genomic Location (Zv9):
Chromosome 20 (position 34079105)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34151618
GRCz11 20 34054497
KASP Assay ID:
2261-4611.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAAGAAGGCCATATTAWTGGCCAAGCAGAAGATCAGTCARCTTACTGG[T/A]GAGAACTGACTCTTTTTGAGAWTAGTATGTGCTTTKAGTCTTTTTCTTTT
Long Flanking Sequence:
AACATTTGACCTGAAGAGATCTTATTTGTGGGTTTTTTTAATACCATTAATTGTTTAAAAACAATTGTGCCAGTGTTCGATCCAAATCAGTTCTTAAAAAAAAATAATATTATTGATGATAGACCTGCTTTCTGCTTACTGACTGGTTTGCTGTTTATCAATCAAGTAAAATATAGCTTGGCATCCCTGTTTTTCTTGTGTGTCTTTGCACATCCTCCCTTACAAACTGAACCTTTTGAGATGAGACTAAAGTTATCGGGTGTCTTTCTCATAATGTGTCATTTCTGTTGTCCTCTGCAGACTGTAGGAGAGCGAGAAATGGAGGCCCGCAGTGCGCAGGAACAAGCCTCTCGTTTGCAGACAGAGTTAACGCGTCTCAGACAAGAGCTTCAGGAGAAATCATCTCAGGAGGAGCGTCTCAAACAGCAGCTGACTGAAAAGGAGGAGAGGACCAAGAAGGCCATATTATTGGCCAAGCAGAAGATCAGTCAACTTACTGG[T/A]GAGAACTGACTCTTTTTGAGAATAGTATGTGCTTTTAGTCTTTTTCTTTTCTTTATTATTTTTCTACATCCAGGTATAAAAGGACAGTTTCAGAAGGAGAACGAGGAGCTGAAGCAACAAAAAGAGGAGTTGGAAGTGCGTGTGAGTGCGCTGAAGTCTCAGTATGAGGGGCGTCTGAGCAGACAGGAAAGGGAGCTACGAGACCTTCGCGAACAGCAGGAGAGACATGGAGAACAGAGGGATGAACCACAAGAGCAGGGCTCCAGCAAGGTAATGCCACACAATCCTATAAATGCAAGCCTATTCGTAGTTTTCAGTCAGGTGATCTGGAGTGTAAAACGTCTATACAACTGTGATAAACACCTTACCATTAGTTTCAAGCCACAAATATTTGGATCAGCCCTCATAAGAAAAAAAAAATGGGGCCAGTAAAATCTTTTAGATGCTTCTGATCCTTATACACTACTTTCCGTCACTAAATATTAAGCTTAATCTGGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18388
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Nonsense 1615 2352 33 50
ENSDART00000109614 Nonsense 1607 2316 34 52
Genomic Location (Zv9):
Chromosome 20 (position 34078906)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34151419
GRCz11 20 34054298
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTGAAGTCTCAGTATGARGGGCGTCTGAGCAGACAGGAAAGRGAGCTA[C/T]GAGACCTTCGCGAACARCAGGAGAGACATGGAGAACAGAGGGATGAACCA
Long Flanking Sequence:
GTGTCTTTGCACATCCTCCCTTACAAACTGAACCTTTTGAGATGAGACTAAAGTTATCGGGTGTCTTTCTCATAATGTGTCATTTCTGTTGTCCTCTGCAGACTGTAGGAGAGCGAGAAATGGAGGCCCGCAGTGCGCAGGAACAAGCCTCTCGTTTGCAGACAGAGTTAACGCGTCTCAGACAAGAGCTTCAGGAGAAATCATCTCAGGAGGAGCGTCTCAAACAGCAGCTGACTGAAAAGGAGGAGAGGACCAAGAAGGCCATATTATTGGCCAAGCAGAAGATCAGTCAACTTACTGGTGAGAACTGACTCTTTTTGAGAATAGTATGTGCTTTTAGTCTTTTTCTTTTCTTTATTATTTTTCTACATCCAGGTATAAAAGGACAGTTTCAGAAGGAGAACGAGGAGCTGAAGCAACAAAAAGAGGAGTTGGAAGTGCGTGTGAGTGCGCTGAAGTCTCAGTATGAGGGGCGTCTGAGCAGACAGGAAAGGGAGCTA[C/T]GAGACCTTCGCGAACAGCAGGAGAGACATGGAGAACAGAGGGATGAACCACAAGAGCAGGGCTCCAGCAAGGTAATGCCACACAATCCTATAAATGCAAGCCTATTCGTAGTTTTCAGTCAGGTGATCTGGAGTGTAAAACGTCTATACAACTGTGATAAACACCTTACCATTAGTTTCAAGCCACAAATATTTGGATCAGCCCTCATAAGAAAAAAAAAATGGGGCCAGTAAAATCTTTTAGATGCTTCTGATCCTTATACACTACTTTCCGTCACTAAATATTAAGCTTAATCTGGTAAGAAATTAATATTAATGCACATAAATGTGGATGTATATGTATATATAATATAATTTTATAGGGTATTTCTCTTTGACTTCAAGCTATTAACCATCTTTAGATACCTAATGTTCTTTTACTTTCAAATGCTTCAAAATGCTGTTTTTTTCCATGTTTAAAGACCCAGGAACCACAAAGGACAACAGAACAGCGACAGATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45709
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Essential Splice Site 1729 2352 35 50
ENSDART00000109614 Essential Splice Site 1721 2316 36 52
Genomic Location (Zv9):
Chromosome 20 (position 34076906)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34149419
GRCz11 20 34052298
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCCACTGCCACAGTCATGCCCACCACACAGGTGGAAAGCCAAGAGCG[T/C]AAGTGAGGTTTTTTTGTTGTACTCATTTATTTGATGGTTTGGACCAGGGT
Long Flanking Sequence:
ATATTTTTTTGTTTATCTTGATTTTTGCAATTTATGAAGATTTTATTTAATATTTTTCTATAGCATACATTTTGGCTACTAATGTTTGAACCATTATTGTTTGTTTTTATGTTAGATTAGCTCCAGATTTGGCTTCAGTACTGACTAAACTAATGTATATGCGCACATATAATATTGTACAGCATCCTATAGAAAAAAATAATTTAAATGAGAGATTTATGGGGGGTGTACTCATATATGCTAAGCACTGTATTTTAAAAAATCAAGCTTCTCCACATTGTTGCTTTTTTTTTTTTTTTTAGTGCTAGCACTTCTGAGCCCCCAACAGCCAACATAAAGCCCACACCTCTGGCAGCAACCCCCAGCAAGCCTCAAGTCATTCCTGGAAACAAATCCACTCCAAGAGCCAGCATCAAACCCATGATCACTCCTGCCCCGGTGCCCACTCCTACACCCACTGCCACAGTCATGCCCACCACACAGGTGGAAAGCCAAGAGCG[T/C]AAGTGAGGTTTTTTTGTTGTACTCATTTATTTGATGGTTTGGACCAGGGTTGTTGTTTTTAACTAAACCATAAAATATACTAAATAAAAAAACATTTAAATAATTAAATATATATATTTTTAATAAACTGGGAAAAAAAGGTTTTGTTGACAACTACTTTTCTATTTTGTTCTGTATAAAATAGCTAAAACTGAAAATATAAAACATGATTAATGATAGTTTGTAAGTAAAGTAATCCAACTGATTAAATTAAGAACCAAAAATGGCAAACAATTCATAAATTTATTTCAAGTTTTTCATTTTTTGTGTGCTTACAAAAAAAAAAATTAAAACCCTTCAAGTTATCTTTTAACTTTAAATTTTTTTTCCTAAACTTGCAGCCATGCAGTCCTCAGAGTCCCCATTGGAGCATGTGACTGTGTATGGCAGTGCCAGTGGTTCAGTAAGGTCCACGAGCCCTAATGTTCAGACCACCCTGGCTCAGCCTCTGCTGAACGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23753
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Nonsense 1929 2352 39 50
ENSDART00000109614 Nonsense 1921 2316 40 52
Genomic Location (Zv9):
Chromosome 20 (position 34073698)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34146211
GRCz11 20 34049090
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGAAATGGATGAGGAACCAGGACCATCTCAGTCTGTCCCTGGAGAT[C/T]GAATGCTGCCCCATCCATCTGAGACCCATCGAAGCCCAGAGGAGCCCGAT
Long Flanking Sequence:
GTTAAAGATGTTGTGTGTTTCATTTCAAGTCCATCATGTTGGTGTATAGAGCCAAAACTTTTTTGTGAATTGTGCAGATGTCCCAATATTTATGGACCTAGCTGTATATATGAGTGAATCATCTCTATATGAGCAAGTTTTAGAAGCATTTATTATCATTAAGATTAATTTACTACTTAAGTGAAGTCTTTAATCAAGAGGTAGTTCAAAAAAGCTGAATCATCCAGTAATGAAATGAGTATTGACAAGTGAGTCGTTGAATCAATTAATAAAAAGCTTTTTAGTTATTTATTCTGAATTGTGGGAAACTCACAGTCTCAAATGGAAGCAAAAAAAAAAAGTGCTTTAATCCAAGATCAGTTCCGGTGAACAGGTCAGAAGTGTGTAACTGACTTAAATGTTTTTTTTCTTCTCATGTCTGTTTGAAGGAGCTGGAGAACTACTCTACTCTGGAAGAAATGGATGAGGAACCAGGACCATCTCAGTCTGTCCCTGGAGAT[C/T]GAATGCTGCCCCATCCATCTGAGACCCATCGAAGCCCAGAGGAGCCCGATCACCACGTCATAGTCATTGTTAGTGACACCGAGAGCGAAGGAGAACAGGAAGAGGAGTCTGAGGAGGAGGAGGAGGAAGAGGAAGAAGAGCAGGTGTGTCCTCGCACTGCAGGTCAAATTCAGTGATATTCAATCCTGTTATATAAACCACTTATCCCTGCTTTAGGATTATGAGGAGGAGGATGAGGAAGAGGAGGAAGAAGATGATGATGATGATGAAGAGGATGGAGGGATTGGGGAAGAGGGAGATGAAAGCAATGAGGAGAGTAGAGACGACAATGAGGCCTACGAAGGAGATGACACAGAGGTAAAGATCTGCACTAGTCAGAATTTAGAAGTGGAGGTTTAAAATTATAAAACTGAGGTCTCGTTTACACTAATACATTTTAGTTTAAAAATAAATAAGTTTTGCTACGGTTACGCCTTTCGTCCAAACTACCCTGGAGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32305
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
ENSDART00000017941 Nonsense 2201 2352 46 50
ENSDART00000109614 Nonsense 2165 2316 48 52
Genomic Location (Zv9):
Chromosome 20 (position 34066676)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34139189
GRCz11 20 34042068
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTTTTGTGCTGTGCAGGTTTAGGCATGTATGAGAGCTCTGTTTTTT[T/A]GGGATCTCATGAGGATGAGTCAGGGGGACGCAGTGTACCCACAACCCCTC
Long Flanking Sequence:
ACCCAATGGTGAAAAACTTGAAAGGCTGATGACTTTTAATTTGCATGTTGTTTATGTATTATTTTTATCTTCTGCAGGTTATGGGTAAAACATGGTAATTCTAATAGTTTGAGAACATGTATGGTAATATTGGAAATCACCAATCTACAAACTGTATATCAGTGTCAATTGTCATGACCAGCTACTACTCATCATGTCATGTTTGCTGTTGTGTTTTGTTATTATTACTTAATCATATTACCACAAAACTGATTTGTTGTTGTCGAATGAAGTTCTCCACAGGTGGCAGGTGTACCACGCTTTCGATTCGGGCTTTTAGATGAGCTCCCGCAGACCAGCTCCTCTCACTCAGACCTCAGTCAGCTGCCCTCACAAGGTCAAACACAATCATTTTAAATTTAGAGATTATCAATTATAATGTCAAACATTAGTTTGTTCAGTTTTTTAAAGGTGTCTTTTGTGCTGTGCAGGTTTAGGCATGTATGAGAGCTCTGTTTTTT[T/A]GGGATCTCATGAGGATGAGTCAGGGGGACGCAGTGTACCCACAACCCCTCTGCAGATCAGCGCTCCTGGTAAATAACGCATGTTTTCTTATTTAGTTTTTTTTAGTCAGACTTTCTTGTTGTTCATCATTTAGGCAGAGTTGTAAAATTCTGTTATGATCTATTATAACCTGTTTATTTATTTAATTATTTTATGATAATTAGATATTTTAATAGCTTCTCTTTTCATTTACATTTATATATAATATTGAACATGCAGGATGAGCATAGACTATATTTTACATCCATCTATTTAGAACTGATAAATAAAGTCTGTGCATCATTGTGTGTGTGCGTGCGCATATCAGTACACAAGTAGTGGTAATAATTTCAAACATTTCAAATTTGTTCAGACCAGAGGTTTTTATTATAGGGGGGTAATTCCCGTTTATAAATGAGTATATAAAACTTTCTGGTGCATAGTGGTGTAACGGATCACAAATCTCACTGTTCGGATCACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23752
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017941 Essential Splice Site 2339 2352 None 50
ENSDART00000109614 Essential Splice Site 2303 2316 None 52
Genomic Location (Zv9):
Chromosome 20 (position 34064252)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34136765
GRCz11 20 34039644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGACAGTGGACTGGTAGTCGAGGTTCTAGAAGCATTGTGAAGAGGGG[T/A]GAGACTTTTGTTTCTTATTTGTTAGTTTCTTAAACTTTTATTTCCTTCCT
Long Flanking Sequence:
ACATGCTTCTCAGTCTGTGCCGATGGTGAGCACCTCTACCCCAGGCCTCAGTGCTCCAGCAGTGGAGGAGAGAGACGACATGTTCCTGGATGCAGGAGACAGGTGAGATTTTTGAGTTTTGAGACTTTTCAACATTTTCTCTTATGATTTTGCCATGACAAGAATCCATATATATTAGTATTTAATGGGAACTTTGATAAATGTTTGTGCAGTGCTGAAGCTTCACTTGAGGCCGTGTCTCAGACTGAGGCAGAAGAAGCAGCGCAGCCTTCAGATGATGCAAATCTGCCTTCAACAAGCCAGGAACCATCATCTAGTTCAGCAGGTACAAACACAATAATATTAGACAAACCACATGCAATCTCTTATTTCTGTTTCACTAACTATGTGTCTCGCTTTTCTCTTTCAGACACAAGCAGCTCTCAGCCTCCTAAAGCCAGGAGCGGCTCTGGCAGACAGTGGACTGGTAGTCGAGGTTCTAGAAGCATTGTGAAGAGGGG[T/A]GAGACTTTTGTTTCTTATTTGTTAGTTTCTTAAACTTTTATTTCCTTCCTTCCTTCATACATTTTCGCTTTTAAGCGGGCTGCATTTACAAAGTATAATTTTAACATCTTTCTTGCTATAGATGGACTGAGTGTTATGGGTGTGAGAGGACGCTTTGCCAGATGAAGCAAAATCCCAGCAGTCTTCATTCTAGTCTTCATCCTGAACTATTGGCTCCACAAGAACAGCTGTGCTTTATTCTGCTTCAGGACTTCAAGTCAGTGTATTATAGCTGTCGTTTGTTAGTTGTATGCTCTGAGCAATCCATTGTTGTTATTTTTAATGATTCTACATCCATAAAATAAATTGTTTTGAAGAAAGAGATTTTTGTTTTGTCTGTGAAGATGTGACCGGTTGTTTTCCACTGCATATTAGACGAGTGCATGAACATGTACTGTGAATGGCAGGAGGTAAGGAGATGGATGACTCAGATTTTCTGAGTGTCTTTGCATTTGAAGAAG
Associated Phenotype:
Not determined