Busch Lab

ZMP

dopey1

Ensembl ID:
ENSDARG00000019962
ZFIN ID:
ZDB-GENE-050309-65
Description:
Dopey1 protein [Source:UniProtKB/TrEMBL;Acc:Q5BLI9]
Human Orthologue:
DOPEY1
Human Description:
dopey family member 1 [Source:HGNC Symbol;Acc:21194]
Mouse Orthologue:
Dopey1
Mouse Description:
dopey family member 1 Gene [Source:MGI Symbol;Acc:MGI:1289294]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa25024 Nonsense Mutation detected in F1 DNA Not yet available
sa2859 Essential Splice Site F2 line generated Not yet available
sa5625 Essential Splice Site F2 line generated Not yet available
sa16205 Nonsense Available for shipment Available now
sa9700 Nonsense Available for shipment Available now
sa36196 Nonsense Mutation detected in F1 DNA Not yet available
sa12398 Nonsense Available for shipment Available now
sa14239 Nonsense Available for shipment Available now
sa36195 Nonsense Mutation detected in F1 DNA Not yet available
sa39117 Nonsense Mutation detected in F1 DNA Not yet available
sa13013 Nonsense Available for shipment Available now
sa42769 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25024
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
ENSDART00000010778 Nonsense 162 2477 3 37
Genomic Location (Zv9):
Chromosome 16 (position 35408187)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33140496
GRCz11 16 33094526
KASP Assay ID:
554-7851.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTCCTGACTGGGGTGCTACCTGGACTGGAAGAGGGCTCAGAGTATTA[T/A]GACAGGTAAAATGAAGGTTTTTAATCTAGAACTGATTCTAAAATGAGCCA
Long Flanking Sequence:
AAGGTATTCTTCTGAAGGCATTTAGAAGTAGTTCATTTAGAAGTTGCATTACTAATCTTATTTTTTTCACAGGTCTTGCAAAACAATGGCAAGTATCAGGTTGTGCCCAAGAAACTGACCATTGGAAAGCGTCTGGCCCAATGCCTCCACCCAGCGCTGCCCAGCGGGGTTCACCGCAAGGCTTTGGAGACCTACGAAATCATCTTCAAGATCATTGGACCAAAGCGCCTGGCGAAGGATCTTTTCCTCTATAGGTAGAGATTATGCAGGATTGAATTTTTCTGCTACTGTAAATTTAAGTGGTTAATATGTCCTTTTATCCCCCTTCTCCTCAGCTCTGGGCTCTTCCCTTTATTATCCAATGCTGCTATGTCTGTGAAGCCAGTATTACTTGGGTTATACGAGACCTACTACCTGCCATTGGGGAAGACTCTTAAACCAGGCTTGCAGGGACTCCTGACTGGGGTGCTACCTGGACTGGAAGAGGGCTCAGAGTATTA[T/A]GACAGGTAAAATGAAGGTTTTTAATCTAGAACTGATTCTAAAATGAGCCAGTTTTTATGCCTGCCAATACTGCATTTATTTGATTCAAAATACATTAAATAAACAGATATTTGCACGTTCAATTTGAGACCTACAGTGCTATTTAATTGGTAATTTGCTTGTGTTTTAAAAAGATTATGATAATTACGTGATAATACATTATATATAAGCAAAGTGAGCATGCACAATCAAATATTATATATATATATATATATATATATATATATATTCATAGCCCAAATTATTAGCCCACAACTGATAATTTTTCTGAAGTGCATCTCAAATTTTAGCACTTCACAATAATTTTCTTTTCGTACTACATTAATTTACATTGGAAATATACCTCTGATGCTATGCTGTGCGTGACCAGTTGTTAACTATTAATGTTTTATTTCAACATTGTATTACTAAGTATTATTTTATGGAACCCAGCTAGCATAAACTAACAATGAACTGTATGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3959
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010778 Nonsense 481 2477 11 37
Genomic Location (Zv9):
Chromosome 16 (position 35402479)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33134788
GRCz11 16 33088818
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACATCAGCACGCTCATTGGTTGAGTTTTGTGAGCTGGTGGACTTCTTGT[T/A]GGACATTGTGTCTTTGGYTGGTAAACATTGGATATGATGATTTATCTACT
Long Flanking Sequence:
CATTTAGGCCCAGCAATCTTAGAGGATGTTCTGATCGAAGTGTTCCGCACCCTGCACACTCAGTGCCGCGCTGAGTTAGACCTGCAGAACCAAAACCCCTTCAGCAAAGATCAAACTCAACTTAGCAGGTCTGTACTGTTTCTGTCTCATTTTATTACAATGTATTTCAATATTTTAAACGTAACTGTCTTGCTGTGTTGTTTTCTTTCAGCAAACTCAGAGAGAACAAGAAAACAGCAGAGCTTATAAAAACAGCCAACCTCTTGTTTAACTCCTTCGAGCCCTACTACATGTGGGACTATATTGCACGGTGGTTTGAGGAGTGTTGCAGGTATGTGTGGGATAATGGAAGAACAATATGAGCTGTCAGTCCATTATAACTTAACTTCTTTCTGATTTTTATAGGTGGACTCAGAGCAGTCATACCCCTGGGCAGACTTTGAGTTCTGAAACATCAGCACGCTCATTGGTTGAGTTTTGTGAGCTGGTGGACTTCTTGT[T/A]GGACATTGTGTCTTTGGTTGGTAAACATTGGATATGATGATTTATCTACTTAGCCTCATTTTCTATTTTATGCTTTAAGGGTGTGTTCACACTTGGCGTGTTTAATTTAAATTGGTTTGATTGCTGTTAGTGAAGTTAATTTAAATAAGGGTAAACTCTGCCATTCAATACTTTGATGCACACCCAAAATTAAACAAATTTTGGGACACTTGGACTTAATTGGAAATGCAACGTAGTCCAAAGACATCTACTGAGCGGTATGGGTCATTCTAATCAGGCTTGCATTTCCAATACCAAGAGTACCCTTGCTTGGTGTGCATGGTGTTTTGTGATCAACGTCATTCTCATTGGAAGGCTTTATGGACCATTTACATATCGTATTTTTTCTGTACTCCAGTTCATTATTTCAAATATCAGGGTTTCTACCGGGGTTTCTTACTTTTTCATCAAGTCAAATTTAATACTTTTTAAGATCTTTTTAAGACCATTATGAATTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2859
Status:
F2 line generated
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
ENSDART00000010778 Essential Splice Site 486 2477 11 37
ENSDART00000010778 Essential Splice Site 486 2477 11 37
Genomic Location (Zv9):
Chromosome 16 (position 35402461)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33134770
GRCz11 16 33088800
KASP Assay ID:
554-3053.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTGAGTTTTGTGAGCTGGTGGACTTCTTGTWGGACATTGTGTCTTTGG[T/C]TGGTAAACATTGGATATGATGATTTATCTACTTAGSCTCATTTTCTATTT
Long Flanking Sequence:
TTAGAGGATGTTCTGATCGAAGTGTTCCGCACCCTGCACACTCAGTGCCGCGCTGAGTTAGACCTGCAGAACCAAAACCCCTTCAGCAAAGATCAAACTCAACTTAGCAGGTCTGTACTGTTTCTGTCTCATTTTATTACAATGTATTTCAATATTTTAAACGTAACTGTCTTGCTGTGTTGTTTTCTTTCAGCAAACTCAGAGAGAACAAGAAAACAGCAGAGCTTATAAAAACAGCCAACCTCTTGTTTAACTCCTTCGAGCCCTACTACATGTGGGACTATATTGCACGGTGGTTTGAGGAGTGTTGCAGGTATGTGTGGGATAATGGAAGAACAATATGAGCTGTCAGTCCATTATAACTTAACTTCTTTCTGATTTTTATAGGTGGACTCAGAGCAGTCATACCCCTGGGCAGACTTTGAGTTCTGAAACATCAGCACGCTCATTGGTTGAGTTTTGTGAGCTGGTGGACTTCTTGTTGGACATTGTGTCTTTGG[T/C]TGGTAAACATTGGATATGATGATTTATCTACTTAGCCTCATTTTCTATTTTATGCTTTAAGGGTGTGTTCACACTTGGCGTGTTTAATTTAAATTGGTTTGATTGCTGTTAGTGAAGTTAATTTAAATAAGGGTAAACTCTGCCATTCAATACTTTGATGCACACCCAAAATTAAACAAATTTTGGGACACTTGGACTTAATTGGAAATGCAACGTAGTCCAAAGACATCTACTGAGCGGTATGGGTCATTCTAATCAGGCTTGCATTTCCAATACCAAGAGTACCCTTGCTTGGTGTGCATGGTGTTTTGTGATCAACGTCATTCTCATTGGAAGGCTTTATGGACCATTTACATATCGTATTTTTTCTGTACTCCAGTTCATTATTTCAAATATCAGGGTTTCTACCGGGGTTTCTTACTTTTTCATCAAGTCAAATTTAATACTTTTTAAGATCTTTTTAAGACCATTATGAATTAAATTTCAGACGTACACAAGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5625
Status:
F2 line generated
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
ENSDART00000010778 Essential Splice Site 486 2477 11 37
ENSDART00000010778 Essential Splice Site 486 2477 11 37
Genomic Location (Zv9):
Chromosome 16 (position 35402461)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33134770
GRCz11 16 33088800
KASP Assay ID:
554-3053.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTGAGTTTTGTGAGCTGGTGGACTTCTTGTWGGACATTGTGTCTTTGG[T/C]TGGTAAACATTGGATATGATGATTTATCTACTTAGSCTCATTTTCTATTT
Long Flanking Sequence:
TTAGAGGATGTTCTGATCGAAGTGTTCCGCACCCTGCACACTCAGTGCCGCGCTGAGTTAGACCTGCAGAACCAAAACCCCTTCAGCAAAGATCAAACTCAACTTAGCAGGTCTGTACTGTTTCTGTCTCATTTTATTACAATGTATTTCAATATTTTAAACGTAACTGTCTTGCTGTGTTGTTTTCTTTCAGCAAACTCAGAGAGAACAAGAAAACAGCAGAGCTTATAAAAACAGCCAACCTCTTGTTTAACTCCTTCGAGCCCTACTACATGTGGGACTATATTGCACGGTGGTTTGAGGAGTGTTGCAGGTATGTGTGGGATAATGGAAGAACAATATGAGCTGTCAGTCCATTATAACTTAACTTCTTTCTGATTTTTATAGGTGGACTCAGAGCAGTCATACCCCTGGGCAGACTTTGAGTTCTGAAACATCAGCACGCTCATTGGTTGAGTTTTGTGAGCTGGTGGACTTCTTGTTGGACATTGTGTCTTTGG[T/C]TGGTAAACATTGGATATGATGATTTATCTACTTAGCCTCATTTTCTATTTTATGCTTTAAGGGTGTGTTCACACTTGGCGTGTTTAATTTAAATTGGTTTGATTGCTGTTAGTGAAGTTAATTTAAATAAGGGTAAACTCTGCCATTCAATACTTTGATGCACACCCAAAATTAAACAAATTTTGGGACACTTGGACTTAATTGGAAATGCAACGTAGTCCAAAGACATCTACTGAGCGGTATGGGTCATTCTAATCAGGCTTGCATTTCCAATACCAAGAGTACCCTTGCTTGGTGTGCATGGTGTTTTGTGATCAACGTCATTCTCATTGGAAGGCTTTATGGACCATTTACATATCGTATTTTTTCTGTACTCCAGTTCATTATTTCAAATATCAGGGTTTCTACCGGGGTTTCTTACTTTTTCATCAAGTCAAATTTAATACTTTTTAAGATCTTTTTAAGACCATTATGAATTAAATTTCAGACGTACACAAGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16205
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
ENSDART00000010778 Nonsense 725 2477 14 37
Genomic Location (Zv9):
Chromosome 16 (position 35395533)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33127842
GRCz11 16 33081872
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATGTCTTCTGAGCAGATGGAATGTCTTGCWGCGTTCACTGCTGCCTG[T/A]CAGCTCTTCCTGGAGTGTTCCAGTTTTCCGGTTTACATCGCTGAGGGCAA
Long Flanking Sequence:
TACTGGTTTGTATACCATGCTGAAGATTTTTTAAAAATTATCTTTCAGATCCTACCAATAACAGGCACTGAGGTATTTGATGATAGCGAGAACGCTTTAAGTGGCCGGTTGTCAGAAAGTGGATTCACTGACTTCATTCAGTACCAAGCAGAGCGTGGTGATCAACCTGATAATGTGCAATGCCTTGAGGATGAGGCATCCAGCCCTGAAGACGTTCCTCTTCAACTCAAACCTAAACCCAAATATGGGTTCAGTAGTTCAGCCAACAGCAAGCCCCAGGACAAACCAGTGATGCAGTCCTGCCTTGAGCATTTCCAGCAGTTCCTTTCTTGCTTAGTGAGGCTATACATCACCCCAGGTGGTCAGACAGAGGCAGGGAAGAGCTGCAGTGCAGAAATGGACACTCTAACAGTGGTGGCTGATAAAAGATGGACAAGTGGCTTTGAGGAGCAGATGTCTTCTGAGCAGATGGAATGTCTTGCTGCGTTCACTGCTGCCTG[T/A]CAGCTCTTCCTGGAGTGTTCCAGTTTTCCGGTTTACATCGCTGAGGGCAACATGAAGTCTTCACCCACTAGAGAGGAGCAGGCAGGTAATAAAAAACACTCCGGCTGCCATTTTTTACTTTATGTACTGATTTATGTCAGTCTGTCAGAAAATTTCCTTCAAGGTATCACTACGACTTTATCTTTGACTGCCTCTGCCACCACAGAACATAAAAAAGACACAAACAATTAAGTATAATTTCAAAGACTAGTTACTATCACACATTTTCTTAGAAGACGCTCAGAAATTTTTTATTTAGTTCAGTTTATTCACATAAAATATAGTCAGGCGTATTTCTTTGTATAACAATAACTTGGGAATTTCAGTTGAAGTGAAAATAAATAAAAATGTCCTGTTTTTGACTTGCCTGCATTATTTAATGCAAAGGGATTGTGGGGCTGTCAAGAAATATAAATTACATGAATACCAGTTTCACACTGACAAACATTCAATGCCACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9700
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010778 Nonsense 1064 2477 19 37
Genomic Location (Zv9):
Chromosome 16 (position 35393702)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33126011
GRCz11 16 33080041
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACAGTCAACCCGTTGAGTGACAGTATTTCTCTCTTGAGYCTTAGCAGT[G/T]AGAACCTGCAGCTGTGTGGCGAATATCAACCACCTGATCAGCAGGGGGAG
Long Flanking Sequence:
GTCCCTGTTCATCATGCTTGATAGTCTCAGTTATTGGGATGGCTCTTCAAGTGCTGTTGGCAGGGCCTGGTTGAACCAGGTTTTGCAAAGACATGACATAGCTCGTGTTCTTGAACCTCTACTACTTTTGCTATTGCACCCCAAAACCCACCGTGTATCCATACAGCGTGTTCAAGCACAGCGACACTGGACCCAGGCCTTTCCTAATCCACCAGAAAATGAACCCTCTGACCCTATTTTCATGAGGGATATTGGCTATACTGAAAGTAAGATTTAAATTTGATTTAAATATATTTGGCATTTGCATTTTTTTTATATTAAACCTAATATATGCTAACAAACATGCACTTGTTTCCTCTGCAGATTATAGCCAGATATCAGGGAATTGCCATAGGGTTGTCCAAGAGTTTGGCAGAAGCCTTCCATTAGATGATATGGAACCCTTTAGCCTCACAGTCAACCCGTTGAGTGACAGTATTTCTCTCTTGAGTCTTAGCAGT[G/T]AGAACCTGCAGCTGTGTGGCGAATATCAACCACCTGATCAGCAGGGGGAGCCCAATAGCTCAGATTCGAGTGGCTCACAATCCTCAACTGTAGACAACGGCAGCTTTGATGAACTGGAGGGAGGTGGCAGCTCTGTTAATATATTGGATCCTATGCTTTGTCAGTCTGTTTCATTAGAGGAAGAGTCCATGCACAAGGCAGTTTCTGCTGTGGTTTTTGAGCTAGTGGACAGGGTGGTGCAAATGGTGGAGAAAGAATCTGAGACACCATCTCCTGATGCCTGGCCTCAGACAGACTCTGACAGTTCCAACTCATCCACAGATACATCAAATGAGCCAGTGGAAAGACTTGCCCCCTTCTCTAACACCCAGCCTAAAACACTTCCAGAACTAGTTGCAGGGGGAACCTTGGAGTTTCTTGCTGTGGCCGCAATTGATGCTTCTGGGGAAGAGGAGCATCGGGAAGGCATTGCTCGGCATAGCTCGTCCCCTTCGATCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36196
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
ENSDART00000010778 Nonsense 1072 2477 19 37
Genomic Location (Zv9):
Chromosome 16 (position 35393676)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33125985
GRCz11 16 33080015
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCTCTCTTGAGTCTTAGCAGTGAGAACCTGCAGCTGTGTGGCGAATA[T/A]CAACCACCTGATCAGCAGGGGGAGCCCAATAGCTCAGATTCGAGTGGCTC
Long Flanking Sequence:
TCAGTTATTGGGATGGCTCTTCAAGTGCTGTTGGCAGGGCCTGGTTGAACCAGGTTTTGCAAAGACATGACATAGCTCGTGTTCTTGAACCTCTACTACTTTTGCTATTGCACCCCAAAACCCACCGTGTATCCATACAGCGTGTTCAAGCACAGCGACACTGGACCCAGGCCTTTCCTAATCCACCAGAAAATGAACCCTCTGACCCTATTTTCATGAGGGATATTGGCTATACTGAAAGTAAGATTTAAATTTGATTTAAATATATTTGGCATTTGCATTTTTTTTATATTAAACCTAATATATGCTAACAAACATGCACTTGTTTCCTCTGCAGATTATAGCCAGATATCAGGGAATTGCCATAGGGTTGTCCAAGAGTTTGGCAGAAGCCTTCCATTAGATGATATGGAACCCTTTAGCCTCACAGTCAACCCGTTGAGTGACAGTATTTCTCTCTTGAGTCTTAGCAGTGAGAACCTGCAGCTGTGTGGCGAATA[T/A]CAACCACCTGATCAGCAGGGGGAGCCCAATAGCTCAGATTCGAGTGGCTCACAATCCTCAACTGTAGACAACGGCAGCTTTGATGAACTGGAGGGAGGTGGCAGCTCTGTTAATATATTGGATCCTATGCTTTGTCAGTCTGTTTCATTAGAGGAAGAGTCCATGCACAAGGCAGTTTCTGCTGTGGTTTTTGAGCTAGTGGACAGGGTGGTGCAAATGGTGGAGAAAGAATCTGAGACACCATCTCCTGATGCCTGGCCTCAGACAGACTCTGACAGTTCCAACTCATCCACAGATACATCAAATGAGCCAGTGGAAAGACTTGCCCCCTTCTCTAACACCCAGCCTAAAACACTTCCAGAACTAGTTGCAGGGGGAACCTTGGAGTTTCTTGCTGTGGCCGCAATTGATGCTTCTGGGGAAGAGGAGCATCGGGAAGGCATTGCTCGGCATAGCTCGTCCCCTTCGATCATTACACTGCCAGATGGCGGTGGCAGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12398
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
ENSDART00000010778 Nonsense 1458 2477 19 37
Genomic Location (Zv9):
Chromosome 16 (position 35392518)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33124827
GRCz11 16 33078857
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTCCGAAGTGCCATGTTCCTGGAGATCATAATCTCCCTTTGYCTCTA[T/A]TTTCTGCGCAGCTATTACTCAGCCCATGTGGCTGCCACGTCACAGGATCT
Long Flanking Sequence:
AGACGTAAGACTAACCAGCCCGAGAAGAACAGGCCACCCAGCATCTTCTTTGGAGACAGTCTTGACTTGGAGAACTGGTACAGCTGTGGGGAAGGTGAAGTATCAGAGATTGAGAGTGATATAGGCTCACCCAGTGGTGGGGCTGCGAGTGGAGGAGGAGGATCTCGCACCTCTGGGACACCTCCTCGTTTTAACATCCATCCCTTATACCAGCACGTGCTGCTTTATCTTCAGCTCTATGACTCCTCTCGGACTCTACATGCTCTCTCTGCTATTGCAGCTATGCTACGTGCTTCACCAACAGGATTTGTGAGCGCCATTTCCACCACCAGCATAAACAATACATATACACCACAGCTCTCTCTACTGCAGAACCTGCTAGCCCGCCATCGCATATCTGTCATGGGCAAGGACTTCTACTGCCCTATCCCGCAGGACTCACATTCCCACTCCTTCCGAAGTGCCATGTTCCTGGAGATCATAATCTCCCTTTGTCTCTA[T/A]TTTCTGCGCAGCTATTACTCAGCCCATGTGGCTGCCACGTCACAGGATCTTTCAGGCAACCATGCCATGCAACTGACCAGCGTGGAGGTGTTGACTCTGCTCTTCAGCGAGCTTGCTAAAGTCACAGGGGGCTCAGCCAAGGGCTTTGCCAGCTTTATTTGTGATGTACTGTCTAAATGCAAAGTGCAGAAGGTAGTGCTACACTGTTTGCTTTCCACCATCTTTAGTGTACAGAAGTGGCATGAACATCGTGTTCGGGGTACTAATGTGGCTGCGGTTGAGGAGGGCCTTTCGGAGGACAGCGTCATCAATCTGTCAGAGGACCAGTTAGACAACTGCAGCTCCATACAGTCACAACTACTGCGTCTGCTGCAGAGCCTGGTGGTTTTGGAGCATCGAGTGATGATCCCAGTGGATGAGGGTGGCGAGGGAGGTCCTGGGACAAATGGGTCTAATGGAGGAGCTAATGGTGCTGGGGCTGGTTTTGAACTGATTGGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14239
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
ENSDART00000010778 Nonsense 1650 2477 19 37
Genomic Location (Zv9):
Chromosome 16 (position 35391944)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33124253
GRCz11 16 33078283
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAACCCATGACTTCCCTGCAATACCTACATGGGCAGCCTATCACAGCA[C/T]AAGGCATGTTTYTATGTGCTGTAATTCGAGCTTTGCAWCAACAYCATGCC
Long Flanking Sequence:
TGACCAGCGTGGAGGTGTTGACTCTGCTCTTCAGCGAGCTTGCTAAAGTCACAGGGGGCTCAGCCAAGGGCTTTGCCAGCTTTATTTGTGATGTACTGTCTAAATGCAAAGTGCAGAAGGTAGTGCTACACTGTTTGCTTTCCACCATCTTTAGTGTACAGAAGTGGCATGAACATCGTGTTCGGGGTACTAATGTGGCTGCGGTTGAGGAGGGCCTTTCGGAGGACAGCGTCATCAATCTGTCAGAGGACCAGTTAGACAACTGCAGCTCCATACAGTCACAACTACTGCGTCTGCTGCAGAGCCTGGTGGTTTTGGAGCATCGAGTGATGATCCCAGTGGATGAGGGTGGCGAGGGAGGTCCTGGGACAAATGGGTCTAATGGAGGAGCTAATGGTGCTGGGGCTGGTTTTGAACTGATTGGGGGCGAGGTAGAGCATGTCAACCCACAACAACCCATGACTTCCCTGCAATACCTACATGGGCAGCCTATCACAGCA[C/T]AAGGCATGTTTTTATGTGCTGTAATTCGAGCTTTGCATCAACATCATGCCTGTAAGATGCACCCACAGTGGATTGGCCTTATTACAACCACTCTGCCATACATGGGAAAAGTGCTTCGGCGAGTGGTTGCATCTGTTACGCTTCAGCTGTGCAAAAACCTCGACAACCTTATCCAGCAATACCGTCACGAGACAGGCCTCACAGACACAAGGTACTGGTCCAGTTCAGTTGTGTAACACAGTAACAGGGTCATACAACAAAGCGTATTAGCTCACAAAGTTGTTAGTACTGGATTCTTTACATTGGCAAACACAAAGTGGCTTGATATCACTTGTGATGAATATTCACACCCATTGAAAGTAACTGTTATAACAAGTTATTTTCCTAACGCTACTTGGAAGGGCTGTATAAAAATTAATTTGACATATTTTTGAACAAATGCTTTGTGAATGAAAACTAATTTGTGTGTGTTTATATTTCTAGGCCCCAATGGATGGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36195
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
ENSDART00000010778 Nonsense 1845 2477 22 37
Genomic Location (Zv9):
Chromosome 16 (position 35390487)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33122796
GRCz11 16 33076826
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCCGATCTCAATGAATCACGGAGCTCACTTTATGGCTGCTATTGCTTA[T/A]GTGTGGAATGAAAGGAAGCAGGTTAAAACTCCATCTAGAAACAAGGTATG
Long Flanking Sequence:
TACCCCAAGGAGACTTAACATTAGTCTTAATATGTAGTGATGAGATTTCCATCCAGATGTAGTCCATGGGAGCAGCATGGTGGCTCAGTGGTTAGTACTCACAGCAAGAAGGTCACTGGTTCGAGTCCTGGTTGGCCCAGTCGGCATTTCTGTGTAAAGTTTGTGTTTAGTTTCCTCCAGGATGCTCTGGTTTCCCCCATTCCAAAAACATTTGGTATAGGTGAATCGAATAAACTAAATTGGCTGTACCCAATACTGGGTTGCCGCTGGAGTGCCATCAGCTGCATAAAACATATGATGGAATAGTTGCCGGTTCATTCCGCTGTGGTGACCTCTAAAATAGAGATTAAGCCGAAGAAAAATGAATGAGTGAATGTAGTCCACGTTCTGCTTACTAGAAGTACTTCTGATTTTTCACAGAATCTCAGGCAGCAAATTTTAGAGCTGCTGGGCCCGATCTCAATGAATCACGGAGCTCACTTTATGGCTGCTATTGCTTA[T/A]GTGTGGAATGAAAGGAAGCAGGTTAAAACTCCATCTAGAAACAAGGTATGAATAACTATAGATGTCTACAGGAGAACATTTCTACACTTGGAGAACAAAACAAACACTGACACGTGTGTCTGTATTTTAGGTAATTCCCACAGCTAGTGAGGAGCAGCTTCTCCTTGTGGAGCTTGTTCGTTCAGTAAGTGCTATGCGAACCGAGACTGTAATACAGACTGTAAAGGAAGTGCTCAAGCAGCCCCCAGCCATTGCCAAAGAGAAGGTATTGCTATGAATATACCCTGACAACTTTCATAATTGCGCCCCAGAAAATGCTGTTAGTTTTTCAGATAGCCCTAGTACTTACTTTTAGCTTTCATTTACAGAAGCATCTATCCCTGGAGGTCTGCATGCTACAATTTTTCTATGCCTATGTGCAGAGGCAAGTGGACCAACCAATTATTGTACTATATCAGTTCAAGCCAAATGCTTTCTTTAAATTACTCTATCAATCTCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39117
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010778 Nonsense 2156 2477 31 37
Genomic Location (Zv9):
Chromosome 16 (position 35383680)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33115989
GRCz11 16 33070019
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTCTTACAGCTGGAGAGCAATCATAGACCACCTGATGACTCATGAC[A/T]AAACCACATTCAGGGACCTAATGAGTGAGTCTTTCCTCTCTGCCAAATAG
Long Flanking Sequence:
TTGGCACAGTTTTGCTCCAACTCAAACACAGCTGATCCAACCACTCAAGGTGTTCAAGACTACCAGAGGCTATTAAGCAGGTGTGATATGGAGGTGGTTGGAGCTAAAGTATGCAAAGCTGTGGCCCTCCAGGAACTGAGTTGGAGACCACTGCTGTATACACAAAATAAGGAATTTACAATAAAGACTTACTCTCTTTCTGTCTGCCAGTGCTCACAATGCGCCCAGTTATCGTGCATGTATCCAGCTGTTGAGCAGCCTCAGTGGATATCAGTACACCCGGAGAGCCTGGAAGAAGGAAGCCTTTGACCTGTTTATGGACCATACATTTTTCCAGATGGACTCTTCCTGCGTCAGCCAGTGAGTCCTGTTATAGCACATCATATATTTTTTGTTGCAGTAGTTTTTCTGCAGCTTAAAGGGCAATGTGACTTCTAGTTGACCACATCTCTCTCTCTTACAGCTGGAGAGCAATCATAGACCACCTGATGACTCATGAC[A/T]AAACCACATTCAGGGACCTAATGAGTGAGTCTTTCCTCTCTGCCAAATAGACTTTCCAGCTGTGCCCATTTTATAGCTCTGTCATTATCATCCTGCTAACATTTTTCTATATGTGCAGCCCGAGTTGCTGTGGCTCAGAGCAGCTCTTTGAGTCTTTTCACCAATCGAGATGCAGAGCTTGAGCAGAGAGCCATGCTACTCAAACGCCTGGCCTTCACCATCTACAGCAGTGAGGTGGACCAGTACCAGAAGTACTTGCCAGACATCCAAGGTACTCAAATCTGCTCATTTCAGTGGTGATGTCGAGTTAAATTGGAAGTTGGGGTATTGGGAAAACCAGTATTCTGCGTTTTCGCTTGACCTGTTTCAAAATTAGGGACTTGAGGACCAATGTCCTGTGTAACCCTTATGTGCGTTTAGGGATGTTTTTATCCACTCTGGGGGGGATTTTTAAGTCTTAATTTGGCTACAACTTACTCTGTATTTCAGTAAATGGAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13013
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
ENSDART00000010778 Nonsense 2180 2477 32 37
Genomic Location (Zv9):
Chromosome 16 (position 35383514)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33115823
GRCz11 16 33069853
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCCGAGTTGCTGTGGCTCAGAGCAGCTCTTTGAGTCTTTTCACCAAT[C/T]GAGATGCAGAGCTTGAGCAGAGAGCCATGCTACTCAAACGCCTGGCCTTC
Long Flanking Sequence:
ATAAGGAATTTACAATAAAGACTTACTCTCTTTCTGTCTGCCAGTGCTCACAATGCGCCCAGTTATCGTGCATGTATCCAGCTGTTGAGCAGCCTCAGTGGATATCAGTACACCCGGAGAGCCTGGAAGAAGGAAGCCTTTGACCTGTTTATGGACCATACATTTTTCCAGATGGACTCTTCCTGCGTCAGCCAGTGAGTCCTGTTATAGCACATCATATATTTTTTGTTGCAGTAGTTTTTCTGCAGCTTAAAGGGCAATGTGACTTCTAGTTGACCACATCTCTCTCTCTTACAGCTGGAGAGCAATCATAGACCACCTGATGACTCATGACAAAACCACATTCAGGGACCTAATGAGTGAGTCTTTCCTCTCTGCCAAATAGACTTTCCAGCTGTGCCCATTTTATAGCTCTGTCATTATCATCCTGCTAACATTTTTCTATATGTGCAGCCCGAGTTGCTGTGGCTCAGAGCAGCTCTTTGAGTCTTTTCACCAAT[C/T]GAGATGCAGAGCTTGAGCAGAGAGCCATGCTACTCAAACGCCTGGCCTTCACCATCTACAGCAGTGAGGTGGACCAGTACCAGAAGTACTTGCCAGACATCCAAGGTACTCAAATCTGCTCATTTCAGTGGTGATGTCGAGTTAAATTGGAAGTTGGGGTATTGGGAAAACCAGTATTCTGCGTTTTCGCTTGACCTGTTTCAAAATTAGGGACTTGAGGACCAATGTCCTGTGTAACCCTTATGTGCGTTTAGGGATGTTTTTATCCACTCTGGGGGGGATTTTTAAGTCTTAATTTGGCTACAACTTACTCTGTATTTCAGTAAATGGAATGATTTTTGGTAACAAATCTAATTTGTACACAAATTGTGGGAAAATGCTTTAAAAGTCTTAAAAAACTCAACAATAGACTCTGGGCAAATTTACTACCCTTTTGTTATGTTGGAAACTGTTTTGCCCCATTGACTTCCATTAAAATGACATTTTTTGATTGCAAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42769
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
ENSDART00000010778 Essential Splice Site 2215 2477 32 37
Genomic Location (Zv9):
Chromosome 16 (position 35383407)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33115716
GRCz11 16 33069746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCAGTGAGGTGGACCAGTACCAGAAGTACTTGCCAGACATCCAAGG[T/C]ACTCAAATCTGCTCATTTCAGTGGTGATGTCGAGTTAAATTGGAAGTTGG
Long Flanking Sequence:
GTACACCCGGAGAGCCTGGAAGAAGGAAGCCTTTGACCTGTTTATGGACCATACATTTTTCCAGATGGACTCTTCCTGCGTCAGCCAGTGAGTCCTGTTATAGCACATCATATATTTTTTGTTGCAGTAGTTTTTCTGCAGCTTAAAGGGCAATGTGACTTCTAGTTGACCACATCTCTCTCTCTTACAGCTGGAGAGCAATCATAGACCACCTGATGACTCATGACAAAACCACATTCAGGGACCTAATGAGTGAGTCTTTCCTCTCTGCCAAATAGACTTTCCAGCTGTGCCCATTTTATAGCTCTGTCATTATCATCCTGCTAACATTTTTCTATATGTGCAGCCCGAGTTGCTGTGGCTCAGAGCAGCTCTTTGAGTCTTTTCACCAATCGAGATGCAGAGCTTGAGCAGAGAGCCATGCTACTCAAACGCCTGGCCTTCACCATCTACAGCAGTGAGGTGGACCAGTACCAGAAGTACTTGCCAGACATCCAAGG[T/C]ACTCAAATCTGCTCATTTCAGTGGTGATGTCGAGTTAAATTGGAAGTTGGGGTATTGGGAAAACCAGTATTCTGCGTTTTCGCTTGACCTGTTTCAAAATTAGGGACTTGAGGACCAATGTCCTGTGTAACCCTTATGTGCGTTTAGGGATGTTTTTATCCACTCTGGGGGGGATTTTTAAGTCTTAATTTGGCTACAACTTACTCTGTATTTCAGTAAATGGAATGATTTTTGGTAACAAATCTAATTTGTACACAAATTGTGGGAAAATGCTTTAAAAGTCTTAAAAAACTCAACAATAGACTCTGGGCAAATTTACTACCCTTTTGTTATGTTGGAAACTGTTTTGCCCCATTGACTTCCATTAAAATGACATTTTTTGATTGCAAAGCCATATAATCGTGCATTCTTAATTGTTGGTGGTTTTTCCTGTTTGAAAGAAGTCAAATTAGCTATTTTTACTGTTAAACAACTGTTGCAGTGCAAAAAGCAAAGTTTCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3954
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010778 Nonsense 2265 2477 34 37
Genomic Location (Zv9):
Chromosome 16 (position 35380817)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 33113126
GRCz11 16 33067156
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCATGTTCTTAAGGCTTGTTTGTATTATCTTTCAGGTTCAGGTGTTTT[T/A]ACTCATGGAGCAGGAACTCACYGCAGATGAGGACATCACTAGGTAYCCAC
Long Flanking Sequence:
GCTTCAGCATTTCTATCACAATGTGTGTGTCCGCAATAGTCAAATCACAGGATATGCAATGTTAAAGGATTGTAGTTGATCAGCCAAACAATTTAGGATTCTCTACATGGGATTTGTGGAGTCATGGCAAAGTATAACCATAACAGAGTGAATCTTTATCATTTGCATGTGTTTTAAAGTCACAAAATGTGTTTTAGGCACAAAAATGTACAACATTTGTAACTTAATAATTTTACTCAATTATTAATACAATGAAGGCTATACAGTGTTATTTTTTTTTCGTTTCACTCTTCTATCTTTAAATTTTTTATCTCAATATAAATGGCAGAAAAGTAAAATATTGCAATGTCAGGTTTTTCCCAAATTGTGCAGCCTTACTTTAACTGTAATATGACATGAAGGAAAGAGAAGTGTTACTTAGTGGACACTTTGTCACATTCATTTTGAATATGTCATGTTCTTAAGGCTTGTTTGTATTATCTTTCAGGTTCAGGTGTTTT[T/A]ACTCATGGAGCAGGAACTCACTGCAGATGAGGACATCACTAGGTATCCACTTATATCCTTTTCATTTGTTTATTTATTTTTTATTTTTTGTGAAGGTCAACCCATGTGCCTATGAATGCTAATGAATTTGGTCTCTGGTGTCTCTATCCAGGACTTCAGGGCCCTCGGTTGCAGGGCTTGAGACAACATACTCAGGGGGCAATGGCTTCTCTACCTCCTACAACAGCCAGCGCTGGCTCAACCTCTACCTGTCTGCCTGCAAGCTGCTGGATCTGGCCCTCGCTCTGCCCTCTGAGAGTCTGCCTCAGTTCCAGATGTGTGTATTCTTGGCATGTTTTTACACATTATGTTTAATATACTATTCAGAATGTGACAGGAGTTCTTTTTAATAAGCGTGCAACTTGAGAAATGTTAATTAAAAACACATCTTCACAGTCTGAAATGCAAGTGGCTTTTATGACTGCACGAAGATGTTCAGATGGATGCTTTTTTCTGTTCCA
Associated Phenotype:
Not determined