Busch Lab

ZMP

zgc:111944

Ensembl ID:
ENSDARG00000009735
ZFIN ID:
ZDB-GENE-050706-185
Description:
PERQ amino acid-rich with GYF domain-containing protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q4KME6]
Human Orthologue:
GIGYF2
Human Description:
GRB10 interacting GYF protein 2 [Source:HGNC Symbol;Acc:11960]
Mouse Orthologue:
Gigyf2
Mouse Description:
GRB10 interacting GYF protein 2 Gene [Source:MGI Symbol;Acc:MGI:2138584]

Alleles

There are 16 alleles of this gene:

Allele Name Consequence Status Availability
sa19882 Nonsense Available for shipment Available now
sa33026 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33025 Nonsense Mutation detected in F1 DNA Not yet available
sa39936 Nonsense Mutation detected in F1 DNA Not yet available
sa18439 Essential Splice Site Available for shipment Available now
sa8785 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39935 Nonsense Mutation detected in F1 DNA Not yet available
sa11852 Nonsense Available for shipment Available now
sa19881 Nonsense Available for shipment Available now
sa39934 Nonsense Mutation detected in F1 DNA Not yet available
sa38357 Nonsense Mutation detected in F1 DNA Not yet available
sa18740 Nonsense Mutation detected in F1 DNA Not yet available
sa19880 Nonsense Available for shipment Available now
sa10322 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa19882
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
ENSDART00000056277 Nonsense 38 1329 3 29
ENSDART00000146705 Nonsense 38 1329 2 28
Genomic Location (Zv9):
Chromosome 2 (position 48359422)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48391086
GRCz11 2 48245250
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGCAGCATTGTGGCCTCCCCTCCGCTCTCGCCTGCATTGCCAAAGTA[T/A]AAACTTGCAGACTATCGCTACGGGAGAGAAGAGATGCTAGCACTTTATGT
Long Flanking Sequence:
TATTGTGATATGTTGAATGGCAATGAAATATAAAAGCCCACAACTTGCATTTAATAAGCTTTAAATCACTTCTGTTAATTTATTTTAATCTGGATGGCTTAAATGTGACATCTTCTTTTCGAGTCTGTTATGTAAATACAGTAGCTTTTGTTTCATTGTATTTTTGATTTACTGATCTGTACATAGAATGCATCACCACACTTTAATTCACTAAACCATTCATTCATTTAGCAGGCGTAAAAGCTTTAACAAAAATTTTAAAACTTCTTAATTTGAATTCATATAACATTTTTAATGAATAGTTTAAAATTTTATTTATTTAAATACTATTTATATTATTTTATTTTTTAAAAGAAAAGTATTTGTTTTACTGTCGCCTTGTATGATTTGGTGACGTAGCATGTTCTCTCTTCTCTGTGTGTCAGGCTCCGTGCTCTGGCTGGTGGGGTGGGCAGCAGCATTGTGGCCTCCCCTCCGCTCTCGCCTGCATTGCCAAAGTA[T/A]AAACTTGCAGACTATCGCTACGGGAGAGAAGAGATGCTAGCACTTTATGTAAAGGATAACATGGTAAGGATGCTGGTTTTAATTTTATTTTCACATTTAGAAGCCTTGTTAATCTTCTAGTTCTGCAAATTTTTAAAGCATATAGTGTTATTTACATTTACAACAAGTTTAAAATGTTTTCGATCATTTTTAGATTCCGGTAGATCTTCATGATAAGGAATTCCTACCTATTTTACAAGAGGAGCCCCTGCCACCTTTGGCATTAGTCCCTTTTACAGAGGAGGAACAGGTAAGAATGGACCTGTTTATGAACTGAACATGTTTTTTTATCAGGGCTTTATAGTAGGGCTGAACAATATATTGTTTGAGCATCATTATTTGCAATAGTCACATCGCAGGATTAGATTATTTTTTAAAGGATATTTAATATTATATATAATATAACGATATTATTAAATTGTAGATATTTTTTTATTTTTTATACAATGATGATCATGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33026
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056277 Essential Splice Site 92 1329 5 29
ENSDART00000146705 Essential Splice Site 92 1329 4 28
Genomic Location (Zv9):
Chromosome 2 (position 48357273)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48388937
GRCz11 2 48243101
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGATGAAGTGGCACTTGCGTTACTATGCATATGTGTGAATCTCTCCGC[A/T]GAGAAATTTCTCCATGTCTGTAAACAGTGCAGCAGTTCTCCGTCTGACAG
Long Flanking Sequence:
TGTATGCAACATTCTTAATTTGTTATCTTAGGCAAGGCAAGATCTCATACTTAATGGGAAATTGTCAATCACCATGACAAGGAATCAGTACTACATATCAGCTGCAAAAATTCTGATTGGAGCATTTCTTAATAGCAGCTCAACATTGCACATCTGGTGATGTGACTATTACAGATTCACACATTGCGATATCGATGCTGAAACGACAGCCCTAATTCTTATTCATTCATGCAAACCGGAACGTCTGATGTGCTTCCTCCACCATCTCTGTTTTCTACGAAACTCAATTCAGTGAAAAAAAAGGATGATGCCGTGCCTACATATTCAGTGTTGTGGCTTCTGTTATTTTCCATATTATGTAATTTACTTGTTTTTGCTATCATTCTGTGGTCAACATCGATAAGGAATATACACCCACTTGCTGTTTCGCTGTCACGCTACCCAAACCTCCATGATGAAGTGGCACTTGCGTTACTATGCATATGTGTGAATCTCTCCGC[A/T]GAGAAATTTCTCCATGTCTGTAAACAGTGCAGCAGTTCTCCGTCTGACAGGAAGGGGGGGAGGGACGGTGGCAGGGGCACCTAGAGGCCGAAGTTCTTCACGAGGGCGAGGTGAGCTACGTTGCAACCGCACAATTACCTTTTTTCCTTCCCCAAAGCTTGTGCAGTCTCTTAAAATGTATCTTTAAGCGGAAATGCTGCACTTTCTGTTGAACCAGAGCAGAGTGTACACCTTTTTTTTTTAGCTTGTGTAACATTTTACTTCCTTTGCAACTATCGTCTCTGTGCACACATTGTATTTCTCATGTACGACTAAGAGAGCAAAGGTCAAACTTGTGTATGTTGGTTTCAATTGCTTGACAGGGAGAGGCAGAGGAGATGGTTTTTACCAAAGAAGTTTTGATGATGTGGAAGGAGGTTTCGGTCGTGGAGGGAGAGAGATGCATCGCTCCCAGAGTTGGGAGGAGAGGTACTGGGTTACTGTCTTTAAGCAGTCATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33025
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
ENSDART00000056277 Nonsense 125 1329 5 29
ENSDART00000146705 Nonsense 125 1329 4 28
Genomic Location (Zv9):
Chromosome 2 (position 48357172)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48388836
GRCz11 2 48243000
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGGGGGGAGGGACGGTGGCAGGGGCACCTAGAGGCCGAAGTTCTTCA[C/T]GAGGGCGAGGTGAGCTACGTTGCAACCGCACAATTACCTTTTTTCCTTCC
Long Flanking Sequence:
CTGCAAAAATTCTGATTGGAGCATTTCTTAATAGCAGCTCAACATTGCACATCTGGTGATGTGACTATTACAGATTCACACATTGCGATATCGATGCTGAAACGACAGCCCTAATTCTTATTCATTCATGCAAACCGGAACGTCTGATGTGCTTCCTCCACCATCTCTGTTTTCTACGAAACTCAATTCAGTGAAAAAAAAGGATGATGCCGTGCCTACATATTCAGTGTTGTGGCTTCTGTTATTTTCCATATTATGTAATTTACTTGTTTTTGCTATCATTCTGTGGTCAACATCGATAAGGAATATACACCCACTTGCTGTTTCGCTGTCACGCTACCCAAACCTCCATGATGAAGTGGCACTTGCGTTACTATGCATATGTGTGAATCTCTCCGCAGAGAAATTTCTCCATGTCTGTAAACAGTGCAGCAGTTCTCCGTCTGACAGGAAGGGGGGGAGGGACGGTGGCAGGGGCACCTAGAGGCCGAAGTTCTTCA[C/T]GAGGGCGAGGTGAGCTACGTTGCAACCGCACAATTACCTTTTTTCCTTCCCCAAAGCTTGTGCAGTCTCTTAAAATGTATCTTTAAGCGGAAATGCTGCACTTTCTGTTGAACCAGAGCAGAGTGTACACCTTTTTTTTTTAGCTTGTGTAACATTTTACTTCCTTTGCAACTATCGTCTCTGTGCACACATTGTATTTCTCATGTACGACTAAGAGAGCAAAGGTCAAACTTGTGTATGTTGGTTTCAATTGCTTGACAGGGAGAGGCAGAGGAGATGGTTTTTACCAAAGAAGTTTTGATGATGTGGAAGGAGGTTTCGGTCGTGGAGGGAGAGAGATGCATCGCTCCCAGAGTTGGGAGGAGAGGTACTGGGTTACTGTCTTTAAGCAGTCATTACTATATAAAGTGGTGTGTTGATTTGACAACTCAGTATATGCAGATGAACTGCTGAAAGAAATACGTTTTGTGAGCTAGATATTATAAATGATAGTAAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39936
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
ENSDART00000056277 Nonsense 289 1329 10 29
ENSDART00000146705 Nonsense 289 1329 9 28
Genomic Location (Zv9):
Chromosome 2 (position 48354349)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48386013
GRCz11 2 48240177
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTAGGCCTCGGTCGGGCAGCGGGAGCGCAGAGGAGGAGAGGGACAGTT[T/A]ACCAGAATGGTGTCTGGAAGATGCAGAGGAGGAGACAGGGACGTTTGACT
Long Flanking Sequence:
ATGGAGGCTTGCAGGCGCTCGTCGGGAAAATGAGCGATGGTGTCCTCCAAGTCCAGGTATGACGCATACAATCATTTGGTATATTTAACTTGCACATTTGGTAACCTTATGTATTACGTACTAACATGAACTAACAATGAACAATACTTGTACATCATTTATTAATCATAGTTCACCATATGCTAATTCATTAATAAAATCTAAATTCATGCTTGTTAATATTAGTTGCGCAACTTTTTTCCAATAGCATAAACAAAGATGAACAACTATAATAAATTTCATTTGTTAATTTTTTATGTTAGTAAATACGTTAACATTTACTACTACAGCCTTATTATGAAGTGTTACTGCAATTTCTTTATTTCCAGATGGTCCACGATCAGCAGGGTGGCGGGAACACCCAGATCAACGTCGACGCTTTGGTTTTGGGGATGAGGAACGCAGTGGTTACCGTAGGCCTCGGTCGGGCAGCGGGAGCGCAGAGGAGGAGAGGGACAGTT[T/A]ACCAGAATGGTGTCTGGAAGATGCAGAGGAGGAGACAGGGACGTTTGACTCCTCAGGGGCCTTCCTCTCACTTAAGGTGAGGGCGCTGGAAGTGAGTGGTTGAGCTTTGATTAATCATTTTACATTTTTGAATGCTCGATAAGGAAGCCTGTTTGAATTAATGTGGGTTTTGATGATTGTTCAATTAGAAAGCTCCTAAGGAGCCAATCCTGGAAGAGGCGGAGCTGGACTTCCGGCCATTGGAGGAGAATGACGAATATGCAGAAAAGGATGACAGTGAAACTGAACAAACCAAAGATACTGACACAAATACTAGGCACGAAAGTGATCGAAATGAAGGTGAGAAGAAAATATGGTTTCCTATAGGCTACTTAAAATCTCCAAATAAACACTTATCAGTTGTTTAGTAGCTTACTGGTCAGTATAAATTTTTAAAATGTCTTTGAAAGAAGTTTTTATATATCATATACTCACTTGCAAATAGTTGAAGCCATAGTGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18439
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056277 Essential Splice Site 319 1329 10 29
ENSDART00000146705 Essential Splice Site 319 1329 9 28
Genomic Location (Zv9):
Chromosome 2 (position 48354256)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48385920
GRCz11 2 48240084
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGACTCCTCAGGGGCCTTCCTCTCACTTAAGGTGAGGGCGCTGGAAG[T/C]GAGTGGTKGAGCTTTGATTAATCATTTTACAWTTTTGAATGYTYGATAAG
Long Flanking Sequence:
ACATTTGGTAACCTTATGTATTACGTACTAACATGAACTAACAATGAACAATACTTGTACATCATTTATTAATCATAGTTCACCATATGCTAATTCATTAATAAAATCTAAATTCATGCTTGTTAATATTAGTTGCGCAACTTTTTTCCAATAGCATAAACAAAGATGAACAACTATAATAAATTTCATTTGTTAATTTTTTATGTTAGTAAATACGTTAACATTTACTACTACAGCCTTATTATGAAGTGTTACTGCAATTTCTTTATTTCCAGATGGTCCACGATCAGCAGGGTGGCGGGAACACCCAGATCAACGTCGACGCTTTGGTTTTGGGGATGAGGAACGCAGTGGTTACCGTAGGCCTCGGTCGGGCAGCGGGAGCGCAGAGGAGGAGAGGGACAGTTTACCAGAATGGTGTCTGGAAGATGCAGAGGAGGAGACAGGGACGTTTGACTCCTCAGGGGCCTTCCTCTCACTTAAGGTGAGGGCGCTGGAAG[T/C]GAGTGGTTGAGCTTTGATTAATCATTTTACATTTTTGAATGCTCGATAAGGAAGCCTGTTTGAATTAATGTGGGTTTTGATGATTGTTCAATTAGAAAGCTCCTAAGGAGCCAATCCTGGAAGAGGCGGAGCTGGACTTCCGGCCATTGGAGGAGAATGACGAATATGCAGAAAAGGATGACAGTGAAACTGAACAAACCAAAGATACTGACACAAATACTAGGCACGAAAGTGATCGAAATGAAGGTGAGAAGAAAATATGGTTTCCTATAGGCTACTTAAAATCTCCAAATAAACACTTATCAGTTGTTTAGTAGCTTACTGGTCAGTATAAATTTTTAAAATGTCTTTGAAAGAAGTTTTTATATATCATATACTCACTTGCAAATAGTTGAAGCCATAGTGGGTGGAGTTGCTCACTATAAATAGTAGAGGTGTGAACCTACACTAGTCTCACGGTTCGGTTACGATTATCATGCCATCGATTCGGTTCAATTCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8785
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056277 Essential Splice Site 519 1329 13 29
ENSDART00000146705 Essential Splice Site 519 1329 12 28
Genomic Location (Zv9):
Chromosome 2 (position 48351519)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48383183
GRCz11 2 48237347
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTGCCATCGGACTTGGATGAGGATGAGGGACTCAAGCACTTTGAGCAG[G/A]TCTGAACCGCTAWGTACTCGACAGTTAAANNCATGCAGCTGAATAGTAAA
Long Flanking Sequence:
CCCTGCACCCATTCAGCCTGTACACCTAGAAAAAGCTGAAGATAAGGAGAGACCGTCAGAGAGAACAACATTACCAGAAATCAGACATGAACTGAGTAAAGCACCACTACACACAGCCCTATCTAACAGCATTGTGGAAGCCATTTCCATACCGCATGTCGCAAACAAACTCCCAGGTAAAAACCATCTGAATAAAACAGATGCAAATGCTTTTGTGTGTAGATATTTACATGTATAATGAGAGCGGTAAGTAGATATTTATTGACAGAGAGTATTTCTAGTTATACCCGTTCCTGTTTCCAGATCTTCCGGTCCCAGCGCCTTCAGTTCTGCCTGTCAAGTCAGTGCCCCCTCAATCCCAACAGGTCAAGCCTATAGAGATGCCAGTGTCAGTTCCTCCTGCTCTGCTACGCTCCACAGGCAGTGTGGGTCCTATCAGTCGACCCTCTGCCCTGCCATCGGACTTGGATGAGGATGAGGGACTCAAGCACTTTGAGCAG[G/A]TCTGAACCGCTATGTACTCGACAGTTAAAAACATGCAGCTGAATAGTAAAGTGCAAGTGAAGCAGTCAGTGAAGTTTACTCATCCACAACTTCACACATTGGGTTAAATTAGGCTTTGCAGTCTCCAAGTTTAGTGCATTATTTCCACTGTATCTGTTCAGCTGAAGGAACGGAACCAACCCCAGTGACGTCAGACACGGTGATATTCCAAGATTGTGGCACCCTTGCGCTAAAAGCTGTAGTACAACATGCCTTTTTCTTGAAAATAGTTACATTAATCGAGTTTGTAATGTATATTTTCAATAAAGTAGACAGCAATTTAGAAAATAACGTAAACATGTCTGACTGCTTCACTTCCACTTTTTTATAATTAGCTCATTTAAGTCCAAATGAGTTTTAACATTTTTGAATCTCTGGCAAGAGCACTTTTAGCGTAGCTTAGCATGGATTATTGAATCAGATTAGACCATTAGCGTCTTGCACAAAAATGACCAGAGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39935
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
ENSDART00000056277 Nonsense 612 1329 15 29
ENSDART00000146705 Nonsense 612 1329 14 28
Genomic Location (Zv9):
Chromosome 2 (position 48346766)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48378430
GRCz11 2 48232594
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGA[C/T]GAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAA
Long Flanking Sequence:
AATCTCCATTTAGTTTGCATAAATGCACAGACTCAACGTGTGGCTGTGAAATGTATGTATATGCAGTAGTTAACCATTGAAGTGGTTCACATTTGGTTCAAAACTTTTTTGATCCACTTCAAATGTTGACTACTGAAGGTATTTGGTTCCACATAATTCTAAGTGTTATTATTTGAATTCTTCTGCTAATGAGTTGTTTTGTGTTTGATTACTCGACTTTAAATTGGTCAATGCATTACAACTTGATTTGTGGCATGTGGCTTCGGCCTTTTCCAGTGATGACTTTATCTAAGCTTCAGAAAATGTAAAAAATTACCATGCAACTCAATATAGTTGCGTTCAGTGACCCCAGTCTGTCTGTCTGTCTTTTTAAAGGACCATTTAATAATCAGGAGATGTCTGAGTGGTTTCAGGCGGGCTATTTCACCATGACCTTGCAGGTAAAGCGAGGATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGA[C/T]GAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAAAGACGCTCACTTTTCAAATCTCTGACCCAAGATGACTTAACACTACTGTTCGGCATCTGAAAAGTTTTGATTTGTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGAAGAGACAACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATGCAATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTTTTTTTATAGCAGTAAAAAATAATAGTTAAAAATACACGACTCTGTTTAATTTATTTGACAATTTTGCACCATATTATGATATGCAGCAAATTATTTGAAACACTTCGCTCCAGTTGGCTACATAATACAGCATTTGCACTATTAATGTGACTTGTAATGCAGAAATGAACTTTTTTTTTTCTCAAATATATTTTTATTAATTTTATTTTAGTGTAAAAACATGTCGGTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11852
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
ENSDART00000056277 Nonsense 636 1329 16 29
ENSDART00000146705 Nonsense 636 1329 15 28
Genomic Location (Zv9):
Chromosome 2 (position 48346592)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48378256
GRCz11 2 48232420
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGRAGAGA[C/T]AACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATGCAATAT
Long Flanking Sequence:
GAATTCTTCTGCTAATGAGTTGTTTTGTGTTTGATTACTCGACTTTAAATTGGTCAATGCATTACAACTTGATTTGTGGCATGTGGCTTCGGCCTTTTCCAGTGATGACTTTATCTAAGCTTCAGAAAATGTAAAAAATTACCATGCAACTCAATATAGTTGCGTTCAGTGACCCCAGTCTGTCTGTCTGTCTTTTTAAAGGACCATTTAATAATCAGGAGATGTCTGAGTGGTTTCAGGCGGGCTATTTCACCATGACCTTGCAGGTAAAGCGAGGATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGACGAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAAAGACGCTCACTTTTCAAATCTCTGACCCAAGATGACTTAACACTACTGTTCGGCATCTGAAAAGTTTTGATTTGTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGAAGAGA[C/T]AACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATGCAATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTTTTTTTATAGCAGTAAAAAATAATAGTTAAAAATACACGACTCTGTTTAATTTATTTGACAATTTTGCACCATATTATGATATGCAGCAAATTATTTGAAACACTTCGCTCCAGTTGGCTACATAATACAGCATTTGCACTATTAATGTGACTTGTAATGCAGAAATGAACTTTTTTTTTTCTCAAATATATTTTTATTAATTTTATTTTAGTGTAAAAACATGTCGGTAATTTATATTGAATAATAAGATAATATACATCTTTCATGTAATTTGAATCCTGCTCCCCACATGAAAAATCTAATAAAAAAAATAATAATAATAACAACAACAACAAATAATTCAATTTGTATTTAATAAATAAACAAATAAATAAATAAGGACATAAATTGCATACATTTTGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19881
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
ENSDART00000056277 Nonsense 651 1329 16 29
ENSDART00000146705 Nonsense 651 1329 15 28
Genomic Location (Zv9):
Chromosome 2 (position 48346547)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48378211
GRCz11 2 48232375
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGACAACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATG[C/T]AATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTT
Long Flanking Sequence:
TAAATTGGTCAATGCATTACAACTTGATTTGTGGCATGTGGCTTCGGCCTTTTCCAGTGATGACTTTATCTAAGCTTCAGAAAATGTAAAAAATTACCATGCAACTCAATATAGTTGCGTTCAGTGACCCCAGTCTGTCTGTCTGTCTTTTTAAAGGACCATTTAATAATCAGGAGATGTCTGAGTGGTTTCAGGCGGGCTATTTCACCATGACCTTGCAGGTAAAGCGAGGATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGACGAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAAAGACGCTCACTTTTCAAATCTCTGACCCAAGATGACTTAACACTACTGTTCGGCATCTGAAAAGTTTTGATTTGTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGAAGAGACAACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATG[C/T]AATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTTTTTTTATAGCAGTAAAAAATAATAGTTAAAAATACACGACTCTGTTTAATTTATTTGACAATTTTGCACCATATTATGATATGCAGCAAATTATTTGAAACACTTCGCTCCAGTTGGCTACATAATACAGCATTTGCACTATTAATGTGACTTGTAATGCAGAAATGAACTTTTTTTTTTCTCAAATATATTTTTATTAATTTTATTTTAGTGTAAAAACATGTCGGTAATTTATATTGAATAATAAGATAATATACATCTTTCATGTAATTTGAATCCTGCTCCCCACATGAAAAATCTAATAAAAAAAATAATAATAATAACAACAACAACAAATAATTCAATTTGTATTTAATAAATAAACAAATAAATAAATAAGGACATAAATTGCATACATTTTGTTTTTGAGCTGTAGTTATATTTAGCAAAGTGTCAAGTTTTTTTTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39934
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
ENSDART00000056277 Nonsense 660 1329 17 29
ENSDART00000146705 Nonsense 660 1329 16 28
Genomic Location (Zv9):
Chromosome 2 (position 48345152)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48376816
GRCz11 2 48230980
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAATTGTTAACCACTAAACTCACTCTCTTTTCTTTTAGGCAACAATA[T/A]GCTCTGCAGCAGAAAGTGTTAAACTCTGCTCCTCCTCCTCCTCCACCACC
Long Flanking Sequence:
ATGCTGAATCACTCTTTCCTGCCACTATATTGGTTCATATAAGCTGTCAATCACTCAAGGCTTTACGCTGTCAGATAACAGAGCTTTTGTAACCGCAGAAAATGTAAACGGCTGAAGTTTAAGGAAGATGCAATGAAAAGTAACGTTACACAGTTTTGCAAACCCACCCAAAGTTACAAATAATGGCACTGATGAGAGCGATCATTGTGAATGTTGATTCAGCAGCCGAGATCAACCGAGTGTTTTTGGAGAGTGGAGAATGACAAAGAACGATATTGCGCAGGCGGTCATCGTGAGAATCCATTTGTGATGATTCTTAGAACGGAGCATTCAAAAGAACTGGGTTTATACAAATACGGTTACATTTTGATCAATTTAAAATATCCATATGTATATTTTTAAGATTTTTTTGTCATACAAACAGTTTACACAACTTTAATTCAATAAATGATTTAATTGTTAACCACTAAACTCACTCTCTTTTCTTTTAGGCAACAATA[T/A]GCTCTGCAGCAGAAAGTGTTAAACTCTGCTCCTCCTCCTCCTCCACCACCACAGCAGCAGCTCAATCTTCTTCTCCATCAGGCGCTGAAGATCAGGTGTGATAACACTGCTTTTGTTTCTGTCACACAATCACACAGTCATCTGCGTAAAGAAAGGACAGTGGCAAATTAGCATAACAATGCGTGGGCGGAGTGTTACATTGCACTGGTATTGTGGTTGATCATCTGTAACCTTATCTTACAGTTTGCTTGATTTGCTCTTGCAGAACTCCTGAGCCGCAGCAGAGCCTCTTACCTCCCGTCACACGCTCCATGTCGGTTCCAGACTCGGGTTCTGTTTGGGAAATGCAGAACCCGTCCACTCAGGCATCCTGTTCTCCAAACATGCAGCCCGCCGCTCCCAGCAGTACGTTAGTGCCTAGATCTGCCCTAAGGCGTAGTGATACACTAATCTTGATTTTGTTTGATGGATAATATCTGTTTCCACTTTTCTTTTTAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38357
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
ENSDART00000056277 Nonsense 815 1329 20 29
ENSDART00000146705 Nonsense 815 1329 19 28
Genomic Location (Zv9):
Chromosome 2 (position 48339649)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48371313
GRCz11 2 48225477
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGAGACAAGAGGAAGAGAGGAAGCGTTTAGAGGAAGAAGAGCTGGCA[C/T]GACGCAAGCAGGTCAGGAGACAACAAAAAATATGCTGTCGACATCAGGCA
Long Flanking Sequence:
GGGAAAGGCGTTTTTTATTCAGACATTTATAAAGAACTTATTCTAGAGTAGTAATCACAATACCCTAATTTAAAAAAATCCAATGTTCTTATTCTCTCGAATCTTATAGCAGTTCATGCCTAGGATGGACTATTCCTTTAAATGGTGAAGTAAATTGAGAAGTTTGACTGTTTTTGTTTGTCTGTTTTAGCTTGGGAAGGGAGTAGCGTATGGGATCTGCCACTAGACAATATGCCTCAAGCGTCTTCCATTGAACAGCTGCAGCTGGAGAAAGCCAAAGCTTTGAAGGTAAGAAAGATATGACACTAGTGCATGAATGCATTTCATTTTGTATGTTTTTTTTTCTTAGTCTTGTCTGTTTTGCTCCAAAGCTGGAGATGGAGAGACGGGAGGCAGAGCTTCGGGCCAAAAGGGAAGAAGAGGAGAGGAAGCGTTTGGAAGAGGCTCTGCGTGCGAGACAAGAGGAAGAGAGGAAGCGTTTAGAGGAAGAAGAGCTGGCA[C/T]GACGCAAGCAGGTCAGGAGACAACAAAAAATATGCTGTCGACATCAGGCACAAAAAACCCAAAAACATGTAAAAATCAGGCTGGAAAAAAAGCAGTGAATGAAAGGATTTTTTTCTATTAGTAGGAATTTATTTTATTTAAGCACACAAGGCACTTTTCATTCCTGGAACACTGTGCTTTGTGTTTACATAAATGATAATTGTTAAATCGGCCTTAAGTATTGACTGCTTTGTTCGGTCATGTAAAAAAAAAAGTGTTTATTGTTTTGTAGTAGGGATGTCTAAAACTACACAGAAAATTGTTGCATCATTGAAATGGCAATGTGCACATTGAATTCTGCAATAGTCCCATCGCAGGATGTTTAATTCCTAGTAGTGATCAAGCACCATGTTTCGAAAATAATTTAATTTCTGTTTTTTTATATTAGAATATGCAAGTAGTGCACAAAATGGGATCACATACAAAGAAAACAAAACCAACAACAAAAACATGAAAAAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18740
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
ENSDART00000056277 Nonsense 909 1329 22 29
ENSDART00000146705 Nonsense 909 1329 21 28
Genomic Location (Zv9):
Chromosome 2 (position 48335623)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48367287
GRCz11 2 48221451
KASP Assay ID:
2259-2654.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGCTGGAGGAGGAGGCTGCGGCCGCTGCAGCAGCACTGCTCAGACAA[C/T]AGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGACAGCAGGAG
Long Flanking Sequence:
GTTTTTAATGACGCTCGACTCACATTGACAGGTAGAAATCCGATCTACCTGCTTGCACAGCAGACACAAGAACACAGATCTGATTCATATTAGATAAATTTCCACATATGAACAAGGTCTGAATATGATTTGAGTTAATCGGAATCCATGTGATTTGTTCCTGCTTACATGTACTTGGGCCATATCCGATCTGTGCCACATGGGAGAAAAAAATCAGAATTGAGTCACTCGAACAGTGCAGTGTTAATGCAGCCATAAAGTGTATTATTTGAAAGCAAAACAATGGCTTTATTAATAATATTTTCATTATACTTTGTGTCATTAATAACCATAGTCCTTCATACAATTGGCAGCATTTAATATTTTTAAATTGATGTTATTAAATTCAGCAGGAAGAGGAGCGGAGGAAGCAGGAAGAACTGGAAGCTCAGAGGCGGCGTGAGGAAGAGAAGAGGCTGGAGGAGGAGGCTGCGGCCGCTGCAGCAGCACTGCTCAGACAA[C/T]AGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGACAGCAGGAGCTGCAGAGACAGAGACAGCAGCAACAGGAGGCACTCCGACGACTCCAGCAGCAGCAGCAACAACAGCAGCTCGCACAAATGAAGGTGAACATCCTGCACACCATATATTTTCTTGCCATGTCATCTTGTAGCCTAATAATAATTATTTATTTTATTAGATTCCATCTTTAGATGGACTTTAGTACAAAATCTTTCTCGTTTCTCTTTCGGTTTCTTGTTAAACTGTTTTCCATTAAGGAGAGTACATTATAAGTCTACCTTTTTAAATTACCAAAATGAGAGCTCTTTAATATTTGTTTTTTACTCTGCTTTATGACATGACTGGATTCAAGGCCTTGAAAGCACTTAAAAACACAGATGCTTGAAAGTGCTTAAATTAAATTTGAAATCAAATTAGATTTTAGTGTTATTTCAACAGATGTCATGCTGCTGTCAAAAACAGAATGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19880
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
ENSDART00000056277 Nonsense 923 1329 22 29
ENSDART00000146705 Nonsense 923 1329 21 28
Genomic Location (Zv9):
Chromosome 2 (position 48335581)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48367245
GRCz11 2 48221409
KASP Assay ID:
2259-2653.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGACAACAGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGA[C/T]AGCAGGAGCTGCAGAGACAGAGACAGCAGCAACAGGAGGCACTCCGACGA
Long Flanking Sequence:
ATCTACCTGCTTGCACAGCAGACACAAGAACACAGATCTGATTCATATTAGATAAATTTCCACATATGAACAAGGTCTGAATATGATTTGAGTTAATCGGAATCCATGTGATTTGTTCCTGCTTACATGTACTTGGGCCATATCCGATCTGTGCCACATGGGAGAAAAAAATCAGAATTGAGTCACTCGAACAGTGCAGTGTTAATGCAGCCATAAAGTGTATTATTTGAAAGCAAAACAATGGCTTTATTAATAATATTTTCATTATACTTTGTGTCATTAATAACCATAGTCCTTCATACAATTGGCAGCATTTAATATTTTTAAATTGATGTTATTAAATTCAGCAGGAAGAGGAGCGGAGGAAGCAGGAAGAACTGGAAGCTCAGAGGCGGCGTGAGGAAGAGAAGAGGCTGGAGGAGGAGGCTGCGGCCGCTGCAGCAGCACTGCTCAGACAACAGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGA[C/T]AGCAGGAGCTGCAGAGACAGAGACAGCAGCAACAGGAGGCACTCCGACGACTCCAGCAGCAGCAGCAACAACAGCAGCTCGCACAAATGAAGGTGAACATCCTGCACACCATATATTTTCTTGCCATGTCATCTTGTAGCCTAATAATAATTATTTATTTTATTAGATTCCATCTTTAGATGGACTTTAGTACAAAATCTTTCTCGTTTCTCTTTCGGTTTCTTGTTAAACTGTTTTCCATTAAGGAGAGTACATTATAAGTCTACCTTTTTAAATTACCAAAATGAGAGCTCTTTAATATTTGTTTTTTACTCTGCTTTATGACATGACTGGATTCAAGGCCTTGAAAGCACTTAAAAACACAGATGCTTGAAAGTGCTTAAATTAAATTTGAAATCAAATTAGATTTTAGTGTTATTTCAACAGATGTCATGCTGCTGTCAAAAACAGAATGAAAATAAATAATTCTTAATTCCGCAATCTTAAATTAAAATCTTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10322
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056277 Nonsense 1296 1329 28 29
ENSDART00000146705 Nonsense 1296 1329 27 28
Genomic Location (Zv9):
Chromosome 2 (position 48321466)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 48353130
GRCz11 2 48207294
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGCANNNNNNACAGCAGCGGTTTGAAACRGTCACTTCCGGCAAGAAGAAGAAR[A/T]AACAGAAGATGGTACGAGCCGACCCAAGCCTTCTAGGTGAGTCATACATC
Long Flanking Sequence:
GGAAAGCTCTATTTGAAGAGTTATCGTTATCGTATATTGCATCAAAATTGCCAAAAACTACTGGAACTTTGTACGATTTTTTTCTGATGTAAGTACTTGTATTTTCAAATGATTTGAGGAATGTTCAAATCCAGAGAAATAAGCAGTTTTAACATGAGACGAGCGTACGCTGTCAATTTCCAATTTAGTTTTATAGATATAAGGGAAACACAGAAGACTTTAATATGCTTTGTGTGTGTTTTATTAGACTGCACAGAGCAGCATTATAACAGAAGCCTAAGATGTATTAAAAAATGAATAAAAGCTCTGCTGCTTTTGTGCCACATTATGTGCATGTTTGAGTGGTTTGTGCTGATCTGTCTGCAATTTTGTGTCAGGAGTCGGTGTGGGGAATAAGAGAAGTGCCACAGTCAGTCCTGCTTCAACAACAACAACAACAACAATTACAGCAGCAGCAACAGCAGCGGTTTGAAACGGTCACTTCCGGCAAGAAGAAGAAG[A/T]AACAGAAGATGGTACGAGCCGACCCAAGCCTTCTAGGTGAGTCATACATCAAGTTTAGAGGTTAAAACGTATTAGACAAATGACTCAACTGAGACTTTGAAATACTGTGACGTGAAGAGAAACTGATGAGTAAGCATGACTTCAGTCAAAACCAGACTAACAGATTGATGGGAAAAACCACATGAGCGTCTGGACCACCAACATCAATTAAAATACTCAAAAGGAAATAAAAAATCATATGAATATACAGTGCTCAGCATATATAAGTAAACCCCCCACAAATCTCTCATTTAAATTCATATTTTTTATAGAAAGCTATACAAAATTATATTTGTGCATATACATTAGATTAGTCCAGTGGTTCTCAAATTTTTTTCATCAAGTACCACCTCAGAAAAAAATTGTCTCTCCAAGTACCACCAAAATGAGCAGTATTGAAATACAGTAGCTAAGTAGGCCCAGTAAAGCAGCTACAACTCTGCACAGTTAAAAAATGTGGC
Associated Phenotype:
Not determined