Busch Lab

ZMP

LOC565591

Ensembl ID:
ENSDARG00000019063
Human Orthologue:
FAT1
Human Description:
FAT tumor suppressor homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:3595]
Mouse Orthologue:
Fat1
Mouse Description:
FAT tumor suppressor homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:109168]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa24961 Nonsense Mutation detected in F1 DNA Not yet available
sa24960 Nonsense Mutation detected in F1 DNA Not yet available
sa7393 Missense Mutation detected in F1 DNA Not yet available
sa39005 Nonsense Mutation detected in F1 DNA Not yet available
sa11100 Nonsense Available for shipment Available now
sa35707 Nonsense Mutation detected in F1 DNA Not yet available
sa42404 Nonsense Mutation detected in F1 DNA Not yet available
sa9979 Nonsense Available for shipment Available now
sa18602 Nonsense Available for shipment Available now
sa35706 Nonsense Mutation detected in F1 DNA Not yet available
sa35705 Nonsense Mutation detected in F1 DNA Not yet available
sa35704 Nonsense Mutation detected in F1 DNA Not yet available
sa8682 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24961
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
ENSDART00000011953 Nonsense 113 4446 1 26
Genomic Location (Zv9):
Chromosome 14 (position 31094755)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29884812
GRCz11 14 30225126
KASP Assay ID:
554-7549.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAAGGAGGCATTTCTGCCTCTCTTAACAGGGAAATAAAAGACCACTA[T/A]CTACTGACTATAAATGCTATTGAAAGACACACTGGTGCAGAGGCACAGAC
Long Flanking Sequence:
AGTATTTCACATGGTTGTCTAATCATTTAGTTTGATTTCTTAAACGTTTTCTCCCAGGCATCAACTGATGAATCACTGATATTTATGTTAATGTGACATTTATTTTCATCCACCTGTTGCTCTGTTTTTTTTTCCCAGTCCTCTCTGAAATCACCTGTAACAATGGGTAAATCCTGGACTAACCATCTTCTAGTGCTCTTTATGTGGATATGCTTAGGTGCCCAGCAAATGGAAGATGCTTTGCCTTTTCAGTTTACTTATCCATTTTATGATGTGACGATATATGAAAATTCAGCAGCAAAAACTTATGTTGAAGGCCCTATAAAAATGGGAATTTTTATGACAAATCAATCTGTGGACATTTGGTACACAATAGAATCTGGAGACCATGATAATTTATTCAAGGCTGAGACATATGTCTTGGGTAATTTCTGTTTCTTGCGAATAAGGACCAAAGGAGGCATTTCTGCCTCTCTTAACAGGGAAATAAAAGACCACTA[T/A]CTACTGACTATAAATGCTATTGAAAGACACACTGGTGCAGAGGCACAGACGCAAGTAAAAGTACAAATTCTGGACATGAATGATCTCAGACCTCTTTTCTCACCGACTACATATAGCTTCTTTGTTCCGGAAAACTCTGCAGCCAGAACAAGCATAGGCAGAGTTTCTGCCACAGACGCTGACACAGGCACCAATGGAGAGTACTATTTCAGCTTCAAAGAGTGGACTGACATGTTCTCCATTCATCCTACTAGTGGGGTTATAACTCTGACAGGCAAGCTGGATTACTCCGAGATGGCTCTTTATGAGATTGATGTGTTGGCTGTGGACAGAGGTCTGAAGCTCTATGGGAGCAGCAGCAGCAGTAGCACAGCAAAGCTAAAGGTGCATGTATTGCAGGCCAATGAACATTCACCTGTTATAACTGCTGTCCCTTTAACTCCTTGGAACACAACCAGCGATCCCACATATGCGCATGTGACTGTGGAGGATGCAGATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24960
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
ENSDART00000011953 Nonsense 402 4446 1 26
Genomic Location (Zv9):
Chromosome 14 (position 31093890)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29883947
GRCz11 14 30224261
KASP Assay ID:
554-7398.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCAAAACTGTAGAGAAACATTCAAAGATTAATTACTTGTTAGAATTT[A/T]AAATGCAACAACACGATAATCCATTTATTATCAATCCAAACACAGGCCTT
Long Flanking Sequence:
GTAGCACAGCAAAGCTAAAGGTGCATGTATTGCAGGCCAATGAACATTCACCTGTTATAACTGCTGTCCCTTTAACTCCTTGGAACACAACCAGCGATCCCACATATGCGCATGTGACTGTGGAGGATGCAGATGAAGGGCAAAATGGTGAAATTGCCTCTCTGAACATTGTAGCTGGAGATCCACTTCAGCAGTTCAAGACCTTTAGAACAAATCCTGGAAGCAAAGAATACAAGATCAAGGCTGTCAAGAAAGTGGAATGGGAGGGTTATAGTTTTGGCTACAATCTTACATTGCAAGCCAAAGATAAGGGAAATCCGCCTAAGTTTTCCTCAGCGATAGTTGTGAGGTTGGGATCACCTAGCGAATACACAGAGATTCCTAGATTCGAGAAAAGTATTTATAGAGTTACCCTAAGTGAGTTTGCGCCACCTCACTCTCCTGTTGTTATGGTCAAAACTGTAGAGAAACATTCAAAGATTAATTACTTGTTAGAATTT[A/T]AAATGCAACAACACGATAATCCATTTATTATCAATCCAAACACAGGCCTTATTTCCACCTCTGGACCTATTAAAGCAGAAAAGGTTAGTCAATATGAATTTGAAGTTGTTATTAGTGACAGACGAGCATCGACAAAGGTGGTAGTGAGTGTAAGTGATATGAACAACAACGCTCCAGTGTTTCAAAAGTCAAATTACGAAGCAAGTATTGCTGAACATGTGCCTATAGGAACCAGTGTCTTAACAGTCAGCGCTACTGACATGGATGATGGAGAAAATGGCTATGTCACCTATAGTATTGTCAATGTGAACAAACAGCCCTTCGTAGTGGATTATTTCACCGGTGTCATAAGCACCACCGAGGATCTAGATTATGAGACCATGCCAAGTAAATTCTCCCTCAGGATTCGAGCCTCAGACTGGGGCTCCCCTTTCCGCCGTGAAGCCGAGACTATTGTTTCAATCTCTCTCACTAACCTAAACGATAATAAGCCACAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7393
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011953 Missense 490 4446 1 26
Genomic Location (Zv9):
Chromosome 14 (position 31093625)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29883682
GRCz11 14 30223996
KASP Assay ID:
554-4124.1 (used for ordering genotyping assays)
KASP Sequence:
ACATGTGCCTATAGGAACCAGTGTCTTAACAGTCAGCGCTACTGACATGG[A/T]TGATGGAGAAAATGGCTATGTCACCTATAGTATTGTCAATGTGAACAAAC
Long Flanking Sequence:
GGGTTATAGTTTTGGCTACAATCTTACATTGCAAGCCAAAGATAAGGGAAATCCGCCTAAGTTTTCCTCAGCGATAGTTGTGAGGTTGGGATCACCTAGCGAATACACAGAGATTCCTAGATTCGAGAAAAGTATTTATAGAGTTACCCTAAGTGAGTTTGCGCCACCTCACTCTCCTGTTGTTATGGTCAAAACTGTAGAGAAACATTCAAAGATTAATTACTTGTTAGAATTTAAAATGCAACAACACGATAATCCATTTATTATCAATCCAAACACAGGCCTTATTTCCACCTCTGGACCTATTAAAGCAGAAAAGGTTAGTCAATATGAATTTGAAGTTGTTATTAGTGACAGACGAGCATCGACAAAGGTGGTAGTGAGTGTAAGTGATATGAACAACAACGCTCCAGTGTTTCAAAAGTCAAATTACGAAGCAAGTATTGCTGAACATGTGCCTATAGGAACCAGTGTCTTAACAGTCAGCGCTACTGACATGG[A/T]TGATGGAGAAAATGGCTATGTCACCTATAGTATTGTCAATGTGAACAAACAGCCCTTCGTAGTGGATTATTTCACCGGTGTCATAAGCACCACCGAGGATCTAGATTATGAGACCATGCCAAGTAAATTCTCCCTCAGGATTCGAGCCTCAGACTGGGGCTCCCCTTTCCGCCGTGAAGCCGAGACTATTGTTTCAATCTCTCTCACTAACCTAAACGATAATAAGCCACAATTTGAGAATATCGACTGTGATGTTAGAGTGCCAAGATCTCTAGGGGTCGATGAGCAAATAATAGTGGTGTCTGCCATTGACGCTGACGATCTTGGTGTAGTGCAGTACAGAATTGACACTGGTAATAACATGAATCTTTTTAAACTGGATTCCACCTCTGGTGTGCTGGCGCTTAAAAAGACACTGAGGGATGGTGATGCTGTGAAACAATCGTTCCACCGTCTGCAAATAACTGCCAGCGATGGAGAAATCTCAAGCACTCCTTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39005
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011953 Nonsense 947 4446 1 26
Genomic Location (Zv9):
Chromosome 14 (position 31092253)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29882310
GRCz11 14 30222624
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCACATTCGAGTGAGAGAAGACATTCCAGTGGGAACTTTAGTGCTCTG[G/A]CTTGAAACTCACGATCCTGATCTTGGCCTGTCTGGACAGGTGAGATACAG
Long Flanking Sequence:
AGAGAAACAACAGACCGCTATACTCTCAAAATCACCGTTTATGACCTCGGCTTACCGCAGAAGTCCTCATCTCACTTGTTAGATGTCAAAATTTTAGATGCCAATGACAACAGTCCTGAGTTCCTCCAGCGCAAGTATATAGTAGATATAAGTGAGGACACGGCTATAGGAACTGATATCATTCAACTTGAAGCGAAAGATAAGGATTTAGGGGTCAATGGAATGGTTAGATACTCATTTCTCACTGAGACTGATAAATTTAACATTCATGAAGAAACAGGGATTGTAAGTGTTATGCGTCTTCTAGACAGAGAAGCCAATCCGGTATTTGTTTTGAGAGTGGCTGCTTTCGATGCAGCAATTGATGAGCCTAAATTAGTATCAACAGTGTTGTTACGCATTAATTTGGAGGATGTGAATGATAATCCCCCTATGTTTGTTCCTCAACATTATCACATTCGAGTGAGAGAAGACATTCCAGTGGGAACTTTAGTGCTCTG[G/A]CTTGAAACTCACGATCCTGATCTTGGCCTGTCTGGACAGGTGAGATACAGTCTAACAGATGGGGACGACGGAAACTTTCAGGTGGATAAAATGTCTGGAGCTGTGTATGTCTCTCAGACTCTTGATTTCGAAACAAGACAGATATACAATCTGACAGCAAAGGCCAAAGACAGAGGCAGGCCAAACCCTTTATCCTCATCCTGCTTCATTCAAGTGGAGATTGTGGCTGTCAATAAGAACATGTACCGTCCAAATTTCCCATTTTTTGTGGATTGGGGAACTGTGCTTGAAGACGCCTCAGTTGGCACCTCTGTATTGAAAGTTGCAGCTCATGATGAGGACAGCGGCAGGGATGGAGAAGTTCGCTACTCCATACGAGGTGGTTCAGGCCTTGGAGTGTTTACCATCAATGAAGAGAGTGGTGAGTTTTTTGTAAGCTATTTTGCTTTTCTAAAAACAAAAAAAGTGAGTCTTGTTCAGTTGTCCATTGACATGCCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11100
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011953 Nonsense 1175 4446 2 26
Genomic Location (Zv9):
Chromosome 14 (position 31088686)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29878743
GRCz11 14 30219057
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATCCAAGCGTTTGACCTGGACTCTGAATCAAGTGAAAATCTCTCATA[T/G]AAAATAAGCAGTGGAAATCCRCAAGGATTTTTTGMYATTGACTTCCAGAC
Long Flanking Sequence:
TTGATTACAGTTTTCATTTCAAAAGAACATTATTAGCATTGCGTCAGTCGTTCCTACTTTGTGTGGTTAATTTCTGCTCCGTCCTTATCTAGACTTCCGAGTTTACAATGCAAAACTTTCAGTCCCACGTGACAAGGTTTTATGGCAGCACCATTGGTGGGATCTGAGTCTAAATATTTCAAGTGCTCTTCGTATGATATGTAGGGCATCATGTTTGTGCTTCTTTTCTTTGTCACAGGCATCATTACAACACAAGAAATCCTTGATCGGGAGACAAATAATCATTATTGGCTCACAGTTTACGCTACTGACCAGGGAATCGTGCCGCTTTCTTCATTTGTGGAGGTTTACATCGAGGTTCAGGATGTCAATGATAATGCTCCGCTGACAACAGAGCCTGTGTACTTTCCTTCTGTATCTGAAAACTCTCCCAAAGGCGTCTCCGTCATCCAGATCCAAGCGTTTGACCTGGACTCTGAATCAAGTGAAAATCTCTCATA[T/G]AAAATAAGCAGTGGAAATCCACAAGGATTTTTTGCCATTGACTTCCAGACAGGTCAGTTAATTCTGCTCATTAATTCTTACCATCTGAAAAAGAAGTAAACTTCACAATGCTTTTATAAAGTGTATTTAATACACAAAAGAGCATTCACATTAGTGTGAATTAAATGTGTTGCTTATAAACACCCAAATGCATATTATTTGTCATTTATTAAAGTTGATCAGACTGTTAATTTATAATACAGTGTAAAAAAACATTGACTCAAATTGTAAGGCAACTTGCTGCACTTGCTTTTGTGTTGACACAACTACAGTACTTGGGTTTAAAGTTAAGTGAACTCAAAAAAGCTGTGAAGCAAGTTGCCTTACAATTTTAAGTTGAGTCAAAAAATTTTTTTACAGTGTAGATGCTATTAGTTGAGCTTGAGAGAATATTTGATACACATTTAGATTAGATTAGATTAGATTAATCTTTATTGTCATTACACATGTACATGTACAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35707
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
ENSDART00000011953 Nonsense 1610 4446 9 26
Genomic Location (Zv9):
Chromosome 14 (position 31071517)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29861574
GRCz11 14 30201888
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCCTCTTTCTTATGGTTAGGAAATCATGGAACTTCCTTCATCATTGAT[C/T]AGTCCTCCGGCATTATAACAGTTGCAAGAGAACTTGATTGTGAGACCAGA
Long Flanking Sequence:
AGAGAGTGATTATGTACAGCCACAGCTCCATTTCAGTCTATCTAATTTGAACATCAGCATTTCTCAAGTAAAATGGGGTCTTCGGTGCTTTAAAATGCTTTGTTATTGTGGGCTGAAAATGTTGTAGTGGAAAATGTTGTAAAGTGGAAAAGTGTTAAAATAACCGCCCTAGTGTAACCTAAATCAACATATTTCCTCATTTTGATGCTCAGTTCAAAGTTTGAGAGATTGCCTTGACCAAATGCCTCTCTAAATGCCTTAATCCATTCAATTGCTTCCATGCAAGAAGGTGAACAGGAGGACACTTAATAAAGTGGCTGGTGATTGTATATATTACACAGACAACCGCAGTGTAAGATACATTCATACTACTGTATTTATGTGTTTTACAGCAGTTGCCAGAGAGATATGTGCAATGAAATTATTATATTGATCTCTGTTTCTTACCTTTCCCCTCTTTCTTATGGTTAGGAAATCATGGAACTTCCTTCATCATTGAT[C/T]AGTCCTCCGGCATTATAACAGTTGCAAGAGAACTTGATTGTGAGACCAGAGACCAGTATGAATTGATAATAAAAGCTTCAGACAAAGGAGAACCTTCGCTCAGTGCAGTTACGGCTGTCAGGATCACAGTCACTATCTCAGATAATACCAAGCCGAAGTTCCCCTCCAATTCTCTATCAGCTGAAGTCAGTGAGAACGTTCCTGTTGGGAGTTTTGTAACTTTAGTCTCAGCCTTCAGTCAATCAACAGTTTTCTATCAAATCATAGAGGGAAATGAGAAAGGCGCGTTTGACATCAATCCAAACTCTGGTGCTGTCATCACAAGGAAGAAGCTGGACTTTGAAACACTTTCATCATATAAACTGATTGTCCAGGGAACAGACATGGCTGAAATGTCAAGCAGTGTCACAGTTAACATTTATTTAAAGGATGAAAATGACAATGCTCCTGTCTTCACCCAATCTGAATATACTGGCTTCATCAGCGAGTCGGCCATCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42404
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000011953 Nonsense 1629 4446 9 26
Genomic Location (Zv9):
Chromosome 14 (position 31071458)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29861515
GRCz11 14 30201829
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATTATAACAGTTGCAAGAGAACTTGATTGTGAGACCAGAGACCAGTA[T/G]GAATTGATAATAAAAGCTTCAGACAAAGGAGAACCTTCGCTCAGTGCAGT
Long Flanking Sequence:
TTTCTCAAGTAAAATGGGGTCTTCGGTGCTTTAAAATGCTTTGTTATTGTGGGCTGAAAATGTTGTAGTGGAAAATGTTGTAAAGTGGAAAAGTGTTAAAATAACCGCCCTAGTGTAACCTAAATCAACATATTTCCTCATTTTGATGCTCAGTTCAAAGTTTGAGAGATTGCCTTGACCAAATGCCTCTCTAAATGCCTTAATCCATTCAATTGCTTCCATGCAAGAAGGTGAACAGGAGGACACTTAATAAAGTGGCTGGTGATTGTATATATTACACAGACAACCGCAGTGTAAGATACATTCATACTACTGTATTTATGTGTTTTACAGCAGTTGCCAGAGAGATATGTGCAATGAAATTATTATATTGATCTCTGTTTCTTACCTTTCCCCTCTTTCTTATGGTTAGGAAATCATGGAACTTCCTTCATCATTGATCAGTCCTCCGGCATTATAACAGTTGCAAGAGAACTTGATTGTGAGACCAGAGACCAGTA[T/G]GAATTGATAATAAAAGCTTCAGACAAAGGAGAACCTTCGCTCAGTGCAGTTACGGCTGTCAGGATCACAGTCACTATCTCAGATAATACCAAGCCGAAGTTCCCCTCCAATTCTCTATCAGCTGAAGTCAGTGAGAACGTTCCTGTTGGGAGTTTTGTAACTTTAGTCTCAGCCTTCAGTCAATCAACAGTTTTCTATCAAATCATAGAGGGAAATGAGAAAGGCGCGTTTGACATCAATCCAAACTCTGGTGCTGTCATCACAAGGAAGAAGCTGGACTTTGAAACACTTTCATCATATAAACTGATTGTCCAGGGAACAGACATGGCTGAAATGTCAAGCAGTGTCACAGTTAACATTTATTTAAAGGATGAAAATGACAATGCTCCTGTCTTCACCCAATCTGAATATACTGGCTTCATCAGCGAGTCGGCCATCATCAGAAGTGTGGTCCTGAACTCTCAGAAAGCTCCTCTTGTTGTTCGTGCAACAGATGCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9979
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
ENSDART00000011953 Nonsense 1806 4446 9 26
Genomic Location (Zv9):
Chromosome 14 (position 31070929)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29860986
GRCz11 14 30201300
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTTCGTGCAACAGATGCTGACCAGCACTCAAATGCCAGACTTGTCTAT[C/T]WGATTATGGAGCCATTTGCTTGTAACTACTTCTCTATCGATTCTAGGACT
Long Flanking Sequence:
GAGAACCTTCGCTCAGTGCAGTTACGGCTGTCAGGATCACAGTCACTATCTCAGATAATACCAAGCCGAAGTTCCCCTCCAATTCTCTATCAGCTGAAGTCAGTGAGAACGTTCCTGTTGGGAGTTTTGTAACTTTAGTCTCAGCCTTCAGTCAATCAACAGTTTTCTATCAAATCATAGAGGGAAATGAGAAAGGCGCGTTTGACATCAATCCAAACTCTGGTGCTGTCATCACAAGGAAGAAGCTGGACTTTGAAACACTTTCATCATATAAACTGATTGTCCAGGGAACAGACATGGCTGAAATGTCAAGCAGTGTCACAGTTAACATTTATTTAAAGGATGAAAATGACAATGCTCCTGTCTTCACCCAATCTGAATATACTGGCTTCATCAGCGAGTCGGCCATCATCAGAAGTGTGGTCCTGAACTCTCAGAAAGCTCCTCTTGTTGTTCGTGCAACAGATGCTGACCAGCACTCAAATGCCAGACTTGTCTAT[C/T]AGATTATGGAGCCATTTGCTTGTAACTACTTCTCTATCGATTCTAGGACTGGAGCGATTCAAACTCTCAGCAACCTGGATTATGAGCAGAGACGGATATTTAACTTTAGAGTTCAAGTTCATGACACTGGGAACCCACGTTTATTTGCTCAAGACACTGCCAATGTGACTATACACATCATTAACATTAATGACTGCGCTCCCAAGTTCACTCAGGATTCATACGAGGCTACTCTTCTCCTTCCGACCTATAAAGGTGTTAAAGTGATAACAGTAAAGGCAACAGATGAGGACTCGCTGCCAGGAAACAAACTACATTTTGAAATTGTGGATGGCAACATAGGGAACAAATTCTGGCTTGATCCAACTTTTGGTGATATTTTTGTACAAAATACTACACAGCTGCGGAGCAGGTACAGATTGACAGTCCAAGTCTCTGATGGAAGTTTCATTGGGTGTGCAAATGTGAAAGTCAATGTTAAAGATAATAAAAGTCACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18602
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
ENSDART00000011953 Nonsense 1909 4446 9 26
Genomic Location (Zv9):
Chromosome 14 (position 31070620)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29860677
GRCz11 14 30200991
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAGTGATAAMAGTAAAGGCAACAGATGAGGACTCGCTGCCRGGAAAC[A/T]AACTACATTTTGAAATTGTRGATGGCAACATAGGGAACAAATTCTGGCTT
Long Flanking Sequence:
CAAGCAGTGTCACAGTTAACATTTATTTAAAGGATGAAAATGACAATGCTCCTGTCTTCACCCAATCTGAATATACTGGCTTCATCAGCGAGTCGGCCATCATCAGAAGTGTGGTCCTGAACTCTCAGAAAGCTCCTCTTGTTGTTCGTGCAACAGATGCTGACCAGCACTCAAATGCCAGACTTGTCTATCAGATTATGGAGCCATTTGCTTGTAACTACTTCTCTATCGATTCTAGGACTGGAGCGATTCAAACTCTCAGCAACCTGGATTATGAGCAGAGACGGATATTTAACTTTAGAGTTCAAGTTCATGACACTGGGAACCCACGTTTATTTGCTCAAGACACTGCCAATGTGACTATACACATCATTAACATTAATGACTGCGCTCCCAAGTTCACTCAGGATTCATACGAGGCTACTCTTCTCCTTCCGACCTATAAAGGTGTTAAAGTGATAACAGTAAAGGCAACAGATGAGGACTCGCTGCCAGGAAAC[A/T]AACTACATTTTGAAATTGTGGATGGCAACATAGGGAACAAATTCTGGCTTGATCCAACTTTTGGTGATATTTTTGTACAAAATACTACACAGCTGCGGAGCAGGTACAGATTGACAGTCCAAGTCTCTGATGGAAGTTTCATTGGGTGTGCAAATGTGAAAGTCAATGTTAAAGATAATAAAAGTCACAATCTGAAGTTCACGCAGGACATTTTCACCGCTCAGGTGCAAGAAAACGCTACAGAAAAGAAAACCCTGGCAGTTCTTTCTGTAGTTGGAAATAGAGTCAACGAGCCTTTGTTTTATTCTATTCTCAATCCTAACAGTAAATTTGAAATAGGACGCACATCAGGAGTGCTTTTCTCTACGGGCATCCCATTTGATCGAGAGGAACAGGATTTGTTTGAAATCATTGTGGAGGTAATAAAAGAGCCAGGGTTGAATGGTCCTGCCCACGTGCTTGTGAAAGTGCAAGTTGAGGACGTGAATGATAATGCCCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35706
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
ENSDART00000011953 Nonsense 2628 4446 9 26
Genomic Location (Zv9):
Chromosome 14 (position 31068461)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29858518
GRCz11 14 30198832
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACAACAGCAGTAGATGAAGATGAGGGAAGTAATGCTGATATCGTATA[C/A]ACTATTGAATCTGATATAGACCACTTTGAAATTCATTCACTTAGTGGTGC
Long Flanking Sequence:
GTGACTGATGGTGTTTTCTGTGCTAGCGCTGAAGCTAACATCTATGTGATGGGTGAAAATAGCCACAGCCCATCATTTACTCAGGACGAGTATCTTATTGAACTTGCTGAGAACTCTCCAGTTGGTACGCTTGTCGGACAAGTTGAAGCCATTGATGAGGACCCAGGGAAATACGGACAACTGACATTCTTCATTATGAATGATATCGCCAGGGATAAATTTAACATCAATGAAGATGGACAGATTTACACAGAAGAGAGCTTTGACAGAGAAAACCCAGAAGAGAAAATAATTAGAATCAGTTTAATGGCTAAAGATGGCGGTGGTCTATTAGGCTTTTGTAATGTCATTGTAATTCTCTCTGATGTGAATGACAATTCGCCTAAATTCAAGCATTCAGAATATAAAGTTACTGTGCCAAGAGATGCCCCTAGCAGCACAACAGTAATCAAAACAACAGCAGTAGATGAAGATGAGGGAAGTAATGCTGATATCGTATA[C/A]ACTATTGAATCTGATATAGACCACTTTGAAATTCATTCACTTAGTGGTGCGATTGTCACAAAAGAAAGCCTAATTGGACTGGAAAATGGCCTGTATTCCTTCTTTGTGAAGGCTAAAGATTCTGGAAGCCCACCAAAGCAATCTATTATTCCAGTTTCAATTAGAATAGTTCCCCCTGAAACATCAATCCCAAAGTTTGCCGAGCCGTCGCTGTGGTTGGAGCTTTCAGAAGACCTGGCTGTCGGAACTGAGATGGATATCTTCCAAGCCGAAAATGAGCTTTCTGTGATCTACAGCCTTGTTGGAGGGAACACCCCAGAGAGTAACAAACATGATGTCTTTGCTATTGACAGCACAACTGGTAAGCTTATACTCACAAAACGACTAGACTATGAAACTATAAAATGGTATCATCTCGCAGTGCAGGTTCGAGATGTCAAAGATGACATGGAAATTATCTCAACTGTAGATGTGAGTGTCCATCTCAAGGATGTCAATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35705
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
ENSDART00000011953 Nonsense 3139 4446 12 26
Genomic Location (Zv9):
Chromosome 14 (position 31060680)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29850737
GRCz11 14 30191051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATCATGTGAGCATTTATCAGAATACACAACCTGGAACATACGTGGCA[C/T]GACTGGAGGCCTTCGACGCAGATATCGGTATGAACAACTTGTTATTTGGT
Long Flanking Sequence:
CTTTTTATGGACAAAGGAAAATTAAGACCTGTTTACAATTATTTAAGACCTACTAGACAACATTTCTGTCAATTAAAGACTTTTTAAGACCCCACTGACACCCTGATAGTGTATCCAATATGAAAGCATGCAGCATTTATTTGCTGTTCTTGCTTTCATTGACTATTTTGGCTATTATGTCAGAGAGAACATTTATGATTTGGGATCTTGCTCAATCAGGAGGCTCCACATATATATTTTTTTCACAAATATAAAGTGCTGATCCTTAATATTGTTTTATTTTTATTTTTCTAGGTGCAGTGAAAACACTGGCAACTCTGGATAGAGAGGTAACAGATGTGTACAACCTAACAGTGCGTGCAGTAGACAAAGACAATCACTTCTGCCAAGCTTCTTTGCTCATCACAGTTGAAGATGCAAATGACAACGCACCCAAATTCACATCTGACCCACATCATGTGAGCATTTATCAGAATACACAACCTGGAACATACGTGGCA[C/T]GACTGGAGGCCTTCGACGCAGATATCGGTATGAACAACTTGTTATTTGGTAACTTTGTTTGTGCATATTGCCTCAAACCATCATGAAGAACGATTAGTTGCAGTAGATACACAATCATCGCTTCCAATAGTGTGTATCTTGATTGAAGCATCAGTAGTTATTAGTCTGTGCCATCTTTTGCTCTGTGTGCCATTTCATTACTCTCATCTCCACTCAGCATGCAGCTTTCCCTGACTGCAGAACAATTGAATATAATCTTCTCATACACGATTGTCTTAGCTCCCTGTGAAGGTAACAATTACTTTCTCACAGTGGTCCACACTCTAATTCAGACAATCTGAACTTTTCTGCCTTCTGGGCAAACTTCAGATCAGGTTTTTTTTTTTCATGGCATTTTAAGCATTGTTGTTTTTTTGTAATGTTTTAATCATTTTTATTGAGTTTACAGAACACTATTAAGTAAAAACAGAAACCTTTTATGGCTATTCATTTTTAAATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35704
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
ENSDART00000011953 Nonsense 3390 4446 15 26
Genomic Location (Zv9):
Chromosome 14 (position 31053393)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29843450
GRCz11 14 30183764
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCCCATTCATCATGGACGCAGTCAGTGGTGAACTGCAACTGGCCCGT[C/T]AGTTAGACAGAGAGATGGTAATGCTTTTTTGATTGATACTTTCCCCTTGG
Long Flanking Sequence:
AACACATTAACAATTACCTAAAAGTGTCTATGCTAAAATATTCTTCAGCTTTACCTTTACCTTAACCTTACCGTGGAAATGACCTGTAACCTTATGAATAGTCTAGCACCTCACTGGCAATCATTAAAGCACTACAGCACCTCTGTGAGAACTACCTAGCAACAACCCAGATCACCCCTATCATCCACGCAGCAACATGCTAAAAAAAACTCTGCTGTACACAACTCCTCCATACTGTACATCTGATACTGTGCCAGTGAGTTTTGGGTGAGGAGGCACCACATGAATCTACTTTAAATTAAATCAATGTACACATCTGTGGAAAGTACTTAATGTTGAGTAAACACATTTTCATGAAGTGTAATGATCCCTGTCCTTAGGTACTTGCGAATGATCTTGATGGGCCTTTAAACAACCAAATCCGCTATTCCATTGAAGAGAGCAACCAGAGCTGCCCATTCATCATGGACGCAGTCAGTGGTGAACTGCAACTGGCCCGT[C/T]AGTTAGACAGAGAGATGGTAATGCTTTTTTGATTGATACTTTCCCCTTGGATAGAGTGGGTTTTAAAAATACCTATAATTCATTGAGCACCAATTTTTTACACATTAAAAATTTATTTGACCTTATGTTTTGTCTATTACATTTATCCATTGTCTCTGAAAATTTTGTTTGTCATAAAAATGTATTGTATAAGATTTTTTCCATTCTTTGCATCCATAGCCAGCATTTTACTGAAGCTAAAGCCAAAAACTAGAATGTCATCTGACAAATTAATCCACTTCATCTCGCAGCACAGATCACTTTGAATAACAAAGTGCAAAAAATAAAGATAAATTGTGGTAGATGGTTGAGCACCACTGCTATTGTATGCTGGTTTCAATGCCTAATCATATGCCACTCATATGTATTTGTGTGTGTTTACATTTGACATACAGCCAGTAAATACAATATTTACTTTTTAAATTTTTCTTTCTTTCTTTTTTTTTTTTATAAAAAAGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8682
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
ENSDART00000011953 Essential Splice Site 4110 4446 23 26
Genomic Location (Zv9):
Chromosome 14 (position 31036239)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 29826296
GRCz11 14 30166610
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCTTGATGGAGCCATTTGTGAGTGTGAGCCAGGATTCAAAGGAGAAAG[G/A]TGTGTTGTTATTGCTAGCACTGTRAACATAACAGTASTCTTTTYAAATAT
Long Flanking Sequence:
TAACTTTAGAGTTAAACTTTGCAATTACTCCCCAATCATGCATGTTATTAACTCATGTGTGTTATTACAGTACATCTTTTTTAACTTCCATATTTATAATGTATAAACTGCCTTATGGTGTTTCTGTATCACTGATATTCTCTCAGGTAACATTTGCAAATGCAGTCCTTCATTCTCTGGGACTCGCTGTGAGGTGAAGATCAGTCCTTGTGACTCAAACCCTTGTCTGTATGGAGGAACCTGCATCCAAAATAACCTGGACTACTCATGTAAATGCCGGGGCAAGTACTCCGGTCAAAGGTACTGCACTGCCAATGTACTGTACAAGTACATTATTGATAATAAAATCTTTCATTACTCTATGTAAAACACTCTCTGTTTGACCGCAGGTGTCAGATAGGTCCCTACTGCAAAGAGAATCCATGCCAAAATGGTGGACAGTGTATAGACAGTCTTGATGGAGCCATTTGTGAGTGTGAGCCAGGATTCAAAGGAGAAAG[G/A]TGTGTTGTTATTGCTAGCACTGTGAACATAACAGTACTCTTTTTAAATATCAGGAATTCCACAGGTCATAGAATTTCAGGAATATCATGGAATTTTTTATGTCCATACTATGTGATGTCCATGTAATGTCCAATGTCCATACCAGACATTGAAAGTCAGGGAATATACTGTATATATTGGCCAAGTAAGGATGTTTTCACACCCGCCTTATTTAGTTCGGTTGAATAGAGTTAATGTTTCCTCTTGGTGTGGTTAGTTTGGGCAGATGTGAATGTTGCAATTGCACTTGAGTGCGCACCAAAAGCAGACGAACAAAGTTTCAAACAAACTTTCAGACGAACCCTAGAGCAGTAAGCTTGTGGTAAGAACATGATGCGAACTAAAACAGACCCACCCGCAAAAAGTACTGTGCCTTTTTGGACTAATCCAGCTGTCATAGTCCGATGCGCTGTCCCATCTCATGGGGTGTGGAGAAAAAATATTGGTAGACAGCGCTTTAC
Associated Phenotype:
Not determined