Busch Lab

ZMP

LOC556748

Ensembl ID:
ENSDARG00000076143
Human Orthologue:
PPIP5K1
Human Description:
diphosphoinositol pentakisphosphate kinase 1 [Source:HGNC Symbol;Acc:29023]
Mouse Orthologue:
Ppip5k1
Mouse Description:
diphosphoinositol pentakisphosphate kinase 1 Gene [Source:MGI Symbol;Acc:MGI:2443281]

Alleles

There are 13 alleles of this gene:

Allele Name Consequence Status Availability
sa30893 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41025 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41026 Nonsense Mutation detected in F1 DNA Not yet available
sa21076 Nonsense Available for shipment Available now
sa10406 Essential Splice Site Available for shipment Available now
sa18894 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18089 Essential Splice Site Available for shipment Available now
sa21077 Essential Splice Site Available for shipment Available now
sa21078 Essential Splice Site Available for shipment Available now
sa34185 Nonsense Available for shipment Available now
sa16976 Nonsense Available for shipment Available now
sa2349 Nonsense Available for shipment Available now
sa8681 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30893
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
ENSDART00000111444 Essential Splice Site 146 1345 3 29
ENSDART00000111444 Essential Splice Site 146 1345 3 29
Genomic Location (Zv9):
Chromosome 7 (position 54229225)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52499075
GRCz11 7 52774145
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCACTGCTTATCAATGATCTTAACATGCAGTATTACATACAGGATAGG[T/C]ATTACCATATTTTTCATTAATCGCAGTTTTGCAAATGATCTCTCATGTTT
Long Flanking Sequence:
ATATATTCTTTTGTGTTTGACAGAATAATGAAACTCAAATAGGTTTTGAACAAGTGAAGGGTGAGTAAATAATGAAAATTGAGAATTTTGGGTGGATAATCCTTTTAACTAATCTAAAGAGATACAATAAAGATGTGACCACGTTGGTAAGGTTTCTGTCTGCCGTTGATAGTGTAGTGAGGTATGACGCACAGCACATTTATTTTCAAACAAAGCAGCTTTCTTTCAAACAATGTTACAAATTTAAGTGGCCGATTTGCCCGTGTAGACTCTTTTTAAAATGACTGGATTTCACCCATTTAAAAAAAAGAGAAATAAGTCTTAAGCCTCTTCTGTGATATATCAATGTAACTGATAAGATGTCTGTGTGTTGCATCTGTGTGACAGTAATGTTTTCTCTTGAACTAGGTTTCCCCTTGGATAAAGCAGTGAGTTATGCAAAGCTCCGTAACCCACTGCTTATCAATGATCTTAACATGCAGTATTACATACAGGATAGG[T/C]ATTACCATATTTTTCATTAATCGCAGTTTTGCAAATGATCTCTCATGTTTGCACACATTTTTGAATTGTAGCTGATGCCTGAATAAGGGATTTGTCTGTTGTTTTCATATTTTAGGAGAGAGGTTTATCGTATCCTGCAGGAGGAGGGGATTGATCTACCACGCTACGCAGTGTTAAACCGTGACCCTGACAAGCCTGATGGTCAGTCAAAGCTTATTTTAAACAAGCATTTGAAAGCTTGGAATATCTAAAGTGTTTTTCTTGATTTTATTTTGAGGAGTTTTAGTTGAAAAGTTTTAGGAGATTAGTCAAAGTAATCGAAATCTGCGTTCAGAACCTATTATTGATCACATTTTTACAGGACAATTTTTTCATTTACTTTCCCTACGTGTCATGTGACCCTACTTTGTTAAAGGCTGTGGCTGATTTCTACTTCTGCGGCCACTTTGCAGCCACATCTTATCTCTGGTCAAGTAGGACAATGGACCCATTTTTGAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41025
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
ENSDART00000111444 Essential Splice Site 146 1345 3 29
ENSDART00000111444 Essential Splice Site 146 1345 3 29
Genomic Location (Zv9):
Chromosome 7 (position 54229225)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52499075
GRCz11 7 52774145
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCACTGCTTATCAATGATCTTAACATGCAGTATTACATACAGGATAGG[T/C]ATTACCATATTTTTCATTAATCGCAGTTTTGCAAATGATCTCTCATGTTT
Long Flanking Sequence:
ATATATTCTTTTGTGTTTGACAGAATAATGAAACTCAAATAGGTTTTGAACAAGTGAAGGGTGAGTAAATAATGAAAATTGAGAATTTTGGGTGGATAATCCTTTTAACTAATCTAAAGAGATACAATAAAGATGTGACCACGTTGGTAAGGTTTCTGTCTGCCGTTGATAGTGTAGTGAGGTATGACGCACAGCACATTTATTTTCAAACAAAGCAGCTTTCTTTCAAACAATGTTACAAATTTAAGTGGCCGATTTGCCCGTGTAGACTCTTTTTAAAATGACTGGATTTCACCCATTTAAAAAAAAGAGAAATAAGTCTTAAGCCTCTTCTGTGATATATCAATGTAACTGATAAGATGTCTGTGTGTTGCATCTGTGTGACAGTAATGTTTTCTCTTGAACTAGGTTTCCCCTTGGATAAAGCAGTGAGTTATGCAAAGCTCCGTAACCCACTGCTTATCAATGATCTTAACATGCAGTATTACATACAGGATAGG[T/C]ATTACCATATTTTTCATTAATCGCAGTTTTGCAAATGATCTCTCATGTTTGCACACATTTTTGAATTGTAGCTGATGCCTGAATAAGGGATTTGTCTGTTGTTTTCATATTTTAGGAGAGAGGTTTATCGTATCCTGCAGGAGGAGGGGATTGATCTACCACGCTACGCAGTGTTAAACCGTGACCCTGACAAGCCTGATGGTCAGTCAAAGCTTATTTTAAACAAGCATTTGAAAGCTTGGAATATCTAAAGTGTTTTTCTTGATTTTATTTTGAGGAGTTTTAGTTGAAAAGTTTTAGGAGATTAGTCAAAGTAATCGAAATCTGCGTTCAGAACCTATTATTGATCACATTTTTACAGGACAATTTTTTCATTTACTTTCCCTACGTGTCATGTGACCCTACTTTGTTAAAGGCTGTGGCTGATTTCTACTTCTGCGGCCACTTTGCAGCCACATCTTATCTCTGGTCAAGTAGGACAATGGACCCATTTTTGAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41026
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
ENSDART00000111444 Nonsense 163 1345 4 29
Genomic Location (Zv9):
Chromosome 7 (position 54229392)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52499242
GRCz11 7 52774312
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAGGTTTATCGTATCCTGCAGGAGGAGGGGATTGATCTACCACGCTA[C/A]GCAGTGTTAAACCGTGACCCTGACAAGCCTGATGGTCAGTCAAAGCTTAT
Long Flanking Sequence:
GATAGTGTAGTGAGGTATGACGCACAGCACATTTATTTTCAAACAAAGCAGCTTTCTTTCAAACAATGTTACAAATTTAAGTGGCCGATTTGCCCGTGTAGACTCTTTTTAAAATGACTGGATTTCACCCATTTAAAAAAAAGAGAAATAAGTCTTAAGCCTCTTCTGTGATATATCAATGTAACTGATAAGATGTCTGTGTGTTGCATCTGTGTGACAGTAATGTTTTCTCTTGAACTAGGTTTCCCCTTGGATAAAGCAGTGAGTTATGCAAAGCTCCGTAACCCACTGCTTATCAATGATCTTAACATGCAGTATTACATACAGGATAGGTATTACCATATTTTTCATTAATCGCAGTTTTGCAAATGATCTCTCATGTTTGCACACATTTTTGAATTGTAGCTGATGCCTGAATAAGGGATTTGTCTGTTGTTTTCATATTTTAGGAGAGAGGTTTATCGTATCCTGCAGGAGGAGGGGATTGATCTACCACGCTA[C/A]GCAGTGTTAAACCGTGACCCTGACAAGCCTGATGGTCAGTCAAAGCTTATTTTAAACAAGCATTTGAAAGCTTGGAATATCTAAAGTGTTTTTCTTGATTTTATTTTGAGGAGTTTTAGTTGAAAAGTTTTAGGAGATTAGTCAAAGTAATCGAAATCTGCGTTCAGAACCTATTATTGATCACATTTTTACAGGACAATTTTTTCATTTACTTTCCCTACGTGTCATGTGACCCTACTTTGTTAAAGGCTGTGGCTGATTTCTACTTCTGCGGCCACTTTGCAGCCACATCTTATCTCTGGTCAAGTAGGACAATGGACCCATTTTTGAGCCTTACTTTGCACTACATTGATGATTATTGAAAGCTGCCCGAGAGATGCCTTTAGATGGCATATACAACTTGTCAGTGAACTATTAGGGCAAATATATATAAATAAATAAATAAAATAATCCAAATCAAGTAAAGAGCCCTATCATACACCCAGATCAATAATGTGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21076
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Nonsense 347 1345 8 29
Genomic Location (Zv9):
Chromosome 7 (position 54236034)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52505884
GRCz11 7 52780954
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGATGTCAATGGATTTAGCTTTGTGAAGAATTCCATGAAATACTA[T/A]GACGACTGTGCTAAGATACTGGGGTAAAAGCTAATAATAAAGACCCAAAA
Long Flanking Sequence:
GTTTAGATCTGTGGAATTATTTTTTTGGAACTTTACTCCCTTTTGTTCATCAGATGAAAATATCCTGTTCATTTTTATTAGTTTTTTGCTTTTTTGTGTGTTTGTTTTATCACAGGTGTACACAGTAGGGCCAGATTACGCTCACGCAGAGGCTCGTAAGTCCCCTGCTCTTGATGGAAAAGTGGAGCGGGACAGTGAAGGAAAAGAAATCCGCTACCCGGTCATGCTCACTGCCATGGAGAAGCTTGTGGCTCGTAAAGTTTGTCTGGCATTCAAGGTAAGAGGATCTTACAAAGAAAATAACTGCAGAATGAAAGCTTCAGCCTGAGCTTCAGCTTCAGAGACATTTTTAGGTTAAGATTTTGATGTGTATTTTATTCTCAAAAACTCTTTGTACTGCAGCAAACAGTGTGTGGATTCGACCTCCTCCGAGCCAATGGCCACTCATATGTGTGTGATGTCAATGGATTTAGCTTTGTGAAGAATTCCATGAAATACTA[T/A]GACGACTGTGCTAAGATACTGGGGTAAAAGCTAATAATAAAGACCCAAAAGTTTGAAAAGTTTGTCTTTCATATATAACATGCAGATATAACAGAGATTAACTTTTTTTTTTTTTTCAGAAATATTGTAATGAGGGAGCTGGCTCCTCAGTTCCAGATCCCCTGGTCCATACCTACGGAGGCAGAGGACATTCCTATTGTACCCACTACATCAGGAACAATGTACTCATCACATGTTGTTCTCATATGTTGGCTTAAACGTATTAGTTTACATCGTTTATTGATAATATTTAAATTCTGGTGAGCATTCAAAGTGTCCTTGTTGACGCTCTTTATAATTCTGTCCTTTAGGATGGAGCTGCGTTGTGTGATTGCTGTAATCCGGCATGGAGATCGCACACCAAAGCAGAAGATGAAGATGGAAGTGCGAAATGCCATGTGCGTTTTTTTTGCCTGTTTGAAATACTAAATAGGAATGATGGATACATAATTAAAATACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10406
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
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Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Essential Splice Site 355 1345 8 29
ENSDART00000111444 Essential Splice Site 355 1345 8 29
Genomic Location (Zv9):
Chromosome 7 (position 54236058)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52505908
GRCz11 7 52780978
KASP Assay ID:
554-6157.1 (used for ordering genotyping assays)
KASP Sequence:
TTTGTGAAGAATTCCATGAAATACTATGACGACTGTGCTAAGAYACTGGG[G/A]TAAAAGCTAATAATAAAGACCCAAAAGTTTGAAAAGTTTGTCTTTCATAT
Long Flanking Sequence:
TTGGAACTTTACTCCCTTTTGTTCATCAGATGAAAATATCCTGTTCATTTTTATTAGTTTTTTGCTTTTTTGTGTGTTTGTTTTATCACAGGTGTACACAGTAGGGCCAGATTACGCTCACGCAGAGGCTCGTAAGTCCCCTGCTCTTGATGGAAAAGTGGAGCGGGACAGTGAAGGAAAAGAAATCCGCTACCCGGTCATGCTCACTGCCATGGAGAAGCTTGTGGCTCGTAAAGTTTGTCTGGCATTCAAGGTAAGAGGATCTTACAAAGAAAATAACTGCAGAATGAAAGCTTCAGCCTGAGCTTCAGCTTCAGAGACATTTTTAGGTTAAGATTTTGATGTGTATTTTATTCTCAAAAACTCTTTGTACTGCAGCAAACAGTGTGTGGATTCGACCTCCTCCGAGCCAATGGCCACTCATATGTGTGTGATGTCAATGGATTTAGCTTTGTGAAGAATTCCATGAAATACTATGACGACTGTGCTAAGATACTGGG[G/A]TAAAAGCTAATAATAAAGACCCAAAAGTTTGAAAAGTTTGTCTTTCATATATAACATGCAGATATAACAGAGATTAACTTTTTTTTTTTTTTCAGAAATATTGTAATGAGGGAGCTGGCTCCTCAGTTCCAGATCCCCTGGTCCATACCTACGGAGGCAGAGGACATTCCTATTGTACCCACTACATCAGGAACAATGTACTCATCACATGTTGTTCTCATATGTTGGCTTAAACGTATTAGTTTACATCGTTTATTGATAATATTTAAATTCTGGTGAGCATTCAAAGTGTCCTTGTTGACGCTCTTTATAATTCTGTCCTTTAGGATGGAGCTGCGTTGTGTGATTGCTGTAATCCGGCATGGAGATCGCACACCAAAGCAGAAGATGAAGATGGAAGTGCGAAATGCCATGTGCGTTTTTTTTGCCTGTTTGAAATACTAAATAGGAATGATGGATACATAATTAAAATACTTTTTCTTTTCTTGCAGGTTTTTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18894
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
ENSDART00000111444 Essential Splice Site 355 1345 8 29
ENSDART00000111444 Essential Splice Site 355 1345 8 29
Genomic Location (Zv9):
Chromosome 7 (position 54236058)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52505908
GRCz11 7 52780978
KASP Assay ID:
554-6157.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGAAGAATTCCATGAAATACTATGACGACTGTGCTAAGATACTGGG[G/A]TAAAAGCTAATAATAAAGACCCAAAAGTTTGAAAAGTTTGTCTTTCATAT
Long Flanking Sequence:
TTGGAACTTTACTCCCTTTTGTTCATCAGATGAAAATATCCTGTTCATTTTTATTAGTTTTTTGCTTTTTTGTGTGTTTGTTTTATCACAGGTGTACACAGTAGGGCCAGATTACGCTCACGCAGAGGCTCGTAAGTCCCCTGCTCTTGATGGAAAAGTGGAGCGGGACAGTGAAGGAAAAGAAATCCGCTACCCGGTCATGCTCACTGCCATGGAGAAGCTTGTGGCTCGTAAAGTTTGTCTGGCATTCAAGGTAAGAGGATCTTACAAAGAAAATAACTGCAGAATGAAAGCTTCAGCCTGAGCTTCAGCTTCAGAGACATTTTTAGGTTAAGATTTTGATGTGTATTTTATTCTCAAAAACTCTTTGTACTGCAGCAAACAGTGTGTGGATTCGACCTCCTCCGAGCCAATGGCCACTCATATGTGTGTGATGTCAATGGATTTAGCTTTGTGAAGAATTCCATGAAATACTATGACGACTGTGCTAAGATACTGGG[G/A]TAAAAGCTAATAATAAAGACCCAAAAGTTTGAAAAGTTTGTCTTTCATATATAACATGCAGATATAACAGAGATTAACTTTTTTTTTTTTTTCAGAAATATTGTAATGAGGGAGCTGGCTCCTCAGTTCCAGATCCCCTGGTCCATACCTACGGAGGCAGAGGACATTCCTATTGTACCCACTACATCAGGAACAATGTACTCATCACATGTTGTTCTCATATGTTGGCTTAAACGTATTAGTTTACATCGTTTATTGATAATATTTAAATTCTGGTGAGCATTCAAAGTGTCCTTGTTGACGCTCTTTATAATTCTGTCCTTTAGGATGGAGCTGCGTTGTGTGATTGCTGTAATCCGGCATGGAGATCGCACACCAAAGCAGAAGATGAAGATGGAAGTGCGAAATGCCATGTGCGTTTTTTTTGCCTGTTTGAAATACTAAATAGGAATGATGGATACATAATTAAAATACTTTTTCTTTTCTTGCAGGTTTTTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18089
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Essential Splice Site 508 1345 13 29
Genomic Location (Zv9):
Chromosome 7 (position 54240469)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52510319
GRCz11 7 52785389
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTAACATACCTTCCTCATGGACAACCCAAAACATCCAGTGAGGARGAAG[G/T]TATGAGGATTGTTGATAGGAAAATTTGTTGGGTTRAAATCGTGTTGTGCA
Long Flanking Sequence:
TGGAACTAAACTGTGCAGAGCTGCGGGCCTTTTGGAACTGAGTTTGACACCTCCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTTGACCAGCCTGGTTTTAGAGGGGTTTTGGCCATTTCCAGGCTGGTTTCTAGCCATTTCCTGTCTGGTCTTAGCTGGTCAGGCTGGAAAATGACCAGCTAAATCCAGCTAAAACCAGCTTGACCAGCCTGGTTTAAGCTGGACATAGCTGGTTTTAGCTGGTCATCTTCCCGCCTGGCCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGTTTTTTTAGTTGGGCTGTGGGATACACCATAATCAAACTATTATCTCTGTATATTTATATTTGATTTATTAAATTTTTTTCAGGTATGGCCATTTCTCTGGAATCAATAGGAAAGTGCAGCTAACATACCTTCCTCATGGACAACCCAAAACATCCAGTGAGGAAGAAG[G/T]TATGAGGATTGTTGATAGGAAAATTTGTTGGGTTGAAATCGTGTTGTGCATGATGGTACTGCTGTGTGTTCAGATACCCGTAAGGAGGGCCCCTCCATACTGCTGGTGCTGAAGTGGGGGGGAGAACTGACTCCAGCCGGCAGAGTACAGGCTGAAGAACTCGGCAGGGCTTTTCGCTGCATGTATCCTGGAGGTCAAGGTACAGTATGGTCAATTACACAGACATTTATTACACTTGTGCCTTTTTCACATCACACTTTAGATGATTTTTTTTTGTCAAAGTCTGCATGAGTCCACAATTTTTGATACGGTACTTAACATTTAAAGTGAATCAAAAAAGTATTTCAAATTAGCCTACGACAATATAAAATCTTTGGATCCACTTCAAATGTTGACTACTATATAATTTATTCTTTTTATTTATTATAAAAGAAACTTGCTATGTGTTCTGTCTTCGACTAACTGGGACTTGACACAGCACTCCTCATTTGTTAACCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21077
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Essential Splice Site 550 1345 14 29
Genomic Location (Zv9):
Chromosome 7 (position 54240669)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52510519
GRCz11 7 52785589
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGAAGAACTCGGCAGGGCTTTTCGCTGCATGTATCCTGGAGGTCAAG[G/A]TACAGTATGGTCAATTACACAGACATTTATTACACTTGTGCCTTTTTCAC
Long Flanking Sequence:
ACCAGCTAAATCCAGCTAAAACCAGCTTGACCAGCCTGGTTTAAGCTGGACATAGCTGGTTTTAGCTGGTCATCTTCCCGCCTGGCCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGTTTTTTTAGTTGGGCTGTGGGATACACCATAATCAAACTATTATCTCTGTATATTTATATTTGATTTATTAAATTTTTTTCAGGTATGGCCATTTCTCTGGAATCAATAGGAAAGTGCAGCTAACATACCTTCCTCATGGACAACCCAAAACATCCAGTGAGGAAGAAGGTATGAGGATTGTTGATAGGAAAATTTGTTGGGTTGAAATCGTGTTGTGCATGATGGTACTGCTGTGTGTTCAGATACCCGTAAGGAGGGCCCCTCCATACTGCTGGTGCTGAAGTGGGGGGGAGAACTGACTCCAGCCGGCAGAGTACAGGCTGAAGAACTCGGCAGGGCTTTTCGCTGCATGTATCCTGGAGGTCAAG[G/A]TACAGTATGGTCAATTACACAGACATTTATTACACTTGTGCCTTTTTCACATCACACTTTAGATGATTTTTTTTTGTCAAAGTCTGCATGAGTCCACAATTTTTGATACGGTACTTAACATTTAAAGTGAATCAAAAAAGTATTTCAAATTAGCCTACGACAATATAAAATCTTTGGATCCACTTCAAATGTTGACTACTATATAATTTATTCTTTTTATTTATTATAAAAGAAACTTGCTATGTGTTCTGTCTTCGACTAACTGGGACTTGACACAGCACTCCTCATTTGTTAACCTGACATTATTAAATACAGTTTTCAGGGTCCAAACCGCTGCACATTTGAAAGTTGAAGTCAGAATTATTAGCCCCCCTTTGAATTCTTTTGTCTTTTAAATATTTCCTAAATGATGTGTAACAGAGCGAGGGAATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGCAAGAAGTCTTATTTGTTTTATTTCTGAAACCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21078
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Essential Splice Site 652 1345 16 29
Genomic Location (Zv9):
Chromosome 7 (position 54243026)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52512876
GRCz11 7 52787946
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGATCATGCAGAAAGATAAAGTCTTCACTGAAGAAGACTATGACAGG[G/A]TACATTTGGAGTGTCTTTTGAACTGTATTTCAGCCCTCCGCTGACTTGAT
Long Flanking Sequence:
TAAGATTAGAGTTGAAGCTGAATCCTACAAGACTGTGTTTCTAGGAACAGGGTTGAATTTTATTAATCTGTTCTGTGAATGTTATTTTCTTGTCCACTTACAGGCGATTACGCTGGCTTTCCAGGCTGCGGTTTGCTCAGGCTACATAGCACCTACCGACATGACCTCAAGATCTACGCCTCTGATGAAGGCAGGGTGCAAATGACTGCTGCTGCCTTTGCAAAGGTCCTCAGCCACAACAAAAACAGGTTATCGAAGGTTTAAAGGTATAAAGTTATCAAAGGTTGTTAAACTGCCGTTGGTTGTTTGCCTGGCAGGGTCTCTTAGCGTTGGAAGGAGAACTGACACCCATCTTGGTCCAGATGGTGAAAAGTGCAAATATGAACGGTCTGCTGGATAACGATATTGAATCGCTCAGCGGCTGTCAGCAGAGGGTTAAAGCCAGACTTCATGAGATCATGCAGAAAGATAAAGTCTTCACTGAAGAAGACTATGACAGG[G/A]TACATTTGGAGTGTCTTTTGAACTGTATTTCAGCCCTCCGCTGACTTGATATGAAAGGCGCATCTGTGTCCACTTCATCTCTTGTGTTTTTTCAGCTGGCCCCAACATGCAGCAGTTCTCTGGTGAACTCTATGAGGGCTGTCGAGAATCCAGTGTGTATATGTGATCAAGTCTACACCCTCGTCCAGAGCCTCACTTCACAGATCCGCAAAAGACTCGAAGACCCCAAATCAGCAGGTGATTGTTCTGTGCTCAATTAAAAACAGTATTTATGCAAAAAATAATTTCATTAATTACTCACCTTTATTTCAGTCCAATCCCCTGAGAATTTCATTCATCTTTAAAACACAAATGAACATATTTTTGATGAAATCTGAGAATTCTCTGGCCCTCCATAGACAGCTCACTTTTCTGGACTTTGAACGTCCTGGGACAGTTGCTGTCTATGAGTAATGAGAGAAATCTCAAATTACACCTAAAATATCTTAACTTGCTATCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34185
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Nonsense 985 1345 24 29
Genomic Location (Zv9):
Chromosome 7 (position 54248367)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52518217
GRCz11 7 52793287
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGTGCCCCATTTGTGTGCACACAGGTCTTGTCAGAAAGCTCTTCCTCT[A/T]AAGGAGGCAGCTATCGCCTCTTCCCCTCCTGCTCACGTCAGTCTCCAGAG
Long Flanking Sequence:
CGCTTCCATGTGGAACTGCATTTCAGCCCTGGGGTTAAAGTGTCTGAGGAAGAGAGCGCTCCGATGGGCTTCGGCTTCCGACCAGCCTCTGCTGAAGTATACAACCCTTTCCTTTGTCCCATTGGAGAACACATTTTTTTAGCTAATAATAGCAATGCTTGCTTGCTGAAGATTCCATGTCTGTGTTTGTGTGTCTTGATGTAGAATGACCAGAAGCAAACAGACCCTGGAAGTTTGGAGAACCTCTCACGGGATGAGCCCGACCGTGCATTGCCCCTTTCAGAGGCCATCAGCACCCAGAGGAAATCCCCTTTGATCCGCAACCGCAAGACTGGCTCTATGGAGGTATCAAAGACAGCATTACACCTACTCTACTTTCTAAAATATGACTGTGAATCTCAGTGGTGTCAAATTGACAGAATCAGGCTGGGTTTTATGTGGCAAAATTCAAAAGTGCCCCATTTGTGTGCACACAGGTCTTGTCAGAAAGCTCTTCCTCT[A/T]AAGGAGGCAGCTATCGCCTCTTCCCCTCCTGCTCACGTCAGTCTCCAGAGATGAAGCAGAGCGGATTAGGTTGGTATCGTGTGTCTGTCCCTCATTCAACCTCAACAACTGCTGTTTATCTCTTCTCCCTGACAGGAAATCACCCTCTGCATCCAAGGCAACACTATATTGAGTCTTATTTCGGGTGTGCCAACCATTAGCTGGGGGCTTTCATTGACATAAAGGAAATTAGTGAATACACAGTGCGTATTGGACACAGTGGAGTTTAGTGCATGTGATGCTGTTCATTTTTAGATCTATTAAAGGGATCATTGTGCGTTTTGCTTTATGCAAACAAATGCTGTGATTTCTGATATGCCATGGTGGTGAAGAGTTCTGAAAGTCCTGCTCAAGTAAAAGTAAAATTACTTGCCATAAAATTTAGTGTGAGTAAAAAGTATCTGTTAAAAATATGAGTAGAATGTTGCTCTTCTAAAGTACTCAAGAATAGTGTTCGTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16976
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
ENSDART00000111444 Nonsense 1191 1345 29 29
Genomic Location (Zv9):
Chromosome 7 (position 54275086)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52544936
GRCz11 7 52820006
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGACACCTCTCCACGCTTCAGCTTCAGTGAGAAGATCACCCTAACGCCT[C/T]AGAGCAGTGAAGAGATCCACCAGATYCCTCAAAACAACAACTGMCACACT
Long Flanking Sequence:
TTTTGGAAAAAGGCTGTAACATCAAATATGTGGAAAAAGTAAAGCGCTATCAATACTTTTCAGATGCACTGTATAATAACTTTAACTGTTAAAAGCTATTAATTAGTTAATTAGTTAAAGTTATTAATAACTAATTTTAAGTTACAGTAACTAATAACCTTAACTTTTCTGAATTTGATTGTAATGCAAGAATGTGCACCTTTTCTATTGCTGCTTTGAAACAACAGTTCTTGTAAAAAGTGCAAATAAACTTGAATGAATGAATACAAAAAAATAGTGAGAACACAGGAGTGAGACTGGGGAAGTTCTCTTGATGACACAAATGGAAAAACTCAAACAAAAGTAGTGTGTTTTGCAGCCAAATGATGGTTTGTGTGTGTTTTGTTTGTACAGACAGCAGTGGTCCTTCCAGCACAGTGTCCAGCGCCGGCCCCTCGTCTCCCACCACGGCTGACACCTCTCCACGCTTCAGCTTCAGTGAGAAGATCACCCTAACGCCT[C/T]AGAGCAGTGAAGAGATCCACCAGATCCCTCAAAACAACAACTGCCACACTGTGTCTTTGACATCCGAACCCAGCATACCCTCAGAGGACCCGCACAGCTCCATACCCTCTCCCATCATGGAGAGACCCAGTCAGATAACATCAGACGGCACAGACTCTGCAGGCCAGTGTCTGACAGAGAGCCCTTCCTGTGATGAAGGGTCAAGTCCAAACACGGCTGAGCCCAGTCCACCCAGTCCTCTCCCAGAGTCCTTCCGCGGGCTGCCCGGCTCCCTGCCTGTTCTCCTGGAGCTCAGAGAAAGCAGTTCTGAGACCGGGTCCAGCGCCCAGACACCGCTCAGCCCTGAGGAGCCCGATGAGTTCTTTGATACGCAGGAAACGGTTGACGCTTGGAGGGAGAACCCGGCATCCCTGCCCCATCCTGGAACTCCTCTGGAGGTGGGAGCTCCACACGTGCCTGAGCCTTGAAGGAAACAGTGCTCCCTTCACCCCATCCCAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2349
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Nonsense 1205 1345 29 29
Genomic Location (Zv9):
Chromosome 7 (position 54275130)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52544980
GRCz11 7 52820050
KASP Assay ID:
554-2614.1 (used for ordering genotyping assays)
KASP Sequence:
ACGCCTCAGAGCAGTGAAGAGATCCACCAGATCCCTCAAAACAACAACTG[C/A]CACACTGTGWCTTTGACATCCGAACCCAGCATACCCTCAGASGACCCGCA
Long Flanking Sequence:
CGCTATCAATACTTTTCAGATGCACTGTATAATAACTTTAACTGTTAAAAGCTATTAATTAGTTAATTAGTTAAAGTTATTAATAACTAATTTTAAGTTACAGTAACTAATAACCTTAACTTTTCTGAATTTGATTGTAATGCAAGAATGTGCACCTTTTCTATTGCTGCTTTGAAACAACAGTTCTTGTAAAAAGTGCAAATAAACTTGAATGAATGAATACAAAAAAATAGTGAGAACACAGGAGTGAGACTGGGGAAGTTCTCTTGATGACACAAATGGAAAAACTCAAACAAAAGTAGTGTGTTTTGCAGCCAAATGATGGTTTGTGTGTGTTTTGTTTGTACAGACAGCAGTGGTCCTTCCAGCACAGTGTCCAGCGCCGGCCCCTCGTCTCCCACCACGGCTGACACCTCTCCACGCTTCAGCTTCAGTGAGAAGATCACCCTAACGCCTCAGAGCAGTGAAGAGATCCACCAGATCCCTCAAAACAACAACTG[C/A]CACACTGTGTCTTTGACATCCGAACCCAGCATACCCTCAGAGGACCCGCACAGCTCCATACCCTCTCCCATCATGGAGAGACCCAGTCAGATAACATCAGACGGCACAGACTCTGCAGGCCAGTGTCTGACAGAGAGCCCTTCCTGTGATGAAGGGTCAAGTCCAAACACGGCTGAGCCCAGTCCACCCAGTCCTCTCCCAGAGTCCTTCCGCGGGCTGCCCGGCTCCCTGCCTGTTCTCCTGGAGCTCAGAGAAAGCAGTTCTGAGACCGGGTCCAGCGCCCAGACACCGCTCAGCCCTGAGGAGCCCGATGAGTTCTTTGATACGCAGGAAACGGTTGACGCTTGGAGGGAGAACCCGGCATCCCTGCCCCATCCTGGAACTCCTCTGGAGGTGGGAGCTCCACACGTGCCTGAGCCTTGAAGGAAACAGTGCTCCCTTCACCCCATCCCAGCATGCTCTCGCTGTAGTGCCTCACACCTTCATTGAGTCCCATACAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa8681
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111444 Nonsense 1332 1345 29 29
Genomic Location (Zv9):
Chromosome 7 (position 54275509)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52545359
GRCz11 7 52820429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAAACGGTTGACGCTTGGAGGGAGAACCCGGCATCCCTGCCCCATCCT[G/T]GAACTCCTCTGGAGGTGGGARCTCCACACGTGCCTGAGCCTTGAAGGAAA
Long Flanking Sequence:
GCGCCGGCCCCTCGTCTCCCACCACGGCTGACACCTCTCCACGCTTCAGCTTCAGTGAGAAGATCACCCTAACGCCTCAGAGCAGTGAAGAGATCCACCAGATCCCTCAAAACAACAACTGCCACACTGTGTCTTTGACATCCGAACCCAGCATACCCTCAGAGGACCCGCACAGCTCCATACCCTCTCCCATCATGGAGAGACCCAGTCAGATAACATCAGACGGCACAGACTCTGCAGGCCAGTGTCTGACAGAGAGCCCTTCCTGTGATGAAGGGTCAAGTCCAAACACGGCTGAGCCCAGTCCACCCAGTCCTCTCCCAGAGTCCTTCCGCGGGCTGCCCGGCTCCCTGCCTGTTCTCCTGGAGCTCAGAGAAAGCAGTTCTGAGACCGGGTCCAGCGCCCAGACACCGCTCAGCCCTGAGGAGCCCGATGAGTTCTTTGATACGCAGGAAACGGTTGACGCTTGGAGGGAGAACCCGGCATCCCTGCCCCATCCT[G/T]GAACTCCTCTGGAGGTGGGAGCTCCACACGTGCCTGAGCCTTGAAGGAAACAGTGCTCCCTTCACCCCATCCCAGCATGCTCTCGCTGTAGTGCCTCACACCTTCATTGAGTCCCATACAAGGGATTTGCCTAAATTTTTAAAGGTATAGTTCACCCAACTCACCATTAGTTTCTGTTAAAGACAAAAAAGAAGTTATTTTAAAGAATGTGAGAACTTCTTGACATCCATAGTAGGAAAAACAATACTTTGGCAGTCAATGGCTACCATTTTTCAAAATTTCCTTGTGAACAGATGCAGGTTGAGTAAATAATGAACAAATCGATATTTTGGGGTGAAATATCCCTTTATGGTAAGTTGAGGAAATGGAGGCCCTCACTTGTTGAAGATGAGAAGCTTAATAAAGTCTCCATGGTTTAATTGTGTAGCGTCATTCAGAGATGCTCCCCGTGTAATGCATCTCTCTCGTTGAATGGCCAGTGGTCAAACATAAGCTGTTAG
Associated Phenotype:
Not determined