Busch Lab

ZMP

apobl

Ensembl ID:
ENSDARG00000022767
ZFIN ID:
ZDB-GENE-030131-9732
Description:
apolipoprotein B, like [Source:RefSeq peptide;Acc:NP_001025233]
Human Orthologue:
APOB
Human Description:
apolipoprotein B (including Ag(x) antigen) [Source:HGNC Symbol;Acc:603]
Mouse Orthologue:
Apob
Mouse Description:
apolipoprotein B Gene [Source:MGI Symbol;Acc:MGI:88052]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa18137 Nonsense Available for shipment Available now
sa43475 Nonsense Mutation detected in F1 DNA Not yet available
sa37070 Nonsense Mutation detected in F1 DNA Not yet available
sa12118 Nonsense Available for shipment Available now
sa43476 Nonsense Mutation detected in F1 DNA Not yet available
sa16833 Nonsense Available for shipment Available now
sa6637 Nonsense Mutation detected in F1 DNA Not yet available
sa6638 Nonsense Mutation detected in F1 DNA Not yet available
sa37071 Nonsense Mutation detected in F1 DNA Not yet available
sa10039 Nonsense Available for shipment Available now
sa32301 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa18137
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028709 Nonsense 1336 3730 23 27
ENSDART00000133353 Nonsense 1336 3730 23 27
Genomic Location (Zv9):
Chromosome 20 (position 31302873)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31374086
GRCz11 20 31276965
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCATGATTGAAGTCACRGGAACAAGTCCAGTGGATCTACTCTCCTTC[A/T]AAATAGAAGGTACTTGTATGYTTTCATATTTTCTGTTAATCACNTTTTTG
Long Flanking Sequence:
TCCTGAATGCGTGAGTGATTCAGAAACAGCTAAACTAATTTTAAATGCAGAACCATTATGAATTATAAATGTTTTGTTACACATTGTACTAATTTATGACATTACATTAATTAAAAAATATTCTGTATTTTAACAGTGAGGGTGCTGCTAAATACAAGTTTGGCCAGAATTATTACACCATAACCATACCTGTTCCTCTTGGTGGAAAAACTTCAAGAGATTTCAACCTCCCTGCTGCTCTGGAAACACCAGTACTGAACGTACCACAGCTTGACCTTCAGGTTAAATCCATTAATATCCCACTTCCAGTGTTCTTTATACCAGAGAGTCTGTCTCTGTCACTACCTCTTGTGGCAAAGGCGGAGGTGTCCAGCAAGCTGAGCAGCAACTTCTATGACATGGAAGCAAAAGCTTCTGCAGGGAGTGAACTTGTAGATAAACCAACCTATTCTGCCATGATTGAAGTCACAGGAACAAGTCCAGTGGATCTACTCTCCTTC[A/T]AAATAGAAGGTACTTGTATGCTTTCATATTTTCTGTTAATCACTTTTTTGTAATCTGTAAAAAATAAATATTGAATGTTGTTCTGTTTATGTTTAGGATCAACCTTCCTGGTAGGTAGACTTGGAGAATCTTTGAAGACTGAGATGAAATCCTCCCTTAATCACAAGCTCCTTGAAGCCAGTGTCAATTATTTTGAGGAAATAACAACTGGAGAAAAAATCACAATGAAATCAAGCAGCAAGATGGAGGCGAAAAGTCCCTTTGGTCTGAAGATTTCTCTGGAACACACGGGCCAGGTTGGACTCGATGAAGATGAGATCTCTGGAGATGGAAATCTGTTGGGCTCTATCAAGGCTGGTCCTTTGAATGGTGAAGTTGCTCTCAGACAATCACTTATCCTTCTTCCATTCAAGCCAGAGCTGAAAATCGACTCTTCTCTGAAAGTAGACTTAGAACAAATCCAAGCAGAGAACATAATTGAAGCAGCTTTTGCCAATGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43475
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
ENSDART00000028709 Nonsense 1591 3730 24 27
ENSDART00000133353 Nonsense 1591 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31303726)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31374939
GRCz11 20 31277818
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACATGTGCAGCCTTTCCCTGACCAGAAACGGCCTAGTCACAATTGGCT[C/A]AACCTTACTAGAGTGCCCAGACATGCCTTTGACACTGCAGAACAAATTCA
Long Flanking Sequence:
GGCTGGTCCTTTGAATGGTGAAGTTGCTCTCAGACAATCACTTATCCTTCTTCCATTCAAGCCAGAGCTGAAAATCGACTCTTCTCTGAAAGTAGACTTAGAACAAATCCAAGCAGAGAACATAATTGAAGCAGCTTTTGCCAATGGAGAGCTCTCTTTCACATCTAAATCAACAGCATTCCAGGACAATCTCATACATGTTGCTGAACTTGCCTATAAAGAATCACAGCTTGCTCTGAAGTCAGATGCAAGGGCAAAGGCTTTCGGCCTAAACATCCAAAATGTAGCTGAGGCTAGTGCTAGTTTTAATTTAGTTAACGTTAAGATTGACACTAATGTTGACACTTTGTTTGGAAATCGTGTCCGTTCCCAGTTTATAGCAGCACTGGACGCCAATGGGCTGGATGTAAAAAGTGATGCCTCTGCAAATCTGGATGAACACACAGCTTCTCACATGTGCAGCCTTTCCCTGACCAGAAACGGCCTAGTCACAATTGGCT[C/A]AACCTTACTAGAGTGCCCAGACATGCCTTTGACACTGCAGAACAAATTCAATGGAGCCCTTGACACTTCAGGGCTTTCATTGTCAGTTGAAACAAAAGGTAAATTCGTTGAAGTGACAATTGAAAACACAAATTCTCTGTCTGCCTCCCTGTCCTCAGTAGATTTCATTTCCAAAGCTAATAGCGATGATGGAACATATGTGCATGACTTCTCCCTTCAGCTTCAGCCATATAGTACCTCGTTGAAAATTAGCAATAATCTGAATGCTCTGAACATCAAACTGATTAATGAGGCACAGTTTAAGGCACTTCCATATGCAGCAGATCTGACTGGCAGTTGGAAGCTTTCCTCTGGAACAGATGAGCTTAAGAACACATATGAGATCAAATATGAAGATCTGGTTGCTACAGCCAAGTGTGGTCTCACTGGAAAACTCATGGGATCTCACATGAGCCAAAACACAGAAATTGAAGTTGCTGGACTTTCAGTTACATACGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37070
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
ENSDART00000028709 Nonsense 1800 3730 24 27
ENSDART00000133353 Nonsense 1800 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31304352)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31375565
GRCz11 20 31278444
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTGATGCAATGGTCAATGCAGATGGGGATTTGTATCTGTATGGAAAA[C/T]AAAGCGCACAAGTCTACTCTAAATTCCTTATGAAGGCAGAACCACTTGCT
Long Flanking Sequence:
ACACAAATTCTCTGTCTGCCTCCCTGTCCTCAGTAGATTTCATTTCCAAAGCTAATAGCGATGATGGAACATATGTGCATGACTTCTCCCTTCAGCTTCAGCCATATAGTACCTCGTTGAAAATTAGCAATAATCTGAATGCTCTGAACATCAAACTGATTAATGAGGCACAGTTTAAGGCACTTCCATATGCAGCAGATCTGACTGGCAGTTGGAAGCTTTCCTCTGGAACAGATGAGCTTAAGAACACATATGAGATCAAATATGAAGATCTGGTTGCTACAGCCAAGTGTGGTCTCACTGGAAAACTCATGGGATCTCACATGAGCCAAAACACAGAAATTGAAGTTGCTGGACTTTCAGTTACATACGGCAGTGAATCCAATTTCAACTCACAGTATCTCCGCTTCAATAGCGACTTACATGCCGCTGCTGTTCCCTTCAGATTCAACGTTGATGCAATGGTCAATGCAGATGGGGATTTGTATCTGTATGGAAAA[C/T]AAAGCGCACAAGTCTACTCTAAATTCCTTATGAAGGCAGAACCACTTGCTTTTGCACACTCACATGAATGCAGAGTCTCAACAACTTACAACCTGTATGATGATCTGGTATTCGAAACCAACCTTGATAATAAAATTGATACTGTGCTGACACCGTCTGAGCAAAAGGCCACAGTGAGAGTAAAATCTAAGTTCAACAACCATGAGTTTAACAAAGACTTGAGTGCTTACAATACCCCTGAAAGACTTGGAGTTGAAATGTCTGGATCCATCATCACCAACATCTTCAATACAGTTGACTCTGACAATCAAGACCACTTTTTCTCTGCCTTCCTAAAATATGATAAAAACAGCAACAGCCGTGCCTTAAGTCTGCCATTTATTGATGAGTTTCCATTTGACCTGCAACACATGAAACTTGCAGTTTTGAGGATTGTTGAGGCCATGCAGAGTTATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12118
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
ENSDART00000028709 Nonsense 1967 3730 24 27
ENSDART00000133353 Nonsense 1967 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31304855)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31376068
GRCz11 20 31278947
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACATA[T/A]GTTAGTGACTTTGTGAATGAACTGAATCTGGAAGAGAAAATCATAAAATT
Long Flanking Sequence:
AGCGCACAAGTCTACTCTAAATTCCTTATGAAGGCAGAACCACTTGCTTTTGCACACTCACATGAATGCAGAGTCTCAACAACTTACAACCTGTATGATGATCTGGTATTCGAAACCAACCTTGATAATAAAATTGATACTGTGCTGACACCGTCTGAGCAAAAGGCCACAGTGAGAGTAAAATCTAAGTTCAACAACCATGAGTTTAACAAAGACTTGAGTGCTTACAATACCCCTGAAAGACTTGGAGTTGAAATGTCTGGATCCATCATCACCAACATCTTCAATACAGTTGACTCTGACAATCAAGACCACTTTTTCTCTGCCTTCCTAAAATATGATAAAAACAGCAACAGCCGTGCCTTAAGTCTGCCATTTATTGATGAGTTTCCATTTGACCTGCAACACATGAAACTTGCAGTTTTGAGGATTGTTGAGGCCATGCAGAGTTATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACATA[T/A]GTTAGTGACTTTGTGAATGAACTGAATCTGGAAGAGAAAATCATAAAATTCAGCAAGGACCTGACTGCGCTGTATGAGGACTATGGAATTACTCTCGACGACCTGGAGGCTTCTCTGATGAATCTAAAGCCTGTTTTGTTGAAGCTAGTCACTGAACTTGACACTTATGTAGTAGAGATAGAAAAGATTGTGAGGGAAATAATTACAAGTGGCACACCATCTGATGCTGCAATACAGAGGTTTACAGATATCCTGAATTCATTCAATGAGAAATATGACGTCAAAGCCATTGTTCTCACTGTTATTGAGGCTATTGAAAAATTTCTTAGGGAAATCGATGTAATGAGTATAAAGGGCAGCAGGGAAGTCTTCAAGCAATATGTTGATGAATATTTTGCTATTAAATCCAAAGTGGAGGAAATTTTGAGTGAACTGAAGCAGTTTGTTGCAAACTTTGACCAAGAAAAGTTCACTGAGGATGTGAAGAACTTTGTTACCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43476
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
ENSDART00000028709 Nonsense 2093 3730 24 27
ENSDART00000133353 Nonsense 2093 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31305231)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31376444
GRCz11 20 31279323
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGGAAATCGATGTAATGAGTATAAAGGGCAGCAGGGAAGTCTTCAAG[C/T]AATATGTTGATGAATATTTTGCTATTAAATCCAAAGTGGAGGAAATTTTG
Long Flanking Sequence:
TTATTGATGAGTTTCCATTTGACCTGCAACACATGAAACTTGCAGTTTTGAGGATTGTTGAGGCCATGCAGAGTTATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACATATGTTAGTGACTTTGTGAATGAACTGAATCTGGAAGAGAAAATCATAAAATTCAGCAAGGACCTGACTGCGCTGTATGAGGACTATGGAATTACTCTCGACGACCTGGAGGCTTCTCTGATGAATCTAAAGCCTGTTTTGTTGAAGCTAGTCACTGAACTTGACACTTATGTAGTAGAGATAGAAAAGATTGTGAGGGAAATAATTACAAGTGGCACACCATCTGATGCTGCAATACAGAGGTTTACAGATATCCTGAATTCATTCAATGAGAAATATGACGTCAAAGCCATTGTTCTCACTGTTATTGAGGCTATTGAAAAATTTCTTAGGGAAATCGATGTAATGAGTATAAAGGGCAGCAGGGAAGTCTTCAAG[C/T]AATATGTTGATGAATATTTTGCTATTAAATCCAAAGTGGAGGAAATTTTGAGTGAACTGAAGCAGTTTGTTGCAAACTTTGACCAAGAAAAGTTCACTGAGGATGTGAAGAACTTTGTTACCTCAGCCAGATTCAGAGACTATGCAGACAATCTGGTGGCTAAAATCCCAACAGAGCAAATCAGCAAGATTCTTGAAAAAGCAAAACAACTGCTTAATCTACTGGGTAACAGAATGAATGCCATCTATACAAATGTGAGAGAAATTCTGGTGAAATCTGGGGTTGACAAGAAGATCGAAACTCTCCTCAAAAAAGTTGTTGAGCTTATCAAGAAGTTCAACATTGAAGAAACTGTTAAGACTCTTGCGGACACTTTGAAATCTATTCTGACCCCTGTCACTGAGCTGGTGGATAAGGCCATCAACTACTTGAAAACAACAGAGGCAAAGGAAATCATTGAAGATCTGAACAACTGCCTAAACCACTGCATTAAATATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16833
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
ENSDART00000028709 Nonsense 2304 3730 24 27
ENSDART00000133353 Nonsense 2304 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31305866)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31377079
GRCz11 20 31279958
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTTGAAATCCGTCAAAAGCTTGAGGCAATCAGAGAGTTTGTTAACTA[T/A]GCTTTGTCATCTATGWGCGCTTGCATCGAAAAGCTGGAAAAAGTCAAART
Long Flanking Sequence:
AGAGACTATGCAGACAATCTGGTGGCTAAAATCCCAACAGAGCAAATCAGCAAGATTCTTGAAAAAGCAAAACAACTGCTTAATCTACTGGGTAACAGAATGAATGCCATCTATACAAATGTGAGAGAAATTCTGGTGAAATCTGGGGTTGACAAGAAGATCGAAACTCTCCTCAAAAAAGTTGTTGAGCTTATCAAGAAGTTCAACATTGAAGAAACTGTTAAGACTCTTGCGGACACTTTGAAATCTATTCTGACCCCTGTCACTGAGCTGGTGGATAAGGCCATCAACTACTTGAAAACAACAGAGGCAAAGGAAATCATTGAAGATCTGAACAACTGCCTAAACCACTGCATTAAATATATTAGATCATTTGACTACAACGCATTTGTGGATGAGGCCAATCAGAAAATCAAGAAGTTAACAAATGATCTTTACACCATGAGTTTGTCACTTGAAATCCGTCAAAAGCTTGAGGCAATCAGAGAGTTTGTTAACTA[T/A]GCTTTGTCATCTATGAGCGCTTGCATCGAAAAGCTGGAAAAAGTCAAAGTTGTGGATGTCGTCAAAAAATTCAGTGACATTGTCGATAGTGTAGTCTTCATTGACACCGAGGCACTCATTGAGGACCTTAGGAAAATACTTGCAGACATTGATATCAGAGAAGAAATCCAGAAGTTTCTGAAGCACGCAAGTAGCATCTCCACCAAGGTTGTGACCACTGCAACAGATGCATGCAGTGCTGTTATGCAAGTGATCCAAAACATCCTTAAAGATCAAGCAGTTGTCAACGAGCTGAAGCAAATCTGTGACAGAGTCAAAACAGTACTGAGAACAGCTGAATTTAAGATTCCATCTTTCATTTTTCCACTGACTGACCTTGTTGTGCCATCCATAAAAATAAGCTTAAAGAATCTTCAGGAAATCAACCTCCCATCTTCACTGATTGACCTTCCAGGGTTTACAATTCTGCAATATTACACTGTGCCACCAATCAGAGTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6637
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
ENSDART00000028709 Nonsense 2696 3730 24 27
ENSDART00000133353 Nonsense 2696 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31307040)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31378253
GRCz11 20 31281132
KASP Assay ID:
554-5428.1 (used for ordering genotyping assays)
KASP Sequence:
TTGCCCTGGCAGGTGGAATATCTGCAAATATCAAAACAACATATAATGAC[A/T]AGTTAAATGCAGWCCTTTGGAACAGTGAATATTATTACGGTAATGATATA
Long Flanking Sequence:
CTAAATACATCAGCAAGCACAAATTTTCTGATCTGACAATCCCAGAATTCACCCTCCCTGGAGTTCCTACTGAGGTCATGGTGCCATGCTTTGGAAAGTTGTATGGTGAGGTTAGAGTCACCATTCCAATTTTCAACATGAGAACTACAGTAGAATTCCTAAACTCTACTGAAAGTGCAGAAACCCCTCAGTTTGTAGGGCACATTACCTCACATGGATCTTCAGAATATGACCTTCTTAAATACACCTTGGACTCCACAGCTCGTGTTGCCATGCCTAAAATGAGTCGTGTGATTCTTGCAGAAACCCTGAAGATCACTCACAGTGTACTAGCCATTGACCATCAATCCTCAGTCTCACTTTATGGCCTCTCAGCCCAGGCTTCTTCCAAGAGCACCATGAAGATTACCTCTTCCACCTATAATGCTAACATCGTTAACACTGCTTTCTTTGCCCTGGCAGGTGGAATATCTGCAAATATCAAAACAACATATAATGAC[A/T]AGTTAAATGCAGACCTTTGGAACAGTGAATATTATTACGGTAATGATATAATTCTAAAGCAGGATGGTCTAAAACTCCTTCTGACCATGGAAGAAGAGGCCAAGGGACATATATCTGTGCTCGAAAAGTCTGATGATATCACTGGCAAGAGTAGTTCATCTATAATTATTACTCCAACAACATTCTCTCTGATCATTTCTGTGGATTCCAGCAGTTCTGTTTCAAACATTAAAAAAAGTATTAAAGCTGACGGTGTTGCTCTGAGCTATGTCGACTTCACTGCCAGCATTGAAGGAACTAGTGATTCTGAGTTATTTTTACTGAATGCAGCTGGAAAGGCGGATCTCAGACAAATGAAAGTAGAGATGAAGGCTGACCTTGACACAAAATATGCTGGACTGCTCAGTGGTACCTTCACCAGTGCCTTTAACTTCTTAGTGCAACCTTTTGAGGTAGTCCTTGATTTCAAGAACAAGGCTAATACTAAGCTCAACCTTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6638
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
ENSDART00000028709 Nonsense 2875 3730 24 27
ENSDART00000133353 Nonsense 2875 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31307579)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31378792
GRCz11 20 31281671
KASP Assay ID:
554-5286.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAACCTTGTAGAGCCCCTGTCTGCTAAGATTGATCTTCAGAACAATTA[T/A]ACTGTCATCCTTAATAGCGACGAGCAGATGTTGAGCACTGGGTTACTTGC
Long Flanking Sequence:
GGTAATGATATAATTCTAAAGCAGGATGGTCTAAAACTCCTTCTGACCATGGAAGAAGAGGCCAAGGGACATATATCTGTGCTCGAAAAGTCTGATGATATCACTGGCAAGAGTAGTTCATCTATAATTATTACTCCAACAACATTCTCTCTGATCATTTCTGTGGATTCCAGCAGTTCTGTTTCAAACATTAAAAAAAGTATTAAAGCTGACGGTGTTGCTCTGAGCTATGTCGACTTCACTGCCAGCATTGAAGGAACTAGTGATTCTGAGTTATTTTTACTGAATGCAGCTGGAAAGGCGGATCTCAGACAAATGAAAGTAGAGATGAAGGCTGACCTTGACACAAAATATGCTGGACTGCTCAGTGGTACCTTCACCAGTGCCTTTAACTTCTTAGTGCAACCTTTTGAGGTAGTCCTTGATTTCAAGAACAAGGCTAATACTAAGCTCAACCTTGTAGAGCCCCTGTCTGCTAAGATTGATCTTCAGAACAATTA[T/A]ACTGTCATCCTTAATAGCGACGAGCAGATGTTGAGCACTGGGTTACTTGCCCGCTTTAACCAGTACAAGTACAGTCACAATTTCACATTGGCCAACAACGAGGATGAGGCTGGCATTTATGCTGCAGTAAATGGCGAGGCTAATTTGGAATTCCTAACAATCCCTTTCAGTATTCCAGCAATGGAATTAGAAACACTAACTATGGTAATTGAAATTCCAGAAATCAGTAACATCAATCTATATGAACAGACTGGGCTTAAGCATGTTTTGACTGACTTCGACCAGGCCATTGATGTAGATGCAAAGATGGTTTACCAGAAGAATGACTTAACCTCTGAGTTGTCTTTCAAGTCCTCCATATTCAATCTTAATGCCAATGCTGGTTTCTATCAGAAGGATAACCCTGTAATTCGTTTTGGAGTCATCACTGCTTCTGAGTTTGAGTCACTGAAGGCCAAGCTTGAAGGAACCAGCAGTCTGAGCACCAAAAGTGGATTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37071
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
ENSDART00000028709 Nonsense 3042 3730 24 27
ENSDART00000133353 Nonsense 3042 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31308078)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31379291
GRCz11 20 31282170
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGCCAAGCTTGAAGGAACCAGCAGTCTGAGCACCAAAAGTGGATTC[A/T]AATTAGCCAATTCTTTGCTTCTAGAAAATCGCCACATTGAAGGAACCCAT
Long Flanking Sequence:
ATACTGTCATCCTTAATAGCGACGAGCAGATGTTGAGCACTGGGTTACTTGCCCGCTTTAACCAGTACAAGTACAGTCACAATTTCACATTGGCCAACAACGAGGATGAGGCTGGCATTTATGCTGCAGTAAATGGCGAGGCTAATTTGGAATTCCTAACAATCCCTTTCAGTATTCCAGCAATGGAATTAGAAACACTAACTATGGTAATTGAAATTCCAGAAATCAGTAACATCAATCTATATGAACAGACTGGGCTTAAGCATGTTTTGACTGACTTCGACCAGGCCATTGATGTAGATGCAAAGATGGTTTACCAGAAGAATGACTTAACCTCTGAGTTGTCTTTCAAGTCCTCCATATTCAATCTTAATGCCAATGCTGGTTTCTATCAGAAGGATAACCCTGTAATTCGTTTTGGAGTCATCACTGCTTCTGAGTTTGAGTCACTGAAGGCCAAGCTTGAAGGAACCAGCAGTCTGAGCACCAAAAGTGGATTC[A/T]AATTAGCCAATTCTTTGCTTCTAGAAAATCGCCACATTGAAGGAACCCATGAAAGCACTGCAACTATGAACCTGAATAACTTTGAAGTTACACTGTCTATGGCCACAGATGCAAAAATGAATCTACCAATTCTTACAGCTAATGCCAACCACCAACTTACTGCTGACAACAAGGCCAACCCAAAAGCAGACTCAACATTTAAGATGGATTACAACTTTGACGTTCCCATTATTAAGCTTGTTGGAAAGGGAAATGCTGAAACCATCTTAAAAGGCGAAGGAACTCGTACGTTTATCTCTGCTGAGACACTTATAAAGAGCAATATTGATGGAACATTCCTAGATCGTGGTATTTTGAAAGGAACTCTGAATTACGATGAATCCCTGTATGTGAATGGTAATAGTTTGCGATATGCCCTTAAGACTGGTGGTAATGGAGACCTGAACTATGGTGATTTCAAGGTGGCTTTTGATGTGGATGAAAACCTGTCTGTAGAGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10039
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
ENSDART00000028709 Nonsense 3214 3730 24 27
ENSDART00000133353 Nonsense 3214 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31308596)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31379809
GRCz11 20 31282688
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTYGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCAYGTATA[T/A]GCTACAATGAAGTTTACTTCCAATAATGAAGCAARTGTTGGATCTTTCAA
Long Flanking Sequence:
CTTCTAGAAAATCGCCACATTGAAGGAACCCATGAAAGCACTGCAACTATGAACCTGAATAACTTTGAAGTTACACTGTCTATGGCCACAGATGCAAAAATGAATCTACCAATTCTTACAGCTAATGCCAACCACCAACTTACTGCTGACAACAAGGCCAACCCAAAAGCAGACTCAACATTTAAGATGGATTACAACTTTGACGTTCCCATTATTAAGCTTGTTGGAAAGGGAAATGCTGAAACCATCTTAAAAGGCGAAGGAACTCGTACGTTTATCTCTGCTGAGACACTTATAAAGAGCAATATTGATGGAACATTCCTAGATCGTGGTATTTTGAAAGGAACTCTGAATTACGATGAATCCCTGTATGTGAATGGTAATAGTTTGCGATATGCCCTTAAGACTGGTGGTAATGGAGACCTGAACTATGGTGATTTCAAGGTGGCTTTTGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCACGTATA[T/A]GCTACAATGAAGTTTACTTCCAATAATGAAGCAAATGTTGGATCTTTCAACACTAAAGGAGTTCATTCCAGCCAGGCTACTCTCGATATGGCTCTTCTGAAGTCACTGGTGGCTGATATGAAAATAGACTTGTCTCAACCGAGCACCTTTGGTGAACTTAGCATCTTCGAGACAATGAAAGTAGATCTCAGTGCTCCCAAGCAGAAAATTGATATCCTTTCAACAATCAAGTCTCCGGTATACACCACAGATGTTCGTGCTAAACTAGACGGTAATGCCCCAGATTACAAAACGGTTCTGAAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAGTAAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGGAAATTAAATCTTGGATTTGTGTGCTTTTACACAAAACAGGCTCCATGAGTTCTACTATGGAGAATGGTGCCCTTGTTGTCGGAGCTAACGCTGTACTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32301
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028709 Essential Splice Site 3331 3730 24 27
ENSDART00000133353 Essential Splice Site 3331 3730 24 27
Genomic Location (Zv9):
Chromosome 20 (position 31308947)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 31380160
GRCz11 20 31283039
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAG[T/C]AAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGG
Long Flanking Sequence:
AATTACGATGAATCCCTGTATGTGAATGGTAATAGTTTGCGATATGCCCTTAAGACTGGTGGTAATGGAGACCTGAACTATGGTGATTTCAAGGTGGCTTTTGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCACGTATATGCTACAATGAAGTTTACTTCCAATAATGAAGCAAATGTTGGATCTTTCAACACTAAAGGAGTTCATTCCAGCCAGGCTACTCTCGATATGGCTCTTCTGAAGTCACTGGTGGCTGATATGAAAATAGACTTGTCTCAACCGAGCACCTTTGGTGAACTTAGCATCTTCGAGACAATGAAAGTAGATCTCAGTGCTCCCAAGCAGAAAATTGATATCCTTTCAACAATCAAGTCTCCGGTATACACCACAGATGTTCGTGCTAAACTAGACGGTAATGCCCCAGATTACAAAACGGTTCTGAAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAG[T/C]AAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGGAAATTAAATCTTGGATTTGTGTGCTTTTACACAAAACAGGCTCCATGAGTTCTACTATGGAGAATGGTGCCCTTGTTGTCGGAGCTAACGCTGTACTTACACATCAGGACTTCACTATGGATATCAGCAATGCTATTCGCATGAGGTAAATAAAAAATCTTTCTGATTTTTTGTTTGAATATTAGTACTATGTTTGCAATTATAATTTATTTTATAAAGCAATTCTGAGTGTAAATCTAAATTCTACTTATCATTAGCGAAAGGAGCCATATTCTGAATGTGGACATCACCAGCCAAACATTTACCGATGTTAACCTTCGCTATGCTGCTCGGAGTGATGGGATAAGTGGCTCTGTTTCCACACCGGGGTCTGGCCTCCTTGGCTTTCAGCTCCAAGGAAATATTCCATCCCAAATGAATGCAAGGCTCTACTGTCGTTATGCTGTAAGT
Associated Phenotype:
Not determined