Busch Lab

ZMP

si:dkey-266j7.1

Ensembl ID:
ENSDARG00000012482
ZFIN ID:
ZDB-GENE-030131-8100
Description:
Novel protein similar to H.sapiens PCLO, piccolo (Presynaptic cytomatrix protein) (PCLO) [Source:Uni
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]

Alleles

There are 18 alleles of this gene:

Allele Name Consequence Status Availability
sa18586 Essential Splice Site Available for shipment Available now
sa36579 Nonsense Mutation detected in F1 DNA Not yet available
sa39190 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45631 Nonsense Mutation detected in F1 DNA Not yet available
sa11698 Essential Splice Site Available for shipment Available now
sa43053 Nonsense Mutation detected in F1 DNA Not yet available
sa9177 Nonsense Mutation detected in F1 DNA Not yet available
sa15776 Nonsense Available for shipment Available now
sa10741 Nonsense Available for shipment Available now
sa43054 Nonsense Mutation detected in F1 DNA Not yet available
sa5793 Nonsense F2 line generated Not yet available
sa1035 Nonsense F2 line generated Not yet available
sa1178 Nonsense Confirmed mutation in F2 line Not yet available
sa13696 Nonsense Available for shipment Available now
sa11836 Nonsense Available for shipment Available now
sa23238 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa18586
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048657 Essential Splice Site 213 4478 4 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9087038)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9664014
GRCz11 18 9633204
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTTAGAAGCTGAATTGAATAAAGAGCCACCAAAAAGCTGCCCCTTAT[G/A]TAAAGAGAYCCTCAAGAAAAYCCCACAAAACTATARCTCTTGCACTTCTT
Long Flanking Sequence:
TTCAGCAGATTTGAAACCACCTACATCAGAAGCCCAAAAGCAGAAAAGTGAAGTCTTACCTGCCAAGTCTGATCAACCACATAAACCCGAACCATCTAAACAAGAAACAGATTTCTTCAGCTTCGGGTTTGGTGGCTCTCAGTCAAGATCACAATCTCCTCAGCCCACTGTGTCTGCTGTCTCTGATAAAGTTTTTGGCTTTGGCTCCTCCTTCCTAAACTCAGCATCAAACTTAATCTCCTCTGCTGAACCATCTAAAACTCCGCCAACATCTCGAAAGGGTTCTACAATTTCTCAGACTTCAAGCAAGACCATACCAACACCTCCCACTTCTCGAAAAGGATCAGTAGCTCCACCAGAGTCAAAACTAAATCCACCTCCAGTGCAGTCTAAGCCAACGTCTACACCAACGCAAGAACAGAAAGGGCCACCAGATGTTCAACCATCCAAACCTTTAGAAGCTGAATTGAATAAAGAGCCACCAAAAAGCTGCCCCTTAT[G/A]TAAAGAGACCCTCAAGAAAACCCCACAAAACTATAGCTCTTGCACTTCTTGCAAGAGCATTGTTTGTAATCTCTGTGGATTTAATCCCAATCCTCATCAAACTGATGTAAGTATATGTGTTTTACATTTTGATGTTGCATTAGCACAGTTCATAAATTAATCATAGTTGAATGATTATAGATTTGATGGTCACATGATACAAATACAATCAAGATATGACTCTATTTGAGGATCTTTTGTATTATCTACAGGTGAAGGAGTGGCTGTGTTTGACTTGTCAGATGCATAAAACTTCAGGACCTCCTCTTCCTCAACCAGAGCCACAATCTAATATAGCACTTGCACCAGCATCTCCACTGAAGGAAAAAACTCAGGTTTCACCTTCTCCTGAGAAAAAGCCAAGTGTTACAGCTGACCAGGACAAGAAGCCTCTTGCAGAGACTAAAGAACTAAAAACACCAAATACTCAAAAATCTAAAGGTGATGTTCCTTCTTCCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36579
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
ENSDART00000048657 Nonsense 926 4478 16 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9096683)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9673659
GRCz11 18 9642849
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTAAGTCCAAACTTGATGAGAATCCAACTGCAGCTCCCACTGAAAAG[A/T]AGGCTGGACCTGCTCAGGAAATAAAGAAAGACATTTCAGTTCAAAAGACC
Long Flanking Sequence:
CCATTCGAATTTCCAGGACATATTCTTTAGTGGTGTGTCTTGCTGCATTTTTGTGTACTTATCTAGTATACAAATAGATTGTTTGACCCTTGCAGGATTTTTCCAGTTCTATACTTTTCACTCACTGATAACCAAATCACTCACTGAAAAGTAAAGGGTAAAACAAGATTAAGGTTAATGATACAAACTGTCTTTTATTATTATCTTAATAACTTATGCTTAAAGACCTGTTTTTTTGTATTTAGAAGGTTTTTAGATATAATTTTAAGAAATAGTTAAGGATGTAATGTCTTATTACATATTTTTTGCAGGTTGATGAATGGCTCTGCCTGAATTGCCAGGTACAACGGGCACAAGGAGGAATAAAAAGTCCTACAGTAAAACCTCAAACAGTTCCTTTAGTAAAGGACAATCAAACTACATCCAAAGCTGACAAGGTAGCTCCAGCTCCAGTTAAGTCCAAACTTGATGAGAATCCAACTGCAGCTCCCACTGAAAAG[A/T]AGGCTGGACCTGCTCAGGAAATAAAGAAAGACATTTCAGTTCAAAAGACCAGCAGTGATGCCAAGCCAACTGATAAGATCACCTCTAGAAAAGATCTACCTGAGCAAGACAATACTAAACCAGAACCCGAGAAAACACAACAACAACCACCCAAGGATACAATTACTCCTGTAAAATCTGCTCCACCTACCAAGACTGAACCCCCAAAACAGGAGTCGGGTTTCTTTGGTTTTGGGTTAGGTGGTCCTAAAGCACAGCCTCCTTCCCCAAAACCAACTGAATCAACCACAGGAAGGTTCTTCGGTGGCCTGACAGAAACAGCGCGATCCCGATCACCCTCACCACAGTCTGTTTCTGCTGTCTCTGGGAAAGTTCTGGGCTTTGGATCTTCATTATTTAGCTCAGCATCTAATCTGATCTCTTCAGCTGTTCAAGATGAGCCGCCCACAACACCACCAACTTCAAGAAAAGGTTCCACAGTTTCTACTGACTCTGGTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39190
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
ENSDART00000048657 Essential Splice Site 956 4478 18 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9101885)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9678861
GRCz11 18 9648051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTTTGCAATAAAAAGGAGTGATTTTTGTTTGTTAGAATCATGTTTAG[G/A]TGAACTGTGACATTAGAGCGATGATTTAAAATGCATGGTCAATGCATGTT
Long Flanking Sequence:
GCATTTTTATGTGCTAAATCTTATTTGGCTCTGTGCTGTTTCCCTGGCCTTTTGGATATGACAGAGTCAGTCTCTTGTAATATGCCCTTAACATGAGCCTATGACTCTGGCTTCTACAATCCTGCACCTTCACACAGGAAAACAGACCTTTTGCTTCCTTTAGAAGACCTTGATGTTAATTGAAAAATACAGTTTATGCCCAAACAACCTTTTTGAATGACGGTGCACGTTTACATATCTGTCATTGTGTAAAGCTGAGGGCATAGCTTGAAACACTGATGTGCCATATTAAGATATTTAGTGATATACTGTGCCCACATCTGGCACACTGTTGGCCAAAAATAGCTTTAAATTTTAATCTACCTCAGCTAGCATTATGACAGTGGCTCTAAGAATGCTGATGGGCCCAAGGGGCTGTATAGGAGCTTGAGCTTACATTTTTGAAACTACAGATTTTGCAATAAAAAGGAGTGATTTTTGTTTGTTAGAATCATGTTTAG[G/A]TGAACTGTGACATTAGAGCGATGATTTAAAATGCATGGTCAATGCATGTTTTTCTATATTTCTTTGTTATTTAATAATTAAAATGCACTTATTATGGAAGTAGTAACGTAACATTTTTTTCATATTATCTTAACAATGTCTAGTTGAAGCTGGCTCTTTTTTGATGATCCTGCAGGTAACTTTTTCAACAGAGATGTACAGTAATGAAATAGAACTACTTCACTACTGTACTTAAGTACTAAAAGGCTGTATCTGTACTGAATTGTTTTTTTCTCCTACAGTAGGTGAGAGTTCAAAGTGGCTATTAACGCCGCAGCATGTACCGCCGCCGTTTGAAATAGGTGCCGCTCTGTTTTTAGTGTATGACCGCAGTTTGTGAATGAGCCGCCAGGGGGCGCAAAGGGACGGGATGCGAACGGACAGAAATAGCCCATACAGCTGCCACTGTGCTTGTAAATGATATTAAACAATAAGTCAAAGCATTATAATTCCTTCATTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45631
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
ENSDART00000048657 Nonsense 982 4478 21 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9121530)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9698506
GRCz11 18 9667696
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATACAGATAGATACCAGTCTTACAGAAATTTCTAAAGTAGATACCT[T/A]GAAAGCAGATACTAAAGAGCAACAAAGAAAGGACATCTTACCAGTTTCAG
Long Flanking Sequence:
TTGTTCCTACCACATATTTGCCACAGACTGAGATGACAGCTGTGGTGGCACCAATACCAGCTGCAGAGTCTCAGAAAGCTGTTGTTACCGCTGCTGAGGTCACTTTGACAGAAACAGGCAGAGACAAAATCCCAGATGAGATAAAAGTTGAGAGAGGACCAATCTCTATGATTCCAGCAGCCACTGTTGAGGCAGATGTAGTAAAGGTATAGTATTTTGTATTCATTATTTAGCAGTGCAAGAAGCAGTTGTTTTTGCACTGTTTTATTCAAGTGTTGTATGATATACTAAAAATAAATGTTTGACATGAAAAGGTGACGATATGTTTTATGATAAAAGCTATACTGCAAATTTTTGTCATTACAGAATTAATTGCATTCGGTCTTCGTTTTTGCAGGTCAAAGAAGATACATACACTCATCCTACAACAGAAGGACAACTGGACAATGTTGTGATACAGATAGATACCAGTCTTACAGAAATTTCTAAAGTAGATACCT[T/A]GAAAGCAGATACTAAAGAGCAACAAAGAAAGGACATCTTACCAGTTTCAGTAGAATCATATAGCTCGGCTGAAGAGGAGCTTAAAGAGATACAGCGGGTCAGTGAAATGGCAATGAAAGAAACTGCTGCAAAACTGTTGCCTGTCAGAGCACAAGATAATGTAAAACAATACCATGAGGACAGCAGTGAGAGTGAACCCTCTCCTCAGATACAAAGAAGAAGAGTGAGGCCTCCATCCTCAAGTAGTGAGGACTACAAAATAGACAGTTCAAATTCTGGAGATGATGAGGAGTTCATCCGTAGACAACTCATGAGCATGGGTGAAGATGAGAACTTACCCTCTGATGAGGAAAACATTGTCAAAGAACAACTAGACGCATCGCAAGAAACCAAAGAAGTCGATTCCATGAAGCCTAAACGTGCCCTAAAGAAACTTACGGTAGAACCTGAGGAGTACCTGTCTTCTCATGATCAAGATGACCAAGTTGTCCAAGTCATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11698
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048657 Essential Splice Site 1831 4478 24 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9124532)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9701509
GRCz11 18 9670699
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTAGAGATGTTCAGCCACCAGCCAGTGTTTCAATTCAAATTCCCATTC[A/G]GAGACTAGTGGAAACCAGATCAGATATTGCACCAYCAKTACWTCAAGCCR
Long Flanking Sequence:
ATCAGCAATTACAGACAAACCAACTGTTGCACCCATGACTGCTGAAAAAGTTGACCATGTGAAAATGTCAACTACACCAGCTCTTACACCTATTGTTCAATCTCAAGAAAAACCTTTAATAGAGACTTCAATTGTTGTTCAAATGCCAGATCATATTTCCTCTTCATTGAAGCACCCAGTTGTAGAACAAACTCCAGTTTCAGCACCTACTCTGCCATCTACTACATTAAAGAATCAAGTACCTACAGCTATCGCCATTGTTGCTACTATGCCAGACACACTCCTATGCCAGGTCACGTCTACATCTCAGTCAGTGGAACAAGCATCAACTTCTGTTCCAACAATGGTACCATCCTCAGTTCCAGCTAGCATCGTCTCTACAGACCCAACAAGCTCAGCTGTTGTACAAGTGGCCACACCACCATCTGCTCATACCACGTTACCTGCTTTGATTAGAGATGTTCAGCCACCAGCCAGTGTTTCAATTCAAATTCCCATTC[A/G]GAGACTAGTGGAAACCAGATCAGATATTGCACCACCATTACATCAAGCCACTCCTATTTCACCCCCAGTGAGTCACATGGAGTGTATTGCTGCAAAGACAGTCTCTGTTGTTTCTCCTACTATTACTACAACTGTTGCTTTTGAAAATTCACTTTCCCATCCCGTTAAATCAATGCTGGCTGATTCTCAGCCAACAATGACACAAATACCGCAGAAAATAATTCCAGATAATGCAATTCCTCCAATTGAACAGAAACCACAAAGCCAGATTAGTTTCAGATTGCCAAATCTAGAAAAAACTGTTAACGATGAGAAAGTCCAACCTGTTATTGTTAGTGTTTCTCCCATTACTTATGCAGCCACAGTATCGAGTTTTGTTTCTCCTTGTGTGGCATCTGCAAAACCTTACATTTCTCAGGAAAGAACGGATAAACCAGTAATTTCATTTCCACCACCTCCCCTTGCTACACCCCCAGAATTACCATATAGCACAGTACCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43053
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
ENSDART00000048657 Nonsense 2094 4478 27 55
ENSDART00000136955 Nonsense 11 1644 1 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9126565)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9703542
GRCz11 18 9672732
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTGACACCTTGCCTAAGCTTGTAACCCAAGTTGTCACGACTGAAGTG[C/T]AAAGAACAACAACTGTGTCAGTTGTCCAGGAGAGGATTCCTGTAGACCCT
Long Flanking Sequence:
AACCATTAGAGGAACTACCAATAACCTTAACCCCCATGTCTGGGGCGCCAGCAGTGTCTGTTCCTCAAAATACAGTGAGTGATGTTCGAAAAGAACTTGAGATGCAACAAGTGCAAACAGCATATTCAGTACCAATAACAATAACCCAGATTCCAATCCAAGCTCAAAATGAAGATATTCCTGGTTTGGATATGGAAGAAGTACTAATAGTCTCAGCCCCAGAAGAGATATTAACTGATCTGGGTCCAACGCCAGTTCCAATAACACAGCAAACAATTTATGAGGAAAAAACTGAAATTCCGTCAATGACTTCTGCAACAGCAGTGCCACCAGTACCAGTCACATTTACCCAATTTACAAAATCTATTGAGAGTCAAGAAATATGTGGACAGGATAAGTTTATTTCAAGCATGAGTCAAGTCTACTCTGCAATTTCAACAACTGAGCAGCATCCTGACACCTTGCCTAAGCTTGTAACCCAAGTTGTCACGACTGAAGTG[C/T]AAAGAACAACAACTGTGTCAGTTGTCCAGGAGAGGATTCCTGTAGACCCTATTCCTGAACCTGTGAGTGCTACAGTCACAATTCAACCAGAAGTCCATCAAAAGTCCAAACAAAATGGAAGAATACATTACCCTACCGATGTCGTAGATCTCACCACATTTAAAGTCAATGTTACAATGACTGACAGTGGAATGGATCTGACAGCCCCAGACTCAAGTAGGTCTTTTCTGTCAAGTGAATCAAGTGGCCGACAGGCTACTGCTGTACAGCCGGAAATTGTGAATCTTAGTGCTGAAATAATCCCCAGTCCAACTCTGTCTGTTGTAAATGATAGCATAACAATAGTCACTTGCACAGCTACAATTGCCTACAATAACAATAGCACAGTTGACAAGCCTCTGGACCTTGGAAATGCTACTTCAGTGCCTCTTTCACTTACCACATACAATCCATTTGAGCCTCTTGCACAGATTGTATATAGACCAGTAAATTCTCAACCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9177
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
ENSDART00000048657 Nonsense 2178 4478 27 55
ENSDART00000136955 Nonsense 95 1644 1 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9126817)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9703794
GRCz11 18 9672984
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCCCAGACTCAAGTAGGTCTTTTCTGTCAAGTGAATCAAGTGGCCGA[C/T]AGGCTACTGCTGTACAGCCGGAAATTGTGAAWCTTAGTGCTGAAATAATC
Long Flanking Sequence:
CAGTTCCAATAACACAGCAAACAATTTATGAGGAAAAAACTGAAATTCCGTCAATGACTTCTGCAACAGCAGTGCCACCAGTACCAGTCACATTTACCCAATTTACAAAATCTATTGAGAGTCAAGAAATATGTGGACAGGATAAGTTTATTTCAAGCATGAGTCAAGTCTACTCTGCAATTTCAACAACTGAGCAGCATCCTGACACCTTGCCTAAGCTTGTAACCCAAGTTGTCACGACTGAAGTGCAAAGAACAACAACTGTGTCAGTTGTCCAGGAGAGGATTCCTGTAGACCCTATTCCTGAACCTGTGAGTGCTACAGTCACAATTCAACCAGAAGTCCATCAAAAGTCCAAACAAAATGGAAGAATACATTACCCTACCGATGTCGTAGATCTCACCACATTTAAAGTCAATGTTACAATGACTGACAGTGGAATGGATCTGACAGCCCCAGACTCAAGTAGGTCTTTTCTGTCAAGTGAATCAAGTGGCCGA[C/T]AGGCTACTGCTGTACAGCCGGAAATTGTGAATCTTAGTGCTGAAATAATCCCCAGTCCAACTCTGTCTGTTGTAAATGATAGCATAACAATAGTCACTTGCACAGCTACAATTGCCTACAATAACAATAGCACAGTTGACAAGCCTCTGGACCTTGGAAATGCTACTTCAGTGCCTCTTTCACTTACCACATACAATCCATTTGAGCCTCTTGCACAGATTGTATATAGACCAGTAAATTCTCAACCTAAGCCTCCAGCTAGTGCAGAGATTCCTGTTAACCTATCAAACAGATCTGCCACAATCAGCGCCCCTCCTCTAATGCCTCTTACTGTAGCCCCAGTGAGCTTCACAAATGGCACTGTTGGTATACCAATGCATACAGAGCCATCAGTGGTTGGACCTGTAGATCTCACCACATCTAAGCCATTGAATACCATGGTTGCTTTGTCCTCATCTTCTGGAGTGGTCACAAATGTTGTGGAAGATGACGGTACACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15776
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
ENSDART00000048657 Nonsense 2352 4478 27 55
ENSDART00000136955 Nonsense 269 1644 1 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9127339)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9704316
GRCz11 18 9673506
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAATGTTGTGGAAGATGACGGTACACCAGTTGATCTKACATCTGGTAGA[C/T]RAACAGTTTGCTGYGATGTTATTTACWGRCTTCCGTTCACAGGGAGCTGC
Long Flanking Sequence:
AAATTGTGAATCTTAGTGCTGAAATAATCCCCAGTCCAACTCTGTCTGTTGTAAATGATAGCATAACAATAGTCACTTGCACAGCTACAATTGCCTACAATAACAATAGCACAGTTGACAAGCCTCTGGACCTTGGAAATGCTACTTCAGTGCCTCTTTCACTTACCACATACAATCCATTTGAGCCTCTTGCACAGATTGTATATAGACCAGTAAATTCTCAACCTAAGCCTCCAGCTAGTGCAGAGATTCCTGTTAACCTATCAAACAGATCTGCCACAATCAGCGCCCCTCCTCTAATGCCTCTTACTGTAGCCCCAGTGAGCTTCACAAATGGCACTGTTGGTATACCAATGCATACAGAGCCATCAGTGGTTGGACCTGTAGATCTCACCACATCTAAGCCATTGAATACCATGGTTGCTTTGTCCTCATCTTCTGGAGTGGTCACAAATGTTGTGGAAGATGACGGTACACCAGTTGATCTTACATCTGGTAGA[C/T]GAACAGTTTGCTGTGATGTTATTTACAGGCTTCCGTTCACAGGGAGCTGCAGAACACAGCCTCCTGTGACAACACAACCAGACACTCAAATTGGCTATGAAATTGATGATGCCGAAATGCCTGTCATTGAAAATCTCAGTACCATGAAGACATCGATATCGGACAGTAATTTCAAAGAGACTGGGCTCCTTAGTTATGAAAGGAAGAATGGATTCACCTATCAGAATGGGGCACCTGAGGGAGCCATGGATTTGACATCAGCTAAAATGTCAATGGGTGTGTATGACAGTGTACATATACGTGTATGTTTTATATTATTTTATTTTTATGCTAATGTTTATTGATTTTGTCTGAGTGTTTTCTGTGATTTACTTTTTGAATGTGTTGATTTTCATTCTTGTCTTTTTCTGTTTCTTTGTTTTTTGAACAGATGCATGCATTTGCCTCCGTGTTGTGCCTCAATGTTTTGGCTTTGCATCCTGCTAATCTGATGACACTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10741
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
ENSDART00000048657 Nonsense 2754 4478 28 55
ENSDART00000136955 Nonsense 671 1644 2 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9128886)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9705863
GRCz11 18 9675053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACAATTCAATGTCWYCTGCGGTTTCCACCCATGACTCCACATTAGTT[C/T]AAAACTGGCAATCAACAACAGYACAGCACAGTTCAAACWTTCCTGWAACA
Long Flanking Sequence:
CCCCAAATTTCCCTGATTTAGATGACAGCAAGAGCCAGCAGTACAAGGCAGAACATGAATTTTTACAATTAGAGAAGCTAAAGCAGCTGTGTCTAGCTGAAGAGCTTGAATGGGAGAGACAAGAGATACAGCGTTATCGTGAACAAGAGCAATTCATTGTGCAGAAGGAGCTGGAGGAACTACAGAACATGAAGCAGCAGCTTCTAATGCAGCAAGAAGAAGAAAGAAAAGCCCAACTGATCCTTCAACAAGAAACCTTTGCACAGCAGCAACATCAGTTAGAGCAGATCCATCGATTACAGAAGCAACTACAGCAACAGTTGGAAGAACAAAAGATATACCCATATGGGTTCGGCCCAATTGAGGGGATGTCCCCACCTATGGGCTCAAACATTATACTTGACTCAAAATATTCTGGGGGAGATAATGGACAGTATTGGCCAGTAAAGGATGACAATTCAATGTCTTCTGCGGTTTCCACCCATGACTCCACATTAGTT[C/T]AAAACTGGCAATCAACAACAGTACAGCACAGTTCAAACATTCCTGTAACAGTGAGTGCACAGACAAAGGAGCAAATGCAGTTGTCCACAAACATGTCTGATTCAGCAAAGCAAGAGCAAAATCTAGGGTTAAGTGGTAAGAAACTGATCGAGAGTGGTGTTCAAACGGATGATGAAGACGAAGTTGAGAAGATTCCATCTGGCAGAAAGAGAAGAAGTAGGAGAAGTGTAGATAGCTGTGTTCAAACTGATGATGAGGATCAGGATGAGTGGGATGTTCCTGTTCGGAGTAGGCGCAGGTCTCGTTCCAGTAGATATGCTGATGGAGAGAAGGGTAAAAGCTCTAAGGTGTCAAGTATTGCGATTCAGACTGTAGCAGAGATTTCAGTTCAGACAGAGCATTCGGGAACCATTAGAAGATCTCCTGTTAGGGCTCAAGTGGACACAAAGGTAGATTTACAGAGAGAGGGCCAAACAGAAAGTGATTCAGATATTACATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43054
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
ENSDART00000048657 Nonsense 2977 4478 28 55
ENSDART00000136955 Nonsense 894 1644 2 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9129556)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9706533
GRCz11 18 9675723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAATGTCCCCTGGGAAAAGTTCACAAAAGATGCTTACAGCTGATTCAT[C/A]AAGGCATCTCAGTAGTCCAAGATCACTACGGGCTTCACAACGATCTCTGT
Long Flanking Sequence:
TGATGAAGACGAAGTTGAGAAGATTCCATCTGGCAGAAAGAGAAGAAGTAGGAGAAGTGTAGATAGCTGTGTTCAAACTGATGATGAGGATCAGGATGAGTGGGATGTTCCTGTTCGGAGTAGGCGCAGGTCTCGTTCCAGTAGATATGCTGATGGAGAGAAGGGTAAAAGCTCTAAGGTGTCAAGTATTGCGATTCAGACTGTAGCAGAGATTTCAGTTCAGACAGAGCATTCGGGAACCATTAGAAGATCTCCTGTTAGGGCTCAAGTGGACACAAAGGTAGATTTACAGAGAGAGGGCCAAACAGAAAGTGATTCAGATATTACATCAGACAAAGATAAAAGACGCCCAGTTCCTACTGGGATAACTGTTAGCACACACCTAACAGCTGATGATGTTGGAACTTCAATGGTTACCAAGTCTCCAAAGGTACTATGCTCCCCAGTCTCACCAATGTCCCCTGGGAAAAGTTCACAAAAGATGCTTACAGCTGATTCAT[C/A]AAGGCATCTCAGTAGTCCAAGATCACTACGGGCTTCACAACGATCTCTGTCTGACCCCAAGTCACTTAGTCCAACAACTGAGGACAGAATGATGTACCAGTACTCAGAAACCTACTCAGTAAGTTAAATCCAGTTAATTCTTTTCTTGTTATGTAAAAAAAAAAAACATTTTTTATTTTATTATATCATATTCATAGCCAATTTACCATTATGTATGTTTCATTTCTATAACTTGCTTGTTTCTTTTCTTATTTCTGTTTCATCATTCTTTATAATTTTTCACAGAGCAAAGGTTCTCAGAGTGGCACACCAGTTGGCTCTTATAAGAAAGTAAAACGCACTCTACCTCATCCACCCCCGGAAGAAGATAACATCATTGGCCTCTCTGGGTACACCACTTCTTCAACCAGAAGACGAATGTGCAGGAACACAACTATGGCACGAGCCAAAATCCTTCAGGATATAGACAAAGAGCTGGATTTAGTTGAACGTGAGTCCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5793
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048657 Nonsense 3108 4478 29 55
ENSDART00000136955 Nonsense 1025 1644 3 3
ENSDART00000142816 None None 231 None 2
ENSDART00000048657 Nonsense 3108 4478 29 55
ENSDART00000136955 Nonsense 1025 1644 3 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9130116)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9707093
GRCz11 18 9676283
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGATACAGGCAGAACTTGATGMGGAGGAGAAAGAGATAGATGCTAAAT[T/A]GAGATATCTGGAGATGGGTATAAATCGAAGAAAAGAGGCTTTATTGAAAG
Long Flanking Sequence:
AGTCACTTAGTCCAACAACTGAGGACAGAATGATGTACCAGTACTCAGAAACCTACTCAGTAAGTTAAATCCAGTTAATTCTTTTCTTGTTATGTAAAAAAAAAAAACATTTTTTATTTTATTATATCATATTCATAGCCAATTTACCATTATGTATGTTTCATTTCTATAACTTGCTTGTTTCTTTTCTTATTTCTGTTTCATCATTCTTTATAATTTTTCACAGAGCAAAGGTTCTCAGAGTGGCACACCAGTTGGCTCTTATAAGAAAGTAAAACGCACTCTACCTCATCCACCCCCGGAAGAAGATAACATCATTGGCCTCTCTGGGTACACCACTTCTTCAACCAGAAGACGAATGTGCAGGAACACAACTATGGCACGAGCCAAAATCCTTCAGGATATAGACAAAGAGCTGGATTTAGTTGAACGTGAGTCCTCCAAACTCCGTAAGATACAGGCAGAACTTGATGAGGAGGAGAAAGAGATAGATGCTAAAT[T/A]GAGATATCTGGAGATGGGTATAAATCGAAGAAAAGAGGCTTTATTGAAAGAGAGAGAGAAGAGGGAGAGAGCCTACTTACAAGGAGTGGCAGAGGAGCGAGACTACATGTCAGATAGTGAGGTCAGCAACATCAGAGAGGCACGAGGCAATGGTCATGGACTAGAAAGGCCACGGACTGCCCCACAGTCAGAGTTTAACCAGTTCATCCCTCCACAAACTGAGTCTGAGTCCCAGTATGCACAGCTTACGAGCCCATACTCCCATTATCAGTATGCATCTCAAACAAGTCAGTACCCTCAGCAGACTTTGTACCAGCAGCAGTCTCTTTACCATCAGCAGGTGTCCCCCTACCAATCCATCTACTCATCAGTGCCCTCACTTAATCAGCAGTCCCAGCAGACTGGCTATGACCATTCCTCACTCCTTCTGATGCAACAAAAGCCCCGTCAGACTACTTTGTCTGACTTAGAGCCAAAAATAACAACAAACTATGAGGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1035
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048657 Nonsense 3108 4478 29 55
ENSDART00000136955 Nonsense 1025 1644 3 3
ENSDART00000142816 None None 231 None 2
ENSDART00000048657 Nonsense 3108 4478 29 55
ENSDART00000136955 Nonsense 1025 1644 3 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9130116)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9707093
GRCz11 18 9676283
KASP Assay ID:
554-0938.1 (used for ordering genotyping assays)
KASP Sequence:
TAAGATACAGGCAGAACTTGATGMGGAGGAGAAAGAGATAGATGCTAAAT[T/A]GAGATATCTGGAGATGGGTATAAATCGAAGAAAAGAGGCTTTATTGAAAG
Long Flanking Sequence:
AGTCACTTAGTCCAACAACTGAGGACAGAATGATGTACCAGTACTCAGAAACCTACTCAGTAAGTTAAATCCAGTTAATTCTTTTCTTGTTATGTAAAAAAAAAAAACATTTTTTATTTTATTATATCATATTCATAGCCAATTTACCATTATGTATGTTTCATTTCTATAACTTGCTTGTTTCTTTTCTTATTTCTGTTTCATCATTCTTTATAATTTTTCACAGAGCAAAGGTTCTCAGAGTGGCACACCAGTTGGCTCTTATAAGAAAGTAAAACGCACTCTACCTCATCCACCCCCGGAAGAAGATAACATCATTGGCCTCTCTGGGTACACCACTTCTTCAACCAGAAGACGAATGTGCAGGAACACAACTATGGCACGAGCCAAAATCCTTCAGGATATAGACAAAGAGCTGGATTTAGTTGAACGTGAGTCCTCCAAACTCCGTAAGATACAGGCAGAACTTGATGAGGAGGAGAAAGAGATAGATGCTAAAT[T/A]GAGATATCTGGAGATGGGTATAAATCGAAGAAAAGAGGCTTTATTGAAAGAGAGAGAGAAGAGGGAGAGAGCCTACTTACAAGGAGTGGCAGAGGAGCGAGACTACATGTCAGATAGTGAGGTCAGCAACATCAGAGAGGCACGAGGCAATGGTCATGGACTAGAAAGGCCACGGACTGCCCCACAGTCAGAGTTTAACCAGTTCATCCCTCCACAAACTGAGTCTGAGTCCCAGTATGCACAGCTTACGAGCCCATACTCCCATTATCAGTATGCATCTCAAACAAGTCAGTACCCTCAGCAGACTTTGTACCAGCAGCAGTCTCTTTACCATCAGCAGGTGTCCCCCTACCAATCCATCTACTCATCAGTGCCCTCACTTAATCAGCAGTCCCAGCAGACTGGCTATGACCATTCCTCACTCCTTCTGATGCAACAAAAGCCCCGTCAGACTACTTTGTCTGACTTAGAGCCAAAAATAACAACAAACTATGAGGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1178
Status:
Confirmed mutation in F2 line
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
ENSDART00000048657 Nonsense 3642 4478 30 55
ENSDART00000136955 Nonsense 1567 1644 3 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9131741)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9708718
GRCz11 18 9677908
KASP Assay ID:
554-1088.1 (used for ordering genotyping assays)
KASP Sequence:
CAACAAGTCTGCCAATCAGTCAGAGCAGAGGTCGAATCCCCATTGTTGCA[C/T]AAAACTCTGAGGAAGAGAGTCCATTGAGCCCTGTGGGTCAGCCCATGGGA
Long Flanking Sequence:
TAAAGAATAAAAAAGCACTCATTGACCCTAAAATTACAAAGTTTTCACCCATCCAGGAGAGCAGGGACATTGAACTAGACTACAGCAACTTTTTGGCCTCTGCCTCATCAGTTGGTGGACTGTCTGCCAGGGCACGGCTCCTGCAGGATGAGATCACATTTGGTCTCAGGAAGAATCTAGCAGAGCAACAGAAATATCTGGGTTCAGCTCTTGGTGCTAACCTGGCTCAGTCCCTCAACTTTGGCCAATCTCTAAATCTAGGGCCTACCATAAGGTCTTCCCTGCATGAAGATGGCACCTACCCCAGCGGCACTCGATCAAGACCTTCCTCTAGGCCTTCATCTGTGTATGGACTGGACCTTTCTATCAAAAGAGACTTATCAAACTCTTCACTACGCTTGAAAACAGAGGGTGAAGGCATGGACTCCCAGTTTGTTTCTAGAGCTAAACCAACAAGTCTGCCAATCAGTCAGAGCAGAGGTCGAATCCCCATTGTTGCA[C/T]AAAACTCTGAGGAAGAGAGTCCATTGAGCCCTGTGGGTCAGCCCATGGGAATGGCCAGAGCATCTGCAGGCCCGCTTCCACCCATATCGGCAGACTTAAGGGACCAATTTGGCTCCAGTCATTCTCTTCCAGAAGTCCAGCAGCACATGAGAGAGGAGTCTAGGACAAGCGGCTATGAGCGGGACATTGCCTTTATAAAGGATGACCTTCAGGGGGCCATGTCAGATAGTGAAGGTAAATTTGTTATGAGATCTGTTATATTTAGTCCCAGCTTCTATTAATGTGCATCTTTGTATGGCCCTGAATGCATTCTTTCTGTGTAAATTCAAATGTTGCATTTTTTCTTTAGTCATCTTTTGTTTCAGAATTGTTTACACGTTGTAGGCTATCACATTTGCATGACGTCATCCTCTTGTATTTAAAATTTCACCTCCATGTGTAAACATAACAGTTTTTATGTATAAAAGCCCCGTGTTTCTCAATGAATTTGCATGCTATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13696
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
ENSDART00000048657 Nonsense 4027 4478 40 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9147477)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9724454
GRCz11 18 9693644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGCTCCGAGAGAAAACAAYGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTARGTGTGTGTGTGTRTNNGTGTA
Long Flanking Sequence:
CCTTCTTGCTGTGAGGCGATAGTGCAAACCACTTAGGCACAGTGCCGTCTATATAATAATAATATAAATTAGAATTAGATTAATTACATTTAATTCAAAATTCCTAAAAATTAAACATTAAAAATCAATTTTCTTGCCTGTTAGTGTTATATAAAATTGATTTAAATATGTCACCATATAGAATTACTACAAATCTACAAAGGCCTTTGAAATATGACATTTGAGACACATTACATTTAGATTATGATGTATCAGCACTAGTGACTCACTTCAGCATTGACTGCCTTATTGGATTTAAATGGCAGCATCTTGGTGCTTATTCTACAGTGAAATCAAATTTGAGTGGATTGCTGGTATTATGCATCTCATAATAAATCTGTCCCTCAGCTTCAAATCAACTACGACAGGAATATGGGCAATCTGATTGTTCACGTGCTACAAGCAAGAAACCTCGCTCCGAGAGAAAACAACGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTAGGTGTGTGTGTGTGTGTGTAAGTTTGGGTGTGTGTGCGTTATAGTGTTAAAGTAAGTGAGTGTAAGTGTGCTGAATGAAATATTTAGAGAGACAAATGTTTGTTTTATGTTTGTTCTTGTCTACATATATAAGTGTTTATGTAATTGTGTTTGATTTACTGTCAGATTTTTTTAGTTATTTTCAGTGATTTCTTTCCCCCGGTTTTATTTAATTTTATATTTTCCGTTGTCGCTTTTCTCCTGGCCTTCCAGAAATCATCTTTTCCCTTTAGTATTAAGATTCTGGGTGTACTCATGAGTATGGTAAAACATCGCTGAAGGCAAAAAAAAAAATATATATATATATATTAGTTATAAATTAGTTGAATGAATGTATATTAAGCATAAAACATAAAAGTAATCGTTACCTGATGAACAAGTGTTTGACGAAATATATAGGCACAGTGTTAAAGAATAGCCATGTCAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11836
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
ENSDART00000048657 Nonsense 4027 4478 40 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9147477)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9724454
GRCz11 18 9693644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGCTCCGAGAGAAAACAAYGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTARGTGTGTGTGTGTRTNNGTGTA
Long Flanking Sequence:
CCTTCTTGCTGTGAGGCGATAGTGCAAACCACTTAGGCACAGTGCCGTCTATATAATAATAATATAAATTAGAATTAGATTAATTACATTTAATTCAAAATTCCTAAAAATTAAACATTAAAAATCAATTTTCTTGCCTGTTAGTGTTATATAAAATTGATTTAAATATGTCACCATATAGAATTACTACAAATCTACAAAGGCCTTTGAAATATGACATTTGAGACACATTACATTTAGATTATGATGTATCAGCACTAGTGACTCACTTCAGCATTGACTGCCTTATTGGATTTAAATGGCAGCATCTTGGTGCTTATTCTACAGTGAAATCAAATTTGAGTGGATTGCTGGTATTATGCATCTCATAATAAATCTGTCCCTCAGCTTCAAATCAACTACGACAGGAATATGGGCAATCTGATTGTTCACGTGCTACAAGCAAGAAACCTCGCTCCGAGAGAAAACAACGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTAGGTGTGTGTGTGTGTGTGTAAGTTTGGGTGTGTGTGCGTTATAGTGTTAAAGTAAGTGAGTGTAAGTGTGCTGAATGAAATATTTAGAGAGACAAATGTTTGTTTTATGTTTGTTCTTGTCTACATATATAAGTGTTTATGTAATTGTGTTTGATTTACTGTCAGATTTTTTTAGTTATTTTCAGTGATTTCTTTCCCCCGGTTTTATTTAATTTTATATTTTCCGTTGTCGCTTTTCTCCTGGCCTTCCAGAAATCATCTTTTCCCTTTAGTATTAAGATTCTGGGTGTACTCATGAGTATGGTAAAACATCGCTGAAGGCAAAAAAAAAAATATATATATATATATTAGTTATAAATTAGTTGAATGAATGTATATTAAGCATAAAACATAAAAGTAATCGTTACCTGATGAACAAGTGTTTGACGAAATATATAGGCACAGTGTTAAAGAATAGCCATGTCAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23238
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
ENSDART00000048657 Nonsense 4219 4478 47 55
ENSDART00000136955 None None 1644 None 3
ENSDART00000142816 None None 231 None 2
Genomic Location (Zv9):
Chromosome 18 (position 9158768)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9735745
GRCz11 18 9704935
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGCCGGAAACGCCATCGCTGCAGCGGAAGCTGCCGTCCATCAATCC[C/T]GACTCCAGCCAAGTAACCCTTACTACTTCACATGAGCTCACAGCCTCTCT
Long Flanking Sequence:
TACAGTCTTCTGTGTCATTTTTATACAATGATTTGATGCTAGGGAAATGTGTATTATTATTATTATTATTATTATTATTATTACTGAAAACTGTTGAGCAGCTTAATATTTTGGTGAAATGCGAAATAAATGATCTCTTTGATAATCAGAAAGTTACAATTTTTCAATCAACTTTCTATTATCTTTTTTTAAATTTTACTGTCACATTTGATCAATTGTATCTATGCAAGTTTAAATCTTATAGACCCCCAACTAAGATCTAAGAGATACTGAAGATCAGTGGTGTATTAATCCAGAGCACATACTGTATGTTTACAGATACACAGGTCCCTACAATAGAAAAGTCCCACAGTAGTCCCGGCAGCTCCAAATCCTCCTCTGAGGGTCACTTGCGCTCACATGGCCCATCACGAAGCCAAAGCAAAGGCAGCGTCACCCAAGCACACTTGGAGGAGGCCGGAAACGCCATCGCTGCAGCGGAAGCTGCCGTCCATCAATCC[C/T]GACTCCAGCCAAGTAACCCTTACTACTTCACATGAGCTCACAGCCTCTCTGTTTTTCTGTCTTTCTTTCTGTCTGTCCTCTTGTTCTCGCACTCTTCCGCTATTTCTTTACCATTCCCTCTCACCCTCACATTTCTGACACTTTCTTTTTTTCAGTAAGTTTAGTTCTTCTTTTCATCGTTTAATGTTAATATTGTAAAACCTACACCTAAAATCACTAATTATAAACATAATAGCGCATAATATAAGAAATCGTATTGTTCAGTGGTGTCCAAACTTGGTCCTGGGGGGCCGTTGTCCTGCAAAGTTTAGTTCCAACCCTAATCAGACACACCTAGGCTGGCTAATCTCTTACTAGGCTTTCTAGAAAAATCTGTGCAAGTATGTTGAGGCAAGTTGGAGCTAAAATCTGCAAGACACCAGCCTTCCAGGACCGAGTTTGGGCACCCTTGGTATAATTGAAGTGCCCCTGTTATGCTTTTTTGAGTTTTGTCCTTTATG
Associated Phenotype:
Not determined