Busch Lab

ZMP

setd2

Ensembl ID:
ENSDARG00000062244
ZFIN ID:
ZDB-GENE-030131-2140
Description:
Huntingtin interacting protein B [Source:UniProtKB/TrEMBL;Acc:Q071D9]
Human Orthologue:
SETD2
Human Description:
SET domain containing 2 [Source:HGNC Symbol;Acc:18420]
Mouse Orthologue:
Setd2
Mouse Description:
SET domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1918177]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa25011 Nonsense Mutation detected in F1 DNA Not yet available
sa45570 Nonsense Mutation detected in F1 DNA Not yet available
sa42691 Nonsense Mutation detected in F1 DNA Not yet available
sa39086 Nonsense Mutation detected in F1 DNA Not yet available
sa22792 Essential Splice Site Available for shipment Available now
sa9194 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36079 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25011
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Nonsense 968 2737 3 21
ENSDART00000131779 None None 285 None 7
ENSDART00000137672 Nonsense 968 2737 4 22
Genomic Location (Zv9):
Chromosome 16 (position 18320188)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16361425
GRCz11 16 16269402
KASP Assay ID:
554-7516.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACAAGGCTGAACCCGCCCCTGCTTCCTCGTTGTTTTCTGGGAATCAG[C/T]AAACTGATACACATGAAAGCATTAATAAAGAATTTCCTTACGGATTTAAC
Long Flanking Sequence:
AAGTAATGTTAGCTCAGAAAATAGAGTTCAGTGATACTACCCCTGATAATTGTAGTCAGAAACTGGACCCAGAAGTACCATCTGAAAAGTCGGTAGAAGTTCATGCAAGAGACACCACCGCAGCTGAATCTCATCAAGAAATAAGTTCTTTCACATCTAATTTTGGAACTAAAGGTACCCATGATGAACTTCAAAAAACTGTTGAAATTCCTCAATCAACAAGTGCCCTGGTTGTTAGTGATTTTCAGCCTAGTAAAGAGAAAGTCAATGTAGACAAAACTAAACCTGAAATTCAAGACCCTGATTCCTTAAATCATGATGGAAAATGTCACAGTGATGATAGTGAGAGTGAAGAATCAGATTCTGATTCAGATGATGGACGGGTCTCCCTAAAGAGGTTGCACTCTGTAGTGGTTGTGCCAAAAAATTCAACCATTGCTCTTGAAACAAATGACAAGGCTGAACCCGCCCCTGCTTCCTCGTTGTTTTCTGGGAATCAG[C/T]AAACTGATACACATGAAAGCATTAATAAAGAATTTCCTTACGGATTTAACAATCAGTCAACACTCAAAGAGTCATCAGCTGCACTTTATAAGGGCAGTGCACAAGCTGCATGTCAAAGTCCAAATGTTAAAGGTGTCTCCTATCAATCGCAGAGCAACATGGTTGACAGCACCAGCCATTTAGAGGTCATGAGTGCCCATGTGGACAAGAACTGGAGTGCTCAAGAAAGACCAAATATCTCTGGCCAGATAAACCAAGAATATGTTCAGAATTTTGAGAAGACTTGCGAGAAACCTGAAACGGATCACCATCAGTACCATGGGAGACCAGATAGCTGGAACGGAAGGAAAGGTGACTTCAGTGTTGGGAGGGGTGACAGCTTGGTCTGGGACTTCAACCAGTCAGAACAGCCCAGCAGCACATTTCAGCAACCGGACAGCAGTTATAGTACACCTCAGCCACTGTTTGATAGTGTTCACAGAGAAGATCCATGGGCCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45570
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Nonsense 1158 2737 3 21
ENSDART00000131779 None None 285 None 7
ENSDART00000137672 Nonsense 1158 2737 4 22
Genomic Location (Zv9):
Chromosome 16 (position 18320758)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16361995
GRCz11 16 16269972
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGACAGTCAACACGCATGTGCCTTTTCAGTATCATGATTTAGTTCAC[C/T]AGATTCATCCAGACTCTCTTACTAATGACCATGATGATGACCGTGAGGGA
Long Flanking Sequence:
AGTCATCAGCTGCACTTTATAAGGGCAGTGCACAAGCTGCATGTCAAAGTCCAAATGTTAAAGGTGTCTCCTATCAATCGCAGAGCAACATGGTTGACAGCACCAGCCATTTAGAGGTCATGAGTGCCCATGTGGACAAGAACTGGAGTGCTCAAGAAAGACCAAATATCTCTGGCCAGATAAACCAAGAATATGTTCAGAATTTTGAGAAGACTTGCGAGAAACCTGAAACGGATCACCATCAGTACCATGGGAGACCAGATAGCTGGAACGGAAGGAAAGGTGACTTCAGTGTTGGGAGGGGTGACAGCTTGGTCTGGGACTTCAACCAGTCAGAACAGCCCAGCAGCACATTTCAGCAACCGGACAGCAGTTATAGTACACCTCAGCCACTGTTTGATAGTGTTCACAGAGAAGATCCATGGGCCCAGCCTGCCATCTCTAAAACCAGCAGGACAGTCAACACGCATGTGCCTTTTCAGTATCATGATTTAGTTCAC[C/T]AGATTCATCCAGACTCTCTTACTAATGACCATGATGATGACCGTGAGGGAAGGATTTTGGGAATTAAACAAGCATCATTATTATCTGCTGGCCTACCAGGACCATCCCCATTTGTTCAAGCGCCTGAGATAAGTAGCAACTGCAGCTTCACAACAGAAAGTCAGAACATCTCGGAAGCACCTAGAGATGACAACCAAAAGCCTCATCGAGGAAGGGGCCCACCTAAGAAGAGACGCCAAGAGTTTGAATCTGAATCAGATAATGAGGCAGAGGCAGGCCTGAGTAAAAGGGAGTGTTTTGATGAGAGCTCAAGGCCTTTGAAAGATGCTAAGGAGTCTTTCCATCAAATTCAAGAGGTTCAGCGACCACTTCTCAGTCTGAAAGAATTTTCGGATCCATTTGTGTGGAGGGATAAAGCCAAGCAGAAAAAAATGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGGTAAATATCTGTTTTGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42691
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Nonsense 1264 2737 3 21
ENSDART00000131779 Nonsense 16 285 1 7
ENSDART00000137672 Nonsense 1264 2737 4 22
Genomic Location (Zv9):
Chromosome 16 (position 18321077)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16362314
GRCz11 16 16270291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGCAGGCCTGAGTAAAAGGGAGTGTTTTGATGAGAGCTCAAGGCCTT[T/A]GAAAGATGCTAAGGAGTCTTTCCATCAAATTCAAGAGGTTCAGCGACCAC
Long Flanking Sequence:
GGACTTCAACCAGTCAGAACAGCCCAGCAGCACATTTCAGCAACCGGACAGCAGTTATAGTACACCTCAGCCACTGTTTGATAGTGTTCACAGAGAAGATCCATGGGCCCAGCCTGCCATCTCTAAAACCAGCAGGACAGTCAACACGCATGTGCCTTTTCAGTATCATGATTTAGTTCACCAGATTCATCCAGACTCTCTTACTAATGACCATGATGATGACCGTGAGGGAAGGATTTTGGGAATTAAACAAGCATCATTATTATCTGCTGGCCTACCAGGACCATCCCCATTTGTTCAAGCGCCTGAGATAAGTAGCAACTGCAGCTTCACAACAGAAAGTCAGAACATCTCGGAAGCACCTAGAGATGACAACCAAAAGCCTCATCGAGGAAGGGGCCCACCTAAGAAGAGACGCCAAGAGTTTGAATCTGAATCAGATAATGAGGCAGAGGCAGGCCTGAGTAAAAGGGAGTGTTTTGATGAGAGCTCAAGGCCTT[T/A]GAAAGATGCTAAGGAGTCTTTCCATCAAATTCAAGAGGTTCAGCGACCACTTCTCAGTCTGAAAGAATTTTCGGATCCATTTGTGTGGAGGGATAAAGCCAAGCAGAAAAAAATGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGGTAAATATCTGTTTTGTTCTCTTGCATCATTTGTATACCTGGTAGTGCTAGGCGATTTGACAAAAAATACTATCTGCTGATATAAGTGCTCTCATATCCTGATATATCACAGTGTAATGTATTTTCTTTATATTCAATTCGTTAGCATAAAATAGTGCACAATAAAATGCTAAATGTTTAGAAATGGTGAGAAAATTGCAAGTAGAGATCTGCGTGGGACTAAATTTTTAATCCCGCTCCCACCAGGTTACAGTCCGAACCCCACCGCTCCCGCTTATATTTAGCATTTGTTGTCCCGCTGCCCGACCCGCCGCATTTTCTACCCGCTGCGACCATTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28617
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1318 2737 3 21
ENSDART00000131779 Essential Splice Site 70 285 1 7
ENSDART00000137672 Essential Splice Site 1318 2737 4 22
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1318 2737 None 21
ENSDART00000131779 Essential Splice Site 70 285 None 7
ENSDART00000137672 Essential Splice Site 1318 2737 None 22
Genomic Location (Zv9):
Chromosome 16 (position 18321241)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16362478
GRCz11 16 16270455
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGG[T/G]AAATATCTGTTTTGTTCTCTTGCATCATTTGTATACCTGGTAGTGCTAGG
Long Flanking Sequence:
ATCATGATTTAGTTCACCAGATTCATCCAGACTCTCTTACTAATGACCATGATGATGACCGTGAGGGAAGGATTTTGGGAATTAAACAAGCATCATTATTATCTGCTGGCCTACCAGGACCATCCCCATTTGTTCAAGCGCCTGAGATAAGTAGCAACTGCAGCTTCACAACAGAAAGTCAGAACATCTCGGAAGCACCTAGAGATGACAACCAAAAGCCTCATCGAGGAAGGGGCCCACCTAAGAAGAGACGCCAAGAGTTTGAATCTGAATCAGATAATGAGGCAGAGGCAGGCCTGAGTAAAAGGGAGTGTTTTGATGAGAGCTCAAGGCCTTTGAAAGATGCTAAGGAGTCTTTCCATCAAATTCAAGAGGTTCAGCGACCACTTCTCAGTCTGAAAGAATTTTCGGATCCATTTGTGTGGAGGGATAAAGCCAAGCAGAAAAAAATGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGG[T/G]AAATATCTGTTTTGTTCTCTTGCATCATTTGTATACCTGGTAGTGCTAGGCGATTTGACAAAAAATACTATCTGCTGATATAAGTGCTCTCATATCCTGATATATCACAGTGTAATGTATTTTCTTTATATTCAATTCGTTAGCATAAAATAGTGCACAATAAAATGCTAAATGTTTAGAAATGGTGAGAAAATTGCAAGTAGAGATCTGCGTGGGACTAAATTTTTAATCCCGCTCCCACCAGGTTACAGTCCGAACCCCACCGCTCCCGCTTATATTTAGCATTTGTTGTCCCGCTGCCCGACCCGCCGCATTTTCTACCCGCTGCGACCATTCCCGCTAACAAAAAATCCACCTAGCTACATGATACAAGAGCTACATGAGTCAAGACAGCCTATAACAAGCTTTCTGTATAAACACACACACACACACACACACACACACACACATAGACACAGAGCACCAAGCAAGCAACACACTGCATCACGTTCTCTCTTATT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa678
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1318 2737 3 21
ENSDART00000131779 Essential Splice Site 70 285 1 7
ENSDART00000137672 Essential Splice Site 1318 2737 4 22
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1318 2737 None 21
ENSDART00000131779 Essential Splice Site 70 285 None 7
ENSDART00000137672 Essential Splice Site 1318 2737 None 22
Genomic Location (Zv9):
Chromosome 16 (position 18321241)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16362478
GRCz11 16 16270455
KASP Assay ID:
554-0586.1 (used for ordering genotyping assays)
KASP Sequence:
TGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGG[T/A]AAATATCTGTTTTGTTCTCTTGCATCATTTGTATACCTGGTAGTGCTAGG
Long Flanking Sequence:
ATCATGATTTAGTTCACCAGATTCATCCAGACTCTCTTACTAATGACCATGATGATGACCGTGAGGGAAGGATTTTGGGAATTAAACAAGCATCATTATTATCTGCTGGCCTACCAGGACCATCCCCATTTGTTCAAGCGCCTGAGATAAGTAGCAACTGCAGCTTCACAACAGAAAGTCAGAACATCTCGGAAGCACCTAGAGATGACAACCAAAAGCCTCATCGAGGAAGGGGCCCACCTAAGAAGAGACGCCAAGAGTTTGAATCTGAATCAGATAATGAGGCAGAGGCAGGCCTGAGTAAAAGGGAGTGTTTTGATGAGAGCTCAAGGCCTTTGAAAGATGCTAAGGAGTCTTTCCATCAAATTCAAGAGGTTCAGCGACCACTTCTCAGTCTGAAAGAATTTTCGGATCCATTTGTGTGGAGGGATAAAGCCAAGCAGAAAAAAATGCCTCCCTACTTTGACCTTATCGAAGAAAATTTGTATTTAACTGAACGG[T/A]AAATATCTGTTTTGTTCTCTTGCATCATTTGTATACCTGGTAGTGCTAGGCGATTTGACAAAAAATACTATCTGCTGATATAAGTGCTCTCATATCCTGATATATCACAGTGTAATGTATTTTCTTTATATTCAATTCGTTAGCATAAAATAGTGCACAATAAAATGCTAAATGTTTAGAAATGGTGAGAAAATTGCAAGTAGAGATCTGCGTGGGACTAAATTTTTAATCCCGCTCCCACCAGGTTACAGTCCGAACCCCACCGCTCCCGCTTATATTTAGCATTTGTTGTCCCGCTGCCCGACCCGCCGCATTTTCTACCCGCTGCGACCATTCCCGCTAACAAAAAATCCACCTAGCTACATGATACAAGAGCTACATGAGTCAAGACAGCCTATAACAAGCTTTCTGTATAAACACACACACACACACACACACACACACACACATAGACACAGAGCACCAAGCAAGCAACACACTGCATCACGTTCTCTCTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39086
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Nonsense 1342 2737 4 21
ENSDART00000131779 Nonsense 94 285 2 7
ENSDART00000137672 Nonsense 1342 2737 5 22
Genomic Location (Zv9):
Chromosome 16 (position 18322470)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16363707
GRCz11 16 16271684
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACATTAAGCGTATGCAGTGTGAGTGTGCTATCCTTTCAAAAGAAGAG[C/T]GAGCCCGAGGAATACTGGCATGTGGGGAAGATTGCCTGAATCGCTTGTTG
Long Flanking Sequence:
ATTTTTTTCCAGCGCTACAAGAAATCTGGTTCTGCAGTGCAGCTCTGGGAATGCAGACCTCTAGTTGCAAGCTTGAAAGTACAATGTTTACATTGTACTTTTAAGCTTGAAACTTTCTCACCATTTTGTTATTTAAGTTTCTGCTTGAATCCAGGTAAATTATCCAAATGATGAAAAAATAAATACAGTAAACAATATGTTTTGCATTATATTATAGAGCATAATGATTATAAATTATAGTAAATATAATTATAATAAATAATAAATTATAGATATTTTATTTTGCCTATACAATATATATTGTCATATTGCACAGCTCTAGTACCCGTCAATAAAATATATGGCTTGGTATGGCCATTCTTTGAAGTAATTTTTTTTTGTTTATTCATTTAATTTCATCATTAATAAAGCTTAAAATCTGTCCCTACAGAAAGAAGAATAAATCTCATCGAGACATTAAGCGTATGCAGTGTGAGTGTGCTATCCTTTCAAAAGAAGAG[C/T]GAGCCCGAGGAATACTGGCATGTGGGGAAGATTGCCTGAATCGCTTGTTGATGATTGAATGGTAGATATTACTTCTATTGTATCATACTAAGTACTGTATCATACTCTCTGCTTTATAGCAGAGAGAACATAAAGAGAAAGCCTGTAGTTAATACTGTGTCATTTTTATGTTACTTGCTGATTTTATATTTGACAGATTGATTCAAATCTTATAGGAACACCCCACTTTTTTTGGAAATAGGCTCATTTTACAAGTCTCCTATTGTTAAACAGTTAAACTACCATTCCCTGCGTCTGGCAGGAGCATTTTTAGCTTAGCATAAATTATTCATTCGATTAAGCTATTAGCATCTCACTAAAAAAAAAAAAAATGGAGTTTCAATAACTTTCTATTTAAAGCTGGACTAATCTGTGGTTACATCATGCACTATAATATGAACAACTAAAAGTTATTACTAAGATGATATGGCCAGGAACTATACTCTAACTCTAATTATCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22792
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1405 2737 5 21
ENSDART00000131779 Essential Splice Site 157 285 3 7
ENSDART00000137672 Essential Splice Site 1405 2737 6 22
Genomic Location (Zv9):
Chromosome 16 (position 18323478)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16364715
GRCz11 16 16272692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACTGAGAGCAAAGGATGGGGTTTACGAGCAGCTAAAGACCTCCAGCC[G/A]TAAGTACCGTATGGTTCAACTAATAGTTTTTTTTGGGGTACATTTAAATA
Long Flanking Sequence:
TGCTGCCAGACCAAGTCAGCAGCAGGCACAATAGTATTATTGCAGAATGAGAGTATAGTTTCTAGTCATATCGGCCTAAAAAGTTATTTTAATTTTTTAATTTTTTTGAGTGAGATGCTAATGGTCTATTCCGATTCAGTGGTCTGTGCTTAGCTAAGCTAAAAGTGCTAGCGCTAGTCTCAGAGATCAGCTGAATGGATTGAAAAAATTTTAAAACTCAACTGTTCAACTCTAGGTGACTTGCAAAATGAGCATGTTTCCCAAAAAAGTTGTTTTTTAATATTTACAAGATTTCAAGATTCAAAATATTTCAAAGCTGTTTATTTAGAATGTGGAAGGTAAGATTTCCCCCTTTTTCTTGTACTTTCAAGCTCTTCCAGGTGTTTAAATGGAGCATACTGCTCCAACCGGCGCTTCCAGATGAAACAGCATGCAGACTATGAGGTTATTTTGACTGAGAGCAAAGGATGGGGTTTACGAGCAGCTAAAGACCTCCAGCC[G/A]TAAGTACCGTATGGTTCAACTAATAGTTTTTTTTGGGGTACATTTAAATATGTCTTTTATGCCTGTTACTTCTAAAATGTAATGATTGATGTATTTTTTCCAGGAACACCTTCGTTTTAGAGTACTGTGGAGAGGTTTTGGATCACCGGGAATTTAAGGCACGCGTGAAAGAGTATGCTCGAAACAAGAACATTCACTATTATTTCATGGCTTTGAAAAATAATGAGGTAAGTCATCAGCGCACTAAAATCTACAAATTAGAACTGTTGGTAATCTACATAAGTGTGATATTGTTTCATATCATTCGATATTGGTAATTATTGAATATTTTTTAGCAGTTCAAATTTAATATTTAATTTTTAATTTCACCACTTTATTGTAATTTACCAACATTACAAAGACAAATAGTTATAAGAGTCAAAAACATGTAAACAAAATATCTAATCTCCTTATAATAAAAAAACAAGTGTTTTAGAGTCTCTTAAACTTGAAAAATACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9194
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
ENSDART00000089776 None None 508 None 7
ENSDART00000111446 Essential Splice Site 1446 2737 6 21
ENSDART00000131779 Essential Splice Site 198 285 4 7
ENSDART00000137672 Essential Splice Site 1446 2737 7 22
Genomic Location (Zv9):
Chromosome 16 (position 18323706)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16364943
GRCz11 16 16272920
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGAAACAAGAACATTCACTATTATTTCATGGCTTTGAAAAATAATGAG[G/A]TAAGTCATCAGCGCACTAAAAYCTACAAATTAGAACWGTTGGTAATCTAC
Long Flanking Sequence:
ACTCTAGGTGACTTGCAAAATGAGCATGTTTCCCAAAAAAGTTGTTTTTTAATATTTACAAGATTTCAAGATTCAAAATATTTCAAAGCTGTTTATTTAGAATGTGGAAGGTAAGATTTCCCCCTTTTTCTTGTACTTTCAAGCTCTTCCAGGTGTTTAAATGGAGCATACTGCTCCAACCGGCGCTTCCAGATGAAACAGCATGCAGACTATGAGGTTATTTTGACTGAGAGCAAAGGATGGGGTTTACGAGCAGCTAAAGACCTCCAGCCGTAAGTACCGTATGGTTCAACTAATAGTTTTTTTTGGGGTACATTTAAATATGTCTTTTATGCCTGTTACTTCTAAAATGTAATGATTGATGTATTTTTTCCAGGAACACCTTCGTTTTAGAGTACTGTGGAGAGGTTTTGGATCACCGGGAATTTAAGGCACGCGTGAAAGAGTATGCTCGAAACAAGAACATTCACTATTATTTCATGGCTTTGAAAAATAATGAG[G/A]TAAGTCATCAGCGCACTAAAATCTACAAATTAGAACTGTTGGTAATCTACATAAGTGTGATATTGTTTCATATCATTCGATATTGGTAATTATTGAATATTTTTTAGCAGTTCAAATTTAATATTTAATTTTTAATTTCACCACTTTATTGTAATTTACCAACATTACAAAGACAAATAGTTATAAGAGTCAAAAACATGTAAACAAAATATCTAATCTCCTTATAATAAAAAAACAAGTGTTTTAGAGTCTCTTAAACTTGAAAAATACAATGTTACAAAATGTGTGCAATGCTAAACCGTAAATACTGAACAATCAAAGCAAACTTTAAGGTCTAAATAAAAATCATACAGTAAACCTCAAACTCTGTCAACAACACAAATTATGATAAGTAAATCTGAGCTTTCAAGTAAATGAACCGACCATCATTATTCAAATACACACTGCAATATTTCAAACAGTGAAGTTGTATGACTATAGTACCCCTATGCTAAAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36079
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
ENSDART00000089776 Nonsense 363 508 4 7
ENSDART00000111446 Nonsense 2592 2737 18 21
ENSDART00000131779 None None 285 None 7
ENSDART00000137672 Nonsense 2592 2737 19 22
Genomic Location (Zv9):
Chromosome 16 (position 18343408)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 16384645
GRCz11 16 16292622
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACTGCTCTATAATGAACTGTGCTCTTGCTTTTAAAGGCAAACGCAGT[G/A]GGATCCTCCCAGCTGGGATGGGACGACAGAGGAAGCTAGTGTTGAACACG
Long Flanking Sequence:
TGTGATGCTTATAAAAGCTGATGCAGCCCTTTAAACAGTTTTCTATTTATTATTAGTTTAATTAAAGCGATCACATGGCTGTATAATATCAAGTTCCTGTTCTACAGCTTCTAATTAGTAGTTTATAGACAACAGGCTTCCAGTAACCTCAGCATGCTGACTAACCTCTCTTGAACTGTGATTCACCACAGGAAATGATTGTACCCAACAACATCATTGACCTGCCGCCTCCATCCCCTCCCAAACCTAAAACCATTATCCTGCCTCCCAGCTGGAAAGTGGCGCGAGACCCAGAGGGCAGAATATATTACTACCACATCATCACCAGGTACCGATACTCCCTATTAAATGAACAATCTGTGTGTTATTAAAACGGGGGGAGCGAGCCACAATCCCATGTCATATATTATGTCATCTAATGAGTTAAGACATTGCTGCCAGATCATATATTTCACTGCTCTATAATGAACTGTGCTCTTGCTTTTAAAGGCAAACGCAGT[G/A]GGATCCTCCCAGCTGGGATGGGACGACAGAGGAAGCTAGTGTTGAACACGAGGCAGAGATGGACCTCGGGACGCCTACGTATGATGAAAATCCCTCCAAGGTATTGAACAGTTCCTTACGCTTTAAGGGGCAAAAAATCATGAGATTTTCATCTAGCTTGAGTTTAAAGTGCTGTAGATATTTTTTTAAAGAAACCTTTTTTGAAAATAGGCTTGAGTTGACTAGAGTTAAACAGTTATGTCTTACCATTTTTTTATTCTATTCAGCCAATCTTCAAGTCTGGCACTTTTAGCTTAGCCTAGCATTGATTATTGAATCAGATTAGACCATTAGCATCTCGCACAAAAAATAAAACAAAAAGTCTTTAGAGTCTGTGTATTTTGCCCTTGCTTAGAAGTCTGTTATCATCCAAATTTATTAGCACAACTGGCACATTGGCGCAGTATTTGCTAGTATGTGTTCATACCAAACCTAGTCTAAATTTAACCTTGTCAACTTAA
Associated Phenotype:
Not determined