Busch Lab

ZMP

ncor2

Ensembl ID:
ENSDARG00000000966
ZFIN ID:
ZDB-GENE-030616-81
Description:
Novel protein similar to mouse silencing mediator of retinoic acid and thyroid hormone receptor (SMR
Human Orthologue:
NCOR2
Human Description:
nuclear receptor corepressor 2 [Source:HGNC Symbol;Acc:7673]
Mouse Orthologue:
Ncor2
Mouse Description:
nuclear receptor co-repressor 2 Gene [Source:MGI Symbol;Acc:MGI:1337080]

Alleles

There are 18 alleles of this gene:

Allele Name Consequence Status Availability
sa21362 Nonsense Available for shipment Available now
sa7154 Nonsense Mutation detected in F1 DNA Not yet available
sa13457 Essential Splice Site Available for shipment Available now
sa14103 Essential Splice Site Available for shipment Available now
sa34468 Nonsense Available for shipment Available now
sa41279 Nonsense Mutation detected in F1 DNA Not yet available
sa41278 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15996 Essential Splice Site Available for shipment Available now
sa11868 Nonsense Available for shipment Available now
sa15101 Nonsense Available for shipment Available now
sa1781 Nonsense Available for shipment Available now
sa21361 Nonsense Available for shipment Available now
sa34467 Nonsense Mutation detected in F1 DNA Not yet available
sa12530 Nonsense Available for shipment Available now
sa38706 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34466 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21362
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
ENSDART00000001092 None None 1999 None 35
ENSDART00000051139 Nonsense 103 2325 3 44
ENSDART00000140618 None None 1989 None 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45544262)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43495198
GRCz11 8 43501985
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCAGGACGCCAGCAGCCAATCAGAAGTGGAGTACTCTGAGATGAAG[C/T]GACCTCGCTTGGAGATTGGGGCGGAGTCTCTTATTCGACACTCATCTCAT
Long Flanking Sequence:
ATTGTCAGTAACGGCAATGGCTTTGTTATGGGGGAAACAGTAACTCATTTGATTACTCAAAGTATTGCCATTATTTATAGTGTTGTTATTCCCATTACTGATCATGAGTATATTTTAAAGTTAGTATGGGCTGTTGCAGCCTAAGTGGAATATCCTCAATAGCACATAAATGCACACTTTTAATAATCTAATTAATCCCTAATGGAGAAAATCAAGTCTTGTTCTCTTAATGAATACGAAGCAACGTATATGTTCTGACATCCTCTTCAGCCATCTGAAGTTTCTGTCGGATGTTGTAACACTTGCTGTTAAATGTCAATTGCAATAAATGATTCGCTAACCTTTTCGTCCTGACATTCTTTCTGATTAGGCTACTGTCTGTATAAATCATCATCTTTATGTTTCTTTTGTCCTCCTACAGAGAGCCCCACATCCGATATGAACACATATACCTGCAGGACGCCAGCAGCCAATCAGAAGTGGAGTACTCTGAGATGAAG[C/T]GACCTCGCTTGGAGATTGGGGCGGAGTCTCTTATTCGACACTCATCTCATCGTCAGGCCCTCACTGTGGGCGGAGCTGAGGAAATGGCAAAGGTCGGCAAATCTAATTTCCATACAGAGTCAACTCCTGATATCCTATCAGTAACTGATAAGATGCTAATTATTGTTATACAAACAAAAGAATAGCCAATTGTAGTCTGCAGTAAATAATATTCACTACCTTAATGTCCAATCTAGACAACTATTCAACACTATTCTGTATTTTTTTGTTATTATAATTATTTATTTATTATTTCTTAAAGATAATTATGCTTTTCACTTTTTTCTGTATTTATTATAAAGTGGTGGATGGAACAAATTGTCTCTTTGCCTTCAAAATAATGTTATGTAATGTCTAATAAGCTGCAAAAAGACAGTCTTATCCTAGCACGGAGTTTTAACTGACTGTTTATGTTTCATTTTGCATCATAAAGGCATTCAATAATACTAGGACGTTTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7154
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
ENSDART00000001092 None None 1999 None 35
ENSDART00000051139 Nonsense 196 2325 4 44
ENSDART00000140618 None None 1989 None 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45528922)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43479858
GRCz11 8 43486645
KASP Assay ID:
554-5459.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGGGAAATCACCATGGTGGAGCAGCAGATCAGCAAACTGAGGAAAAAA[C/T]AGGTAAACKTCACCCCGACCTTCTTGAAGCTGTAAATATGTGATCGAAGG
Long Flanking Sequence:
TATTGTCTACTCACCCTTGTGTTTGGTTATCAAAAACCAATTAGTTATGACAAATCATATTGGCTCCACCCTGAAATCCATTATTTAAAACATTTTATTAAATGCATGATAATGTTTTCATTTTATTATACCAGTAAACAATATTAACTTCTTTTTGATATTATTATGAGATAGTATTAATAATTTCGGATAAGAGTTGAAATGATTACAACCACAGAGTAAATGTTTTTAAAAATCCTTTAAATCTACACCCTTTACAAACAGCATAAAGCATCTATTAGGTCTGAATGAGTACAATTTGTGTGTTTACACAGGAGCACAGCAGCAGCAGCTCTATTGGGAAGATTGAGCCCATCTCTCCTGTGAGCCCGGTGCCCATGGAGGCCGACCTGGACCTGGTGCCCTCCCGCCTCTCCAAAGAGGAACTAATCCAAAACATGGACCGCGTGGACCGGGAAATCACCATGGTGGAGCAGCAGATCAGCAAACTGAGGAAAAAA[C/T]AGGTAAACTTCACCCCGACCTTCTTGAAGCTGTAAATATGTGATCGAAGGGCTGTGCAGTAAAAATGATAACTGTATCGATCATTTATAGAAATGATCATTTATAAAACAGTGTTGCATGTTTGTTAAATGTCCAATACACTGTTTGCGCTTCAAAATATTACGCTTATTTGTATCACATGGACTCTTTACCTATTTATGTAAATCGTGTTCAACATAGTGTGAGTTTTGGTTCATTTACATGCTTATTGATCTCAAATCAAACACACAACCGGCTCCAAAGAGAATCGCATGAATTTAGTGAAGAACTCAAATGTCTTTGTGGTTTAGTTTAAAACCTTATGAAACCGCATTGACATTCTCAATGACACTGAAAAACTGGGGAGGAATGGGGCGGAAAGTGCAGTGTGCCATGAACGATCCATCTTGAAAGCTTTTGCATGGATTTGCTGTAGTACCAGCAAATGCACCACAGTGTTGTGGCAGGATTGGTAGATATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13457
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 None None 1999 None 35
ENSDART00000051139 Essential Splice Site 196 2325 4 44
ENSDART00000140618 None None 1989 None 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45528918)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43479854
GRCz11 8 43486641
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAATCACCATGGTGGAGCAGCAGATCAGCAAACTGAGGAAAAAAHAGG[T/G]AAACKTCACCCCGACCTYCTTGAAGCTGTAAATATGTGATCGAAGGGCTG
Long Flanking Sequence:
GTCTACTCACCCTTGTGTTTGGTTATCAAAAACCAATTAGTTATGACAAATCATATTGGCTCCACCCTGAAATCCATTATTTAAAACATTTTATTAAATGCATGATAATGTTTTCATTTTATTATACCAGTAAACAATATTAACTTCTTTTTGATATTATTATGAGATAGTATTAATAATTTCGGATAAGAGTTGAAATGATTACAACCACAGAGTAAATGTTTTTAAAAATCCTTTAAATCTACACCCTTTACAAACAGCATAAAGCATCTATTAGGTCTGAATGAGTACAATTTGTGTGTTTACACAGGAGCACAGCAGCAGCAGCTCTATTGGGAAGATTGAGCCCATCTCTCCTGTGAGCCCGGTGCCCATGGAGGCCGACCTGGACCTGGTGCCCTCCCGCCTCTCCAAAGAGGAACTAATCCAAAACATGGACCGCGTGGACCGGGAAATCACCATGGTGGAGCAGCAGATCAGCAAACTGAGGAAAAAACAGG[T/G]AAACTTCACCCCGACCTTCTTGAAGCTGTAAATATGTGATCGAAGGGCTGTGCAGTAAAAATGATAACTGTATCGATCATTTATAGAAATGATCATTTATAAAACAGTGTTGCATGTTTGTTAAATGTCCAATACACTGTTTGCGCTTCAAAATATTACGCTTATTTGTATCACATGGACTCTTTACCTATTTATGTAAATCGTGTTCAACATAGTGTGAGTTTTGGTTCATTTACATGCTTATTGATCTCAAATCAAACACACAACCGGCTCCAAAGAGAATCGCATGAATTTAGTGAAGAACTCAAATGTCTTTGTGGTTTAGTTTAAAACCTTATGAAACCGCATTGACATTCTCAATGACACTGAAAAACTGGGGAGGAATGGGGCGGAAAGTGCAGTGTGCCATGAACGATCCATCTTGAAAGCTTTTGCATGGATTTGCTGTAGTACCAGCAAATGCACCACAGTGTTGTGGCAGGATTGGTAGATATACCGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14103
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
ENSDART00000001092 Essential Splice Site 462 1999 9 35
ENSDART00000051139 Essential Splice Site 842 2325 19 44
ENSDART00000140618 Essential Splice Site 462 1989 9 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45460088)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43412870
GRCz11 8 43419657
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYATGCAGCGCCGATGAGGTGGAGGAGACKGAGAGCTCAGAGAAGAGCAG[G/A]TGAGAGTGTGCACGTGTGTRTGGCTGTGTGTTGATTGGTTACTTGGGTGG
Long Flanking Sequence:
ATCAAGCAAACGGCACACACCAGATCAGCTGGCATCAGTGTTCTGCCCTATCGTGACGTTTCCCATCACCTCTTTATTTCAGGTGGAGCCAATAACAGCTCAGACACAGAGAGCCTCCCTTCCCCACGCTCCTCAGATGACAGCAAGGTCAAAGAAGAGGGCTCGGCTCGGCCCAAAACTGCACCCAACGCCACTTCCTCCTCTTCCTCCACGGACAAGGACATGGCAGCTGCAGAGACGGGGATGGACGAGAAGCCAAAAGTGGAGAAGGGAGACGGGGAGCAGGCAGGAGTGAAGCAGGAGGTGAAGACCGAGCCAGGGGAAGGCGCTTCAGAGTCAGCCGGAGAGGATAAGAAGCCTCCTGCCCTGGAGGTGGAGGAGGGCAAGAAAGAGGTCAAGAAGAAAGAGCACGGGGGAAAGAGTGGAGCTCACGACAGCGACTCCAGCGCCACATGCAGCGCCGATGAGGTGGAGGAGACGGAGAGCTCAGAGAAGAGCAG[G/A]TGAGAGTGTGCACGTGTGTGTGGCTGTGTGTTGATTGGTTACTTGGGTGGGGTCTGATGTGGTTAAGAAGGCTGGGATTGTTGATCTGTCCTGTAGGATTTTTTTTCCATGACAGCAAACACTGTATATGTTGGCTGAGTCGGGGGAAACATTAGCTTGTGAGCTTGCCAAACATATCAGAGTGAGAAGTGTGTGTGTGTCTGTCTGGTTCCGTCTTTTGTGTATTTTGCGTTTTACATTTCCATACGACTGCAAGTGGAAAGGCTGTGTTTGTTTATGTGTGGCGGGATGATGATTAAGCGTGTGTGTTTGTGGTTTTGTGGCATTAACGGGCTGTTTACAAAGAGCGTAAATAAGAGAGAATGAGCCTCTGACCATATTAAGCAATAACTCTTCTCTCTCTTCTCACAATGACGTCTCCTAGGCCCAGCTTGTTGAGTTTTAGCCACGATGGAGTGATCTCTTCTCAAGCTCAGAAACCGCTGGACCTCAAACAGCTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5501
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Essential Splice Site 575 1999 11 35
ENSDART00000051139 Essential Splice Site 955 2325 21 44
ENSDART00000140618 Essential Splice Site 575 1989 11 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45454054)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43406836
GRCz11 8 43413623
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTCGGGTCAGGACTCGCAGCCCTGGTATCTCTGACAGAGAGAGAGAAG[G/A]TAAGCTGCTCTCTGTTCTTTAYCTTTCTTGTKTTCTTTCAGTACATTTCT
Long Flanking Sequence:
ATTCTTTTTTTTTATGCACCTTGGTGGGAGGTACTTTAGTTTAGCAATCTGCTAAATCTAATAACAGAATTGAAAACCTCTTAGTGACGGGCATAAAGAGATGATCGCACAGAACATGTTATTGCTCTCAATGTTGTGAGAAACATAATTAGTCATAATGCTGTTTTTACGATAATAGTACTATACCTCAGTCAATGAGTAGAAAAGATTGCAGAGTCTAGAGATGCAGTAATGTATAATAAGCAATATCTGTCGGTTTGTGTAGTTGCCAGAGGTGTCAGGACGTGATAACCGGCCTGGTTTGCCAGGAAAGCAGGCTATGCCGGACGCTCTTGCGTTGTACCAGCAGCAGATTACCATGGCACATGAATCCTCCCAGGAGGCCAAACAGCAGCAGCAACAACAGCCAACCAAATCACAGCATTACCCTGCGGCAGGGGACTCCGGCAGCCCTCGGGTCAGGACTCGCAGCCCTGGTATCTCTGACAGAGAGAGAGAAG[G/A]TAAGCTGCTCTCTGTTCTTTACCTTTCTTGTGTTCTTTCAGTACATTTCTCTCCCCAGCTTTCTCAAGCACCCTGGATTTCCACACCAGCAAGTTCTGATGTGTGTGTATGTGCTGTGCTGTGCTGTGCTGTGCTGTGAATGAAGCTGACTGGATCCAACCTAGACAGTCAGTTAGTGAACAACCAGCAAACCCCAGTTCACGTTGGTTTTTAGTTGCTTCTTACAAAAAGATTAAGACACCAGGTCTAGGTAGGAATGTGTTCCCTCATCTGCTTGTGATCTGATGGACCAAAATGCATCTTAATAGCTGGTGTAAACAGGGTCTTGCATGTGCAAATCTGAAATTGATGCAGACTCTTCAATATGCATATGTTCAATAAAAAGTGGTGCCTTTTTTTAGGCAAAAGGTGCAATTCTACAAATATTTACAGACAAAATCCTGTTATATAGATAAGAATTCATGTGTTCAGGGATTTAGTGGGAGGGGGAAAGAATTTGC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27255
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 642 1999 13 35
ENSDART00000051139 Nonsense 1006 2325 22 44
ENSDART00000140618 Nonsense 632 1989 13 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45451160)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43403942
GRCz11 8 43410729
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCGCCCAGAGACATGGCCAAATTCAGCCAAGAACAGCTGCTACACTA[C/A]AATCCCTGTAAGAGAGCACTGCCTTGTCAATTGAATTAAAGTGTTACATA
Long Flanking Sequence:
TAGGTTTACACTTTTACACACGCATACCCGCACACTATTGGAGCAGCCTCTAATCAAGCGTGTTGATTTCTGGGAGTGTGAATGATCTGCAGATGTGTTTGCATGCCGCTACGCTCACAGATTTCAGCTTACAGAGTGCCGATGAGCCTGGTGATTTGTAGACTCTTGGAGTCTGAATAACTGCTGTCTGCGTGTTTTCACATACTACTTTTCATACAGGGGTTGTGTTGATTTGAGCTTTGACATCTTTACCTTTGGCAAAACAAAAAAAAAAACAAGGTGTGACAGACTGCAATCCAGTCATCATCTGGTTGACAGTCACTTCTGTGTGTTTTGTTCATGTGCGCAGATAAATCCCGGGCGTTCTCTCCTCTTGCAGATGGCAAGAAGAATCCCGGGGCTGATGACATTCGGGCTTTAGGTCTAGGCCGGCCAGTGATGTCATCGTACCTCTCGCCCAGAGACATGGCCAAATTCAGCCAAGAACAGCTGCTACACTA[C/A]AATCCCTGTAAGAGAGCACTGCCTTGTCAATTGAATTAAAGTGTTACATAGTCACACCCATCAATATTGATGATAGTACACATTAATATAAGTTGTGCATGTCACGTTTTATTCAGAAATGATGTTGAATAGGCTGTTTGGATTAACTATACAAGGAAAAATAAATATATTTATGCAGTTTGAAGCTTTATGTTTGAGAAATTATAAAGGATCACTAACTTTATAAAGTCATTCACTGTTTTGTTTTGTTTTTTAACACATTTTTACTGACCTTATGCACCTTAAATGAGTTCTCTGGTGTGACAGTGCAATATATTAATGAAACCAACTCTTAATAATATACAAATAGTGGGAGAGCTTCTTATCTTCTTTGTTGGACACTTATCCTCATATAGCGCTATATACTTTATATGAAATAACCAATTTTTTTTTCATCATGACTTAGGGCTGGGCGATTAATTGAAAAGTAATTGAAATCAACATTTAGAACCTATAATCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34468
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 696 1999 15 35
ENSDART00000051139 Nonsense 1060 2325 24 44
ENSDART00000140618 Nonsense 686 1989 15 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45448974)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43401756
GRCz11 8 43408543
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATTGCAGGGTACTCCAGTGCAACTGCACAATCCATCCCATGGCTCT[G/T]AGCATGGGAAAGTCCCAGCTCCAGGATCACTGGCTCTCTCCTGGGTGGAC
Long Flanking Sequence:
ATTTAAAATTTGTTTAATAATTACATTTATTATTAATAATTACTGATATATAAAATTTTTTAACAAATGCCAACTTGATGAACAGATTTATTTTCTGAAAAAAAAAAACTGACCCCAAACTTTTGACCAGTAGTGTAGATATCTGTCATCTGTGACAGTGAAAATACAATGCCATGTCAACAATCCTACATATACATTTCTAATAATTTATTTATCTCTTTTAGCGTTAGCTTCCACTTTACAGCCACAGGACAGAATGGCTGCAGTGCGGCCTCTCCATATTCCAGAACCCCCTCCCCTCATCTCCTCTGCCAAACCTGGTGGCTCCATCACACAGGTGAGAGCGACACTTTATCTTGATATGCCAGTCTTATGAGTTAGCGTTACTGTGACCGTTCATCAATACTGTAGGGTTTTAATGTGCATAATTAAGCTGTTGTTCATGTTGTATTAAATTGCAGGGTACTCCAGTGCAACTGCACAATCCATCCCATGGCTCT[G/T]AGCATGGGAAAGTCCCAGCTCCAGGATCACTGGCTCTCTCCTGGGTGGACCAGAGGAAAATGGGTAAGCGCGAGACCCGAGCCATCACAAGTCAGCTATCTGTTTTCCATATCCAACATCTCTTTCTGTCTCCTCAGGCGGGTTTCCAGTTGTTAAACAAGAGCAGTTGTCTCCTCGTGGGGCTTCCTCCTCCTCCTCTCAGGCTGAGAATCTTTCCACACAGGACAGTTCTACATCACGGGGTGAGTTTGGGCCAAATCATCATCCCTCATCTCAATTTAATCTTAGCCCAAAGAGATTAAAGTGGAGGACTAAAGTTCATGCACAAATAGATTTCAAACATCATTAACTCTTGTGTCTCTTAGGACCCATGCCAGCTGTTCAGGGTGGCAGCATTACAAAGGGCATCCCTGGCACACGTGTGCACCAGGATTCTCCCATATCATATCGAGGTGGTTCTATCACTCAGGTGAGAATCTCACACAGTGAAAAGGGTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41279
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
ENSDART00000001092 Nonsense 724 1999 16 35
ENSDART00000051139 Nonsense 1088 2325 25 44
ENSDART00000140618 Nonsense 714 1989 16 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45448816)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43401598
GRCz11 8 43408385
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATCCAACATCTCTTTCTGTCTCCTCAGGCGGGTTTCCAGTTGTTAAA[C/T]AAGAGCAGTTGTCTCCTCGTGGGGCTTCCTCCTCCTCCTCTCAGGCTGAG
Long Flanking Sequence:
TGAAAATACAATGCCATGTCAACAATCCTACATATACATTTCTAATAATTTATTTATCTCTTTTAGCGTTAGCTTCCACTTTACAGCCACAGGACAGAATGGCTGCAGTGCGGCCTCTCCATATTCCAGAACCCCCTCCCCTCATCTCCTCTGCCAAACCTGGTGGCTCCATCACACAGGTGAGAGCGACACTTTATCTTGATATGCCAGTCTTATGAGTTAGCGTTACTGTGACCGTTCATCAATACTGTAGGGTTTTAATGTGCATAATTAAGCTGTTGTTCATGTTGTATTAAATTGCAGGGTACTCCAGTGCAACTGCACAATCCATCCCATGGCTCTGAGCATGGGAAAGTCCCAGCTCCAGGATCACTGGCTCTCTCCTGGGTGGACCAGAGGAAAATGGGTAAGCGCGAGACCCGAGCCATCACAAGTCAGCTATCTGTTTTCCATATCCAACATCTCTTTCTGTCTCCTCAGGCGGGTTTCCAGTTGTTAAA[C/T]AAGAGCAGTTGTCTCCTCGTGGGGCTTCCTCCTCCTCCTCTCAGGCTGAGAATCTTTCCACACAGGACAGTTCTACATCACGGGGTGAGTTTGGGCCAAATCATCATCCCTCATCTCAATTTAATCTTAGCCCAAAGAGATTAAAGTGGAGGACTAAAGTTCATGCACAAATAGATTTCAAACATCATTAACTCTTGTGTCTCTTAGGACCCATGCCAGCTGTTCAGGGTGGCAGCATTACAAAGGGCATCCCTGGCACACGTGTGCACCAGGATTCTCCCATATCATATCGAGGTGGTTCTATCACTCAGGTGAGAATCTCACACAGTGAAAAGGGTGTTTGCAATTGCTTTTAATGACTGATGAAAATGTTTATTCACAATAAATATATTTTATTTTTGTAAGTAGTAGGGCTGCAGTATATTGGACAAATCAGACATTGCAATATTTAGCTTTTCTGTAATAAATATTGTGATATACAGTCTATACAATTTCACCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41278
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
ENSDART00000001092 Essential Splice Site 786 1999 17 35
ENSDART00000051139 Essential Splice Site 1150 2325 26 44
ENSDART00000140618 Essential Splice Site 776 1989 17 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45448503)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43401285
GRCz11 8 43408072
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCACCAGGATTCTCCCATATCATATCGAGGTGGTTCTATCACTCAGG[T/C]GAGAATCTCACACAGTGAAAAGGGTGTTTGCAATTGCTTTTAATGACTGA
Long Flanking Sequence:
TGCAACTGCACAATCCATCCCATGGCTCTGAGCATGGGAAAGTCCCAGCTCCAGGATCACTGGCTCTCTCCTGGGTGGACCAGAGGAAAATGGGTAAGCGCGAGACCCGAGCCATCACAAGTCAGCTATCTGTTTTCCATATCCAACATCTCTTTCTGTCTCCTCAGGCGGGTTTCCAGTTGTTAAACAAGAGCAGTTGTCTCCTCGTGGGGCTTCCTCCTCCTCCTCTCAGGCTGAGAATCTTTCCACACAGGACAGTTCTACATCACGGGGTGAGTTTGGGCCAAATCATCATCCCTCATCTCAATTTAATCTTAGCCCAAAGAGATTAAAGTGGAGGACTAAAGTTCATGCACAAATAGATTTCAAACATCATTAACTCTTGTGTCTCTTAGGACCCATGCCAGCTGTTCAGGGTGGCAGCATTACAAAGGGCATCCCTGGCACACGTGTGCACCAGGATTCTCCCATATCATATCGAGGTGGTTCTATCACTCAGG[T/C]GAGAATCTCACACAGTGAAAAGGGTGTTTGCAATTGCTTTTAATGACTGATGAAAATGTTTATTCACAATAAATATATTTTATTTTTGTAAGTAGTAGGGCTGCAGTATATTGGACAAATCAGACATTGCAATATTTAGCTTTTCTGTAATAAATATTGTGATATACAGTCTATACAATTTCACCAGATAACTTGAAAACTACTATTTGAAAGGAATTTATTAGATTAGTCTGATTGGGATAATTCTTTAGGTAAGTTAATTATGCTTAAAATATAATAAACAAATTTCAAGCATAGATAAATTCAAAAGAGCAAAGATAAACATGTGATTAAATAGTGTTTATGTTTTTCAGGGCAGTCAAATACTGTAGTATTCAGTCATCCTTGGACTAATCAATGTAAAATAACACTGTAAAAGTCTTTACTGTATAAATAATTTAATAAAATATACATTAATAAAGTTACAAAGGGGTAAAATATCTTGTGGCTGAAAACTTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15996
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
ENSDART00000001092 Essential Splice Site 1159 1999 23 35
ENSDART00000051139 Essential Splice Site 1523 2325 32 44
ENSDART00000140618 Essential Splice Site 1149 1989 23 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45441548)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43394330
GRCz11 8 43401117
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAACRTTTGATGCYGCAGCTCTGCCCAGGGGYATCCCGATTGACTCAG[G/A]TATTCCAYATATTTGCAGATTAGCAGAAAATGTCASTGTGCAATTTTCCA
Long Flanking Sequence:
GGGGGCAAATCTCGACCCAGTGCTGTAGTCAGTGCCCCCAGCTCTCTGTCCCGTGTCTCTCCATTGGCACTGAGTGGAGAGCAGAGCAGCAGGCCTCACCACAGTCCAGTGGGGTATGAAGATCATAAAAGATCCAGCTACCCTCCGCCCTCACACAGAGCCTCTCCACTGTCTGGCAGAGAAAACTCACAGCGCGCTCATGAAGGTATCATGATCATCCAGTCAGAGAAAATTCAGTAGCTAATGTCCTTTCTTTGAGGTTTGAACATTGTTTCTCTGTGTATATTTAGGCTCTAGTAAACCCCAACAGCAGGAGAGAAAGGCCACCCCCACCCCAAGAGAGATGGGCTCCACTAAGTCTCCATTGGCAGTGGGTGAGCACACTGCAAATTTAGCCTTCGAGAGGATCCTTGGGTTGGGACCGGACATGTACCGTAGCCAGATGTCTCATTTAACATTTGATGCTGCAGCTCTGCCCAGGGGTATCCCGATTGACTCAG[G/A]TATTCCACATATTTGCAGATTAGCAGAAAATGTCAGTGTGCAATTTTCCATGATCATTAATTATACTTGGAAACATTAAAATTTTCATGTATTATGTTATGCATCATCTCAGTTTGTCTTTGCTTTCCCACAGCGTATTACCTGCCTCGTCACCTGGCTCCTGGCCCTGGCTACCCACACCCCTATCCACCCTACCTGATCAGAGGCTGTTTCCCTGAAACAGCAGCCCTGGAAAACAGACAAACGCTTTTCAATGACTACATTACCTCTCAGCAGATGCACCAGTGGCCTGCTGCCGCTGCAATGGCTGCCCAGAGACCTGACCTGCTCAGAGGCCTCACACCTAGAGAGCAGTCCTTAAACTTAGCCTATTCACCCACGCCTAGAGGTGAGCCTTTCTGAAAAGCGTCAAATCTTACAATTAACATAGTATTCACTTCTTATTTGTTTTTGTCTGTCAGTCAAGTCAGTCATCAAGCAAAGATTCAACACAGGAATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11868
Status:
Available for shipment
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Availability:
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 1177 1999 24 35
ENSDART00000051139 Nonsense 1541 2325 33 44
ENSDART00000140618 Nonsense 1167 1989 24 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45441362)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43394144
GRCz11 8 43400931
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTACCTGCCTCGTCACCTGGCTCCTGGCCCTGGCTACCCACACCCCTA[T/A]CCACCCTAYCTGATCAGAGGCTGTTTCCCWGAAACAGCAGCCCTGGAAAA
Long Flanking Sequence:
TCACAGCGCGCTCATGAAGGTATCATGATCATCCAGTCAGAGAAAATTCAGTAGCTAATGTCCTTTCTTTGAGGTTTGAACATTGTTTCTCTGTGTATATTTAGGCTCTAGTAAACCCCAACAGCAGGAGAGAAAGGCCACCCCCACCCCAAGAGAGATGGGCTCCACTAAGTCTCCATTGGCAGTGGGTGAGCACACTGCAAATTTAGCCTTCGAGAGGATCCTTGGGTTGGGACCGGACATGTACCGTAGCCAGATGTCTCATTTAACATTTGATGCTGCAGCTCTGCCCAGGGGTATCCCGATTGACTCAGGTATTCCACATATTTGCAGATTAGCAGAAAATGTCAGTGTGCAATTTTCCATGATCATTAATTATACTTGGAAACATTAAAATTTTCATGTATTATGTTATGCATCATCTCAGTTTGTCTTTGCTTTCCCACAGCGTATTACCTGCCTCGTCACCTGGCTCCTGGCCCTGGCTACCCACACCCCTA[T/A]CCACCCTACCTGATCAGAGGCTGTTTCCCTGAAACAGCAGCCCTGGAAAACAGACAAACGCTTTTCAATGACTACATTACCTCTCAGCAGATGCACCAGTGGCCTGCTGCCGCTGCAATGGCTGCCCAGAGACCTGACCTGCTCAGAGGCCTCACACCTAGAGAGCAGTCCTTAAACTTAGCCTATTCACCCACGCCTAGAGGTGAGCCTTTCTGAAAAGCGTCAAATCTTACAATTAACATAGTATTCACTTCTTATTTGTTTTTGTCTGTCAGTCAAGTCAGTCATCAAGCAAAGATTCAACACAGGAATAGACACTTTACAAAAAGATTGAGCATTTATATAACATTTTTATTTAAATTAAACAAATGGTATTAAATTTTTAGAGGTACATTTTTATGTTTTCTTGCAGGAACATCTGCATCTCCCATGGATCGTATCACATATATCCCAGGAACTTCTCCAGGTTTCCCTAGCGGAGCCTACAACACCTCTCCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15101
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 1211 1999 24 35
ENSDART00000051139 Nonsense 1575 2325 33 44
ENSDART00000140618 Nonsense 1201 1989 24 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45441260)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43394042
GRCz11 8 43400829
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACAAACGCTTTTCAATGACTACATTACCTCTCAGCAGAWGCACCAGTG[G/A]CCTGCTGCYGCTGCAATGGCTGCCCAGAGACCTGACCTGCTCAGAGGCCT
Long Flanking Sequence:
AGGCTCTAGTAAACCCCAACAGCAGGAGAGAAAGGCCACCCCCACCCCAAGAGAGATGGGCTCCACTAAGTCTCCATTGGCAGTGGGTGAGCACACTGCAAATTTAGCCTTCGAGAGGATCCTTGGGTTGGGACCGGACATGTACCGTAGCCAGATGTCTCATTTAACATTTGATGCTGCAGCTCTGCCCAGGGGTATCCCGATTGACTCAGGTATTCCACATATTTGCAGATTAGCAGAAAATGTCAGTGTGCAATTTTCCATGATCATTAATTATACTTGGAAACATTAAAATTTTCATGTATTATGTTATGCATCATCTCAGTTTGTCTTTGCTTTCCCACAGCGTATTACCTGCCTCGTCACCTGGCTCCTGGCCCTGGCTACCCACACCCCTATCCACCCTACCTGATCAGAGGCTGTTTCCCTGAAACAGCAGCCCTGGAAAACAGACAAACGCTTTTCAATGACTACATTACCTCTCAGCAGATGCACCAGTG[G/A]CCTGCTGCCGCTGCAATGGCTGCCCAGAGACCTGACCTGCTCAGAGGCCTCACACCTAGAGAGCAGTCCTTAAACTTAGCCTATTCACCCACGCCTAGAGGTGAGCCTTTCTGAAAAGCGTCAAATCTTACAATTAACATAGTATTCACTTCTTATTTGTTTTTGTCTGTCAGTCAAGTCAGTCATCAAGCAAAGATTCAACACAGGAATAGACACTTTACAAAAAGATTGAGCATTTATATAACATTTTTATTTAAATTAAACAAATGGTATTAAATTTTTAGAGGTACATTTTTATGTTTTCTTGCAGGAACATCTGCATCTCCCATGGATCGTATCACATATATCCCAGGAACTTCTCCAGGTTTCCCTAGCGGAGCCTACAACACCTCTCCTATCTCACCAGGTACAGAGTAGCATGCTAATTTCAAACATATTTTTTGAAACAAGTTCAGTTCCCTCACCTTAATTATTGCTTATCTTCTTAACAGTAGGAGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1781
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 1321 1999 26 35
ENSDART00000051139 Nonsense 1685 2325 35 44
ENSDART00000140618 Nonsense 1311 1989 26 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45440637)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43393419
GRCz11 8 43400206
KASP Assay ID:
554-1774.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAGCAGAGAGAGCGAGAAAGAGAAAGAGAGCGAGAGAGGGACAGGGAG[C/T]GAGATCGAGACCGGGAGCGTGAGAAAGATCGAGACAGGGACAGAGAAAGA
Long Flanking Sequence:
AAATCTTACAATTAACATAGTATTCACTTCTTATTTGTTTTTGTCTGTCAGTCAAGTCAGTCATCAAGCAAAGATTCAACACAGGAATAGACACTTTACAAAAAGATTGAGCATTTATATAACATTTTTATTTAAATTAAACAAATGGTATTAAATTTTTAGAGGTACATTTTTATGTTTTCTTGCAGGAACATCTGCATCTCCCATGGATCGTATCACATATATCCCAGGAACTTCTCCAGGTTTCCCTAGCGGAGCCTACAACACCTCTCCTATCTCACCAGGTACAGAGTAGCATGCTAATTTCAAACATATTTTTTGAAACAAGTTCAGTTCCCTCACCTTAATTATTGCTTATCTTCTTAACAGTAGGAGCCTCTCACATGAGCAAGATCCAAGGTGGTTCATCATCTGCTGAAAGAGAAAGAGAACGGGAGAGAGAGAGAGAAAGAGAGCAGAGAGAGCGAGAAAGAGAAAGAGAGCGAGAGAGGGACAGGGAG[C/T]GAGATCGAGACCGGGAGCGTGAGAAAGATCGAGACAGGGACAGAGAAAGAGACAAGTCTCTCAGCCATGGTAACGTGGAGCACGCACCTATATGGAGACCAGGTGAGACCCCCTCAGCACCTCTTTATTTTAAATGGGTACAATCATTCTTAAATATCTGATAGTTAATTTATTTGGAACATATGTATTTCTTTTAATGTTTCTTTTTTTCATATTTTACATATTTCAGTAACTGAATTTCTTGGTAATAGCTTAAGTTAACAACATTGTTGTATAGTTAAAATTAATTTAATATGAAGTTGAAAGTGAACCGAAAGCATTTCTTCTTCAAGCAGTCAATTGTAGAATTAGCTTTAGTGCACTTCGGTGAATCTTTTAAATGCATCTCAGTATTGCTAAAAATCTGAACTTTGTTTCTGAGCAGGAGCACCTGAACAGATGAGCGGCAGCAGTTCTCGTCCCCCTTCTCATCCTTACAGTCACCAGTCCCCGCTCTCGCC
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:
sa21361
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 1437 1999 28 35
ENSDART00000051139 Nonsense 1801 2325 37 44
ENSDART00000140618 Nonsense 1427 1989 28 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45439868)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43392650
GRCz11 8 43399437
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGCTTCAGTGGGCACCTCCAGAGGTCTGGTTTACCCGGTGAGGGTTA[C/A]CCATCTGGAACGGACCCAAGTGCTAAAGACTTGAGCAGAGATGGGGGCAA
Long Flanking Sequence:
GTTGTATAGTTAAAATTAATTTAATATGAAGTTGAAAGTGAACCGAAAGCATTTCTTCTTCAAGCAGTCAATTGTAGAATTAGCTTTAGTGCACTTCGGTGAATCTTTTAAATGCATCTCAGTATTGCTAAAAATCTGAACTTTGTTTCTGAGCAGGAGCACCTGAACAGATGAGCGGCAGCAGTTCTCGTCCCCCTTCTCATCCTTACAGTCACCAGTCCCCGCTCTCGCCCCGTCCCCAGGACAGCTTGCAGCAGAGACCAAGCGTCCTGCACAACACCAGCTCCAAGAGCCTGTCAAACTCTGAGCACAACAATCCTTCTGTGCTGCGGTGAGTCTTCCCCACTCAAACTGCTGTCTGAAGCTCCATCTAGTGAGATCAACATGTTAAAGCTGGCTCTAATTTGTTTCTGCTTTTCTTCCTTCAGACCACCAGGCTCTGCTCGCTACCAGGGCTTCAGTGGGCACCTCCAGAGGTCTGGTTTACCCGGTGAGGGTTA[C/A]CCATCTGGAACGGACCCAAGTGCTAAAGACTTGAGCAGAGATGGGGGCAAAAGCCATGGGCGAGGAGGTCTGCCCAAACACCAAGACCTTTCATCCTCTTCTAAATCTGACTCCAAGCTCGCCAGTCCTGGTGCCGGTGGTACATATCCCTCTCCATACAACCAGGCCCCTGTTGCCCACCTGCCCACAAGTCGAGGGCACCCCTTGTTGGCGCCCGAAAGTGGCGGCGGCGGCAGTTCCATCCAATCCCGTGGCGGGGACAGCGGCAGCAGCGCGTCAAGTAGGGAAAAGACTCAAAACAAAGTGATGTCCATACAGGAACACGAACTTCGAGCACTCGGTAAGACCACCATGACAGCGGCCAACTTCATAAACGCGATAATCATGCATCAAATTTCTTGTGATGCGGCGATGCCAGAGACTGGTGCGCTCGCGACCAACGGCACCTGTGATGGTAAGATGCTCTGGGACCTTTGGGCCGTTAACGCCACATCCAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34467
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
ENSDART00000001092 Nonsense 1490 1999 28 35
ENSDART00000051139 Nonsense 1854 2325 37 44
ENSDART00000140618 Nonsense 1480 1989 28 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45439709)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43392491
GRCz11 8 43399278
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCCAAGCTCGCCAGTCCTGGTGCCGGTGGTACATATCCCTCTCCATA[C/A]AACCAGGCCCCTGTTGCCCACCTGCCCACAAGTCGAGGGCACCCCTTGTT
Long Flanking Sequence:
CACCTGAACAGATGAGCGGCAGCAGTTCTCGTCCCCCTTCTCATCCTTACAGTCACCAGTCCCCGCTCTCGCCCCGTCCCCAGGACAGCTTGCAGCAGAGACCAAGCGTCCTGCACAACACCAGCTCCAAGAGCCTGTCAAACTCTGAGCACAACAATCCTTCTGTGCTGCGGTGAGTCTTCCCCACTCAAACTGCTGTCTGAAGCTCCATCTAGTGAGATCAACATGTTAAAGCTGGCTCTAATTTGTTTCTGCTTTTCTTCCTTCAGACCACCAGGCTCTGCTCGCTACCAGGGCTTCAGTGGGCACCTCCAGAGGTCTGGTTTACCCGGTGAGGGTTACCCATCTGGAACGGACCCAAGTGCTAAAGACTTGAGCAGAGATGGGGGCAAAAGCCATGGGCGAGGAGGTCTGCCCAAACACCAAGACCTTTCATCCTCTTCTAAATCTGACTCCAAGCTCGCCAGTCCTGGTGCCGGTGGTACATATCCCTCTCCATA[C/A]AACCAGGCCCCTGTTGCCCACCTGCCCACAAGTCGAGGGCACCCCTTGTTGGCGCCCGAAAGTGGCGGCGGCGGCAGTTCCATCCAATCCCGTGGCGGGGACAGCGGCAGCAGCGCGTCAAGTAGGGAAAAGACTCAAAACAAAGTGATGTCCATACAGGAACACGAACTTCGAGCACTCGGTAAGACCACCATGACAGCGGCCAACTTCATAAACGCGATAATCATGCATCAAATTTCTTGTGATGCGGCGATGCCAGAGACTGGTGCGCTCGCGACCAACGGCACCTGTGATGGTAAGATGCTCTGGGACCTTTGGGCCGTTAACGCCACATCCAAGCCCTCCCCTGCCCATTCTTCCTGTTCTCTACCAGTCCACCAAAACCCTCTCCCTCCCTTCCTCCCTCCCTCCCTCCCTCATCATTCCTCTGCCCATCCTGCACCCCTGCCCCTTACGTCTGTGGCCTAGTGCACGCTTGTGGTGGTTGGCATTAATGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12530
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001092 Nonsense 1687 1999 30 35
ENSDART00000051139 Nonsense 2013 2325 39 44
ENSDART00000140618 Nonsense 1677 1989 30 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45430694)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43383476
GRCz11 8 43390263
KASP Assay ID:
2260-0990.1 (used for ordering genotyping assays)
KASP Sequence:
CCACCTAGCACCCCTCAAGCCCAAACCCCCACAGAGCCCAATTCCCGCTA[C/A]ACCCCWGAGGGCACTTCTGCAGARAGGGGCARAGACAGGTCTCCTCCTCA
Long Flanking Sequence:
ACAGCAAAGATACAAACTAAATAAGCGGTATTTCATGCATTTGTGGAAATCAAGCAGTATACAGTGCAAAATGGATAATCAAATGTAAAATGACCCAGTATAGCCTTCATTGTATTTAGACACCAATACAATTAGAGTTTCTTAAAGTTACAGGCACTATCATTTTGTGTGCTGAATGCTCCACATTGCAGAGATGCCCAGTGCCCACATTGCAATATCAATGCCAAAACCATATATTGTGAAGCCCTAGACAAGCTGTGGTGCTGTATTTCTCAGTGTAAACATGTACCTGTCTCCTGCATGCACATCACTAAATCAAACTTTCCCTTTTTACAGGAGGTGATCACTAAAGATTACACACGCCAGTCACAGCAAAACCAGATAGGAGGTCAACCATCTCTCCCGCCTGGTTATGGGTATCACAGCTCTCCTGTGCTGGATCTCACCCGTCCACCTAGCACCCCTCAAGCCCAAACCCCCACAGAGCCCAATTCCCGCTA[C/A]ACCCCAGAGGGCACTTCTGCAGAAAGGGGCAGAGACAGGTCTCCTCCTCAGAATAAAACCTCTCCAGTGAGTCTGGCTGCTGATGGGATTGAACCAGTTTCACCACCAGGGGCCATTTCAGAGCCTGAGACGCCAGGAGCCAACTACCCCAATGAACAAGCTGAGCAGGGGTATGTAGCACACATTGTCACCAATCAGGGCTTTTGGAGAGCTTAACCATAAACTGTTGAAAACTGCAATTCAGAGGTTGCTAGGGCACTTAATCAGGGCGAGCTGAAAACTGAAGCCAAAATGCTAAAAAAAAAATGTGGATTCTGGCAGTAAGCCCCTCACTCCACAGCTAAAAGGAAAAATAGTCTGAAAAAACATCTCATTTTAAAATGTTGGCAAAACTGGTTGCTCTTCACATCTTCCCTTCAGACTCAGTGAGGAAAGCGAGGCTTTCACTTTTGACAGATTAAATGAGCTGATCTGGGTAAACTTTATCAACTCACCTAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38706
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
ENSDART00000001092 Essential Splice Site 1788 1999 None 35
ENSDART00000051139 Essential Splice Site 2114 2325 None 44
ENSDART00000140618 Essential Splice Site 1778 1989 None 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45427048)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43379830
GRCz11 8 43386617
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGCAAGAAGGAAATGATCAAAAAGATCAGCGCAGAGGCTGAGTTCAG[T/C]AAGTCTATGGATTCCATTTATTGTTTCTGTTTTGCAGAGAAAACGCCTGG
Long Flanking Sequence:
CCTGCCAGTGCTGTAAAAACTGAAAAATAGCATCTGTGGTATTACACAGAATGTCACATAATTTCACAAAAATTTGGAGAATAAACTAAAAGTAGGAGTGTTAGGACACCTAATCAAATTGACACTGAGAATGATTATAATAATGCATGTATTTACGGATATATTTAAAAATTAGTTACACACATTTTTTCGTGTATTCATTTTAGCACAGGAATTTGGAACATGGAAGAGGTGTATTTTATACTTTATGGCTGGTTACTTCCAATTGATTAACATTCCACCTAAGAATGGTTCATTTAGGAATTAAGTTATGTCAAACCAACCGAAGAAATGTCCAGATTTTCTGACTGGTTCTGTCTGTTTCTCAGTATGGGATCTCGTTCTCCGGCCAGTAGCTCTCAGCCCCCAGCCTTCTTCAGTAAACTGACTGAGAGCAACTCAGCCATTGTCAAGAGCAAGAAGGAAATGATCAAAAAGATCAGCGCAGAGGCTGAGTTCAG[T/C]AAGTCTATGGATTCCATTTATTGTTTCTGTTTTGCAGAGAAAACGCCTGGTATTGATATACACGATTGTCTTGCTGGGTAAACAGACTTAAACCTGTCTCTTCTATCTCCTCTTTAGACCAGAGCCAACCTGGGACAGAAATCTTCAACATGCCTGTCTCTACAAATGCAGGTGAGCAGTTCAGGACAGTCTATGTGTGTTTTGTTTTTCCTGCACAACAGTCTCAAGAAAGGTTTCTGTTCCATTAACACAAGCATTATGGCAATTCTTTCAGGACCCGTGAGTGTGCGCAGCCACCCGCCACCAGAAGCCAGCGGTAATACTATCGGTCTGGAGGCCATCATCAGGAAAGCCCTCATGGGCAAGTATGATGAACAGATGGACGAGCGCTCGCCGTCCAACTCTGTCAACTCGATGGCTGCCGGAGGGGCAGCTGCAGTCGTGCCACCAGCTTCAGCAGATGGGCGTTCAGAAGACCCCTACTCCCTGCCAGGTGTGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34466
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
ENSDART00000001092 Nonsense 1972 1999 35 35
ENSDART00000051139 Nonsense 2298 2325 44 44
ENSDART00000140618 Nonsense 1962 1989 35 35

The following transcripts of ENSDARG00000000966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 45422458)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43375240
GRCz11 8 43382027
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCGGGACCCTCACCTTCCCCAACACATCCTGGCGCTTCTGCACCCACA[C/T]AAGGCCAGACCCAACCCCGCACCTGGGAGGAAGAACCCAAACCTCTGCTG
Long Flanking Sequence:
TTCAAACAAAACTCAAGGACATGCACAGAACAACATGCACATTTATAGCAAATAAACGAATGTATTTGTAAATAAATGTATTATCCCGCTTGCTTTTTGAGCATTGTCGAGCGAGCTGTTAAACCCCTGTGATTGGTCATTGTCTTCCCGCACTCAACAGAAAGGGCTTATTCTCCAAGGCTGCAGACAGTGCACGTTACTAATGTTTACAGGTGTGCCCAGCTATGCTCTAACAAACTCTGTCCTGTTTTTAGTTTGTCTTGATTTTCTCTTAGAAACATTTATGCTCGTGGGGTGTAATAAATAAATAAATCAGGTCAGGTACTAACAGATAACATCTTGTATGTATTATAATGTTTGCTGATGTGCTCTTCTGGTTCCTCCTCTCAGGCCCCACTCCATTCCCCTGCAACCCCCTGACCATGGGGATGCGTCTCCCCAGCGGGATCATGCCGGGACCCTCACCTTCCCCAACACATCCTGGCGCTTCTGCACCCACA[C/T]AAGGCCAGACCCAACCCCGCACCTGGGAGGAAGAACCCAAACCTCTGCTGTGCTCTCAATACGAGACCCTGTCAGACAGCGAGTGAACACACACACACCGAGAACGTTTGCTGCTTTCTGAACAGAAACTTGTTACTGTAAACAGGGGTGTTTGTGAGCACACTCACTCATATCCATACTGACACACACACACATACTCACACTCTCTTACGGGAACATACGTCCATCCATGCTCATGCCCTCTGATACCTCCACACATATGCATACATGCACACATCCCATAATGCTCTCCAAGCGGGCACATTCACACTGTCAGTGAAAGTGCATTACATGGCTGCAGTGTTCGTAGATGTGTTTGTGAATGTGCACACTTGCATTAGTGTGTGCAGTCACTCCAGGACTACTTGTAGGAAGAATCACTTTTGAATTTTTATATGTATATATATATATAAATGCATATACATACAATTCTATATATACTTCTATTGGTGTCGTCTTGC
Associated Phenotype:
Not determined