si:dkey-7c22.2

Ensembl ID:

ENSDARG00000009549

ZFIN ID:

ZDB-GENE-090313-341

Description:

Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:Q98SN0]

Human Orthologue:

UBR4

Human Description:

ubiquitin protein ligase E3 component n-recognin 4 [Source:HGNC Symbol;Acc:30313]

Mouse Orthologue:

Ubr4

Mouse Description:

ubiquitin protein ligase E3 component n-recognin 4 Gene [Source:MGI Symbol;Acc:MGI:1916366]

Allele Name	Consequence	Status	Availability
sa1352	Essential Splice Site	Confirmed mutation in F2 line	Not yet available
sa24308	Essential Splice Site	Available for shipment	Available now
sa18557	Essential Splice Site	Available for shipment	Available now
sa24309	Essential Splice Site	Available for shipment	Available now
sa24310	Essential Splice Site	Available for shipment	Available now
sa24311	Nonsense	Available for shipment	Available now
sa17768	Splice Site, Nonsense	Available for shipment	Available now
sa10455	Nonsense	Available for shipment	Available now
sa10225	Nonsense	Available for shipment	Available now
sa43965	Nonsense	Mutation detected in F1 DNA	Not yet available
sa45795	Nonsense	Mutation detected in F1 DNA	Not yet available
sa18073	Nonsense	Available for shipment	Available now
sa18017	Nonsense	Available for shipment	Available now
sa3235	Nonsense	F2 line generated	Not yet available
sa6733	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37687	Nonsense	Mutation detected in F1 DNA	Not yet available
sa17134	Splice Site, Nonsense	Available for shipment	Available now
sa18331	Nonsense	Available for shipment	Available now
sa16066	Nonsense	Available for shipment	Available now
sa37688	Nonsense	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa1352

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Essential Splice Site	40	5152	1	105
ENSDART00000033970	Essential Splice Site	28	5129	1	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21573216)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21352523
GRCz11	23	21279074

KASP Assay ID:

554-1266.1 (used for ordering genotyping assays)

KASP Sequence:

CTTTCGAAACGAAAGAGCTACCTCAGCTTATAGGATCCATCATAAACAGG[T/G]CAGAYGAGGGCTTGTTTGTTTAGTTGGCCCGTGCGGGTCTGAAATAAACT

Long Flanking Sequence:

AAATAAAGTCTCCATGTTTATTGCAGAAAGTACACAAATTAGATATATAAAAATAATTAGCAATTTGGGAATTTGTAAGATATGCATTATGCAAGATCTTAAAATGTATCTCTTTTATTTTGTTGGAAATGCTGAATTTATCAGGTAATAACCATGCCCTCTTCCACTGAATGCAATCAGAAAAATTGGTCCAGAAAAATGTACATCTTGGGGAGGTGTATACAGAGTAATGTAACAATCGTCTGACATGTCTGTTGTCACATGACACAACACATACAAGACTTTTCATGTTTATCTCTGACGACAGTTCCTGTTTTTTGGCGTCTGATGATTAACCTCATTTCCGCTCTTGGATTCTAATAGAGGATCTCAAGATGGCGTCGAGTGGAGGAGATGGAGAACCTGAGTGGACCGCAGCCGTACGGCCACTTTTATCAGCGTCCTACACGGCTTTCGAAACGAAAGAGCTACCTCAGCTTATAGGATCCATCATAAACAGG[T/G]CAGACGAGGGCTTGTTTGTTTAGTTGGCCCGTGCGGGTCTGAAATAAACTGTTGAGTGACTCTGCATTAGCTGTGATGCTATGGCAGTACATAGGTTGTGTCTCAAAACCTAGTCAGCTGACTACCTTGACAGCATGTCGGAGTATCACGAAACGATTTAGGCCGTTCCAAATGCAACAGTAACGCCTTAAAAATGCTGTCTAAATAGATGTTCAATGACAAACAAATAAATTTGATCGCCTATTGTTTGGCATGATGCCTGGAAATGCTGTCTTCGTAGTCAGCTCGCTGGCTATTGAGTCACAGACCGAGTGTTACTGTGCCATTACAGTAGCAGATACATGAGATTCTGCTTCATCATCAGGCCGGAGATCCACACTTTTACGTTAACATTATCACCTGGACTGATATTTTAACAACGCCGCCTACTTCTAATGAACACTCATGATCTCACGACTTCAACCCCTAAATAAAGTGATATTATATTTGTGGCGGACGTG

Associated Phenotype:

Not determined

Allele Name:

sa24308

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Essential Splice Site	107	5152	3	105
ENSDART00000033970	Essential Splice Site	95	5129	3	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21578917)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21358224
GRCz11	23	21284775

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCATTGCTGCGTCTGGAGAATCCTGATGAAGCATGTGCAGTCTCTCAGG[T/G]CAGACTTTCACCTTTTAAGCAGAAAACAGTTTGATTGTTTGATTAAGCAT

Long Flanking Sequence:

CTAATATTGAGAGCATTGTTTTAGCAGTCATGCAGTTTACAAATGGAGCAATATAGTAAAATGTTACATTTGTTTCCTTTTTTGAGTCAAATTACAGAAATGAAATCTCAAACTCCATTTTTCAACTGTTTTCCTCCTTTTATTTTTACAGTGAATCTGAGATTCTTCACCATGACAAACAGTATGAGCCATTCTACTCCTCTTTTGTGGCACTATCTGCACATTACATCACCACAGTTTGTGGACAAAGTATGTCAAATTTCAGTTTTTTTTTTTTAAACTATAATTTTCTTAATTTGTTGGTCTGTCATGTCATGTATTTCTAGCTTAACACAGATTGAACATGCTCTTCAAAATGTCCCTATTTCAAATAACAAATGTTCTGTTTTAATTAGTCCCCAGAAATCAGTTGCTGTCAGTAGCTGCAGCCTGTAAAGTATTGATTGAATTCTCATTGCTGCGTCTGGAGAATCCTGATGAAGCATGTGCAGTCTCTCAGG[T/G]CAGACTTTCACCTTTTAAGCAGAAAACAGTTTGATTGTTTGATTAAGCATTGCATTTTCTTATAGACTGGCTTGCTTTGTGTTTCCCCTACACAGAAGCACCTGATCCTCTTAATAAAGGGCCTTTGCACTGGCTGCAGTCGATTGGATCGGACAGAAATCATCACCTTTACTGCGATGATGAAGTCGGCTAAACTTCCCCAAACTGTCAAGACCCTTTCTGATGGTAAGAGCTGCTTTAGATCATCTTTCTTGGCTTAATGGCTTGTATGTAAGATGTAATCTCTGTGATTTTAGATATTATAGACATGGTATTTCAGCATGTGAATATGCTGCAGCAGCGTTTTGGTTTGTTTTAATGTTGAGTCTGTTGTCCGGAATGTCAACACAGCTGTTCAGATGTAAACACAGCTTGAGACGATGTTCCGTTTTGTTGGATTTTCATGTTTGCTTTGCCGTTTTGACTTTTACTTTGGCCCAATCCCAATTCTTTTTTTGTAC

Associated Phenotype:

Not determined

Allele Name:

sa18557

Status:

Available for shipment
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Availability:

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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Essential Splice Site	321	5152	8	105
ENSDART00000033970	Essential Splice Site	309	5129	8	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21585693)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21365000
GRCz11	23	21291551

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGGAGACTACTTGATGTGACTGTGTTAGCACTAAGCTGCCTCTAYGCAGG[T/C]GGGTTCATTTGGGAAAAAAATCTGTTCTTGTTGAYYTCAGAGGAAAACAG

Long Flanking Sequence:

TAAGTACAATATGTATATTGGTTTAAAAATTTACAATTTTGTATATTTACAATAGGAAATGTAGAGCATTTCAAAATTTTCTGTTATTAAGTCCTTATATCGATCCTGTTATTGAAACATTTTTTTGTTATTCCACTCATTCCAGGGGGCTCTGAAAAGTTGCTGCGTGTGTGCCTCAACCTCCCCTACTTCTTACGGTATATCAACCGCTTCCAGGACGCGGTATCCGCCAACTCTTTCTTCATCATGCCGGCCACTGTGGCAGACGCCACCGCAGTCCGAAATGGGTAAACCACAAAGACCCTCGGCTCACTTCTGTTTATTGAATCTAGTGAATGTGAGATGAGTGTGATGACTCTGCCCTCCGGTTTCAGTTTTCACTCCCTGGTGATTGATGTGACCATGGCCTTGGACACTCTTTCCTTGCCTGTACTGGAGCCTTTGACCCCTGGGAGACTACTTGATGTGACTGTGTTAGCACTAAGCTGCCTCTATGCAGG[T/C]GGGTTCATTTGGGAAAAAAATCTGTTCTTGTTGACTTCAGAGGAAAACAGAGAACTTGATTTACGCGTGTGTTTTCTTTTCCTCAGGTGTGAGTGTGGCAACTTGCATGGCTATATTGCAGGTGGGGAGCGGATTACAGCTTCGGTCAGCCTCCACCGGCTCCAAGGAGGAAGACTATGAAAATGACGCTGCTACCATTGTGCAGAAATGTGTAGGTGTCAGATTCAAGCACTTATTTTATAATGTTACAACATGTGCCGTGAGTAACATTCTGTTATAAATATGATATGGATTTCAAACTTTTTAAACTTTAGCTAGAGTGTGATGTTGCTGTTTGAGCATAAACATCTGCGCTTAAATGTTGCTGTTTGAGCATAAACATCTGCGCTTAAAGTTCAATGGAAAGAGAAATGTTTTCTTTTATATTATTAGCTTTTTATGGCATACAACAAATGGCTGGTAGGAACTACAACAAAGTTTTTCCTGGTTTGAGACATCAC

Associated Phenotype:

Not determined

Allele Name:

sa24309

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Essential Splice Site	382	5152	10	105
ENSDART00000033970	Essential Splice Site	370	5129	10	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21587892)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21367199
GRCz11	23	21293750

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAGATGATTGGACAGGCCATCAGTAACTCTCGCAGAGCTGGAGGAGAG[G/A]TAGAAATATTATTTTACAGAGTATATACATATAACATGAAAGGAAAGTGG

Long Flanking Sequence:

TTGGTCAAGATTTGATGAAAAACATAAGAATAAGGTTACATGAAGAAAACGTTGATCCATTTAGGAGGAAGTGGCAAACTACAAGCTTTGAAAGTTTATATGGTTTTATATATTTTGGAGCACAATAGCTTATAGACATCCTTAAAACTAACATACTGATTCTAACTTCCAAAAAACTAATTTCACGGGACCTGTAAATCCACTGGCGTAGATATAAACAAATTTTCTTATCAATTATTATTACAGATATGGTGGGAGGAAATATTGTCAAAAGCACAAATGACCATCATCATTGTAACATTTGCTAAAATTTCCTTCAAATGTGGCAAAACATTGCATGTGAATTAATCGGTGAAATCAGACACAAATTGCCCAGCCCTATATTATGTGTTATTGTCTATGATACAGAGCTGATCTCTGTTTTTTGACTTTTTCAACAGCTGGAAATCTATGAGATGATTGGACAGGCCATCAGTAACTCTCGCAGAGCTGGAGGAGAG[G/A]TAGAAATATTATTTTACAGAGTATATACATATAACATGAAAGGAAAGTGGCCCACATCTAAGATCCTGGTTTGTGTTTCGACAGCATTATCAGAACTTTCAGCTCTTGGGCGCCTGGTGCCTGTTGAACAGCCTGTATTTGATACTAAACCTGAGCCCCACAGCCCTGGCTGATAAAGGAAAGGAGAAAGATCCCTTGGCAGCTCTGCGGGTCCGAGACATTGCCACCCGAACCAAGGACGGAGCAGGATCTCCTAAACTTGGCCCAGGGAAAGGGTAAGTGCCTTTTTCTGTTCTGCGAGTATAGCGATTTGTCTTTTAAAATATATTTTTTGGGTGAAATATAAATATGTTCTGAAACTCCTGGGTCATTTTGGTATCAAATTAGTCATATACAGTGAAAGCATATTAAATGCAAGTAAAGTTTCTTTTTTTAATGATTAAATTAACATCTATTGCAATGATCTATTATCATCATTCAGTATAAATTTATATTAAATG

Associated Phenotype:

Not determined

Allele Name:

sa24310

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Essential Splice Site	709	5152	None	105
ENSDART00000033970	Essential Splice Site	696	5129	None	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21597619)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21376926
GRCz11	23	21303477

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTTAATCACTCTCTGGTTACATCAGACCTGCCCTCTCCATCCCTGCAGG[T/A]AAAGTTGAGATATTCTTTAAAACGTATTCAAAATTTGTGACAGACATATT

Long Flanking Sequence:

AGATGTAAAAGAGCGGGGTCACATGACTCCACAGATGTTAGGGAAGGTAATTGAAAAAAAATCAATGGATTATATTTTCAGAATGTCGATTTCGATTTCTTTACGATTAATTTATTAATAATTAAATGGTATTTACATTGATGACTCGAATGCATGTTTCTTGTTTCAGTTTTTGAGTTTGGCCTCAAGCATATTGAACTTCATTACCACTTCCATGCTAAAGTCCAGAAATAACTTCATTCGCAACTACCTGAGCGTGTCACTCACAGAGCAGCACATGGCAACCCTCGCCAGTATCATCAAAGATGTCGACAAGGATGTCAAAGGTTTTCCGTCATTTTGATCTAAATCTTAAACTTAGGCTTACATTTAGGCTTTTACCAACGTTTCTTTACCCCTCCCCCCACCCCCAGGTTCCTCTGATGACGAATTTGCCTCAGCCCTCTATCACTTTAATCACTCTCTGGTTACATCAGACCTGCCCTCTCCATCCCTGCAGG[T/A]AAAGTTGAGATATTCTTTAAAACGTATTCAAAATTTGTGACAGACATATTGTGTCTGATGACTTGTTTTCTCCAACGTTTCTTTAGAACACTCTTCTGCAGCAGTTAGGTGTTGCCCCGTTCTCAGAGGGTCCTTGGCCCATGTACATCCACCCTCAGTCTCTCTCAGTGCTCTCCAGGTTGCTGCTGATTTGGCAACATAAAGCCAGTCAGCAGGGGGAGCCTGATGTACCCGAGTGCATGAAGGTCTGGGAGAGGTGAGACATTACTCAACCTTAAAGAGTGACTTCTTTTTGCTAAAATGCTGCTTTGTTTACTAGTTTGAGTTGTATTTGAAATGTGTTAACCAGCCAGAGCAAAATTTTTATGATCAAAGTTCATTAAAGAGTTCGTTCACCAAAAAAATCCTTATTTATTCACACTCAAGTTGTTCATGAATTTTCTTCTTCTGTTGATCAAAACAAAAACAGGCTATTCTGAAGATTGACGGGGAAAAAAGTT

Associated Phenotype:

Not determined

Allele Name:

sa24311

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
ENSDART00000024846	Nonsense	745	5152	18	105
ENSDART00000033970	Nonsense	732	5129	18	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21597812)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21377119
GRCz11	23	21303670

KASP Assay ID:

2261-7624.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTACATCCACCCTCAGTCTCTCTCAGTGCTCTCCAGGTTGCTGCTGATTT[G/A]GCAACATAAAGCCAGTCAGCAGGGGGAGCCTGATGTACCCGAGTGCATGA

Long Flanking Sequence:

TTGAACTTCATTACCACTTCCATGCTAAAGTCCAGAAATAACTTCATTCGCAACTACCTGAGCGTGTCACTCACAGAGCAGCACATGGCAACCCTCGCCAGTATCATCAAAGATGTCGACAAGGATGTCAAAGGTTTTCCGTCATTTTGATCTAAATCTTAAACTTAGGCTTACATTTAGGCTTTTACCAACGTTTCTTTACCCCTCCCCCCACCCCCAGGTTCCTCTGATGACGAATTTGCCTCAGCCCTCTATCACTTTAATCACTCTCTGGTTACATCAGACCTGCCCTCTCCATCCCTGCAGGTAAAGTTGAGATATTCTTTAAAACGTATTCAAAATTTGTGACAGACATATTGTGTCTGATGACTTGTTTTCTCCAACGTTTCTTTAGAACACTCTTCTGCAGCAGTTAGGTGTTGCCCCGTTCTCAGAGGGTCCTTGGCCCATGTACATCCACCCTCAGTCTCTCTCAGTGCTCTCCAGGTTGCTGCTGATTT[G/A]GCAACATAAAGCCAGTCAGCAGGGGGAGCCTGATGTACCCGAGTGCATGAAGGTCTGGGAGAGGTGAGACATTACTCAACCTTAAAGAGTGACTTCTTTTTGCTAAAATGCTGCTTTGTTTACTAGTTTGAGTTGTATTTGAAATGTGTTAACCAGCCAGAGCAAAATTTTTATGATCAAAGTTCATTAAAGAGTTCGTTCACCAAAAAAATCCTTATTTATTCACACTCAAGTTGTTCATGAATTTTCTTCTTCTGTTGATCAAAACAAAAACAGGCTATTCTGAAGATTGACGGGGAAAAAAGTTGACATTAGGGGTGCAATGGTTCAATATACTCACGGTTCGGTATGCAACACTGTTTTAGGGTCACGGTTTCGATACTGTACAGTTTGTGATATGCTTTGGAAAAAAAATGCCTACAGAACATTTAAAGAACAATAAACATATTTATTGATTAACAAACACCTGACAATGCCGGAGCTTCACATATATGACTAGA

Associated Phenotype:

Not determined

Allele Name:

sa17768

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Splice Site, Nonsense	859	5152	19	105
ENSDART00000033970	Splice Site, Nonsense	846	5129	19	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21600317)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21379624
GRCz11	23	21306175

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGACTACCTGCTRCACCAGTACTCAAAAGCTCCCGTCTACTTGTTTGAG[C/T]AGGTACGAATGCTAATGTKGCTGTATKTTAACTGRAATCAAGCCACTGTA

Long Flanking Sequence:

AATTCTGGACCCTTTGTCAGTCTTGCGAATAATAAATGTCTGGAAGTCAGCCGCTAGGATTTCCCAGTATATCTTCCTCTGTATTCAATAGAAGAAAGAATGTTAGGGTTAACCTAACCTAAAAGACTGAAACTCAAACATGTTTGAAACGAGTAACCCCAACCCTACCCTGAGATGTCTTTAATTGCAAGTCAAATTCACAACCTAAATCTGCTTTCCATAGGTTTGTGGGCACTCTGAAACAGCATACCCTACAGGGAGCCGTGCCTGCGGATGAGGATCTCAATGTTGAGCACCTCCAGCTGCTTCTGCTCATCTTCCACAACTTCTCAGAAAAGGGCCGCCGCACAGTTCTGACCCTCTGCATGCAGGCAATAGCTGAAATCGCATCCAATGCCGACTCCCAACTTCAGGCGGTGCCCCTCAACCTAGCCCGCATCTTACTTGTGTTTGACTACCTGCTGCACCAGTACTCAAAAGCTCCCGTCTACTTGTTTGAG[C/T]AGGTACGAATGCTAATGTGGCTGTATGTTAACTGAAATCAAGCCACTGTATTGTGACATGCTGTTTGTAATGATTTTGTTCACACACTCAGGTCCAATACAATCTTCTGACACCCCTGGCATCCAGCGCTAGTGCCGGACAGGATGGGGGAAAGAGAGGTGCCGTTCCTCTTTATTATGGTTTTAAAGAGGTGGAGGAGAACTGGGCCAAGCACTGCTCGGCAGGTAGGAGTAAGTCAGACCTTTTCTATTTTGTCTATATTTTACCCTAAAATTAAGAATAAATATTACCTCCTACCTTTAAAGTTTGTTTCTTTACAAAAGCAGACAAAGTGTTCTGGTTGCTGGCACCCATTGACTTATATAGTATGAAAAAAATGATGATGTGGAAGTCAATGGGTGCTAGTGATAATCATTTTTCAAAATGTCTTTTGAAAAATGAGAAGAAAGAAGCCGAAGAAAGAAAATGAGAACTGAAGAAAGAAACTCAAATAAACTTTG

Associated Phenotype:

Not determined

Allele Name:

sa10455

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Nonsense	1175	5152	26	105
ENSDART00000033970	Nonsense	1162	5129	26	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21607822)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21387129
GRCz11	23	21313680

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGCCAGAGGAAGGAGAAAACAAGCCCACTGAAGCTAAACTGCAGGGCTA[T/A]GCTGCCGTGTTGTCCATTGGATCTACGCGCTGCAAAGCCAACTTGCTTGG

Long Flanking Sequence:

CTTTAGATGAGCATTTCTCCAAAATAGCTGCGGACACAGATCCCAATAAATCCTCTGAGATCACCAAAAACCTGCTGCCCGCCACGCTGCAGCTCATCGACGTCTACACAGCCTTTACTAGGTATTGATTCCACCACATTTACTGAGGATTGTTGCACATATTAAGGGATCATTCCCATGATAATGAGAATTCTGCCATCTTTTAATCACCATCATGGTATTTAGTGGAATTATTTTATTATTTATTGGAACAGTAACATACAATTTGTTCCACACTTCCCACACTTCTTTGTTGCATAATGTTCTCTGATGTTTTTTTTATGATTGGAAGATGTAGAAGCATTCTGCCTTGATATCTTTGTGTGAAATTTAGGTTGTCAAAAACTCCAAAGAAACTTTCTGACTGGTTTGCTGTTTGTTTGTTTGCTCAGGTCATACCTGCTGATGAGCCTGCCAGAGGAAGGAGAAAACAAGCCCACTGAAGCTAAACTGCAGGGCTA[T/A]GCTGCCGTGTTGTCCATTGGATCTACGCGCTGCAAAGCCAACTTGCTTGGTAAGAATTTTGAATGACATTTAATAGACATGGTAACTTGCCTAAAGTGATCAGTGCAAAGTACAATTCATGTGTGGTGTTTTTACTTTTTCAGGTCAGACCGTGATGCAGAATCTGCCCTCCGCCGTGCAGACACTGTGTGAAACATGGAACAACATTCACACTAATGAATTCCCAAACATCGGTTCATGGGTAAGCAATGCATTTCCTTCAGCTCTTAGAGTAAGCATGCTGTCTGTGCCTCACTGTATACTGAATGCTTCTTTATCCACAGCGAAACGCCTTTGCCAATGACACCATCCCATCAGAAAGCTACATCAGCGCGATTCAGGCTGCACACTTGGGCACCCTCAGTAACCAATCGCTGCCCTTGGCCTCTTCTCTCAAGCACATTCTGCTCTCATTGGTTCGCCTCACGGGGGACCTCATTGTGTAAGTATTGAGTGCAGTG

Associated Phenotype:

Not determined

Allele Name:

sa10225

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Nonsense	1547	5152	33	105
ENSDART00000033970	Nonsense	1534	5129	33	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21611572)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21390879
GRCz11	23	21317430

KASP Assay ID:

2261-7628.1 (used for ordering genotyping assays)

KASP Sequence:

CTTAAAACTAAATCCAACTTTTTCCTATTTATCTTTCAGTAAAAAATACT[T/A]GTATCAGAAGAACGTTGTGGAGAAAGTAACAGCCAACGTGTCACAAGGCA

Long Flanking Sequence:

GTTCTCTCTCTCTCTGTATATTACTTACATTATACTTTTGTATATGGATTGATATATATTGTTATGCCTGTAGGCAATTATGTTAATAATAGTGTAATTCTATAAATTAATTGTGTATAATGAATTTTAATGTAATGATGTTAGTACTACCCAGAAGAATATTGTAACAAATAATAAATGTTTTTAATATAATGTGTTTTTAAATAGTTGTACGACAACTTGGCTTAAAGTTTGGCTTTTGCATTAGAAGGTATGCATTAGAAATAGAAAAAAATAATGATATTAATATTAAAGTAATATTATAAATGTTACAAATTTAACGAAAAAATTATACAATATTTTTAGCATTTAGCAGTGGGTTGTTGGGCAAATTTTTGAAGTGTGAAACTACTACATATACTGTAGATTGAACCTAAAAAGCTCTACTCTTATGTGCATTTGTTACCCACACTTAAAACTAAATCCAACTTTTTCCTATTTATCTTTCAGTAAAAAATACT[T/A]GTATCAGAAGAACGTTGTGGAGAAAGTAACAGCCAACGTGTCACAAGGCAAGGTAGGCACCAGATATGTTTAGTTTTTTTATACAACCATTTACATCCCTTCTATTTTTATCAGAGCATAATTAAATTTTATTCGCAGCATGCTAGTATGCTGGAGTGTGCCTGTCACATCATCTCCTACCTGGCGGATGTGATGAACGCATTAAGGCAAAGCAGTGGCCAGGGCTCGTCCCAGCTCCTGATGGATGGAGAGGAGAAGGCCATCGAAGTGGACTCTGACTGGGTCGAGGAGCTGGCTGTTGAAGAAGATGACTCGCAGGCCGAAGACTCGGTCAGAAAAAACCCTGCTCACTTCAGTTTCAGAGATTACTTTTATTTGCTAATCTATTTAGCCTTTGGATAGTCAAATAATCCCGGACGAGCCCCCAAAAATCATACAAAACCATTTTTGCCACACAAAAGTTAAATCAAAAACTGAGTGAAGGGAAAAAAAATCAGATA

Associated Phenotype:

Not determined

Allele Name:

sa43965

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
ENSDART00000024846	Nonsense	1842	5152	39	105
ENSDART00000033970	Nonsense	1829	5129	39	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21620027)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21399334
GRCz11	23	21325885

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCAAAATTGCTTAATGTGTTTTTATCCTCCAGGTTCCAACACTGGGCTCA[C/T]AAGAGGGTGCTTTTGAAAATGTCAGGATGAACTACAGTGGAGATCAAGGA

Long Flanking Sequence:

TTTGAGGTTGCGGAAACATATTGAAATAATGCCACAGCGAATGCATGCCATAAACAAAGCTAAAGGCAGTCCAACAAAACATTAGAATGTGTGACTTTTTGGAAAGGGCAGTGTATTTACAAATGCATCTTGCTACTTTATATATTCATCACTCTACAGCACAGGTGTTAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATTAACTAATTGAGTCCTTCAGGCTTATTTGAAACCTACAGGTAAGTGTGTTGGAGCAGGGTTGGAACTAAAGTGTGCAGGGCTTCGGCCCTCCAGGGATTGAGGTTGACACCCCTGCTCTACAGTAATCATTCCTCAGGTCTTTTAAACACTCTTTTTAACCGCAACAAAAAAACAACAATGTGATCTCTTTAAGTAAATTAGGACATTATTGGTTCAAAATTGCTTAATGTGTTTTTATCCTCCAGGTTCCAACACTGGGCTCA[C/T]AAGAGGGTGCTTTTGAAAATGTCAGGATGAACTACAGTGGAGATCAAGGACAGACCATCCGGCAGCTCATCAGCGCTCATGTGTTGCGTCGAGTGGCCATGTGTGTTCTGTCCTCTCCTCACGGACGTAGACAACACCTCGCCGTCAGCCATGAGAAGGGCAAGGTGGTCATAAAACCTCAACGCCGGTTTGTGTCTATGCTGCTTGTGTTTAATTGTAACTTCATACCATTTGTCTGTATTTGATTTGCAGATCACAGTCCTGCAGTTGTCTGCTCTGTTGAAACAAGCTGACTCCAGTAAGAGGAAGCTGACTTTGACTCGACTGGCCTCTGCCCCGGTTCCCTTCACTGTGCTCAGTCTCACAGGAAACCCCTGTAATGAAGATTATCTGGCTGTGTGTGGACTGAAGGTAACCATGTAGACAGAACTGTTGAAGAATTAATTGACAAGATTGTTGCCACTGATTGTTTTGTGTCTGATTTCTCTGTAATTCTCATC

Associated Phenotype:

Not determined

Allele Name:

sa45795

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
ENSDART00000024846	Nonsense	2202	5152	45	105
ENSDART00000033970	Nonsense	2189	5129	45	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21624950)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21404257
GRCz11	23	21330808

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCAGATTCAGGACATGGTTGCGATCCGTCACACAGCTAGCAACGAGCAG[C/T]AGCGCACAACCATGATTCTGCTGTGTGAGGATGGCAGCCTTCGTATTTAC

Long Flanking Sequence:

TTTTTTACAAAAAAATCTTTTTTTTTTTTTTTTTACAGCGCATTAACAATGAAAGAAGTACCAAAAAAAAACATTTAAAAAAACCCTTACATATGCTTTAGGCACGGTATAACAGAAAATTCTAGCAGTTTTAAAAAGTTGACATTTCCAAACTGCAGGAAACCTTGAAACCGGTTATCGTCCCTTGCTTAGCATCAACATATTTAAAGAAATGTCATAAGTTATAAATTTAGATAGAAAAGACATTTATTTTGGCTGCTATTGTATTTTAAGATATATATTTTTTAAATGTCAAAATTGCTGTTTTGTTTATTTGTGTATTTATCCTGAGTTCATATTTAAATCATTTTGGTAATTAATGAATGTCGAGGTTATTAGGCAAAGTTTGTTTTAGTTGTGAAATATTGTTATTTACGTGAAGCAAAGACAAATAAACAAATCTCTCCTCTTTTCAGATTCAGGACATGGTTGCGATCCGTCACACAGCTAGCAACGAGCAG[C/T]AGCGCACAACCATGATTCTGCTGTGTGAGGATGGCAGCCTTCGTATTTACATGGCTAATGTGGAGAACACGTCCTATTGGCTTCAGCCCTCACTTCAGCCCAGCAGCGTAATCAGTATCATGAAACCTGTTCGCAAACGCAAGACCGCTACGGCCAGTGAGTCACGCCACACATTCACTCTGACTCATCACGTGCTGTTTACTCACATTTATGTGTCATTTTTGTGTTCCCTCATCAGCCACCCGCACATCCAGCCAAGTCACTTTCCCTGTGGACTTTTTCGAGCACAACCAGCAGCTGACAGAGGTGGAGTTTGGAGGCAATGACCTTCTGCAGGTCTACAATGGCCAACAAATCAAACATCGGCTGAACTCTACAGGGATGTATGTGGCCAACACCAAGGTAACAAACGTGATCCTACATACTGATTTTTTTTTTTTTATTGCTGATTCCAATTGCTGATTTTGTGTCACTTTTAATATGAATTCTCAGCAGTCTAT

Associated Phenotype:

Not determined

Allele Name:

sa18073

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
ENSDART00000024846	Nonsense	2288	5152	46	105
ENSDART00000033970	Nonsense	2275	5129	46	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21625292)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21404599
GRCz11	23	21331150

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGCAGCTGACAGAGGTGGAGTTTGGAGGCAATGACCTTCTGCAGGTCTA[C/A]AATGGCCAAYAAATCAAACATMGSCTGAACTCTACAGGGATGTATGTGGC

Long Flanking Sequence:

ATCATTTTGGTAATTAATGAATGTCGAGGTTATTAGGCAAAGTTTGTTTTAGTTGTGAAATATTGTTATTTACGTGAAGCAAAGACAAATAAACAAATCTCTCCTCTTTTCAGATTCAGGACATGGTTGCGATCCGTCACACAGCTAGCAACGAGCAGCAGCGCACAACCATGATTCTGCTGTGTGAGGATGGCAGCCTTCGTATTTACATGGCTAATGTGGAGAACACGTCCTATTGGCTTCAGCCCTCACTTCAGCCCAGCAGCGTAATCAGTATCATGAAACCTGTTCGCAAACGCAAGACCGCTACGGCCAGTGAGTCACGCCACACATTCACTCTGACTCATCACGTGCTGTTTACTCACATTTATGTGTCATTTTTGTGTTCCCTCATCAGCCACCCGCACATCCAGCCAAGTCACTTTCCCTGTGGACTTTTTCGAGCACAACCAGCAGCTGACAGAGGTGGAGTTTGGAGGCAATGACCTTCTGCAGGTCTA[C/A]AATGGCCAACAAATCAAACATCGGCTGAACTCTACAGGGATGTATGTGGCCAACACCAAGGTAACAAACGTGATCCTACATACTGATTTTTTTTTTTTTATTGCTGATTCCAATTGCTGATTTTGTGTCACTTTTAATATGAATTCTCAGCAGTCTATTTGTGTATTGCCTTGTTACAAAAATATGTAAATTTTTACAATATACACATTAAACAAAAGATACATTTAATTTGACCTAATGCTGAAAAACAAAGCACCCAATACATCTTAGCATATATAAGTTCTTCTTAGATACCATTTTCTTATAAATAATACCACCCTCCCTAAATTGATCAGTGCATCAATAATTCTAAATGCACAAACGATCATCAGTTTGTGCATTTAAGCTACTTTTTCCACTATATTTATTTATTTATTTAATCCATTATTTTGTTTTCAGCCTGGAGGATTCACTGTTGAAGTGGTGAACAATAATAATTCAATGGTAATGACTGGAATGAG

Associated Phenotype:

Not determined

Allele Name:

sa18017

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
ENSDART00000024846	Nonsense	2292	5152	46	105
ENSDART00000033970	Nonsense	2279	5129	46	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21625302)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21404609
GRCz11	23	21331160

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGAGGTGGAGTTTGGAGGCAATGACCTTCTGCAGGTCTAMAATGGCCAA[C/T]AAATCAAACATMGSCTGAACTCTACAGGGATGTATGTGGCCAACACCAAG

Long Flanking Sequence:

TAATTAATGAATGTCGAGGTTATTAGGCAAAGTTTGTTTTAGTTGTGAAATATTGTTATTTACGTGAAGCAAAGACAAATAAACAAATCTCTCCTCTTTTCAGATTCAGGACATGGTTGCGATCCGTCACACAGCTAGCAACGAGCAGCAGCGCACAACCATGATTCTGCTGTGTGAGGATGGCAGCCTTCGTATTTACATGGCTAATGTGGAGAACACGTCCTATTGGCTTCAGCCCTCACTTCAGCCCAGCAGCGTAATCAGTATCATGAAACCTGTTCGCAAACGCAAGACCGCTACGGCCAGTGAGTCACGCCACACATTCACTCTGACTCATCACGTGCTGTTTACTCACATTTATGTGTCATTTTTGTGTTCCCTCATCAGCCACCCGCACATCCAGCCAAGTCACTTTCCCTGTGGACTTTTTCGAGCACAACCAGCAGCTGACAGAGGTGGAGTTTGGAGGCAATGACCTTCTGCAGGTCTACAATGGCCAA[C/T]AAATCAAACATCGGCTGAACTCTACAGGGATGTATGTGGCCAACACCAAGGTAACAAACGTGATCCTACATACTGATTTTTTTTTTTTTATTGCTGATTCCAATTGCTGATTTTGTGTCACTTTTAATATGAATTCTCAGCAGTCTATTTGTGTATTGCCTTGTTACAAAAATATGTAAATTTTTACAATATACACATTAAACAAAAGATACATTTAATTTGACCTAATGCTGAAAAACAAAGCACCCAATACATCTTAGCATATATAAGTTCTTCTTAGATACCATTTTCTTATAAATAATACCACCCTCCCTAAATTGATCAGTGCATCAATAATTCTAAATGCACAAACGATCATCAGTTTGTGCATTTAAGCTACTTTTTCCACTATATTTATTTATTTATTTAATCCATTATTTTGTTTTCAGCCTGGAGGATTCACTGTTGAAGTGGTGAACAATAATAATTCAATGGTAATGACTGGAATGAGGGTGCAGGTG

Associated Phenotype:

Not determined

Allele Name:

sa3235

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Nonsense	2685	5152	54	105
ENSDART00000033970	Nonsense	2672	5129	54	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21635456)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21414763
GRCz11	23	21341314

KASP Assay ID:

554-3216.1 (used for ordering genotyping assays)

KASP Sequence:

TTGCTTGCAAACAGGCTCTGATTAGAGTACTTAGACCCAGGAATAAGCGC[A/T]GACATGTGACCTTACCATCGCCGCCTCGCTCCAACACACCCATGGGTATG

Long Flanking Sequence:

CAACAGAGATAGAGAGCTCACACAATTTTCTAAATGTTGCTAGAATTGTTTTTTATGTATGGGCAATATATATTGCATCACCAAAAGTAATTTAGGTCATGTCCATGACCTGTGCGATAAGTCAATATATTGATTATGGTGACAGGCCTAGTTGAAACACTGATTTTAGTCATCTTTGGAGCTTATCTGCTTTTTTTTTTTTTTTTTTTTTTGTTATTTTTGTCGGTCTCCTAGGTCTAACTCACATTGAAGCCACAGTAAACGCACTGGTTGATATAATTCATGGCTACTGCACCTGTGAGCTGGATTACATCAACGTGGCCTCCAAAATCTACATGCAAATGCTGCTCTGCCCTGTATGTATTTTTTTATTAAATAGAAGCACATCCTTTGAGTTTATCGTCATTTTAATCTAACTTCTTTCTGATCTACAGGACACCTCTGTGAGCTTTGCTTGCAAACAGGCTCTGATTAGAGTACTTAGACCCAGGAATAAGCGC[A/T]GACATGTGACCTTACCATCGCCGCCTCGCTCCAACACACCCATGGGTATGAGATTCTCATTTCAGCATTGGGACCTAAATTGTGTTTACACCTCCTAATGGTTTAAACCTAAAAATGCCTACTGGGCTTTGTATCTCAGGAGATAAAGATGACGACGACGATGATGATGCCGATGACAAAATGCAGCCGTCCAACATGACTGGAGGAGAAGGTGGCAGACAGGAGAGTCAAGAGCAAAATGAGGTGGACCATGGGGACTTTGAGATGGTGGTGAGTTTCGCAGCCACTACGAGTCCAACTGTTGGACACCTGGATTTGAAAACTCCAATGTGTATATGCTGTAATGTCAATGAAGAAATGTGTATTATTATTGATTATTATTTTATTATTATTTTTATCAAAGTTGTTAAGTAAACTTCTTTATTTACTATTAAATTATGTAAATTATTTATTTGTTTACTATTAAACTATTACTGTTTATTTTTTTACTATTAGTTTTA

Associated Phenotype:

Not determined

Allele Name:

sa6733

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
ENSDART00000024846	Nonsense	3249	5152	65	105
ENSDART00000033970	Nonsense	3223	5129	64	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21644508)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21423815
GRCz11	23	21350366

KASP Assay ID:

554-4538.1 (used for ordering genotyping assays)

KASP Sequence:

TTCCTGAGGGGCGGAATCGTGACTGCCACATCTGGCTCTGCTCTGCAGTA[C/A]GACACTCTGATTAGTCTGGTGAGTAGCGCTCTCAGCAGTCTTCTGTGACR

Long Flanking Sequence:

ATGTTTTTGAGAATCAAATATCATAGCCTAATAAATGCTGGTGTGTTTCTTAGGGTCATGCTGCTGATGTGTTCGAGGCGTACTCTCAGCTCCTCACCGAGATGGTTCTCAGACTGCCGTACCAGATCAAGAAAATTGCAGATGCCAACCCTCGCATCCCGCCACCAATCTTTGATCACTCCTGGTTCTATTTCCTGTCAGAGGTAATGCAGTCTATTTACTTTTGCCCTCAGCTGAGGAGTTTTCAATAAATAATTTAGCAGGAATCAACCTTCTTCGATCATCTTCCAGTATCTGATGATCCAGCAGACGCCGTTTGTGAGGCGACAAGTGAGGAAGCTCCTGCTGTTCATCTGCGGCTCCAAAGAGAAGTACCGCCAGCTCCGAGACCTCCACACACTTGACTCGCATGTGCGCGGCATCAAGAAGCTTCTGGAGGAGCAGGGCATCTTCCTGAGGGGCGGAATCGTGACTGCCACATCTGGCTCTGCTCTGCAGTA[C/A]GACACTCTGATTAGTCTGGTGAGTAGCGCTCTCAGCAGTCTTCTGTGACATTCTATGACTTCGACTAATTTTCCACTTTGGATTTGTGCTTACCTTTTGGTTGTTTTCTTGTTTTTTTTTTCATTTTACACAGATGGAGCATCTTAAAGCATGTGCTGAAATAGCCACTCAGAGGACCATCAACTGGCAGAAGTTCTGCATGAAGGATGACTGTGAGTGAACATATTTTCTGACCTTTACATTATGTCAGACACCAGATAGACATGTAGATATGTCTACATCAGATAAAACCACCCTGACAGCAAAACCAATCTATCTGACAGCAAACCAATCCCAGTCTATTCCTCGCTTAAGCAAAGTGCTACTTCTCACTTCTCACACAAAGAACAATTTGATTTGGAAGTTTCCTTTGTTAATAACTTGTATTTTTACTGATCTCATACAATTATATACATTTACATTTAGCAGGCTTTTATCCAAAATGACATGCATTATATTTA

Associated Phenotype:

Not determined

Allele Name:

sa37687

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
ENSDART00000024846	Nonsense	3402	5152	68	105
ENSDART00000033970	Nonsense	3376	5129	67	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21646782)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21426089
GRCz11	23	21352640

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTTTCTGCTGGAGTCCAATTCCTCATCTGTGCGCTGGCAAGCTCACTG[C/A]CTCACACTGCATATCTACAGGTACGTAAAATCAATTTTCTACCTTTGAGC

Long Flanking Sequence:

CATATTTTCTTTTTGTGTAGCTGTGTTGTACTTCCTGCTGCAAGTGAGTTTCCTGGTGGATGAGGGTGTTTCTCCAGTCCTGCTGCAGCTGCTTTCTTGCGCCTTATGTGGCAGTAAAGTCATGGCAGCCTCTTCTGGATCTTCTGGTGGAGGTTCAGGAACATCCCAGCCCTCTCAGAGCAAATCCTCAAGCAAAAAGAGCAAGAAAGAGGACAAGGAAAAGGATAAAGAAGGTCTGATGTTTTTTCAACTACTTTTGGCTTTTTTTGATCATTGATACCACATTCACTCACTGTAGTGTTCAGTATAAGGTTTTTTTTTTTCAGTTCTATTTCTCTTGTGTTTCCTGCAGGTGATGGAGCTGGCAGTCAGGAAGATCAACTGTGCACGGCTCTGGTTAGTCAGCTCAATAAATTTGCAGATAAGGAGACGCTCATCCAGTTTCTGCGTTGCTTTCTGCTGGAGTCCAATTCCTCATCTGTGCGCTGGCAAGCTCACTG[C/A]CTCACACTGCATATCTACAGGTACGTAAAATCAATTTTCTACCTTTGAGCTTGATCCAGAAGTTCAATCATGTTAAATCTAACAGAAAATTTGCCTTTATAGGAACTCAAACAAATCCCAGCAGGAGTTGCTGCTCGACCTGATGTGGGCCATTTGGCCGGAATTACCTGCTTATGGGCGTAAAGCAGCTCAGTTTGTGGACCTGCTTGGATACTTTTCTCTTAAAACTCCTCAGACAGAAAAGAAGGTAGTCCAACTCAATTTTTTTCAGAATTCTTCAAATGAACTGCATTTTTTTTAATTAGAAATCTCTTGTAACCTTAATCAAGTGTTTCAAGTAAATCTATCTTTGCTTTAAGTTTTCATTTTTTACAACAGAAAATATGACTAACCGTAAACAGTCATTTGTAGTAGGCTAGCCTTTGCAAAATTTGAAATGTGCAAATGTTTTGCTTCCTACTTTTCTAGTTAAAGGAATACTCTCAAAAGGCTGTAGAAAT

Associated Phenotype:

Not determined

Allele Name:

sa17134

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Splice Site, Nonsense	3485	5152	70	105
ENSDART00000033970	Splice Site, Nonsense	3459	5129	69	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21647334)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21426641
GRCz11	23	21353192

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGAGGGCACAGAACCACATTCTGACCAATCACCCTAATTCAAACATATA[C/A]AAGTAAGTGTTCTCATCATTGGATGAAAATATTCTGCTTCACCGATGTAA

Long Flanking Sequence:

TGATCCAGAAGTTCAATCATGTTAAATCTAACAGAAAATTTGCCTTTATAGGAACTCAAACAAATCCCAGCAGGAGTTGCTGCTCGACCTGATGTGGGCCATTTGGCCGGAATTACCTGCTTATGGGCGTAAAGCAGCTCAGTTTGTGGACCTGCTTGGATACTTTTCTCTTAAAACTCCTCAGACAGAAAAGAAGGTAGTCCAACTCAATTTTTTTCAGAATTCTTCAAATGAACTGCATTTTTTTTAATTAGAAATCTCTTGTAACCTTAATCAAGTGTTTCAAGTAAATCTATCTTTGCTTTAAGTTTTCATTTTTTACAACAGAAAATATGACTAACCGTAAACAGTCATTTGTAGTAGGCTAGCCTTTGCAAAATTTGAAATGTGCAAATGTTTTGCTTCCTACTTTTCTAGTTAAAGGAATACTCTCAAAAGGCTGTAGAAATTTTGAGGGCACAGAACCACATTCTGACCAATCACCCTAATTCAAACATATA[C/A]AAGTAAGTGTTCTCATCATTGGATGAAAATATTCTGCTTCACCGATGTAAGAACATCTCTTAATTTTCATCTTGTCACACTTTCTTTCCAGCACCCTGTCTAGACTAGTGGAATTTGATGGATTTTACCTAGAAAGTGATCCCTGCTTGGTGTGCAACAACCCTGAAGTGCCCTTCTCTGTAAGTGTTGTCCATGACATGTGATGTTGAAATGCTTGCTTTGGTTGCTGCTGGCTGTAAATTCTGATCTACTTTATTCCCTGTACTATTAGAACATCAAACTCTCATCTATCAAAGTGGACACGCGTTACACCACCACTCAGCAAGTGGTGAAGTTGATTGGCAGCCACACTATCAGCAAAGTGACCGTGAAGATTGGTGATCTCAAGAGAACCAAGATGGTCCGCACAATCAACCTGTACTACAATAACAGGACTGTACAGGCCATTGTAGAGCTGAAGAATAAGTGAGAATTTTAAACACACTTTTAGAAGTTAGAGA

Associated Phenotype:

Not determined

Allele Name:

sa18331

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
ENSDART00000024846	Nonsense	3931	5152	78	105
ENSDART00000033970	Nonsense	3905	5129	77	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21652620)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21431927
GRCz11	23	21358478

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATGAATGATCTCATTATTGCCAAGGTGTCTGCAGCCCTTAAAGGACACT[G/A]GGCCAACCCTGATCTGGTATTTACCCTTTGTTATTGCATAGTAAGGATTG

Long Flanking Sequence:

AGTGCTTGCGTCACGTAAGGAGCTGCTGGAGTATGACCTTCATCAGCGAGAAGCAGCAACCAAATCATCACGCACCTCCGCTCAGCAAACATTTACAGCCAGTCAGTATCGAGCCCTGTCTGTGCTGGGCTGCGGACACACGTCCTCCACTAAGTGCTACGGCTGTGCGTCTGCTGTCACAGGCCACTGTATCACTCTTCTGCGTGCACTGGCAACTAACCCTGCCATCAGGCAGATACTGGTACTGCAGGGACTCATCCGAGAGCTGTTTGAGTACAACCTGCGCCGCGGCACCGGAGCCATGAGGGAAGAGGTTCGCCAGCTTGTCTGTCTGCTCACCAGGTATGGTAAATTCACAAACCTGTGAAGACGCAGTGGTGAACAGAATACTCTGCTAACAACTGTCATGCCCATGTATTTTTGCAGAGATCATCCAGAGGCCACACAGCAGATGAATGATCTCATTATTGCCAAGGTGTCTGCAGCCCTTAAAGGACACT[G/A]GGCCAACCCTGATCTGGTATTTACCCTTTGTTATTGCATAGTAAGGATTGGTGCACACGACAATCTGTAGCACTTGCCTAAAAAGCTTAGTTTTTCCTGTTTTCCTATCATTCAGGTTAGCAGTTTGCAGTATGAAATGCTGTTGCTCACTGACTCCATTGCTAAGGAGGGGGGATGCTGGGAGCTTAGACTTCGCTGTGGTGAGTCTTGTGGTGAAGCTGAAAATCTGAACTTTATAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTGTGTGTGTGTAAGCTGAATCAAATTAATTATCTGAGATGTTGATTTGTGTATTTTGAGTATTTCGTATTTTGAAGATTTTGTAACATTGAGTTTCCAGTCAATAGTGAATGTATATCAACCAGTAAAGCTTTTTTTAATTATAAATG

Associated Phenotype:

Not determined

Allele Name:

sa16066

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024846	Nonsense	4719	5152	97	105
ENSDART00000033970	Nonsense	4696	5129	96	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21662167)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21441474
GRCz11	23	21368025

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTCCTYCTTGTAGATGCTWATCGGAACAGATTCAATAACCAATTTGCAC[A/T]AGCTGGAGCAGGTGTCCAGCGACGAGGGTATCGGCACTTTAGCAGAGAAT

Long Flanking Sequence:

TAATTATTCAACTTGATTTGTTTTGCCAAACTAATAATTTTTTACGTTTCCCATATTTAGAAATCCATTTTTTTGGTACTGTATCTATAATTATCTTTGAAACATGTTTCTAGATCTGATCAAATACACTGTATAATACATTAAATAAACATTTTGTTTTAATGTCTTTTTATTGAAAAATTGGTTGTTTTTAACTACTCTATTAAATAAATAACATTGTTTTTGATGCGAGTGATTAACCTGAATATAAATATTTTGTAGCCTGGATGCAGATGTTTGGAAGAAATTCCTTGCTCGTCCAGCCCTTCCGTTCATCCTTAGACTGCTGCGTGGTCTAGCCACCCAACACCCCCCTACACAGGTAACATTTCCATTACTAGCTTTAATCGCATCTTTTCTTTTGTAAATTTTATTCTGTATTCCTGTACACACACAGCTCACATAAATTGATCTCCTTCTTGTAGATGCTAATCGGAACAGATTCAATAACCAATTTGCAC[A/T]AGCTGGAGCAGGTGTCCAGCGACGAGGGTATCGGCACTTTAGCAGAGAATCTCCTGGAGGCTCTGAGGGAACATGCAGATGTGAACCTGAAAATCGATGCAGCAAGAAGAGAGACTCGCGCAGAGAAGAAACGCATGGCTATGGCTATGAGGCAGAAGGCTCTCGGCACACTGGGAATGACAGTGAGTTTCATATATCGATGACACATGATGCTCAGACCATGAAATCAAAACCACTTTGAACTTATGTTGTCTTTCCTTCTTTACTTCAGACCAATGAGAAGGGTCAGGTGGTCACAAAGACATCTCTGCTTAAACAGATGGAGGAGCTCATCGAAGAACCGGGCTTGACTTGCTGCATTTGTAGAGAGGGCTACAAGTTCCAGGTCTATTTATTTACCATTTGTGTTTAAGCGTGTTGTAGTTTATTGTGTTATTAACAATTAGCAACATTTTATTCTGTACCCCATAGCCAACAAAAGTTCTGGGCATCTATACTTT

Associated Phenotype:

Not determined

Allele Name:

sa37688

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
ENSDART00000024846	Nonsense	4911	5152	101	105
ENSDART00000033970	Nonsense	4888	5129	100	104

The following transcripts of ENSDARG00000009549 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 23 (position 21663724)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	21443031
GRCz11	23	21369582

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAGTTGGAGTGTAAACTTGTTTTTTTACCATTTTACAGGCACAACACATA[T/A]CTGCAAGAGTGCACAGGGCAAAGGGAACCCACATACCAGCTCAACATTCA

Long Flanking Sequence:

AATGGGCTCCTTCCAGTATGGGGGCCACATGTGCCCGAATCTGCGTTTGCCACATGCCTGGCAAGGTATGTTCTGCTTGCATATAGATTAAATGGATACTTTCTACGTTCTGCTTGCATATAGATTAAATTGTTCCAGTTACTGAACCACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGAATTGAATACAGGGGTCACCAATCTCGGTCCTGGAGGGCCGGTGTCCCTGCAGAGTTTAGCTCCAACTTGCCTCAACACACCTGCCCGGGTGTTTCAAGTATACCTAGTAAGACCTTGATTAGCTTGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAAATCTGTAGGACACCAGACCTCCAGGAACAAGTTTGGTGCCTCTGCTTTAATAGTTGGAGTGTAAACTTGTTTTTTTACCATTTTACAGGCACAACACATA[T/A]CTGCAAGAGTGCACAGGGCAAAGGGAACCCACATACCAGCTCAACATTCATGACACCAAGCTGCTGTTCCTGCGTTTTGCAATGGAGCAATCCTTTAGTGTGGACACAGGAGGAGGAGGCCGAGAGAGCAACATCCACCTCATCCCTTACATCATTCACACAGTCCTCTACGTCCTCAACACGTATGTTACACAAAAATGCAATCTCAGATCAACTGCGTTTTTCAGATGTTATGTTTTTTTGAAGTACTCCTAAAGTCAAAATTATTCCTATTTTTAGTTTGTGTATGTTTGAGCTGTGGCAAAAAATTGTTCGAGAAATCGATTCTGCAGAGAGATTTTCAAAATGCATTACTGTTTCACAACAGATGGCCCTCTAGGCTAGTTTTTAAACGCACACTGAAATAATTACAAGAAAAAGCTCTTGTGCATTCAGTAGTTCATGCAAGTTGGTTTTTATGTCACAGCATTCAAGTAGACACAGCTCACTATGAACACCCT

Associated Phenotype:

Not determined

ZMP

Alleles

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