Busch Lab

ZMP

C10orf71 (1 of 2)

Ensembl ID:
ENSDARG00000086970
Description:
chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:26973]
Human Orthologue:
C10orf71
Human Description:
chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:26973]
Mouse Orthologue:
3425401B19Rik
Mouse Description:
RIKEN cDNA 3425401B19 gene Gene [Source:MGI Symbol;Acc:MGI:3588196]

Alleles

There are 21 alleles of this gene:

Allele Name Consequence Status Availability
sa42226 Nonsense Mutation detected in F1 DNA Not yet available
sa35522 Nonsense Mutation detected in F1 DNA Not yet available
sa16604 Nonsense Available for shipment Available now
sa12297 Nonsense Available for shipment Available now
sa42225 Nonsense Mutation detected in F1 DNA Not yet available
sa38950 Nonsense Mutation detected in F1 DNA Not yet available
sa42224 Nonsense Mutation detected in F1 DNA Not yet available
sa35521 Nonsense Mutation detected in F1 DNA Not yet available
sa17126 Nonsense Available for shipment Available now
sa28133 Nonsense Mutation detected in F1 DNA Not yet available
sa44790 Nonsense Mutation detected in F1 DNA Not yet available
sa42223 Nonsense Mutation detected in F1 DNA Not yet available
sa35520 Nonsense Mutation detected in F1 DNA Not yet available
sa18475 Nonsense Available for shipment Available now
sa18600 Nonsense Available for shipment Available now
sa4510 Nonsense F2 line generated Not yet available
sa35519 Nonsense Mutation detected in F1 DNA Not yet available
sa44789 Nonsense Mutation detected in F1 DNA Not yet available
sa13671 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa42226
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 853 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31157115)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30803063
GRCz11 13 30933513
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAAGCCCAAAAGAATGAAGAACTGTACTCTTATCAGCCATATAAGTAT[G/T]AGCATAACAAACAGTGGCACATGTCAACAAGTGAAGACAGGCACACCAAG
Long Flanking Sequence:
AAAGAGATGACCGATTTGAATCAGGGCCATTTAGAGGAGAAATAGCAGCTCTGATTGAGATGGACAAACAGAGGAAGGCCACTGCCAAGCAATATTCTGCCAATGATAATTATTCTGTCCGAAAGGAAACTTATATGCAAAAAGTGAATGAAGACATTAAACTTGGTCGACTTTCAAAGGAGGAAGCGAAAGAGGTCAGAGAAGACTCTATATCACCCAGGAAAACATCTTACAGTGACAGTCAATTGAACACATTTTCAAAGCATACTGAATCATATGGAATGCTAAAAAAACAGAATACAACACATCCTCTAAAAGAGGTCTATGGTGGTTTACAAAGCCTTAATGTAACAAATGATCATGTTAAAGCACCAGAACAGAACGTGTCTTCTAACAGCATGGCAATGCAAAAGACATTTGATCAGAGAGTGTATGCACCTTTACAAGACCATAAAGCCCAAAAGAATGAAGAACTGTACTCTTATCAGCCATATAAGTAT[G/T]AGCATAACAAACAGTGGCACATGTCAACAAGTGAAGACAGGCACACCAAGGAAAGCATGTGGATGCAAAAAAAATTAGAGACAATGGAACAAACTGATGCCAAGAGTTATAATGTTTCTAATACATTGTCAACTACAACTGAGTTTGTTACCTGCAATGGTGCACCAAAACCCAGATTGCAGGATGGAGAATCAGCCTCATCAACTGACACCTCAGATCAAAATAACTCAACTAAACAAGACAGGTTCAGCATTAATGATATTCTTGCCATCAGAGATAACGAGCAGGCAAGAAGACTAAAGGATAATTCAGTTAGTATGTCTAAATCAGAAAATTCACAAAGTCAAGTGAAATTGGATGCAGCTGAAAAACTAACCACAACAGATCTTGCTAAGGAGCAAGAACAACAAGGCTACAAAGTGCAGGAAGTTATAAGTCCATCGCCTGGCTATATTAGAAAAGAATTCCACAATGCAACAAATATCAGCAATGACAGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35522
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 961 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31156791)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30802739
GRCz11 13 30933189
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATAACGAGCAGGCAAGAAGACTAAAGGATAATTCAGTTAGTATGTCT[A/T]AATCAGAAAATTCACAAAGTCAAGTGAAATTGGATGCAGCTGAAAAACTA
Long Flanking Sequence:
ATGGTGGTTTACAAAGCCTTAATGTAACAAATGATCATGTTAAAGCACCAGAACAGAACGTGTCTTCTAACAGCATGGCAATGCAAAAGACATTTGATCAGAGAGTGTATGCACCTTTACAAGACCATAAAGCCCAAAAGAATGAAGAACTGTACTCTTATCAGCCATATAAGTATGAGCATAACAAACAGTGGCACATGTCAACAAGTGAAGACAGGCACACCAAGGAAAGCATGTGGATGCAAAAAAAATTAGAGACAATGGAACAAACTGATGCCAAGAGTTATAATGTTTCTAATACATTGTCAACTACAACTGAGTTTGTTACCTGCAATGGTGCACCAAAACCCAGATTGCAGGATGGAGAATCAGCCTCATCAACTGACACCTCAGATCAAAATAACTCAACTAAACAAGACAGGTTCAGCATTAATGATATTCTTGCCATCAGAGATAACGAGCAGGCAAGAAGACTAAAGGATAATTCAGTTAGTATGTCT[A/T]AATCAGAAAATTCACAAAGTCAAGTGAAATTGGATGCAGCTGAAAAACTAACCACAACAGATCTTGCTAAGGAGCAAGAACAACAAGGCTACAAAGTGCAGGAAGTTATAAGTCCATCGCCTGGCTATATTAGAAAAGAATTCCACAATGCAACAAATATCAGCAATGACAGAAAAGATAGAATAATGAGTAAAGACACTGAGAAGGCTACTACAAGAGCAATGTCTTACAAAGAAAGAGGCCAAAGCAAACAAGAAATACTGACGTCGAAATTGAAAGCACATGCTCAAAAGGAAATATCAGCAATTAAAGAAAAGGGACTTGCCAGACAAGGCATTCTTGCAAGAAATACAACAAAACCAAGTATGACTATCAATAATGAAGGTCAAGAAGGTCATTCAAATAAGAAGGAAATCACAGCAGACAAGCTAAATCACCTGTTTCAAGATATCACTTATTCCAGTGTAACCCAGTACAAAGAACAAAATAAAACGCAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16604
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1622 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154808)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800756
GRCz11 13 30931206
KASP Assay ID:
2260-6577.1 (used for ordering genotyping assays)
KASP Sequence:
GARATGAAGACATKACAAAGTCTTTGCTCTATTTCAATAAWGAAGATGTA[C/T]AAGCATTARCTAWCAAAAACATTAAAWCAAAGGAAAATGTTTTGGATAAY
Long Flanking Sequence:
TGATCAAAAACAATACGACACCGGAAAATGTTTTATTTAACCAACAAAACAATCCATTGCAAGTGAAGGCTAATGACAGTACCACTGCAAACCAAATAAAGGATAATCAGTCAAGCTTAGGAACAAGTAAAGAATCTCTAACACAAATGGCATCAGTTAGAGCGAAAGAAAACTGTTTACAAAAAGATCTTCCTCAAGATGATGAAAATACAAAGTCTCTGCTACGTTTCAATAAGGAAGATAAACAAGCATTAATAATTGGAAACAATAAAACAAAACAACATATTATGGATGACCAACAAAGCAATGCATCTCAAGTAAAGTCTCCAGAAACTACCACTGCAAACCAAATGGTGGACAGTCAGTCAAAGCCAGGATCAGATAAGGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAAGAAAACTGCGAGCAAGAGAAACTCCAAAGAGATGAAGACATGACAAAGTCTTTGCTCTATTTCAATAATGAAGATGTA[C/T]AAGCATTAGCTATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACAAGGAAAGGCTGTAAAAACTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAAACTAGAAACAAGTAAAGAATCCCTAGCACAAATGGCATCAGTTAAAGCAAAAAAAAAATCTATGCAAAAAGAACTCCATCAAGATGATGAAAATGATAAGGTGCTACTATGTTTTAACAATGAAGATGGACAAGCAATAATGATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACGGGGAAAGGCTGTAGAAGCTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAATCTTGGAATGAGTAAATACTTACTACCACAAATGGCATCAATTAAAGGAAATGAAAACTGCGAGCAAAAAGTACTCAATCAAGATGATGAAAATACAAAGTCTCTGCTATGTTTTAATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12297
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1673 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154655)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800603
GRCz11 13 30931053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGATGGACAGTCAGTCAAAACTAGAAACARGTAAAGAATCCCTARCA[C/T]AAATGGCATCAGTTAAAGCAAAARAAAAANTCTATGCAAAAWGAACTCCAT
Long Flanking Sequence:
CAGTTAGAGCGAAAGAAAACTGTTTACAAAAAGATCTTCCTCAAGATGATGAAAATACAAAGTCTCTGCTACGTTTCAATAAGGAAGATAAACAAGCATTAATAATTGGAAACAATAAAACAAAACAACATATTATGGATGACCAACAAAGCAATGCATCTCAAGTAAAGTCTCCAGAAACTACCACTGCAAACCAAATGGTGGACAGTCAGTCAAAGCCAGGATCAGATAAGGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAAGAAAACTGCGAGCAAGAGAAACTCCAAAGAGATGAAGACATGACAAAGTCTTTGCTCTATTTCAATAATGAAGATGTACAAGCATTAGCTATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACAAGGAAAGGCTGTAAAAACTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAAACTAGAAACAAGTAAAGAATCCCTAGCA[C/T]AAATGGCATCAGTTAAAGCAAAAAAAAAATCTATGCAAAAAGAACTCCATCAAGATGATGAAAATGATAAGGTGCTACTATGTTTTAACAATGAAGATGGACAAGCAATAATGATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACGGGGAAAGGCTGTAGAAGCTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAATCTTGGAATGAGTAAATACTTACTACCACAAATGGCATCAATTAAAGGAAATGAAAACTGCGAGCAAAAAGTACTCAATCAAGATGATGAAAATACAAAGTCTCTGCTATGTTTTAATAATGAAGATAGACAATCATTAATGATCAAAAATATTAAAACAAAAGAAAAAGTTCTGGATAGCCAACAAAACAGTGCATCACAAGGAAAGGCTATAGAAAGTACCACTGCAAATCAAAAGATGGACAGTCGGCCAAATCTTGGAACTAGTAAATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42225
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
ENSDART00000128847 Nonsense 1707 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154553)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800501
GRCz11 13 30930951
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATGATGAAAATGATAAGGTGCTACTATGTTTTAACAATGAAGATGGA[C/T]AAGCAATAATGATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAAC
Long Flanking Sequence:
TAATTGGAAACAATAAAACAAAACAACATATTATGGATGACCAACAAAGCAATGCATCTCAAGTAAAGTCTCCAGAAACTACCACTGCAAACCAAATGGTGGACAGTCAGTCAAAGCCAGGATCAGATAAGGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAAGAAAACTGCGAGCAAGAGAAACTCCAAAGAGATGAAGACATGACAAAGTCTTTGCTCTATTTCAATAATGAAGATGTACAAGCATTAGCTATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACAAGGAAAGGCTGTAAAAACTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAAACTAGAAACAAGTAAAGAATCCCTAGCACAAATGGCATCAGTTAAAGCAAAAAAAAAATCTATGCAAAAAGAACTCCATCAAGATGATGAAAATGATAAGGTGCTACTATGTTTTAACAATGAAGATGGA[C/T]AAGCAATAATGATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAACCAACAAAACAGTGCATCACGGGGAAAGGCTGTAGAAGCTACCACTGCAAACCAAAAGATGGACAGTCAGTCAAATCTTGGAATGAGTAAATACTTACTACCACAAATGGCATCAATTAAAGGAAATGAAAACTGCGAGCAAAAAGTACTCAATCAAGATGATGAAAATACAAAGTCTCTGCTATGTTTTAATAATGAAGATAGACAATCATTAATGATCAAAAATATTAAAACAAAAGAAAAAGTTCTGGATAGCCAACAAAACAGTGCATCACAAGGAAAGGCTATAGAAAGTACCACTGCAAATCAAAAGATGGACAGTCGGCCAAATCTTGGAACTAGTAAATATTCACTAACCCAAATTACATCAGTTAAAGCAAAAGAACACTGTGAGCAGAAAGAACTCCATCAAGATGATAGGAATACGGAGTCTATGCTATGTTTGTACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38950
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1959 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153797)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799745
GRCz11 13 30930195
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAGTTGATGAAAGTACAAAGTCTTTGCTAAGCTTTAATAAGGAAGAT[G/T]GACAAGCATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGAT
Long Flanking Sequence:
AATCATTAATGATCAAAAATATTAAAACAAAAGAAAAAGTTCTGGATAGCCAACAAAACAGTGCATCACAAGGAAAGGCTATAGAAAGTACCACTGCAAATCAAAAGATGGACAGTCGGCCAAATCTTGGAACTAGTAAATATTCACTAACCCAAATTACATCAGTTAAAGCAAAAGAACACTGTGAGCAGAAAGAACTCCATCAAGATGATAGGAATACGGAGTCTATGCTATGTTTGTACAATGAAGATGGACAAGCAGTGAAAAACATTAAAACAAAGGATGATGTTTTAGTTGATCAACAAAACAGTGCATCAAAAGGAAATGCTGTAGAAACTACCATTGCAAACCAAAAGAAGGGCAGTCTGTCAAAACTAGAAACAAGTAAAGAATCCCTAACACAAATGGCATCAGTTACAGCAAAAGAAAGCTTTGAGCAAAAAGATCTCCATCAAGTTGATGAAAGTACAAAGTCTTTGCTAAGCTTTAATAAGGAAGAT[G/T]GACAAGCATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGATAATCAACAAAGCAATGCATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGACAGTCGGTCCAAACCAGGATCAAATAAAGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAGGAAAATGATCATCAAAAAGAACCACATAAAGATAAAGAAAATACAAAGAATTTGGTGTTATTCGACAAAAAGGAACTTTCTAAAAGCCAAAACATGTCCAGAATAATAGATAGTTCAGCAACTGTAAGTAACAGTCAACAGGTAGAGAAAAGGCCAGAAAGTGCAATGTCAAAACAAAAAGAACTTCCTAGACCATTGGAAATATCAAAAGAGAACAACAATCACAAGACAACAAAAGAATCTCAAGAAAAGAACCCAAGCAATTCTGAACCCAAAAAAGCTATAGATAAACTAGAACCAAATGTTTCCTCACAACATAAAGTAAAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42224
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
ENSDART00000128847 Nonsense 1978 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153740)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799688
GRCz11 13 30930138
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGATAATCAA[C/T]AAAGCAATGCATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGAC
Long Flanking Sequence:
ACAGTGCATCACAAGGAAAGGCTATAGAAAGTACCACTGCAAATCAAAAGATGGACAGTCGGCCAAATCTTGGAACTAGTAAATATTCACTAACCCAAATTACATCAGTTAAAGCAAAAGAACACTGTGAGCAGAAAGAACTCCATCAAGATGATAGGAATACGGAGTCTATGCTATGTTTGTACAATGAAGATGGACAAGCAGTGAAAAACATTAAAACAAAGGATGATGTTTTAGTTGATCAACAAAACAGTGCATCAAAAGGAAATGCTGTAGAAACTACCATTGCAAACCAAAAGAAGGGCAGTCTGTCAAAACTAGAAACAAGTAAAGAATCCCTAACACAAATGGCATCAGTTACAGCAAAAGAAAGCTTTGAGCAAAAAGATCTCCATCAAGTTGATGAAAGTACAAAGTCTTTGCTAAGCTTTAATAAGGAAGATGGACAAGCATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGATAATCAA[C/T]AAAGCAATGCATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGACAGTCGGTCCAAACCAGGATCAAATAAAGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAGGAAAATGATCATCAAAAAGAACCACATAAAGATAAAGAAAATACAAAGAATTTGGTGTTATTCGACAAAAAGGAACTTTCTAAAAGCCAAAACATGTCCAGAATAATAGATAGTTCAGCAACTGTAAGTAACAGTCAACAGGTAGAGAAAAGGCCAGAAAGTGCAATGTCAAAACAAAAAGAACTTCCTAGACCATTGGAAATATCAAAAGAGAACAACAATCACAAGACAACAAAAGAATCTCAAGAAAAGAACCCAAGCAATTCTGAACCCAAAAAAGCTATAGATAAACTAGAACCAAATGTTTCCTCACAACATAAAGTAAAACTAGATGAGGGTGCAACTCAAAAGGACAATACAAAGCCTGTTTCAACACAGAATGTAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35521
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1998 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153680)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799628
GRCz11 13 30930078
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGACAGTCGGTCC[A/T]AACCAGGATCAAATAAAGAATCACTAAAACACAAGACTTCAGCTAAAGCT
Long Flanking Sequence:
GGCCAAATCTTGGAACTAGTAAATATTCACTAACCCAAATTACATCAGTTAAAGCAAAAGAACACTGTGAGCAGAAAGAACTCCATCAAGATGATAGGAATACGGAGTCTATGCTATGTTTGTACAATGAAGATGGACAAGCAGTGAAAAACATTAAAACAAAGGATGATGTTTTAGTTGATCAACAAAACAGTGCATCAAAAGGAAATGCTGTAGAAACTACCATTGCAAACCAAAAGAAGGGCAGTCTGTCAAAACTAGAAACAAGTAAAGAATCCCTAACACAAATGGCATCAGTTACAGCAAAAGAAAGCTTTGAGCAAAAAGATCTCCATCAAGTTGATGAAAGTACAAAGTCTTTGCTAAGCTTTAATAAGGAAGATGGACAAGCATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGATAATCAACAAAGCAATGCATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGACAGTCGGTCC[A/T]AACCAGGATCAAATAAAGAATCACTAAAACACAAGACTTCAGCTAAAGCTAAGGAAAATGATCATCAAAAAGAACCACATAAAGATAAAGAAAATACAAAGAATTTGGTGTTATTCGACAAAAAGGAACTTTCTAAAAGCCAAAACATGTCCAGAATAATAGATAGTTCAGCAACTGTAAGTAACAGTCAACAGGTAGAGAAAAGGCCAGAAAGTGCAATGTCAAAACAAAAAGAACTTCCTAGACCATTGGAAATATCAAAAGAGAACAACAATCACAAGACAACAAAAGAATCTCAAGAAAAGAACCCAAGCAATTCTGAACCCAAAAAAGCTATAGATAAACTAGAACCAAATGTTTCCTCACAACATAAAGTAAAACTAGATGAGGGTGCAACTCAAAAGGACAATACAAAGCCTGTTTCAACACAGAATGTAGAATCTACAGCCGGTGTATCAAACATCATTCATACACCTAGCAAAGTGGAGTCTGCAGAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17126
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2171 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153159)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799107
GRCz11 13 30929557
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACCTAGCAAAGTGGAGTCTGCAGAGGAGCCGAWGATTTACAATATYTG[T/A]GTGTCAAGCAAAACGGAAGCAGCCTCAGAYGATGAGCCCATGATCTACAC
Long Flanking Sequence:
TCACTAAAACACAAGACTTCAGCTAAAGCTAAGGAAAATGATCATCAAAAAGAACCACATAAAGATAAAGAAAATACAAAGAATTTGGTGTTATTCGACAAAAAGGAACTTTCTAAAAGCCAAAACATGTCCAGAATAATAGATAGTTCAGCAACTGTAAGTAACAGTCAACAGGTAGAGAAAAGGCCAGAAAGTGCAATGTCAAAACAAAAAGAACTTCCTAGACCATTGGAAATATCAAAAGAGAACAACAATCACAAGACAACAAAAGAATCTCAAGAAAAGAACCCAAGCAATTCTGAACCCAAAAAAGCTATAGATAAACTAGAACCAAATGTTTCCTCACAACATAAAGTAAAACTAGATGAGGGTGCAACTCAAAAGGACAATACAAAGCCTGTTTCAACACAGAATGTAGAATCTACAGCCGGTGTATCAAACATCATTCATACACCTAGCAAAGTGGAGTCTGCAGAGGAGCCGATGATTTACAATATTTG[T/A]GTGTCAAGCAAAACGGAAGCAGCCTCAGACGATGAGCCCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAACAAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGTGTTAAGGATGATAGCTTTCGTATTGAAAATGACAGAGCAGAAAATGAACCTGAGGTTGTTCGCAGAAAGACTGAAGTATCTTCAAACGTTGAAGAAAAAGAAGACAAGATTGGAAAATGTGAACTGACGACAACTATGAATAAGTCAAATGTCATGGGAAGAATCACTACATCATACGAGGACCTCTTAGCTAAATATGGGCTTCCAGCAAGTGATTACCATGGTCATCTCATGTCAAAACGTACTCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCTCAAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAAAAAGCTCAGGTGACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28133
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
ENSDART00000128847 Nonsense 2201 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153071)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799019
GRCz11 13 30929469
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAA[C/T]AAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGT
Long Flanking Sequence:
TGTTATTCGACAAAAAGGAACTTTCTAAAAGCCAAAACATGTCCAGAATAATAGATAGTTCAGCAACTGTAAGTAACAGTCAACAGGTAGAGAAAAGGCCAGAAAGTGCAATGTCAAAACAAAAAGAACTTCCTAGACCATTGGAAATATCAAAAGAGAACAACAATCACAAGACAACAAAAGAATCTCAAGAAAAGAACCCAAGCAATTCTGAACCCAAAAAAGCTATAGATAAACTAGAACCAAATGTTTCCTCACAACATAAAGTAAAACTAGATGAGGGTGCAACTCAAAAGGACAATACAAAGCCTGTTTCAACACAGAATGTAGAATCTACAGCCGGTGTATCAAACATCATTCATACACCTAGCAAAGTGGAGTCTGCAGAGGAGCCGATGATTTACAATATTTGTGTGTCAAGCAAAACGGAAGCAGCCTCAGACGATGAGCCCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAA[C/T]AAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGTGTTAAGGATGATAGCTTTCGTATTGAAAATGACAGAGCAGAAAATGAACCTGAGGTTGTTCGCAGAAAGACTGAAGTATCTTCAAACGTTGAAGAAAAAGAAGACAAGATTGGAAAATGTGAACTGACGACAACTATGAATAAGTCAAATGTCATGGGAAGAATCACTACATCATACGAGGACCTCTTAGCTAAATATGGGCTTCCAGCAAGTGATTACCATGGTCATCTCATGTCAAAACGTACTCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCTCAAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGACAAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCAGAGGGAAAAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44790
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
ENSDART00000128847 Nonsense 2316 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31152725)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30798673
GRCz11 13 30929123
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCT[C/A]AAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAA
Long Flanking Sequence:
ATCAAACATCATTCATACACCTAGCAAAGTGGAGTCTGCAGAGGAGCCGATGATTTACAATATTTGTGTGTCAAGCAAAACGGAAGCAGCCTCAGACGATGAGCCCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAACAAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGTGTTAAGGATGATAGCTTTCGTATTGAAAATGACAGAGCAGAAAATGAACCTGAGGTTGTTCGCAGAAAGACTGAAGTATCTTCAAACGTTGAAGAAAAAGAAGACAAGATTGGAAAATGTGAACTGACGACAACTATGAATAAGTCAAATGTCATGGGAAGAATCACTACATCATACGAGGACCTCTTAGCTAAATATGGGCTTCCAGCAAGTGATTACCATGGTCATCTCATGTCAAAACGTACTCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCT[C/A]AAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGACAAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCAGAGGGAAAAATCAAGCAATTGCAACACTGTGATATCCCTTCAAACAACGTTGCTGAAAAGCAACAGAGTTCAGGAAATAGTATACCAAGCCTTGGCCATTCTACAAGTGATACCACCCTAATACCAAAAGATATAAATAGACATGTTGAACAAGACAGAGTTACACAAAATATTGAACCATCAAGTCAGAGTAGGGGAAGCAATATTCAATCGAAGGAAAAGAAAGTTGAAGAGCAAGTGAGAAACAGTGAGAAAGTGCAAAGTATGAAAAATACAGGAAATATTACTGATGACGTATCCAGAAAGTCCACAAAGAAAACAGACAATGAATCCCTAATGACTAAACAATCGGTAATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42223
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
ENSDART00000128847 Nonsense 2347 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31152633)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30798581
GRCz11 13 30929031
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGA[C/T]AAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCA
Long Flanking Sequence:
CAGACGATGAGCCCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAACAAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGTGTTAAGGATGATAGCTTTCGTATTGAAAATGACAGAGCAGAAAATGAACCTGAGGTTGTTCGCAGAAAGACTGAAGTATCTTCAAACGTTGAAGAAAAAGAAGACAAGATTGGAAAATGTGAACTGACGACAACTATGAATAAGTCAAATGTCATGGGAAGAATCACTACATCATACGAGGACCTCTTAGCTAAATATGGGCTTCCAGCAAGTGATTACCATGGTCATCTCATGTCAAAACGTACTCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCTCAAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGA[C/T]AAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCAGAGGGAAAAATCAAGCAATTGCAACACTGTGATATCCCTTCAAACAACGTTGCTGAAAAGCAACAGAGTTCAGGAAATAGTATACCAAGCCTTGGCCATTCTACAAGTGATACCACCCTAATACCAAAAGATATAAATAGACATGTTGAACAAGACAGAGTTACACAAAATATTGAACCATCAAGTCAGAGTAGGGGAAGCAATATTCAATCGAAGGAAAAGAAAGTTGAAGAGCAAGTGAGAAACAGTGAGAAAGTGCAAAGTATGAAAAATACAGGAAATATTACTGATGACGTATCCAGAAAGTCCACAAAGAAAACAGACAATGAATCCCTAATGACTAAACAATCGGTAATGTGTGAATCAACAAGAGCAGCAAAATCTGATGTTTTAAAAGCATCCGTTTCCAACACATCCTTGGCAAAGGACACAGCCAAGACCAAACTCACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35520
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2410 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31152444)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30798392
GRCz11 13 30928842
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTGGCCATTCTACAAGTGATACCACCCTAATACCAAAAGATATAAAT[A/T]GACATGTTGAACAAGACAGAGTTACACAAAATATTGAACCATCAAGTCAG
Long Flanking Sequence:
TATCTTCAAACGTTGAAGAAAAAGAAGACAAGATTGGAAAATGTGAACTGACGACAACTATGAATAAGTCAAATGTCATGGGAAGAATCACTACATCATACGAGGACCTCTTAGCTAAATATGGGCTTCCAGCAAGTGATTACCATGGTCATCTCATGTCAAAACGTACTCAAGAAGAGAGAGAGAGAAAAGAAAAGGAGGACACTGAAACTCAATTCTCAAACAAACCAATAAAACATGGTATTACCAAACCTCTGACACCCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGACAAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCAGAGGGAAAAATCAAGCAATTGCAACACTGTGATATCCCTTCAAACAACGTTGCTGAAAAGCAACAGAGTTCAGGAAATAGTATACCAAGCCTTGGCCATTCTACAAGTGATACCACCCTAATACCAAAAGATATAAAT[A/T]GACATGTTGAACAAGACAGAGTTACACAAAATATTGAACCATCAAGTCAGAGTAGGGGAAGCAATATTCAATCGAAGGAAAAGAAAGTTGAAGAGCAAGTGAGAAACAGTGAGAAAGTGCAAAGTATGAAAAATACAGGAAATATTACTGATGACGTATCCAGAAAGTCCACAAAGAAAACAGACAATGAATCCCTAATGACTAAACAATCGGTAATGTGTGAATCAACAAGAGCAGCAAAATCTGATGTTTTAAAAGCATCCGTTTCCAACACATCCTTGGCAAAGGACACAGCCAAGACCAAACTCACTGAAAGTAAAATTCCCAAAAAGACAATACCCCAAGCTGAAAAGAAGCTTGAAGAGGTGGAAGGTAAAGAGAAAATGTTTAATCAAACTGATACATTAATGCTACATCCGAATAAAATACACAGAAGGGAAACGTTTAATTCAGAAAATCAGAAAAGTATTCATGAGGATAAACAACAGGATTCTACAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18475
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2829 3591 1 1
ENSDART00000128847 Nonsense 2829 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151187)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797135
GRCz11 13 30927585
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAG
Long Flanking Sequence:
TTCACTTAGAGGACATAAAAGTGTCTACAGAGGAAGTGTCATCAAACAAAGAATTCATGGTAGGCCACAAAAACCAACATGAAGTGATAAAGAGGAAAACTCTACAAGGAAAGAAAGTAACTGTTGTGGCTGAACATGTGGGTGAAAAAGACTTTGCAGAGCTAAAGAAGTTACCAATAAAGACCCTTGCAGCCCAAAATGAACCCAAAACTGTGGACATTATGAAAGGGCTCTGTGAAACGGCACCCAAACCACTTAAGAGAGATTGTCCAAGTGAATCAGAAAAGCCAGAAATTAATCAACAAGATGCATTAGTTCAGTCTCAACATATAAAAGTCTGTGATAATAAACAACCTGCACTGAATAGTGAGGAAAGGAAGATTGAACAGCCTGTATTAAGTAAAAATGGACAAAAGGATGGTAATTTGAAAGTTCGAAATGAAAACAGAAGCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAGCCTGAAAAAGAAAGAAGTGCAAGCTATGAACTAGAACATGCACAGATATATCAAAAGGACGCCAAGAAAGAAGGTATGTTATCCAAAAATGAGGCTACACAGAGGAACAAAAAGGTGACTAGACCTGAAATATCAGCAATCGCAGACTATGCTCGACTGAAAGTTATTGCTGCAGAAGATGACACAAAAGAGCTTGATATATTTCCAAAAACGGACTTCTACAACAGTTATGATCAGCCGGCTTCAAGAATTTCTAAAGATTCTCATAGAAAGGTGTCAGGAGATATATGGGAAGATTCAAAACGAGAGGCCATTTTAAGAGAAAAAGGTCAAAATCTCAAGCAAACACCATCATTAGCCCAAAAGCACAATCCCAGTACGAATATAGCTGAAGCAACGCCTGTATCACTGGTAGCATCAGGTTCACAAGGTAGAGCTGCTTCAACTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18600
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2829 3591 1 1
ENSDART00000128847 Nonsense 2829 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151187)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797135
GRCz11 13 30927585
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAG
Long Flanking Sequence:
TTCACTTAGAGGACATAAAAGTGTCTACAGAGGAAGTGTCATCAAACAAAGAATTCATGGTAGGCCACAAAAACCAACATGAAGTGATAAAGAGGAAAACTCTACAAGGAAAGAAAGTAACTGTTGTGGCTGAACATGTGGGTGAAAAAGACTTTGCAGAGCTAAAGAAGTTACCAATAAAGACCCTTGCAGCCCAAAATGAACCCAAAACTGTGGACATTATGAAAGGGCTCTGTGAAACGGCACCCAAACCACTTAAGAGAGATTGTCCAAGTGAATCAGAAAAGCCAGAAATTAATCAACAAGATGCATTAGTTCAGTCTCAACATATAAAAGTCTGTGATAATAAACAACCTGCACTGAATAGTGAGGAAAGGAAGATTGAACAGCCTGTATTAAGTAAAAATGGACAAAAGGATGGTAATTTGAAAGTTCGAAATGAAAACAGAAGCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAGCCTGAAAAAGAAAGAAGTGCAAGCTATGAACTAGAACATGCACAGATATATCAAAAGGACGCCAAGAAAGAAGGTATGTTATCCAAAAATGAGGCTACACAGAGGAACAAAAAGGTGACTAGACCTGAAATATCAGCAATCGCAGACTATGCTCGACTGAAAGTTATTGCTGCAGAAGATGACACAAAAGAGCTTGATATATTTCCAAAAACGGACTTCTACAACAGTTATGATCAGCCGGCTTCAAGAATTTCTAAAGATTCTCATAGAAAGGTGTCAGGAGATATATGGGAAGATTCAAAACGAGAGGCCATTTTAAGAGAAAAAGGTCAAAATCTCAAGCAAACACCATCATTAGCCCAAAAGCACAATCCCAGTACGAATATAGCTGAAGCAACGCCTGTATCACTGGTAGCATCAGGTTCACAAGGTAGAGCTGCTTCAACTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4510
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2854 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151110)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797058
GRCz11 13 30927508
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAGCCTGGGAGAGGTTTGGAGCCTGAAAAAGAAAGAAGTGCAAGCTA[T/A]GAACTAGAACATGCACAGATATATCAAAAGGACGCCAAGAAAGAAGGTAT
Long Flanking Sequence:
CATGAAGTGATAAAGAGGAAAACTCTACAAGGAAAGAAAGTAACTGTTGTGGCTGAACATGTGGGTGAAAAAGACTTTGCAGAGCTAAAGAAGTTACCAATAAAGACCCTTGCAGCCCAAAATGAACCCAAAACTGTGGACATTATGAAAGGGCTCTGTGAAACGGCACCCAAACCACTTAAGAGAGATTGTCCAAGTGAATCAGAAAAGCCAGAAATTAATCAACAAGATGCATTAGTTCAGTCTCAACATATAAAAGTCTGTGATAATAAACAACCTGCACTGAATAGTGAGGAAAGGAAGATTGAACAGCCTGTATTAAGTAAAAATGGACAAAAGGATGGTAATTTGAAAGTTCGAAATGAAAACAGAAGCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAACAAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAGCCTGAAAAAGAAAGAAGTGCAAGCTA[T/A]GAACTAGAACATGCACAGATATATCAAAAGGACGCCAAGAAAGAAGGTATGTTATCCAAAAATGAGGCTACACAGAGGAACAAAAAGGTGACTAGACCTGAAATATCAGCAATCGCAGACTATGCTCGACTGAAAGTTATTGCTGCAGAAGATGACACAAAAGAGCTTGATATATTTCCAAAAACGGACTTCTACAACAGTTATGATCAGCCGGCTTCAAGAATTTCTAAAGATTCTCATAGAAAGGTGTCAGGAGATATATGGGAAGATTCAAAACGAGAGGCCATTTTAAGAGAAAAAGGTCAAAATCTCAAGCAAACACCATCATTAGCCCAAAAGCACAATCCCAGTACGAATATAGCTGAAGCAACGCCTGTATCACTGGTAGCATCAGGTTCACAAGGTAGAGCTGCTTCAACTCAATCAAGGACTCCAGCAATTCATAGGAAATCAAATACTAAACAAACTTTGGAGCAAACAAAAACAGGAGAAAGTTACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35519
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
ENSDART00000128847 Nonsense 3029 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31150587)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30796535
GRCz11 13 30926985
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAAACAAAAACAGGAGAAAGTTACAAAACATACCAGTCCAGGAATCCC[C/T]AAGGAGACAATATTGCAGCATTGCAAGCTGAGAGTACAATAAACCGATCA
Long Flanking Sequence:
ATCAAAAGGACGCCAAGAAAGAAGGTATGTTATCCAAAAATGAGGCTACACAGAGGAACAAAAAGGTGACTAGACCTGAAATATCAGCAATCGCAGACTATGCTCGACTGAAAGTTATTGCTGCAGAAGATGACACAAAAGAGCTTGATATATTTCCAAAAACGGACTTCTACAACAGTTATGATCAGCCGGCTTCAAGAATTTCTAAAGATTCTCATAGAAAGGTGTCAGGAGATATATGGGAAGATTCAAAACGAGAGGCCATTTTAAGAGAAAAAGGTCAAAATCTCAAGCAAACACCATCATTAGCCCAAAAGCACAATCCCAGTACGAATATAGCTGAAGCAACGCCTGTATCACTGGTAGCATCAGGTTCACAAGGTAGAGCTGCTTCAACTCAATCAAGGACTCCAGCAATTCATAGGAAATCAAATACTAAACAAACTTTGGAGCAAACAAAAACAGGAGAAAGTTACAAAACATACCAGTCCAGGAATCCC[C/T]AAGGAGACAATATTGCAGCATTGCAAGCTGAGAGTACAATAAACCGATCAAGACAACCGGCTCATGATAAAAGAATGGAGAAGACTAGCTTTTCTCATTCAGGAAGACAAGTGTTGGGTAATGTAAAACAAGCAGACAACCAAATAAATATGGCATCACCACCAGAAGAAGAAATGGAAGAACTACAATATTACACCGTGAATGCTCTTGACATTGAACCAAAGCCAAATTACACACCCGAGCCACCTCATGAAAGTCCCAAAATTTACCAAAACAAATTAGAGGAAGACAAAAAGGAAGATAGCTTGTCTTTGCAAAGTCTAACAGAATATGGTAAAGCTAACATGACAGGACCCCGATCCAACTCTTCTTCTCCAGCCATGGGAAAACCCACCATGTTCAGAGTGAAGGATAATACCATCAGACCGTCTTCTGTGACCAAAACTGTGAAGCCACGCTTTCACAGGTCATTCTCTGATGACTTGAGGATTGGTTCTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44789
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 3460 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31149294)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30795242
GRCz11 13 30925692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATGGTGGACGTACCACTACCGGTTAAGACAAAGACTTTTTATGACCCT[G/T]AAACTGGTAAATATGTACAGTTGAATGTCCGTCAGAGGTCTCAGGGTGCT
Long Flanking Sequence:
TCATGCCTAAGAATGAATTTTACAGAGATTCCTACCGAAGGCCTGCATCCGCCTGCTATGAACGACCAGATTCAGTCTGCTACGAAAGGCCAGAATCAGCCTGTAGTGATATAAGATCATTGGGGAAACCTCCAGCGGTGCCCCCCAAATCTGAAAAAGCTCTTCGGCGAGCGCAAAGACTTACAACAAGACGTCTCAAAAAGTCTGAGTCTCCGAAGTTAGCACCTGAAAACCAAGAACAACCAGAACCCAAATCAATCAGCAACATCTCCAGCGTTCCCTCTTCACCATCGGATGTACCGTCATCACATCAAGAGGTGCATGCCTCACCCCCTCTTTCACAATATGACACCCAGCCAAATTACTCCCCCCCTGCACACAGTATAGTGGCGCAACCTTTCCCAATGACACAGAGAAAGCTTTTGCAAGACCCAAACTCAGGGCAGTACTTTATGGTGGACGTACCACTACCGGTTAAGACAAAGACTTTTTATGACCCT[G/T]AAACTGGTAAATATGTACAGTTGAATGTCCGTCAGAGGTCTCAGGGTGCTTTAACACAGCCAGCACAAGTTGAAATGTTAAATGCTCCTTACATGCTGTATCGTGGCTTTCTGCCAATGGCTGCATCCTCATTATCACCCTTGAGGTCATCATCTGAAATGTCAACACCGGCTGCGCTAACAGTTCATCGGGATATGCTTGAGACGGGTAGCGAAGCGTGGACTCAGAATGTTCATCACAGCAGAGATTCTCAGCAATACCCTGAAACACAGTATGGGTCACACGAGCAAATTCACAACCCGGCTTTGTATGCAGAAAACAATGTTGATGACAATGACAGACACAGAGATATTATAACTATGAGTGAATTAGAGGACTTTGCAATGGAGAGCACATGACAAGAAAAGATAGTTTAAATAGGTAAATGCTGTTTGTACACAAATCTATCCTTTTATGACTGTATATCTAAGCTATTTAAATGTGACTTTTAAATTAAAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13671
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 3490 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31149202)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30795150
GRCz11 13 30925600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGGTGCTYTAACACAGCCAGCACMAGTTGAAATGTTAAATGCTCCTTA[C/A]ATGCTGTATCGTGGCTTTCTGCCAATGGCTGCATCCTCATTATCACCCTT
Long Flanking Sequence:
GAATCAGCCTGTAGTGATATAAGATCATTGGGGAAACCTCCAGCGGTGCCCCCCAAATCTGAAAAAGCTCTTCGGCGAGCGCAAAGACTTACAACAAGACGTCTCAAAAAGTCTGAGTCTCCGAAGTTAGCACCTGAAAACCAAGAACAACCAGAACCCAAATCAATCAGCAACATCTCCAGCGTTCCCTCTTCACCATCGGATGTACCGTCATCACATCAAGAGGTGCATGCCTCACCCCCTCTTTCACAATATGACACCCAGCCAAATTACTCCCCCCCTGCACACAGTATAGTGGCGCAACCTTTCCCAATGACACAGAGAAAGCTTTTGCAAGACCCAAACTCAGGGCAGTACTTTATGGTGGACGTACCACTACCGGTTAAGACAAAGACTTTTTATGACCCTGAAACTGGTAAATATGTACAGTTGAATGTCCGTCAGAGGTCTCAGGGTGCTTTAACACAGCCAGCACAAGTTGAAATGTTAAATGCTCCTTA[C/A]ATGCTGTATCGTGGCTTTCTGCCAATGGCTGCATCCTCATTATCACCCTTGAGGTCATCATCTGAAATGTCAACACCGGCTGCGCTAACAGTTCATCGGGATATGCTTGAGACGGGTAGCGAAGCGTGGACTCAGAATGTTCATCACAGCAGAGATTCTCAGCAATACCCTGAAACACAGTATGGGTCACACGAGCAAATTCACAACCCGGCTTTGTATGCAGAAAACAATGTTGATGACAATGACAGACACAGAGATATTATAACTATGAGTGAATTAGAGGACTTTGCAATGGAGAGCACATGACAAGAAAAGATAGTTTAAATAGGTAAATGCTGTTTGTACACAAATCTATCCTTTTATGACTGTATATCTAAGCTATTTAAATGTGACTTTTAAATTAAAGGTGTTCAATTTGTATTCAAAGATTGCTATTAAACTGCATTGTGTTTTGTAGCCGAGGGGAAGGGCATGGGCTCTTTATTGTCAGAAAAATCAAT
Associated Phenotype:
Not determined