Busch Lab

ZMP

myo5c

Ensembl ID:
ENSDARG00000013782
Human Orthologue:
MYO5C
Human Description:
myosin VC [Source:HGNC Symbol;Acc:7604]
Mouse Orthologue:
Myo5c
Mouse Description:
myosin VC Gene [Source:MGI Symbol;Acc:MGI:2442485]

Alleles

There are 16 alleles of this gene:

Allele Name Consequence Status Availability
sa16770 Nonsense Available for shipment Available now
sa11146 Essential Splice Site Available for shipment Available now
sa14963 Essential Splice Site Available for shipment Available now
sa12025 Nonsense Available for shipment Available now
sa11888 Nonsense Available for shipment Available now
sa6792 Nonsense Mutation detected in F1 DNA Not yet available
sa6793 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa3291 Essential Splice Site F2 line generated Not yet available
sa37990 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9570 Nonsense Available for shipment Available now
sa25221 Nonsense Mutation detected in F1 DNA Not yet available
sa3298 Essential Splice Site Available for shipment Available now
sa44223 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa16770
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
ENSDART00000045539 Nonsense 241 1746 6 51
Genomic Location (Zv9):
Chromosome 25 (position 4805201)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4666443
GRCz11 25 4792871
KASP Assay ID:
2261-9296.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAGTTTCGATAAAAGATACCAAATCATTGGTGCCAACATGAGGACGTA[T/A]CTTCTGGAAAAGTCCAGGGTGRTGTTTCAGGTGAATATCATTCGAGAGAC
Long Flanking Sequence:
CAAAAAATGTAGATAAAGCATTTTTCGCATTGAAGAAATGCAGAATAACCAACAAACTTTATAGGCTGAGCTCAAAATGAGTGAGCTCATATTTTAGTGAAGCATCTTTTGTTCAACTTTCAGGAATAACAAAAATCAGTCCATCATTGTGAGCGGTGAGTCCGGGGCCGGAAAGACTGTATCTGCTCGCTATGCTATGAGATACTTTGCCATGGTCAGCAAATCCGGCAGCAAAACCCGAGTGGAGGACAAAGTTTTGGCGTCCAATCCGATCACTGAGGTAAAATGTTCGAAATCTAAGATCAGATCTTAGAATCATCATACAATTTCTTTTTTACTGATCTTATTATTATTATTATTAATTGGGATAATCGAATGCGCCTGCAGGCCATTGGAAATGCAAAAACAACCCGAAATGACAACAGCAGTCGATTTGGAAAGTACACTGAGATCAGTTTCGATAAAAGATACCAAATCATTGGTGCCAACATGAGGACGTA[T/A]CTTCTGGAAAAGTCCAGGGTGGTGTTTCAGGTGAATATCATTCGAGAGACGTGCTGAATAATAAATGTAGATTTCTCATTGTGTCTCGTTTGTTCTCCCTGCAGTCGGAGAACGAGAGAAATTATCACATCTTCTACCAAATGTGTGCTTGTGCAAATCAGCCGGAGTTCAAAGGCTTACGACTGTGTGAGTGTCTCTCTCCTGCACGTGTTACATCAGTCTTTAACGCAGCACAGAAATCAGCGGAGTTAAAAAATGGTTTGAGAGGTGTCGGCACCAGTGGTGTAGTGGTTAGTGCGTCAACACATGCACTCCGGTGCTCAGGGTGACCCGAGTTCAATACCTCCCTCGAAGACCTATGCTCATCCTTCCCCTTTCTCTGCTCCCCATGCTTTCCTGTCAATACTCTACACTGTCCTATCCATTACAGGTGAAAACCCAGAGAAAAAAAAAACTGTTTTGAGAGGATTGTGCACAATCCAGTCATAATTATAAGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11146
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
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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
ENSDART00000045539 Essential Splice Site 439 1746 10 51
Genomic Location (Zv9):
Chromosome 25 (position 4809498)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4670740
GRCz11 25 4797168
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTCCCTGGSAAACAGCATTCGTTTATTGGGGTCTTGGATATTTACGGG[T/A]ACGTCAAATTMAATTMAATTCAATTCAATTTAGCTTTATTTGTATAGCGC
Long Flanking Sequence:
CAAAAACAAAACGAAAAAACTGTGAGAAATTCTTAATTTAAAGATTCATTCATTCATTTTCCTTCGGCTTAGTCCCTTATTTAGCAGGGGTCTCCACTGCGGAATGAACCACCACCTATTCCAGCACACATACAAAAGTGTGTGATTTGAAATCAATGGTGCTTTAAAAACTCCTTATATCTGCTGTTCGTGAAATAGTGGGAACCCTGATGTTTACTCTGCTCCTTCTCCAGTCCAGAGACCCTCACCTGGCCATATTCTGCGACCTCATGGGCGTCAGCACGGAAAACATGAGCCGCTGGTTGTGTCATAGACGGATAGTCCTGTCAACAGAGACCGTAGTCAAACCGCAGCCCCGGGAACGTGCTGTCAATGCACGCGACGCTCTTGCTAAACACATCTACGCCCATCTTTTCAACTGGGTCATTCACAAAATCAACCACGCGCTGATGGTCCCTGGCAAACAGCATTCGTTTATTGGGGTCTTGGATATTTACGGG[T/A]ACGTCAAATTAAATTCAATTCAATTCAATTTAGCTTTATTTGTATAGCGCTTTTACAATGTATATTGTGTCAAAGCAGCTTCACATAAATGGTCATAGTAACTGGATCAGGGTAGTTCAGTTTTTAGTGTTTAAGTTCAGTTCAGTTTAGCTCAGTTCAGTGTGGTTTTAAGTCATTACTGAGAGTCCAAGCACTGAAGAGCAAATCCATCGATGTGTAGCTCTACAGATCCTGAACCATGGCGAAAGCGGAGAGGGAAAAAAACTTCACCAATAGGAGAGTGAAGAAAAAAAACCTTGAGAGAAACCACACTCAGTTCGGCAAGACCATTTTAAATTAAAAGAAATTTAATTTTTAAATTAAAGAAATCAGAATTTACTATGTTTACTTTAGCTAGTGAATTGAATTAATAAAAAAAAAAAAGTTTGCTTTTGGTAATCTTCAATCTGCTTCTGTGTTTTGATTGGCTGCTTCTCTGATGATGTTCAGCCACAGTATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14963
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
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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
ENSDART00000045539 Essential Splice Site 514 1746 13 51
Genomic Location (Zv9):
Chromosome 25 (position 4813036)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4674278
GRCz11 25 4800706
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTATTGTGTTAGTTTGTTTAYTARCAAAGTCTTTTYTGATATCYCGCA[G/A]TTCCCGCAAGGCACTGATAAAAACTGGCTGCAAAAACTGTACAATTTTCT
Long Flanking Sequence:
ATGAGGAGTGTCTGGTGAGAAGAAGAATAATGTGGAGAAAATATTCAGTCCTAACTAAAATGAAGAAAGGGATGGTTTATATTTAATTGCATAGCCCCGCCCACACTGTAATCTCATTGGTTTAAAACATATAAATCAAAACCTGAATATTAAGCAGCTGTGTTTTGATTGGCGGTTTTAAAAGATACAACTTCTAAATATATCACAGAAAAAATGTATCAAACATTTAAAATGTCTGTCGGTAAAATATTCTGTCTTAACTGTGATAAAAGAATGTGAAGAAGAGCTGGTTTATATTGTGTTGAGTAGCCCCACCCACATCAAATCATTGGTTCAAAACACCTCCCTGCTGAATATTAAGTAGCTATGTTCCGATTGGCTGTTTTAGAAGATACACATTCTGAAATGCATATAAATTAGATTTTAATAAACAGAATATGATTGATTTGTGTGTATTGTGTTAGTTTGTTTACTAACAAAGTCTTTTTTGATATCTCGCA[G/A]TTCCCGCAAGGCACTGATAAAAACTGGCTGCAAAAACTGTACAATTTTCTAGGCTCAAAGCCGCTGTTTGAGAAGCCTCGTTTGTCTAATGACTCTTTCATGATTCAGCATTTTGCTGATAAGGTGAGAAACTATTCATTTATTTGTTTGTTTGTTTATTTATTAAAAAAAATTAATTGCCATTTGATTGGCAACTCTAAAAATGCATTAAAAATAGTTTGGCAAAACTTTTAAAATTCCAAACCTATTATTTGAAAATTACAAACTTGTTCTGAAACATTGAAACATCAGGGGCTCTATTTTGACGGTCCATGCGCAGAGCGCAAAACGCAGGGCACAAACGCTTTCAGGGCGTGTCAGGACTTTTTTTAAGGACAATTTAAGGACGGGAAATCTGCCTTGCGCTTCAGTGCATGATCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTATAGGTGTGTTTTGAGAATAAACCAATTAGAGTCTCATCTCCCATTCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12025
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
ENSDART00000045539 Nonsense 785 1746 19 51
ENSDART00000045539 Nonsense 785 1746 19 51
Genomic Location (Zv9):
Chromosome 25 (position 4818358)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4679600
GRCz11 25 4806028
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGACARAGACGCAGCTTTCTGAACATCARACAGGCGGCTCTCATCAYR[C/T]AGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGASAGTTAAAACTTTCT
Long Flanking Sequence:
TTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAAGTCCAAACACATGCGCTAGAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGGATGTTTTACAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACGTGCTGGATTAGTTGGCGGTTCATTCCGCTGTGGTGACCCCGGATTAATAAAGGGACTCAGCCAACAAGAAAATGAATGAATAAAAATAACGTTGCTTTGAACAAAATCTCTTCTGCTCCATTTCAGGACTCCAATCAGTACAAGTTTGGTCGGACCAAGATCTTCTTCCGGGCCGGGCAGGTGGCGTATCTGGAGAAGCTGCGTTTAGATCATCTGCGAGCGGCTTGTGTGACCATCCAGAAGCACGTGAGGGGCTGGAGACAAAGACGCAGCTTTCTGAACATCAGACAGGCGGCTCTCATCATA[C/T]AGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGACAGTTAAAACTTTCTCTTTTTTCAATTTAATTAAATTTATTTAGCTTTTTTGGGGTATTTAGTATTGACGTACGGATGTAATTCCTGCAATAATTCAATCCTGGCATTGCCATGCAGAAAACAAATAAACCTTACACCTTAGATGCACAGTGACAGCTCAGGCGTTGAAGCAGGGCTGGGCTGCAATAGTGATCCAAAGACACTGCCGCGGTTTTCTGGTACGGAGGATTTACCAGCTCGTCCTGAGAGCTGCGGTCACCATACAGGCCTTCACCAGAGGATGGATGGCTCGCAAACGCTACAAAAAGGTAAAATGACTTCTTATTCTTTGTTTAATACCTTATTATTTGATATTGCTCTGTAATGATTATGTGTCTTTTTTGCGTCGTTGTAGATGGTGGCAGAACATAAGGCTCTGGTTCTGCAGAAATATGCTCGAGCGTGGCTGGTGCGCCGGCGGTTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11888
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045539 Nonsense 785 1746 19 51
ENSDART00000045539 Nonsense 785 1746 19 51
Genomic Location (Zv9):
Chromosome 25 (position 4818358)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4679600
GRCz11 25 4806028
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGACARAGACGCAGCTTTCTGAACATCARACAGGCGGCTCTCATCAYR[C/T]AGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGASAGTTAAAACTTTCT
Long Flanking Sequence:
TTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAAGTCCAAACACATGCGCTAGAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGGATGTTTTACAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACGTGCTGGATTAGTTGGCGGTTCATTCCGCTGTGGTGACCCCGGATTAATAAAGGGACTCAGCCAACAAGAAAATGAATGAATAAAAATAACGTTGCTTTGAACAAAATCTCTTCTGCTCCATTTCAGGACTCCAATCAGTACAAGTTTGGTCGGACCAAGATCTTCTTCCGGGCCGGGCAGGTGGCGTATCTGGAGAAGCTGCGTTTAGATCATCTGCGAGCGGCTTGTGTGACCATCCAGAAGCACGTGAGGGGCTGGAGACAAAGACGCAGCTTTCTGAACATCAGACAGGCGGCTCTCATCATA[C/T]AGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGACAGTTAAAACTTTCTCTTTTTTCAATTTAATTAAATTTATTTAGCTTTTTTGGGGTATTTAGTATTGACGTACGGATGTAATTCCTGCAATAATTCAATCCTGGCATTGCCATGCAGAAAACAAATAAACCTTACACCTTAGATGCACAGTGACAGCTCAGGCGTTGAAGCAGGGCTGGGCTGCAATAGTGATCCAAAGACACTGCCGCGGTTTTCTGGTACGGAGGATTTACCAGCTCGTCCTGAGAGCTGCGGTCACCATACAGGCCTTCACCAGAGGATGGATGGCTCGCAAACGCTACAAAAAGGTAAAATGACTTCTTATTCTTTGTTTAATACCTTATTATTTGATATTGCTCTGTAATGATTATGTGTCTTTTTTGCGTCGTTGTAGATGGTGGCAGAACATAAGGCTCTGGTTCTGCAGAAATATGCTCGAGCGTGGCTGGTGCGCCGGCGGTTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6792
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
ENSDART00000045539 Nonsense 840 1746 20 51
Genomic Location (Zv9):
Chromosome 25 (position 4818669)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4679911
GRCz11 25 4806339
KASP Assay ID:
554-4622.1 (used for ordering genotyping assays)
KASP Sequence:
GGATTTACCAGCTCGTCCTGAGAGCTGCRGTCACYATACAGGCCTTCACC[A/T]GAGGATGGAWGGCTCGSAAACGCTACAAAAAGGKNNNNTGACTTCTTATT
Long Flanking Sequence:
CCATTTCAGGACTCCAATCAGTACAAGTTTGGTCGGACCAAGATCTTCTTCCGGGCCGGGCAGGTGGCGTATCTGGAGAAGCTGCGTTTAGATCATCTGCGAGCGGCTTGTGTGACCATCCAGAAGCACGTGAGGGGCTGGAGACAAAGACGCAGCTTTCTGAACATCAGACAGGCGGCTCTCATCATACAGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGACAGTTAAAACTTTCTCTTTTTTCAATTTAATTAAATTTATTTAGCTTTTTTGGGGTATTTAGTATTGACGTACGGATGTAATTCCTGCAATAATTCAATCCTGGCATTGCCATGCAGAAAACAAATAAACCTTACACCTTAGATGCACAGTGACAGCTCAGGCGTTGAAGCAGGGCTGGGCTGCAATAGTGATCCAAAGACACTGCCGCGGTTTTCTGGTACGGAGGATTTACCAGCTCGTCCTGAGAGCTGCGGTCACCATACAGGCCTTCACC[A/T]GAGGATGGATGGCTCGCAAACGCTACAAAAAGGTAAAATGACTTCTTATTCTTTGTTTAATACCTTATTATTTGATATTGCTCTGTAATGATTATGTGTCTTTTTTGCGTCGTTGTAGATGGTGGCAGAACATAAGGCTCTGGTTCTGCAGAAATATGCTCGAGCGTGGCTGGTGCGCCGGCGGTTTCAAACCATGCGGCGGCTGGTCATTAATGTTCAGCTATCATACAGAGTCCAGCAGCTGCGTAAGAAAGTAGAGGAGCAGGTACAGTCATTCAAAAACACAGAGGAAAATGCGTATGTCAGTATGTCATTTTGACCACTAGAGGGCGGGTATTCACAACAAACAAAGACGTAGTTTGATCACAGCATGACTGGGTTTGGAATCATGGGAGTTGTAGTCTTCATTAAATCCTACAGGAGTACTGTATCTAGCGATCAATGCCATAAACCACTCAAACACCCTAGTAACTAACAATTAATGCCCTTAAACTAAACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6793
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045539 Essential Splice Site 850 1746 20 51
Genomic Location (Zv9):
Chromosome 25 (position 4818703)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4679945
GRCz11 25 4806373
KASP Assay ID:
554-5467.1 (used for ordering genotyping assays)
KASP Sequence:
YATACAGGCCTTCACCWGAGGATGGAWGGCTCGSAAACGCTACAAAAAGG[T/G]NNNNTGACTTCTTATTCTTTGTTTAATACCTTATTATTTRATATTGCTCT
Long Flanking Sequence:
GGACCAAGATCTTCTTCCGGGCCGGGCAGGTGGCGTATCTGGAGAAGCTGCGTTTAGATCATCTGCGAGCGGCTTGTGTGACCATCCAGAAGCACGTGAGGGGCTGGAGACAAAGACGCAGCTTTCTGAACATCAGACAGGCGGCTCTCATCATACAGCTGTACGTGCGCGGGAAGAAGCAGATCAGGTGACAGTTAAAACTTTCTCTTTTTTCAATTTAATTAAATTTATTTAGCTTTTTTGGGGTATTTAGTATTGACGTACGGATGTAATTCCTGCAATAATTCAATCCTGGCATTGCCATGCAGAAAACAAATAAACCTTACACCTTAGATGCACAGTGACAGCTCAGGCGTTGAAGCAGGGCTGGGCTGCAATAGTGATCCAAAGACACTGCCGCGGTTTTCTGGTACGGAGGATTTACCAGCTCGTCCTGAGAGCTGCGGTCACCATACAGGCCTTCACCAGAGGATGGATGGCTCGCAAACGCTACAAAAAGG[T/G]AAAATGACTTCTTATTCTTTGTTTAATACCTTATTATTTGATATTGCTCTGTAATGATTATGTGTCTTTTTTGCGTCGTTGTAGATGGTGGCAGAACATAAGGCTCTGGTTCTGCAGAAATATGCTCGAGCGTGGCTGGTGCGCCGGCGGTTTCAAACCATGCGGCGGCTGGTCATTAATGTTCAGCTATCATACAGAGTCCAGCAGCTGCGTAAGAAAGTAGAGGAGCAGGTACAGTCATTCAAAAACACAGAGGAAAATGCGTATGTCAGTATGTCATTTTGACCACTAGAGGGCGGGTATTCACAACAAACAAAGACGTAGTTTGATCACAGCATGACTGGGTTTGGAATCATGGGAGTTGTAGTCTTCATTAAATCCTACAGGAGTACTGTATCTAGCGATCAATGCCATAAACCACTCAAACACCCTAGTAACTAACAATTAATGCCCTTAAACTAAACAAACACCCTAAAAACTTAGGATAAATCCCCTAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3291
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045539 Essential Splice Site 899 1746 21 51
Genomic Location (Zv9):
Chromosome 25 (position 4818935)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4680177
GRCz11 25 4806605
KASP Assay ID:
554-2474.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAGCTATCATACAGAGTCCAGCAGCTGCGTAAGAAAGTAGAGGAGCAG[G/A]TACAGTCATTCAAAAACACAGAGGAAAATGCGTATGTCAGTATGTMATTT
Long Flanking Sequence:
TAGCTTTTTTGGGGTATTTAGTATTGACGTACGGATGTAATTCCTGCAATAATTCAATCCTGGCATTGCCATGCAGAAAACAAATAAACCTTACACCTTAGATGCACAGTGACAGCTCAGGCGTTGAAGCAGGGCTGGGCTGCAATAGTGATCCAAAGACACTGCCGCGGTTTTCTGGTACGGAGGATTTACCAGCTCGTCCTGAGAGCTGCGGTCACCATACAGGCCTTCACCAGAGGATGGATGGCTCGCAAACGCTACAAAAAGGTAAAATGACTTCTTATTCTTTGTTTAATACCTTATTATTTGATATTGCTCTGTAATGATTATGTGTCTTTTTTGCGTCGTTGTAGATGGTGGCAGAACATAAGGCTCTGGTTCTGCAGAAATATGCTCGAGCGTGGCTGGTGCGCCGGCGGTTTCAAACCATGCGGCGGCTGGTCATTAATGTTCAGCTATCATACAGAGTCCAGCAGCTGCGTAAGAAAGTAGAGGAGCAG[G/A]TACAGTCATTCAAAAACACAGAGGAAAATGCGTATGTCAGTATGTCATTTTGACCACTAGAGGGCGGGTATTCACAACAAACAAAGACGTAGTTTGATCACAGCATGACTGGGTTTGGAATCATGGGAGTTGTAGTCTTCATTAAATCCTACAGGAGTACTGTATCTAGCGATCAATGCCATAAACCACTCAAACACCCTAGTAACTAACAATTAATGCCCTTAAACTAAACAAACACCCTAAAAACTTAGGATAAATCCCCTAAAACCACTTAAACACTCTATTAATTAACAATCAATGCCCTAAAATCACTCAAACACCCTAGTAACTAACAAGCAATGCCTTAAAACCACTCAAACACTCTAGTAACTAACAATCAATGCTCTAAAACCACTCAAACACCCTAGTAACTAACACTCAATGCCCAAAAACCACTCAAACACCCAGGTAACTAACAATCAATGCCTTAAAAGCACTCAAATACCCTTAGTAACTAACGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37990
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045539 Essential Splice Site 954 1746 22 51
Genomic Location (Zv9):
Chromosome 25 (position 4821395)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4682637
GRCz11 25 4809065
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGCTTTAGTGCAGAGGGCGAAAACAAACTCAGAGGAGGCCAATCAG[G/A]TAAAAGTGCTACGCAATATCTTTGTAATATTGAAGATAATTTTGAGGATC
Long Flanking Sequence:
ACCCCTTCCAGTTGTTTAGCTTGTTTGTTTCGTTTCCAACCCAGGGGTATGAATAATTTCAGGCTTGACTGTGTATACTTTGCATTATACACTTAAAAAATGACTTTTGCTGTCAAACTATTTATTTAAAATTTGCTGAAACAACACAATCATTGACATTTTTTGGGGCAACAACTTAATTGTTTTATGTTCAATCCACTAAAATTTGTAAACTAAATTCCTTCATGTCGTTCCAACACAAATTGATTGCGTGGAACTCAGCATTTTTTACAGTGCACTTGTATCCTTTGAATGGTCTTTACAGTAAGTTATTTTATACAAAAACGTCTTCTTAGAATAAAGAGAACTGTGGCCTGATGGAGAAACTCACCAGCTTGTCTAACGCACGGGCTCAAGGGTTAGAAAAGATTCAGGCTCTGGAGGCGGAGCTGGGAAAACTGACCAATGAGATGTCAGCTTTAGTGCAGAGGGCGAAAACAAACTCAGAGGAGGCCAATCAG[G/A]TAAAAGTGCTACGCAATATCTTTGTAATATTGAAGATAATTTTGAGGATCTTCACTTTGCTTTCTTCTCTCGAAGGCAATCGATGTGCTTCAGAATGACAAAGAGAAGCTTGTTGAGGAAAATAAGGCTTTGGAGCGGAAACTCAAAGATACGACTGTGCAGATGCAAGGTAAAGAGTGGTCTGACTGATTTCAGAACAGTCAAAACGAAGACTGTAACTTTTGAAAAATCTGTTTTTCAGATCAATTTGAGGATGTGAAGCGGAAGCTGATGGAAGATTTAGAAAGAGAGGAAAGACTAAGAAAGTAAGATCTCTTTCTTAAAGCGACAGTTCACCCCAAAATCAATGTTGTTGCCCATCAATCTGATTTTCCAAATCTGTTCTCTGTTTTGTCAGGGTGGCAGAGCACAACAGTGAACTGCAGAAGGAAGACTCGGACAAAGAAATTGTGGCGATAAAAGAGGAAAACCGTAGACTGAGAGAGGAGCGAATCAGACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9570
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
ENSDART00000045539 Nonsense 1016 1746 25 51
Genomic Location (Zv9):
Chromosome 25 (position 4821818)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4683060
GRCz11 25 4809488
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAATCTGTTCTCTGTTTTGTCAGGGTGGCAGAGCACAACAGTGAACTG[C/T]AGAAGGAAGACTCGGACAAAGAAATTGTGGCGATAAAAGAGGAAAACCGT
Long Flanking Sequence:
CGGAGCTGGGAAAACTGACCAATGAGATGTCAGCTTTAGTGCAGAGGGCGAAAACAAACTCAGAGGAGGCCAATCAGGTAAAAGTGCTACGCAATATCTTTGTAATATTGAAGATAATTTTGAGGATCTTCACTTTGCTTTCTTCTCTCGAAGGCAATCGATGTGCTTCAGAATGACAAAGAGAAGCTTGTTGAGGAAAATAAGGCTTTGGAGCGGAAACTCAAAGATACGACTGTGCAGATGCAAGGTAAAGAGTGGTCTGACTGATTTCAGAACAGTCAAAACGAAGACTGTAACTTTTGAAAAATCTGTTTTTCAGATCAATTTGAGGATGTGAAGCGGAAGCTGATGGAAGATTTAGAAAGAGAGGAAAGACTAAGAAAGTAAGATCTCTTTCTTAAAGCGACAGTTCACCCCAAAATCAATGTTGTTGCCCATCAATCTGATTTTCCAAATCTGTTCTCTGTTTTGTCAGGGTGGCAGAGCACAACAGTGAACTG[C/T]AGAAGGAAGACTCGGACAAAGAAATTGTGGCGATAAAAGAGGAAAACCGTAGACTGAGAGAGGAGCGAATCAGACTGCAAACGCAAGTGGAGGAGGACGTGAAGACCAACACAGAACTGCAAGAGCAAATGCTGCAGCTCACCAAACACGTCAAGGTGGCGTATATAAAATGACAAGGCTTTAAAACACATTCTAGTAACGATATGAGGATTTTTAAACAGAAACTTAAAATAAAGTCCTTAACCTAGGAGGAGGAGTTCAAGTATTTTGGGGTTTTGTTCACAAGTGAGAGAAGGATGGAGCATGGGATTGACAGGTCGATCAGTACATCGACGTACCGGTCCATTGTGGTAAAGAAGGAGCTGAACCGAAAGGCAAAGCTCTCGATTTACAGGTCAATCTTTGTTCCTACTCTCACCTATGGTCATGAGCTTTGGGTCATGACCTAAAGAACAAGATCTCGAATACAAGCAGCCAAATTAGTTTGGTCTTCGCAGGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25221
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
ENSDART00000045539 Nonsense 1107 1746 27 51
Genomic Location (Zv9):
Chromosome 25 (position 4822912)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4684154
GRCz11 25 4810582
KASP Assay ID:
554-7422.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTATTGTTGTTGTTTTTGTTAGCTAAGATGAATCTGATCACGAGG[C/T]AGCTGCTTGGTGATGCTACAGAGCAAGATCTCATCCAGAGGTGTGTCAGA
Long Flanking Sequence:
TCTCACCTGTGACCCGACCCCAGAAAAGCAGATGAAAATGAATAAATGAACTTAAAAGACACATTTTTGAGATTCCCTATTATGTTTTTAAGTACTTGTGATGCATTTAAGATTGAAACATGGAATAAATGATACACGAATCAATAAATTTGTGCGTAAATATATAAAACTGAAAAAATTAATCTGAGAACATTTCCAAATAATCCATTCATTAAATGGCAATAAGTAAATGACTTATAGTGCAGATCATTTTTTTAGATATAAATGTTTTTATTTTTTGTATCATTTAAAGGTCATACCAGATTTACGTAAAGAAATCAACAACCTGCAGATTCAACGAGCTGAAGCTGAAAAAACCCTGAGAGCTCAAAATCTACAAGCCAGAGGTGCTAAACATTATTTAGCTCACATTCATGGTTTATGATTTGTCTTCTGAGCCATTTTCATATATTTTTTTATTGTTGTTGTTTTTGTTAGCTAAGATGAATCTGATCACGAGG[C/T]AGCTGCTTGGTGATGCTACAGAGCAAGATCTCATCCAGAGGTGTGTCAGAATATTAGGATTAACATTGCTAATTGTTATTAGGCAGTTTGGATTAGCTTCATTTGAATTTTCTTTTTTTTTTCCAGGCTCAATGAAGAAGCCTCTGATAATAACGATGATGGAGCTGATCTAATCACTGCTTTTGATGGCATGGAGCGAGCTGCTAAGTATGATTTAAATCTGCTTTTTTATTTTCTTGGACCAAATTTCGAAATTCATCTCTTGCAAAACTAGCTTAGGGAAAGCTAACAATGCCAACCATGATAGAAACATGCTTGTACAATCAAATTCATGTTAGCATTTCACTTTCTTAGACCATATTTCAAAACGCATCTCTCTTGTAAAACTAGCCCAAGGCATGCTAACAATGCTAATCATTTAAGAAACATGCTAGTAACATTGGTATTAATTCTAGCATTTTTATTTTCTTAGGCCAAATTTCAAAATGCATTTCTTGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3298
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045539 Essential Splice Site 1120 1746 27 51
Genomic Location (Zv9):
Chromosome 25 (position 4822953)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4684195
GRCz11 25 4810623
KASP Assay ID:
554-2739.1 (used for ordering genotyping assays)
KASP Sequence:
ATCACGAGGCAGCTGCTTGGTGATGCTACAGAGCAAGATCTCATCCAGAG[G/A]TGTGTCAGAATATTAGGATTAACATTGCTAATTGTTATTAGGNNCAGTTTGG
Long Flanking Sequence:
ATAAATGAACTTAAAAGACACATTTTTGAGATTCCCTATTATGTTTTTAAGTACTTGTGATGCATTTAAGATTGAAACATGGAATAAATGATACACGAATCAATAAATTTGTGCGTAAATATATAAAACTGAAAAAATTAATCTGAGAACATTTCCAAATAATCCATTCATTAAATGGCAATAAGTAAATGACTTATAGTGCAGATCATTTTTTTAGATATAAATGTTTTTATTTTTTGTATCATTTAAAGGTCATACCAGATTTACGTAAAGAAATCAACAACCTGCAGATTCAACGAGCTGAAGCTGAAAAAACCCTGAGAGCTCAAAATCTACAAGCCAGAGGTGCTAAACATTATTTAGCTCACATTCATGGTTTATGATTTGTCTTCTGAGCCATTTTCATATATTTTTTTATTGTTGTTGTTTTTGTTAGCTAAGATGAATCTGATCACGAGGCAGCTGCTTGGTGATGCTACAGAGCAAGATCTCATCCAGAG[G/A]TGTGTCAGAATATTAGGATTAACATTGCTAATTGTTATTAGGCAGTTTGGATTAGCTTCATTTGAATTTTCTTTTTTTTTTCCAGGCTCAATGAAGAAGCCTCTGATAATAACGATGATGGAGCTGATCTAATCACTGCTTTTGATGGCATGGAGCGAGCTGCTAAGTATGATTTAAATCTGCTTTTTTATTTTCTTGGACCAAATTTCGAAATTCATCTCTTGCAAAACTAGCTTAGGGAAAGCTAACAATGCCAACCATGATAGAAACATGCTTGTACAATCAAATTCATGTTAGCATTTCACTTTCTTAGACCATATTTCAAAACGCATCTCTCTTGTAAAACTAGCCCAAGGCATGCTAACAATGCTAATCATTTAAGAAACATGCTAGTAACATTGGTATTAATTCTAGCATTTTTATTTTCTTAGGCCAAATTTCAAAATGCATTTCTTGTAAAACTAGCCCAGGGCATGCTAACAATGTTAATCATTCAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44223
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
ENSDART00000045539 Nonsense 1558 1746 38 51
Genomic Location (Zv9):
Chromosome 25 (position 4836943)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4698185
GRCz11 25 4824613
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGAGACTCCAGCACGTCTGAGGCCTTCAGCGTCAGCTCCATCCTGCAG[A/T]AGCTCAGCACCTTTAACTCCAGCATGTGTCAGCAGGGCATGGAGCCGCAG
Long Flanking Sequence:
AAACTAAACTAAGTTAAAGTAATTAGGCAAGTCATTGTATAACAGCAGTTTGTTCTGTAGACGATCAAAAATAAATATTGCTTAAGCGGGCTAATAATATTGACCTAAAATGCTTTTAAAAAAGTAAAAACTGATTTTATTCTAGCCTAAATAAAACAAATAAGGCTTTCTCCAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAATGCATTCAAAGATAAAACTAATTTTCCCTTCAACTGTAAACGATGACAGAATATTCATCTCAAGGTGAACAAAGCCTTTAGGCGATCTTCTCTTGTCTCTCTCTTTAGTCCCAGGGATGCTGGAGCATGAAAGTCTCCAGGGAATCTCCAGCATGAAGCCCACCGGTCTCCGCAAGCGCTCCAGCAGTGTGTTTGAGGATGGCGGAGACTCCAGCACGTCTGAGGCCTTCAGCGTCAGCTCCATCCTGCAG[A/T]AGCTCAGCACCTTTAACTCCAGCATGTGTCAGCAGGGCATGGAGCCGCAGCTGCAGGGGCAGATCGTCAGACAGCTCTTCTACCTCATTGGCTCCTCATCCGTCAACTGCATCCTGCTCCGCAAGGACCTGTGCTCCTGCCGCAAGGGCATGCAGATCAGGTGCGTACATGTGTGTTCAAAGGTCACAGTAAAGACTAACCTAATGGTTAGAAAGTTGGACTTGTGATCGAAAGGTTGCAGGTTTGAGTCCCGGCCTTTGGGGCAGACTAATGGTTGGAGAGTTGGACTTGTGATTGAAAGGTTGCTGGTTCGAGTCCCGGCATTTGGGGCCACCATGGCCTAACTGTTAGAGAATTAGACTTGTGATCGAAAGGTTGCAGGTTGGAGAATTTGACTTGTGATCAAAGGTTGCGGGTTTGAGTCACAGCATTTGGGGCAGCCTAATGGTTTGAGAGTTATACTTGTGATCAAAAGGTTGCAGGTTCAAGTTCTGGCATTT
Associated Phenotype:
Not determined