Busch Lab

ZMP

flncb

Ensembl ID:
ENSDARG00000018820
ZFIN ID:
ZDB-GENE-041008-175
Description:
Novel protein similar to vertebrate filamin C, gamma (Actin binding protein 280) (FLNC) [Source:UniP
Human Orthologue:
FLNC
Human Description:
filamin C, gamma [Source:HGNC Symbol;Acc:3756]
Mouse Orthologue:
Flnc
Mouse Description:
filamin C, gamma Gene [Source:MGI Symbol;Acc:MGI:95557]

Alleles

There are 19 alleles of this gene:

Allele Name Consequence Status Availability
sa12735 Nonsense Available for shipment Available now
sa15601 Nonsense Available for shipment Available now
sa6929 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31379 Nonsense Available for shipment Available now
sa40229 Nonsense Mutation detected in F1 DNA Not yet available
sa20216 Essential Splice Site Available for shipment Available now
sa26231 Nonsense Mutation detected in F1 DNA Not yet available
sa33399 Nonsense Mutation detected in F1 DNA Not yet available
sa11171 Nonsense Available for shipment Available now
sa5246 Essential Splice Site F2 line generated Not yet available
sa45167 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11278 Essential Splice Site Available for shipment Available now
sa40230 Nonsense Mutation detected in F1 DNA Not yet available
sa7556 Missense Mutation detected in F1 DNA Not yet available
sa33400 Nonsense Mutation detected in F1 DNA Not yet available
sa20217 Nonsense Available for shipment Available now
sa38425 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12735
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Nonsense 65 2743 1 48
ENSDART00000134286 None None 2248 None 40
ENSDART00000026492 Nonsense 65 2743 1 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9129464)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10066222
GRCz11 4 10067032
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGAYCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGG
Long Flanking Sequence:
TTTTTGTGACGACGACAGAAAAGTGGCGAATGGAAGACTTTAAATACGATTGTTTTTAAACTGTTCGTGGCTTGAAGGTAATTCCAAGTGGTCTCTGTATGACAGATACTTTATTACTACTGACTTTTTTCGCAAACGCTTCCAACTTTCTTTCGTTTCTTTCCTTCTTTTTTCATCAGAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCGCGCCTGCCCCACTCCCCCCTCACGCTGTAAGAGTCTCGTAGTTTGTAGAATAAAAGGGGGCACGAAAACATCGGAAAAACATGATGAGCAATAATACATACTACGACCAGCAGCTGCCGCCGCAGTATTACCAGGGCACCGACAACGGCGAGGACGGAGACGAGGAGATGCCGGCCACGGAGAAGGACCTGGCCGAGGATGCGCCCTGGAAGAAGATCCAGCAGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGATCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGGCTCCTGGAAGTTCTCAGCCAGAAGAAAATGTACAGAAAGTACCACGCCAGACCCAATTTCAGGCAGATGAAGCTGGAGAATGTGTCAGTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGGTAAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCGAACGCACTTTGGTACAATGCCATGCCACTTAACTATTTATAACTATCATAAAAGTGTTTAAAAGGTTACAGAGTGCTTGTTACAAGTGATGTTTGAATGATCAATTAAGTGATGTGCTCGAGCTGCGTACTGTCGCTATGGTTACCTCATCAATTCGTCATGGTTTCTACTAAGTGCACTAGTAAGCTGACTTGTGTGGTTAGTGAAACGTTTCTAATCTTTCAACGTGTACTTATATAATGTAAACCTACTTTTAAAAGCCTCCTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15601
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Nonsense 65 2743 1 48
ENSDART00000134286 None None 2248 None 40
ENSDART00000026492 Nonsense 65 2743 1 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9129464)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10066222
GRCz11 4 10067032
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTRGAYCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGG
Long Flanking Sequence:
TTTTTGTGACGACGACAGAAAAGTGGCGAATGGAAGACTTTAAATACGATTGTTTTTAAACTGTTCGTGGCTTGAAGGTAATTCCAAGTGGTCTCTGTATGACAGATACTTTATTACTACTGACTTTTTTCGCAAACGCTTCCAACTTTCTTTCGTTTCTTTCCTTCTTTTTTCATCAGAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCGCGCCTGCCCCACTCCCCCCTCACGCTGTAAGAGTCTCGTAGTTTGTAGAATAAAAGGGGGCACGAAAACATCGGAAAAACATGATGAGCAATAATACATACTACGACCAGCAGCTGCCGCCGCAGTATTACCAGGGCACCGACAACGGCGAGGACGGAGACGAGGAGATGCCGGCCACGGAGAAGGACCTGGCCGAGGATGCGCCCTGGAAGAAGATCCAGCAGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGA[A/T]AGATCCTGGATCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGGCTCCTGGAAGTTCTCAGCCAGAAGAAAATGTACAGAAAGTACCACGCCAGACCCAATTTCAGGCAGATGAAGCTGGAGAATGTGTCAGTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGGTAAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCGAACGCACTTTGGTACAATGCCATGCCACTTAACTATTTATAACTATCATAAAAGTGTTTAAAAGGTTACAGAGTGCTTGTTACAAGTGATGTTTGAATGATCAATTAAGTGATGTGCTCGAGCTGCGTACTGTCGCTATGGTTACCTCATCAATTCGTCATGGTTTCTACTAAGTGCACTAGTAAGCTGACTTGTGTGGTTAGTGAAACGTTTCTAATCTTTCAACGTGTACTTATATAATGTAAACCTACTTTTAAAAGCCTCCTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6929
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Essential Splice Site 127 2743 1 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9129652)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10066410
GRCz11 4 10067220
KASP Assay ID:
554-4723.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGG[T/A]AAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCSAACGCAC
Long Flanking Sequence:
AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCGCGCCTGCCCCACTCCCCCCTCACGCTGTAAGAGTCTCGTAGTTTGTAGAATAAAAGGGGGCACGAAAACATCGGAAAAACATGATGAGCAATAATACATACTACGACCAGCAGCTGCCGCCGCAGTATTACCAGGGCACCGACAACGGCGAGGACGGAGACGAGGAGATGCCGGCCACGGAGAAGGACCTGGCCGAGGATGCGCCCTGGAAGAAGATCCAGCAGAACACCTTCACCAGGTGGTGCAACGAACACCTGAAATGCCTCAACAGAAAGATCCTGGATCTGCAGAAGGACCTGACCGACGGGCTCAAGCTCATCGGGCTCCTGGAAGTTCTCAGCCAGAAGAAAATGTACAGAAAGTACCACGCCAGACCCAATTTCAGGCAGATGAAGCTGGAGAATGTGTCAGTGGCGCTGGAGTTTCTGGAAAGGGAACACATCAAACTGGTTTCAATAGG[T/A]AAGTGCGCTTTCCTGGCATACATATGCGCTCAATGCGGTGGCGAACGCACTTTGGTACAATGCCATGCCACTTAACTATTTATAACTATCATAAAAGTGTTTAAAAGGTTACAGAGTGCTTGTTACAAGTGATGTTTGAATGATCAATTAAGTGATGTGCTCGAGCTGCGTACTGTCGCTATGGTTACCTCATCAATTCGTCATGGTTTCTACTAAGTGCACTAGTAAGCTGACTTGTGTGGTTAGTGAAACGTTTCTAATCTTTCAACGTGTACTTATATAATGTAAACCTACTTTTAAAAGCCTCCTCAAACGCTTTGGTTTAACTTTCTTTGGGGGGCCTCAAGATCCTAATTAGGGTGCTCAGACCCCACAAATCACAGATAATAAGCTGTTATGGCTCATAATGGGTGTGTTTTCTATTTTAACTGTAAATATTGTTTTTCATTCTTGTAATTCTGTTAATTATAATTTTGGACAATGTAAATCTTCTTCGGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31379
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Nonsense 278 2743 4 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9161999)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10098757
GRCz11 4 10099622
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACCTGTCGCAGTTCCCCAAAGCCAAACTCAAGCCTGGTGCACCACTG[C/T]GACCCAAAACTCTGCACCCCAAGAGAGCCAAGGCCTACGGACCAGGTCAG
Long Flanking Sequence:
ACGGGACTGAAGGGAGCGTAGAGACAGAAAATATTTTCCACAGCTCTCCTTAAGTGTACTTCATCAGTTTGTGCCGTAGACCATCACTATGTTTATATCTGACGATCGATTCTGGCAGTAGAAGTACTCAAAGGAAATGTCAAATAAAGACAGTGAGATGTGCTTCTTCATCTGTTTTAGCTCCTGAGGGCTGCGGCAATGGACATTTATGGTGTTTTGCCATCTGATAAAGCTATTATAGGTCAATGTTTCACTAATAGTAAATAAAATGACTTGTATTGAAGTGTTTGATGAGGAAAACATCCAAAATGTTGTACTAGTTTCCCCAAGAGCTTGACAGAGGAATTGGCACTATGACTGATCTCTAAGTTTGCACTCTGCTCTGTTTCATCCAGGTCATTGCTCCAGAGGAGATTGTGGATCCTAATGTGGACGAGCATTCGGTGATGACCTACCTGTCGCAGTTCCCCAAAGCCAAACTCAAGCCTGGTGCACCACTG[C/T]GACCCAAAACTCTGCACCCCAAGAGAGCCAAGGCCTACGGACCAGGTCAGACCAAAAAAAGATGATGTTAAAACTTTTGATTGGCAGACAGTGGTTATGAATCACGACTTTTACTGTAACACAAACTTCTGCATCTTTCATCTTCCTATAGGTATTGAGCCCAGAGGGAACGTTGTGTTGAAGCCAGCCGAGTTTGTGGTGGAGACCGTGGAGGCCGGGCTTGGAGAGGTGTTGGTCTACATTGAAGATCCAGAGGGACACACAGAAGAGGTCATCTACTAACTCAGCTCAACTTCTTTCATTGTCAAAGTCAAACGTCTTTCAGCCAGGGGTATTTACACATCGACTGGGTTTCTGGTTGCATTGGCTAAATTTAAGGCTATGTTTACACAGAAGTTTTACCATTGCATTTTAAAAGTTTCACTTTTAAGCAAGACCATTTTAAACAAAATCATTGGCATTTACATGTCCATGTAAATAGGTAAAAATGCTGAATTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40229
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
ENSDART00000026492 Nonsense 349 2743 6 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9163338)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10100096
GRCz11 4 10100961
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTAGAGTAATTCCCAACAATGACAGGAACAGGAGTTACTCTGTGGTGTA[T/A]GTTCCGAAAGTGGAGGGTTTGCATAAGGTACCAGTAAAATTAAGTAATAA
Long Flanking Sequence:
GAATCCTCAAAAATGTCTCAATTTATGTGCTTCCAGTCACAAAAATGCTCTTGCTGTGTAAACAAACAGGCAAAACACACAAAAGTTTCCAGTTTTGGGATAAAAATGTTGTAGTGGAAATGGCTCCTTACGTTAAATGAAATACTAGGATTTAATACAAACACATTTCATATTTCTTTTTAATGAACGGCACTTGTATTTTTTTTTTTTTTAAACTATTTTGCATTGTGGATCAAAAAATGTTACAAACAAATCACATGAATATAACTGAAAAATGGTCAAAACTTGTCGAAAAGGGCGGATTAAATGGGAATGTGTCTCTTTATGATGTGATGATTTAATCAAAATATATTACCGTGTACCGAGTGTACATACGATTAAAAAATATATGTTTTGACATCTAACTGATGAAATTAATCAAATCTAACTGATGAAAATTATTTTTCACAGGCTAGAGTAATTCCCAACAATGACAGGAACAGGAGTTACTCTGTGGTGTA[T/A]GTTCCGAAAGTGGAGGGTTTGCATAAGGTACCAGTAAAATTAAGTAATAACCAGTGTTAAAAATTTTGCTAATCATAAATTTCCAGGTGTATAATTATTTACAGTCTTCTTAAGTCTTCATATCAGTAGTTTTATTTCTGTTTTATTGTCTTGCAGGTGAAAGTTTTGTTTGCTGGACAGGACATTGACAGAAGCCCTTTCTTAGTAAATGTGTCTAAAGCACTGGGAGACCCAAACAAGGTGCAGGCCAGAGGGCCAGGTTTGGAACCGGTGGGCAACGTGGCCAATAAACCCACCTATTTTGACATCTACACTGCAGGTAATGTCAGGCAAATAATTCTGTTTGTTCTTAGACCCGAGAGCAGTTTAAGATCATCTGTGTATTTGTGACTCCTCAGGTGCAGGAGCAGGTGATGTTGGTGTGATCATTGTGGACTCTCAGGGCCGTAGAGACACAGTGGAGATCATTCTGGAAAACAAGGGTGACAGTGTTTTCCGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20216
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Essential Splice Site 479 2743 8 48
ENSDART00000134286 None None 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9163938)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10100696
GRCz11 4 10101561
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCGGCCAGCAAATACCCAGAAGTCCTTTCACTGTGCACATCTCAGAGG[G/T]TGAGACCCATGTCCTCACTTCTGGACTTAATTCCTTTAAGAAATGTATTG
Long Flanking Sequence:
TACAGTCTTCTTAAGTCTTCATATCAGTAGTTTTATTTCTGTTTTATTGTCTTGCAGGTGAAAGTTTTGTTTGCTGGACAGGACATTGACAGAAGCCCTTTCTTAGTAAATGTGTCTAAAGCACTGGGAGACCCAAACAAGGTGCAGGCCAGAGGGCCAGGTTTGGAACCGGTGGGCAACGTGGCCAATAAACCCACCTATTTTGACATCTACACTGCAGGTAATGTCAGGCAAATAATTCTGTTTGTTCTTAGACCCGAGAGCAGTTTAAGATCATCTGTGTATTTGTGACTCCTCAGGTGCAGGAGCAGGTGATGTTGGTGTGATCATTGTGGACTCTCAGGGCCGTAGAGACACAGTGGAGATCATTCTGGAAAACAAGGGTGACAGTGTTTTCCGTTGCACCTATGGCCCCATTCTGGAGGGCCCTCACACTATATATGTGACATTCGCCGGCCAGCAAATACCCAGAAGTCCTTTCACTGTGCACATCTCAGAGG[G/T]TGAGACCCATGTCCTCACTTCTGGACTTAATTCCTTTAAGAAATGTATTGATTTTCTGGAGTCATTTTGCAGTCACGTTGTTCTTTGGTACCTAAGCTGTTAATGCACCAAGAATACAACAAGTTCTTTGTTGACTTGATGTTTTTTGCTGCATTAAAAGCATGTCATGTGCTTTTTAAAATGTTTACTGCCCTCTCTGAAAAGGCCAGCTCAGACTAGTGTGGTAAAACTGCTTTACTTGCTGGTTTAGACGACTGGTGAAAACTCAAGGGCTAAATTCCGGATCTAATAAGTTTTATCAAGCTGGCTTTTTCAATGGGGGCATTATGCACAAATGGAGCTAGATTTTCCAAACTAAAGGTACGGTCACACTTATGATTAAATTTAATTAATCAAACAGGCAAAATTTACTCATTGGTAAAAGAGTGAAACGTTACACATGCAGACTTCTCTCATAATCATATTGTTTACAGAACTTCACCATGCTGACCAACAGAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26231
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Nonsense 509 2743 9 48
ENSDART00000134286 Nonsense 30 2248 1 40
Genomic Location (Zv9):
Chromosome 4 (position 9166894)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10103521
GRCz11 4 10104386
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGCCCAAGGGTGTACGTGTGAAGGAGGTGGCTGATTTTAAGGTTTA[C/G]ACGAAGGGAGCAGGCAGTGGAGAACTACGTGTTCATGTCAAGGGGCCAAG
Long Flanking Sequence:
CAAAACCCAACAGTAAGCCACACATTTCACATAAAAAAGCTGTTTTATTTGAGTAGAATATTGTTAAAGTTTGGTTATATGTTTCACAGCTGGCTCTTGTATCTAATTGCAAACATTGTATTCGTTTTAAGCTCGTGAAAACACTGCTCAGCTTGCCTGTAGTTTTACTATAGTGGTATCATACATTCCTAATGGGATTTTCATGAGATTGCTAATTGCATTGTCAACGAAACTTTCTGTCTTTGGTTGTTCTTCATTGCTCATTCTTTTGCTGGGCTCATATGCTGGACCATGCATCTAAACTAACTTTGACAAACATGTCTACGTTCATGTATGTACATTTCATGAGTCTTTTTCGCCTTCTTGTGCTTTTCTTTTGTGATCAGGAATAACCACAATTTGTTCTTTCTAGCAAGTAACCCCAATGCTTGTCGGGCAATTGGTCGTGGCCTGCAGCCCAAGGGTGTACGTGTGAAGGAGGTGGCTGATTTTAAGGTTTA[C/G]ACGAAGGGAGCAGGCAGTGGAGAACTACGTGTTCATGTCAAGGGGCCAAGTATGTATGCAACTGTTTTGACTTTAGCAATATTTGTGGAACTTATCAGTTTAAACAAAGTTAGTTTAGTTAGTTAGTCTGAATTAAACCCTGTCTTTTTAGCAGGTGGCGATGAGCCTGTGAAGGTGGAAGATTTGGGAGACGGTGTGTATGAATGTGATTACTATCCTATTTTCTGTGGAAAATACATCATCACCGTTACTTGGGGTGGCCATGCCATTCCCCGCAGGTAAGGGCCATTAGAAAACTCCAACAGTTTAACATAAGAAACAATTTGGAAATGTTATTTCCGAGCATTAAGCCTAACTATTTTCTGATTAAAAAAATATTTGTGCATAGTCCATTTGAGGTGATCATAAGTGAAGATGCAGGACCTCAGAAGGTGAGGGCATGGGGTCCAGGCTTGGAGACGGGCATGGTGGGCAAATCAGCTGATTTTGTGGTTGAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33399
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
ENSDART00000026492 Nonsense 711 2743 13 48
ENSDART00000134286 Nonsense 230 2248 5 40
Genomic Location (Zv9):
Chromosome 4 (position 9168046)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10104673
GRCz11 4 10105538
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTAAATAAACCTGCAGAGTTTACAATTGATGCCCGTGGAGCTGGAAGA[G/T]GACAGCTACAAATTTATGCTCAGGTACATTTTCATACAAGTCCCAGATGC
Long Flanking Sequence:
AGTTATAGGCAGATGTGTTTGATCACGGTTGGAGCTAAACTCTACAGGAAAGTGCCCAAATTGAGACCTACTCTATTATTGTAATAAAAATGCCTGAATAATTGGTCCAAACTTCCTTTCATGCACAGGCTTTTCCATCGAAGGGCCCTCGCAGGCTAAGATAGAGTGTGATGACAAGGGTGATGGCTCTTGTGATGTTTTGTACTGGCCCACTGAGCCAGGGGACTATGCAGTCCATGTCATCTGCGATGATGAAGATATTAAAGACAGCCCCTTTATGGCCCACATCCTCCCTGCAGCCAGTGACGTTTTCCCTGAGAAGGTCTGTTTTGTGGTGCTTGGCAATAATGATTGTACATTCAATAGGGATAATAAATAACTGTGGTACTGAAAGTCATGTTTTTATGCAGGTTAAGTGTTACGGCCCCGGGCTGGAGCCAACCGGGTGCATCGTAAATAAACCTGCAGAGTTTACAATTGATGCCCGTGGAGCTGGAAGA[G/T]GACAGCTACAAATTTATGCTCAGGTACATTTTCATACAAGTCCCAGATGCCTCATGCTTCACTTCACTGGTGCAAAAACCTTTTTGTCCTTCTTTTATCCAAGGACTCAGAAGGGTTTCCCATCAACATCCAGATCACAGATAACGGCGACAGCACATATTTCTGCGTCTATATACCCATCAAGCCCATCAAACACACTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGGGTGAGAGCTCACTGTCAACAGGCAAATTTCACCCGGCTGATGACATTTTTATGATGCTGTTGGTCAAGAACGTTCATAAATTGGATCTGCAGCAAGCTTAGCCTTTCAATGAAAGTTCATGACCACATTTTTCCAGTGTTAGATTTCACACTTTGCCTTTGCGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11171
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
ENSDART00000026492 Nonsense 728 2743 14 48
ENSDART00000134286 Nonsense 247 2248 6 40
Genomic Location (Zv9):
Chromosome 4 (position 9168177)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10104804
GRCz11 4 10105669
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTGTCCTTCTTTTATYCAAGGACTCAGAAGGGTTTCCCATCAACATC[C/T]AGATCACAGATWAYGGCGACAGCACATATTTCTGCGTCTATATACCCATC
Long Flanking Sequence:
TTTCCATCGAAGGGCCCTCGCAGGCTAAGATAGAGTGTGATGACAAGGGTGATGGCTCTTGTGATGTTTTGTACTGGCCCACTGAGCCAGGGGACTATGCAGTCCATGTCATCTGCGATGATGAAGATATTAAAGACAGCCCCTTTATGGCCCACATCCTCCCTGCAGCCAGTGACGTTTTCCCTGAGAAGGTCTGTTTTGTGGTGCTTGGCAATAATGATTGTACATTCAATAGGGATAATAAATAACTGTGGTACTGAAAGTCATGTTTTTATGCAGGTTAAGTGTTACGGCCCCGGGCTGGAGCCAACCGGGTGCATCGTAAATAAACCTGCAGAGTTTACAATTGATGCCCGTGGAGCTGGAAGAGGACAGCTACAAATTTATGCTCAGGTACATTTTCATACAAGTCCCAGATGCCTCATGCTTCACTTCACTGGTGCAAAAACCTTTTTGTCCTTCTTTTATCCAAGGACTCAGAAGGGTTTCCCATCAACATC[C/T]AGATCACAGATAACGGCGACAGCACATATTTCTGCGTCTATATACCCATCAAGCCCATCAAACACACTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGGGTGAGAGCTCACTGTCAACAGGCAAATTTCACCCGGCTGATGACATTTTTATGATGCTGTTGGTCAAGAACGTTCATAAATTGGATCTGCAGCAAGCTTAGCCTTTCAATGAAAGTTCATGACCACATTTTTCCAGTGTTAGATTTCACACTTTGCCTTTGCGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5246
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
ENSDART00000026492 Essential Splice Site 766 2743 14 48
ENSDART00000134286 Essential Splice Site 285 2248 6 40
Genomic Location (Zv9):
Chromosome 4 (position 9168294)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10104921
GRCz11 4 10105786
KASP Assay ID:
554-3500.1 (used for ordering genotyping assays)
KASP Sequence:
CTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGG[G/A]TGAGAGCTCACTGTCAACAGGCAAATTTCACCYGGYTGATGACATTTTTA
Long Flanking Sequence:
ATGATGAAGATATTAAAGACAGCCCCTTTATGGCCCACATCCTCCCTGCAGCCAGTGACGTTTTCCCTGAGAAGGTCTGTTTTGTGGTGCTTGGCAATAATGATTGTACATTCAATAGGGATAATAAATAACTGTGGTACTGAAAGTCATGTTTTTATGCAGGTTAAGTGTTACGGCCCCGGGCTGGAGCCAACCGGGTGCATCGTAAATAAACCTGCAGAGTTTACAATTGATGCCCGTGGAGCTGGAAGAGGACAGCTACAAATTTATGCTCAGGTACATTTTCATACAAGTCCCAGATGCCTCATGCTTCACTTCACTGGTGCAAAAACCTTTTTGTCCTTCTTTTATCCAAGGACTCAGAAGGGTTTCCCATCAACATCCAGATCACAGATAACGGCGACAGCACATATTTCTGCGTCTATATACCCATCAAGCCCATCAAACACACTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGG[G/A]TGAGAGCTCACTGTCAACAGGCAAATTTCACCCGGCTGATGACATTTTTATGATGCTGTTGGTCAAGAACGTTCATAAATTGGATCTGCAGCAAGCTTAGCCTTTCAATGAAAGTTCATGACCACATTTTTCCAGTGTTAGATTTCACACTTTGCCTTTGCGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACAGTGGACTGCAGTGAGGCTGGACAGGGTCAGAACCAACATCATTGATATCATTATTCTAATCTGCATTTTACATTTATTTAGTGATCATTACTTATTTGTCTTTTCCGATTCCATAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45167
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 None 803 2743 15 48
ENSDART00000134286 Essential Splice Site 322 2248 None 40
Genomic Location (Zv9):
Chromosome 4 (position 9168689)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10105316
GRCz11 4 10106181
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACAGTGGACTGCAG[T/C]GAGGCTGGACAGGGTCAGAACCAACATCATTGATATCATTATTCTAATCT
Long Flanking Sequence:
AACGGCGACAGCACATATTTCTGCGTCTATATACCCATCAAGCCCATCAAACACACTATCATCATCACATGGGGAGAGGTCAACGTTCCCAACAGTCCTTTCAGGGTGAGAGCTCACTGTCAACAGGCAAATTTCACCCGGCTGATGACATTTTTATGATGCTGTTGGTCAAGAACGTTCATAAATTGGATCTGCAGCAAGCTTAGCCTTTCAATGAAAGTTCATGACCACATTTTTCCAGTGTTAGATTTCACACTTTGCCTTTGCGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACAGTGGACTGCAG[T/C]GAGGCTGGACAGGGTCAGAACCAACATCATTGATATCATTATTCTAATCTGCATTTTACATTTATTTAGTGATCATTACTTATTTGTCTTTTCCGATTCCATAGGAGATGTAAGCATTGGGATTAAGTGCGCTCCTGGTGTGGTGGGACCTGCGGAAGCAGATATTGATTTTGACATCATTAAAAATGACAATGACACATTCACAGTGAAGTATACACCCCCTGGTGCTGGACGCTACACAATCATGGTGCTATTTGCAGATCAAGTAAGGCTCAGTCAATAATGTGATATGACTCATAAGCAATCTAAAATCTGAAATCTAAAATCTACTTTTTCAATTTACCAACAGGAAATTCCCATCAGCCCCTTCCGTATCAAAGTTGATCCATCTCATGATGCTAATAAGGTCAAAGCAGAGGGTCCTGGCCTCAACAAGACAGGTCTGTTTTATAGACAATGACTGAAAGTTTGCAAAATAATAGGTGAGGATATCTAATCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11278
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Essential Splice Site 861 2743 16 48
ENSDART00000134286 Essential Splice Site 375 2248 8 40
Genomic Location (Zv9):
Chromosome 4 (position 9168955)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10105582
GRCz11 4 10106447
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACCCCCTGGTGCTGGACGCTACACMATCATGGTGCTATTTGCAGATCAA[G/A]TAAGGCTCAKTCAATAATRTGATRTGACTCATAAGCAATCTAAAATCTGA
Long Flanking Sequence:
CGTGACCATGTTAGATCATAGGTTCCATATTGGATCATAAGCTTTACTAGAATCACTGTCCTCCATAAGATTTCAGTTACTACTTTTACAATATATTTATAAATATATAATTGACATATCTCAGGTGACCATTGGAGAAGGCAGTCACCCTGAGAATGTGAAGGTTCATGGACCAGGAGTAGAAAAGACTGGCTTAAAGGCCAACGAACCCACATACTTCACAGTGGACTGCAGTGAGGCTGGACAGGGTCAGAACCAACATCATTGATATCATTATTCTAATCTGCATTTTACATTTATTTAGTGATCATTACTTATTTGTCTTTTCCGATTCCATAGGAGATGTAAGCATTGGGATTAAGTGCGCTCCTGGTGTGGTGGGACCTGCGGAAGCAGATATTGATTTTGACATCATTAAAAATGACAATGACACATTCACAGTGAAGTATACACCCCCTGGTGCTGGACGCTACACAATCATGGTGCTATTTGCAGATCAA[G/A]TAAGGCTCAGTCAATAATGTGATATGACTCATAAGCAATCTAAAATCTGAAATCTAAAATCTACTTTTTCAATTTACCAACAGGAAATTCCCATCAGCCCCTTCCGTATCAAAGTTGATCCATCTCATGATGCTAATAAGGTCAAAGCAGAGGGTCCTGGCCTCAACAAGACAGGTCTGTTTTATAGACAATGACTGAAAGTTTGCAAAATAATAGGTGAGGATATCTAATCTCATCATAATTTATATGTCTATATCACAGGTGTGGAAGTGGGCAAGCCAACCCACTTTACAATCTACACTAAAGGAGCAGGCAAGGCCACACCTGAGGTTCACTTCACTGCATCTGGTAGAGGAGATGCTGTCAGTGACTTTGAGATCATCGATAACCATGACTATTCTTTCACTGTGCGCTACACTGCATTACAGCAGGTGAGACATTCTGGCACCAGGTTATAGTTCATATAAATGGACACTAAAGCCTGATTAATTCTTCTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40230
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
ENSDART00000026492 Nonsense 1267 2743 21 48
ENSDART00000134286 Nonsense 781 2248 13 40
Genomic Location (Zv9):
Chromosome 4 (position 9172420)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10109047
GRCz11 4 10109912
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGGGTTCAGGTAGATCCCGCTCTTGACACCAGTGGGATCAAGGTCTA[C/A]GGACCAGGAGTGGAGCCCAGAGGTAATATTAGATTTGTTTATGTGTGTAT
Long Flanking Sequence:
GCTGGCACAGGTGGTCTCGGTCTGACTGTGGAAGGCCCATGCGAAGCCAAAATCGAGTGCCAGGACAATGGAGATGGATCTTGCTCTGTGTCTTATCTGCCAACCGAACCTGGAGAGTATTCCATCAACATCCTGTTTGCTGATGCTCATATCCCAGGTTCCCCATTTAAAGCTATGGTGCAGTCCGTCTTTGACCCAAGCAAGGTCACAGCTAGTGGACCAGGTCTGGAGAGAGGAAAGGTTAATGAAGCGGGATCATTCACAGTCGATTGCTCTAAAGCCGGCGAGGCAGAGTTGACCATCGAGATTATTTCAGATTCAGGAGCGCAGGCGGAGGTTCATGTCCAGAACAACAGCGACGGGACATATTCGATCACCTACATCCCTCCTTTCCACGGAATGTACACTATCACAATTAAATATGGAGGACATGCAGTGCCAAAGTTCCCTGCAAGGGTTCAGGTAGATCCCGCTCTTGACACCAGTGGGATCAAGGTCTA[C/A]GGACCAGGAGTGGAGCCCAGAGGTAATATTAGATTTGTTTATGTGTGTATTTAGCATCACTGTGTTTAGCAATGTGCTATAAAATGGTATGTTTTTACAGGGGTGCTCCGAGAAGTTACTACACACTTCATTGTTGACACTCGGGTTCACAACAAAATGGGTGGAAACCACATCAAAGTTCGTATTGTTAACCCTTCAGGTGCCAACACTGATGCGTATGTCACTGACAAAGCAGACGGCACTTACAGAGTGGAGTATACTGCCTATGAGGACGGTAAGATTTCCAGTGAATAAATCAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTACATTACATTACATTACATTACATTACATTACATTACATTCAATTCAATTCAATTCAATTCAATTCAATTCATTTCATTACAATTCAATTCAATTCAATTCAATTAAAAAGTCCAACTGTTTGCATTGCCATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7556
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Missense 1287 2743 22 48
ENSDART00000134286 Missense 801 2248 14 40
Genomic Location (Zv9):
Chromosome 4 (position 9172556)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10109183
GRCz11 4 10110048
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTATGTTTTYACAGGGGTGCTCCGAGARGTTACTACRCACTTCRTTGTT[G/T]ACACTCGGGTTCACARCAARATGGGTGGAAACCACATCAAAGTTCGTATT
Long Flanking Sequence:
TTGCTGATGCTCATATCCCAGGTTCCCCATTTAAAGCTATGGTGCAGTCCGTCTTTGACCCAAGCAAGGTCACAGCTAGTGGACCAGGTCTGGAGAGAGGAAAGGTTAATGAAGCGGGATCATTCACAGTCGATTGCTCTAAAGCCGGCGAGGCAGAGTTGACCATCGAGATTATTTCAGATTCAGGAGCGCAGGCGGAGGTTCATGTCCAGAACAACAGCGACGGGACATATTCGATCACCTACATCCCTCCTTTCCACGGAATGTACACTATCACAATTAAATATGGAGGACATGCAGTGCCAAAGTTCCCTGCAAGGGTTCAGGTAGATCCCGCTCTTGACACCAGTGGGATCAAGGTCTACGGACCAGGAGTGGAGCCCAGAGGTAATATTAGATTTGTTTATGTGTGTATTTAGCATCACTGTGTTTAGCAATGTGCTATAAAATGGTATGTTTTTACAGGGGTGCTCCGAGAAGTTACTACACACTTCATTGTT[G/T]ACACTCGGGTTCACAACAAAATGGGTGGAAACCACATCAAAGTTCGTATTGTTAACCCTTCAGGTGCCAACACTGATGCGTATGTCACTGACAAAGCAGACGGCACTTACAGAGTGGAGTATACTGCCTATGAGGACGGTAAGATTTCCAGTGAATAAATCAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTACATTACATTACATTACATTACATTACATTACATTACATTCAATTCAATTCAATTCAATTCAATTCAATTCATTTCATTACAATTCAATTCAATTCAATTCAATTAAAAAGTCCAACTGTTTGCATTGCCATTCAGGATAATTAGTTTAATTACAAAAAAAAGTGAAATGTCAGGCCATAGTCAAACTCTGAATGTTGGTTTGTTGTTTCATAACTGAAGCTTATATGGCTTTCATAAAGTCTGTTATGCTGAAGCTGGTCCACCCTAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33400
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
ENSDART00000026492 Nonsense 1530 2743 26 48
ENSDART00000134286 Nonsense 1044 2248 18 40
Genomic Location (Zv9):
Chromosome 4 (position 9174543)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10111170
GRCz11 4 10112040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGTCTACACTCCTGCTAAAGATGGACCTTACACTGTGTGTGTCAAGTA[T/A]GCAGACCAAGAAGTGCCACGAAGGTGAGCGGACTGCTTTAATGTATTAAT
Long Flanking Sequence:
AAGACATTTAGAAGACATGATCATTTAATTTAGCAGTTGAATACTTACATACTTACAATACTTAGTTGAACATACCTGATTTATTGTTTTATAAAGAAAAACTAACCGTATGATTTCTGTGGGTATTTAGGTAGTCCATTTAGGGTGCCTGTAAGGGAGCTGGTGGACCCCAGTAAGGTCAAATGCACTGGTCCTGGTCTGGGCAGTGGAGTAAGAGCCCATGTCCCACAAACCTTCACTGTGGACTGCAGCAAGGCTGGACTCGCCCCACTGGAGGTTCTGCTGTATGGACCTACAGGTAAACAAAACATACTGGAATAGATTCATCAAGAGTGTTTTACAGTCGACTGGACAAGATGACAAACATGCAGAGAGACTAATTGTGTTGTTATTATTTTAGGGATGACAGAGCCGGTGAATATCACAGACAACGGCGATGGCACACATACAGTGGTCTACACTCCTGCTAAAGATGGACCTTACACTGTGTGTGTCAAGTA[T/A]GCAGACCAAGAAGTGCCACGAAGGTGAGCGGACTGCTTTAATGTATTAATCAAGTATTAATATTAATGCAGCACATAGACTGTGTGGTCAGACCAAAATGTCAATGCTGACTTTTTAACAAAAAGAGCACTTCAAGATCAAGGATGTATGTTTTTAGGATTATGAATCAAATTTGATTGTTGTGAATAATTGCTGAAACTATCATGATGTAGGGTATTATCACGATATTGGCCTAAGTTGCGAAGAAGGTTACTAAAATAATTAGCATATTGCTTCATGTTTATACATGTTTAGGACAGACAAATGCATCAACCAAACTGAAAAGCAAAAGAGTTATAAAGTACAATAGGTCACACTTTATAATCAAGTATCATTAGTAAATGTTAGTTAATGGAAACGGCAGATTTATTACAGTTGCTATGCTAATAATAGTTAAAAATACAACCCAAATATATTAGTTTTTAAGTCGTATTTAATAAAACAATCATGACTATTATTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20217
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026492 Nonsense 1936 2743 35 48
ENSDART00000134286 Nonsense 1449 2248 27 40
Genomic Location (Zv9):
Chromosome 4 (position 9180477)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10117104
GRCz11 4 10117974
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATGGCACCTGCACTGTATCCTACCTGCCAACGGCCCCGGGAGACTA[C/A]AACATAATCGTCAAATTTGATGACAAGCACATCGCTGGAAGCCCCTTTAC
Long Flanking Sequence:
TACTTGCTCTCTTTAGATCCCAATATTGAATGTTAAATTGAATACATAAACTGTCTTTTCTTTGTGATTATTCAAAAATATTAAAATTTAAAACTTTTTATTTTAAACTTTCAGTTAAATGATTAAAAAATACACTTTTAATAACTATTCCACAAATTCTGGCTCTCTTTTATTATTTCCCTACAGGAAGCCCACTGCAGTTCTATGTGGATGCCATTAACAGCGGGCATGTGAATGCATACGGCCCTGGTCTGAGTCACGGGATGGTCAACAAATCCGCTACATTCACAATCGTCACTAAGGATGCTGGAGAAGGTAATGCCCACAGCAAACCTACAATCCCCCCATTCACATTGCATTAGTTTCACATTGCACTCTCATCTTCTCCCAGGTGGTCTGTCATTGGCAGTGGAAGGACCCTCCAAGGCAGAGATCAGCTGTAAGGATAATAAAGATGGCACCTGCACTGTATCCTACCTGCCAACGGCCCCGGGAGACTA[C/A]AACATAATCGTCAAATTTGATGACAAGCACATCGCTGGAAGCCCCTTTACAGCCAAGATCACAGGTTTGTGTGTGCCCATATTTGGGTATGAGTAAGAGAGCAGGAGGATGAACAAGAGAGGGCAAAGTTATGTCTCTCCATAATGTCTGTGAATCACTAAATTAGCTGGCATGTGTGTTTATGTGTGTGCGCGTGCATTCACACCGGGAGAATTTAACCACATCTGTAAAGTGCTTCTAAAAGTAGGAGGCCCTTTCAGAGAGTTTTAAGAAACAGGAAGCAGCTGTTTCCCCCCTCCTTTAGTCTCACTCTCACTTTGCCCCTCAAAAAACGGTTCTAGTCTGCGGAAATAGGGTTGCACCCACAGAGCAAATGCTTATTTTAATAATTATATCATATTTGTTAATTATAATAATTATAAAAGAACTATTTTTACGTTTTGGCTAGGTTTACATGTTTGAATAAACTCACAAAGATTGCATTTGTTTGATCAGGATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38425
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
ENSDART00000026492 Nonsense 2558 2743 46 48
ENSDART00000134286 Nonsense 2063 2248 38 40
Genomic Location (Zv9):
Chromosome 4 (position 9190549)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 10127176
GRCz11 4 10128046
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCAGATTTCATTGTGAACACATGTAATGCTGGGTCAGGAGCTCTGT[C/A]GGTCACTATTGACGGCCCGTCCAAGGTGAAGATGGATTGTCAGGAGTGTC
Long Flanking Sequence:
TTTTAATGGGAGCCACATCCCAGGCAGCCCCTTCAAGATCCGAGTCGGGGAACCTGGTCAGGCAGGAGATCCAGGAATGGTGACTGCTTTTGGGCCTGGACTGGAGGGAGGAACGACAGGTATGACACCAACAAAAAGACCGTCTGTTAGTCAGGATTCTTGGTCCATGTGCTCATCAGATGGCAAAAGCAAATAATAAGATCATGATGACAATATTTTTATCATAATAAAAAGCCTAATCTCATATGGTTGGACAGTGATTCGTCTTAAATAAATGTTTAAAATATTGGACTGTAGTGTAAAATAATTTGCTTTAATGTGTGATATGATTAAACAGTGCTCATTTCTCAATTGGTTTGAGTAGAAGTTAGGACCTGGTAAAAGCAGTTTATGAGTGTTGAAATCCAAATGCAAAGGAACTCATTTGGTTGGGTCTTCTGTCTCAGGCGTACCATCAGATTTCATTGTGAACACATGTAATGCTGGGTCAGGAGCTCTGT[C/A]GGTCACTATTGACGGCCCGTCCAAGGTGAAGATGGATTGTCAGGAGTGTCCGGAAGGATACAAGGTCACCTACACACCTATGGCTCCCGGCAGCTACCTCATCTCCATCAAATATGGTGGACCGCAGCATATCGTGGGCAGCCCCTTCAAAGCCAAAGTCTCTGGTGAGTCACCAAACACCATATTTTTACTATGTATTTACCCTCGGAACTAAAATGTTTGGTGTAAGATCGGTGCAAGGACACACTCATGAAGCACATCTGAAGGTTTTAAGTTAATCTATATATATGTATTTAATTTAATATAATTAGTTTTATATTAGTTTATTTTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTAGTCTTGC
Associated Phenotype:
Not determined