Busch Lab

ZMP

f5

Ensembl ID:
ENSDARG00000055705
ZFIN ID:
ZDB-GENE-030131-5531
Description:
coagulation factor V [Source:RefSeq peptide;Acc:NP_001007209]
Human Orthologue:
F5
Human Description:
coagulation factor V (proaccelerin, labile factor) [Source:HGNC Symbol;Acc:3542]
Mouse Orthologue:
F5
Mouse Description:
coagulation factor V Gene [Source:MGI Symbol;Acc:MGI:88382]

Alleles

There are 13 alleles of this gene:

Allele Name Consequence Status Availability
sa13037 Nonsense Available for shipment Available now
sa21530 Essential Splice Site Available for shipment Available now
sa21531 Essential Splice Site Available for shipment Available now
sa41467 Nonsense Mutation detected in F1 DNA Not yet available
sa7198 Nonsense Mutation detected in F1 DNA Not yet available
sa13751 Nonsense Available for shipment Available now
sa13402 Essential Splice Site Available for shipment Available now
sa2508 Nonsense F2 line generated Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27434
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 41 2101 1 25
ENSDART00000128539 None None 406 1 26
Genomic Location (Zv9):
Chromosome 9 (position 35098486)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34317997
GRCz11 9 34127182
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTGGAGAGACATTACTATATTGCAGCTGTTAATATTAACTGGGACTA[C/A]ACATCTGGACAGCAAAGGTATGGCTTTCCATTGCTTGATCAGTGTATTTT
Long Flanking Sequence:
TAACCTGCATAGACATATTTTAAAATACACTGGCAAACATTTCCAGTAGAAGGAACTAATATGTGAATGACTAAATTTGCTCATGGCAACTTTCATGGTTTCATTCTTGCCAACAAAACATTTAATTACAATTCTTCCATTAAACAAAAGCCTCAGAGTACTAATGACTAAACAAAAACAAGAAGTTTCAGTTTTTTTTGATAATGATAGTGCACTGCCCTCGAACACAGTGTTTAAACATGCAAGTGCAGTGTGTCTGTGTGTGTGTACGCAATAGGGGGGTGGAGGGGAGATAAAACTCACTGCCATTTCTCTGAAAGTTCATACTTCTCTTCACTCCAGAACAGAACGTTTCTACCTGGAGTTTCATTTTTAAATATGAAACTCCGCTCCTGGCCAGGGGCCCTTCATGGTTTGGCCCTCCTGGCATTCCTGTGTCATTGTGCAACAGCTGTGGAGAGACATTACTATATTGCAGCTGTTAATATTAACTGGGACTA[C/A]ACATCTGGACAGCAAAGGTATGGCTTTCCATTGCTTGATCAGTGTATTTTAGAGATATTTATAGATTCTAGATATTTTTAAAGAGTTTTATGTATTGAATAATAACATATTTGTTTTAAAATGATTCGCTAGTGGAAAATTGCATTTTTCTAATTAATTAACATTGGTGTTTGGAATGAATATTTTAATCATGGTTGGAAAAACATTTAAATTTTTTTTAAAACTGTTAAACGTTACACTTTATTGATTGACAAAAATAATAATTGTTTAAAATAACAGAATCTTTCATAGAGTTTGTTATTTTGTTGTAATATTATACATGTACAGTCAATTTACTTTCCCTTTTGATTAATTTAACAAGCTTTTTATAAATAAATATATTTTAAGAGAGAGAAAGAAACTTCTACATTCTTTTTAATGGTATTTTATTACAGCACACTCAAAAATTCAATGCAGCACAACCTGAAAATAATAAGCAACGTTTCTTAAGCAGCAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13037
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
ENSDART00000078065 Nonsense 66 2101 2 25
ENSDART00000128539 None None 406 2 26
Genomic Location (Zv9):
Chromosome 9 (position 35101085)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34320596
GRCz11 9 34129781
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTAYACCGRTCACTTAACTTTAA
Long Flanking Sequence:
AATTTCAAATATCTATGTAACAAAATAGTTTTGTATACATATTTTTTCTATGTATGTGTATCACATATACATAATAATTACATATATATATATATATATATATGTATATGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21530
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Essential Splice Site 75 2101 None 25
ENSDART00000128539 Essential Splice Site None 406 None 26
Genomic Location (Zv9):
Chromosome 9 (position 35101193)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34320704
GRCz11 9 34129889
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGT
Long Flanking Sequence:
TGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21531
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
ENSDART00000078065 Essential Splice Site 115 2101 3 25
ENSDART00000128539 Essential Splice Site None 406 3 26
Genomic Location (Zv9):
Chromosome 9 (position 35101318)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34320829
GRCz11 9 34130014
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTT
Long Flanking Sequence:
AACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCCTTCAATGTTTCCATTAGGGTCTTTATACTTTGACAACACGTCACTCCTTGAGAAAAATGATGATGTAATTCAACCTGGTGAAGAGCACACTTACCAGTGGGACGTGACGTCTGATGTGACCCCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41467
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
ENSDART00000078065 Nonsense 195 2101 5 25
ENSDART00000128539 None None 406 5 26
Genomic Location (Zv9):
Chromosome 9 (position 35104061)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34323572
GRCz11 9 34132757
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGATTAATGTGTCCTTGTCCCACAGGCACCCTAGACGACTCAGGAAAT[C/T]AGATTCATTTCCATCAAGAGTCTGTGCTGCTGTTTGGAGTATTTGATGAG
Long Flanking Sequence:
ATGTAGCTTTCTTCAAAATATTTTCTTTTGTGTTTAACAAAATAGTTAATCAAATAGTTTTAAACAAGTAAAGGGGGTGAGTAAATGATGATGGCATTTTCATTTTTGGTTGAACTATTTCTTTAAACTAGACTAGATTCTAATGCATATCAATGAAGTCTCCATGGCTGATTCTGAAATGTTATTTCATAGTTAGTAAGAGAGGCTTAAGCCATGTTTGTTTCTCCTTTATGAAAGATCGAAGACACAGTACTCAACACAGTGTCTAACAAAGTGTGCAGTGTAAATTGGTCTTAATAAACCAATATACTGAATGATGCATCATCATAATCATCATCATTAACATCATCCTGCACAAGCTGAACTCATTTTCAAGCGTTACAGTGTAAATGCGTGCAGTTTTTTGAGTTTCCCAGAACTTATGCAACTATAAACAGCTCTGTTTGTTTAGATGATTAATGTGTCCTTGTCCCACAGGCACCCTAGACGACTCAGGAAAT[C/T]AGATTCATTTCCATCAAGAGTCTGTGCTGCTGTTTGGAGTATTTGATGAGAACAAGAGCTGGTACAGCACTGGGGACTCTCCACAGCCTCTGAATGTCAAATACACAATAAACGGCTACACAAATGGCTCAGTACCAGGTTGGTTCGATACAGTTTTTTGCAAAAGTCTTAGGCCACTAGCATTTTCACCAACAAAAAAAGTTTTGGTGTAGTATGCGAGTAGAAATATATTTTCCAAACATTATTTTTGCTATTTTTGATATTTATAGTCACCATCATCGAATACAACTTGAAAAACATGACGAAATAGAACAAACTGATACAGACTAAATCCAGTAGAACATCTTCAAGACACTTCAGGAACCTGACACTGTAAAAAGGTTTTAGGCACTTGTGTAAGAATGCTGTAAAGTGTGTATGCTTCAAAAATAATGCCTTAAAGGGGACCTATCATGCCGATTTTCTCAAGATGTAAAGTAAGTCTCTGATGTCCCTAGAGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa8345
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 325 2101 7 25
ENSDART00000128539 None None 406 7 26
Genomic Location (Zv9):
Chromosome 9 (position 35106910)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34326421
GRCz11 9 34135606
KASP Assay ID:
2260-2100.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTGATTATCWTGTGTGTAGCTGGTTTGCACGGGTACCTAAAKATCAGG[A/T]AGTGTGATGAGTATACGGCGCCAAAAAGACGGCTTACCATTGAACAGAAA
Long Flanking Sequence:
TACACCAACAAGACTTTTGCACAGTACTGAATTTCTCACATAACACGTTCATTTCTTGCAATCTGCTTACATGTAAAACTCCTCTCTGTCGTCCTCCAGATCTGGACATCTGTGCCCACTCTAAAGTCAGCTGGCACCTGCTGGGAATGAGCTCAGAGCCAGAGCTTTTCTCTGTACACTTCAATGGGCAAGTCCTTCTGCACGATGGGCACAAAACTTCAGCTGTTGGCATTATTAGTGGAACTGCCACCAGTGCCAGTATGACCGGTGTCCACCCTGGCCGCTGGCTCGTTTCCTCGCACATTAGCAAGCACTTGGAAGGTAAAACCTGCCAGAGAATACATGACACATTTATTCAATAAAAATCAACATTTGCATCCTGAACTCCACAGTTTCAGTATTAATGCTTATAGTTCGTACTTAAGGTGATTGCAGCGGCATTTGCTGAAAATGTGATTATCTTGTGTGTAGCTGGTTTGCACGGGTACCTAAATATCAGG[A/T]AGTGTGATGAGTATACGGCGCCAAAAAGACGGCTTACCATTGAACAGAAAAAAGAGAGTCAAGAGTGGACTTACTATATGGCAGCAGAAGAGGTCATCTGGGATTATGCGCCAAATATGCCAGAAAACATGGACGGGTATGTACATCATGACTTATCAAATAAGACAAGCTCTTGTATGACAATCTTATGGGTGTGTTTTTATCTCTTTTAAACTTAGGGATTTCCGGTCAAAATATTTAAAGCAGGGGCCTCAGCGGATAGGTAAAAAATATAAAAAAGCTGTGTTTACTCAGTATAAAGATGGCATGTTTAAAGAGAGAGCGGAAGATAAGCAGAGGAAGAGAGAGCTTGGAATTCTTGGCCCAGTGATTAGAGCTCAAATCAGAGACATCATTAAGGTAAACGGCTTCTCACGTTCATTTTACTTCAGGATAAAACGTAAACAGAATGTCTGATGGTTTTGGTCAGGATTCATGATTATTGTGATGTTGTTTCAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7198
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
ENSDART00000078065 Nonsense 630 2101 12 25
ENSDART00000128539 None None 406 12 26
Genomic Location (Zv9):
Chromosome 9 (position 35110453)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34329964
GRCz11 9 34139149
KASP Assay ID:
554-4876.1 (used for ordering genotyping assays)
KASP Sequence:
ATTACATCCAGACTGCTACTTTCTATGGTCATACATTTGAGCTAAAAAAC[A/T]GAGAAGAGGATATACTCAGTCTATTTCCTATGACKGGTGAAACTATCACG
Long Flanking Sequence:
CTTTTTTTTTTTTAGCTCACTGACAAACTACCATTAAAATGTTTGTAAAAGAGTTGCTCCTTATGTTAAATGTTTCAAAAAATGTGGCTTAAGCTGCTGTCAACACTTCTCTATTTCAGCTAAAAGCTGACAAGGAGCAGCATGCCATGTTTACCGTTTTTGATGAGAACAAGAGCTGGTACCAAGATGAGAACATTAACACATACTGCAGTGATCCCAAAAAAGTGAAGAAAGACGATCCCGAGTTTTACAAGTCAAATGTCATGCACAGTGAGTGATTTTCTGCTATTATTTCTGATATCATCATATTGCTGTTGATTGATATATGCTACGATGTGTTTATAAAAACTCTTACAGCAATCAATGGTTATGTATATGAAAGCGGCCAAGAATTGGGATTTTGTCATGGTGAAATTGTGACTTGGCATGTGTCGAGTGTTGGGGAACAGGATTACATCCAGACTGCTACTTTCTATGGTCATACATTTGAGCTAAAAAAC[A/T]GAGAAGAGGATATACTCAGTCTATTTCCTATGACTGGTGAAACTATCACGATGAACATGGTTAATATAGGTATGTTTGTCTGATTAGACTATCCAAATTACTTGTAATAAATTAGTTTTAGAATTTAAATATTAACTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGGAAATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5551
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 692 2101 13 25
ENSDART00000128539 None None 406 13 26
Genomic Location (Zv9):
Chromosome 9 (position 35110768)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34330279
GRCz11 9 34139464
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTYGAATGCTTCAGAGATTATGTAATAGAATATGWTTATGAGGAYGGG[A/T]AATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAA
Long Flanking Sequence:
TGATTGATATATGCTACGATGTGTTTATAAAAACTCTTACAGCAATCAATGGTTATGTATATGAAAGCGGCCAAGAATTGGGATTTTGTCATGGTGAAATTGTGACTTGGCATGTGTCGAGTGTTGGGGAACAGGATTACATCCAGACTGCTACTTTCTATGGTCATACATTTGAGCTAAAAAACAGAGAAGAGGATATACTCAGTCTATTTCCTATGACTGGTGAAACTATCACGATGAACATGGTTAATATAGGTATGTTTGTCTGATTAGACTATCCAAATTACTTGTAATAAATTAGTTTTAGAATTTAAATATTAACTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGG[A/T]AATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGTTTGTTGCCCATTGTTGAAGAAAAAAGCCTGGGATCAAGCAACGAGAACTTACACAATGCTACTTTACAATCTTTCATTGAGACTCATGGTTTATTAATGGAGGAAGGTGATTTAGACAAGGGAGAATCTTCTAATAAAGTCTTGAATGACAGCACAGACAAGGCATTGCTAGAGACAACAACTACTTTTGATTCCAATAGAGTTGTCGCATTAAACAACGAAACGGACAGTATAATTTTAGATTTTCCAATTGTAGAAAGAAAGGTTCGTAGTGCACCATCAAAGCCAATGAACGAACCTGAAAGTGTCACTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13751
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
ENSDART00000078065 Nonsense 799 2101 13 25
ENSDART00000128539 None None 406 13 26
Genomic Location (Zv9):
Chromosome 9 (position 35111089)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34330600
GRCz11 9 34139785
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTTTATTAATGGAGGAAGGWGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGWCTTGAATGACAGCACWGACAAGKCATTGCTAGAGACAACAACTACT
Long Flanking Sequence:
CTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGGAAATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGTTTGTTGCCCATTGTTGAAGAAAAAAGCCTGGGATCAAGCAACGAGAACTTACACAATGCTACTTTACAATCTTTCATTGAGACTCATGGTTTATTAATGGAGGAAGGTGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGTCTTGAATGACAGCACAGACAAGGCATTGCTAGAGACAACAACTACTTTTGATTCCAATAGAGTTGTCGCATTAAACAACGAAACGGACAGTATAATTTTAGATTTTCCAATTGTAGAAAGAAAGGTTCGTAGTGCACCATCAAAGCCAATGAACGAACCTGAAAGTGTCACTATGAACTTTAAAACAACAGAACATATCAATTCATCATTAGAGAGAATCAATGCTATATATTCCCCAATAACTGAAACAAACATCAACACAATGACTGAGACACACACTGATTTCAGTATCACTCCATTTGATGGTTCAACTGGAGAAATGAACTTCACACTAGAGGATGACACCGCACTTCTAAATTCATCTGAATCAGAGCCCCTGCAATCAAACCAAAACTCCGAAAACAGAATAGCTTTTCAAGAAGAGCTAAATGCAAAAGATGGCACAGATGTTGACAGTAATAATTCTGTGAAAAATCAGATCTTCAAATACAACGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13402
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Essential Splice Site 1467 2101 None 25
ENSDART00000128539 Essential Splice Site None 406 None 26
Genomic Location (Zv9):
Chromosome 9 (position 35114295)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34333806
GRCz11 9 34142991
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACRTTTTMAATAAATRAATCTAAARCTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAA
Long Flanking Sequence:
AAATTTACTGTAAAATAACAGTCCTTAAATTACAGAAATTTACCATAAAACAACGGCTGTTAAATTACAAAATTTCCTTAAATTTTTAATTTCCGGTAAATTTCTGTTTTTTAATATCTGTTATTTTACAGTAAATTTCTGTAATTTAACGGACGTTATTTTATGTCTTTTTCCAGTACCCTAGTACTAAACCGAAGGAGATGAATGAATAAATAGTGTTTTTTTTTTAAGTGAGACATTTAATTCCTAACTGAATTTGATGAGCCAAGACAAGTTTAGCATTTTTAACATATTAGGAATACAAATAAGACTGAATGTGTGCATGTTTTAAAATAATATTTGGAAATAATTAAAAATTATAACTTCCCACCTAGAATTCGACTACATCATTCTGTTTCTTCAAATGTTATTTAAAAATAAGTCCCTCAAAATCATCAGAATTTCTGGAGAACGTTTTAAATAAATGAATCTAAAACTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTACCTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACACCTGGGAATTCTTGGTCCGCTCATTAAAGCGGAAGTTGATCAGACCGTTATGGTAAACCACACACTTGTGAAGAAATCAGAATTGGAAAGCATCACGTCTATAAAATGAATATTAACAATTGCATTCTGGTTTTCCATGCTAGGTATTTTTCAGGAACCGTGCAAGTCGTCCATACTCTTTGCATGCAAATGGAGTAAAATACTTAAAACAAATGGAAGGCCTGAGTTATGATGATGAATCTCCATACTGGTACAAACAGGACGATGCTGTTCCACCCAATGGCACCTTTACCTACATGTGGACCATAAATCCCAAATCTGGACCTCAAAATAATGAATCTGACTGCCGAACTTGGACCTACTACTCTGCAGTGAATCCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2508
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 1489 2101 14 25
ENSDART00000128539 None None 406 14 26
Genomic Location (Zv9):
Chromosome 9 (position 35114363)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34333874
GRCz11 9 34143059
KASP Assay ID:
554-3064.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTA[C/A]CTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACA
Long Flanking Sequence:
AAAATTTCCTTAAATTTTTAATTTCCGGTAAATTTCTGTTTTTTAATATCTGTTATTTTACAGTAAATTTCTGTAATTTAACGGACGTTATTTTATGTCTTTTTCCAGTACCCTAGTACTAAACCGAAGGAGATGAATGAATAAATAGTGTTTTTTTTTTAAGTGAGACATTTAATTCCTAACTGAATTTGATGAGCCAAGACAAGTTTAGCATTTTTAACATATTAGGAATACAAATAAGACTGAATGTGTGCATGTTTTAAAATAATATTTGGAAATAATTAAAAATTATAACTTCCCACCTAGAATTCGACTACATCATTCTGTTTCTTCAAATGTTATTTAAAAATAAGTCCCTCAAAATCATCAGAATTTCTGGAGAACGTTTTAAATAAATGAATCTAAAACTAATTTGCTAATTCCTGTTTGCAAAGGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTA[C/A]CTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACACCTGGGAATTCTTGGTCCGCTCATTAAAGCGGAAGTTGATCAGACCGTTATGGTAAACCACACACTTGTGAAGAAATCAGAATTGGAAAGCATCACGTCTATAAAATGAATATTAACAATTGCATTCTGGTTTTCCATGCTAGGTATTTTTCAGGAACCGTGCAAGTCGTCCATACTCTTTGCATGCAAATGGAGTAAAATACTTAAAACAAATGGAAGGCCTGAGTTATGATGATGAATCTCCATACTGGTACAAACAGGACGATGCTGTTCCACCCAATGGCACCTTTACCTACATGTGGACCATAAATCCCAAATCTGGACCTCAAAATAATGAATCTGACTGCCGAACTTGGACCTACTACTCTGCAGTGAATCCTGTACGCATGAATCTTATCATAATATGGTTTTTATTCCTCCAAGGAGCAAGCCAATAATCACAGATTGCTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa373
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 1878 2101 21 25
ENSDART00000128539 Nonsense 197 406 22 26
Genomic Location (Zv9):
Chromosome 9 (position 35117681)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34337192
GRCz11 9 34146377
KASP Assay ID:
554-0245.1 (used for ordering genotyping assays)
KASP Sequence:
GCACTGACAAAAAGAAGTGGATCTACTACAAGGGAGACAGTGATGCTGTC[A/T]GAAAGGCAAGTGACTATTTTTGTGTATTAACCCATTGAATGCATGGATCA
Long Flanking Sequence:
ATAACAGCATCTGACACTAGAGGTAGGATCTGAAAGCATAGTTTGTGTTTATTTATTTGGGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGATGATATTAAAATTTACCTTTTTGATTAAGGACAATGGTATCCTCATTTGGCCAGACTTCATAATACAGGGAAATACAATGCATGGAGTACATCGTCAGAGCCAGGACAGTACTTACAGGTATAACCACTCACTTAGGATGGCGTGCAGATAATTAGCCCATAAATTGAGAAATGCTAATGACCAGTTATTTGAGAAGAGTGTATCCTGCTTTTCCAGGTGGACTTCCAGAGGCCGGTGGTGATTAGTAAAGTCGCCACACAAGGAGCCAAACAATTTTTGACACACAACTTTGTGTTGAACTACACCATTTCCTACAGCACTGACAAAAAGAAGTGGATCTACTACAAGGGAGACAGTGATGCTGTC[A/T]GAAAGGCAAGTGACTATTTTTGTGTATTAACCCATTGAATGCATGGATCACCATATATGGGCTGTTCACACTGAATGCATTTTTCCAATCCACTGTTGTGGTTCTCAACACTAGGGGGCCTCGGGAAACTTCTAAGGTCACCCTTCAAAATGACTTTACAACTGTTTAAAACAAACTAAATGGAGAAAAACAAAACCAGATGATAATTCTTTTCATTATCCTCCCCATCATAGCGTTTTTAAAAACTAGATAACACATATAATATAGTGTGAATTTTGGTAAAATAATGTGATACAATCATAAAAACAAATGCACATTTATTGGTTAAGTTTTAGAACATTTTATTGGGCTATTTTTTAAAAATCTGTATCCTTAAAGGGGTGGCTGACCCAAAAAAAGATTTTTTTGTAACATTATTTGCTGAAACTGTGGTTCTGGCCATTTAAAAAAGATGCAAGCCATAAAGCCAATAAATACCAGCACTCAAATTAATGATAATA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27435
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078065 Nonsense 1976 2101 23 25
ENSDART00000128539 Nonsense 281 406 24 26
Genomic Location (Zv9):
Chromosome 9 (position 35118668)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 34338179
GRCz11 9 34147364
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCCAGTTCTGTGGCATCCAACTGGTACTCCGGACAGTGGCATCCTTG[G/A]TATGCTCGCCTAAATAAACAAGGAACCGCCAATGCATGGCAAGCAAAGGT
Long Flanking Sequence:
AATTAATGATAATAGTTAAATGATGTTTTTACATAGCAGTATGTTTTTACGCTGATAATTTAAATGTATCAGTTTTTTTCTAAATCTGAACACATTCTGTGTGTGTGGCCCATAAGATATACACAAAACTAATGTATTTTTCAATGCCCGGCAGACTTTTGAAGGAAATGCTGAAGCTTATGAGACGAAGGAAAATATATTTTTCCCACCTCTGATTGGTCGATATGTGAGACTGCATCCTTTACATTCTTACAACTTCCCGACTGTCCGTTTGGAGTATTATGGTTGTGAGCTTGATGGTATGGATGAAAATAAAACAGATTTTTTTTATTCATATTACTTTTTAAACACAAAATCTGTCTTTGTTGTCATTAATGTCTTCATTGTGTGCTGGCAGGCTGCTCTGTGCCATTAGGAATGGAAAAAGGTCTTATTGATGACAGTAAAATCACTGCCAGTTCTGTGGCATCCAACTGGTACTCCGGACAGTGGCATCCTTG[G/A]TATGCTCGCCTAAATAAACAAGGAACCGCCAATGCATGGCAAGCAAAGGTAAAGACATTAAGAAATCATTAATTAAGCCTTTGGTATCGCATTAATACCATAAAACTTCAACTGATGGTCTTAATAACTGTCTGCAATCTACAGAACAATGACATTCAGCCTTGGATCCAGGTGGAACTCAAAGAAGTAAAGAAGATAACTGGAATTGTAACACAGGGAGCCAAATCAATGGGCAATGAAATGTTTGTGAGATCTTATATTTTGGAATATAGTGAAGATGGCAGGCGATGGATGAAGTACACAGATGATGATGATTATGAGCAAAAGGTATGAGGCTTCTCATGTGTTCGTTTATTTACATTTTTTGGTTTCTTCACAATGACAAAGTGACTTCTTGACTTTTACAGCTATTTCAAGGCAACACAGATAACAATGGCCAAATAAAGAACTACATCTACCCGCCGATATTTTCCAGATTCATCAGAATAATACCAAAACAA
Associated Phenotype:
Not determined