Busch Lab

ZMP

LOC100331716

Ensembl ID:
ENSDARG00000078270
Human Orthologue:
MAST4
Human Description:
microtubule associated serine/threonine kinase family member 4 [Source:HGNC Symbol;Acc:19037]
Mouse Orthologue:
Mast4
Mouse Description:
microtubule associated serine/threonine kinase family member 4 Gene [Source:MGI Symbol;Acc:MGI:19188

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa5747 Nonsense F2 line generated Not yet available
sa2208 Nonsense F2 line generated Not yet available
sa25312 Nonsense Mutation detected in F1 DNA Not yet available
sa13693 Essential Splice Site Available for shipment Available now
sa9036 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15684 Nonsense Available for shipment Available now
sa33719 Essential Splice Site Available for shipment Available now
sa20534 Essential Splice Site Available for shipment Available now
sa30865 Nonsense Mutation detected in F1 DNA Not yet available
sa40562 Nonsense Mutation detected in F1 DNA Not yet available
sa16213 Nonsense Available for shipment Available now
sa13456 Nonsense Available for shipment Available now
sa26579 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa5747
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088325 Nonsense 61 1327 3 29
ENSDART00000088325 Nonsense 61 1327 3 29
Genomic Location (Zv9):
Chromosome 5 (position 55555431)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54359742
GRCz11 5 54982578
KASP Assay ID:
554-2624.1 (used for ordering genotyping assays)
KASP Sequence:
GGTATATGGACTAAGAGTTTTCTGYGTTTGTAGAACTGATGGGCGACGCT[G/A]GTCCTTGGCATCTCTTCCCTCTTCTGGCTATGGAACAAACACACCCAGCT
Long Flanking Sequence:
TGAGACCTGGACGTAAGATTCATGAGATTCACTCTGTTATACTTGTACATATTTCTCAGAATTCAACCATAGTGCATCGCAACCTCACTTGACATGATATTGACATCAAGTGTCTGCACAACCATTTTTGGGCATTTTCTGTATGTATTCGGCACATGCAACTCTCCTCCCTGTGTTTGTGGCATTTGTCTTCCTGTGATTATCATTAGATCATTCAGTCAGCCAGAAGAAATGGCTCACAGCGCACTGCTCCAAAAGATAGCAGCCCCAGCTCATGGGTTACACTGCCACTGTCTTTCATCTGCTCTACTCTGAAAATGAATGACAAACTCAGCATTTTCTTTTTATCTAGTGTACCACTTGCTTCTCATGTCTTTGAGCCAATGGAATGCAATCTAGTATATACAGTTTGCAGATGATGATTCTAAACAGTGGCAATAACTATTTAAAGGTATATGGACTAAGAGTTTTCTGCGTTTGTAGAACTGATGGGCGACGCT[G/A]GTCCTTGGCATCTCTTCCCTCTTCTGGCTATGGAACAAACACACCCAGCTCTACAGTCTCTGTAAGTACTCCATGTTTTTCATACTGTATTGGTTAAGTGTGCATACACGTTTCCACCATAAGAAAATCTAGAAGACCAACCTGCAAGCAAAAGCAAACATATAAAGAATAAAAAGTTGGTATCAAGCCAATAAATCACTCTTAGTATGAATGCACCCCTAAAGCCCAGGCATACTTTTTTGTTCTCTATGGGCTCTATTTGACGGTCCATGCGCAGAGCGCAAAACGCAGGGCACAAACGCTTTCAGGCCGTGTCAGAACGCATTTTTGCTAATTTAAGGACGGGAAAACCCGCTTTGCGCCATGGCGCATGGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTATAGGTGTGTTTTGAGAATAAACCAATTAGAGTTTCATCTCCCATTACCTTTAAAAGCCAGCTGCGTTGTGCGCCATAAGCGCATTTTAACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2208
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088325 Nonsense 61 1327 3 29
ENSDART00000088325 Nonsense 61 1327 3 29
Genomic Location (Zv9):
Chromosome 5 (position 55555431)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54359742
GRCz11 5 54982578
KASP Assay ID:
554-2624.1 (used for ordering genotyping assays)
KASP Sequence:
GGTATATGGACTAAGAGTTTTCTGYGTTTGTAGAACTGATGGGCGACGCT[G/A]GTCCTTGGCATCTCTTCCCTCTTCTGGCTATGGAACAAACACACCCAGCT
Long Flanking Sequence:
TGAGACCTGGACGTAAGATTCATGAGATTCACTCTGTTATACTTGTACATATTTCTCAGAATTCAACCATAGTGCATCGCAACCTCACTTGACATGATATTGACATCAAGTGTCTGCACAACCATTTTTGGGCATTTTCTGTATGTATTCGGCACATGCAACTCTCCTCCCTGTGTTTGTGGCATTTGTCTTCCTGTGATTATCATTAGATCATTCAGTCAGCCAGAAGAAATGGCTCACAGCGCACTGCTCCAAAAGATAGCAGCCCCAGCTCATGGGTTACACTGCCACTGTCTTTCATCTGCTCTACTCTGAAAATGAATGACAAACTCAGCATTTTCTTTTTATCTAGTGTACCACTTGCTTCTCATGTCTTTGAGCCAATGGAATGCAATCTAGTATATACAGTTTGCAGATGATGATTCTAAACAGTGGCAATAACTATTTAAAGGTATATGGACTAAGAGTTTTCTGCGTTTGTAGAACTGATGGGCGACGCT[G/A]GTCCTTGGCATCTCTTCCCTCTTCTGGCTATGGAACAAACACACCCAGCTCTACAGTCTCTGTAAGTACTCCATGTTTTTCATACTGTATTGGTTAAGTGTGCATACACGTTTCCACCATAAGAAAATCTAGAAGACCAACCTGCAAGCAAAAGCAAACATATAAAGAATAAAAAGTTGGTATCAAGCCAATAAATCACTCTTAGTATGAATGCACCCCTAAAGCCCAGGCATACTTTTTTGTTCTCTATGGGCTCTATTTGACGGTCCATGCGCAGAGCGCAAAACGCAGGGCACAAACGCTTTCAGGCCGTGTCAGAACGCATTTTTGCTAATTTAAGGACGGGAAAACCCGCTTTGCGCCATGGCGCATGGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTATAGGTGTGTTTTGAGAATAAACCAATTAGAGTTTCATCTCCCATTACCTTTAAAAGCCAGCTGCGTTGTGCGCCATAAGCGCATTTTAACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25312
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
ENSDART00000088325 Nonsense 110 1327 4 29
Genomic Location (Zv9):
Chromosome 5 (position 55549903)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54354351
GRCz11 5 54977187
KASP Assay ID:
554-7698.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCCAGCCCACACCAGATGAGCTGCACTTCCTGTCCAAGCATTTCTA[C/A]ACAGAGAGCATTTCTGGAGATGACCACAGAAGAGTCACTCCTATGCGGCC
Long Flanking Sequence:
ACAATTGAGAACTCAAAGTTAAATTCACTCATAAAGAACCATAGTTTTAGGTCAATTACGATTAACACGATTTTCGACTAGTGTTGACTATAGATGGAGCTTCTCGGTATAGTTTAAAAAGAACATCAGAAAGTTAATTTTGGATTAAAATGAATTAACTACCCCGTATCTCGACCTAAATGCATATTGACAGCGTTTTTTTTTCTGCCCTACACCATTGTAGGATCACATCATCTTTAAGAAGCAGGAAAACAATAAACCTCCATTGCTGCATTTTAATTTTAATCCATCATCCGCATTATCATCACGTGATGTGTAATTAAACACATCAATAGTCATTGTTCTCGTGTTTTCATTCCATTTCATTTCTCTTCTTTTCTTTTCTTTTTCAATGTATTTTCGTTTCATTTCCAGTCGTCCTGTTCATCACAGGAGAAGCTCCATCAGCTGCCTTTCCAGCCCACACCAGATGAGCTGCACTTCCTGTCCAAGCATTTCTA[C/A]ACAGAGAGCATTTCTGGAGATGACCACAGAAGAGTCACTCCTATGCGGCCACGGTCTCGCAGTCTCAGGTACAGAAAACAGTGTGCTTTTTTTTTCTGTTCTGTTAACTTCCTACATCTAATTTTTCATACAAACTGCTCTGTAAATATGCAACTCAAAGGATATTTAATGCAAATTCAATTCTTATGCTAATTGAAAAGCTAATGCATATGCTTGTTTATTTTTTGTAATTTTACCATCTTTCCAATGAAAAGAAATGACATTAAACATACATATTTTTGGTAGTGACGTTGTGCGCCGAGGTTTCGAAGCATGTTCCAAAAAAAAACATACATTTCACAATGAAGCAGTGTACCGGAGCTTGATTTGTTTTGCCATCATCACTTGTTCAGTGATGTCCGAAGCTTAATTTTCGCCTATACCCACGTGACAGCTTGGAATTCTGATTCAAAAGTTTAAACACCCTCATGGGTTAGTAAAGTGTATAGTGAGAGATTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13693
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
ENSDART00000088325 Essential Splice Site 229 1327 7 29
Genomic Location (Zv9):
Chromosome 5 (position 55547159)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54351614
GRCz11 5 54974450
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGCATGCGTTTAGATGGCCACTTCTGATGTGTTCTGTCATTGTAAWGC[A/C]GTCGACTGAGCGATCGGAGAGTGCAGAGGTGACCTTCATTAAGGAGCTAG
Long Flanking Sequence:
AACCATGTGTACAAAGAAAGATTTCCCAAGGTGAGTGTTCACCAATCCTCCTCGGTGTCAAGTGATTGCATATTTAAAGGGGAATTCATTGTGGGTTTGTTTTTTCCACCCTTCAGGCCACAGCTCAGATGGAGGAGCGCATCAAGGAGATCATTCAAAGCAACTCCCCTGAGAACGTCTTGCCTCTGGCTGATGGTGTCCTCAGCTTCGCACACCATCAGATCATTGAACTGGCCAGAGACTGCCTGGAAAAGTCCCGCCTTGGCCTCATTACCTCACGATACTTTTGTGAGCTCACAGATAAACTGGAAAGGCTCTTTCATGAGGTAAATGAAACCTCCAGGGACGGCGCTTTCTTGATTCTTTTGAGCTGAAACTAGCTTTCTGTTTTTAAAACACGTTTCCCCATGTGTATACTTTTATCTCAAGTCTCTGATCATTGGTTTTATTGATGCATGCGTTTAGATGGCCACTTCTGATGTGTTCTGTCATTGTAATGC[A/C]GTCGACTGAGCGATCGGAGAGTGCAGAGGTGACCTTCATTAAGGAGCTAGTGAAGAAGATTCTCATTGTCATCGCCAGGCCTGCGCGACTGCTTGAATGTTTGGTAGGTTGTGTTTTTGCTTCTGTCCGTTGTCAGATCAGTATGACAAAATGAGACCTAATGGACATTTTTGTACATTTCATTTTATATATTAGCAGTGGGACAGTTTGGTTAGGTTTGTATGATGGTTATGTAGTCACTGTTTTCATTTTGATTCAGTTTACATTGAAATAAATGGGTCTCCTAACCAAGGTTATTATAGTTAATGAAAAAGAACAAAAAAACGGAACCGGAGTCACGTTCTTGGCAGGGTCATTGAACCCTGTATAAATTATGAATAAGGTCAAAGATTACTGGCTTTGAATGTTGTTTTTTAATTCTTTATTCAAACACTTTATAAAAAAGAAACCTTTTTTTCAATTGGTTGTTGTTTTTGTACAGAGATAAAATTAGCTTGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9036
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088325 Essential Splice Site 229 1327 7 29
Genomic Location (Zv9):
Chromosome 5 (position 55547159)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54351614
GRCz11 5 54974450
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGCATGCGTTTAGATGGCCACTTCTGATGTGTTCTGTCATTGTAATGC[A/C]GTCGACTGAGCGATCGGAGAGTGCAGAGGTGACCTTCATTAAGGAGCTAG
Long Flanking Sequence:
AACCATGTGTACAAAGAAAGATTTCCCAAGGTGAGTGTTCACCAATCCTCCTCGGTGTCAAGTGATTGCATATTTAAAGGGGAATTCATTGTGGGTTTGTTTTTTCCACCCTTCAGGCCACAGCTCAGATGGAGGAGCGCATCAAGGAGATCATTCAAAGCAACTCCCCTGAGAACGTCTTGCCTCTGGCTGATGGTGTCCTCAGCTTCGCACACCATCAGATCATTGAACTGGCCAGAGACTGCCTGGAAAAGTCCCGCCTTGGCCTCATTACCTCACGATACTTTTGTGAGCTCACAGATAAACTGGAAAGGCTCTTTCATGAGGTAAATGAAACCTCCAGGGACGGCGCTTTCTTGATTCTTTTGAGCTGAAACTAGCTTTCTGTTTTTAAAACACGTTTCCCCATGTGTATACTTTTATCTCAAGTCTCTGATCATTGGTTTTATTGATGCATGCGTTTAGATGGCCACTTCTGATGTGTTCTGTCATTGTAATGC[A/C]GTCGACTGAGCGATCGGAGAGTGCAGAGGTGACCTTCATTAAGGAGCTAGTGAAGAAGATTCTCATTGTCATCGCCAGGCCTGCGCGACTGCTTGAATGTTTGGTAGGTTGTGTTTTTGCTTCTGTCCGTTGTCAGATCAGTATGACAAAATGAGACCTAATGGACATTTTTGTACATTTCATTTTATATATTAGCAGTGGGACAGTTTGGTTAGGTTTGTATGATGGTTATGTAGTCACTGTTTTCATTTTGATTCAGTTTACATTGAAATAAATGGGTCTCCTAACCAAGGTTATTATAGTTAATGAAAAAGAACAAAAAAACGGAACCGGAGTCACGTTCTTGGCAGGGTCATTGAACCCTGTATAAATTATGAATAAGGTCAAAGATTACTGGCTTTGAATGTTGTTTTTTAATTCTTTATTCAAACACTTTATAAAAAAGAAACCTTTTTTTCAATTGGTTGTTGTTTTTGTACAGAGATAAAATTAGCTTGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15684
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
ENSDART00000088325 Nonsense 293 1327 8 29
Genomic Location (Zv9):
Chromosome 5 (position 55545501)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54348875
GRCz11 5 54971711
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGGTCATGCCAAAGAGGGCCAAGGCATCAAGACAGACATCCCACGATR[C/A]ATTATCAGCCAACTTGGCCTGACAAGGGACCCACTTGAGGGTAAGAGGAC
Long Flanking Sequence:
AAGATAAATTTTGATATTTTAAAAACACGTGTGGAAAAAATAAATAAATGCAGCGCTTATTGTACATTCTGAGGCCCACTTTATATCATATATCAATTAGGCAGTGACTATTTTGAAAAAAAAACAGACTTTAAATGTGTCAATTTTACAACAGCATGCAATTCACCGTAAGTGCTTTAACTGGGTTACTGAGAATGAAAAGTCCCTCTGCATATAACACAGTGAGCAATTGGCTGCATATCAAGCTGCCATTCTTTAAACAAAGTAACATTTAAGGATTACAATTCTGAAAATTTATGAAAAACTTTTTCTAAACCGATGCATAAGCGTTAAATTATACAAGAAATGAAAATCTATGGTGCAGCCTAGTTTGAGTCTTGCATTAACAGTGTGCTTTTCCTCTTGTAGGAGTTTGACCCAGAAGAGTTCTATCATCTCCTGGAGGCTGCAGAGGGTCATGCCAAAGAGGGCCAAGGCATCAAGACAGACATCCCACGATA[C/A]ATTATCAGCCAACTTGGCCTGACAAGGGACCCACTTGAGGGTAAGAGGACCTTCATAAATGGTTTTTCATAGTCTTTTCCAATGGTCTCTAGCCTCGGATGGCACACACATGGGTTATAAACAAACTGAAAATAAAAATGGCAAGAGGGTGTAACAAGTGTGTTTTCATTTCATTGGGTGATTATTATTATGCTTCCTTTGGGAGTCTAGACACATTAGATTTTATCAGCTCATCAGTAAATAAAGTTTTATTTACAGGCTATCAGGCTGAGTGCTTCCAAGAAAGAAGTCTTTGCTGGAATTGACCCAGTTTGCATCAAACATTCATTCATTCATTTTCTGTCGGCTTAGTCCCTTTATTTATTAGAGGTCGCAACGGTAGAATGAACCGCCAACTTATCCAGCATATGTTTTATACAGCGGATGTCCTTCCAGCAGCAACCCAGCACCTGGAAACATCCATACACTCATTCACAGACACACACACACACACACACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33719
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088325 Essential Splice Site 474 1327 12 29
Genomic Location (Zv9):
Chromosome 5 (position 55538841)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54342267
GRCz11 5 54965103
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATCTCCACAACTATGGAATTGTCCATCGAGATCTCAAACCAGACAAG[T/C]GAGCTGTGCCTAACAATTACTGATTAACAATTACTAATTACTGAAATTTG
Long Flanking Sequence:
GATATAGATAGACCTGCCATTCTCAAAAAAAAAAAAAAAAAACTCATAACAAAAATATAAATAATATAGCTTTTGTTTTGCTAAATAGTTTATTTATTTATTTACTTATTTTTTTTTTTACTTATTTACTGATTTATTTATTCCATACAATGATGATGATATATCCCATACAATGTAAGATTTTGTCCTAGTCTTTGTCTTTGATCACTATATACTGTATGTTTGTCTTTCTTAAATATATATATAAATATACAACGAACGTGAAGCTTCTAAAAATTGTTTAATTTGACACGGTTTAACCCAGGAGTCAAAAATCTGTGTTTTACGCAGCATTATTTTGCATGTTTCTTATTCGCACAGGAGGGGACTGTGCTACTTTGCTGAAGAACATGGGTCCTCTCCCTGTGGACATGGCCAGAATGTACTTTGCAGAGACTGTGTTAGCCCTGGAATATCTCCACAACTATGGAATTGTCCATCGAGATCTCAAACCAGACAAG[T/C]GAGCTGTGCCTAACAATTACTGATTAACAATTACTAATTACTGAAATTTGACATAGCATACACAATAAAAATGAAATGAGCTGACCTAACAATATTTCTACATGGTGGTTTTATTAGCTGGTCTTGAACAGGGGTTTTCAACCTGGCCTATTAAGGGGGCCATGAGAATTTGAAGCATGTACTCGAGTGTATCATGATGATGATTTTTATGTGTTCACTAGAGTGAATCTGATTAGCGTTTCACAGCTAACTATTGAGTGAAATTGGTCAAACTTGAGGGTGTGTCCTAAAAGGTTGAAAACCCCTTGTCTAAAATGTTGACATCTTTATTCTAATTAAAGGATGCAGACAAGTTACAGCCACTAGGTTAATAGCATCATAAGCTGATATGACCAAGATAATATTATATTGTGCCTCTTATATCTTATCATATTTTCCATAGTTTGTTAGTCACTTCAATGGGACACATCAAGCTGACAGACTTTGGCCTATCGAAAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20534
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088325 Essential Splice Site 608 1327 15 29
Genomic Location (Zv9):
Chromosome 5 (position 55534760)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54338186
GRCz11 5 54961022
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCACTCTGCTGCTCAGACAGAACCCTATGGAGCGCCTTGGCACTGG[T/C]AAGGGTCCAGAATACTTACAGTGATACTTGCCAAGCACCAAATGTGAGTA
Long Flanking Sequence:
TCCCTGTCCTCTTCCTTCAGATCGAACACGTTTTGTTATTCCACAGTAATCATTTAAGTCATGATTTCATCAAGGGTCTGCTCTTTGATTAGTGAGAAATGCGAAATAACCTGTGGTACTGGATGCTCGTTCCTAGAATTCATGCATGTGAAAGTGGATATGATAATGTTTGGCATGCCTGTTTATGTGTAGTAGGCAGTTTGATGCATTTTAATTATTACATTTGATTCATATGTAAAAATATTCTCTGTATTCATTAATGTAGTGTTGTGAATGTGTAATGGGTTTGTGTTACAATGGAGGCACAACAAAAGTGGTGTGGATCTGTCATGTTGAATGATTTTTGGAAAAGACTTTGGTTAATGAGGATAAAACTGTTGTCTTCTGCTTGCCTTAGATGAAATAAACTGGCCTGAGGGAGAGGAAGCGCCACCAGCTGATGCTCAGGAGCTGATCACTCTGCTGCTCAGACAGAACCCTATGGAGCGCCTTGGCACTGG[T/C]AAGGGTCCAGAATACTTACAGTGATACTTGCCAAGCACCAAATGTGAGTAAACATAATTTTGGCAATTAAATAAAATGCCTATTTGGCCAGTAAAATGTTGTAGAAATTTCAAAGTCATATAGATTTAAATGCTTTAAAATGCTTATACAAATAAATTCATTCATTTTCTTTTCGGCTTAGTCCCTTTATTAATCTGTGGTCGCCAAAGCGGAATGAACCACCAACTTATCCAGCATATGCTTCGGCAGCGGATGGTCTTCCAGCCGCAACCCAACACTGGCAAACATCCATTCACACACATACACTACAGACAAATTAGCTTACCCAATTTACCTATACCACATGTCTTTGGACTTGTGGGGGAAACCGGAGCACCCGGAGAAAACCCACGCAAACATAGGGAAAACATGCAAACTCCACACAGAAATGCCAACTGACTCAGCCAGGGCTTAAACCAGCGACCTTCTTGTGCTACCCACTGCTCTTTCTTGTGCCTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30865
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
ENSDART00000088325 Nonsense 1014 1327 25 29
ENSDART00000088325 Nonsense 1014 1327 25 29
Genomic Location (Zv9):
Chromosome 5 (position 55523284)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54326710
GRCz11 5 54949546
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTTGAAAACACTTCTATCAAAACTGGGCCAGCTAGAAGAAACAGCTA[C/A]AGAAGTAAAATGGTGAGAAGAACCAAAAAACCCAAGAAAGAGAAAACTCA
Long Flanking Sequence:
TCCTATGCCTTACCCAGAATATAAAAAGACATAAAAATAAATTTAGATAATTTACGTTAATCATTAATACCAGAATGTGAAGAGCATTGTACCCAGCGCAGCAAAACATTAAAAAAGACAATCACCTACTGCACCTTTAAGAGACAAATAAAATATTTTGAGCTATGCATGATTTAAAATAAATACTGGTCTAATTTGGTATAGAATGTGGAGGATGGTGGACCTGCTCACAAGGCTGGTCTTAAGGCTGGAGATCTAATAACTCATGTGAATGGAGAAACAGTTCATGGGTTACTTCACACAGAAGTGGTGGAGCTGTTGCTGAAGGTACATACCATTGTTACAAACACAGCATTATTCCCTCTTTTCTATGCCATTTCATTGTTATTGTGTCTGTAAGTAACACGTGTTGTTTTTCAGAGTGGAAGTAAAGTTGCAATATCTACAACCCCATTTGAAAACACTTCTATCAAAACTGGGCCAGCTAGAAGAAACAGCTA[C/A]AGAAGTAAAATGGTGAGAAGAACCAAAAAACCCAAGAAAGAGAAAACTCAAGAAAGGTAAGAAAAAATGATGATCATCACTGACTGTGTCAGCTTTTAAAGTTGTGTATTAAAAATACCATTTAATTTTGGATCCCTAAAGTACATCTCAGTAGAAAAGGCACTCGACTCCCACTAGATGTAGCTGTTGTTGCTTTTGTTTTTGTAGTATACTGTACAAATGCAAACTTCATTTAGAATTGGAAGTTTTTGTACTTTCTAATGCATACCGTGCAGTGTATAAAGTATATCGCTAACAGTTTCTGTCTATATCCCTTAAAGGTAGTTTGAATAGTATGATACCGTTGTGTTATGTTGCAGTATGGTTGTTTTTCAGTCAAACATATTTTCTTCTCCAGACGGCGTTCAGTATTCAAGCGCTTTGCCATGCAACCCTCTCCACTTTTACACACCAGTCGCAGTTTCTCCTCCCTGAATCGTTCACTGTCTTCAGGAGAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40562
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
ENSDART00000088325 Nonsense 1014 1327 25 29
ENSDART00000088325 Nonsense 1014 1327 25 29
Genomic Location (Zv9):
Chromosome 5 (position 55523284)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54326710
GRCz11 5 54949546
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTTGAAAACACTTCTATCAAAACTGGGCCAGCTAGAAGAAACAGCTA[C/A]AGAAGTAAAATGGTGAGAAGAACCAAAAAACCCAAGAAAGAGAAAACTCA
Long Flanking Sequence:
TCCTATGCCTTACCCAGAATATAAAAAGACATAAAAATAAATTTAGATAATTTACGTTAATCATTAATACCAGAATGTGAAGAGCATTGTACCCAGCGCAGCAAAACATTAAAAAAGACAATCACCTACTGCACCTTTAAGAGACAAATAAAATATTTTGAGCTATGCATGATTTAAAATAAATACTGGTCTAATTTGGTATAGAATGTGGAGGATGGTGGACCTGCTCACAAGGCTGGTCTTAAGGCTGGAGATCTAATAACTCATGTGAATGGAGAAACAGTTCATGGGTTACTTCACACAGAAGTGGTGGAGCTGTTGCTGAAGGTACATACCATTGTTACAAACACAGCATTATTCCCTCTTTTCTATGCCATTTCATTGTTATTGTGTCTGTAAGTAACACGTGTTGTTTTTCAGAGTGGAAGTAAAGTTGCAATATCTACAACCCCATTTGAAAACACTTCTATCAAAACTGGGCCAGCTAGAAGAAACAGCTA[C/A]AGAAGTAAAATGGTGAGAAGAACCAAAAAACCCAAGAAAGAGAAAACTCAAGAAAGGTAAGAAAAAATGATGATCATCACTGACTGTGTCAGCTTTTAAAGTTGTGTATTAAAAATACCATTTAATTTTGGATCCCTAAAGTACATCTCAGTAGAAAAGGCACTCGACTCCCACTAGATGTAGCTGTTGTTGCTTTTGTTTTTGTAGTATACTGTACAAATGCAAACTTCATTTAGAATTGGAAGTTTTTGTACTTTCTAATGCATACCGTGCAGTGTATAAAGTATATCGCTAACAGTTTCTGTCTATATCCCTTAAAGGTAGTTTGAATAGTATGATACCGTTGTGTTATGTTGCAGTATGGTTGTTTTTCAGTCAAACATATTTTCTTCTCCAGACGGCGTTCAGTATTCAAGCGCTTTGCCATGCAACCCTCTCCACTTTTACACACCAGTCGCAGTTTCTCCTCCCTGAATCGTTCACTGTCTTCAGGAGAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16213
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
ENSDART00000088325 Nonsense 1183 1327 28 29
Genomic Location (Zv9):
Chromosome 5 (position 55522261)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54325687
GRCz11 5 54948523
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTCWGYGTTCCCCGTCTCCCTTGYTGACTCATACTGTCGGAAGCTCC[A/T]AAACTTCTCAGYCCTTCCCTGCCAAAATGCWCTCACCCCCCAMTATTRTA
Long Flanking Sequence:
GCCTCTCACCACGCTCCCCCACTGCTGCCTTTCGCCCAGCACCAGATTTTACCCAGTCAGGTTGTATGTTTTACCCTGTCAATGATCCTGATAAAAGAGCATATATTAATCATGTTTCATGTCAAGAAGTGTAAATAGATATTAAGTGTTCAGTGCATTTTATTCCTGTTCAATTCAAGGTGGAATATTAAACCTAAATGACAGTAACTTCAAAGGTTGACACTATACATTTTCTTGTTGTAGGTGGCACTTCATCACAGAGTAGCTCCCCCAGTTCCAGTGCACCTAACTCACCTGCAGGCTCTGGCCACATTCGGCCCAGTACTCTGCATGGCCTGGGACCCAAACTTCCTGGACGGCTCCGTCAAGGCCGACGTAAATCAGCAGGGAGCATTCCCCTATCACCATTGGCTCGCACACCCTCCCCAACACCTCAGCCTCAGCCAACATCTCCTCAGCGTTCCCCGTCTCCCTTGTTGACTCATACTGTCGGAAGCTCC[A/T]AAACTTCTCAGCCCTTCCCTGCCAAAATGCACTCACCCCCCACTATTGTACGCCATATGGTTCGACCTAAAAGTGCTGAGCCTCCTCGATCACCACTATTGAAGCGTGTCCAATCTGAGGAAAAACTGTCCCCCTCTTATGCTGGAGACAAAAAACATTTATGCACTCGAAAGCACAGTTTGGAGGTCACCCAAGAGGAATCTCAAGGGGAGGCTTCATCTAAAGGGGAAAATGTCCAACCTTGCATAGAGGAGAGCACTTCTTGTGATCCGCCCACCATTACCCGGGTGAGGCCTGCTGAGCAGGGTTGCCTAAAGCGGCCTGTGACGCGCAAAGTTGGCCGACAGGAGTCAGTAGAGGAGCTCGACAAGGAGAAGCTAAAGGCCAAAGTGGTGGTGAAGAGGCAGGACTGGCCTGAGAGACGAGAGTCCATGCCAAAACAAGACACTGTGCAAGATGTGGAAGGTCCTACTGCTGAAGATAAGGAATGGGGTGTGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13456
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
ENSDART00000088325 Nonsense 1212 1327 28 29
Genomic Location (Zv9):
Chromosome 5 (position 55522174)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54325600
GRCz11 5 54948436
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCCAMTATTGTACGCCATATGGYTCGACCTAAAAGTGCTGAGCCTCCT[C/T]GATCACCACTATTGAAGCGTGTCCAATCTGAGGAAAAACTGTCYCCCTCT
Long Flanking Sequence:
CTGATAAAAGAGCATATATTAATCATGTTTCATGTCAAGAAGTGTAAATAGATATTAAGTGTTCAGTGCATTTTATTCCTGTTCAATTCAAGGTGGAATATTAAACCTAAATGACAGTAACTTCAAAGGTTGACACTATACATTTTCTTGTTGTAGGTGGCACTTCATCACAGAGTAGCTCCCCCAGTTCCAGTGCACCTAACTCACCTGCAGGCTCTGGCCACATTCGGCCCAGTACTCTGCATGGCCTGGGACCCAAACTTCCTGGACGGCTCCGTCAAGGCCGACGTAAATCAGCAGGGAGCATTCCCCTATCACCATTGGCTCGCACACCCTCCCCAACACCTCAGCCTCAGCCAACATCTCCTCAGCGTTCCCCGTCTCCCTTGTTGACTCATACTGTCGGAAGCTCCAAAACTTCTCAGCCCTTCCCTGCCAAAATGCACTCACCCCCCACTATTGTACGCCATATGGTTCGACCTAAAAGTGCTGAGCCTCCT[C/T]GATCACCACTATTGAAGCGTGTCCAATCTGAGGAAAAACTGTCCCCCTCTTATGCTGGAGACAAAAAACATTTATGCACTCGAAAGCACAGTTTGGAGGTCACCCAAGAGGAATCTCAAGGGGAGGCTTCATCTAAAGGGGAAAATGTCCAACCTTGCATAGAGGAGAGCACTTCTTGTGATCCGCCCACCATTACCCGGGTGAGGCCTGCTGAGCAGGGTTGCCTAAAGCGGCCTGTGACGCGCAAAGTTGGCCGACAGGAGTCAGTAGAGGAGCTCGACAAGGAGAAGCTAAAGGCCAAAGTGGTGGTGAAGAGGCAGGACTGGCCTGAGAGACGAGAGTCCATGCCAAAACAAGACACTGTGCAAGATGTGGAAGGTCCTACTGCTGAAGATAAGGAATGGGGTGTGCTAACACGTCCAAGTGTGAGACCCCAAATTTTAGAATCTGGATCCTTGGACAAATCTACAAATGCTAGTTTAAAAGATGTCCTCTACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26579
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
ENSDART00000088325 Nonsense 1312 1327 29 29
Genomic Location (Zv9):
Chromosome 5 (position 55521820)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 54325246
GRCz11 5 54948082
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTGAAGAGGCAGGACTGGCCTGAGAGACGAGAGTCCATGCCAAAA[C/T]AAGACACTGTGCAAGATGTGGAAGGTCCTACTGCTGAAGATAAGGAATGG
Long Flanking Sequence:
AGCCAACATCTCCTCAGCGTTCCCCGTCTCCCTTGTTGACTCATACTGTCGGAAGCTCCAAAACTTCTCAGCCCTTCCCTGCCAAAATGCACTCACCCCCCACTATTGTACGCCATATGGTTCGACCTAAAAGTGCTGAGCCTCCTCGATCACCACTATTGAAGCGTGTCCAATCTGAGGAAAAACTGTCCCCCTCTTATGCTGGAGACAAAAAACATTTATGCACTCGAAAGCACAGTTTGGAGGTCACCCAAGAGGAATCTCAAGGGGAGGCTTCATCTAAAGGGGAAAATGTCCAACCTTGCATAGAGGAGAGCACTTCTTGTGATCCGCCCACCATTACCCGGGTGAGGCCTGCTGAGCAGGGTTGCCTAAAGCGGCCTGTGACGCGCAAAGTTGGCCGACAGGAGTCAGTAGAGGAGCTCGACAAGGAGAAGCTAAAGGCCAAAGTGGTGGTGAAGAGGCAGGACTGGCCTGAGAGACGAGAGTCCATGCCAAAA[C/T]AAGACACTGTGCAAGATGTGGAAGGTCCTACTGCTGAAGATAAGGAATGGGGTGTGCTAACACGTCCAAGTGTGAGACCCCAAATTTTAGAATCTGGATCCTTGGACAAATCTACAAATGCTAGTTTAAAAGATGTCCTCTACAAAAAACTAAATCCAAGAGTCTGTGAGAGCATTGCAGAGTCAGTCACTACTGGTGATTGTGCATCCTTTTTAAGTGAGAATATTAGGTCACCTTCATGTCAAGCAGAGCGACAGATGTCTTGGTCAATGAAGGAAGGTAACAAGCCAGAGAGGCTAGATTTCAAAGCTTCCAAAATGGAGTTTGTCCGAAAGAGGCAGTCCTTTGAAGAGAGAGAGGACTCCTTGTGTCGAATATCCTCTGGGGTTCATGACAGTATTCATTTTAACACAACCAGGTCCAAAAGCCTTCAGCTGGATTCTGCGTTGGCTTTAGAACATGTAAAAGGAGGCATGTGCAACATCCATGTCACTTCTGAA
Associated Phenotype:
Not determined