Busch Lab

ZMP

MAST2

Ensembl ID:
ENSDARG00000074311
Description:
microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:19035]
Human Orthologue:
MAST2
Human Description:
microtubule associated serine/threonine kinase 2 [Source:HGNC Symbol;Acc:19035]
Mouse Orthologue:
Mast2
Mouse Description:
microtubule associated serine/threonine kinase 2 Gene [Source:MGI Symbol;Acc:MGI:894676]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa33890 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20733 Nonsense Available for shipment Available now
sa489 Essential Splice Site Available for shipment Available now
sa7584 Missense Mutation detected in F1 DNA Not yet available
sa40725 Nonsense Mutation detected in F1 DNA Not yet available
sa40724 Nonsense Mutation detected in F1 DNA Not yet available
sa11672 Essential Splice Site Available for shipment Available now
sa8985 Nonsense Mutation detected in F1 DNA Not yet available
sa26773 Nonsense Mutation detected in F1 DNA Not yet available
sa26772 Nonsense Mutation detected in F1 DNA Not yet available
sa31517 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa33890
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
ENSDART00000115409 Essential Splice Site 276 1934 9 30
Genomic Location (Zv9):
Chromosome 6 (position 33388508)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33706173
GRCz11 6 33690863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGGGAGACGATCCCCAGCCATGCGTCCGCGCTCCCGCAGTCTCAGG[T/C]ACAAACACGTACACATTCCCATTTCACAGCAATCAGAAGCTGGCCTTCAA
Long Flanking Sequence:
AAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATACCTACAACTACAATAAATCTATTAAAAAAACTAAACATTTTCATTTGAACCTGGACATTTTCAGTAGATAAAAAAAGAAACTTTACGTGTGATTAAATACAAATAAAAAAAATACTGTTTAAGTATTCCCCCCTCTATTTGGCCTAAAGTTTTCAGTCACATTTTCAAAATCGGTCAGCGTTAGCCAACAAAGGCAGTTGACTGACAGTCAGGGCAGCCTATGCAATGCCTTCTGTCCTTGTAATCCCTCCCTCTCTGCTTCTCACAGTCATCATGTTCATCTCAGGAGAAGCTGCACCAGTTGCCCTTCCAGCCCACTGCAGACGAGCTGCATTTCCTCACCAAACACTTCAGCTCGGAGAGCATCACGGATGAGGATGGGAGACGATCCCCAGCCATGCGTCCGCGCTCCCGCAGTCTCAGG[T/C]ACAAACACGTACACATTCCCATTTCACAGCAATCAGAAGCTGGCCTTCAAGTGAACATGACGGTTGTGAGTGTGTGATGTCAGCTGAGCCCTCAGGCTTTCACTCACTCGCTGTTAAAGGCCAGATCTGCAGCCCTGACAGGAAAACTGCCACACTTCATTCTCTAGACTCTGACTCTCTTCTTCAAGGTTGCAGACATTTATCATTCAGCCTCTCTGCCCTTCACTCAGCTGCCTTCACGTGTTCTTTATGATTCTGTCCATCTGTCAGTACTATGCACAAGTTTCACTGCACCTCAAAATCCAAAGAAATATTACAATTCTGTTTTCATGGGAAGTCTAATAGTATTTGCAAATGCATTATCAAAGTTTTTTAACGGTAATCACCAGTTTTTATTACTTTAATGAAAAAATATACACTACCAGTCAGTTTTTGGTCAGTTTTTAGCTGCATTTATTAAATGTAAAAAAAAAAGATAATTGTTAAATATTTATAAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20733
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
ENSDART00000115409 Nonsense 295 1934 10 30
Genomic Location (Zv9):
Chromosome 6 (position 33382887)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33700552
GRCz11 6 33685242
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCACCAATATCATTTGACCATGAGATTGTCATGATGAACCATGTCTA[C/A]AAGGAGCGTTTTCCTAAGGTGAGGTCTTAAACTGAAATACTAGATAGATT
Long Flanking Sequence:
TTCAGTCAGGTGGTCTAATAGGCTTCGATTGATGACTTATAGCATTACCTCATCCACAAGGTCACATGACCAGCTTACCTTCACTAACCGGGTGAGTCATACAGCACCATCTGCAATCTGTGTCCCTGAAACACACACACATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATAGTTACTTATCTACTCTGTATCTCTCAATATTCCCTATGGGACATCTCAAGTTGAAGATGCTACTTTGACATGAATGAGGTTTGATATGCCAAAAAATCACAGGTGCTTCAGTCTATCATCCCCATTAGATTTTAGGTATGGACACTGCTAATCAACTTCTGCTCAGTGACCCTAGGGTTTTGTCCACTTACTGTATGTCTTTCTTTTCTCTGTTTTTCAGCCCTGGACGGTCACCAATATCATTTGACCATGAGATTGTCATGATGAACCATGTCTA[C/A]AAGGAGCGTTTTCCTAAGGTGAGGTCTTAAACTGAAATACTAGATAGATTATTTTAACAAAGTAATGTACGTTATTGTCATGACCTGGGTAAGGCATCAATACACATCACAACGGAAAAAGGAGATTTAAAAAAAATCACAAATTTAAAATGAGTAAATCTGCTAGAATGTTAAAGGGATGGTTCATGCAGATATGAAAATCACTACTGACTATAGACCCTTTTCACATTTGTGGGTTTCTCAGTAGTGGAAGTCATCATAGTTAGATACACTAAAAGCACAGTGAATCTGAGAGTACAACCAATGATTTTTTTACAATCTTATTTGCTGAAATAATAAAAGAAAAATGCCACGTTGGTGTTATCAAGACTTTCAGAAAAGGAAATAAATAGTGTGAGACTAATAACGGCAGCCAGAGGAGAGAATACTGTCAAATTTACTGTCTTATATACACTCCATTAGAAACAGCTCGCACAAGCGGTACTTCGATTTTGGGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa489
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
ENSDART00000115409 Essential Splice Site 301 1934 10 30
Genomic Location (Zv9):
Chromosome 6 (position 33382868)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33700533
GRCz11 6 33685223
KASP Assay ID:
554-0342.1 (used for ordering genotyping assays)
KASP Sequence:
ACCATGAGATTGTCATGATGAACCATGTCTACAAGGAGCGTTTTCCTAAG[G/A]TGAGGTCTTAAACTGAAATACTAGATAGATTATTTTAACAAAGTAATGTA
Long Flanking Sequence:
AGGCTTCGATTGATGACTTATAGCATTACCTCATCCACAAGGTCACATGACCAGCTTACCTTCACTAACCGGGTGAGTCATACAGCACCATCTGCAATCTGTGTCCCTGAAACACACACACATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATAGTTACTTATCTACTCTGTATCTCTCAATATTCCCTATGGGACATCTCAAGTTGAAGATGCTACTTTGACATGAATGAGGTTTGATATGCCAAAAAATCACAGGTGCTTCAGTCTATCATCCCCATTAGATTTTAGGTATGGACACTGCTAATCAACTTCTGCTCAGTGACCCTAGGGTTTTGTCCACTTACTGTATGTCTTTCTTTTCTCTGTTTTTCAGCCCTGGACGGTCACCAATATCATTTGACCATGAGATTGTCATGATGAACCATGTCTACAAGGAGCGTTTTCCTAAG[G/A]TGAGGTCTTAAACTGAAATACTAGATAGATTATTTTAACAAAGTAATGTACGTTATTGTCATGACCTGGGTAAGGCATCAATACACATCACAACGGAAAAAGGAGATTTAAAAAAAATCACAAATTTAAAATGAGTAAATCTGCTAGAATGTTAAAGGGATGGTTCATGCAGATATGAAAATCACTACTGACTATAGACCCTTTTCACATTTGTGGGTTTCTCAGTAGTGGAAGTCATCATAGTTAGATACACTAAAAGCACAGTGAATCTGAGAGTACAACCAATGATTTTTTTACAATCTTATTTGCTGAAATAATAAAAGAAAAATGCCACGTTGGTGTTATCAAGACTTTCAGAAAAGGAAATAAATAGTGTGAGACTAATAACGGCAGCCAGAGGAGAGAATACTGTCAAATTTACTGTCTTATATACACTCCATTAGAAACAGCTCGCACAAGCGGTACTTCGATTTTGGGCATTTGAAGCAAAGATGATATAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa7584
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115409 Missense 615 1934 17 30
Genomic Location (Zv9):
Chromosome 6 (position 33371558)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33689223
GRCz11 6 33673913
KASP Assay ID:
554-4157.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGCACGCATGTACTTTGCTGAAACCGTTCTTGCATTGGAATACCTTCA[C/A]AACTATGGTATTGTGCACAGAGACCTCAAACCTGACAAGTAAGGAAACCA
Long Flanking Sequence:
TCATCATCGATTGTATCTCCTGTGCTTTTTCATAGTCGAGTAAAAAGAAACTGATTTGCGTAAAACATACCTTTTTTCACTCAGGGCTGTGTTTCTGGTGAGGCATAAAGAGACCCGTCAGCGATTTGCCATGAAGAAGATCAACAAGCAGAACCTGATCCTAAGAAACCAGATCCAGCAGGCCTTTGTGGAAAGAGACATCTTGACATTTGCAGAAAACCCTTTTGTTGTCAGCATGTTCTGCTCCTTTGAGACAAGGAGACATCTTTGCATGGTTATGGAGTATGTGGAGGGTAAGATATATGGCATCCTTTTGAAGATGTAACTGTTCTGTGGAGGATTTCAGTATGGCATACACCACAAAGTGATGCTCTAGTTGAATTGGTTTGTATGTCTAAAGGTGGGGATTGTGCCACTCTCCTGAAGCACATTGGAGCTCTGCCTGTGGATATGGCACGCATGTACTTTGCTGAAACCGTTCTTGCATTGGAATACCTTCA[C/A]AACTATGGTATTGTGCACAGAGACCTCAAACCTGACAAGTAAGGAAACCAGCTTGTTTGCAGTTGACTTTCTGTCAATTTAGTTTGCTTTGGTTTATACAGCAATTCTTTTTAATGGATAAATGGTCCTCAAATACCGACTAAAGAACAAAATGTCTGTTTTCTGCAGTCTCCTGATTACCTCAATGGGACACGTCAAACTGACTGACTTTGGCCTGTCCAAGATTGGTTTAATGAGCTTAACAACTAATCTGTATGAGGGCCACATTGAAAAAGATACTCGAGAATTCTTGGACAAACAGGTAGAAGTGACCTGTTAGACTATATATTTTCTTCTCTTTCGTTTATTCTTTTCTTTTTTTTAATACAAGGACAATATTCTCTCTTTCTCTCTTAGGTGTGTGGTACTCCTGAATACATTGCTCCTGAGGTTATTCTGCGACAGGGTTATGGAAAACCAGTTGACTGGTGGGCCATGGGAGTCATCTTGTATGAGTTTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40725
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
ENSDART00000115409 Nonsense 766 1934 21 30
Genomic Location (Zv9):
Chromosome 6 (position 33369841)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33687506
GRCz11 6 33672196
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATATTTAAAGAAATCTTCTCTTTTTATGTCTAACAGGGAGTGCGTTT[G/T]AGGTAAAACAGCACCGCTTCTTTACTGATCTGGACTGGAACAGCCTCCTG
Long Flanking Sequence:
AAATAAACAGGGGGCCTAATAATTCAAGGGGGCTAATAGTTCTGACTTCAACTGTATGTACTAACCTGTAATCTTGCTTGTCTTTGAGTTATCTGGGATACAATAGTACTCTGAAGTCTGATCTGACCTAACAGTCCTCTGGGAAATGTGGTTATGTATGTTTTGTTCAACAGATGAGATAATCTGGCCAGAAGGTGATGAAGCTTTGCCTCCGGATGCTCAAGATCTCATCTCCAAACTTCTTCGGCAAAACCCTCTAGAGCGTCTTGGGACAGGTCCTCTTGCACATTTACTCTTACTTGCACAGATGCTGACTTCTTAATGTATTCCCTGGAAGACAATTAGAGGAGTAACTTGGCTATTATGATTAATAGTATATAAATAAACCTCATCAGAAAATCTTGGGAAGTCTTTGTTTTTTTTATATAATGCTACATCATTGCTCGCTAAGAAATATTTAAAGAAATCTTCTCTTTTTATGTCTAACAGGGAGTGCGTTT[G/T]AGGTAAAACAGCACCGCTTCTTTACTGATCTGGACTGGAACAGCCTCCTGAGGCAGAAGGCTGAGTTCATTCCTCAGCTGGAGTCGGAGGATGACACTAGCTACTTTGACAGTACGTCTTCAGGCAGAAGATACTAGAGTGAAATTTATGATAAGACTTTTTTCTTTACCTGCAATGCAAATAAATACCACTCGTGCATACAGTCTGGAAAACACAATCTAAGATCTCTCTCTCTCTTTTTCACTCTTTAGCACGCTCAGATCGTTATCATCATGTGGACTCAGAGGAAGAAGATGACACAAATGATGACGACCATTTGGAGATCCGTCAGTTCTCCTCCTGTTCGCCACGATTCAGCAAGGTGGATTTTACAAATGCATGTTAACTCAACACAACAGAAACTGAATAGTATAAAATTAAGGATGCCCGATTGATCAGCCGAAGATCAATTTTGGACGATAATCACATTTAATGACTCGATCAGTACTCGCCAATCTGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40724
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
ENSDART00000115409 Nonsense 825 1934 22 30
Genomic Location (Zv9):
Chromosome 6 (position 33369523)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33687188
GRCz11 6 33671878
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCATGTGGACTCAGAGGAAGAAGATGACACAAATGATGACGACCATT[T/A]GGAGATCCGTCAGTTCTCCTCCTGTTCGCCACGATTCAGCAAGGTGGATT
Long Flanking Sequence:
TTAATGTATTCCCTGGAAGACAATTAGAGGAGTAACTTGGCTATTATGATTAATAGTATATAAATAAACCTCATCAGAAAATCTTGGGAAGTCTTTGTTTTTTTTATATAATGCTACATCATTGCTCGCTAAGAAATATTTAAAGAAATCTTCTCTTTTTATGTCTAACAGGGAGTGCGTTTGAGGTAAAACAGCACCGCTTCTTTACTGATCTGGACTGGAACAGCCTCCTGAGGCAGAAGGCTGAGTTCATTCCTCAGCTGGAGTCGGAGGATGACACTAGCTACTTTGACAGTACGTCTTCAGGCAGAAGATACTAGAGTGAAATTTATGATAAGACTTTTTTCTTTACCTGCAATGCAAATAAATACCACTCGTGCATACAGTCTGGAAAACACAATCTAAGATCTCTCTCTCTCTTTTTCACTCTTTAGCACGCTCAGATCGTTATCATCATGTGGACTCAGAGGAAGAAGATGACACAAATGATGACGACCATT[T/A]GGAGATCCGTCAGTTCTCCTCCTGTTCGCCACGATTCAGCAAGGTGGATTTTACAAATGCATGTTAACTCAACACAACAGAAACTGAATAGTATAAAATTAAGGATGCCCGATTGATCAGCCGAAGATCAATTTTGGACGATAATCACATTTAATGACTCGATCAGTACTCGCCAATCTGGGCGTTCTCGTAAACCAATAGCAGGGGTTTGTTAATGAGCTTACAAGCAAAGGAAGACACACATGTCCTCCTTTATATTATACATAGCCTACAGCAGCCACAACACGTAAGGAGGTAAATAATGTTTGGAGGCATGAGCGTTTGCTGTGCTCGCATCACATAAACTAAAAAATATACCAATGCGGTGCGACCTGTCTATTGGCGCAACTCGTGTGAGTGATGTTCTCTGTGCAGCCAATGTACATCCAGTGTTTTGAGCTGCTATGACGCGAGCAGAGCGATTGCCCCTATCTAGCGTCTTATCCAACCTTATGACTTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11672
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115409 Essential Splice Site 1059 1934 25 30
Genomic Location (Zv9):
Chromosome 6 (position 33366666)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33684331
GRCz11 6 33669021
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCATCAAATCAGCTTCAGCAACAACCCTGTCACTCATGATCCCTGCTGG[T/C]AAGTGTACAGTATATGATTGACCATCATGATTTTACAATRTAAGACATRA
Long Flanking Sequence:
AGAGCTCAGGCTGGATGAATCGCCCACCACGCCAGGATCCACTTCCAGTCAAATCAGCCAGTCCACACTCACACGTGAGTCTTGCTGAATTAGACTCTGGCATATGGTATAGGTTCTAGATTTAACTGGAAATTGTTTGAAATGTTTTAATGAGATGTACAAATCTCACATAAAGGGATTTAAAAAAAAAAAGCGTATTATTATTGTTTAAAATAACACCGTAATTGATAATTTTGATAGTTGAAATTTTTCTGTATATTTATATGGTTGTTTTTGTGTGTGATTTCAGCTGGTAGTTCTGGTGATGTGTTAGATCGTGCTTCTCGCTATAGTGCTGAAGTTTCTGAAAACTCCACTCCAAGAGCCATCAGTGATTTGGCGGCTCGAAGAGCTCGCCACAGACTGCTTTCAGGAGATACAGATAAACACACATCACGTCCACTTAGCAAAGTCATCAAATCAGCTTCAGCAACAACCCTGTCACTCATGATCCCTGCTGG[T/C]AAGTGTACAGTATATGATTGACCATCATGATTTTACAATGTAAGACATGATCCTATATCAACCTTTTGAATCTTAGATCTACTGTCCACATGATTGGGAACATGACACAATCATCTAGTTAACATCACAGTCACTTGATTGGATTTGCTGCCTTTATATATTCAGAAGAAATGTGTGAAGTGAGCTAACTTCTTGTTTTTTAGATCACCATGGTGCTTCTCCACTGGCCAGTCCCATGTCGCCTCACTCTCTCTCTTCGAACCCCTCATCACGTGACTCCTCGCCCAGCCGTGACCTTTCCCCAGCTGTCTGTAGTGTTAAACCTGCCATAATCATCCATCGAGCTGGAAAGAAATATGGTTTTACTTTACGTGCAATCCGGGTTTACATGGGAGACACAGACATATATACTGTCCATCACATGGTCTGGGTGAGTAGTACTGGGTGAATGTAGTTATTGTCGAAAAATACAGTTTGTAAATACAGCAATTTGTAGCGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8985
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
ENSDART00000115409 Nonsense 1127 1934 26 30
Genomic Location (Zv9):
Chromosome 6 (position 33366257)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33683922
GRCz11 6 33668612
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTTTACTTTACGTGCAATCCGGGTTTACATGGGAGACACAGACATATA[T/A]ACTGTCCATCACATGGTCTGGGTGAGTAGTACTGGGTSAATGTAGTTATT
Long Flanking Sequence:
CAGGAGATACAGATAAACACACATCACGTCCACTTAGCAAAGTCATCAAATCAGCTTCAGCAACAACCCTGTCACTCATGATCCCTGCTGGTAAGTGTACAGTATATGATTGACCATCATGATTTTACAATGTAAGACATGATCCTATATCAACCTTTTGAATCTTAGATCTACTGTCCACATGATTGGGAACATGACACAATCATCTAGTTAACATCACAGTCACTTGATTGGATTTGCTGCCTTTATATATTCAGAAGAAATGTGTGAAGTGAGCTAACTTCTTGTTTTTTAGATCACCATGGTGCTTCTCCACTGGCCAGTCCCATGTCGCCTCACTCTCTCTCTTCGAACCCCTCATCACGTGACTCCTCGCCCAGCCGTGACCTTTCCCCAGCTGTCTGTAGTGTTAAACCTGCCATAATCATCCATCGAGCTGGAAAGAAATATGGTTTTACTTTACGTGCAATCCGGGTTTACATGGGAGACACAGACATATA[T/A]ACTGTCCATCACATGGTCTGGGTGAGTAGTACTGGGTGAATGTAGTTATTGTCGAAAAATACAGTTTGTAAATACAGCAATTTGTAGCGTTACAACATTTAAAATATGTCTTTGCAGCATGTGGAGGATGGAGGACCTGCTCATGAGGCTGGACTGAGAGAGGGAGATCTCATCACACATGTTAACGGAGAGCCTGTCCATGGACTTGTGCACACAGAAGTTGTTGAGCTCATTCTTAAGGTACATTTGTAGCCAAGTTCTTATGAGCCTTTTTGCTGATATTGATATTAAGATTCATTTTTATTTTTTCTGTTCCAGAGTGGCAGTAAGGTGTCCATCTCTGCTACACCCTTTGAAAATACATCAATTAAGGTTGGTCCTGCTCGCAAAACTAGCTACAAGTCCAAAATGGCCCGTCGCAACAAAAGAACCAAAACTAGAGAAGGACAAGACAGGTGAAGTTTAACATATAGCATAATTTAAATTACACCTATATTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26773
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
ENSDART00000115409 Nonsense 1402 1934 30 30
Genomic Location (Zv9):
Chromosome 6 (position 33364896)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33682561
GRCz11 6 33667251
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGATATCTCGGCCAAAGAGTGCAGACCCTCCTCGCTCTCCTCTGCTC[A/T]AACGAGTCCAGTCCGCAGAGAAACTCGCCGCCTCTCTTTCTTCTTCATCC
Long Flanking Sequence:
ATACTGCCATGTCAGATATTATAATCATTGATTTTTTTTTTTTTTACTTAATATTAGTTCCCCGTGAGATCATGCATATCATTTTGCTCATTATTTTTGGTAGTATTAATATGTAACCTTGAACCTTCTTTTTTCCTAATACAGTTGGTGGAAACTCATCCCAAAGTAGCTCGCCTAGCTCCAGTGTGCCAAACTCTCCTGCCAGCTCTGGCCAGATCAGACCCAGCTCCTTGCATGGTCTGGCCCCCAAGCTGCAGCGCCAGTACCGATCCCCCCGCCGGAAGTCTGCAGGCAACATCCCTTTATCCCCTCTGGCCCGTACACCATCGCCCACTCCACAGAGCACTTCTCCCCAGCGTTCCCCTTCTCCCCTGCCAAGCCACGGGCTCATCACTTCTTCAATAGGCCAGTCTTTTCCTGTCAAACTGCACTCTTCACCTCCATTAGTAAGACAGATATCTCGGCCAAAGAGTGCAGACCCTCCTCGCTCTCCTCTGCTC[A/T]AACGAGTCCAGTCCGCAGAGAAACTCGCCGCCTCTCTTTCTTCTTCATCCTCCTCTCCTTCTCCCTCTTCGGCTGCTGATAAAAAGCTTCCAGTTGGTGCCAGCCGCAAACACAGTCTTGATACCTCACATTCAGAGTTTAAAAAAGAGATGCTGCAGCGAGACCCTAGTCTACAGAGCCTGCAAGAGTCAGCCAGTGAGACTCTTATGGGAGGAAGAGTGTCTCCTGCAGAAAAGGGAAGCCTGCAGAAAAGTTCAGTGCGTAAACTGGGCAGGCAAGAAGGTCCCGAGTCTGGAACAGGAACTCTGGGACTTGTTCCTGGAAAGAGTAAATTGAAAGACAAGCTGTCTGCCATACGTGCTGAACGCCGCGAATCTCTTCAAAAGCAGGATGCCATCCATGAAGTGGATTCATCTGAAGATGAGACAGACGAAGGGTCGGAAGACAGCCAAGATGGGCGCAGAACTTGCTATGCTCCTCCTAGCCATGTCTTGAGGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26772
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
ENSDART00000115409 Nonsense 1403 1934 30 30
Genomic Location (Zv9):
Chromosome 6 (position 33364893)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33682558
GRCz11 6 33667248
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATATCTCGGCCAAAGAGTGCAGACCCTCCTCGCTCTCCTCTGCTCAAA[C/T]GAGTCCAGTCCGCAGAGAAACTCGCCGCCTCTCTTTCTTCTTCATCCTCC
Long Flanking Sequence:
CTGCCATGTCAGATATTATAATCATTGATTTTTTTTTTTTTTACTTAATATTAGTTCCCCGTGAGATCATGCATATCATTTTGCTCATTATTTTTGGTAGTATTAATATGTAACCTTGAACCTTCTTTTTTCCTAATACAGTTGGTGGAAACTCATCCCAAAGTAGCTCGCCTAGCTCCAGTGTGCCAAACTCTCCTGCCAGCTCTGGCCAGATCAGACCCAGCTCCTTGCATGGTCTGGCCCCCAAGCTGCAGCGCCAGTACCGATCCCCCCGCCGGAAGTCTGCAGGCAACATCCCTTTATCCCCTCTGGCCCGTACACCATCGCCCACTCCACAGAGCACTTCTCCCCAGCGTTCCCCTTCTCCCCTGCCAAGCCACGGGCTCATCACTTCTTCAATAGGCCAGTCTTTTCCTGTCAAACTGCACTCTTCACCTCCATTAGTAAGACAGATATCTCGGCCAAAGAGTGCAGACCCTCCTCGCTCTCCTCTGCTCAAA[C/T]GAGTCCAGTCCGCAGAGAAACTCGCCGCCTCTCTTTCTTCTTCATCCTCCTCTCCTTCTCCCTCTTCGGCTGCTGATAAAAAGCTTCCAGTTGGTGCCAGCCGCAAACACAGTCTTGATACCTCACATTCAGAGTTTAAAAAAGAGATGCTGCAGCGAGACCCTAGTCTACAGAGCCTGCAAGAGTCAGCCAGTGAGACTCTTATGGGAGGAAGAGTGTCTCCTGCAGAAAAGGGAAGCCTGCAGAAAAGTTCAGTGCGTAAACTGGGCAGGCAAGAAGGTCCCGAGTCTGGAACAGGAACTCTGGGACTTGTTCCTGGAAAGAGTAAATTGAAAGACAAGCTGTCTGCCATACGTGCTGAACGCCGCGAATCTCTTCAAAAGCAGGATGCCATCCATGAAGTGGATTCATCTGAAGATGAGACAGACGAAGGGTCGGAAGACAGCCAAGATGGGCGCAGAACTTGCTATGCTCCTCCTAGCCATGTCTTGAGGCCTACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31517
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
ENSDART00000115409 Nonsense 1813 1934 30 30
Genomic Location (Zv9):
Chromosome 6 (position 33363663)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33681328
GRCz11 6 33666018
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAGCTCAATATCCCAGGTACTAAAGAGACCATGGAACGAACAAAGGAC[C/T]AGCGTACCCAGGCAGATGCCACCCACCCAAAGATAAAAGAATGTCGCCTG
Long Flanking Sequence:
GTTCAACGATAATTGATGATTCGAAAAAACAGTCACAGGCACAAGACATTCAGTCCAGACCTTCTCCACATCAACCCAGTCCTCTGTCTAGTACCTTTTCCACCCAAGGCAGCGCCTTTACCTCTGTTAGTAAAGACCCATTTGTCAAGCCCACCACACCTCCATTGGATCCCCGGAGGACCCCAAAAATGTCTGAGCCAAGGTCAAAAACCAGTGGTAGAACTGATTCTAGCACTACTTCTGGAGTAGCCAGGGATACCCCAGTTGCGACTACCCCAACAGGAGGAATCACTAAGGAGATGAAGGAGGCTGACAATCGCAGACAGGCTGCAGCTGCTGCTGCTGCCTCTGCCGCCGCTGCTACCACCTCTGCATCCACTGCCTCTGAAAGTGGAATGGATAAAGTTGTGTCTCAGCTCGCCACTGTGGCCAAGAGTGTGCTTGGACCTGTCAAGCTCAATATCCCAGGTACTAAAGAGACCATGGAACGAACAAAGGAC[C/T]AGCGTACCCAGGCAGATGCCACCCACCCAAAGATAAAAGAATGTCGCCTGGAGCACCCTGATTCTCCTGACCAATTGAGTCCATCTGCTGCTTCGGGCTCCCAGTCTCCACGACTGACTGAATCTCCATCTAAACAAACATCATCCAAATCTGAGCCAGCCTCAACTTCTCAGAGACCTTTAGAGGTCCCAGGGACTTTCAAAAGACAAACTTCTCCAATCCCTCAAGCTAGGGAAGAGCATCAGGATAGGTCAGGAACTCTGCAAAGTGGCACCACATCAAGGCCTAGGTCTGAAGCACAATCACAGACCCAGCAGGCAAAGCCCAGTTCCACTACGTCACGAGATAAATCCAACAAGACAACGTAGCAGCCTTGCAGAAGACCCAGCTTTAATTGAACATGCCTATTAACAGACAAATACATATTGTAACGCAAGGCTGTTGTGTTGCTTAATGTCAATATCCCTGTGAAAAGATTGTGGAAGAGAGATGATGTTTAC
Associated Phenotype:
Not determined