Busch Lab

ZMP

zgc:171671

Ensembl ID:
ENSDARG00000016763
ZFIN ID:
ZDB-GENE-071004-18
Description:
hypothetical protein LOC100002269 [Source:RefSeq peptide;Acc:NP_001098611]
Human Orthologue:
ZNF292
Human Description:
zinc finger protein 292 [Source:HGNC Symbol;Acc:18410]
Mouse Orthologue:
Zfp292
Mouse Description:
zinc finger protein 292 Gene [Source:MGI Symbol;Acc:MGI:1353423]

Alleles

There are 13 alleles of this gene:

Allele Name Consequence Status Availability
sa9274 Nonsense Mutation detected in F1 DNA Not yet available
sa8386 Nonsense Mutation detected in F1 DNA Not yet available
sa9571 Nonsense Available for shipment Available now
sa10055 Nonsense Available for shipment Available now
sa8910 Nonsense Mutation detected in F1 DNA Not yet available
sa18214 Nonsense Available for shipment Available now
sa28931 Nonsense Mutation detected in F1 DNA Not yet available
sa23187 Nonsense Available for shipment Available now
sa43006 Nonsense Mutation detected in F1 DNA Not yet available
sa23186 Nonsense Available for shipment Available now
sa23185 Nonsense Available for shipment Available now
sa10631 Nonsense Available for shipment Available now
sa10167 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9274
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
ENSDART00000004424 Nonsense 45 2313 1 8
ENSDART00000111678 Nonsense 45 200 1 9
Genomic Location (Zv9):
Chromosome 17 (position 49594493)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49355577
GRCz11 17 49438552
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCCGAGTCGACGCTAGATGCCTCCAATAGTTTTTGTCAGGATTTCTGC[C/T]AAGTACGGTTTTATTCATGCGCTTWAGTCTGTCAGTCTTTGTTCGCGGAC
Long Flanking Sequence:
AGAGGGAAAGAAAGACTTTTGTCAATGACGTGACTGTTTTTGAGGACAGACGCCCCCTCCCCTAACCCCCCTGCGCCATAGTCGAAACGGTAGTTTCGAATTTCGAACACTACTATGACTAAAGATTGACTCATGAATATTAATTATGCCGCTTTGACGTACTTCATAACAGTTACTATGGCGACTGCTTCACAGGCACACATATTAAATATGTCTAGTAGTAGGTAAACCGCAAATTTTCTCTTGAATATTAATTAGCCAGTGCTGACGTTGCTCGGTCAGCGAACGCACGGGTCATGAATATTTGGATCAGGCCTTGGCCGTAGTAGTTTGAGATATTTGGGCTGCTGTGTGTGAATGCAGCGAAGATGGCGGAGGAGGAGGGCAGCGCGAATGAGGCTGTGGCCCTCAAACACAAATTCCAGGATCTCATCTCTGAATTAAAAAGGAGCTCCGAGTCGACGCTAGATGCCTCCAATAGTTTTTGTCAGGATTTCTGC[C/T]AAGTACGGTTTTATTCATGCGCTTAAGTCTGTCAGTCTTTGTTCGCGGACGATGCTGCATGTTTGCATCGCTGCACCAACGATAACAAAACTAACAATACTCGTGCAGTTGTTGATCAATATGATGGGGGAAAACCTAAAATCTGTGCGCTGGAAAGAGGGAGCGTGATTGTTTAACAGTTTTTAAAGCTTATGCTCATTAGGTTAGTATGGATGGCATGGTCACAGCTCCTGATGGCTAACACATTAGCTTATTGTAGCAGCAGTAGCCCTTACTTTCCACCCAAAACATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAGCATGCATGTGTGTTTTCATAATTTAAAAACATAGAAACTAAAATCTAAAGTTAAGTCTTTTTTTGTTAAAGAAAACTGCTATGAAATAAGCTTATGCATGTATTATAAATGTATTAACTTAGAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8386
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
ENSDART00000004424 Nonsense 299 2313 7 8
ENSDART00000111678 None None 200 8 9
Genomic Location (Zv9):
Chromosome 17 (position 49577694)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49338778
GRCz11 17 49421753
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGAGCTGACACTGTTTTGGAGTAAGCTTCTAATAAGGCTGGAATCAAAA[C/T]AKGCCTTTTTGGAGCAATGCAGACTGTTAGCAYGCCTCTYTGAGAGCGTG
Long Flanking Sequence:
TCAGCGTCAGCGCTTGACTGAAGGCATGTCTGAAGTTGGGGCTGAAACGATCGTCATAGAAGCGTCTGATTGGCTGACGCTTCCGTCGGCGCTTGAAAAGTTGAGCTAGTCCCAACTTCAGCAGCAAGCAACGCCTTTGAAGCGGCGCCGACGGATCCACAATGATGTTCGGCAACGCCTGACGTCATCCATTCAAAGTGAACGGGAAGCGTTGACACTGACGCCCCATGTGAATGGGGTGTAAATGCATAACAACACGCAAAGCATGCGCCGTGGGTCACACCGATCAGTTGACGCAGAAGTATAAACCAGGCTTAAGCTTTCACTGAAAGTTTGTTTGCTTTAAAACTCTAGCTGGGCATAGAGCTCAGTAAAAAACTTGAGAATCACTAAACATTGTAGTGCTTGTTTTCATTTGAAATCAATACATTAATCATTGTATACCTTCCAGGGAGCTGACACTGTTTTGGAGTAAGCTTCTAATAAGGCTGGAATCAAAA[C/T]AGGCCTTTTTGGAGCAATGCAGACTGTTAGCACGCCTCTCTGAGAGCGTGTACCATATTCTGCTCCTCATCAAAGTCATCCAGGCTGAGGTTAGAAAACCTTTCTTTTTTTTTATGCCAGCATGTTATGGAATCCAAATCTTTGGCAATCTGATGACTGACATTTTTGTTTCCCTAGGTTGACACCGATGGGCTTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9571
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004424 Nonsense 424 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49577230)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49338314
GRCz11 17 49421289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCT[T/G]AAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAAYTCTAA
Long Flanking Sequence:
TTTTGGAGTAAGCTTCTAATAAGGCTGGAATCAAAACAGGCCTTTTTGGAGCAATGCAGACTGTTAGCACGCCTCTCTGAGAGCGTGTACCATATTCTGCTCCTCATCAAAGTCATCCAGGCTGAGGTTAGAAAACCTTTCTTTTTTTTTATGCCAGCATGTTATGGAATCCAAATCTTTGGCAATCTGATGACTGACATTTTTGTTTCCCTAGGTTGACACCGATGGGCTTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCT[T/G]AAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAACGAATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10055
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49577000)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49338084
GRCz11 17 49421059
KASP Assay ID:
2261-1579.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTTACGAACTCTTTGAAGTTGGARCAGAAAGAAAGAAGAAGAAGAAY[G/T]AAWTTAAGAAGGTRAAGGAGAAGGGATTWGTTTCTGCTCGATTCCGCAAT
Long Flanking Sequence:
TTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAAC[G/T]AATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8910
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
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49577000)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49338084
GRCz11 17 49421059
KASP Assay ID:
2261-1579.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTTACGAACTCTTTGAAGTTGGARCAGAAAGAAAGAAGAAGAAGAAY[G/T]AAWTTAAGAAGGTRAAGGAGAAGGGATTWGTTTCTGCTCGATTCCGCAAT
Long Flanking Sequence:
TTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAAC[G/T]AATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18214
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
ENSDART00000004424 Nonsense 501 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49577000)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49338084
GRCz11 17 49421059
KASP Assay ID:
2261-1579.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTTACGAACTCTTTGAAGTTGGARCAGAAAGAAAGAAGAAGAAGAAY[G/T]AAWTTAAGAAGGTRAAGGAGAAGGGATTWGTTTCTGCTCGATTCCGCAAT
Long Flanking Sequence:
TTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAAC[G/T]AATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28931
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
ENSDART00000004424 Nonsense 703 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49576394)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49337478
GRCz11 17 49420453
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCATGTTAAGGCCCATAAAAACGAGCAGGAAGCAACAGACTTCCTT[C/T]AACTACAGAGCCGGAAGGCAATGTGCCAATATTGTCACCGCCAGTTTGTT
Long Flanking Sequence:
GAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGATTGTTGCTGTCCTGTTACAAGCTGTCAAAAGGTTTTTAAATACTTTAGGAATTTGGTTGCTCATGTTAAGGCCCATAAAAACGAGCAGGAAGCAACAGACTTCCTT[C/T]AACTACAGAGCCGGAAGGCAATGTGCCAATATTGTCACCGCCAGTTTGTTAACTTGACCCATCTTAACGATCACGTACAAATGCATAGTGGCGATAAGCCATACTTTTGCGTTCAGCTTGGATGTAATTGCCGCTTTTCCTCTCACGCTGAGCTTCTGATGCACAGAAAATTACATGCTGAATTTCAGGCGCAGTGCGCATATCCAAACTGTGAGCGAATCTTCAATGAGACCTACTTGCTGTATGATCATGAAGCACAGCACTACTTGACGTTCCCCTGCAAAAGTCATAACTGTGACAAGGTGTTCTACACATTGGCTGAGCTAGATTTGCATCAGAGAGGGCATGCAAAGCAGGTGGACCACTCTGCCATCGATAGGCGCTCACATTTACACTTGGAAGTAGCGCCTCAGGCTTGTCCTGCTTCCGAGCTGCCTCAGAACCAGATTAAAGATTTTACCCCAGTAGAAATTAAATGCTCAGTTCAAAACATTGCAGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23187
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004424 Nonsense 1342 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49574475)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49335559
GRCz11 17 49418534
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGAAAATAGGAAATGCAAAAAAATTAAATCATCAAAAAGAACCAAATG[G/A]CCTGCCATAATACAGGATGGGAAGGTCATTTGCTGCAGGTGCTACAGAGA
Long Flanking Sequence:
CCCTCAGGCGTGATGAATGAAGCCTCAAAATATGTCTCAAGCTCTCTTAGGGTGCTGCATGCTCTTAATGGCGATCAGACTTGTGACCTGTCACAGGTTGAGTCGAGCGTTAATCTCGAAGATATTTCCATCAGCAATGATTTGCATGCAGGAGCTCTGTCCGGACAGAACGTCAGCCTGTATTTTCCTTCAGAGGCAAGTTCTGTTTCAATGCAGTCAATGGAAAATTCGAACAAAGAAATGAGCTCGGAGTGTACCGATGCAGCGTTCGCATCAGAAATCAAATGCATGTCAGATATTTTAAACCCTAACTTTAAGGAATCATCAGAAGATTTCTTTGGTGCTACCCCTGTGAACGATGATAAAACTCCAGATGATTTTTGTAATCATGAAATGGCCCTGGAAGGACCGGAAGGAATCACTTCAGATGATCAGACTGTTTTAGATTCTGGTGAAAATAGGAAATGCAAAAAAATTAAATCATCAAAAAGAACCAAATG[G/A]CCTGCCATAATACAGGATGGGAAGGTCATTTGCTGCAGGTGCTACAGAGAGTTTTCAAGCACAAAGTCTCTAGGAGGTCATTTGTCAAAACGTTCCCAGTGCAAACCTGTAGACGAAATAGATCTTACTGCTGATTTACCAGTATCGTTTCTCGATTTTCTAAATGATCCTGACATTTCAACAGTACAAATGCCTCTACCAGCTAATGATATACTTGAGGACAATCACAAATCCTTCATCTATGCACCATCAGAATCAAGTACCTTTAACGATAACACCTTAACAAGTGTGCATGGCACAGAGAGCATCCCCAACATTAATGCTAATGAGCCCTCTCAAGACCACTCTGAGATAGCTACAAATCCCAATTTGTTTAATTCCCCTGTATCTAACACAGCCACAGAAATGATAGCTGATACTGAAATTATCCCTGAAAATGCTGGTGAGGATGGAATTATCTTAGAAATTGAAAGGGCATTACAACGCCTTGATTTAGTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43006
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
ENSDART00000004424 Nonsense 1833 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49573004)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49334088
GRCz11 17 49417063
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCATATCGATGCATTCATGAGGGATGTGTGGCTGCCTTTTCAATCCAA[C/T]AAAATCTCATCCTCCATTATAGGGCTATGCATCAGTCAGAATGTGATGAA
Long Flanking Sequence:
TTCAACACCAAGTCGATCCCAAATTGACTGTTTCAACAGTTAAATCAAATGTTGATGGCAAACCTAAGATTGTTAGCAAAAAAAAGAAACAAGCCACAAAAAGCTCCCTTACAGTCGGCACCACTAAGTCTTGCAAAACTACGGAAGAGACGCAGAAAAATGTTGGAAACCTTGATCGACTTTCGACCACATGTATAAAACTAGAAGCCCCAGCTCAAAATGCTGAGAGTCATGCTAGTGATTTAAACCATCCAGGTATATTTGGAGCACAGGAGTTGAGTGGTCTTAGTAGTCCCCATCTTTTTAACAAAGTAAATGCCACGAACGAAGAATATGCAACTCCACAATTTTTCGGACAAATTGGGACAAAATCAAGTGTGACTGAAGATACTCAGGAGAAAACGATGGCAGTTGGTAACACTGATTGTGGTGATTCGGTTGATGTGTATCGGCCATATCGATGCATTCATGAGGGATGTGTGGCTGCCTTTTCAATCCAA[C/T]AAAATCTCATCCTCCATTATAGGGCTATGCATCAGTCAGAATGTGATGAAAAGAACAGCGCTAAAGCTACCGATGGAGTGTTCCCGGTGCAGGAATACAGATGCCAAGTCAAACAATGCTCAAAAGTTGTGTCGAAAGTTACCAGCTTGCTGAAACACTATCTTTTGCTCCACAGATGCACATTGGAAAAGGCAAGTGCGTTGCTCTCTGGTGTTGAGGTAGGCACGTTTCAGTGTGACCAGTCCAAATGTTCTGCTCACTTCACGTGCCATTTGAAGTACATTGATCATATCAAAAACGATCACAAAGCAATAAAGGTTTCAGTCGATGGGGACTTTGAGAGCGTGAACCTCACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGTCGAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCATGAAAGCGAAACAAGAACATGTGGGGGACAGTGTTCAAACCAAGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23186
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
ENSDART00000004424 Nonsense 1967 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49572601)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49333685
GRCz11 17 49416660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGT[C/A]GAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCA
Long Flanking Sequence:
GATGGCAGTTGGTAACACTGATTGTGGTGATTCGGTTGATGTGTATCGGCCATATCGATGCATTCATGAGGGATGTGTGGCTGCCTTTTCAATCCAACAAAATCTCATCCTCCATTATAGGGCTATGCATCAGTCAGAATGTGATGAAAAGAACAGCGCTAAAGCTACCGATGGAGTGTTCCCGGTGCAGGAATACAGATGCCAAGTCAAACAATGCTCAAAAGTTGTGTCGAAAGTTACCAGCTTGCTGAAACACTATCTTTTGCTCCACAGATGCACATTGGAAAAGGCAAGTGCGTTGCTCTCTGGTGTTGAGGTAGGCACGTTTCAGTGTGACCAGTCCAAATGTTCTGCTCACTTCACGTGCCATTTGAAGTACATTGATCATATCAAAAACGATCACAAAGCAATAAAGGTTTCAGTCGATGGGGACTTTGAGAGCGTGAACCTCACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGT[C/A]GAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCATGAAAGCGAAACAAGAACATGTGGGGGACAGTGTTCAAACCAAGAAGTCAAGTGCAAATCCTAATTCCAACAATGGGAAGGAAAATATTGCGAAAGACAAAACTAAAACGAAGAAGAAAAGTTCCAAAAAGAAAGAGGACAAGGCTCAAAGCCAACGGGTAACCTTAGAGAAGCCTGCGCTTAAATCCAACGAGGAAGCATCTGCTTTGTGCACTCAAACATTTCCTCTACAGTACCCATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTACACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23185
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
ENSDART00000004424 Nonsense 2083 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49572252)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49333336
GRCz11 17 49416311
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTA[C/A]ACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTT
Long Flanking Sequence:
TCTGCTCACTTCACGTGCCATTTGAAGTACATTGATCATATCAAAAACGATCACAAAGCAATAAAGGTTTCAGTCGATGGGGACTTTGAGAGCGTGAACCTCACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGTCGAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCATGAAAGCGAAACAAGAACATGTGGGGGACAGTGTTCAAACCAAGAAGTCAAGTGCAAATCCTAATTCCAACAATGGGAAGGAAAATATTGCGAAAGACAAAACTAAAACGAAGAAGAAAAGTTCCAAAAAGAAAGAGGACAAGGCTCAAAGCCAACGGGTAACCTTAGAGAAGCCTGCGCTTAAATCCAACGAGGAAGCATCTGCTTTGTGCACTCAAACATTTCCTCTACAGTACCCATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTA[C/A]ACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTTCAGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10631
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
ENSDART00000004424 Nonsense 2230 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49571813)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49332897
GRCz11 17 49415872
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTT[C/T]AGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAA
Long Flanking Sequence:
CATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTACACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTT[C/T]AGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAAACTCAAACCGATCATCCGAACGAAAGATCAAGTCAAGCGCGTCGTTAATTTCCGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTATAAAAACCAGTCCCCTGGTTCTAGACTTCTGCTGAAGCAACTTCAAGATATGCAGCCTAGGGTCATCCTGGAAAAGAGGCTGCACAGTTGATGGTTAGAGTAGAGACGTTAAAAACAAGGCCTTGCTCTCAGGACCACATACTGTGTCACATGCTGCTGACAGGTACATCCAGATACTCTCTTGCATTTATAGTAGTTCCAACACATTGTTAATGACTTTTAATTAGTAGAAGAGAAAGCAAAGTTTTGTACAATATTTAACGTTTTGATGTACTATTATGGTTGTGCTAAAAAAAAAACCTTTTGTATTTCTGAAATTCTCTGATGAAAATTAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10167
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004424 Nonsense 2284 2313 8 8
ENSDART00000111678 None None 200 None 9
Genomic Location (Zv9):
Chromosome 17 (position 49571649)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49332733
GRCz11 17 49415708
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTA[T/G]AAAAACCAGTCCCCTGGTYCTAGACTTCTGCTGAAGCAACTTCAAGATAT
Long Flanking Sequence:
AATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTTCAGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAAACTCAAACCGATCATCCGAACGAAAGATCAAGTCAAGCGCGTCGTTAATTTCCGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTA[T/G]AAAAACCAGTCCCCTGGTTCTAGACTTCTGCTGAAGCAACTTCAAGATATGCAGCCTAGGGTCATCCTGGAAAAGAGGCTGCACAGTTGATGGTTAGAGTAGAGACGTTAAAAACAAGGCCTTGCTCTCAGGACCACATACTGTGTCACATGCTGCTGACAGGTACATCCAGATACTCTCTTGCATTTATAGTAGTTCCAACACATTGTTAATGACTTTTAATTAGTAGAAGAGAAAGCAAAGTTTTGTACAATATTTAACGTTTTGATGTACTATTATGGTTGTGCTAAAAAAAAAACCTTTTGTATTTCTGAAATTCTCTGATGAAAATTAGATGAATTTTTTTTAAATGTACAGTTTTGTGTAGAATGAAAAAGTTATCATCTATCCCTGTGGGATTTTTTTTTCTTTATTTTTTTTCCTTTATTCGAAAGTATTTATTTTTAACTTAACAGTAGTGTTTCAACGTACTTGTCTTCCACCTAACATTCAATTTAAGT
Associated Phenotype:
Not determined