Busch Lab

ZMP

si:ch211-285n22.1

Ensembl ID:
ENSDARG00000034555
ZFIN ID:
ZDB-GENE-070912-290
Description:
Novel protein similar to human and mouse par-3 partitioning defective 3 homolog B (C. elegans) (PARD
Human Orthologue:
PARD3B
Human Description:
par-3 partitioning defective 3 homolog B (C. elegans) [Source:HGNC Symbol;Acc:14446]
Mouse Orthologue:
Pard3b
Mouse Description:
par-3 partitioning defective 3 homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1919301]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa18025 Nonsense Available for shipment Available now
sa34592 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21451 Essential Splice Site Available for shipment Available now
sa14053 Nonsense Available for shipment Available now
sa11131 Nonsense Available for shipment Available now
sa27364 Nonsense Mutation detected in F1 DNA Not yet available
sa45350 Nonsense Mutation detected in F1 DNA Not yet available
sa15430 Nonsense Available for shipment Available now
sa6111 Nonsense Mutation detected in F1 DNA Not yet available
sa16200 Nonsense Available for shipment Available now
sa25419 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18025
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061062 Nonsense 33 1172 1 22
ENSDART00000131512 Nonsense 33 131 2 4
ENSDART00000137043 Nonsense 33 178 2 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15483446)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15236011
GRCz11 9 15207214
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAAGGATGGACAGTGCGKGATCTCATCCTGCAAGCCACACAGAGATA[T/A]AGAAAACTACTGGAGCWGGTGAGTTTAGTGATCTTATCAGATTTAAAGGC
Long Flanking Sequence:
AGTTAGCCGCAACAAACGGTACACTTACCGCCTTCATCTCTAACTGTAATAACAAATCCAGGCTGAAAATGTATTTGGATCGTTATTATCTATCCATAGACAGTTTTTTTTTACTTTCTCACCAGCTGTTGATATTGAGCACCCAAGTGTCTATCCAACCATCAACAAGCTGTTTATTAAACATTTTAATAAACACTGCCGTATAGTTATAAATCATATAACGTTATCTGAAACATGTTTCTCGTTTATTTGTTTTACATGCAGTATTTGTTTTTCTTTGTATAGAATTATGTCATCTCTGATGCTGTGAAGTTTGCTGCAAAAAAGCAAATACCACAAACACCTGCTGCTGGAGTTTCTGTAGGGACACATCTGTATTAATCTTCGCTCTCTGGATTAAATATGAAAGTGACAGTGACTTTTGGAAGGACTGGTGTTGTTGTACCTTGTAAGGAAGGATGGACAGTGCGGGATCTCATCCTGCAAGCCACACAGAGATA[T/A]AGAAAACTACTGGAGCAGGTGAGTTTAGTGATCTTATCAGATTTAAAGGCAGGCACACTGGTTGTATAGTTCTTTTCTTTCTTTCTTTCTTTCTTTCTTTAAAATTCTTTCTTTCTTTTTTTTTTACTTATGTTGTTTTAAATCAACATAATTTGCTTTATTACATGCATCATGACAAAGTAGATTTTTAGCAAACTTATTTTGGTCAACAATGTTAGGATAACTAATAAATCTACAGTAGTGTTCAGATTTTTTACGTTTTTGAAACATTTAGTTTCTTATCCTAACCAAAAGTAAAAACTCTAATTTATTAGTCCTTCCAGGTTTTTTTGCAGAGATATTATATTGACTTTTTGCAGGCTAAAAGCACATTTTAAGCCTAAAATTCATGCATTAATTTTCCTTCGGCTTAGTCCCTTTATTCATCAGGGGTTGCCACAGCAGAATGAACTGCAAACTTATCCACCATATGTTTTAAACAGCGGATGCCCTTCCAACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34592
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
ENSDART00000061062 Essential Splice Site 161 1172 4 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 Essential Splice Site 161 178 5 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15316284)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15068849
GRCz11 9 15040052
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGCCCTTGGAGCTTCTCAGATGGAAGATATGAACAGCAGAGCGATGG[T/C]AAAACCAAACTCACCCATTCAGCCTCTCACATTTCAAACACCACATATAT
Long Flanking Sequence:
CATGTTACAAACATGTCTATTTTTTTTTTTTCTGTATGAATTTGGTTTATTGTGTTATTTCAACAGTACAGTACACTGCAAGTAAAAACAGTACAAACAAAAATAACTATGACAAATAATGCAAATGTTATCAATATTTTAGTATTTATTTTATTAAAGTTCTTTGACCATGACGGTTTAAAAACTAAATTTTAATTAAAATTTTCTTTAGACAATGACACATTCAAAATATCACTTTTTAAATGTAAATATAAAGTGTAACTAATATGTTAAGTGCAGTAAAGGACTGCCATTACACTACATACAGTATGCTGAGGGTGTGAATTACCAAGGTGTTTTAAAATGAAAGGTGCTATAAAACATACTTTATACTACTCTATATTAGTAGTATATTGATCAGCTGTGTGTTTGTGTTGCAGGTACTCCTCTACTAGTGCGCAGCAGCAGTGATTCTGCCCTTGGAGCTTCTCAGATGGAAGATATGAACAGCAGAGCGATGG[T/C]AAAACCAAACTCACCCATTCAGCCTCTCACATTTCAAACACCACATATATGTCTTCTGAAAGCACTGATCTGATGTCATCACATGAGAAGATAACAGCCACAAACTATTATTAGAGACCACCGTTGTGTCTAATGATCAATCAGTGTGCCTGCTATAAATACTTACAACCTTAGACCCTGCTAAAATCATCAGAGAACAGCTAAGTAAAACATACAGGTGCTGAGCAGCTCACATTGCAGTTAAAACCTATTGATCATATAGGCTGTGTCTCATGCTTTTTTTAACCATTCTGTCATTGCCAATACATTAATCAGCTTGATCTAGCAGTCTGTTAACAGAGGTTTATAGCGTTAGAAGAAAATACAATTTAGTGATAACTTACAGCATTTCTTACTATGCTGTGATAGGACATACTTGAGTTATTTCTTGAGTTAATTTGCTAAGTAATTTTTCTTGAGTATATATTTTACATGAAATTAAACTTTTTAAATAGGTTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21451
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
ENSDART00000061062 Essential Splice Site 214 1172 6 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 Essential Splice Site 37 629 2 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15268767)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15021332
GRCz11 9 14992535
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCCTTTAGGAATACACGTGGTGCCGTATTGCTCCTCTCTCAGCGGAAG[G/A]TTAGTACAGCACATTTCCCATTTTTCCATATTCACACACACACAAAACAC
Long Flanking Sequence:
TCTAACTGTACTCGCTCATGTATGACTCTGCAAATATTCCAGCATGATGAGCTATTAGTTGTGGATTAAAGGCGGATGATCACTGGCCCGCTCTGTCCACAGTTATCCACTTACTCTCCCACTATATCATCACACCTCATGCCAGGAACATTTGCAGAAATAGAGAAAAAAAAGAGGAACATCTGAAAATTAGTCAGAAAGGCAGACATCATGGAAACGATTTCAGCAGGGAATGTAGGAAAACAGGATCATGTGGTAGAAAGCTGACTAACTCAAACATGTACGGCAGCCCGGCAGCCCTGCATGCAGTAGATCTGAGGGCCATGAGACAGTGAGTTTACACTGGTTTGTATTGTGCTGTCTTACTTCTTAATAACGTGACTGATGTGTTTTTTTTTTTGCTGTTGTGTTTTCAGCCTCACAAAGACGGTGGAGATTTCTGGGGAACAAGGGCCTTTAGGAATACACGTGGTGCCGTATTGCTCCTCTCTCAGCGGAAG[G/A]TTAGTACAGCACATTTCCCATTTTTCCATATTCACACACACACAAAACACACTTTGGTGATACATGTCTTAGCTAAAGCATGTTGACGTGCGTTGGAGAAATCTAAAGCTCCACTGCAAACATCCAGAGCTTTGTTTGTGTCTACATGTTTTTGTTGCGGGGGATTATGGGAATGTTCTGTGCTGCTCTGTTGGTTTTGAAGTGATGAATCAGAATGTTGTAGCTTTTAGTTCAAGTTTTTGGGCTATCTTTATACTAGCGTATGAAGGTAAGGTTGACAAAATAAAGTTTAGTTTAAATATTCAAAGTTGCTTTGAATGGAAAAACTGGCTAAAAGTTTTGATGACTCATTTTATGCCAGTTATATTTACTCTTGAATGATAATGACCCTCTCCCATCTGCAAATATATATAATCCAATATGATTTCGATAGAATGTATGATTCGTATGTACTGTGAGTATACATGTGGCTACGAGCCGACATCTTATGTTGCTTGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14053
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061062 Nonsense 236 1172 7 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 Nonsense 59 629 3 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15256362)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15008927
GRCz11 9 14980130
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATTCGAGGGGTGGAGGAGAACAGTCGCTCCAAACGGGAAGSCATCTTT[C/T]AGGACGATKAGTGTATCGTTAAAAYTAATGATACTGAATTAATGGACAAG
Long Flanking Sequence:
TTGAATGCCAGCCTATAAAAACACAATGCATTTGAAACACAAAAACACCATACAGTATGTGCACTTTAAATATTCATCCTAGTCCCATCCTGCATGCCAAAATCAAGATCAGGTGAATCTCTTAGTATTTGTTTAAGTTAGATTTGCAGGTATCTTTAAATCTTCTAAACATTCATAAGTGACTCTGGAATATAAATGCATACTCTTTTCCTCATTTTAGCAGTTTAAAGACTCCACGCTATAATGATATGCACTGTTTAATGAGTACTTTTTCTAATTATTATGTAATTACCTTGCAATTACTTTGTAATTATTGGTATTTGTCATGTGCTGTTGTTTTATTATGTTACAGTGGCACAGTCTGTCATGGTCAGTTGCTGGCTAGTGCTGTGCTCTGTTTTTGCTGCTAATTTATGATTTGCTCTATTTTTCTCAGGCCTCTGGGTCTTCACATTCGAGGGGTGGAGGAGAACAGTCGCTCCAAACGGGAAGGCATCTTT[C/T]AGGACGATGAGTGTATCGTTAAAATTAATGATACTGAATTAATGGACAAGTCTTTTTCACAGTGAGTCTTAGAGCTAAAGGCTTTCTGCTCTGCTTTCTCTGTCACCACTTCCCGATATCCTTTCCTTTCTGTCGTGTTACTTAGTTTTAAGCTCTATCCTTTCATTTCATGGTTGTAAAAACAAGCAAGTGTCCATTGTTGTGCTCTGTTTATGGCTATCAACCCTGGACGGGTGTCAGAAAAGCAAAAAAAAAAAAAAAAAAAAACACTGGACCCGTGGTGTCAAAGCCCATTCAGCAGTCACGGTCATTTGCTGAGCTCTGTTTGTTGTGTGTAGCAGACCTCCTCATCTTACAGAGCATTACTGCACACTGTCATGCAGATTAGAGATGTGCTACCTGACCTACAGATAGCAGGATATAAAAAAGTGATATGGGGTTTGAGCTATTTTTAACATATAATTTTAGATTTGGGCCTGTTTCAGTGAGGACAGCATTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11131
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
ENSDART00000061062 Nonsense 239 1172 7 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 Nonsense 62 629 3 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15256353)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15008918
GRCz11 9 14980121
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTGGAGGAGAACAGTCGCTCCAAACGGGAAGGCATCTTTCAGGACGAT[G/T]AGTGTATCGTTAAAAYTAATGATACTGAATTAATGGACAAGTCTTTTTCA
Long Flanking Sequence:
AGCCTATAAAAACACAATGCATTTGAAACACAAAAACACCATACAGTATGTGCACTTTAAATATTCATCCTAGTCCCATCCTGCATGCCAAAATCAAGATCAGGTGAATCTCTTAGTATTTGTTTAAGTTAGATTTGCAGGTATCTTTAAATCTTCTAAACATTCATAAGTGACTCTGGAATATAAATGCATACTCTTTTCCTCATTTTAGCAGTTTAAAGACTCCACGCTATAATGATATGCACTGTTTAATGAGTACTTTTTCTAATTATTATGTAATTACCTTGCAATTACTTTGTAATTATTGGTATTTGTCATGTGCTGTTGTTTTATTATGTTACAGTGGCACAGTCTGTCATGGTCAGTTGCTGGCTAGTGCTGTGCTCTGTTTTTGCTGCTAATTTATGATTTGCTCTATTTTTCTCAGGCCTCTGGGTCTTCACATTCGAGGGGTGGAGGAGAACAGTCGCTCCAAACGGGAAGGCATCTTTCAGGACGAT[G/T]AGTGTATCGTTAAAATTAATGATACTGAATTAATGGACAAGTCTTTTTCACAGTGAGTCTTAGAGCTAAAGGCTTTCTGCTCTGCTTTCTCTGTCACCACTTCCCGATATCCTTTCCTTTCTGTCGTGTTACTTAGTTTTAAGCTCTATCCTTTCATTTCATGGTTGTAAAAACAAGCAAGTGTCCATTGTTGTGCTCTGTTTATGGCTATCAACCCTGGACGGGTGTCAGAAAAGCAAAAAAAAAAAAAAAAAAAAACACTGGACCCGTGGTGTCAAAGCCCATTCAGCAGTCACGGTCATTTGCTGAGCTCTGTTTGTTGTGTGTAGCAGACCTCCTCATCTTACAGAGCATTACTGCACACTGTCATGCAGATTAGAGATGTGCTACCTGACCTACAGATAGCAGGATATAAAAAAGTGATATGGGGTTTGAGCTATTTTTAACATATAATTTTAGATTTGGGCCTGTTTCAGTGAGGACAGCATTGACTGGCAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27364
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
ENSDART00000061062 Nonsense 280 1172 8 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 Nonsense 103 629 4 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15252084)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15004649
GRCz11 9 14975852
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATGCGTTCATCCATCGTTCGTTTAGAAGTGGTTCCGGTCTTTAAT[A/T]AAGAACGTTTTGAGAAGAGTGTGATCAGCCACCTGTTTAACCCAGAAACC
Long Flanking Sequence:
CTGTTGAAACATTACCCAGTTGTTCTGTGGTCATCATGTACATTACACATATATTACATATACACATTTGTGCTAAGTAGAATTACTTCTATCCAGTAGAAGGTCACATTAATCTTATTAGACTCGGGATGGATGGACGGCTTTTAAATTAAATCAGTCAAGCAAAAATGAAGGAGGTGGATTGCTTTGTCATTTGTAATGCGTAGGACTCATTAGTCATAACCCCAATTATGCTGTCAGAATAAATGTCAGAGCGAGTTTTATCTAAGCCAAGACTATTCAAAGTATTACAATTTCCACCTTTTTTTTTTTTAGTTTCCAGGTTCATTTGTTTCATCAAACAACCTGCAAATAATTATAAAAAATTGATTGTCTCCTAATTGCTTTTTCTATTTCTTGCGTCCCTTATCTCTCCTTCGTCTTTTTCCAGAGCTCAGGAAATATTCCGGCAAGCCATGCGTTCATCCATCGTTCGTTTAGAAGTGGTTCCGGTCTTTAAT[A/T]AAGAACGTTTTGAGAAGAGTGTGATCAGCCACCTGTTTAACCCAGAAACCCCTGACGCATCAGCACAGACCAAAGAGCCTCCGCCGCTGAAAGTGAAGCCCATGGTGAGGCCTGTAGAGTCTTCCTCAGGATGGCAAGCCGAATTTCAGGAGTCCAGCAGTAGTCTTGAGAGTCGCTCTTTGGGCTCTCCTTTACCCATCAACCTCTCTCCCACACCCAGAGGCAAGAGTGCTGAGAGCTCTCTCCTAAAAAATAGCCTGGGACCGTCACCTCTACAGAACCACAACAAGAAGGGTGGAAAGAGACTCAGAATCGACCTTAAGAAAGGTAAACAGTTGGGAAACATTTACTGAAAAAAAATGAGAAAATGGAAATATGTGGTATCTCTGCCTACATGTTTGAGAAACATAAAATTTGTAGCTCAAGGGACATTTCGTTGCATGTTTCAAATGACAAAGCCACTAGAGCAGGGGTGTCAAACTCAATTCCTGGAGGGCCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45350
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
ENSDART00000061062 Nonsense 325 1172 8 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 Nonsense 148 629 4 13
ENSDART00000144022 None None 184 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15251949)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15004514
GRCz11 9 14975717
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGAAAGTGAAGCCCATGGTGAGGCCTGTAGAGTCTTCCTCAGGATGG[C/T]AAGCCGAATTTCAGGAGTCCAGCAGTAGTCTTGAGAGTCGCTCTTTGGGC
Long Flanking Sequence:
GACGGCTTTTAAATTAAATCAGTCAAGCAAAAATGAAGGAGGTGGATTGCTTTGTCATTTGTAATGCGTAGGACTCATTAGTCATAACCCCAATTATGCTGTCAGAATAAATGTCAGAGCGAGTTTTATCTAAGCCAAGACTATTCAAAGTATTACAATTTCCACCTTTTTTTTTTTTAGTTTCCAGGTTCATTTGTTTCATCAAACAACCTGCAAATAATTATAAAAAATTGATTGTCTCCTAATTGCTTTTTCTATTTCTTGCGTCCCTTATCTCTCCTTCGTCTTTTTCCAGAGCTCAGGAAATATTCCGGCAAGCCATGCGTTCATCCATCGTTCGTTTAGAAGTGGTTCCGGTCTTTAATAAAGAACGTTTTGAGAAGAGTGTGATCAGCCACCTGTTTAACCCAGAAACCCCTGACGCATCAGCACAGACCAAAGAGCCTCCGCCGCTGAAAGTGAAGCCCATGGTGAGGCCTGTAGAGTCTTCCTCAGGATGG[C/T]AAGCCGAATTTCAGGAGTCCAGCAGTAGTCTTGAGAGTCGCTCTTTGGGCTCTCCTTTACCCATCAACCTCTCTCCCACACCCAGAGGCAAGAGTGCTGAGAGCTCTCTCCTAAAAAATAGCCTGGGACCGTCACCTCTACAGAACCACAACAAGAAGGGTGGAAAGAGACTCAGAATCGACCTTAAGAAAGGTAAACAGTTGGGAAACATTTACTGAAAAAAAATGAGAAAATGGAAATATGTGGTATCTCTGCCTACATGTTTGAGAAACATAAAATTTGTAGCTCAAGGGACATTTCGTTGCATGTTTCAAATGACAAAGCCACTAGAGCAGGGGTGTCAAACTCAATTCCTGGAGGGCCGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTATGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTACAGAGCTGCGGCCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15430
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
ENSDART00000061062 Nonsense 858 1172 18 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 None None 185 None 3
Genomic Location (Zv9):
Chromosome 9 (position 15017108)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14769673
GRCz11 9 14740876
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTCTTTCTATGCCCTCCCCTTCTCTGTCTCTCCTTTAGATTTGGAAAG[A/T]AAAAGGAAGAGAAGAGCAAGYCAGAGACAAAAGTGAATGCRTTGAARCAG
Long Flanking Sequence:
TGTTTGTGCGTGAGTAGCATATAGGATACTGGGGTGATTCCATTTCCTCTGACTTTCCTCTGTGTGTTAGATGAGTCCTGGTGTGTGTATATTTGTGTGTGTGTGTGTTTGTAGCCGCAGGCCACGGCCCCTGCTCGCTGTGACATTGATACACTGCGTTGAAGCCGAGTGCTGTGCTGCTCTACTGGGCGACAGTGGGTTTGAGACACAGGCACATATGAGAAATGACCTTCTATGAGCAGGGAAAATGGAGACGGGTGCAGGACTCAATCACTGGTGCAGAAATGATGCATGTTAACAGAGCATCTCTACTGACACGCTCTGGCCCCTACAGCGATTTAGGAACTCCCCGATGTACACACACACACACACATACATGCACACAGACTAGATAGACTCTCTGCCTGTTTTCCTAGATAAACGTAATTTGCAAACAGTGATCATTCAGTGATGTCTTTCTATGCCCTCCCCTTCTCTGTCTCTCCTTTAGATTTGGAAAG[A/T]AAAAGGAAGAGAAGAGCAAGCCAGAGACAAAAGTGAATGCGTTGAAGCAGACGACAGAGATTCTGAGCGAAGAGGAGTTGGAAAGGATGAAGGAAGAGAGAGAAAGGTGAGACTGGTTTCTTTACACTGTCACAATTTAAAAGAGTGGATCCCTACAAAAAATATTGATAACATAAAAGTTAAACACTGGACATTAGTACCCCTATATGTCATAGAAATATCTGTCATCATGCAAATCACACAGCAAACTTGATAAATATATGTTTATTTATTTATACCAAATCAATGCTTTACTCAGCAAATATGCATTAAGTTGGCCATAAGTAACAGTTAAAATATTCATTAAGTATTTGTTAATTAATTAATTAATTTATTTATTTGTTTCATTATTTATTTATTTATTTATTCGTTTCATTATTTATTCATTCATTCATTCATTCATTAATTCATTCATTCATTCATTCATTCATTTCTTGTTCATCAAAGAATTCAGGGGAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6111
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061062 Nonsense 1041 1172 21 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 Nonsense 55 185 2 3
Genomic Location (Zv9):
Chromosome 9 (position 14875463)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14628028
GRCz11 9 14599231
KASP Assay ID:
554-3943.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTACCAGATGCCGATGAGAAACCCTGACCCCAGACTGGCACCCCGCTA[T/G]GAGGACGTCGAGCGAMAGTATGCCTCCTTGCCCAGGTAACAAYATCCACT
Long Flanking Sequence:
TCGAGGCTCGAACCAGCGACCTTCTTGCTGTGAGGTGACAGCACCACCTACTGCGCCACTGCGTAGCCCATACTGGAATTTGTTTGGTAAAAATGTTTCCATCGTAGTTTATGCTTTTTTTTAAAGTTTTGCGCATACGTTTTTTTGTGCGCATTTTCTAAATTTATGCACATCTTGGCGATTCCATTAGCCGTTTTTTTATGCGCATATCTAAAATGTCATAAAAAATAGGTGGATAGAAACATAGCTACAGATATTAATTAAACAAATAGCATTTTGTAGTTAATAGCCTCACATTGACCATTTGCTTTTACAAACATGTTTTCTGTATACAGAATGCTACCTTGTTGACATTGCTATGAACAGTACTATAGCTGCACTGCAGTCCAATATGATTTGATGTGTCATGTAAACCTTTCGGGCTATTTTTCACTCTGCTCTCTTCTTGCCTTTTACCAGATGCCGATGAGAAACCCTGACCCCAGACTGGCACCCCGCTA[T/G]GAGGACGTCGAGCGACAGTATGCCTCCTTGCCCAGGTAACAACATCCACTCATTAATCCCACACCCTTCGTGACAAAACAGAAGAGGTGGAGAGCTAAAAACAGAAAAGATGGGATGGAAAAGAGGGGGAGAGCAGGTAGTCATCTGTCTCTCTCATGCAGAGCTGAATAATCCTCTTTAAAGCGTATAATTAAATCTGGAGTGTCTGCCTTCTGAGGCCCCCCTATCCTGGGAATTCACCTGATCCTCTCCGGGGAGATGGCCATGCGGTCGCAGCTCTGTAACCCGATCATACAGCGTGTTTCTGGAGCCGCCTAAAGTTACGGCTGCCTCTTTCTGTCTGTCTGTCTGTCTGTCTCTTTCCTCACCATCATTTCTATCGTTCTCAATCACATCTTTTCATGTTTGCTGAGCCTGACGAACCACAACGGCCAGCGTAAACAAACAGACAAACGCACAGGCGTGAATGTTGGCTCGTAAAGTCCACAGCCTGTTTGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16200
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
ENSDART00000061062 Nonsense 1047 1172 21 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 Nonsense 61 185 2 3
Genomic Location (Zv9):
Chromosome 9 (position 14875447)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14628012
GRCz11 9 14599215
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WGAGAAACCCTGACCCCAGACTGGCACCCCGCTAKGAGGACGTYGAGCGA[C/T]AGTATGCCTCCTTGCCCAGGTAACARYATYCACTCATTAWTYCCACACCC
Long Flanking Sequence:
CGACCTTCTTGCTGTGAGGTGACAGCACCACCTACTGCGCCACTGCGTAGCCCATACTGGAATTTGTTTGGTAAAAATGTTTCCATCGTAGTTTATGCTTTTTTTTAAAGTTTTGCGCATACGTTTTTTTGTGCGCATTTTCTAAATTTATGCACATCTTGGCGATTCCATTAGCCGTTTTTTTATGCGCATATCTAAAATGTCATAAAAAATAGGTGGATAGAAACATAGCTACAGATATTAATTAAACAAATAGCATTTTGTAGTTAATAGCCTCACATTGACCATTTGCTTTTACAAACATGTTTTCTGTATACAGAATGCTACCTTGTTGACATTGCTATGAACAGTACTATAGCTGCACTGCAGTCCAATATGATTTGATGTGTCATGTAAACCTTTCGGGCTATTTTTCACTCTGCTCTCTTCTTGCCTTTTACCAGATGCCGATGAGAAACCCTGACCCCAGACTGGCACCCCGCTATGAGGACGTCGAGCGA[C/T]AGTATGCCTCCTTGCCCAGGTAACAACATCCACTCATTAATCCCACACCCTTCGTGACAAAACAGAAGAGGTGGAGAGCTAAAAACAGAAAAGATGGGATGGAAAAGAGGGGGAGAGCAGGTAGTCATCTGTCTCTCTCATGCAGAGCTGAATAATCCTCTTTAAAGCGTATAATTAAATCTGGAGTGTCTGCCTTCTGAGGCCCCCCTATCCTGGGAATTCACCTGATCCTCTCCGGGGAGATGGCCATGCGGTCGCAGCTCTGTAACCCGATCATACAGCGTGTTTCTGGAGCCGCCTAAAGTTACGGCTGCCTCTTTCTGTCTGTCTGTCTGTCTGTCTCTTTCCTCACCATCATTTCTATCGTTCTCAATCACATCTTTTCATGTTTGCTGAGCCTGACGAACCACAACGGCCAGCGTAAACAAACAGACAAACGCACAGGCGTGAATGTTGGCTCGTAAAGTCCACAGCCTGTTTGCCCTCTCCGGTCTGTGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25419
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061062 Nonsense 1054 1172 22 22
ENSDART00000131512 None None 131 None 4
ENSDART00000137043 None None 178 None 6
ENSDART00000137117 None None 629 None 13
ENSDART00000144022 Nonsense 68 185 3 3
Genomic Location (Zv9):
Chromosome 9 (position 14845795)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14598360
GRCz11 9 14569563
KASP Assay ID:
554-7370.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCTTCCTTCCCCTAACTATATTTCCTTCACTTTCACTCTCTTGCAGA[A/T]GAGCACCAGCTGACCCTAATGAGTATCCTGTGCAGCAGTGGTCAGCACAC
Long Flanking Sequence:
TGCGGAGATATGACTGAGGTCTCTCTCTGCGCGCTCTAGGTGTCACGTGCATTCGCTCTCTCGGGCACTCTGTCCCTCTGCTTTCACGGTCAGTTCGGTGCTGTGCGCATTAGCCTCCAAAAGTATTAATTCACGGACCGTTTCGGCACCGGTGCTGTCTTAAAAGTATTGATTTAGCACCAGTATCGAAATAAAAATTAAAAGTATTGTAGTCAACTCATAGCAAACTTGACTTTAACCCTTTGTTGATATGTGATCCAAATATTTGTAGCTTGAAACTGAAGGAAAATGACCGGTTTGTGCTGCGTTTCAAATGGAAATCCCAGTATAGATGCCATAATGACCCATTGTTTATTTGTCCGCCAGCCTCCGCACTGGTCATGTGACTGAAAACTAATAATTGGGCAGTGAAAATAAATGGGTTGTTAGAACAGTTGACCAGTGTTACCATCTCCTTCCTTCCCCTAACTATATTTCCTTCACTTTCACTCTCTTGCAGA[A/T]GAGCACCAGCTGACCCTAATGAGTATCCTGTGCAGCAGTGGTCAGCACACAGAGAACCAGCACAATACCCAAACCCCCAGTCAGGTTACCACCCCGGCTACCCTCCTCCTCCCAGAGAGGCCTACCCTCGCCCGTTGGATCCTCGTCAAGGCGACGCCGGCTTCTACCACCCTCTTCCACAGCAGAGAGGCCCACTTCGACAGGATGTCCCCCCATCTCCCACCATACCCATCAGAGGCCCTCGATTTGACACCATGAGCCGCGGCGGCTACCGAAACACCAGCCCAGAGCGCTATGCTTACGGAGACCAACGGCACTCCGACCCAAGACAGAAGAGTCCCATGACGGCAGCTGTTTAACACAATCATTCCTTTTCCACTGTGTGTACGAAGTTTCTGGAACAAACACCAAACACAGCCACCATTATCTACAGGTGTTTACATGCTTTTACTAACAGTTTTTCCTTAATAGCCAAAGCTGCGTCTTAGGGTTTTGACGCA
Associated Phenotype:
Not determined