Busch Lab

ZMP

zgc:171763

Ensembl ID:
ENSDARG00000077582
ZFIN ID:
ZDB-GENE-070928-30
Description:
hypothetical protein LOC100126016 [Source:RefSeq peptide;Acc:NP_001099166]
Human Orthologue:
ANK3
Human Description:
ankyrin 3, node of Ranvier (ankyrin G) [Source:HGNC Symbol;Acc:494]
Mouse Orthologue:
Ank3
Mouse Description:
ankyrin 3, epithelial Gene [Source:MGI Symbol;Acc:MGI:88026]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa22032 Essential Splice Site Available for shipment Available now
sa41965 Nonsense Mutation detected in F1 DNA Not yet available
sa22031 Essential Splice Site Available for shipment Available now
sa35212 Nonsense Mutation detected in F1 DNA Not yet available
sa22030 Nonsense Available for shipment Available now
sa16119 Nonsense Available for shipment Available now
sa8513 Nonsense Mutation detected in F1 DNA Not yet available
sa4451 Nonsense F2 line generated Not yet available
sa41964 Nonsense Mutation detected in F1 DNA Not yet available
sa35211 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22032
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088100 Essential Splice Site 394 3888 10 39
Genomic Location (Zv9):
Chromosome 12 (position 8433762)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7737360
GRCz11 12 7771343
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGAGCTGCTGCTGAAACACGGAGCGTCCATTCAGGCTGTGACTGAG[G/C]TGAGTAGAGAGAGAGTTTGCTTGAACGTGAAATAACACTGGATGTAGGAT
Long Flanking Sequence:
ATTTTTTTCTTTGGCTTTCATATTAGATGCTGTTGCCAAAATGATAATATCTGCACACTCAGATTGGAAAGTTATAACATGTAGCATGTTTGTTTACGCACAGTGCCATGGCGATCCGTAAAAAGCCACTCTTGGCACAGAGCACGCATACTGTCATGCTCTGAAGTAACGGTTAGAGAGCGGGCGTGTCGCAGCAGTTTATGAGGGAAAAAAAGGAAGAAAGAAAGAAAACTGTAGAAAGACAAGAAGTCTGCCAAGCATCGAGCAGCAGGAGCCACGTGTTTTCATTCGTCTGGAAACAAAGCTTTCTTAACTCTTCAGTCATCTGGTTATGGTCAAAGCACAAGCAGACTTTCAGTAGTAAGCTGGAGTAAAAATACCCTTGTTTTTTTTTTTTGTAGAATGGTTTTACACCACTTCACATCGCTTGCAAGAAGAACAGGATTAAAGTGATGGAGCTGCTGCTGAAACACGGAGCGTCCATTCAGGCTGTGACTGAG[G/C]TGAGTAGAGAGAGAGTTTGCTTGAACGTGAAATAACACTGGATGTAGGATAGTTTGCTCAGGCTTTTGTAAGAGATATTGGTTGTCTGTGGACACCAGGCTCATAGCAACTGTGATAAATGGAGGGAGGTTGGTCTCACTCACTTTTCAGGACATCATTTATTACAAAAGAAAATAATAAAGTGTGAAGAGCATTGTCTTGAGAACAGTTAGGTTGCATTTCTCAGAGGTTTTAATGTCAAATTTAAGGGTTGTTTCTAGATCAGTTACCGTTGCGGCTGAAAGTTAACGAGAATTATTCATATTATTTATTAAATTTCCCATTTGTTGTATTTTATTAACGTCTACCCCTACCCCAACCCTAAACCCATCCTTCATAGTAATGTAAAAAGAGTAGCTGTAGCTGTGTTATTAATATCATCTATTAAATTACCCAATTTTTTTTTAACGTCTATGCTCACCCTAACCCTAAACCCAACCGTCAAAGTAATGTAAAAACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41965
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
ENSDART00000088100 Nonsense 1107 3888 28 39
Genomic Location (Zv9):
Chromosome 12 (position 8338951)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7642639
GRCz11 12 7676865
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCACTAAGGACTTCCCACAATACTTTGCGGTTGTATCACGGATCAAA[C/T]AGGAGAGTAATCAGATGGGTCCTGATGGAGGCGTCCTGTCCAGCATGACA
Long Flanking Sequence:
AGTGAAGGAATTATCTACACACAATATGAATTCCCAATTAGAAAAATACTACAAGCTAAAAAATACTATTCATGAAAATACTTAAATAGCACAAATCCAAATGCCCAACGCAAGCGAGCTGCGCTCCAGACTAGATCAGCTGGATGACGTTGAATGTCATTTATATATTATGCTGCCTATGGAGAGTGACACATCGCTAAAATCTCAGAAAAAGTTTATTTCTGGGTGAGGTAATCCTTAAGGTAAAAGCTTAGATTAAACTATCATTACAACCCCTTAGCAACACATTTAAAACCAGCACAAGACAACTCCAACTTAAGGAAACATCATAAAATCAAGTTTGTATGTTTTCTCCAAATACTTTCGCAGCCCTTCAAACTCACAAAATACTGGTGTGTCTTACAGAGCTGGACAGCTCAGGTGATTTGGAGAAGAAGCGCATCTGCCGGATCATCACTAAGGACTTCCCACAATACTTTGCGGTTGTATCACGGATCAAA[C/T]AGGAGAGTAATCAGATGGGTCCTGATGGAGGCGTCCTGTCCAGCATGACAGTACCTATGGTACAGGCCTCGTTTCCTGAGGGTGCTCTCACCAAGAAGATCAGGGTTGGACTGCAGGTAGATTATGGTCTAGGTCAGGGGTGCCCAAACTTTTCCTTATAGAAAGCCAAAAGCCAAAAATCATTGAGAGCCTTGGGTGGAAGTTAATTTACTGAGCTATATTACATTAAAGTTGCCATGGGTAATTTCCTAAATTGTATGGATTATATGAATGAATTTGTTAAATTCTATTTAAACTAATGCAGGATAATGTTTAAAATGATAACGTATTGCAATAAAACATAAACAATACACTAGTCAAGCAGAATCTACCTTTGCCTTGATCTGAAATCTGATTAATTTACACCATTTAATTGTAACATTTACTTCAGTTAGCTTTTAACAATAAAACAAACAAACAAAAGTTTACATCCTATTTGAAATGACAACCTCTAAACCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22031
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
ENSDART00000088100 Essential Splice Site 1323 3888 31 39
Genomic Location (Zv9):
Chromosome 12 (position 8334007)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7637689
GRCz11 12 7671812
KASP Assay ID:
2260-4969.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAACAACAGGAAAACTTTGAGGAGGTGGCCAGAAGCAAAGACATAGAG[G/A]TAGATATATTTTAATGTGATTTTTCTAAACCTTTCATGATGAATATTTAT
Long Flanking Sequence:
AAAATCCTATTAATAAAGGATCTATTGACAGGTGGCACATCACCAGCTCAATGGGAGGACATCACCGGCACTACACCTCTCACCTTCATGAACGACTGCGTGTCCTTCACCACAAACGTGTCTGCCAGGTACAAGGACAACTCATGTCCTTCTCTGTCATGAAGTCCTCTTCATGACAGATCTATTTTCCAATGATCTATTTGTACGATCTATTTTCCAAATCTCCAAATTTTAAAAAAGAGATTTTTGTTACTGCCAACTTTGTGTCCAGGTTTTGGCTCGCTGACTGCCATCAGACCCCAGAGACTGTACCTTTGGCCACCCAGCTCTACAGAGAGCTTATCTGTGTGCCCTACATGGCCAAGTTTGTAGTGTTTGCCAAAATGAATGACCCCGTGGAGTCCAACCTGCGCTGCTTCTGCATGACGGATGATAAAGTGGACAAAACTCTGGAACAACAGGAAAACTTTGAGGAGGTGGCCAGAAGCAAAGACATAGAG[G/A]TAGATATATTTTAATGTGATTTTTCTAAACCTTTCATGATGAATATTTATTGTACGAAGTAAAACTGTTACGATTTTTGCACATTAACAGTAAATAAAATGTCATACGGCTTGTAAACATGACTGGCAATTTTAAAGGTCCTGGAAGGGAAGCCCATCTACGTGGACTGCTACGGCAATTTGGCCCCTCTGATCAAAGCTGGACAGCAGCTGGTTTTTAACTTCTATGCTTTCAAAGAAAACAGACTCCCATTCTGTGTGAAGGTAGTTTTTTTTTTCTCCTACGATTTCCATCTTTTGGTTTGACTTTTTTCATTATTAAATGCTTTTTCTTTATTAAATAAATCAGCTTAAATTATATTATTCAGCACAATGAATACTGCTTAAAAACATATTGTTATTAAATAATTGTTATTAAAATAATATCTCAAATGCACATTGTTTGACTTGGGAAAGTAAATGCATGAATAGATATGATAGAAAGACCTTTTACAAATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35212
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
ENSDART00000088100 Nonsense 1818 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8325438)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7629120
GRCz11 12 7663243
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGACACACAACCAAACACAGTCCTCTACAACACGAAAGAAACCTGCA[A/T]AGCCCTCACTTTTCATTTCTCCAACAGTCCTCAAAGCAGCAGCCACACCC
Long Flanking Sequence:
CAGCCAGGGGGACATTTTTGTCATCACTTTCTTCATCAGCTAAGCCTACAACAGCCAGTACTGAAACAGTCATGTTAAATGGATCCGTTTCACCATTAAAATATCCCATATCCTCCTCTTCATCTTCCCGTCTGTTTTCAGGAGGGGCTTATAGCTTACAAGAACGGATACAGGCCACAACACAAGCAGCGACAGCCAGTGTTGGTGCAGCCTTCAGTGAGGCTGAAAGAACAGTTACTGGTGGCTCGAAGTCAAACTACAGTACACTAAAATCTGTATCGTCACCTTTAAGATCACACTTAACAAGTTCTGTTTATGAGTCCCTTCGATCACCAGTCACCACTACCACGCCAATGACATCTGTTTCCATGTCTGTTCCAGTATTTTCTGTGGTCAGTGTGCTTCCTGAAACACAGGGGAGGAAACTTCCAGAAAAAATAACAATCACACCTCAGACACACAACCAAACACAGTCCTCTACAACACGAAAGAAACCTGCA[A/T]AGCCCTCACTTTTCATTTCTCCAACAGTCCTCAAAGCAGCAGCCACACCCACATTGACTTCCAATCAAGAGATTCTTAAGGATGTAGCAGATATGAAGGAAGATCTGATGAGAATGACAGCAATCTTACAAACTGACTCTTCAACTTCACCCAAAAGTTTCCATTCAAAGGTTTCTAAAGAACCCAAGATAGAAGATGAAGAAACTTTCAGTTTGGTCGAGAAAGTTAAAGAGGACCTTGTCAAAGTTAGTGAAATTCTTAAGAAAGATGTTCTGAGTGAGGCCAAAAACTCTCGAAAAGAGAGGGCATCAGAAGATGAATGGGAAGAGTTCTCTAAAGATGAAATTGAGGAGGCACGACACAGTGCCCTGCGATCCCTGCCAACATTCGAATCAACACTTCCAGTTGGGCCACAGTCAGTGCCAGACAAAGATCTCAATTTAGCCAAAGTGGTTGATTACTTAATGAATGATCTTGGTGCTAGTTCCCTTTCAAAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22030
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088100 Nonsense 1906 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8325174)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7628856
GRCz11 12 7662979
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCGAGAAAGTTAAAGAGGACCTTGTCAAAGTTAGTGAAATTCTTAAG[A/T]AAGATGTTCTGAGTGAGGCCAAAAACTCTCGAAAAGAGAGGGCATCAGAA
Long Flanking Sequence:
CACTAAAATCTGTATCGTCACCTTTAAGATCACACTTAACAAGTTCTGTTTATGAGTCCCTTCGATCACCAGTCACCACTACCACGCCAATGACATCTGTTTCCATGTCTGTTCCAGTATTTTCTGTGGTCAGTGTGCTTCCTGAAACACAGGGGAGGAAACTTCCAGAAAAAATAACAATCACACCTCAGACACACAACCAAACACAGTCCTCTACAACACGAAAGAAACCTGCAAAGCCCTCACTTTTCATTTCTCCAACAGTCCTCAAAGCAGCAGCCACACCCACATTGACTTCCAATCAAGAGATTCTTAAGGATGTAGCAGATATGAAGGAAGATCTGATGAGAATGACAGCAATCTTACAAACTGACTCTTCAACTTCACCCAAAAGTTTCCATTCAAAGGTTTCTAAAGAACCCAAGATAGAAGATGAAGAAACTTTCAGTTTGGTCGAGAAAGTTAAAGAGGACCTTGTCAAAGTTAGTGAAATTCTTAAG[A/T]AAGATGTTCTGAGTGAGGCCAAAAACTCTCGAAAAGAGAGGGCATCAGAAGATGAATGGGAAGAGTTCTCTAAAGATGAAATTGAGGAGGCACGACACAGTGCCCTGCGATCCCTGCCAACATTCGAATCAACACTTCCAGTTGGGCCACAGTCAGTGCCAGACAAAGATCTCAATTTAGCCAAAGTGGTTGATTACTTAATGAATGATCTTGGTGCTAGTTCCCTTTCAAAAATAGCTGATGTAAAGAGCAGATATGATGAAATAAAGAAAGAAGGTGAGGAAAAACAGAAGCGCACCATGAAGCCTGAGCACAAGCTCAAAATGCCACCCACCGGTATGAGGACCTCACCTTCAGAGAAAGACTTAAGTAAATTAACTCAAGAAACATATAGTGGCACTGACGCTATCTTGGAATCTCCTGATGACTTTTCCCATGAGCAAGATAAAAGTCCTCTCTCAGATAGTGGTTTTGAAACCAGAAGTGAAAAGACCCCATCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16119
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
ENSDART00000088100 Nonsense 1937 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8325081)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7628763
GRCz11 12 7662886
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCAGAAGATGAATGGGAAGAGTTCTCTAAAGATGAAATTGAGGAGGCA[C/T]GACACAGTGCCCTGCGATCCCTGCCAACATTCGAATCAASACTTCCAGTT
Long Flanking Sequence:
CATCTGTTTCCATGTCTGTTCCAGTATTTTCTGTGGTCAGTGTGCTTCCTGAAACACAGGGGAGGAAACTTCCAGAAAAAATAACAATCACACCTCAGACACACAACCAAACACAGTCCTCTACAACACGAAAGAAACCTGCAAAGCCCTCACTTTTCATTTCTCCAACAGTCCTCAAAGCAGCAGCCACACCCACATTGACTTCCAATCAAGAGATTCTTAAGGATGTAGCAGATATGAAGGAAGATCTGATGAGAATGACAGCAATCTTACAAACTGACTCTTCAACTTCACCCAAAAGTTTCCATTCAAAGGTTTCTAAAGAACCCAAGATAGAAGATGAAGAAACTTTCAGTTTGGTCGAGAAAGTTAAAGAGGACCTTGTCAAAGTTAGTGAAATTCTTAAGAAAGATGTTCTGAGTGAGGCCAAAAACTCTCGAAAAGAGAGGGCATCAGAAGATGAATGGGAAGAGTTCTCTAAAGATGAAATTGAGGAGGCA[C/T]GACACAGTGCCCTGCGATCCCTGCCAACATTCGAATCAACACTTCCAGTTGGGCCACAGTCAGTGCCAGACAAAGATCTCAATTTAGCCAAAGTGGTTGATTACTTAATGAATGATCTTGGTGCTAGTTCCCTTTCAAAAATAGCTGATGTAAAGAGCAGATATGATGAAATAAAGAAAGAAGGTGAGGAAAAACAGAAGCGCACCATGAAGCCTGAGCACAAGCTCAAAATGCCACCCACCGGTATGAGGACCTCACCTTCAGAGAAAGACTTAAGTAAATTAACTCAAGAAACATATAGTGGCACTGACGCTATCTTGGAATCTCCTGATGACTTTTCCCATGAGCAAGATAAAAGTCCTCTCTCAGATAGTGGTTTTGAAACCAGAAGTGAAAAGACCCCATCGGCTCCTCAAAGTGCAGAGAGCACAGGGCCCAAACCCCCATTCACAGATGTGCCTATTCCCCCTGTCATAACAGAAACCAGAACTGAGGTTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8513
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
ENSDART00000088100 Nonsense 2615 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8323047)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7626729
GRCz11 12 7660852
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAGACATCTAAAGTGAGTTCTTTTAGGCAGAAGTTTGAAACAGAAGCA[C/T]AGAAACAGGATAAGAATMTACCTATAGCACAATCCAAAAAATCACCAGAA
Long Flanking Sequence:
GAAGCCCTAAACATGCCGTCTGGATGCGATTTACCCAAGATAGGCAAGACAGGAATAGAGAGAAACTTATTTATGAGGACAGAGTTGATCGGACTATTAAAGAGGCAGAGGAAAAACTGAGTGAGGTCTCACAGTTTTTTAGAGATAAAACTGAAAAGCTAAATGATGAGCTTCAGTCTCCCGAGAAAAAGAAACCAACAAGACTTTCACGGGAGACACTGTCAGGGCCGAGCTCAATGTGCAGCAGCCCTGAGAAAAAGCAAAAGAGCACAGCTGATGAATGGGAGAAAGGCAGGCAGAAAATGTTTGGGAGTACAGCTGAAAGGAAAAGTGCGAGCCTCCCAAACAGTCCCGAGAGGCATAAGCTGTCACAGTTCAGTGAGGATAAGCCAAAACAGCATGAATCTCCTCAGCAGGCAAAGACAGGTAATACAGGCCCCCCAGTCCCAGTTAAGACATCTAAAGTGAGTTCTTTTAGGCAGAAGTTTGAAACAGAAGCA[C/T]AGAAACAGGATAAGAATATACCTATAGCACAATCCAAAAAATCACCAGAAAGTAAGTTACCAGTTTATCAATTTTTCACTGGTTCAAAACCGTCAAAGTCAGACTCTGCAGATGTAGGACAGTCACCTTCTAGAAAACTAACAGAAATCGATAAAAGTAAAGTAGACCCTCAGAGTTGTAAATCTCAAGGTCCTCAAAGAACTACTGTTTCAAAGCAATCCGGTGAAAAAGCTTTACTTGAAAAATCGACTACATCAAATAATGTTGCAAAAAAAGCCTCGCTGTTTGAGAAGATTAAGGATCAGGGGCTTGATACAACTCTAGAGAGCTCTACTAAAGTGCAAGACTTGAAAGATGGATATAGTGCAGACAGACATAGTGCAGTTAATGATATTAAAGAACAACGGTACCTAAAAAGTGACATTAAAAATGACTCCTTTAAAACAGATGCCTTATCGAAGGATAATGTCAGTAGAAACGACAGCCAGATAAAGACCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4451
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088100 Nonsense 2992 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8321916)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7625598
GRCz11 12 7659721
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATTACAAGCCCGATAGCTGAGGTTTCAGAAGAATCTGAAGATAGTGAA[C/T]AAGGTAAAGATCATTCTTTGAAAAAATCTGGACCAGAAGTTCAGGAAACA
Long Flanking Sequence:
TGACAAGACCAAGGGTCCAGGGCCGTTTAGAGTTACAGAAAGAAGATGCTTCAACAACGAAACCGGAAGAAGTCTCTGTTGAAAGTAAAACAAGTGACACTAGTTCAGTGGAAAAATTCACAGTTACAACAAGAGAAAGTTTCAAAGGGCTTAAAACTTTACCAGTTTATGTAAGTGTGCAAATGGGTAAGCAGTCTGATAAAGACATGGGAGGAGGAACAAATGGAACAATAAAAAAGGTATCTGGTTCAGAAAGTCGGACAGTTTATGCAGTTAAACAGAAACAGCCCACATCTCCTCAAGGCAGCCCAGATGATGACACCTTAGAACAGTTCTCTTTTATCGATAGCTCTGGCAAAAGTCCTATGACCCCAGAGACCCCAAGCTCAGAAGAGGTCAGCTATGATCTCACTTCGAGAACTCCTGATCCATTTATTGCATTTATGCCAGGTATTACAAGCCCGATAGCTGAGGTTTCAGAAGAATCTGAAGATAGTGAA[C/T]AAGGTAAAGATCATTCTTTGAAAAAATCTGGACCAGAAGTTCAGGAAACAAAAGACAAAAGAGTTGCATATATAGAGTTTCCTCCTCCACCACCCTTAGATTCTGATTCATCACAGCCTGAGAAAAAAGGGTCGACTCCTTCCTCAGAAGCTGAGACTGAAATGATGGAAGTAAATCTCCAAGAGGAGCATGATAAACATCTTCTTGCCGAACCCATAATAAGAGTCCAACCTCCATCCCCTGTGCCCCCAGGAGCTAATGATAGTGATTCAAGTGACGAGGAATCAGTCTTTAAACCCATTCCAATAAAGAAATATACCTTTAAAATTGATGAGAACCAGGACTTGACAGACAGCCAATCAAAAAAACAAGACAAGAATGGTAATGATAAAGAACCAGGGGAAAATGGTAATGGAAAAACAGAAGATTATGATTATGAACAAAATGGCAATGATCAGTCCATCACAGACTGTTCAATAGCAACAACAGCAGAGTTCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41964
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
ENSDART00000088100 Nonsense 3183 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8321343)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7625025
GRCz11 12 7659148
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACTCACTGGATGGATATGAACTTCAGGATGAGGATGATGGCTTAAGT[G/T]AACCTATAGCCAAACCTTTTGGATTTCCCAATGACAACAGAAAAGACATT
Long Flanking Sequence:
TAGAGTTTCCTCCTCCACCACCCTTAGATTCTGATTCATCACAGCCTGAGAAAAAAGGGTCGACTCCTTCCTCAGAAGCTGAGACTGAAATGATGGAAGTAAATCTCCAAGAGGAGCATGATAAACATCTTCTTGCCGAACCCATAATAAGAGTCCAACCTCCATCCCCTGTGCCCCCAGGAGCTAATGATAGTGATTCAAGTGACGAGGAATCAGTCTTTAAACCCATTCCAATAAAGAAATATACCTTTAAAATTGATGAGAACCAGGACTTGACAGACAGCCAATCAAAAAAACAAGACAAGAATGGTAATGATAAAGAACCAGGGGAAAATGGTAATGGAAAAACAGAAGATTATGATTATGAACAAAATGGCAATGATCAGTCCATCACAGACTGTTCAATAGCAACAACAGCAGAGTTCTCTCATGATACAGATGCCACTGAGATTGACTCACTGGATGGATATGAACTTCAGGATGAGGATGATGGCTTAAGT[G/T]AACCTATAGCCAAACCTTTTGGATTTCCCAATGACAACAGAAAAGACATTTGGGCATCAGATAATATGTCTAGACCAAGTGACCGTTGCCAAAGTAAACTTGAAGTAATTCAAGAAGAATCACCAGCTGAGGACTGCAAAAAGACCAAAGCTAAGATTGATCCTTCAAACAGAACGAATGGAAAAGACGAAAAGGATGGAAAACAATCTGATCAAGGACTTTCGGACACTTATTTTAGTTACAAGTTAGATGAGGAGTTTAATACTCCTTTTAAAACTGTTGCAACAAAAGGCTTTGATCCTTGGTCAAGCAAGGGAGGAGAAGATGAAGTAGTGGATGCTAGAATTAAAGACGATGAACCCAAGCCATTTGGGTTAGCAGTAGATGACAAGTCTGCTGCAACAACCCCTGACACAACTCCTGCAAGAACCCCAACTGATGAAAGCACACCAACTAGCGAGCCTAACCCTTTCCCCTTCCACGAAGGGAAGATGTTTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35211
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088100 Nonsense 3284 3888 36 39
Genomic Location (Zv9):
Chromosome 12 (position 8321039)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 7624721
GRCz11 12 7658844
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGTTTAATACTCCTTTTAAAACTGTTGCAACAAAAGGCTTTGATCCTT[G/A]GTCAAGCAAGGGAGGAGAAGATGAAGTAGTGGATGCTAGAATTAAAGACG
Long Flanking Sequence:
GAATGGTAATGATAAAGAACCAGGGGAAAATGGTAATGGAAAAACAGAAGATTATGATTATGAACAAAATGGCAATGATCAGTCCATCACAGACTGTTCAATAGCAACAACAGCAGAGTTCTCTCATGATACAGATGCCACTGAGATTGACTCACTGGATGGATATGAACTTCAGGATGAGGATGATGGCTTAAGTGAACCTATAGCCAAACCTTTTGGATTTCCCAATGACAACAGAAAAGACATTTGGGCATCAGATAATATGTCTAGACCAAGTGACCGTTGCCAAAGTAAACTTGAAGTAATTCAAGAAGAATCACCAGCTGAGGACTGCAAAAAGACCAAAGCTAAGATTGATCCTTCAAACAGAACGAATGGAAAAGACGAAAAGGATGGAAAACAATCTGATCAAGGACTTTCGGACACTTATTTTAGTTACAAGTTAGATGAGGAGTTTAATACTCCTTTTAAAACTGTTGCAACAAAAGGCTTTGATCCTT[G/A]GTCAAGCAAGGGAGGAGAAGATGAAGTAGTGGATGCTAGAATTAAAGACGATGAACCCAAGCCATTTGGGTTAGCAGTAGATGACAAGTCTGCTGCAACAACCCCTGACACAACTCCTGCAAGAACCCCAACTGATGAAAGCACACCAACTAGCGAGCCTAACCCTTTCCCCTTCCACGAAGGGAAGATGTTTGAGATGACCCGCAGTGGTGCGATTGACATGAGCAAGAGGGATTTTGTTGAAGAGAGGCTGCAATTTTTTCAGATTGGTGAGCATACATTTGGAGGGAGGATAGGGAATGGGGTCAGAAAACCAAATGTAGTCACCTCAAATTCACAAATAGTTGAGAGGGCACAAGTTAAGTTGGAGGACAACACTGTTATGTCATACAATATCATTCAGATATGCACTGACCACTCAGACACATCTCATGACATGGAGCCTCCCCCCTACTCAGAAGTCAGTAGTTTGTGTTCTTCTTTTAAGATAGGACTGAAGT
Associated Phenotype:
Not determined