Busch Lab

ZMP

magi1

Ensembl ID:
ENSDARG00000003169
ZFIN ID:
ZDB-GENE-030131-5110
Description:
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 [Source:RefSeq peptide
Human Orthologues:
MAGIX, SAV1
Human Descriptions:
MAGI family member, X-linked [Source:HGNC Symbol;Acc:30006]
salvador homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:17795]
Mouse Orthologues:
Magix, Sav1
Mouse Descriptions:
MAGI family member, X-linked Gene [Source:MGI Symbol;Acc:MGI:1859644]
salvador homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1927144]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa15448 Nonsense Available for shipment Available now
sa45424 Nonsense Mutation detected in F1 DNA Not yet available
sa35064 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9078 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16729 Essential Splice Site Available for shipment Available now
sa17306 Essential Splice Site Available for shipment Available now
sa2611 Nonsense F2 line generated Not yet available
sa41810 Nonsense Mutation detected in F1 DNA Not yet available
sa24890 Nonsense Mutation detected in F1 DNA Not yet available
sa35065 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15448
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 None None 1276 None 24
ENSDART00000103968 Nonsense 263 293 5 5
ENSDART00000103969 None None 1109 None 20
Genomic Location (Zv9):
Chromosome 11 (position 19439948)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18857262
GRCz11 11 19019604
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGGAAGGAAAGGGGGAAAGAGCGCCATCTGGCTGTGGCGGAGRGGTT[T/A]GTTTGTGTTAGAAAGCAGCAAGATGGACTNNNNCTGTCCTTATGTATTGA
Long Flanking Sequence:
AAACTTAAACATAGGATTTAAAAAAAATCAAATAATGTAATCAATCAACTGGGGAAATATAGTGACAACTATTATTTTGGAATCATCCTATCCACCCTATGTCTTTCCTTGAATTCTGCCAATATCCTCTTGTTTCTAGGTAACTATTATGGCACACCCAAGCCGCCTATTAAGCCCCCTAGTGGCAAAGTGATCACTGGCGATGCTCTTCAAGACAGCCTTCCCGGATCCCAGCCGTCCACCCCGCGTCGCACCAAGTCCTACAATGAGATGCAAAATGCTGGAATAGTGCCTACAGAGACTGAGGATGATGACGAGGTTCCTGAAATGAACAGCAGCTTCACAGGTCAGCACTGAGACGCTTTGTTTGCATTTGTGTCTGGCACATGGAGGAAGAGATGAGTGAGTGATGCCTCTTTGTTGCTTTTCCTCTTCCTTCGCCATTGCCCGTTCAGGAAGGAAAGGGGGAAAGAGCGCCATCTGGCTGTGGCGGAGGGGTT[T/A]GTTTGTGTTAGAAAGCAGCAAGATGGACTCTAGCTGTCCTTATGTATTGATCGGACAGTTATGCGATGCCAACTTTCACAACAGTGTTGAATGAGGTGCATTTTTTGTGTCGAACTGAGGTGTTTACAGGCTTGCGGTCTGATTACTAATAGGCAACAGTAAGTACAGATTGTGGAAATGGTTAAACATTAAAGTAGGTGCATTTCGTTGTTTTGAAATGCAAATTAATGGCCCTGTTTGCAACTGGTAAGATGTGTTTTTGTTCATGAGATTTAATGCTGGTTTTACTGATTTTTCTGACCGCTTTTGATTACTTTGGCATTGTCACCTGGTATTAGATGGATAGGGAGTTAATAATATGCCAAAACAATATGAATTTGAATTGTGTTAATTTGAATTATTGACAATTGACAAATCTGAATTTTCATATGACATTAAAAATCCTTTTGAATTTGAATTTCTTAATTTGAATTTGGGCGAGGCAGTGGCGCAGTAGGTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45424
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
ENSDART00000044423 None None 1276 None 24
ENSDART00000103968 Nonsense 267 293 5 5
ENSDART00000103969 None None 1109 None 20
Genomic Location (Zv9):
Chromosome 11 (position 19439959)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18857273
GRCz11 11 19019615
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGGGAAAGAGCGCCATCTGGCTGTGGCGGAGGGGTTTGTTTGTGTTA[G/T]AAAGCAGCAAGATGGACTCTAGCTGTCCTTATGTATTGATCGGACAGTTA
Long Flanking Sequence:
TAGGATTTAAAAAAAATCAAATAATGTAATCAATCAACTGGGGAAATATAGTGACAACTATTATTTTGGAATCATCCTATCCACCCTATGTCTTTCCTTGAATTCTGCCAATATCCTCTTGTTTCTAGGTAACTATTATGGCACACCCAAGCCGCCTATTAAGCCCCCTAGTGGCAAAGTGATCACTGGCGATGCTCTTCAAGACAGCCTTCCCGGATCCCAGCCGTCCACCCCGCGTCGCACCAAGTCCTACAATGAGATGCAAAATGCTGGAATAGTGCCTACAGAGACTGAGGATGATGACGAGGTTCCTGAAATGAACAGCAGCTTCACAGGTCAGCACTGAGACGCTTTGTTTGCATTTGTGTCTGGCACATGGAGGAAGAGATGAGTGAGTGATGCCTCTTTGTTGCTTTTCCTCTTCCTTCGCCATTGCCCGTTCAGGAAGGAAAGGGGGAAAGAGCGCCATCTGGCTGTGGCGGAGGGGTTTGTTTGTGTTA[G/T]AAAGCAGCAAGATGGACTCTAGCTGTCCTTATGTATTGATCGGACAGTTATGCGATGCCAACTTTCACAACAGTGTTGAATGAGGTGCATTTTTTGTGTCGAACTGAGGTGTTTACAGGCTTGCGGTCTGATTACTAATAGGCAACAGTAAGTACAGATTGTGGAAATGGTTAAACATTAAAGTAGGTGCATTTCGTTGTTTTGAAATGCAAATTAATGGCCCTGTTTGCAACTGGTAAGATGTGTTTTTGTTCATGAGATTTAATGCTGGTTTTACTGATTTTTCTGACCGCTTTTGATTACTTTGGCATTGTCACCTGGTATTAGATGGATAGGGAGTTAATAATATGCCAAAACAATATGAATTTGAATTGTGTTAATTTGAATTATTGACAATTGACAAATCTGAATTTTCATATGACATTAAAAATCCTTTTGAATTTGAATTTCTTAATTTGAATTTGGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35064
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 Essential Splice Site 359 1276 7 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 221 1109 5 20
Genomic Location (Zv9):
Chromosome 11 (position 19449976)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18867290
GRCz11 11 19029632
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTGATGAGAAGAAGGGGTCCATACAGAGGAGCTGGACAATGAACTAG[G/A]TAGGCCACAATCCCACTGGGAAACTTTTTTTTAACTTGTAAACCCAGCCT
Long Flanking Sequence:
GTATTTATAATATAAAATATAATTATATGTTATGAATTTAAGTTTATTCTAAAAAGGCTTATTTTAGTAAGCAATTTAATTTCATTTCCATTTTATATTGATTATTTACATTTTCAAGGTTTATTATTATGTGTTGCAGCAATACATGTCTAAACTAAAATAAAGTCAATGAGAATCCATAAACATGATGCACTGTTTTCCAGTACAGATATGTATGAAATATTCTGAAATAATTTTACTGTAAAATCCTTCTGTAATGGGTCGCTACAGCCCTACTAAATAATAGATTTGATCTAAAAGTGATTTCCACTCTATTTTTTGTAGTTTTTTGGGATAATTAAAGGGCTTCAAGCTTTTATTTTGCTTCTGATCAACAACTAACCCTCTCTGCCTCTCTGCCACCCTTCCTCTTTTTCTCTGGTCCTGCTTGCGTGCACCTGCCCCTTTTATTCCCTGATGAGAAGAAGGGGTCCATACAGAGGAGCTGGACAATGAACTAG[G/A]TAGGCCACAATCCCACTGGGAAACTTTTTTTTAACTTGTAAACCCAGCCTACATGTTTTTTATTTTTTTGAGTGTAGACCGATCCTTCTGTGCTGCTTTGGGACCAGATGTTTTCTCTGAAATACTGGATTTAATTATGAAAACAGAGCCCACAATTGATCCCAGATCAGCGCAGAAGGAAACGTCTACCCACAGTGCACGTGCAATGCCACGCTTTGTAGATGTAGAATCATTTTTCATTTTGAAATTGTTTATAAATTTAATGGCAAAAAAATGCATAGAATTAAACAAGCAATTTCGAAGTAGAAAAATGAAAATTGTTATCTTAAATTGATGAAGTGAAAATGAAGTGTTATCTTATTAAAGGGACAGTCCACCCAAAAAAGACAAATCTGTCATTATTTACTCACCTAAAAAGAACACAAAATAAATTTGTTAGTATTTTCAAATCCAGTAGCCACTGACATCTATAATATTTGTTTCTCTATAGACCATTTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9078
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 Essential Splice Site 360 1276 7 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 222 1109 5 20
Genomic Location (Zv9):
Chromosome 11 (position 19449977)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18867291
GRCz11 11 19029633
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTGWTGAGAAGAAGGGGTCCATACAGAGGAGCTGGACAATGAACTAGG[T/G]AGGCCACAATCCCACTGGGAAACTTTTTTTTAACTTGTAAACCCAGCCTA
Long Flanking Sequence:
TATTTATAATATAAAATATAATTATATGTTATGAATTTAAGTTTATTCTAAAAAGGCTTATTTTAGTAAGCAATTTAATTTCATTTCCATTTTATATTGATTATTTACATTTTCAAGGTTTATTATTATGTGTTGCAGCAATACATGTCTAAACTAAAATAAAGTCAATGAGAATCCATAAACATGATGCACTGTTTTCCAGTACAGATATGTATGAAATATTCTGAAATAATTTTACTGTAAAATCCTTCTGTAATGGGTCGCTACAGCCCTACTAAATAATAGATTTGATCTAAAAGTGATTTCCACTCTATTTTTTGTAGTTTTTTGGGATAATTAAAGGGCTTCAAGCTTTTATTTTGCTTCTGATCAACAACTAACCCTCTCTGCCTCTCTGCCACCCTTCCTCTTTTTCTCTGGTCCTGCTTGCGTGCACCTGCCCCTTTTATTCCCTGATGAGAAGAAGGGGTCCATACAGAGGAGCTGGACAATGAACTAGG[T/G]AGGCCACAATCCCACTGGGAAACTTTTTTTTAACTTGTAAACCCAGCCTACATGTTTTTTATTTTTTTGAGTGTAGACCGATCCTTCTGTGCTGCTTTGGGACCAGATGTTTTCTCTGAAATACTGGATTTAATTATGAAAACAGAGCCCACAATTGATCCCAGATCAGCGCAGAAGGAAACGTCTACCCACAGTGCACGTGCAATGCCACGCTTTGTAGATGTAGAATCATTTTTCATTTTGAAATTGTTTATAAATTTAATGGCAAAAAAATGCATAGAATTAAACAAGCAATTTCGAAGTAGAAAAATGAAAATTGTTATCTTAAATTGATGAAGTGAAAATGAAGTGTTATCTTATTAAAGGGACAGTCCACCCAAAAAAGACAAATCTGTCATTATTTACTCACCTAAAAAGAACACAAAATAAATTTGTTAGTATTTTCAAATCCAGTAGCCACTGACATCTATAATATTTGTTTCTCTATAGACCATTTTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16729
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 Essential Splice Site 360 1276 8 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 222 1109 6 20
ENSDART00000044423 Essential Splice Site 360 1276 8 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 222 1109 6 20
Genomic Location (Zv9):
Chromosome 11 (position 19458053)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18875367
GRCz11 11 19037709
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGARTTACAATGAGCTGAAAAACCTYTTCTGTTTTGCTTCCTTTTTTCC[A/T]GAGCTGCCAACAGGCTGGGAGAAGATYGATGATCCAGTGTACGGGGTGTA
Long Flanking Sequence:
ATTCAAACCATAACCCATACAATTTCACAGGCCTTTACCTTGGACTTTTTGTGTCTTTTTTCAAAGAATTTGTGTCAAATGAACGTTTGTAATGTTGTGATTCTCCTCATAGATATTTGGCTTGGTTTATGGCTTAGAATGCTTAAGTGAATACATTTTTAAAATAGATGGTGAAAAACAATTCTGGATGTAGCATGGCTGAAAAAGTGGGTGGATACTAATGAACCCCATAAGCAAACCCTTTAGAACATCTGCCAACCAATCAAAATCAAGCATTTTGTAGTGCACTTTTAAAATCATGCTAAACGATGCAGTTAAGATTCAATTTGCGTAATATAATCTGCTCATCGTGGTCATTATAGTTTTAAAACGCCTGGCTTGTTAGTTGGAAAGCTCTTGAATGTTAATCAAAACATCAAATTACAAAGGACTCCATAAAAGCCTTATTAAATGAGTTACAATGAGCTGAAAAACCTCTTCTGTTTTGCTTCCTTTTTTCC[A/T]GAGCTGCCAACAGGCTGGGAGAAGATCGATGATCCAGTGTACGGGGTGTATTATGTTGAGTAAGTGACTCATCAATATTATCTTCAAATCATCTTTAATAAACTGTGTGACATCATCTGGAAACATCAAAGAGGCGGCCACTGTTCCTCCGATCGGGCCTGTTGTGTTTTCGGCTGTGCACACCCTTTGTTACTGTTACCATTTTGAAATCTTGTTCTCTCTCTCTCCCTCCCCTTCAGAGGGACCCTTGGGTTTGTAGTGCATAAATATGAATGCATTCATATGTTTTGATGTTGTTTCAAAGCAATACCTCAGAGGCTGGAAGCCTTCCGGTTTTTGTCTTTGGAGATGTTTACGCATGTTTCAAGCCGTATTTGCCTAGTAAATTGTGCAGGCCTTTTGGAAAGTGGCCTGGATCGCAGCTGGGCGTGATCTGATTTATTTTGTAATTGTGCCGATGGAGTTTTATTTATTTTTATTTGTTTTTTTTTTTTACTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17306
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 Essential Splice Site 360 1276 8 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 222 1109 6 20
ENSDART00000044423 Essential Splice Site 360 1276 8 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Essential Splice Site 222 1109 6 20
Genomic Location (Zv9):
Chromosome 11 (position 19458053)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18875367
GRCz11 11 19037709
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGARTTACAATGAGCTGAAAAACCTYTTCTGTTTTGCTTCCTTTTTTCC[A/T]GAGCTGCCAACAGGCTGGGAGAAGATYGATGATCCAGTGTACGGGGTGTA
Long Flanking Sequence:
ATTCAAACCATAACCCATACAATTTCACAGGCCTTTACCTTGGACTTTTTGTGTCTTTTTTCAAAGAATTTGTGTCAAATGAACGTTTGTAATGTTGTGATTCTCCTCATAGATATTTGGCTTGGTTTATGGCTTAGAATGCTTAAGTGAATACATTTTTAAAATAGATGGTGAAAAACAATTCTGGATGTAGCATGGCTGAAAAAGTGGGTGGATACTAATGAACCCCATAAGCAAACCCTTTAGAACATCTGCCAACCAATCAAAATCAAGCATTTTGTAGTGCACTTTTAAAATCATGCTAAACGATGCAGTTAAGATTCAATTTGCGTAATATAATCTGCTCATCGTGGTCATTATAGTTTTAAAACGCCTGGCTTGTTAGTTGGAAAGCTCTTGAATGTTAATCAAAACATCAAATTACAAAGGACTCCATAAAAGCCTTATTAAATGAGTTACAATGAGCTGAAAAACCTCTTCTGTTTTGCTTCCTTTTTTCC[A/T]GAGCTGCCAACAGGCTGGGAGAAGATCGATGATCCAGTGTACGGGGTGTATTATGTTGAGTAAGTGACTCATCAATATTATCTTCAAATCATCTTTAATAAACTGTGTGACATCATCTGGAAACATCAAAGAGGCGGCCACTGTTCCTCCGATCGGGCCTGTTGTGTTTTCGGCTGTGCACACCCTTTGTTACTGTTACCATTTTGAAATCTTGTTCTCTCTCTCTCCCTCCCCTTCAGAGGGACCCTTGGGTTTGTAGTGCATAAATATGAATGCATTCATATGTTTTGATGTTGTTTCAAAGCAATACCTCAGAGGCTGGAAGCCTTCCGGTTTTTGTCTTTGGAGATGTTTACGCATGTTTCAAGCCGTATTTGCCTAGTAAATTGTGCAGGCCTTTTGGAAAGTGGCCTGGATCGCAGCTGGGCGTGATCTGATTTATTTTGTAATTGTGCCGATGGAGTTTTATTTATTTTTATTTGTTTTTTTTTTTTACTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2611
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044423 Nonsense 395 1276 9 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Nonsense 257 1109 7 20
Genomic Location (Zv9):
Chromosome 11 (position 19458924)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18876238
GRCz11 11 19038580
KASP Assay ID:
554-3283.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGTCATATTAACAGGAAGACGCAGTATGAGAACCCAATTCTGGAAGCT[A/T]AAAGGAAGAAGCAACTGGAGCAGTCTCAGCCCGCTGAAGGTGAGCGGWTT
Long Flanking Sequence:
GTATTTGCCTAGTAAATTGTGCAGGCCTTTTGGAAAGTGGCCTGGATCGCAGCTGGGCGTGATCTGATTTATTTTGTAATTGTGCCGATGGAGTTTTATTTATTTTTATTTGTTTTTTTTTTTTACTGAGCTTGTCTAGTCTGCTGGATAGATTTTGCTTTTAAGCACATGGGATGAGAGAGAATTGCACACTTTTTTTTTCTCCCCCAAATTTCAAATGAATTTTAAATGAATGCAGAGGCTTTCAGCTGTACTTGAAGCTGTCTTTATTGCCTTTTCTCTGAATGAATTCACTTTATTTCTCCGCTTACCTGCTCTCCTTTGGCTCAACCTTTACCTGCCCTCTCATTCTATTTCCCGTTTCTCCCTCTGCTTCTGTTATTGACTGTGTCCTCTGCTCACTCATCTTCATCACCTCTTTCTCTTTCTCTCTCACTCTCTCTCCACCTCTCAGTCATATTAACAGGAAGACGCAGTATGAGAACCCAATTCTGGAAGCT[A/T]AAAGGAAGAAGCAACTGGAGCAGTCTCAGCCCGCTGAAGGTGAGCGGTTTATCCAAGGTTCGTTTCAGGCCCAACATGCTATCATTTTTTTTCTTATATGATTTGTCACTATTTAGCCTTAGAATTATGTTGCTGATCTGGTTTTGAAATTATTGTTTATTATGGTTAACCATATTCATATTATCTATAATTTGTTTAATTTCTTATCACTGCTTTTTGTAGATCTTTCTATTTCTTTATTTTTATTTATGTATTTATTTTGCATAAGTGTAATATTTAATAAAAAAAATAAGAGAACTTTAAAATATTGTTTGATTAAATGTTTATGTTTTGGGCCAGTGTTATAGAAACAGCTTGAAAAGGGAAATAAACCAATCGCAGTTGCGAAATGTTAAAATTTTCAAGTGAAACTAAATATTCAAAAATGTCTACATGAACTCATAATCAATCTCATTGACTTATTTAAAGGGATGTTTCAATCAAAAAATATTTATTTCTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41810
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
ENSDART00000044423 Nonsense 527 1276 12 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Nonsense 389 1109 10 20
Genomic Location (Zv9):
Chromosome 11 (position 19462152)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18879466
GRCz11 11 19041808
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTATTGTAAGTGTGAACGACACTTGCGTTTTGGGTTACACACACGCC[C/T]AAGTTGTGAAGATCTTCCAGTCAATCCCTATTGGCTCTATGGTCGACCTT
Long Flanking Sequence:
TGCTCGTGAAGTTAACTTTGCTGCACAGCTTTTTCTTGAAACAAAATATTCTCAAGATTTGCTGTGTCCTAATACTCAAAGGTATACATAATAATCTTCTACACAGGGGCCAACAGATTTACCGTTGCCGATTGCCATAGCTCACTAGTTGTGCATCGCTTTTCTCATTGCAGGAGGTAAGCCATTTTTCACAAGGAACCCTGCAGAACTGAAGGGGACATTTATTAACACCAAGCTCAAGAAGAGCAGGCGTGGGTTCGGCTTCACTGTAGTAGGAGGAGATGAACCCGATGAGTTCTTGCAGATTAAGAGTCTTGTGCTCGATGGACCCGCTGCCCTTGACGGAAAGATGGAAACAGGTACATCTGAAAACCATGAACTCATAAACGCGTGATGTAGTCTAATCTTTGTACTTTGCTCATCGCAAGTTTTTTTTTTCTCCCTCAGGTGATGTTATTGTAAGTGTGAACGACACTTGCGTTTTGGGTTACACACACGCC[C/T]AAGTTGTGAAGATCTTCCAGTCAATCCCTATTGGCTCTATGGTCGACCTTGAACTCTGCCGTGGCTACCCTTTGCCCTTTGACCCTGATGACCCCAACACCAGCCTGGTGACTTCAGTGGCCATTCTGGACAAGGAGCCAATCATTGTCAATGGAAAAGAAAGCTACGACTCACCATCCAGCCACGGGAGCGAAACTACAGCTGGAGGCAGTAGCTTAAATGGCTCCAGTGATCCTCCTCGCCCCCATAGCCCTTCAGCAGAGGTGGCTTCCAATGGCTCTCATGGTTATCCCAGTGATGTGGTGACTTTGGCGTCCTCGATCGCCACCCAGCCCGAGCTTATTACTGTCCACATGGAAAAAGGCGACAAGGGATTCGGCTTCACAATAGCAGACAGCCCGTCTGGAGGAGGCCAGCGAGTAAAGCAGATAGTGGATTACCCACGATGCAGAGGCCTGAGGGAAGGTGACATCATCATGGAGGTGAACAAGAGGAACGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24890
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
ENSDART00000044423 Nonsense 666 1276 12 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Nonsense 528 1109 10 20
Genomic Location (Zv9):
Chromosome 11 (position 19462569)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18879883
GRCz11 11 19042225
KASP Assay ID:
554-7673.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGGGATTCGGCTTCACAATAGCAGACAGCCCGTCTGGAGGAGGCCAG[C/T]GAGTAAAGCAGATAGTGGATTACCCACGATGCAGAGGCCTGAGGGAAGGT
Long Flanking Sequence:
CTCATCGCAAGTTTTTTTTTTCTCCCTCAGGTGATGTTATTGTAAGTGTGAACGACACTTGCGTTTTGGGTTACACACACGCCCAAGTTGTGAAGATCTTCCAGTCAATCCCTATTGGCTCTATGGTCGACCTTGAACTCTGCCGTGGCTACCCTTTGCCCTTTGACCCTGATGACCCCAACACCAGCCTGGTGACTTCAGTGGCCATTCTGGACAAGGAGCCAATCATTGTCAATGGAAAAGAAAGCTACGACTCACCATCCAGCCACGGGAGCGAAACTACAGCTGGAGGCAGTAGCTTAAATGGCTCCAGTGATCCTCCTCGCCCCCATAGCCCTTCAGCAGAGGTGGCTTCCAATGGCTCTCATGGTTATCCCAGTGATGTGGTGACTTTGGCGTCCTCGATCGCCACCCAGCCCGAGCTTATTACTGTCCACATGGAAAAAGGCGACAAGGGATTCGGCTTCACAATAGCAGACAGCCCGTCTGGAGGAGGCCAG[C/T]GAGTAAAGCAGATAGTGGATTACCCACGATGCAGAGGCCTGAGGGAAGGTGACATCATCATGGAGGTGAACAAGAGGAACGTGCAGAACCTGACGCACAATCAGGTGGTCGACCTGCTCAGCAAGTGTCCTAAAGGCAGTGAAGTGACCATGTTGGTGCAACGAGGTAAGCTCACCAAAATGTTATGACATGAAAGGAAAAGTGAGAAAGGAAATCCAAAAGCATTAAAAAAAAAACAAAAACAAAAAAAAAAACGGTTGCTTGCATGGAAAAATGCTAATTTGCTGTTGATTTACTTATCCTCAGGTCAGACAAGATCCAGGTGACTTACAGTAGAGCATTAATAAAAGGTTTTTGTCTTGAACCTGGTGGCTTGGTTTTTCTTTAAATACAAATCATTGACTACAACACTTTCAGAATCACTATTATTTAATTTGTTTTGTCTGTTTTTCATTTATTCATTCTGAAAGTGCCGGTAGCCATTTACTTCCATTTTATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35065
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
ENSDART00000044423 Nonsense 720 1276 12 24
ENSDART00000103968 None None 293 None 5
ENSDART00000103969 Nonsense 582 1109 10 20
Genomic Location (Zv9):
Chromosome 11 (position 19462731)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 18880045
GRCz11 11 19042387
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCTCAGCAAGTGTCCTAAAGGCAGTGAAGTGACCATGTTGGTGCAA[C/T]GAGGTAAGCTCACCAAAATGTTATGACATGAAAGGAAAAGTGAGAAAGGA
Long Flanking Sequence:
TTGACCCTGATGACCCCAACACCAGCCTGGTGACTTCAGTGGCCATTCTGGACAAGGAGCCAATCATTGTCAATGGAAAAGAAAGCTACGACTCACCATCCAGCCACGGGAGCGAAACTACAGCTGGAGGCAGTAGCTTAAATGGCTCCAGTGATCCTCCTCGCCCCCATAGCCCTTCAGCAGAGGTGGCTTCCAATGGCTCTCATGGTTATCCCAGTGATGTGGTGACTTTGGCGTCCTCGATCGCCACCCAGCCCGAGCTTATTACTGTCCACATGGAAAAAGGCGACAAGGGATTCGGCTTCACAATAGCAGACAGCCCGTCTGGAGGAGGCCAGCGAGTAAAGCAGATAGTGGATTACCCACGATGCAGAGGCCTGAGGGAAGGTGACATCATCATGGAGGTGAACAAGAGGAACGTGCAGAACCTGACGCACAATCAGGTGGTCGACCTGCTCAGCAAGTGTCCTAAAGGCAGTGAAGTGACCATGTTGGTGCAA[C/T]GAGGTAAGCTCACCAAAATGTTATGACATGAAAGGAAAAGTGAGAAAGGAAATCCAAAAGCATTAAAAAAAAAACAAAAACAAAAAAAAAAACGGTTGCTTGCATGGAAAAATGCTAATTTGCTGTTGATTTACTTATCCTCAGGTCAGACAAGATCCAGGTGACTTACAGTAGAGCATTAATAAAAGGTTTTTGTCTTGAACCTGGTGGCTTGGTTTTTCTTTAAATACAAATCATTGACTACAACACTTTCAGAATCACTATTATTTAATTTGTTTTGTCTGTTTTTCATTTATTCATTCTGAAAGTGCCGGTAGCCATTTACTTCCATTTTATGAAACACCAGGGACCAAGGTTTGAGCTAAAAATCTTTTAAATGTTCTGCTGAGGAAAAGAGTTACCTTCATCCTGAATGAACTGAGTAGGGAGGGAAACACTTTCAAATTTCACAACATTCCAAAGTTCATGTTTTGTAAACTCCAACTGGCAAATTTTTGTCT
Associated Phenotype:
Not determined