Busch Lab

ZMP

MEGF6 (2 of 2)

Ensembl ID:
ENSDARG00000074808
Description:
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Human Orthologue:
MEGF6
Human Description:
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Mouse Orthologue:
Megf6
Mouse Description:
multiple EGF-like-domains 6 Gene [Source:MGI Symbol;Acc:MGI:1919351]

Alleles

There are 16 alleles of this gene:

Allele Name Consequence Status Availability
sa41912 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24897 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9346 Nonsense Mutation detected in F1 DNA Not yet available
sa19013 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9355 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41911 Nonsense Mutation detected in F1 DNA Not yet available
sa2600 Essential Splice Site Available for shipment Available now
sa15275 Essential Splice Site Available for shipment Available now
sa41910 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15985 Nonsense Available for shipment Available now
sa21975 Essential Splice Site Available for shipment Available now
sa35153 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41912
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
ENSDART00000109204 Essential Splice Site 296 1318 9 35
Genomic Location (Zv9):
Chromosome 11 (position 42858860)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41149355
GRCz11 11 41761585
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATGTCATCCAGGTTATCAGCTCGCTGAAGACGGCAAGACATGTGAAG[G/A]TAAAATACACCTGCCTGTCTTATATTTTAAGATCACAGAGAGTTCTCAGT
Long Flanking Sequence:
CACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCTGGAGGAAACCCACGCGAACATGGGAGAACATGCAAACTCCACACAGAAACACCAACTGAGCAGAGGTTCGACCCAGCGACCTTCTTGCTGTGAGGCGAAAGAACTACCTACTGCACCACTTCCTCGCCATAAACTTACTAATGAAAATCAAAATGTGAAAAAGAAACTGAAATCTTCATCGTAAGCAAGGCCAATAACACAAGCTCCCTGAAACAATAAACAAAAACACAAAAACCACTAAACTAGCAAAATGAGCTGAAAAAAATCAATATGGTTAGTTTTGATATCATGTGTACTTTAATACCTGATATCCTGTATTGACCATCATCAGTGGTGAACCCGTGTGCGGAGCAGAATGGCGGATGTTCTCAGATGTGTCATAGGGATGGAGCTCAGGCCCGCTGTGAATGTCATCCAGGTTATCAGCTCGCTGAAGACGGCAAGACATGTGAAG[G/A]TAAAATACACCTGCCTGTCTTATATTTTAAGATCACAGAGAGTTCTCAGTGTTACACTGCTCATATTAATGTCTTGTGTTTTTGAAATTGGATGTGTTTATGCTGTGTGTTTTTGGTGCATCAGACATTGATGAGTGTGCGTTGGGTCAGACGGACTGTGCTCATGGCTGTCGTAACACCAGAGGATCCTTCATGTGTGTGTGTTCTGCTGCCTATGAGCTCGGGGTGGACGGTAAACAGTGCTATCGTGAGTATGAGCTGAGAGACTCACATACACTGAAAAAAAAAAAAGATTCACTCGATTTACATATTTTTAATGTAAAAATGTCTGAATTTAAATATTGATGTTTGAATATTGATATTAATATTAAATGAGTTATACAATCATAATAATATTATATAATGCAAATATGCAATATTTAAAAAAAAATGCTGGAAACTATTAGCTCTAAACTGCATATACAATAAATTACAATGATTATAGAATTTATGTATTTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24897
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
ENSDART00000109204 Essential Splice Site 427 1318 12 35
Genomic Location (Zv9):
Chromosome 11 (position 42857052)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41147547
GRCz11 11 41759777
KASP Assay ID:
554-7681.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGTACAGCCGGATATCGACTGAACACTGACGGATGCAGCTGTGATGG[T/C]AACACACATAAACTCACCAGGCCAGATTTTAAGAGAAGCTCATTACTTTT
Long Flanking Sequence:
ATATTGTTTTTTCAAAGGTCTACAGAACAAACAATCGTTATACAATGACTTGCCTAATTACCTTAACTTTAACTTAATTAACCTAAATGAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGTCATGGCAAAAATAAATTAAATAATTTATTAGAGATTCTTTATTAAAACTTTTATGTTTAGAAATGTGTTGAAGAAATCTTCTCTCCGTTAAATAGAAATTGGGGAAAATTTACAGGGGGGCTAATAATTCAGGAGGGCTAATCATTCTGACTTCAACTGAATGCACAGTAATGCTGTTAGCTGAAGGTGTGTGTATTCTCTCCTGTCAGATATAAACGAGTGTGTCGACGGCAGCTCGTGTTGTGAACATGACTGTACGAACTATCCTGGAGGATACGAGTGTTACTGTACAGCCGGATATCGACTGAACACTGACGGATGCAGCTGTGATGG[T/C]AACACACATAAACTCACCAGGCCAGATTTTAAGAGAAGCTCATTACTTTTGTTCTTTAGTTGAAATGAAATATATATATATGTTTTGTTGTTTAGAAATATGTTCCAGAGTTTTTCTCTACTGTATATACACTGACAAAAGTGAAACTACACTGTAAAAGCAATATATTGTCTATAAAGGTCATGTGAAGTGCTTTGAAATGTGCATTTTTATTCGATGTTTGACATAATCTCAACCGAAAAATGAAGAGAGGGTGGGACATAGTGTAGCTCCTCCCCTTTTTAAATCAGCTAATAGTGTTTTGTTTTATCACAGCTCTGCCAGCAGGCCCGGATTGGCTAATTGGGAGGACCGGGAGAATACCCGGGGGGCCGCTCCGTTTTTTTGGCCGCGAGGGCCTGTGTCCCTAGCTGCTTGCGCTCTCAGCAGTCGCACTTTAAAAAATGTTTTATTTATTTGACCATAGTCTCACTCTTTTTATTCATTATTTTGCCGCAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9346
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
ENSDART00000109204 Nonsense 491 1318 15 35
Genomic Location (Zv9):
Chromosome 11 (position 42850337)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41140832
GRCz11 11 41753062
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAAACAAMCMTGYGTGTGTGTCAGTGATGGAGGAGTCAGTGGAGGCGT[T/A]GAGCAGCGGTCAGACAGTCAATAAACCTGGACCAGGACCTCAGCTCRCCA
Long Flanking Sequence:
ACGTCTCACATCAGCACGTTCTAGACGTGCACGCACACTTTCCGGCAATCTTCCTTCTGCATTCACACAGCGCAGCATTTCTGCAAATTACCGGTAATGTTACAACTTCTCTTTCCGGAAAATAGCCAGAACGAATTTACCAGTATTTTCAAAAAGGACCTGTTCACACATACACACCTTTCCGGAAAATTGCCGGTAATTTTCCGGAAAGGTCTGTATGTGTGAAAGGGGCTAATGTCATGGGTCAGGTGTTACAAGTAGATGTTGGATTATGAGGACGTTCCTGATTTTTTTAAGAGGTCTATAAATCATACAGAATTAGTTTTATTTTCAGAAAGTAAAGCAAAATCAGACAGTAAAACCTCAGAAAGGAAAACCTTTTCCTAGTGTAAAAAAATTGTACAGTATAAAAACAATTGAAAACAATGGAATGTCCCCACAATTCACAAAAACAAACAAACCTGTGTGTGTGTCAGTGATGGAGGAGTCAGTGGAGGCGT[T/A]GAGCAGCGGTCAGACAGTCAATAAACCTGGACCAGGACCTCAGCTCACCATCCTGCAGGACTTCGATCAGATCCTGGAGAAATACGAGGACTACGAGGACGACACTGGAGAACTGCGTGCCGAGAGCACTTTAGCTGAGAAATTCAGTGAGAAACCCTTTCCTTCTGTTCTGTAACACTGCTGGGATTTCATTTACTGAGGAATATTCATCACAATGCAAACTGCCCTTACCTTATCATTTGTTGTGTGCAGTTTGTTTGAACGATTCGTTCGGCGTTGACTGCAGTCTGTCCTGTGAGGACTGTGTGAACGGAGGAGTGTGTAACAAACACAGAAATGCCTGTGACTGTCCTGACGGATGGACTGGAGTCGTCTGTAATGAGAGTGAGTTTGCCATGATGCTATAAATGGTTTCATTTAGAAATGTGAACCTGGACCACAACATCTTAACAGGATAGTTCACCCAAAAATGAACAGTTCCTGTTAAAGGGCACCTATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19013
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Essential Splice Site 539 1318 15 35
ENSDART00000109204 Essential Splice Site 539 1318 15 35
Genomic Location (Zv9):
Chromosome 11 (position 42850190)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41140685
GRCz11 11 41752915
KASP Assay ID:
2260-4670.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACGACACTGGAGAACTGCGTGCCGAGAGCACTTTAGCTGAGAAATTCA[G/T]TGAGAAACCCTTTCCTTCTGTTCTGTAACACTGCTGGGATTTCATTTACT
Long Flanking Sequence:
TTCAAAAAGGACCTGTTCACACATACACACCTTTCCGGAAAATTGCCGGTAATTTTCCGGAAAGGTCTGTATGTGTGAAAGGGGCTAATGTCATGGGTCAGGTGTTACAAGTAGATGTTGGATTATGAGGACGTTCCTGATTTTTTTAAGAGGTCTATAAATCATACAGAATTAGTTTTATTTTCAGAAAGTAAAGCAAAATCAGACAGTAAAACCTCAGAAAGGAAAACCTTTTCCTAGTGTAAAAAAATTGTACAGTATAAAAACAATTGAAAACAATGGAATGTCCCCACAATTCACAAAAACAAACAAACCTGTGTGTGTGTCAGTGATGGAGGAGTCAGTGGAGGCGTTGAGCAGCGGTCAGACAGTCAATAAACCTGGACCAGGACCTCAGCTCACCATCCTGCAGGACTTCGATCAGATCCTGGAGAAATACGAGGACTACGAGGACGACACTGGAGAACTGCGTGCCGAGAGCACTTTAGCTGAGAAATTCA[G/T]TGAGAAACCCTTTCCTTCTGTTCTGTAACACTGCTGGGATTTCATTTACTGAGGAATATTCATCACAATGCAAACTGCCCTTACCTTATCATTTGTTGTGTGCAGTTTGTTTGAACGATTCGTTCGGCGTTGACTGCAGTCTGTCCTGTGAGGACTGTGTGAACGGAGGAGTGTGTAACAAACACAGAAATGCCTGTGACTGTCCTGACGGATGGACTGGAGTCGTCTGTAATGAGAGTGAGTTTGCCATGATGCTATAAATGGTTTCATTTAGAAATGTGAACCTGGACCACAACATCTTAACAGGATAGTTCACCCAAAAATGAACAGTTCCTGTTAAAGGGCACCTATGGTGAAAAATCTACTTTTCAAGCTGTTTGGACAAACATGTTTGTAAGTATAGTGTATATACTAGGGATGGGAAGATTAACCGATATGTATCGATACGCGGTCATGCGCGTGCACGATGCGAGTGCATCGGTTGAGCAGCAGAGGATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9355
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Essential Splice Site 539 1318 15 35
ENSDART00000109204 Essential Splice Site 539 1318 15 35
Genomic Location (Zv9):
Chromosome 11 (position 42850190)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41140685
GRCz11 11 41752915
KASP Assay ID:
2260-4670.1 (used for ordering genotyping assays)
KASP Sequence:
GGACGACACTGGAGAACTGCKYGCYGAGAGCACTTTAGCTGAGAAATTCR[G/T]TGAGAAACCCTTTCCTTCTGTTCTGTAACACTGCKGGGATTTMATKTAYT
Long Flanking Sequence:
TTCAAAAAGGACCTGTTCACACATACACACCTTTCCGGAAAATTGCCGGTAATTTTCCGGAAAGGTCTGTATGTGTGAAAGGGGCTAATGTCATGGGTCAGGTGTTACAAGTAGATGTTGGATTATGAGGACGTTCCTGATTTTTTTAAGAGGTCTATAAATCATACAGAATTAGTTTTATTTTCAGAAAGTAAAGCAAAATCAGACAGTAAAACCTCAGAAAGGAAAACCTTTTCCTAGTGTAAAAAAATTGTACAGTATAAAAACAATTGAAAACAATGGAATGTCCCCACAATTCACAAAAACAAACAAACCTGTGTGTGTGTCAGTGATGGAGGAGTCAGTGGAGGCGTTGAGCAGCGGTCAGACAGTCAATAAACCTGGACCAGGACCTCAGCTCACCATCCTGCAGGACTTCGATCAGATCCTGGAGAAATACGAGGACTACGAGGACGACACTGGAGAACTGCGTGCCGAGAGCACTTTAGCTGAGAAATTCA[G/T]TGAGAAACCCTTTCCTTCTGTTCTGTAACACTGCTGGGATTTCATTTACTGAGGAATATTCATCACAATGCAAACTGCCCTTACCTTATCATTTGTTGTGTGCAGTTTGTTTGAACGATTCGTTCGGCGTTGACTGCAGTCTGTCCTGTGAGGACTGTGTGAACGGAGGAGTGTGTAACAAACACAGAAATGCCTGTGACTGTCCTGACGGATGGACTGGAGTCGTCTGTAATGAGAGTGAGTTTGCCATGATGCTATAAATGGTTTCATTTAGAAATGTGAACCTGGACCACAACATCTTAACAGGATAGTTCACCCAAAAATGAACAGTTCCTGTTAAAGGGCACCTATGGTGAAAAATCTACTTTTCAAGCTGTTTGGACAAACATGTTTGTAAGTATAGTGTATATACTAGGGATGGGAAGATTAACCGATATGTATCGATACGCGGTCATGCGCGTGCACGATGCGAGTGCATCGGTTGAGCAGCAGAGGATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41911
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
ENSDART00000109204 Nonsense 725 1318 21 35
Genomic Location (Zv9):
Chromosome 11 (position 42843406)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41133901
GRCz11 11 41746131
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTGTCCCCCTAATAGAGTGTGAATCAGGGTTTTTTGGCTCTGCTTG[T/A]GAGAATAAATGCTCTTGTCCGCCTGGAGTGACCTGTGATCATGTGACTGG
Long Flanking Sequence:
AAGGAAAGATTATAATATTTTCCAAGTGCTGTTTAACAGAGAGTTTTTTTTTCAACACATTAGTTTGAATAACTAATTTTTTAAAATTTTTATTACCAGAGAGTATAAAACAAAATTTTCTCCCCATTTTGGACTGTTAAAATAGTTTTTGGGACATTTCATATGCTGCAAAACAGTTGCAGGACCACACTGTATGTCTGTAACAGAATATAAAACATTCATTTAAAAACATTTAAATAGCCACTTAAGAGCTAAAAATGTTCTGCCCTTGGAGGTTAATAAAATACGAGAAGAATAAAAAATGATTAATAAAGAAATAAAAAGAAGAAGAAAAATGCAATTAAAAAAATGTTGTCAGTGTAGCATTGTTGTCTTATTCATTTTAAACCTACACCTTTTTAAAGTTTGCTCTGAATGTATCTAAACTATCTAAAAATATATGATCTCTGTTATTTTGTCCCCCTAATAGAGTGTGAATCAGGGTTTTTTGGCTCTGCTTG[T/A]GAGAATAAATGCTCTTGTCCGCCTGGAGTGACCTGTGATCATGTGACTGGAGCTTGTCAACCCAAATGTCCAGCTGGAAAAACAGGCGACAAATGTGACCAAGGTTTTTCAGAGTACTCATACACAACGTGTCTGTAGTTCATTATCTAAATTGTTTGGATGTTTGTCGAAGCACACTGGATGTTTTCCTATTACTTTGATAGATTGTGTGGAAGGGAGATTTGGGATTGGATGCTCTCAGTCTTGTGACTGCTCTGGCGCACCATGTGACAAAGTGACTGGTCAATGCACGTGTCCTGCTGGAACGTTTGGAAAGCGCTGTGAAAAAGGTAAAATGATTATATTGATGTCTGCATGTCACAATTATCTTGTACTGAATTAGGGCTGTGTGACATTTAGGGCTTGCGGTCCATGCGCAAAGCGCAAAACGCAGGGCGCAAACGCTTTTAGGGCGTGTCAGGACGCCTTTTTGCTAATTTAAGGACGGGAAAATCTATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2600
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
ENSDART00000109204 Essential Splice Site 759 1318 21 35
Genomic Location (Zv9):
Chromosome 11 (position 42843302)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41133797
GRCz11 11 41746027
KASP Assay ID:
554-2880.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTCAACCSAAATGTCCAGCTGGAAAAASAGGCGACAAATGTGACCAAG[G/C]TTTTTCAGAGTACTCATACACAACGTGTCTRTAGTTCATTATCTAAATTG
Long Flanking Sequence:
ATAAAACAAAATTTTCTCCCCATTTTGGACTGTTAAAATAGTTTTTGGGACATTTCATATGCTGCAAAACAGTTGCAGGACCACACTGTATGTCTGTAACAGAATATAAAACATTCATTTAAAAACATTTAAATAGCCACTTAAGAGCTAAAAATGTTCTGCCCTTGGAGGTTAATAAAATACGAGAAGAATAAAAAATGATTAATAAAGAAATAAAAAGAAGAAGAAAAATGCAATTAAAAAAATGTTGTCAGTGTAGCATTGTTGTCTTATTCATTTTAAACCTACACCTTTTTAAAGTTTGCTCTGAATGTATCTAAACTATCTAAAAATATATGATCTCTGTTATTTTGTCCCCCTAATAGAGTGTGAATCAGGGTTTTTTGGCTCTGCTTGTGAGAATAAATGCTCTTGTCCGCCTGGAGTGACCTGTGATCATGTGACTGGAGCTTGTCAACCCAAATGTCCAGCTGGAAAAACAGGCGACAAATGTGACCAAG[G/C]TTTTTCAGAGTACTCATACACAACGTGTCTGTAGTTCATTATCTAAATTGTTTGGATGTTTGTCGAAGCACACTGGATGTTTTCCTATTACTTTGATAGATTGTGTGGAAGGGAGATTTGGGATTGGATGCTCTCAGTCTTGTGACTGCTCTGGCGCACCATGTGACAAAGTGACTGGTCAATGCACGTGTCCTGCTGGAACGTTTGGAAAGCGCTGTGAAAAAGGTAAAATGATTATATTGATGTCTGCATGTCACAATTATCTTGTACTGAATTAGGGCTGTGTGACATTTAGGGCTTGCGGTCCATGCGCAAAGCGCAAAACGCAGGGCGCAAACGCTTTTAGGGCGTGTCAGGACGCCTTTTTGCTAATTTAAGGACGGGAAAATCTATGGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTACAGGTGTGTTTTAAGAATAAACCAATCAGAGTCTCATCTCCCATTCCCTTTAAGAGCCAGCTGCGTCACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15275
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Essential Splice Site 760 1318 21 35
Genomic Location (Zv9):
Chromosome 11 (position 42843301)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41133796
GRCz11 11 41746026
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCAAMCSAAATGTCCAGCTGGAAAAASAGGCGACAAATGTGACCAAGS[T/A]TTTTCAGAGTACTCATACACAACGTGTCTRTAGTTCATTATCTAAATTGT
Long Flanking Sequence:
TAAAACAAAATTTTCTCCCCATTTTGGACTGTTAAAATAGTTTTTGGGACATTTCATATGCTGCAAAACAGTTGCAGGACCACACTGTATGTCTGTAACAGAATATAAAACATTCATTTAAAAACATTTAAATAGCCACTTAAGAGCTAAAAATGTTCTGCCCTTGGAGGTTAATAAAATACGAGAAGAATAAAAAATGATTAATAAAGAAATAAAAAGAAGAAGAAAAATGCAATTAAAAAAATGTTGTCAGTGTAGCATTGTTGTCTTATTCATTTTAAACCTACACCTTTTTAAAGTTTGCTCTGAATGTATCTAAACTATCTAAAAATATATGATCTCTGTTATTTTGTCCCCCTAATAGAGTGTGAATCAGGGTTTTTTGGCTCTGCTTGTGAGAATAAATGCTCTTGTCCGCCTGGAGTGACCTGTGATCATGTGACTGGAGCTTGTCAACCCAAATGTCCAGCTGGAAAAACAGGCGACAAATGTGACCAAGG[T/A]TTTTCAGAGTACTCATACACAACGTGTCTGTAGTTCATTATCTAAATTGTTTGGATGTTTGTCGAAGCACACTGGATGTTTTCCTATTACTTTGATAGATTGTGTGGAAGGGAGATTTGGGATTGGATGCTCTCAGTCTTGTGACTGCTCTGGCGCACCATGTGACAAAGTGACTGGTCAATGCACGTGTCCTGCTGGAACGTTTGGAAAGCGCTGTGAAAAAGGTAAAATGATTATATTGATGTCTGCATGTCACAATTATCTTGTACTGAATTAGGGCTGTGTGACATTTAGGGCTTGCGGTCCATGCGCAAAGCGCAAAACGCAGGGCGCAAACGCTTTTAGGGCGTGTCAGGACGCCTTTTTGCTAATTTAAGGACGGGAAAATCTATGGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTACAGGTGTGTTTTAAGAATAAACCAATCAGAGTCTCATCTCCCATTCCCTTTAAGAGCCAGCTGCGTCACGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41910
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Essential Splice Site 804 1318 23 35
Genomic Location (Zv9):
Chromosome 11 (position 42838134)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41128629
GRCz11 11 41740859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACGTCATGAATGTTACAGTATTTGTCATGTGTTTACGGAATCTGTCCC[A/T]GAATGCCCGGCTGGCTCGTTTGGGCCCGGCTGTAAGCATCGCTGCCAGTG
Long Flanking Sequence:
GCCAGTTTGTTTTCTGTATTTTACATACATTTTGTATACAGTAGAAATTAAAATGATTTTTGTTAATATTTCAAATATTTCCTAAGAGATGTTTCTTTTGGAGAAACTCTTATTTGTTTTATTTTGGCTAGAATAAAAACTTTTCATTTTAGTTTAAAATTTTTTAAAACTATTTGAAGGTCCATATTATTAGTCTCCCTAAGCAATATTCGATTGTCTACAGAACAAACCATCATTGTACAATAACTTGCCTAATTACCCTTATTTTTACCTAATTAACCTAATCAAGCCTTTAAATGTCACTTTAAGCTGTATACTGGTATCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGGCAAAGAGAAAAGAAATGTTTAGAAATGTGTTAAAAAAACTCTCTGTTAAACAGAAAAAAATATACAAATAATTCTGACTTCAACTGCACGTCATGAATGTTACAGTATTTGTCATGTGTTTACGGAATCTGTCCC[A/T]GAATGCCCGGCTGGCTCGTTTGGGCCCGGCTGTAAGCATCGCTGCCAGTGTGAAAATCAGGCATCATGTGACCACGTGGGCGGAGCTTGTACCTGTAAGACCGGCTGGACCGGAACCTTCTGTGAAAAACGTATGATTGTTCCACTAAACCCATATTAACATCTGGCCTGATAGAGGATCTACTTAACATCTGCTAATGTGTTTGTGTATGTTCAGCCTGTCCGCAGGGTTTCTATGGTCTGGACTGTCAGCAGAAGTGTGTGTGTTTGAACGGCGGTCTCTGTGATCATGTGAGCGGTCAGTGTTTCTGTAAGGCCGGATGGATCGGGACGCGCTGTAACCAGAGTGAGTTCATTGTTATGGTAGTTTCTTTAAAGTCAGTGGGAACCAGAAGATCAGTGGTTAGCACTGTTTTCAGCAAGAAGGTCGCTGGTTTGAATCCTGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGCGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15985
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
ENSDART00000109204 Nonsense 962 1318 26 35
Genomic Location (Zv9):
Chromosome 11 (position 42832266)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41122761
GRCz11 11 41734991
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGTGAATGTGTGAATGGAGCTCAGTGTGATRGTCAGACGGGTSGCTG[T/A]GTTTGTCCGCCGGGCTGGRCAGGAGAGCGCTGTGAGAATGGTGAGCTCAT
Long Flanking Sequence:
CAGAAAAAACAAAACAGCAGAGAAGAAGCTCGACACAGAGGAACATTAACACCTCACTGCCAACTAGCGTTTCGGAAGTGTTAATGCAGACCAACAGAGACAGCGCGCAGAATTATTAATGCACAGCTACGCGAGTTGCATGCGCGGTGGGTTACACCGATCACTTGATGCAGAAGTATAAACCAGGCTTAAGACCTAGTTGAACGCTATAGCGGTTTATGAGGACTGATGTCCTTGTAATTCAAAACATTTCAAAATCATACCTAATGGGGTCTTTTAAATTTTACCACAGGCGCTGGAGGGGTGCTGTGTAGGACTATATAATACTACATGTTTTAAAACTACATTACACCTATAGAGAGTCCCTGTAAACCACAAAAACCAACATGTGTGCATGTGTGTGTGTTGTCAGAATGTCCAGCGGGGAGGTTCGGCTCAGACTGTCAGGACAGATGTGAATGTGTGAATGGAGCTCAGTGTGATGGTCAGACGGGTCGCTG[T/A]GTTTGTCCGCCGGGCTGGACAGGAGAGCGCTGTGAGAATGGTGAGCTCATCTACACACAAAACACACTCTGGAAAACACACTCTGAGTAAAGACAGCCCTTCAGCCTCAACTTAATAGTACAATAGAACAGTGTTTGACAGCAAAGTTTGATTTAGTTTTAGTCTTAGTCTTTTAACTAAAATTCCCTTTTAATTTCAGTCATGTTTTAGTTTTCTGAATCATTTTAGTTGTAGTCGACTAAATTTCAAAAGATTTTAGTCGACTAAATCTACTCTAGGCAGTGGCGCAGTGGGTAGCACATTCGCCTCACAGCAAGAAGGTCGCTGGGTCGCTGGTTCGATCCTCGGCTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTCGTTGCATGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGTTAAATTGTCCGTAGTGTATGAGTGAATGAATCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21975
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Essential Splice Site 1019 1318 27 35
Genomic Location (Zv9):
Chromosome 11 (position 42827191)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41117686
GRCz11 11 41729916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCAGTGTCTCTGCCCTGCTGGATGGAGAGGAAGACGCTGTGAGAAAGG[T/C]CAGCTCATTAAAAAAAATCAAATATATATAATAAATGACTTTATAAATAT
Long Flanking Sequence:
GGTTTAATATTTTTTTGTTATTAAAATTGAAGTTCCTGTTTCAAAGCTTACAGATAGATGGCTAATTTGTATGTCATTGACACTTTTGGCACTTTTTTTGGATTATTTTCATAAGTTTTGTTTTTTCCTGTAAATGATTCAATAAATACCGTACCATGACATTCATACCGAGGTATTACCGTACCGTGAAATTCTGATACCGTTACATCCCTAGTAATATGCCAATAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTGTGTGTAAGGAAGAATGAGGGAATAATGATCATAATCAACCCATAGGATCAGCAGTAGTCATTAGTGATCGTGTGTGTGTGTGTGTTCAGAGTGTGAACGGGGCTGGTTTGGCGTGGGTTGTGAGGACCGCTGTCAGTGTGATCACGGTGCTGTCTGCCATCACGTGAGCGGTCAGTGTCTCTGCCCTGCTGGATGGAGAGGAAGACGCTGTGAGAAAGG[T/C]CAGCTCATTAAAAAAAATCAAATATATATAATAAATGACTTTATAAATATTATTACTAGAATATATTTCACCCATAATGAATAGTTAAATGTCATTAAATAATACATAATTTAAATTTCTTTAAATATTTATTTATTAATTATACATGTATTATGTTTGAAATGACATTAATTATATACGAGCAATTATTAAATATTTAATATATGTGAAACTGTACCTTTATTTGAAGTGTGTGTAACATATGTTGTGTCTCTGCATGTTGTGTGTGTGTGCATGTGTCGTGTGTCTCTGTGTGTGTCTGTCTGGGTGTGTAATGTGTGTGTGTGTGTGTTTCTCTCTCTCTGTTGTCTCTTTCTTTCTCTCTGTCTCTCTCTCTTTCTCTGTGTGTGTGTGTGTGTGTGTGTTGTAGCATGTCTGCCGGGCTCATTTGGTCAGGATTGTGTCCAGCGCTGCTCTTGTCCGTCCGGCTCCTCGTGTCATCATGTGACCGGTCACTGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35153
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109204 Nonsense 1233 1318 33 35
Genomic Location (Zv9):
Chromosome 11 (position 42814861)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41105356
GRCz11 11 41717586
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGATACAGGACAGTGTGTGTGTCCCGCTGGAGTCCACGGCCCGCGCTGT[C/T]AGCACGGTCAGACCTACAGTATATACATCAGTCAACACACACTTGAATAT
Long Flanking Sequence:
ACACACACACACACACACACACACACACTCACTCAACAATTTAGTTTATCAATTCACCTGTACCACTTGTCTTTGGACTGTGGGAAAACGGGAGCACCTAGAGGAAACCCACGCGAACACAGGGAGAACATGCAAACTCCACACAGAAATGCCAACCAAACCAGACTCGAACCAGCAACCTTCTTGCTGTGACACCACAGTGCTAACCATTGAGCCACCATGATAACTTGATATAATTCGTTTTTCTTTTTTTTTTAAATTACAATTATTTTTGTTTTCAAAAATAATAAGACGGTTTAGCTTGGAAATAGAGAAGTACCCACAATTCCACAATCATGCATACACATGCTGAATGACTGTGATTTGTGTGTGTTTCAGCGTGTCCGGCTGGTCTCTTCGGCTCTGGGTGTCAGCAGCAGTGTGACTGTATGAACGGAGCCTCCTGTCATCCGGATACAGGACAGTGTGTGTGTCCCGCTGGAGTCCACGGCCCGCGCTGT[C/T]AGCACGGTCAGACCTACAGTATATACATCAGTCAACACACACTTGAATATGTGCTTTACAGGGACTCACCGCAGACGTACTGTAATGATTTTTCTACTACAGTAAACACACTGAATATTCTGTCCTCCAATCAAACACTGTCAAACAATATTCCTAAATTAGCAGTTTTCTGTATTTTCCCTGTTTATTTCTGCATTTGAGTTGCATTATGGGAGCTTACGAAACCCCGGAGGGGACGTAGTGGAGGAGAAAAAAATTGGCTGGGTGAAAATAAAATAATGGGTGATAGAAAAAAAATGGGTGGAAGGAAAATATATATTTCTAAGTTTTTGCGGTCCCTGGCAAAGATGTTATGCGTTATCTTGCAAAACTGTTTCTCCACAAACACTTCCTGTTCACTCACATGAACCCTTCCGTTTTTGCCGAAATTCTCCCGTATTTCACCATTCTATCCCACTTTCTTTACATTAATACTGTGCGTCGTTTGTCGACTTTCATAT
Associated Phenotype:
Not determined