Busch Lab

ZMP

ADAMTSL3

Ensembl ID:
ENSDARG00000027903
Description:
ADAMTS-like 3 [Source:HGNC Symbol;Acc:14633]
Human Orthologue:
ADAMTSL3
Human Description:
ADAMTS-like 3 [Source:HGNC Symbol;Acc:14633]
Mouse Orthologue:
Adamtsl3
Mouse Description:
ADAMTS-like 3 Gene [Source:MGI Symbol;Acc:MGI:3028499]

Alleles

There are 15 alleles of this gene:

Allele Name Consequence Status Availability
sa40844 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11069 Essential Splice Site Available for shipment Available now
sa10958 Nonsense Available for shipment Available now
sa40843 Nonsense Mutation detected in F1 DNA Not yet available
sa34013 Nonsense Mutation detected in F1 DNA Not yet available
sa38594 Nonsense Mutation detected in F1 DNA Not yet available
sa25354 Nonsense Mutation detected in F1 DNA Not yet available
sa17662 Essential Splice Site Available for shipment Available now
sa20869 Essential Splice Site Available for shipment Available now
sa26898 Nonsense Mutation detected in F1 DNA Not yet available
sa40842 Nonsense Mutation detected in F1 DNA Not yet available
sa34012 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26899
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Nonsense 359 1760 10 30
Genomic Location (Zv9):
Chromosome 7 (position 13348215)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12276329
GRCz11 7 12529290
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATTTGATCTTGATGTCTGACAGTGTTTAATCTCTCTCCTGCAGGTTA[T/A]CAGCTGAATTCAGCCGACTGCGTGGATATCCGCTATAACAGATCGGTTGC
Long Flanking Sequence:
ATGATTTGCGCCTTATTGCACCAGGTATATGATAGGGTCCAATGTTTTATACAACTATAAAATGCCTCTGTACACACTACACTACACACAGTTGAAGTCAGTATTATTATCGCTCTTGTGAAATATTTCTCAAATGATGTTTAACAGAGCAACGAATTTATCACAGCATTTCCTATAATATTTTCTCTTCTAGAGAAAGTCTTATTTGTTTTATTTCATCTACAATAAAGCAGTTTTAAAACCATTTTAAAGTCAATATTATTAGCCCTCTAAAGCAATTTTGTTTTTGTTATTTCTGACTTCAACTCTACATGTCTGTCCAAACAGCTTCCAATGGTTGATTTTGCATGGTAGGTGCCTTTAAAAATGCTGCAAGGGATGAAAGTTTCATGAATTGTAACTTGAAAGTGGTCTGATGTTGTATATCTCAGCTAAGATTGATCTATGAAAAGCATTTGATCTTGATGTCTGACAGTGTTTAATCTCTCTCCTGCAGGTTA[T/A]CAGCTGAATTCAGCCGACTGCGTGGATATCCGCTATAACAGATCGGTTGCGGAGCACTTGTGCCACAGTTTCCCAGAAAACACCAAACCCACACCCAAACTCAAAGAGTGCAACATGGAACCCTGTCCTGAAAGGCTGGTTCTGCCATATTAATGCACACACATCTAATTAGAGCATACAGTAGCTGTGATGATGATGATGATGATAATAACGCTTTTTGTTTCTCTTCCAGTGATGGATTTAAGGAAGTGATGCCGTATGACCATTTCCAGCCTCTTCCTCGGTATGAAATCATTTACTTACTGCTCTCATACTGATAGAGATCAACCCTGATAGAGATACAGTTCAGCACTATAAAAAAAATTACATAAAAACACATTTTTATGTTGCCTTAACTAATTTTACTAGGTTAATCAAGTTTCAACTGCATTTTTACGGACAAAGTGAAACTAAATATGTTTTACTCAGTTTGACTGATGAAATGAGATGATGGCGGCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40844
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
ENSDART00000052750 Essential Splice Site 489 1760 12 30
Genomic Location (Zv9):
Chromosome 7 (position 13343978)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12272092
GRCz11 7 12525053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCAACACCTTTGACTGTCCGCAGTGGATGGCCATGGAGTGGTCTCAG[G/A]TTAGTGCAGGGTTTCCGCACTATATACACAATATTATCGAATTTAAAAGA
Long Flanking Sequence:
ACACTCATACCGCAATTATTTGGACTGAGGAGGAAACTGGAGCACCAGGAGGAAACCAACGCCAACACAGGGAGAGATATGCCTATATATACTGTATATATATATATATATATATATATATATATATATGAATAGTTGGCGGTTCATTCCACTGTGGCAACCCCTGATAAATAAGGGACTAAGCCGAAGGAAAATGACTGAACTTTGGCTGCTTTTCCAGGTTGTTGAGAGCCTGTATGTAAGCTAGCATTGATCCAGTAATGTGATCAAGTGTTGTTGTGTCCTCTTGGTTCAGATGGGAGCAGAACCCGTGGACGTCGTGCTCGGTGTCGTGCGGAGGGGGATCTCAGGAGAGGAGTATCGTGTGTGTGGAGGAGGACGTTCATGGTCAGATTGTGCAGGTGGAGGACTGGAAGTGCACACACTCACCTCGACCAATCAGCAAACAGAACTGCAACACCTTTGACTGTCCGCAGTGGATGGCCATGGAGTGGTCTCAG[G/A]TTAGTGCAGGGTTTCCGCACTATATACACAATATTATCGAATTTAAAAGAACTATTCCAGACATATACAAGGGTTGGACAATGAAACTGAAATGCCTGATTTTAGACCATGATAATTTATTAGTATGGTTTAGGGCCCACTTTTGCGGCCAACACAACATCAATTCATCTTGGGAGTGAAAGACACAAGTCCCGCACAGTGACCAGAGAAATTCTGATCCATTACAGGATGCTGGTGGAGGAAAAGGTTTGCTGACTCGCTCCTTCCAAAACAACCCAAAGGGACTCAATAGTATTTAGGTCGGGTTACTGTGCAGGCCACAGGAGATGTTCAACTTCCCTTTCGTGCTCATCAACCCATTCTGTCTCCAGTCTTGCTGTGTGTATCGGTGCATTATCATCCTGATACACGACACCGCCTTCGGGATACAATGTTTGACCCATTGGGAGCACAGCGTTCTTCAGAATGGTTCGGTAGTCCTTGGCAGTGACTCAGAGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11069
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Essential Splice Site 489 1760 12 30
Genomic Location (Zv9):
Chromosome 7 (position 13343977)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12272091
GRCz11 7 12525052
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCAACACCTTTGACTGTCCGCAGTGGATGGCCATGGAGTGGTCTCAGG[T/G]TMGTGCAGGGTTTCCGCACTATWTACACAATATYATCGAATTTAAAAGAA
Long Flanking Sequence:
CACTCATACCGCAATTATTTGGACTGAGGAGGAAACTGGAGCACCAGGAGGAAACCAACGCCAACACAGGGAGAGATATGCCTATATATACTGTATATATATATATATATATATATATATATATATATGAATAGTTGGCGGTTCATTCCACTGTGGCAACCCCTGATAAATAAGGGACTAAGCCGAAGGAAAATGACTGAACTTTGGCTGCTTTTCCAGGTTGTTGAGAGCCTGTATGTAAGCTAGCATTGATCCAGTAATGTGATCAAGTGTTGTTGTGTCCTCTTGGTTCAGATGGGAGCAGAACCCGTGGACGTCGTGCTCGGTGTCGTGCGGAGGGGGATCTCAGGAGAGGAGTATCGTGTGTGTGGAGGAGGACGTTCATGGTCAGATTGTGCAGGTGGAGGACTGGAAGTGCACACACTCACCTCGACCAATCAGCAAACAGAACTGCAACACCTTTGACTGTCCGCAGTGGATGGCCATGGAGTGGTCTCAGG[T/G]TAGTGCAGGGTTTCCGCACTATATACACAATATTATCGAATTTAAAAGAACTATTCCAGACATATACAAGGGTTGGACAATGAAACTGAAATGCCTGATTTTAGACCATGATAATTTATTAGTATGGTTTAGGGCCCACTTTTGCGGCCAACACAACATCAATTCATCTTGGGAGTGAAAGACACAAGTCCCGCACAGTGACCAGAGAAATTCTGATCCATTACAGGATGCTGGTGGAGGAAAAGGTTTGCTGACTCGCTCCTTCCAAAACAACCCAAAGGGACTCAATAGTATTTAGGTCGGGTTACTGTGCAGGCCACAGGAGATGTTCAACTTCCCTTTCGTGCTCATCAACCCATTCTGTCTCCAGTCTTGCTGTGTGTATCGGTGCATTATCATCCTGATACACGACACCGCCTTCGGGATACAATGTTTGACCCATTGGGAGCACAGCGTTCTTCAGAATGGTTCGGTAGTCCTTGGCAGTGACTCAGAGCCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10958
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
ENSDART00000052750 Nonsense 508 1760 13 30
Genomic Location (Zv9):
Chromosome 7 (position 13342965)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12271079
GRCz11 7 12524040
KASP Assay ID:
2259-8494.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACCTGTGGTCCAGGTTTGCGCTACAGAGTTGTTCTGTGTGTGGATTA[T/G]AATGGTCAACACGCCGGTGGCTGCAATCYTCACCTCAAACCTCATATCAA
Long Flanking Sequence:
TATTGGGCCTCAGGAATACTATAATATTGCTGCCCAATATAACCCCCCCCCCATGCTTTACTCTGGGCATGCAACAGTCTGCGTGGTACACTTCTTTGGAGCTTCTCCACACCGTAACTCTCCCGGATGTAGGAAAGACAGTGAGGGTGGTCTCATTAGAGAACAATACATGTCTCACCTTGTCCACCGCTCAAGTTTTCGCTGCTGGCCCTTTTGAAACTTACGTTTAGTACCCGGATATCTCTTTCAGACAGCTTCCTCTTGCATCCACAGTTGAATTTGGCTTGTCCATCATCGTGATATACTGACATTACTCTGGATATCGTGGCAGTTTATACATCACAAAGATAAGCGGTCTTAGTCACAGATCCGCCAGTGAGATGAGCACTAACAATGATTTGTCCTCTTTCGAATTCTGAATATTTGTGTATGTGTGTTTTCCAGTGCACGGTCACCTGTGGTCCAGGTTTGCGCTACAGAGTTGTTCTGTGTGTGGATTA[T/G]AATGGTCAACACGCCGGTGGCTGCAATCCTCACCTCAAACCTCATATCAAAGAGGACTGCCTCGTCCCCATCGCATGCCACAAACCACGAGGTAAAAGACCACATCTGTACACCTTCAAGAGCAATGGACATAGATGAACACATAGGGCTCTATTTTAACGGTCTAGGCACACAGTCTGAAGCGCAGGGCGCAAAAGCATTAAGGCATGTCCGAATCCACTTTTGCTATTTTAAGGACAGGAAAATCCGCTTTGCGCCGTGGCGCATGGTCTAACAGGGTTGAGCTAATTCTTTTAATGAGTTATGGGTGTAATTTGAGAATAAACCAATCAGATCACCGATCATCTTATCTCCAATTCCCTTTAAGAGTCAGTTGCTTCGCTCCATGGCACATTTGCTATTTACATGACGGTTTTAGAGGGGTTTTGGCCATTTCCAGGCTGGTTTCCAGCCATTTCCAGCCTGGTTTTAGCTGGTCAGGCTGGGAGATGACCAGCTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40843
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
ENSDART00000052750 Nonsense 634 1760 15 30
Genomic Location (Zv9):
Chromosome 7 (position 13308690)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12236804
GRCz11 7 12489765
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAGCTGTGATTCAGGGCCCTGTTTGGCAGCTCCAGACTCCTCGCGGT[G/A]GCCCCTGAGGACCCCTGAGGGCCCCAATCAGCATGGTTATGCTTGGGAGT
Long Flanking Sequence:
AAAGCCTGGTAAGGTCTAACAGTGTAGTTAACCTAATTAACCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCAAGTAAAATATTATTGACTGTCATCATGGCAAAGATAAAATAAATCAGTAATTAGAGATGAGTTATTAAAACTATTATGTTCAGAAATGTGTTGAAACAATCTTCTTTCCATTAAACAGAAATTATTGGAAAAAATAAATAGGGGCGTTAATAATTCAGGGGGGCTAATAATTCTGCCTTTAACTGTATATGTGTGTGTGTAGGTTTGTCCCGGAGCCGTGGTCATCCTGCAGTGTGTCTTGTGGTCTGGGCATCCAGCGGCGTCAGGTGAAGTGTAAAGTGCTGCTGTCCTTCACTCAAGCTGAGGTCGAACTGCCTGATGAAGAGTGCCATGAAGAAAAGCCTTCCTCTCAAAGGAGCTGTGATTCAGGGCCCTGTTTGGCAGCTCCAGACTCCTCGCGGT[G/A]GCCCCTGAGGACCCCTGAGGGCCCCAATCAGCATGGTTATGCTTGGGAGTACATTGGCTTCACTGCTTGCTCTGCATCATGTGCTGTCGGTGAGTCTCCACTGAGGTACACATGAAATCAAAACGGTAACACTTTACAATAAGGTTCATTAGATAATGCATTTACTAACATGAACTAATCATGAACAACACATGTGCAGCATTTATTAATCATAACTGAACATTTACTAACGCATTATTAACATCCAAGTCCATGCTTTTTAACATTAGTTAATGCACCATGGGTTAACATGAACTAACAATGAACTACTGTATTTTCATTAACTAACGTTAACTAACATGAACAAAAACAGTAGTAAATGTGTTGTTCATTGTTTGTTCATGTTAGTAAATGCATTAATTAACAATAACTAATGAACCTTATTGTAAAGTGTGACCATCAAAACTAACCATAATGATTGTGTTAGCTCATATTGCTAGATTTGTGGTGAACAATTCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34013
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
ENSDART00000052750 Nonsense 1169 1760 20 30
Genomic Location (Zv9):
Chromosome 7 (position 13282456)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12210570
GRCz11 7 12463531
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTGAACTTTTTGGTACGGAGGTTTCAAAAATAGCAGCAATCGTTCGA[C/T]AGAAGCATCACGGATCTGTTATGAGCTTCCAGCGGGATCTCAGGATCCAT
Long Flanking Sequence:
GGCTCCTGGATCATCCGAGTTTGGGAAAGGAAAGAAGGGGGAACTTTCATCCATACCTCAACAAAGAAGGAGGTTTTGTTAGTTCGAAATGCAATGAAGGATTCACGAATGGAAACAAGGCTTCGAAATCAAGTTGGATGCAAAAAAACGAATTCTACAGAGACGATGATGGACATCCCAAGGAGATGCTTTGGGATACTCTTGCTTTGGGAAACTATGCTTTGGCTTCAAGCACTAGTAGCCACACAGGAGCCTTCGTTCTTGAACCTGCACAATTTGAGGAGCTTGTGAAAAACATCAGTCAGCTTGCAGAGAGTGGCGATGTGACGGATGAAATGGCGTCGCAACTAATTGGGAAACTACTAGAGGACTTGGCTGCTGCAGGGCAAGGGCAAGTTCCTATTGAGGAAAGCACTACAGTGGACAATTATTTAGATAGGACGTCAAACACTTCTGAACTTTTTGGTACGGAGGTTTCAAAAATAGCAGCAATCGTTCGA[C/T]AGAAGCATCACGGATCTGTTATGAGCTTCCAGCGGGATCTCAGGATCCATGTGGGAAGGACTGCTTACCTGACCAATGCAACCCACAGCCTTACACTGTTGTGTCCCAGTAAGGGATCACCAAAGCCAAAGCTCTCCTGGACCAAAGATGGAGCTCCACTGCAGGACATCAACAGGTAAGAGCTGCAATGTGTTGTTGAAAAAGCATTGGTGTTGCAGAATCTCTCTTTCTACATACAGGTGAACTGAAAATTAATCGTCCTCCTCTGAAATATTTCCCAAACAATGTTTGATAGAGTAAGGAGGAAGAAAAGCCTATTCCCAGCCACTAGACCTTTTTGACAGGGAATTCGAGTGTCAGATGTGTGAAAGTTTGACTACTATACAGGAGTTATTATTATGTAATGTAATGTGTATTTATATAGCGCATTTATTGTGTATGGCCATACACCCAAAGCGCTTCACAATCATGAGGAGGGTTTCTCCACACCACTGCCAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38594
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Nonsense 1252 1760 21 30
Genomic Location (Zv9):
Chromosome 7 (position 13265485)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12193599
GRCz11 7 12446560
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACTGCACATCTCCAGCCCTGGTGCCAGTGATGTGGGCATCTACAGGTG[C/A]ACCTCCACCAATGAACTGGGCTCAGATTCAGAAACAACACAAGTTCTGTT
Long Flanking Sequence:
GTTTGATCAACTAGTTACTTTAAATCTCTATACTAAAAAAAAAAGATTAAACCAGCCTAGGCTGGTTGGCTGGTTTAAGCTGGTCGACCAGGCTGGTTTTAGAAGGGTTTTGAGCATTTCCAGGCTGGTTTCCAGTCATTTCCAGCCTGGTCAGGCTGGGAGATGACCAGCTAAAATCAGCTTGACCAGCCCTAATTAAATAGATAATTGTGGTTTTCTGTTGGTAGATCTCACACCGCTAACATGTGACCGCTAACATGTCATCTTAGAAGAGACAGAAGTCTGTCAATTAAAGATTCATATAAACATCAAAAAACATTGTAATATTTTCTGTTGACGTTAATAGTACATATGTGTAAATGGGAAATGTAATAAAGCTATTTGCCAATAATAGGACAGTATAGCTGATCTCTCACTCTCCCCAGGGTATCATGGGACAGCAGTGGTGGAGAACTGCACATCTCCAGCCCTGGTGCCAGTGATGTGGGCATCTACAGGTG[C/A]ACCTCCACCAATGAACTGGGCTCAGATTCAGAAACAACACAAGTTCTGTTAGCCGGTGAGACACTGCACACTTTTATCACAAGGACTCTCAAAATCTATTGTTTCAGAATGTCATGAAATGCATGAAATAAATCATGTGTAATAATAAGTGCTAGTTTACTCAGAATAAAGCTTAAGGTAACACTTCAACTCAAGTACCAATTCTCCCTATTGAATCGTTGCTTATGAGCTGCCTAATATTAAGACATTGCCTGTTTTGTAGTACTTGTACATATTCTGCATGACTTTATTCTACCTTTCTATATCTTGCCTCAATCAAACCTTAACTATTAATAAGCAGAAAATTAGGAGTTTATTAAGGCGACAATAATAGATGGTTTATTATAAAATGAGCTAGTTTTATTTTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25354
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
ENSDART00000052750 Nonsense 1269 1760 21 30
Genomic Location (Zv9):
Chromosome 7 (position 13265435)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12193549
GRCz11 7 12446510
KASP Assay ID:
554-7550.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTCCACCAATGAACTGGGCTCAGATTCAGAAACAACACAAGTTCTGT[T/A]AGCCGGTGAGACACTGCACACTTTTATCACAAGGACTCTCAAAATCTATT
Long Flanking Sequence:
ACCAGCCTAGGCTGGTTGGCTGGTTTAAGCTGGTCGACCAGGCTGGTTTTAGAAGGGTTTTGAGCATTTCCAGGCTGGTTTCCAGTCATTTCCAGCCTGGTCAGGCTGGGAGATGACCAGCTAAAATCAGCTTGACCAGCCCTAATTAAATAGATAATTGTGGTTTTCTGTTGGTAGATCTCACACCGCTAACATGTGACCGCTAACATGTCATCTTAGAAGAGACAGAAGTCTGTCAATTAAAGATTCATATAAACATCAAAAAACATTGTAATATTTTCTGTTGACGTTAATAGTACATATGTGTAAATGGGAAATGTAATAAAGCTATTTGCCAATAATAGGACAGTATAGCTGATCTCTCACTCTCCCCAGGGTATCATGGGACAGCAGTGGTGGAGAACTGCACATCTCCAGCCCTGGTGCCAGTGATGTGGGCATCTACAGGTGCACCTCCACCAATGAACTGGGCTCAGATTCAGAAACAACACAAGTTCTGT[T/A]AGCCGGTGAGACACTGCACACTTTTATCACAAGGACTCTCAAAATCTATTGTTTCAGAATGTCATGAAATGCATGAAATAAATCATGTGTAATAATAAGTGCTAGTTTACTCAGAATAAAGCTTAAGGTAACACTTCAACTCAAGTACCAATTCTCCCTATTGAATCGTTGCTTATGAGCTGCCTAATATTAAGACATTGCCTGTTTTGTAGTACTTGTACATATTCTGCATGACTTTATTCTACCTTTCTATATCTTGCCTCAATCAAACCTTAACTATTAATAAGCAGAAAATTAGGAGTTTATTAAGGCGACAATAATAGATGGTTTATTATAAAATGAGCTAGTTTTATTTTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTATTTATTTATTTATTTTTTTTTTCTGTGCAAACTGATGCATTTTAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa7059
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Nonsense 1310 1760 22 30
Genomic Location (Zv9):
Chromosome 7 (position 13263490)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12191604
GRCz11 7 12444565
KASP Assay ID:
554-4862.1 (used for ordering genotyping assays)
KASP Sequence:
STTGGAGGTGTTATCCGGGTCCGTTCTGGTGCCAACCTCACCCTGGAGTG[T/A]CCCGTCAAAGGTGAGTGAAGATTNNTACAGAAATTACTTTTTACATATTT
Long Flanking Sequence:
ATGACAGCGACACATTTGTAGGATTGAGTCCAAACAATGCCACTAAAAGACACGGTTCAATTTTTATAAGAGCTAGTTTTATTTTAGACAACTAATTTAGCTTCATTTTAATATATTTAGTGAATGAAAGATTGCAAACAGTTCAGTTGTTTGCTGTTTTTGTTTGTTTGTGTTGTTTTAGATACTGTAAGTATAGAATGATGAATATTTATGTTTTGGTGTACTGTTTAATCTGATGGAGAAAGAAAGAAAGATCTAAAGAAAAGCCCAATTTTAAAGTCTCACGAGCTTATTGTTTTCTAAAATAAGTATTGTGGATTGAACTCAGTTGTGTTCTGCTAGACCCCCAATAGTGACTCCATTTCATGCCATTTTTAAACAGAAAGTCCCACGATCGCTGCCTCACGCAGAAACACATCAGATCTGAAGAGTACGAGCCTGAAGGTGGTGGTTGGAGGTGTTATCCGGGTCCGTTCTGGTGCCAACCTCACCCTGGAGTG[T/A]CCCGTCAAAGGTGAGTGAAGATTATTACAGAAATTACTTTTTACATATTTAAAGAAGTCATCATATGTCTATACAGGGCCGGAGTGGGACTCCTTTTCAGCCCTGGAGTTTCAAGCCTCAGACCGGCCCACCTCATTTCACGACTGACTATATTAAAATAAGGTCGTTTCCAAATCAGTTTCTAATGACACTATCACGTCTTGTTTTTTGAGAAAACAGCTGCTTTAGAACTTCAAATGTTTAACAACCCTAACAGTATTACATGTCTTAACAATAAAAATGAAAACAATAAATTGCTCTAATGAGGATCGAACCTGGGTCTGCAGTGTCTTAACCTAACGTGTTAACCGCTGGACCACAACAGCTGTGTATGGTGCTGAGACACAACTGAGTTTTATCATATGAATAAAAAGGCTGTGGTCAAGTAAATAAATAAATTTAAAAAGTGTGACTGCTGAGAGCAACAGATTCTGGAGCTAGGGACACCGGCCCTCGCGGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17662
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Essential Splice Site 1313 1760 22 30
Genomic Location (Zv9):
Chromosome 7 (position 13263479)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12191593
GRCz11 7 12444554
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCCGGGTCCGTTCTGGTGCCAACCTCACCCTGGAGTGTCCCGTCAAAG[G/A]TGAGTGAAGATTNNTACAGAAATTACTTTTTACATATTTAAAGAAGTCAT
Long Flanking Sequence:
ACATTTGTAGGATTGAGTCCAAACAATGCCACTAAAAGACACGGTTCAATTTTTATAAGAGCTAGTTTTATTTTAGACAACTAATTTAGCTTCATTTTAATATATTTAGTGAATGAAAGATTGCAAACAGTTCAGTTGTTTGCTGTTTTTGTTTGTTTGTGTTGTTTTAGATACTGTAAGTATAGAATGATGAATATTTATGTTTTGGTGTACTGTTTAATCTGATGGAGAAAGAAAGAAAGATCTAAAGAAAAGCCCAATTTTAAAGTCTCACGAGCTTATTGTTTTCTAAAATAAGTATTGTGGATTGAACTCAGTTGTGTTCTGCTAGACCCCCAATAGTGACTCCATTTCATGCCATTTTTAAACAGAAAGTCCCACGATCGCTGCCTCACGCAGAAACACATCAGATCTGAAGAGTACGAGCCTGAAGGTGGTGGTTGGAGGTGTTATCCGGGTCCGTTCTGGTGCCAACCTCACCCTGGAGTGTCCCGTCAAAG[G/A]TGAGTGAAGATTATTACAGAAATTACTTTTTACATATTTAAAGAAGTCATCATATGTCTATACAGGGCCGGAGTGGGACTCCTTTTCAGCCCTGGAGTTTCAAGCCTCAGACCGGCCCACCTCATTTCACGACTGACTATATTAAAATAAGGTCGTTTCCAAATCAGTTTCTAATGACACTATCACGTCTTGTTTTTTGAGAAAACAGCTGCTTTAGAACTTCAAATGTTTAACAACCCTAACAGTATTACATGTCTTAACAATAAAAATGAAAACAATAAATTGCTCTAATGAGGATCGAACCTGGGTCTGCAGTGTCTTAACCTAACGTGTTAACCGCTGGACCACAACAGCTGTGTATGGTGCTGAGACACAACTGAGTTTTATCATATGAATAAAAAGGCTGTGGTCAAGTAAATAAATAAATTTAAAAAGTGTGACTGCTGAGAGCAACAGATTCTGGAGCTAGGGACACCGGCCCTCGCGGCCAAAAAACGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20869
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
ENSDART00000052750 Essential Splice Site 1374 1760 23 30
Genomic Location (Zv9):
Chromosome 7 (position 13246572)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12174686
GRCz11 7 12427647
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAACACCATCGGCAAATCCGCTGCCTCCAGCCGGATCAGTGTGGAGG[G/A]TGAGTAAAGACCACGGGATACTTCAAAGAAAGGTTTTTTTGTGGGCAAAA
Long Flanking Sequence:
GGAAAGAAATCTGTGAACTCAATCAATGATTATTTTAAATTAATTAGCCTGACATGTTTACTGTTCCAAAATGTTTTCAGTACATCTTAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATGTTCAATGTGAAAAAAGTTGCTGTTTTTGGGATAGTAGTAATCCCAATACCGTGATATTTTTTTCCAAGGTTTTCATACCGTCAGAGTCTATCGGCCCATGCCTAGTGAATGGACTGATTTGCTGTTTGTCTCTGGGCAGGTGTCCCCCATCCAGCAGTGAGTTGGCACCGAAAGGAGGGTCCGCTGGACGCCCGTGCTAGTCCTCTCCTGAGCGGATCACTGCTCCTTACAAACCTCACACAGCAGGATGAAGGCACCTACTCCTGCATCGCTGCCAACACCATCGGCAAATCCGCTGCCTCCAGCCGGATCAGTGTGGAGG[G/A]TGAGTAAAGACCACGGGATACTTCAAAGAAAGGTTTTTTTGTGGGCAAAAAGAAGTTTGAAAAGTCTGTTTTTGCACTAAGTTGCAGTGGGTGTGGTTGTAAATGTGTCACGCTGCTTACATGTACCTATAAACACAATGATGGTTTCATAAGCAACAGCCTTTCGCAAATCAGACGATAAAGCCTGTTTCACACTGCAGGCGTAAGCAGTGCATGAGCAGCGCATGAGCTGTGCGTGTTTTTTTCAGCATCCATGTTAACAGATTAGAGCTTTCATATGACACGCAGAGAGAGGCAGGAGTGTCGCTGAAGCAGCAGTGCCGCGATAGTTTCGGCACTGGGTCTATTTTTACCACGCTGCTCACGCTCAATTAAAGTGACAGTGTATTGATAATGACCAAAACACATTGAATGACAGTAAAAAGTAGCAATTTTACCCTTTAAATGCAGCGATAATATCAGCGATAGACTTATATATGGTCAATCAAATGAACTTAAAC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5398
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052750 Nonsense 1513 1760 26 30
Genomic Location (Zv9):
Chromosome 7 (position 13237173)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12165287
GRCz11 7 12418248
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGCTCGTCCTGTGGAAACAGAGGGAYTCAGATGAAGAAGATTAAATG[T/A]GTGTCGTCAGAGGGCAGAGAGTCTTCTCATGCAKCCTGTCATTATCTCCC
Long Flanking Sequence:
CTAGGCAAGTTGGGGTAATTAGGCAAATTATTGTATAACGATGGTTAAAGGGGCTAATAATTTTGTCCTTAAAATGGCTTTTAAAAAATTAAAAACTGCTTTTATTCTTGCCGAAATAAACCAAATAAGACTTTCTCCAGAAGAAAAAATATTAACAGACATACTGTGAAAATGTCCTTGTCCTGTTGAACATAATTTAGGAGATATTAAAAAAGAAAAAAAAATTAAAAGGGGCTAATAATTCTGACTTCAATTGCACATACAAATACTTGGAAGTATAGATGCGATTAATCTTTGCCCAGTGTTACAAAAAATATTAAAAATAAGGCAATAACACAAATCAATAGTCAGTTTTTTTTTTTGGAGTCAGAATGTGAAAAATGCCTCTAAGCGTGTGTGTTTTTTCTGTGTGTTGTAGAGTTTGAGTGGCGTTTGGGCGACTGGAGCACGTGCAGCTCGTCCTGTGGAAACAGAGGGACTCAGATGAAGAAGATTAAATG[T/A]GTGTCGTCAGAGGGCAGAGAGTCTTCTCATGCAGCCTGTCATTATCTCCCCAAACCCAGCAGTCAAACGCGCCCCTGCAACCTCCTGCACTGCCCGCCCAGGTATAACTGCTCTACTCAAAGAAATAGTTCATCCAAAAATCTAAATTACCCCATAATTTACTCACCCTTAGAGCCAGCCTGAAGCAAAAGCAAACTAAGTGGCTGCTTAGAGACCAGTGGCCACCAGGGGGCCTCAAGAGTGCATAAAATAAAAATTAATGTTTTGGTTATGATAGATCATGTTAGGGACATGGCAACATTAAGCACTAGAATCCAGTCTCTCTAAACCCTGCTTTTCCAATAGCCTGCTTCTGTTGGTTAGATGTTGTACCGTGTATGATTTTAATCAATTATTCATTCATTCATTCATTCATTTTCCTACGGTTAAGTCCCTTATTTATCAGCGGTTGACACAGCAGAATGAACCGCTCACTATCCCAACATATGTGTTATATAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26898
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
ENSDART00000052750 Nonsense 1573 1760 27 30
Genomic Location (Zv9):
Chromosome 7 (position 13220655)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12148769
GRCz11 7 12401730
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCAGCTCCTGTGGGCGGGGCTTCAGAGAGAGGCGGGTCTCCTGTCAG[C/T]AGGTGGAAGCTTCTGGAAGTGTGAAGGTTTTGCCTAGTAGTGAGTGTGAG
Long Flanking Sequence:
CCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCAAGTAAAATATTATTTACTGTCATCATGTCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTGTGTTTAGAAATGTGCTGAAAATTTTTTATCCTCGTTAAACAGAAAACGGGGAAAAATAAACAGGGGCGAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGAAGGAAATCTGGATACATCATGCAATACTGAAAACTCCCAACTAAATGATTTCTCCTCTCTGTATGTGCTCAGCTGGGTGTCAACAGTGTGGTCGAGGTGTTCCAGCTCCTGTGGGCGGGGCTTCAGAGAGAGGCGGGTCTCCTGTCAG[C/T]AGGTGGAAGCTTCTGGAAGTGTGAAGGTTTTGCCTAGTAGTGAGTGTGAGGGCTCTCCTCGACCCGAAGACCGACAGGAGTGCAGCTCTCAGGCCTGTGTTGAGTGGATCTCTGGCCCCTGGGGGAAGGTACATTCACTAATGCTTTTATATGATCATTCTGATCTCTTTAATGTGGAACAGTCATCTAAAATAGTGGTCATAAGTACATTACCTGACAAAAGTCTTGTCGCCTATCCAAGTTTTAGGAACAACAAATAATAACTGGACTTCTAGTTGATCATTTTGTATCAGAAGTGGCTTAAATGAAAGGCAAAGGCCTCTATATGCTTATTTTACCAAAATAAAATATGATCATGCCTTTATTTTGAATGATTTGAGATCTGACTTTGCTTAGACACGTCTTGTCACTTAACAGAAATAATGTACAGTATAGAATGTAAAGTTTTTGCTTCCCATTTCAAAAACTAATGCAAAGCAACGTACTGTGATGTATAGAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40842
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
ENSDART00000052750 Nonsense 1599 1760 27 30
Genomic Location (Zv9):
Chromosome 7 (position 13220577)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12148691
GRCz11 7 12401652
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGCCTAGTAGTGAGTGTGAGGGCTCTCCTCGACCCGAAGACCGACAG[G/T]AGTGCAGCTCTCAGGCCTGTGTTGAGTGGATCTCTGGCCCCTGGGGGAAG
Long Flanking Sequence:
ATTTACTGTCATCATGTCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTGTGTTTAGAAATGTGCTGAAAATTTTTTATCCTCGTTAAACAGAAAACGGGGAAAAATAAACAGGGGCGAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGAAGGAAATCTGGATACATCATGCAATACTGAAAACTCCCAACTAAATGATTTCTCCTCTCTGTATGTGCTCAGCTGGGTGTCAACAGTGTGGTCGAGGTGTTCCAGCTCCTGTGGGCGGGGCTTCAGAGAGAGGCGGGTCTCCTGTCAGCAGGTGGAAGCTTCTGGAAGTGTGAAGGTTTTGCCTAGTAGTGAGTGTGAGGGCTCTCCTCGACCCGAAGACCGACAG[G/T]AGTGCAGCTCTCAGGCCTGTGTTGAGTGGATCTCTGGCCCCTGGGGGAAGGTACATTCACTAATGCTTTTATATGATCATTCTGATCTCTTTAATGTGGAACAGTCATCTAAAATAGTGGTCATAAGTACATTACCTGACAAAAGTCTTGTCGCCTATCCAAGTTTTAGGAACAACAAATAATAACTGGACTTCTAGTTGATCATTTTGTATCAGAAGTGGCTTAAATGAAAGGCAAAGGCCTCTATATGCTTATTTTACCAAAATAAAATATGATCATGCCTTTATTTTGAATGATTTGAGATCTGACTTTGCTTAGACACGTCTTGTCACTTAACAGAAATAATGTACAGTATAGAATGTAAAGTTTTTGCTTCCCATTTCAAAAACTAATGCAAAGCAACGTACTGTGATGTATAGAGGAATGAAACTATGGAATGAATTGCCATCAGACATTACATGCATTGTAACAAGTAAAATGAGGTTTAAAAAATCATTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34012
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
ENSDART00000052750 Essential Splice Site 1615 1760 27 30
Genomic Location (Zv9):
Chromosome 7 (position 13220525)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 12148639
GRCz11 7 12401600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAGCTCTCAGGCCTGTGTTGAGTGGATCTCTGGCCCCTGGGGGAAGG[T/C]ACATTCACTAATGCTTTTATATGATCATTCTGATCTCTTTAATGTGGAAC
Long Flanking Sequence:
ATTAAAACTATTGTGTTTAGAAATGTGCTGAAAATTTTTTATCCTCGTTAAACAGAAAACGGGGAAAAATAAACAGGGGCGAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGAAGGAAATCTGGATACATCATGCAATACTGAAAACTCCCAACTAAATGATTTCTCCTCTCTGTATGTGCTCAGCTGGGTGTCAACAGTGTGGTCGAGGTGTTCCAGCTCCTGTGGGCGGGGCTTCAGAGAGAGGCGGGTCTCCTGTCAGCAGGTGGAAGCTTCTGGAAGTGTGAAGGTTTTGCCTAGTAGTGAGTGTGAGGGCTCTCCTCGACCCGAAGACCGACAGGAGTGCAGCTCTCAGGCCTGTGTTGAGTGGATCTCTGGCCCCTGGGGGAAGG[T/C]ACATTCACTAATGCTTTTATATGATCATTCTGATCTCTTTAATGTGGAACAGTCATCTAAAATAGTGGTCATAAGTACATTACCTGACAAAAGTCTTGTCGCCTATCCAAGTTTTAGGAACAACAAATAATAACTGGACTTCTAGTTGATCATTTTGTATCAGAAGTGGCTTAAATGAAAGGCAAAGGCCTCTATATGCTTATTTTACCAAAATAAAATATGATCATGCCTTTATTTTGAATGATTTGAGATCTGACTTTGCTTAGACACGTCTTGTCACTTAACAGAAATAATGTACAGTATAGAATGTAAAGTTTTTGCTTCCCATTTCAAAAACTAATGCAAAGCAACGTACTGTGATGTATAGAGGAATGAAACTATGGAATGAATTGCCATCAGACATTACATGCATTGTAACAAGTAAAATGAGGTTTAAAAAATCATTTAAAAAATATTTAATGGAACAATATTAAGTGGATTGTTGATTTGGATGTTATGTA
Associated Phenotype:
Not determined