Busch Lab

ZMP

CADPS (1 of 2)

Ensembl ID:
ENSDARG00000043661
Description:
Ca++-dependent secretion activator [Source:HGNC Symbol;Acc:1426]
Human Orthologue:
CADPS
Human Description:
Ca++-dependent secretion activator [Source:HGNC Symbol;Acc:1426]
Mouse Orthologue:
Cadps
Mouse Description:
Ca2+-dependent secretion activator Gene [Source:MGI Symbol;Acc:MGI:1350922]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa27764 Nonsense Mutation detected in F1 DNA Not yet available
sa31824 Nonsense Available for shipment Available now
sa35069 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa27765 Nonsense Mutation detected in F1 DNA Not yet available
sa21886 Nonsense Available for shipment Available now
sa15647 Essential Splice Site Available for shipment Available now
sa41815 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa14101 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa27764
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
ENSDART00000029680 Nonsense 96 1316 1 30
Genomic Location (Zv9):
Chromosome 11 (position 20201706)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19619020
GRCz11 11 19781362
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGAAGAGGCTCCAGCTGTACGTCTTTGTGATGCGGTGTATTGCCTA[T/A]CCTTTTAATGCAAAACAGCCGACCGACATGGCGAGGCGACAGCAAAAGGT
Long Flanking Sequence:
GTTAAACACGTAAGCAGCAACAATTTAATTCGGTGGAAGACTACTGGCTGTTGGAGCAGCTTTTTTCACTCGCAGTGAGGGTAAGTGACACTTTTGATGTCGCGTTTGGATGGAAATAAGCGCCTTCGGTACTTTTCCGAGTTACCGAGGGGCTTTTGATAGTAAACAACATTTCTCTCGTTTGATTTCAGGGAAGCGAGAACTTGCGTTGAAATGTTGGACCCGTCATCCAGCGAGGAGGAGGCGGATGAGGTTGTGGAAGAAGAGCGAAAAGTGGTGGCGGCGCCCAAGGCTGGTGGTCCTCGGGTGTCTTCAAGCCGGACCAGCGAAAGCTCTGGTGGGCTGCAGCCGAGCCGAAGCACCAATGCCCGGCCGACGAGCCCCAGTCCCTCAGTGGCGGTCGAGAAGGAAAAGGATGATTTAGAAAAGATGCAGAGGGAGGAAGAGGAGAGGAAGAAGAGGCTCCAGCTGTACGTCTTTGTGATGCGGTGTATTGCCTA[T/A]CCTTTTAATGCAAAACAGCCGACCGACATGGCGAGGCGACAGCAAAAGGTAAGAGGGCAAAGTCGCATGCAACAGATTGCTGTGCAAATGAATTGAAGAATGGGTGAGCAGCAACTGCAGGCTGTGGAAAAACACAGTTTTAGCGTATTGGGGATGATTGTTTCAGCCCTAAACTAATGCAACATGAAGATGCATCAGGAAATTTATTTATTCATATTTTCCAGTGCATAAGAAATCAACATTATGCTTGATTTGTTTTTTCATAATCAAGAAGAAATTAATGTTTACCTTGCATTAGTAGCTTTCATTTGTACTTTTAGATTGTGTTAAAGATGAAAGTGGGTTTTTAGTATAGTATCAGAACAATAAAAGTGTAATATACATTTAATTTCCCCCATACTTTAGAATGTGTCCAGTTTAATTAAAAGGAAATATCAGAATCACTATCATACATTTTTACAGTGATTTATGGAAGAGAACCACTAAAATTTGCACCGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31824
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Nonsense 149 1316 2 30
Genomic Location (Zv9):
Chromosome 11 (position 20251084)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19668398
GRCz11 11 19830740
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCAGATTGTAGCCGATGAGGCCTTCATCAATGCAGTCCAAAGCTACTA[T/A]GAGGTTTGGCTTCAATTTTATTCATCAACGCAACAAGTCTGGACTTGCAC
Long Flanking Sequence:
AGCCACACAATATTTGCAATTCTGTTTGCGAATGTTTAGTTCACTCAAAAATTCTCCATGTTTCAAACTTTTATGAGTTACTTTATTCTCTTTAACACAAAATATTTATTTAAGAATGTTGGAAAGCAGCAGCCATTTACTTGCAAAATAGTTTCTGTTCTTATACTGTCGATGTCAGTGATTACCGGTTTTCCAGCATTCTTCATAATATCAGATAACAATAATAACAGAAGAAATAAATGTATAACTTGAAAACTTGAGAGTGAGTAAATGATGAGAAACATCTGGATTCTTAAAAGTTTTTTAATAGTTTTTTCTTTTTTTTTGGTGTCACATTGTATACATAATAAATGAAAATCTGTCTCTCTCTCCGATGATTTCTCTTCTCAGATCAGCAAGCAGCATCTTCAAACAGTGAAAGAGCGTTTCCAGGCCTTTCTCAATGGAGACACTCAGATTGTAGCCGATGAGGCCTTCATCAATGCAGTCCAAAGCTACTA[T/A]GAGGTTTGGCTTCAATTTTATTCATCAACGCAACAAGTCTGGACTTGCACTGGATCTCAAACCAATTCTTCTTTCGATAAAATCCTTTGCACGCAAACCTTGTATAATGTCATCAAAAAAGATGTTTACTAAATTGAAAGAGCGTTTCTGTGTGTTTTTAATAGAAGATTCCTAAACTCAAGAAAGACTGTATTTATTATATAGCTGTGGTAAAAAATAAATAGAAAGAACTAAAAAAAAGTTTTTTCGAAAAAGGCTAGATCATTTATTTTCTCATATTTAAAATAAAATTGTCATTTATGTCAAAAATGTCAATTTTATGTAATGTTTTTGCAAACAGTCTGACTAATTTCTATTTTCTGAATACCAAAAATGCCCTAAATGACAATATTTTTAATTTAAATTAGGAAGAAATGTTATCAGATCTTAATCTAAAACTAATTTAAACGTTTTAAACATGTAGTTAAAACAATTCTTGTCAGTTTTGATCAGTTTAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35069
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Essential Splice Site 366 1316 5 30
Genomic Location (Zv9):
Chromosome 11 (position 20297384)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19714698
GRCz11 11 19877040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGAACCAGCTCTCCAAGTCTGACGTTGTTTTGTCTTTCACACTGGAGG[T/A]AAGTGTTCCTGTTTAACTGCATGGATTAGAGTGTCACTTTTTCCGGGAAT
Long Flanking Sequence:
AGAATTTTTAGATATTTGGACTAGAAACAAGACAAAACATCCAAGTAAAAAAACATTTATTGCAATGTTGTCATTGCTTGCTGTACTTGCCTTGCACTATTTGCTCTATATTTCTTTACATGTTTCACTTGCCATTGTATGTGTGTGCTTGTTGATTTTTTGTACTGGAAGTCAAAAAAAAAAATGTAGATGCACATTGTACAATGCCAATTAAGACATTCTAATTCTAAAGAATTGTTTTTTCTCTCTTTACCTGCTTGAACAGGCTGGCCGCTTCCCTAAGTTTGTGTCCAGGGACATGGAGGCCATGTACATTGAGGAGCTGAAGTCATCGGTGAACCTGCTGATGGCCAATCTGGAAAGCATGCCAGTGTCCAAAGGAGGAGAGTTTAAACTGCAGAAGCTCAAAAGAGGCCACAACACATCCATCATTGACATGGGCCAGGAGGACGAGAACCAGCTCTCCAAGTCTGACGTTGTTTTGTCTTTCACACTGGAGG[T/A]AAGTGTTCCTGTTTAACTGCATGGATTAGAGTGTCACTTTTTCCGGGAATGTTGTTCAAAACATGACCTCGTGACACTCTAAACAAGGAGATCTCATAGGTATCGATGTCAAGACTGCAGTTTATAACGGATTGGCTGATCACCAAGCATGTAGAAGTTCATTTCTACAATGAACAAAATGCTGTTTAAAGTTTATATTATAGAAAGTGTGGTGTATATTTCTGGATTAGTGTAATATCCCTGTCTAAAAAAGCACTGACTGTATTCAAACCACAAGAGACAAACACTTTGATATACATCATTTATCTTTCAGCTTAGGGTGAAATTATTTTGTGGGTTGACAACAATTTAGGACAAATATGGCGGCATATGAAGGAAAAGCAGGATGTTATGGATAGTTTGTAACTTATTAGCATGATGTTAGTTTTATAAAACGTCTTTGAGTTTTTTTAGATCCTTTTTGTCAAAATTTAGCTATAGCTGAGGTAAGTGACAAAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27765
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
ENSDART00000029680 Nonsense 386 1316 6 30
Genomic Location (Zv9):
Chromosome 11 (position 20304069)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19721383
GRCz11 11 19883725
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTG[C/A]ACCATGGAGGTGGAAGGAGGACAGAAACTTCAGACAGATCAAGCAGAGGC
Long Flanking Sequence:
TGTATGTATCCTTGTTATTGTATGCTTTATCACAAACATCTAACAATAATTACAATTTAGTTCAGTAGCAGATTGTAGACAGTCTTTTGTGGCTGTTTGTGGCATTATATTTCACCAAATTAGTTTTTAAAAGCAATTGAAAATGAAAACAATTCAATACAGTGCATTTTGACTACCTCTAAAAGTGTTTAAATCATATTAGATCCTGTGTACTGCTACAGCATGTACAGCATTATCCGTTTGTGATTGGATTGACAAAAACACATATTACTACTAGGTGTAAAGAGAGCCTTGAATGACAGAAATAACTACTGTACGGCTGCCAACGCAACACATTTTCCTTGACTTTGATAACATCAGCTATTTTTGATTGTATTTTCTACTAGGCAGTCATTTTTTAAGAGTCTTTTTTTCATTGCTCTTTTCATGTTTACTTCACAGGTGGTGATCATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTG[C/A]ACCATGGAGGTGGAAGGAGGACAGAAACTTCAGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCATAATTTTTTTGTTTCTACCTCAACGTTATATGATGTGCATTGTTGCATGCTCCCATTTTCAGAAGCGCTGATTCTGGAAGAATTTTCCATTAATTTTTCTCATAGGGATTTTTATAAAAGTCTTTAAGCATTACAATCAACGAACCAAACCAACCAGTCCTAAGAAACATCACAACATTAACAATTATTGATTTAAAGGGCTATGAAACCCCCCACTACATGTGCACTACATCTGATTTTCACACCGGCAACACAAACACAGATGCAGGGGAGATAGACAGAGAGCAGCATTTACAGTGGATCTGAGAGCTGTGTGGAAGTGGAGGATTTTTAGTCCATAATATTGTAGAGATATTACTGTAAACTTAGTAACGAAATCATTTTGACTAAATTATGTCTTTAAAAACTAAGAGTAATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21886
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Nonsense 397 1316 6 30
Genomic Location (Zv9):
Chromosome 11 (position 20304100)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19721414
GRCz11 11 19883756
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACCGAATTGTTTACTGCACCATGGAGGTGGAAGGAGGACAGAAACTT[C/T]AGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCA
Long Flanking Sequence:
ACAAACATCTAACAATAATTACAATTTAGTTCAGTAGCAGATTGTAGACAGTCTTTTGTGGCTGTTTGTGGCATTATATTTCACCAAATTAGTTTTTAAAAGCAATTGAAAATGAAAACAATTCAATACAGTGCATTTTGACTACCTCTAAAAGTGTTTAAATCATATTAGATCCTGTGTACTGCTACAGCATGTACAGCATTATCCGTTTGTGATTGGATTGACAAAAACACATATTACTACTAGGTGTAAAGAGAGCCTTGAATGACAGAAATAACTACTGTACGGCTGCCAACGCAACACATTTTCCTTGACTTTGATAACATCAGCTATTTTTGATTGTATTTTCTACTAGGCAGTCATTTTTTAAGAGTCTTTTTTTCATTGCTCTTTTCATGTTTACTTCACAGGTGGTGATCATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTGCACCATGGAGGTGGAAGGAGGACAGAAACTT[C/T]AGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCATAATTTTTTTGTTTCTACCTCAACGTTATATGATGTGCATTGTTGCATGCTCCCATTTTCAGAAGCGCTGATTCTGGAAGAATTTTCCATTAATTTTTCTCATAGGGATTTTTATAAAAGTCTTTAAGCATTACAATCAACGAACCAAACCAACCAGTCCTAAGAAACATCACAACATTAACAATTATTGATTTAAAGGGCTATGAAACCCCCCACTACATGTGCACTACATCTGATTTTCACACCGGCAACACAAACACAGATGCAGGGGAGATAGACAGAGAGCAGCATTTACAGTGGATCTGAGAGCTGTGTGGAAGTGGAGGATTTTTAGTCCATAATATTGTAGAGATATTACTGTAAACTTAGTAACGAAATCATTTTGACTAAATTATGTCTTTAAAAACTAAGAGTAATGCTGACTTCACTTACTAACTTTGCCATCAAGTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27766
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Essential Splice Site 407 1316 7 30
Genomic Location (Zv9):
Chromosome 11 (position 20333930)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19751244
GRCz11 11 19913586
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTATAATTAGATACCTGATTTAAATTCTCTTCCTCTCTCTCGTCTA[G/A]TTGGGGTACTCAAGGAGATTTCACCACCACTCATCCACTTCCAGCAGTGA
Long Flanking Sequence:
AGTTTGACTATTTTTCTTCAACAAATTAATCCGTGCATTTCTGGCTTTAATATTTGCATTGTGTGGCAACCATTTTATTATATGGTATTATAACAAATAGACCCACACAGCCCACATCTGCCCACAGAAATCAACAGATAAATATGAGTGATTATTCTGATTTTATTTTAATTTTAGCAATATTATTGAAAAATATGCAAATCTATTGTTTAAGTACAGATCAGATAGTAAACTATTGTTTCCATCTTTTAACCAATGTATTTTATGAGAGACATTATTTACCAAATAAGGGGATCTAATTGGATTTAAACTTTAAACTTAGATTAGCAGTTAAAAAGTGATTGTTTCTTTATTTAATGCATTAAATCTTAGCTTCTATAATTTTGCTGTATTGTGAATAATACTTGATCTGTGTACACTTTAAATATGTAAATATTTTTTAAAATCTATTTTTTTATAATTAGATACCTGATTTAAATTCTCTTCCTCTCTCTCGTCTA[G/A]TTGGGGTACTCAAGGAGATTTCACCACCACTCATCCACTTCCAGCAGTGAAGGTGAAACTCTTCACAGAGAGTACAGGAGTGCTGGCGCTGGAGGATAAAGAGCTGGGCCGGGTCAGAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGACACACACAAACACACACACACACACTAGCTTGTTTATGATCACAAACGAACAAAACTAAATTCAGGTGGTTTTTTAAGTTTTTTTTTTTTTTTTACACTTTTTTTTTTACTTAATGTCCACTTTGACCACTTTCAGAGGTAGCTGAGAACAAGGCAAGTCATTGGACAGCAATGGTTTATTCTGTAGCTAATTGGAAAAACATTTAGGTGGCTACAATTTTTTACATTATAAATTCTTGTAAAAAAATAAAAACTACTTTTACCTTAGCCAAACTAAATAAAGACTTTTTCCAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27767
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
ENSDART00000029680 Nonsense 521 1316 10 30
Genomic Location (Zv9):
Chromosome 11 (position 20354709)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19772023
GRCz11 11 19934365
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTGCTCATTTTTTTTCCACAGGTGAGCCAGTACACCTTTGCCATGTG[T/A]AGCTACAGGGAGAAGAAAGCAGAGCCGGTTGAACTTCTCCAACTGGACGG
Long Flanking Sequence:
GAATGTATTATTACAGTGAACTCTCTACACAAGCATGTTGAAAAAAACGTGTCTCCACCTAGTTTTGTGTCAGAAACATGCTTGATAGAGATGCATGATATTATCGGATTGTTCAGCCTATAATTAATAGAAGTGTAAACACTGGCATCAGCCAGATATGGAAAATTTCCTTCCTAGCTGATGTGTTGATTATGTGTGGATGATGAGCCTGCATTATTTTACTTGTGCTCATTGCCAAATTTGCATTGTCACAGTCACTTCTATCTGTTTCTGATAAAACACACTTTTTAGTACCACTCGGACATTTCACTGTCAGGAAACATTCAAGAATCAACGTATAAATGTTTTTGCTTAAATGACACCAAATTTTTTTTATGAGCCTGGGTTGGATATTGCTCCTCTTCCAGTTCAAAATAGTGTGGTTCATTATTTAAATTCATAGAAATATATGTTGTGCTCATTTTTTTTCCACAGGTGAGCCAGTACACCTTTGCCATGTG[T/A]AGCTACAGGGAGAAGAAAGCAGAGCCGGTTGAACTTCTCCAACTGGACGGATACACTGTGGATTACACCGACCCTCAGCCAGGTCACTTAGCCGATCAGAATGCAACAATCATAATGAATACAATGCAAAATACAAATTTTCCATACAAATATGCAAATTAGAAGCAAAACTAGAATAGCTCATAAAACACTTGTGAACAAAGAATTGTTTTCATCCAAACTTTCAAAGAGTTAAAGAGAACAAAATCATCATAGGAGAAGCCACCGTGGGCCTTTTTTATATACAACTTGCCACTCAGAAGACATGCAATGAAGATGTATAGTAGCTTCTTGAGGTGTGAGACCTTTCGTTAGGAGTTTTGACAGTTCTGGGTGGTAATGATACTCAACCACTTTAATGATGGACATTGGCTAAGGGATTTTAAAATGACCAAGACAACATTTCAGATATTTTACAATGTGGTTTGTCCATTAATGTCTTTTAAAACAAAATCACATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15647
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
ENSDART00000029680 Essential Splice Site 784 1316 16 30
Genomic Location (Zv9):
Chromosome 11 (position 20385170)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19802484
GRCz11 11 19964826
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCCAGCTACTCTCAAAAGTGAGCATGCAGTTGATTTGTGRTGTTTTTC[A/T]GGTCCTGATGAARGACATTGTGACCCCGGTTCCTCAGGATGAGGTAAAGG
Long Flanking Sequence:
TAAACACATTTTAAATCTAATATTTTATAACTAATTTATTTTTTTCTTTGTCATGATGAAGGTACAAAATGTTTTCCTAGTTATTTTGCAAGATACTAGTATTCCGCTTAAAGCGCACTTTAGAGACTTAACTAGGCAATTTAGGTCACTCAAGTTAGTTTAAGCAAGTCCTGGGATAACTGTGGTTTATTTTATAGCCAATTGTAAAAAATAAAACAATTTAGGGGCCTAACAATATTGACATTTTCTTTTATAAACTGTTTTTATTCCAGCCAAACTAAATGAAACAAGGCTCTTTTTTACAGAAGAAAATAGTTATTAAATAATATAGGAAATTTTGTGAAAATGTCCTTGTTCAGAACTTGGTAATTGAAAATAATTGTAACTAAAAATACAGGAGGGCTATTATGTTAATTATATTGAATAAGTAAATATTTGATAAGTTTAAATAACCCAGCTACTCTCAAAAGTGAGCATGCAGTTGATTTGTGATGTTTTTC[A/T]GGTCCTGATGAAGGACATTGTGACCCCGGTTCCTCAGGATGAGGTAAAGGCTGTGATCCGCAAGTGTCTGGAGCAGGCAGCTTTAGTCAATTATCAGCGCCTCTCAGAATATGCCAAGGTGGAAGGTAGGAAGCTTGTGTTTCTACTCCTCTTCAGCAACACAGTGCATATTCCTGTCTCTGAAACTGTGCTTAACAACAGTGATGATTAACTAACCCCCATTATACAGAAGTCGTGCTGAAATGCAACTGATATTGTTTATTTCAAAACAGGAAAGTTCAGGAGAACTCATTAAAAGTCAATATGTTATTTTGGGATTTTTCAAATAAGTTTATAAGTTAAATAAATAAATATAATATTATGAATCAATTTTTTTTATTTGTAATGTTTATATGATTTCATGTTGTTATTATTATTATTATTATTATTATTATTGTTATTATTATTATTATAGAAGCTATAAGCTGCAGATTTATAAAACTGTGTGGTAATAAATATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41815
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Splice Site, Nonsense 927 1316 21 30
Genomic Location (Zv9):
Chromosome 11 (position 20412030)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19829344
GRCz11 11 19991686
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTGCTGTATGTCAGCACACATTTAGTCTGTTCTTCCCTCTTTCAGA[T/A]AATCTGTGTAATGGGAAGTTTCACAAGCACCTGCAGGATCTGTTTGCTCC
Long Flanking Sequence:
ATCAGCAGCACCGCTCAAATGGCTAATAGAAGAAGAGCAATCAGAAAGACAAACAAACAAACAAACACACACACACACTGCATACAAACCAGTTAACTTCACTATAGTTTCACTATAATAAGTTATAGTTATACTCTATAGTTTCACTAAAGTTAGACCTTTATTTACTGAAGCACAAGACAATGTTTATGACAATTCTGTATAAAAATATAGGGTTTTTTTTTGCATTTTTGAGGTTATTTTTATGAGCAATTGTGCATTGTATGTTTGGTAAAGCGTTCTGTTGTATATAGTTTTTGTTTATTTTGTTTCATTTGAATTGTTTGCTCAAAGTTTTGTAACAATTTAGCACTTTACTATTTGCTATAAAACACATTTCAGAGCATTAAGAGAGATCATAAAAACATCATAATAAGTCAAAAAAGAAAACAGGTTGAGCTCGTAAAATGTAGGTTTGCTGTATGTCAGCACACATTTAGTCTGTTCTTCCCTCTTTCAGA[T/A]AATCTGTGTAATGGGAAGTTTCACAAGCACCTGCAGGATCTGTTTGCTCCTCTGGTGGTGAGGTATGTGGATCTTATGGAGTCGTCCATCGCTCAGTCCATTCACAGAGGATTCGAACGAGAGTCTTGGGAGCCTGTCAAGTAAGCAGAACACTTCTTTGCTGATCAATCCAACACTGATTAAATGGGTGTTCTTCATTACTAAAACAACTAAAACTTAATCATGCTTATCCGCAGTCTCACTATTCACACACGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGCACACACACACACAGTAAAAGCATTTATTTATATGTTGTTGTTTGTTTGTGTGTGTGTGTGTGTGTGTGTGTTCAAAATTCAGAATTCAAAACAGAGTTTGAACAGCACTGGAACATGTTTCAGTTATTTTTTTATTGAGTTGTTTTACTTATTTTTAGTATTATTGTTATCGTTATTATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14101
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
ENSDART00000029680 Nonsense 1034 1316 23 30
Genomic Location (Zv9):
Chromosome 11 (position 20419477)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19836791
GRCz11 11 19999133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACYGTGTTCTGTGGTGWTTTCAGCAATGGTTCGGGGACGTCTGAAGAYT[T/A]GTTTTGGAAGCKGGACGCTCTGCAAACATTCATTAGAGACCTGCACTGGC
Long Flanking Sequence:
ATGCCTTGATGGCCTGCTGGCTGTTTGAGGACTTAGGCTGTAAGGAATAGTGCCAGAGTCAGTCTCTGCTTTTTACCATTTATTACAAAAGGATTGAATTTTTGATTGAATATCAGGGACCGTCTCTCCTCCTTCCACACACATTAACCTTAACATTGTGATCCTGCTGTTTTCCTTTGACAACATTGTGCATGTTTAACCTTCCCTGTTCTCAAACAACCAAAAGATTGTTTATACTATTTTGTTTCAGAGTTAACCCTTTATTTTTTCCATGGACTGATCAGCACAAACATCTGCAACGATCGGGAAGTGGTAAAAAATAACCAAACCAAATGTATGTGGACATGAAACAGTTTTTGTCTTCTTTAACAACCCGCCTTCCTCTGAGCTGTCCCGTATTCCTGACATTTTTGGGGCTGTCCTTTCCTGATTTACAGTTGTGGTTGAATAAACTGTGTTCTGTGGTGTTTTCAGCAATGGTTCGGGGACGTCTGAAGATT[T/A]GTTTTGGAAGCTGGACGCTCTGCAAACATTCATTAGAGACCTGCACTGGCCAGAAGAAGAGTTTGCCAAACATTTGGAGATGCGACTTAAACTCATGTCCAGTGATATGATCGAGTCCTGTGTTAAAAGGTGAGAACAGAACACACAAATACATATACATATACACTCACACTCACAGGCCACTTTATTAGGTACACCTTACTTGTACCGGGTTGGACCCCCTTTTGCCTTCACAACCACCTTAATCCTTATTGGCATAGATTCAACAAGGTACTGGAAATATTCCTCAGAGATGTTGGTCCATATTGACATGACAGCAGTTGCTGCAGATTTGCCAGCTGCACATCCATGATAGCCATCAGAAGATGGCTACACTAAGGTCATAAAGAGATGGATATGGTCAACAACAATACTCAGGTAGGCTGTGGTGTTGACATGATGCTCAATTAGTACTAATGGACCCAAAGTGTGCCAAGAAAATATCCCCTACACCATTACAC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27768
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029680 Nonsense 1283 1316 30 30
Genomic Location (Zv9):
Chromosome 11 (position 20460024)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 19877338
GRCz11 11 20039680
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCCGACTGCAAGGCGTATTAGACTCAACTCTGAACAGCAAGATGTAC[G/T]AGACTGTGAGAAACAGGCTGATTCTAGAAGAGGCCACAGCATCTGTGAGA
Long Flanking Sequence:
ACAATTTATTTGGGCTGAATTTAAACAAATAAATTAAGTTGAACAAAATTGTATTTGTTTGTGTAAATTTAGCTCCTATACTGTAAATAGTTTGCAACAAAAGTTCAGTTTCACAAAAAAGTATCAGCCAATACCAATTATTGGACAATAAATTTGTGCAACTCTACTCATAATTAATTTTAATTAATCAAAAGTATTCAAAATATTATCATTTAGAGCATTTTAAAAATATATATTTTTAGAAAATGACAGTTGGTCAGTGTTCATTTGTTGTGAACATTTTTTCTACCAAATATTGCTTTCTTAACTCTTCTGAAATTAAAACATTGGGATTGTGTTTTAATAAAAGAATGTCATGACTATTATTACTGTTATAAGTAATGAAAGGAAAATTGAGCTAGATGTACCTAAATCCACAATTCTCCTTGTTTACACAGAAAAAGTATCGTGATTTCCGACTGCAAGGCGTATTAGACTCAACTCTGAACAGCAAGATGTAC[G/T]AGACTGTGAGAAACAGGCTGATTCTAGAAGAGGCCACAGCATCTGTGAGAGAAGGAGGGATGCAGGGGATATCAATGAAAGATAGTGATGAAGAAGACGACTAGATCCTGCTGGAGACACTTCAGTCACAGCCACGGTTATCGTGGCCTAAAATAATGCATGTACACCACTGTCCATCACTCGTACAGGTCTGGATGTTGATAAAGTCATGTTTGATGACAGACAAGAGACCAATTTCAATTGAAGTGACACAACAATTTATTAATCTCCATTTAGATGATGAAAACAACATACTAATTTAAATTTAAATTACTTTTCAAAAACATTCTGGGTTGTTTCAAGCCACATTTGGGTCAATTTTTGACATATTGATATTAATAAATGTGATCCTAGACCTCAAAACCAGTCTAAGGCTGCAGTCACACTGCACATTTCTTCACATAGACTTCCATTCATACGCATGCTAATGCGACACACCAGAAACGCAAACTCATGCAACA
Associated Phenotype:
Not determined