Busch Lab

ZMP

cacna1ab

Ensembl ID:
ENSDARG00000006923
ZFIN ID:
ZDB-GENE-090514-3
Human Orthologue:
CACNA1A
Human Description:
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit [Source:HGNC Symbol;Acc:1388]
Mouse Orthologue:
Cacna1a
Mouse Description:
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit Gene [Source:MGI Symbol;Acc:MGI:10948

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa12560 Essential Splice Site Available for shipment Available now
sa12516 Essential Splice Site Available for shipment Available now
sa35120 Nonsense Mutation detected in F1 DNA Not yet available
sa15403 Essential Splice Site Available for shipment Available now
sa7292 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa5845 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10764 Essential Splice Site Available for shipment Available now
sa35121 Nonsense Mutation detected in F1 DNA Not yet available
sa9062 Nonsense Mutation detected in F1 DNA Not yet available
sa41872 Nonsense Mutation detected in F1 DNA Not yet available
sa41873 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12560
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
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Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008139 Essential Splice Site 38 2101 1 51
ENSDART00000008139 Essential Splice Site 38 2101 1 51
Genomic Location (Zv9):
Chromosome 11 (position 31781540)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30658902
GRCz11 11 30906086
KASP Assay ID:
2260-4470.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGCAGTCAGAGTRTTACGGCCGCTAAAACTGGTGTCAGGAATTCCTAG[T/C]AAGTTTTCCATCTGTGTCAGTTTTTTTCTGTCTTTTTTCCCCCAACATGC
Long Flanking Sequence:
ATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATGGATGGATGTAAACTTAGCTAATTAATGCATCAGCTTTAGTTAGCCTTGGATGAACAACCACTCATGCACACACATTCACTCACATTTAAAGATCAGACAATTTGAACAGTGTGTGATGCGAGAACCCAGCAGTGTGTGATCAATTATTTACCTTCAACTGACCTCTTCTCCTGATAGTGTGTTTCTTTGACACATGACATGTTTTCTCATTTTTCCTCAAAAATGAATGATGCATGATTGCAAAAATAACTATTTCCTGGCTTGTTCTTCTGTCCTCCAGTATCCTGTCCTCCGTGGGGTCAGAATTAGACCTGCGGACGCTGCGAGCAGTCAGAGTGTTACGGCCGCTAAAACTGGTGTCAGGAATTCCTAG[T/C]AAGTTTTCCATCTGTGTCAGTTTTTTTCTGTCTTTTTTCCCCCAACATGCATTAATACCATTACTCTCCAGGCCTGCAGGTGGTGCTGAAGTCCATCATGAAGGCCATGATTCCACTGCTGCAAATTGGTGTGCTTTTATTCGTGGCCATTCTTATGTTTGCCATTATTGGCCTGGAGTTCTACATGGGCAAATTCCACACCACCTGCTTCAACACCATCACTGGTGAGCTTTTCTCAAAGAGAGAAGACAAAAAAAACATGTTGTAGTAGTTTTACCTAACCATGAAACTTTATGTTGACCAGGTGAGATGTATGATGAACGGCCATGTGGAGCTCGGACATGTGATGCAAACAATACGCAATGCCAGGGCTACTGGCTTGGGCCCAACTATGGGATCACACAGTTCGACAATGTACTTTTTGCTGTGCTCACTGTATTCCAGTGCATCACAATGGAGGGCTGGACTGATATGCTTTATTATGTAAGACTTAAAGGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12516
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008139 Essential Splice Site 38 2101 1 51
ENSDART00000008139 Essential Splice Site 38 2101 1 51
Genomic Location (Zv9):
Chromosome 11 (position 31781540)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30658902
GRCz11 11 30906086
KASP Assay ID:
2260-4470.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGCAGTCAGAGTRTTACGGCCGCTAAAACTGGTGTCAGGAATTCCTAG[T/C]AAGTTTTCCATCTGTGTCAGTTTTTTTCTGTCTTTTTTCCCCCAACATGC
Long Flanking Sequence:
ATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATGGATGGATGTAAACTTAGCTAATTAATGCATCAGCTTTAGTTAGCCTTGGATGAACAACCACTCATGCACACACATTCACTCACATTTAAAGATCAGACAATTTGAACAGTGTGTGATGCGAGAACCCAGCAGTGTGTGATCAATTATTTACCTTCAACTGACCTCTTCTCCTGATAGTGTGTTTCTTTGACACATGACATGTTTTCTCATTTTTCCTCAAAAATGAATGATGCATGATTGCAAAAATAACTATTTCCTGGCTTGTTCTTCTGTCCTCCAGTATCCTGTCCTCCGTGGGGTCAGAATTAGACCTGCGGACGCTGCGAGCAGTCAGAGTGTTACGGCCGCTAAAACTGGTGTCAGGAATTCCTAG[T/C]AAGTTTTCCATCTGTGTCAGTTTTTTTCTGTCTTTTTTCCCCCAACATGCATTAATACCATTACTCTCCAGGCCTGCAGGTGGTGCTGAAGTCCATCATGAAGGCCATGATTCCACTGCTGCAAATTGGTGTGCTTTTATTCGTGGCCATTCTTATGTTTGCCATTATTGGCCTGGAGTTCTACATGGGCAAATTCCACACCACCTGCTTCAACACCATCACTGGTGAGCTTTTCTCAAAGAGAGAAGACAAAAAAAACATGTTGTAGTAGTTTTACCTAACCATGAAACTTTATGTTGACCAGGTGAGATGTATGATGAACGGCCATGTGGAGCTCGGACATGTGATGCAAACAATACGCAATGCCAGGGCTACTGGCTTGGGCCCAACTATGGGATCACACAGTTCGACAATGTACTTTTTGCTGTGCTCACTGTATTCCAGTGCATCACAATGGAGGGCTGGACTGATATGCTTTATTATGTAAGACTTAAAGGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35120
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
ENSDART00000008139 Nonsense 206 2101 5 51
Genomic Location (Zv9):
Chromosome 11 (position 31783731)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30661093
GRCz11 11 30908277
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGCGTGTAGAGAACAGGAGTGAGTTCCTCAAGCTCAAACGGCAGCAG[C/T]AGATCGAGAGAGAGCTCAACGGTTACCTGGAGTGGATCTGCAAAGCAGGT
Long Flanking Sequence:
AAACCTTAGAGATGGTTGTGCATGAAAATCCCAGTAGATTAGCAGTTTCTGAAATACTCAGATAAGACCGTCTGGTACCAACAACCATACCTCTTTCAAAGTCACTTAAATCACCTTTTTTCCCTATTCTGATGCTCAGTTTGAACTGCAACAAATCGTCTTGATCATGTCTACATGCCTAAATGCAATGAGTTGCAGTCTTGTGAGTGGCTGATTAGAATTTTTTGTTAACAAGCAGTTGGATAGGTGTACCTAATAAAGTGGCCGGTTAGTGTATATATTGTCTGCATAACTAGTATTATTCTAGTTCCCTTTCTATATCTGCATATCCTTCAATTCTATTATGTTTTTCTTCTGTCTGTTGTTCTATCGATCCATCCATACACACACCATCTTAACAAAGTGCTAACTAGCAGCTGTCTGTTTCTCTCAGTGAGTTTGCCAAAGAAAGAGAGCGTGTAGAGAACAGGAGTGAGTTCCTCAAGCTCAAACGGCAGCAG[C/T]AGATCGAGAGAGAGCTCAACGGTTACCTGGAGTGGATCTGCAAAGCAGGTCTGTGCTTTAAACTAATATGGGACGGACATAAATACATAACCTGAAGTATGTGCAGAATCCAACTCTGTTTCTTTTTCCAGAAGAGGTCATACTCGCAGAGGATGACAATGACACCGGTGAGAATATTAATGTTTTTTGCATGCTAAATAAAGCCACCAAATTGAAACATATTACGTCTGAAATGCAGTAAATGCTAAATTTGCTTTGTGCACAGGATCTCGACGAAGACCCACATTAAAGAAAAATAAAGCTGACCTGTTAAATCCACAAGAGGGAGTGGACCACATGGGAGATTCAGTTGGTGGGAATTACTTAATATGTTTCTCTGTTTTTGAAACGCATATTAATAGCTTATATACAGCTGAAGTCAGAATTATTAGCCCTCCTGAATTGTTAGCCATTTCTATCCCCAATTTCTGTCTAATGGAAAGATTTTTCACATAATAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15403
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
ENSDART00000008139 Essential Splice Site 340 2101 8 51
Genomic Location (Zv9):
Chromosome 11 (position 31785271)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30662633
GRCz11 11 30909817
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGCTGYAGTACACTACGATCAGCCTGAGCTACTGTCAGACTTCCTCTG[T/A]AAGTTCTGAYTCTTACTGAGTTGTTTGTTTTTACTTGCATGTTCAAAAAT
Long Flanking Sequence:
TTAAGGCAGCTAATATTATTGACTTTAAAATGGTTTTAAAAAAATAAAAAACTGCTTTTGTTGTATCCGAAATAAAACAATTAAGACTTTCTTCAGAAGAAAAAATATTATCAGACATACTGTAAAAACTTCCTTGCTCTGTTAAACATAATTTAGGAAATATTTGAAAAAGAAAATACACTTCACAGGAGGGCTAATCATTGTGACTTCAGCTGTATATATAATATCATATAGTGTTAATGCTAGGGTAGGAGATTTGAATGGTGCCTCACAATGTTATGCTATTTATTCTCAGGCTCACCTTTTGCTCGTGGAAGCATGAGCGGGAAGGGTGATGAAACCCCATTTAGCAAGAAAGAGCGACGTCTTCGCTTCCTTATTCGAAAGATGGTAAAGACTCAGGCGTTTTACTGGACCGTCATTAGCCTGGTTGCACTCAACACACTGTGTGTGGCTGTAGTACACTACGATCAGCCTGAGCTACTGTCAGACTTCCTCTG[T/A]AAGTTCTGATTCTTACTGAGTTGTTTGTTTTTACTTGCATGTTCAAAAATGTCATACAGATGGAATCAGCATAAAACACATGAAACACTGCTGTTCTGATGAAATGTGTCAGTGTCAGGACTCGCAGGGGTCATAATATCTACATCAGAAGTCAACTGTAGAACTTAAGACCATGGTTGCAAATTAATAGTATTTTGTGGAAAAATTTACACCAGCAAGAACAAGATTAAGGAAAATTTGAAGAAAATGTTTCAATAATTATCTTATCTTTGGAAAGAGGCTTCATCTTCTTCTTCTGAAACAATTTTTAAAGTCTATTTCCTTCTAAGCCTTTTAAGCTATATCCTTCAAACTTTCATCATAGCTTCATACTGGTCTGATTTGGGTTGCTTTTAACTTTTCCAACTGATCTAACTTTCAGATTTCTGATAAACGACCCGGAAAATTCCTGTTGACTCATCTCATTGGACCACACTTGGGTCAAACTTTGTACAGACTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7292
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008139 Splice Site, Nonsense 775 2101 19 51
Genomic Location (Zv9):
Chromosome 11 (position 31801777)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30679139
GRCz11 11 30926323
KASP Assay ID:
554-5368.1 (used for ordering genotyping assays)
KASP Sequence:
GYAATAAGAAGTCAGTGTTGCTTTGTTTTTTCTTTATTTTAACCCTTTCA[C/T]GTACAAGTTCTAAATCTTCAGCTGACCCCCCACCCCTGTGAGTTTTTTTT
Long Flanking Sequence:
TGAAGACCCACTTGGACCGTCCACTAGTTGTCAATCCTCAGGAGAACCGCAACAACAACACCAACAAGCCCCGACCCGATGACCCAAACCCCCAGGAGCGAAGCGAAGAACACCCGTCCAGATCCCATCACCATCACAGCCACCATCACCACCACCACCACCACCACACTCACCACTCCAGCCGCCAGTCTCTGCACCTCCCAGAGCTGGCCGAGACCGGTTTTGAATGTGATGTGGAGGGCGCAGGTGAGCACAGGCGACCCCGACACCACCAGCACAGGCGGAGGGATGAAGATGGAGGAGAGAGAGGAAGGAAACACAGAGATCATCACAGCAGAGGAGAGACGGCTGGAGGAGATGCAGAGGACGGACAGGAGAAGCGGCAGAGGAGACATCGACATGCTAACCATGGGGATGGAGACGGGAGAAGGGAGAGGAGTCGACTGCATCGCAATAAGAAGTCAGTGTTGCTTTGTTTTTTCTTTATTTTAACCCTTTCA[C/T]GTACAAGTTCTAAATCTTCAGCTGACCCCCCACCCCTGTGAGTTTTTTTTACGGTGAATATTATTTAGATCTCTTCTCTTTAAAGTTCTCATAGGGGCACATCAAGATTTATGCATAGATTGTTTTTGTCTCTATTTTTCTAACGTCAGAATTATAGTGCTCCATATATATAAGTAAACCCCTTACAAATCTTTTTAAATTCATATTTTTAATAGGAAGCTATACAAAATTATATTTGTGCATATACATTAGATTAGTAAATACTGAAGCCAAATCTGGAGCTTTTCTAACAAAATAACTTGCGATAACTGTCCAAAAACTAGTACACCCAAATGTATATGTATAGAAAAATATTAAACACCATTTAAAAAAAAAGAGGAAAATTCAGCAAAAAATATGAAAAATTTTGTTGAATATCTTTGATGACTAAAATATAATTTCAATAAATTTGAAAACAAAATGTTTTGTTTAAATGCACCAAAATACATTGCCTATATTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5845
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
ENSDART00000008139 Essential Splice Site 962 2101 22 51
Genomic Location (Zv9):
Chromosome 11 (position 31806410)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30683772
GRCz11 11 30930956
KASP Assay ID:
554-3714.1 (used for ordering genotyping assays)
KASP Sequence:
CGCGTTAGCAGCAGAAGATCCCGTCTCACAGGATTCAGAGAGAAACAAAG[T/A]GAGCAAAAAGATTTTAAATATATGTTTACTGTCGTAAYTAATATTTATGC
Long Flanking Sequence:
ATTTAATGCTGTTCGTATCATATGGAATTGAATTAACAGTTAACAGTTTCAACACCTGACAGTTCAAAACTAGACATTGGCTTGTTAAAAACCAATATGTAATTGTGTTTAAAGCCTGTTATTGAGCATTCCCTTTTTTCCTACATTGTTCAGTGAACAAGAATGCCAACACAGAGCCAGCTAAAGAAGGGGAGAAGAAAGAGGAGGAAGAAGACGATGGTGGCGATGAAGAAGGCCACAAGCGCATTCCACCTTTTAGTTCTTGTTTCATCCTATCCACAACCAACCCGTAAGAGTGTCCTTGTGTGTTTGTTTGTGAGAGTTAGTGCCAAGCAAATGTCATTCATCTCAACCGGTGTGTGTTTTCAGCTTCCGGAGATGCTGTCACTACATCCTCACTCTACGTTATTTCGAGATGTGTATTCTGTCCGTTATCGCTATGAGCAGCATCGCGTTAGCAGCAGAAGATCCCGTCTCACAGGATTCAGAGAGAAACAAAG[T/A]GAGCAAAAAGATTTTAAATATATGTTTACTGTCGTAACTAATATTTATGCAAGTATTTTGTTGACCAATAATAGATACATACTGTAGAAATGCAGGGTTTCTCACAATTCTGTCATGTTGTCCCAACACAAATTAAGTTAACAAATGTAAGTGTATTGAACATAAAACAATAAAGTTGTCCAGTGCATATAGTTTATAGATCCATAATTGTATACTGTAATTCAATAATAGTAACATGTGACCCTGTCAAAATGTATATAATCGCCACAGAGTACCATCTGAATGGTTTCATGTTAAATATCATGCGAATGTGCGCATCTGGTGTGCAATACTTTGAGCGCACCGTGTTGCGGCGCCGAGAGTTTGACCTGCTTCACAGTTTTATCACAAGTCTGAAAGCAAGTCTAAAATGAATCTAATTTTGTGTTTTAGGAAGAGGGGAGTGTCTAGGAAAAGGCGTAGAAAACAGGCATGACTAGATTAGTTGAAGATCTTGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10764
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008139 Essential Splice Site 983 2101 24 51
Genomic Location (Zv9):
Chromosome 11 (position 31808013)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30685375
GRCz11 11 30932559
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTYTGTGTGTGGTTTCGCCTCTTTGCTTTATTCCTCTGCTTTGTGTTTC[A/G]GATGGTGGTGTTAGGCTTGATTTTGCACGAGGGCTCATATTTTCGTGAYC
Long Flanking Sequence:
GCCAAATATTATGCTATCACTACAAACCATCAATCAATTAAATTTATTTATTTATTTATGTATTTCCAAATTGACACATATAACTGGTTTTGTGGCACAGGGTCACATTTACGTTTATGTTCATTTTTCCAAATCAAATGATATTTTGAGGGAAATGTCTTAGACAAGTCACTTATTAGTTCAGACAAAAACATTTTTAAATAAATAATTATATAAATAAATAAATAAATAAATGCCAATAGTTTCAACTACTTAGCCTCAAATCTCAGGTTAAGTGGATGTCGTGTGATTTAATCTCAAATAGACTTTGCATTTTATAGAACACATTTGTAATCAATTTTTTTCCTGTTATCCAGGTTTTGCGTTATTTTGACTACGTCTTTACTGGAGTGTTCACCTTTGAGATGCTTATCAAGGTAAATCCTTGGTCAAATGACTTCCGTGATTGAGTTTCTGTGTGTGGTTTCGCCTCTTTGCTTTATTCCTCTGCTTTGTGTTTC[A/G]GATGGTGGTGTTAGGCTTGATTTTGCACGAGGGCTCATATTTTCGTGACCTGTGGAACTTTCTGGACTTTGTAGTGGTTAGTGGTGCCCTGGTAGCCTTTGCCTTCACGTAAGTGCCCTTTTACCCCCTGCGTCTCCTGCCGCACAGTGCCTGCCTGCTGCCCCTTATCTTCTCCTCTGCCACCCTGGAGCCTTGTCAATACTCTCTCTTCTGGTCTCTTTTTCTTCTCCTGTCAGCACTGTTTTGCTCTTTTCAGCTTTCTATCTCTGTTATTTATTTTTTTGTCACTTTGCTTTCTGTCTCACTCAATCAGTCACACAAATGAAGGCCTTTCTCTCTTTCCACACACTCAAGCGCACCCACTATCTGTCCAGACCAACCTGTCTGTCTCTCTTTTCTCTCTGGCCAATCAGATCCCCAGCTTTTAAATTGTTCACTCCTCTGTTTCTTTGTCATCCAACTGCTGCCATTAGCCTGTGTTTGTCTTTAGTCTCACATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35121
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
ENSDART00000008139 Nonsense 1131 2101 27 51
Genomic Location (Zv9):
Chromosome 11 (position 31822427)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30699789
GRCz11 11 30946973
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGAGGTCAAATCTCAGAAGAGGGAGTGGAAGAAGTACGATTTCCACTA[C/A]GACAATGTGCTTTGGGCCCTGCTTACTCTCTTTACTGTGTCCACCGGAGA
Long Flanking Sequence:
TTTTAAGAAATAATATGTCAAAATTAAGTTGTTTTTTTATTAAAACAAGCAAAATAATGTACCAGTTGGGTAAGAAAAATTATCTTAATTCAAAGTGAAAACAAAACCCTGCTGGCAGATTAACTTGCTTGTTTTAAGAAAAAACTCACTTTATTTTGTCATATTATTTTTGAAAACAAGATAATATTTTTGCGTGTCTAGAAAATGCTTTTTGATTTAAGAATTTTTAGATATTTGGACTAAAAACTATACCAAAACTCTAAGCAGGAAAAGCATTTTAGCAGCGTATATTGTTTATCTTTTTTTATTCTTTAATATAGAACAACAATAGTTGTTAAACCTTTATAATTATTATCCTCAGTGTGAACAGCCTTTATCCTCACCCGTTCTTAAGAAAATGTGTATGTGCATTTCTGATTCAGGGGCGAATATTTGGTGTACGAGCGCGATAACGAGGTCAAATCTCAGAAGAGGGAGTGGAAGAAGTACGATTTCCACTA[C/A]GACAATGTGCTTTGGGCCCTGCTTACTCTCTTTACTGTGTCCACCGGAGAGGGATGGCCAGAGTGAGTTAACATGCATTCACTTATCTCCTGTTATCTCTCCTTTTGTGTCATCGCCTCTTATTTGGTCCTTTCTTTCAGTGTGTTGAAGCACTCTGTGGACTCCACTTACGAGAATCGGGGCCCGAGCCCGGGATACAGGATGGAAATGTCCATCTTTTACGTGGTGTACTTCGTTGTCTTCCCCTTTTTCTTCGTAAACATATTTGTAGCTCTCATCATCATCACCTTCCAAGAGCAAGGAGACAAGATGATGGAGGACTACAGCCTCGAAAAAAATGAGGTACTTACTACTTTGTTCACATGAGTCATTTAAGGTCCTATTTAACACCGGCTAAAATGTAATTTGCTTGTAATGATAGCTTATGTACCAAAACAATGTGATATATTTACTACAAAGACTGTATTTTAGGATTACAGCGCAGCCCCAATAATTTATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9062
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
ENSDART00000008139 Nonsense 1246 2101 29 51
Genomic Location (Zv9):
Chromosome 11 (position 31825675)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30703037
GRCz11 11 30950221
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAACCTCTAACGCGCCACATGCCTCAGAACAAGCAAAGCTTTCAGTAC[C/T]GAATGTGGCAGTTTGTGGTGTCGCCTCCGTTTGAGTACAGTATCATGTCT
Long Flanking Sequence:
TTGGATTAAAAAAAAACACATATATATGGTTGAGAGAGACAGTTATTGAATAAATAATACAAATTAAAAACACACAGTTTTATATAATAATGATTAAAATAAGCAGGATTTTATGATAACCACTATATAAATAAATATAAATGCATATTTAGCAACAATGAGGAAAAAACTAAACCATTCAAAAGCTAAGACTTTTCATATTTGTGTGGATTATACCTAGAAAATTCCTATGTATGTTTGTTTGATTATTTTGCCACATGCTAATATATGAAAAAGCTCTGAGCATTAGTCGCAAATTCAAGCATGATGTCTACTTTAGAGAGAAGGTTTCACTTTTCACTTCAATTTCCAGAGCAACAAACATGCAATGTGATACGTAAGATGCTTTTGTTCACTGTTTTCCCTTGTTCTGTTTCTTCTAGAGAGCCTGTATTGATTTTGCTATAAATGCCAAACCTCTAACGCGCCACATGCCTCAGAACAAGCAAAGCTTTCAGTAC[C/T]GAATGTGGCAGTTTGTGGTGTCGCCTCCGTTTGAGTACAGTATCATGTCTCTCATTGCGCTCAACACCATCATCCTTATGATGAAGGTACAAGATTTTTTCCACCCAACATTAGTAAACTGTAAATTAACTAACAGTTGGCTATAGTTTTTGATTCATGGGTTTTAAATTAGTTAATGCTTTTGAATAGCAATACTGGAACTTTATCTCTGCTCAGACTATTTTGATAGTTTCAAGCTCCAATTGTCTTTTACTGACAATTTTAATAGTTTGAAACAATAACTTGTCTGGGATATTTATTTCAATTCCAGTACTAAAATGAATGAAGTAGCTGTAATTTTTTGAATATGGCAGTTGGTGAGAATATTTTTTTAGTTTTTTTAGTTGTTGATGTATTCTTTTCCACCAAATATTGATTTCTTAACTTTTTTAAGTTACGACAGTGATATTTGTCGTCTAAAATACATAAACATGTCTGAAAACTGAAAACATGGCACTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41872
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
ENSDART00000008139 Nonsense 1282 2101 30 51
Genomic Location (Zv9):
Chromosome 11 (position 31826477)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30703839
GRCz11 11 30951023
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATTTTTTTAACTGTGTGTTTTCAGTATAATGGGGCTTCCGATGCATA[T/A]GACAAAGTCCTGAAGAACCTGAATATAGTGTTCACCACATTCTTCTTCAT
Long Flanking Sequence:
CAATTCCAGTACTAAAATGAATGAAGTAGCTGTAATTTTTTGAATATGGCAGTTGGTGAGAATATTTTTTTAGTTTTTTTAGTTGTTGATGTATTCTTTTCCACCAAATATTGATTTCTTAACTTTTTTAAGTTACGACAGTGATATTTGTCGTCTAAAATACATAAACATGTCTGAAAACTGAAAACATGGCACTTTTTTATATTTTATAAAATAAATGCTCTGAAATAAAACATTTTAAATTTTGAATATGGAAAAAAACGTTCTCTGTTGTTAATTAAACAAAACAAAAATGTGATTTACTCTAGCATAAAAAGCTGCTCAGATCAGAGCATAACACAACTAGAAAATTCGTAATACAATTTAAATGTTTAAATAAACAAAAAGTCACCCATGAATCACAAGATACAGTCATACAGATATTTTTTGCACTAAAGCTTTTGTCATGTTCTTATTTTTTTAACTGTGTGTTTTCAGTATAATGGGGCTTCCGATGCATA[T/A]GACAAAGTCCTGAAGAACCTGAATATAGTGTTCACCACATTCTTCTTCATGGAGAGTATTCTGAAAATCATTGCCTTTGGTGTCAGAGTAAGTGTCATACAATTTTTTTTTTTTTTAACACTGTCTTTATCCGTTTTTAGGAACTTGTACTAAAGAAAAGAAAAACAAAACATACAAAATTATTTAAATTAAATACATTTAAAATAAAATAATTATAATTACAGGTATATAAATAAATAAATAAATAAATGCATGTACATCCACATAAAAATAAAGGTGTCAAAAAAGTCTATTATTAGCAGGTGATACAAGATACAAGTTATTTGGACAAAAGATTTGTATCAGCTTCGTATCAATTCCATATTTAGAAAAGATTTCCATTCTCACAATGAGTTTCTGAGTTTTCTTAGCCTTTCAACCGAGTTCGTTCTTCCAATGTAATCTGGCAGCATGTTCAGTGCTGCGAATACATTTTAAAAGCCGATCTTGCTTATTTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41873
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
ENSDART00000008139 Nonsense 1897 2101 47 51
Genomic Location (Zv9):
Chromosome 11 (position 31897105)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 30774467
GRCz11 11 31021651
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACACAGTCGGGTGACCTCCCACCTAAAGAAAGGGAACGAGAACGGGGT[C/T]GAGCAAAAGACCGTCGCCACCACCACCACCATCATCACCACCACGGCTCG
Long Flanking Sequence:
GCAATATACAGAGCTGATGCGGTACCAGCCGTGTTCAATCATAAGCATGTGATCCTCTCTAAATTAATTTATAAATAAACCGCACTTATATGTCGTTTCTGACTTTATAATGCAAAATTGCAAGAGAAAATAATTCGATTTCTAAGAACTGCATCATTTCTGTGTTCCAAATTACAAATGCAGCCTGAATTGCTAGTAAGCCTATCAACTTGCGGTTTTTGTCTATTCTATATACGCTTGCAGTTTTCCAGCAATTCTTATGTTTTTCACACAAATCTGAGCACAATTGAGAATATTAGAGCTGTATTGGTTATACTGCTATTCAGAGTTTCATCTCACAATTCTGTGTTTATAATATTTGAGGTTTTCTCTTTTCAGTTTATATCTCATAACTTGCTGTGATAACTCATAACTTGGTCTTGTTAGGTCTGGGTACAGATCTTAGCACCACTACACAGTCGGGTGACCTCCCACCTAAAGAAAGGGAACGAGAACGGGGT[C/T]GAGCAAAAGACCGTCGCCACCACCACCACCATCATCACCACCACGGCTCGGTGGATAAAGATCGGTACAGTCACGAGCGCGACTACCATCGTCATCCTCAAGACAGATCAGATCGCCAATGGTCCCGCTCTCCGAGTGAGGGCAGAGGGCACAGACAGGTGGGACACACACTCACTGAAGTACACACAAATTAAACATTCATCTTTAGATTAAACACACACTACTGCTTAAAAGGGGTCATGTTAAATCTTTTTCTTTCAATAATCTTCGCTAAACCAAAAACACCTAAACCCAAAAGTTTTTTTGCTGCAGATCCTACTTGAAGTTGTTATGAATACATTTTTTTCTCAGATATAAAATAAATAACAGCACATATGAGTTCCAGGTTTGCTCTCAGATCTACTGTAGTAGTAGCCTGCTCTCTTTGCACATTTTAAGCCCAATCCTAAATCTATTTTATACCCCCTACCCCTCCGCCTACCCTCACCCCTTCGCCTTTC
Associated Phenotype:
Not determined