ZMP
lama5
Ensembl ID:
ZFIN ID:
Description:
laminin subunit alpha-5 [Source:RefSeq peptide;Acc:NP_001034260]
Human Orthologue:
LAMA5
Human Description:
laminin, alpha 5 [Source:HGNC Symbol;Acc:6485]
Mouse Orthologue:
Lama5
Mouse Description:
laminin, alpha 5 Gene [Source:MGI Symbol;Acc:MGI:105382]
Alleles
There are 21 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24260 | Essential Splice Site | Available for shipment | Available now |
sa9662 | Nonsense | Available for shipment | Available now |
sa25193 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18267 | Essential Splice Site | Available for shipment | Available now |
sa9446 | Nonsense | Available for shipment | Available now |
sa43919 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16193 | Essential Splice Site | Available for shipment | Available now |
sa16078 | Essential Splice Site | Available for shipment | Available now |
sa37625 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18231 | Essential Splice Site | Available for shipment | Available now |
sa43918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43917 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24259 | Nonsense | Available for shipment | Available now |
sa29878 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6725 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16872 | Nonsense | Available for shipment | Available now |
sa13881 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24260
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 311 | 3664 | 6 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9813078)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9771219 |
GRCz11 | 23 | 9706189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCCACGCTGAGGCCTGTAATGCTCAAGACCCCAATGATCCCTACAAG[T/C]AAGTGACCTTTAAGAATGTTTCATTTATTTATGTGTTTTTAAATGTCAGG
Long Flanking Sequence:
CATTCACCCGATCTCTAAGTCTGGCAGGAACACCTTTAGCTTAGCTTAGCATAAATCATTGAATCAGATTAGACCATTAGCATCTCATTCAAAATGACAAAATAGTTTTGATAATTTTACTATTTAAAGCTTGACTTATCTGTAGTTACATTGTGTCTAAGTGTAAGAGTCAAGCTTTAAATAGTAAAATAATTTTTTTGAGGGGGATGTTAATGGTCTAATCTGCTTCAATGATTTATGCTAAGATAAAAGTGCTCCTGCCAGGCCCCGAAAATCAACTGAATGGATTCTGAAATGCTAAAATTCAACTAGGGAATTGTAAAATGAGCCTAATACTCTCAAAAAAGTGGAGTGTTTCTTTAAACCTAAATTCTAAAACATCTTGTGCATTTGTTCCTCAGTATTACTACAGTATTAAAGACATCAGTATCGGAGGGAGATGTGTGTGTAATGGCCACGCTGAGGCCTGTAATGCTCAAGACCCCAATGATCCCTACAAG[T/C]AAGTGACCTTTAAGAATGTTTCATTTATTTATGTGTTTTTAAATGTCAGGCTCAAACTTCAGGTCAAATGGATAAGCATTTCAACGCATGTGAATATGCCACAACCTTGGAAAACCTTTTTTAAATGCACTATTCTGTTGACATAGAGATAAGACTTCATTCAAGAGTTCATAGTTAGATGATGATTGATAATAAAGCTGTTTTGCATGCTGTTCCAGAAGAGAACCCTGAGATTATAAGATCCTTGAGCCCTGGGCTCTCTTCCATTATCAGGGTGAGAGGGGAGGTTGAGTTCAGGTAGATCTTTATGAACAACCCTGACTTGTTTACGAATAATGGCAGATTGTAGGGTTAGCTACAGTATGCTGCTTACTGAGGGCTCGTCTATAGTGCCAAATTGCTTATATTGCGTGTTTTTGGATTGTGGGAGGAAACCGGGAAACCCACACAAGCATGGGGAGAACATGCAAACTCCGCACAGATATGTCGACTGGTCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9662
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 388 | 3664 | 8 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9790070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9748211 |
GRCz11 | 23 | 9683181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCTGGACATGCAGGGAGAATACAATGGCGGTGGAGTGTGTGTCGAGTG[C/A]CAGGTGGGCTCAGGTGTACAAACATACAATTATKAAGCAATTGKAGTAAT
Long Flanking Sequence:
TTTTGTTGTAACAGAAACAACTGTTAGTAATATTTTGGTCTCTGGTAGGTCTTGTAAGATTAAATACAAATTATAAAAGTACGATTAAAAAGTTTAAAGACATTTTCTCATCTCTAACTTCCCTCCAAGCTAATCACTGTTCTCTTTCTTCTTCCCTTCTCTGCTGTCATTCACATTTGGACAGTCTGAACTCTTCAGGGGTTCTGACTGAAGTGTGTATGTCTTTTATTTCCTCCGCTTGGGTATTTTGTCTCTGTGCTGCCAGAAGAGTTATTAACCTCAGCATGATTTATTTTTTTAAGCTGATTATATGGTGTTCTCACTCCCTCTCTCTCTCTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTGCAGCATGTAACTGCCACAGACACTCTTCAGAGTGCTACTACGACCCAGAGATCGATCAACGCAGATCCAGTCTGGACATGCAGGGAGAATACAATGGCGGTGGAGTGTGTGTCGAGTG[C/A]CAGGTGGGCTCAGGTGTACAAACATACAATTATGAAGCAATTGTAGTAATAAAGGCATTGGTTGTGGTTTACAACTTGCCAAGGCATCATTTCGGGCCAACAAACAGACTTCGTACAGGTGCTGGAAATTCTTGAAAATGTTTTCATTTTTAATTGAGTGTTTCTGAGGTTTGAAAAGTGCCTGAAATTGCTTGAAAATGAAGTTATGTTGCTTTCTCAATTTTTCTTTGAGTTATGATTTATGTTCTTCTGTACGATAAAGTGCAGAAAATGTTTGGTTTATGTGTTCATTTGCTTTCGCTCTTATACGAGAGATTATTTGTGTTGAACACTCTGGGCTCTCTTTTAAATATCTAGGCGCAAAGTCTGAAGCGCAGGGTGCAAAAGCATTAAGGGCGTATCCGAATCCACTTTTGCTGTTTTAAGGACGGAAAAATCCGCTTTGCGCCACTGTGCATGACCTAACAGGGTTGAGCTTATTCTCTTAATAACTTCTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25193
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 664 | 3664 | 16 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9775068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9733209 |
GRCz11 | 23 | 9668179 |
KASP Assay ID:
554-7863.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAGACCTTCTTGAGCAACAGGGGATTAAGTTCAAACCTGTCTGTTTC[A/C]GCATGTGATTGCTCAGTGGAGGGCTCTCGCTCCAGCTCCTGTGATCCAGT
Long Flanking Sequence:
TACCTTTAGGATTCCTGTATATATCCTGTATTTGGTCCCCTTACAACAACCTTATCACTAAACCCAATCCTCAAAAGAAAAATAGGTTTGATTGATCAATTTCCTTAAAAAATGTCTCCACAATATCAAAATGTACTTTTACTGCTCTATGTGTGGAACATTCGGTCACCACAACTTGAGGAATACAATACAGTAATGTATTACACATTTTAATGAATACACATGTATTCTGATCACCGTCTGTATTATATAGACTGTAACATTTTTTATTTCCTATTATTTCCCAGTGTGCACTTGTGACCCCCGCACATCTTTGGACTCCAGCTGTAGTGAGTTGGATCAGTGTAACTGCAGACCAAACTACAGCGGCCCCAGATGTCAGCAGTGCGCACCAGGATACTACTCTTATCCCAGCTGCACACGTAAGTCTATGACTATTATCAGCACTTGGGAAAGACCTTCTTGAGCAACAGGGGATTAAGTTCAAACCTGTCTGTTTC[A/C]GCATGTGATTGCTCAGTGGAGGGCTCTCGCTCCAGCTCCTGTGATCCAGTGTCAGGACAGTGTGTGTGTCTGCCGAACATCGAGGGTCAGAGGTGTGACAGCTGCAGTCCTGGGTCATATGGCTTCCCCCTTTGCCAACGTGAGAGAGACAATCAAATATAATCATGTTTATTAAATTAACATACTTTTGTTCTGATGTTTTTATTGTGTTTCTGTACTTTAGTGGGGACTTGTAACCCAGCAGGTTCTGTTCATAATGACATTCTACCCACTGTGGTAAGTGTTTGTTTCCAATTACTGTACACCTTTTCTATTGTTATTTCTTTCTTAACGCTGTACTTGAGGATCTTGTTGTCTTTTTCAAATATCATTCTTGGTCCAGGCTCTCAGATTTTGTTGTTTTTGCTTTCTCAGGGCTCTTGTGTGTGTCGGCCGTATGTGGAGGGAGTGGCGTGTGAACGCTGTAAACCTCTCTACTGGAATCTGTCTCCTGATACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18267
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 1904 | 3664 | 44 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9727666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9685807 |
GRCz11 | 23 | 9620777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGCCTCTGTCATAGAGTAAAAGATGTTNNNTGTTTGGTCTTGTTYAC[A/C]GTTTTGCTATTCGCWGTGTGGAGAAGCCCAATAATATGCGGTGCCTGTGY
Long Flanking Sequence:
CATCTCAAACATTCTTTTTCTTCTGATGATCTGTGTGGAATTGAAATTTAGTCAGACTTTTGTTTTCTTTCTGATTTATTAGGCTTTTACCCCCTGTAAGAGCCATAATTTGATTGAATATAATAGTGCTCAAATTCATATACAGTTTATATATGTTCATATGTTCAGTTGTGTACATTCGCTATTTCACCCCTACTCTTTTGTTTGTAATGGTTTGCTCCGCTTTTATTGGACTGATTCAAGTTATATTACGAAACTGGAAAGTGAAAGAAAAAGACAGAGCAGCACATTTTTATTTTTTTTTAACCGGAGCTAATAGTTATGACGCTTAAGAATTCAGTAAACATCTTTAATTGTAAAGAAACCAAAGTCAATTTATTGGCTGACTGATTTTTTGAAATTCTGATAATACTCCCTTAAAATAAATTCATTTCAGTGCTGGATATCTCAACATGCCTCTGTCATAGAGTAAAAGATGTTATTTGTTTGGTCTTGTTCAC[A/C]GTTTTGCTATTCGCTGTGTGGAGAAGCCCAATAATATGCGGTGCCTGTGCATGCCTGGCTATGCTGGATCTAAGTGTGAAAGGTACACATGTGAAACATTCATTCGATCATTCATTTTCTTGTCAGATTAGTCCCTTTATTAATCCAGGGTCACCACAGCGGAATAAACCACCAAGTTATCCAGCATGTTTTTACGCAGCGGATGCCCTTCCAGCCACAACCCATCTCTGGGAAACATCCACACACACTCACTCATCCACTACAGACAATTTAGCCTACCCAATTCACCTGTACTGCATGTCTTTGGACTGTGGGGGAGCACCCGGAGGAAACCCACATGAACGCAGGGAGAACAAATATTTTTATTATATTTATATATATATATATATATATATATATATATATATATATAAACAATGCCAATAAAGAAAACATTAATTTCCAAGTTGGATTCTAAGTGGACTGCAAAAAACGAAATACAGGCATTGCAAATATGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9446
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 2164 | 3664 | 49 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9721582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9679723 |
GRCz11 | 23 | 9614693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGTGTGATGGTGCTGCTGGAAGATYTGGACAGGATCMGTCATTTTTA[T/A]GAGTCCGTTGCCAATCAGCTGACCAGCCTCAATGCCAGCACCTTCGCCTG
Long Flanking Sequence:
ACTCACTCACATATGTTTAATCACTATCTCACCAACTCTCTAACTCACCCTCTCACTCACTAACTCACTCACTCACTCACTAACTCATCCATTCAGTCACTCATTCATTCGTACTCTTACTCACCCATTCATTCACTCACTCACGTTCATTAACTCACCCACTCACTCACTTACTCACTCATTCACTAACTAACCCATTCACTCGCTCAGTCATTCAATCACTCACTTACTTATGCGCTTACTCATTCACTCACTGGCCAACTCACTCATTCATTAACTCACCTATTCATTCAGTCATTCACACACTCACTCTTTCATTCACTCCCTAACTCATGCATTCAGTTACTTATTCACTCATTTGCTAACTCCCCGATTCAATCACTAACTCACAGACATCAGCATTCACACATCAGATGGTGATTGCGGTGCATTATGTTTTCAGCCTGTGACAGCTGTGTGATGGTGCTGCTGGAAGATCTGGACAGGATCAGTCATTTTTA[T/A]GAGTCCGTTGCCAATCAGCTGACCAGCCTCAATGCCAGCACCTTCGCCTGGACTCAACTAAACCGCCTTAATGCCTCCATTGCGGACATTGCTGTGAGTCTCTTTCTAACATAAACACTATCAGACTTTTGCCGTTAACTTTCAGTCATGTGCATTAATATATATAGTTGAAGTCAGAATTACTATCCCCCCTTTTAAATTTTCTTTCTTTTTTGAATATTTCCCAAATTATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTCTTTTGGAGAAAGTCTTATTTTGTTGTTTTATTTCGGCTGGAATAAAAGCAGTTCTTAATTTTTTATTAATCATTTTATGGTCAAAATGATTAGCCTCTTTAAGATTATCTTTTCGACTGTCTTTCAGAACAAACCAGCAGTACACAGTAACTTGCCTAACTACCCTATCCTGCCTAGCTAACCTAATTAACCTAATTAAGCCTTTAAATGTCACTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43919
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 2195 | 3664 | 49 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9721487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9679628 |
GRCz11 | 23 | 9614598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTGGACTCAACTAAACCGCCTTAATGCCTCCATTGCGGACATTGCTG[T/C]GAGTCTCTTTCTAACATAAACACTATCAGACTTTTGCCGTTAACTTTCAG
Long Flanking Sequence:
GTCACTCATTCATTCGTACTCTTACTCACCCATTCATTCACTCACTCACGTTCATTAACTCACCCACTCACTCACTTACTCACTCATTCACTAACTAACCCATTCACTCGCTCAGTCATTCAATCACTCACTTACTTATGCGCTTACTCATTCACTCACTGGCCAACTCACTCATTCATTAACTCACCTATTCATTCAGTCATTCACACACTCACTCTTTCATTCACTCCCTAACTCATGCATTCAGTTACTTATTCACTCATTTGCTAACTCCCCGATTCAATCACTAACTCACAGACATCAGCATTCACACATCAGATGGTGATTGCGGTGCATTATGTTTTCAGCCTGTGACAGCTGTGTGATGGTGCTGCTGGAAGATCTGGACAGGATCAGTCATTTTTATGAGTCCGTTGCCAATCAGCTGACCAGCCTCAATGCCAGCACCTTCGCCTGGACTCAACTAAACCGCCTTAATGCCTCCATTGCGGACATTGCTG[T/C]GAGTCTCTTTCTAACATAAACACTATCAGACTTTTGCCGTTAACTTTCAGTCATGTGCATTAATATATATAGTTGAAGTCAGAATTACTATCCCCCCTTTTAAATTTTCTTTCTTTTTTGAATATTTCCCAAATTATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTCTTTTGGAGAAAGTCTTATTTTGTTGTTTTATTTCGGCTGGAATAAAAGCAGTTCTTAATTTTTTATTAATCATTTTATGGTCAAAATGATTAGCCTCTTTAAGATTATCTTTTCGACTGTCTTTCAGAACAAACCAGCAGTACACAGTAACTTGCCTAACTACCCTATCCTGCCTAGCTAACCTAATTAACCTAATTAAGCCTTTAAATGTCACTTTAAGCTGTAAAGAAGTGTCTCCAAAAATATCTAGTAAAATAATATGTACTGTCTTCATGGCAAAGATAAAATAAATCAGTTATTAGAAATTAATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16193
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 2270 | 3664 | 52 | 80 |
ENSDART00000045126 | Essential Splice Site | 2270 | 3664 | 52 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9720373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9678514 |
GRCz11 | 23 | 9613484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGAAATRYCACAGACAAAGTCAAGTGATGGCATTTGTGCATCTGCTC[A/T]GACATYATACAGCAGGTGAAYCGGACAGCRCAGAATGAGACGCAGGTGAT
Long Flanking Sequence:
CTCTAATTTCATGTCTCAGAATGCGATAACAAACTACAACAGCACTCTGGACAAGAGCAGGAATCGGGCCAGTGTGTTGGAGGGAGAGCTGGAAATCATCGACTCAGATATTAAAGATTTAGAAAAGAAGGTACGAGAACATATCAGATGATCATATTCTGGTTAAAAATATCAGTTTATAGTTTTTTCTAAAATACTTACTTATTTTGACCACACCAACTATATCTATATTATTAACAAATTACTATTTAATAAATTACTATATTAATAATTATTTGTATTGCATGTCTTTATTAGGCCTCAGTCACACAAAAGAAAAAAGATGCTTTAGAGGACAACATTAACTCGACACACACTAGAGCACAAGAGCTGTTTGGATTCATCAAAGGCATCATGAGAGATGTGAAGGGTGGGAATTTGACAGTACAGTTGTACTACTACTCTTACTGTATTTGAAATGTCACAGACAAAGTCAAGTGATGGCATTTGTGCATCTGCTC[A/T]GACATTATACAGCAGGTGAACCGGACAGCGCAGAATGAGACGCAGGTGATGGATGAGAAGGACCTGGCCAGAAAGATAGCAGAAGTGGAGTCCATGCTCAGAGACATGCGCTTCAGGGGCTTTGACTACCAGAAGAACAAAGCAAAAAATGAGCTGGACCAGGCCAATAACTGTAAGTGACCAGAACACATCTACTAGAAATGTAACGGCAGAGAACAATCATGAATTTAAAAGCGACATATTATTCACAATTGTGTGTCAAATGGTGAAAATTAGTTAAGTGCTATTTAAAATCACACTTGATAAAAAACAAAGTCTGCAGAAACACTTTGATTGACATTCTCCCTTTTATACATGTCATCAGGGGAAAGCTCCGCCCATTAGTCACGCCCATCTCTATCTGATTAGCATAAACCACCTTGAATGAGAAGCAGCCATCAGCCATTAGTGTTTGCATTCTGCCACTATGCTGACACATAGGCACTTGCAGCTCCACCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16078
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 2270 | 3664 | 52 | 80 |
ENSDART00000045126 | Essential Splice Site | 2270 | 3664 | 52 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9720373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9678514 |
GRCz11 | 23 | 9613484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGAAATRYCACAGACAAAGTCAAGTGATGGCATTTGTGCATCTGCTC[A/T]GACATYATACAGCAGGTGAAYCGGACAGCRCAGAATGAGACGCAGGTGAT
Long Flanking Sequence:
CTCTAATTTCATGTCTCAGAATGCGATAACAAACTACAACAGCACTCTGGACAAGAGCAGGAATCGGGCCAGTGTGTTGGAGGGAGAGCTGGAAATCATCGACTCAGATATTAAAGATTTAGAAAAGAAGGTACGAGAACATATCAGATGATCATATTCTGGTTAAAAATATCAGTTTATAGTTTTTTCTAAAATACTTACTTATTTTGACCACACCAACTATATCTATATTATTAACAAATTACTATTTAATAAATTACTATATTAATAATTATTTGTATTGCATGTCTTTATTAGGCCTCAGTCACACAAAAGAAAAAAGATGCTTTAGAGGACAACATTAACTCGACACACACTAGAGCACAAGAGCTGTTTGGATTCATCAAAGGCATCATGAGAGATGTGAAGGGTGGGAATTTGACAGTACAGTTGTACTACTACTCTTACTGTATTTGAAATGTCACAGACAAAGTCAAGTGATGGCATTTGTGCATCTGCTC[A/T]GACATTATACAGCAGGTGAACCGGACAGCGCAGAATGAGACGCAGGTGATGGATGAGAAGGACCTGGCCAGAAAGATAGCAGAAGTGGAGTCCATGCTCAGAGACATGCGCTTCAGGGGCTTTGACTACCAGAAGAACAAAGCAAAAAATGAGCTGGACCAGGCCAATAACTGTAAGTGACCAGAACACATCTACTAGAAATGTAACGGCAGAGAACAATCATGAATTTAAAAGCGACATATTATTCACAATTGTGTGTCAAATGGTGAAAATTAGTTAAGTGCTATTTAAAATCACACTTGATAAAAAACAAAGTCTGCAGAAACACTTTGATTGACATTCTCCCTTTTATACATGTCATCAGGGGAAAGCTCCGCCCATTAGTCACGCCCATCTCTATCTGATTAGCATAAACCACCTTGAATGAGAAGCAGCCATCAGCCATTAGTGTTTGCATTCTGCCACTATGCTGACACATAGGCACTTGCAGCTCCACCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37625
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 2433 | 3664 | 55 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9714961)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9673102 |
GRCz11 | 23 | 9608072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGAGCTCACACTCAGACTCGTGCATGCTCTCGTCTCTGTCAGGATTA[T/A]GAGCATCTGGCCGCTCAGCTGGACGGAGCGAGACAGCCCCTAGCTGAAAA
Long Flanking Sequence:
CAGTTGAAGGATGTTGTGTTTAAATCAATTATTTATCTGACTACATTGTAATTAATCTGACTCCATTAAAGTTGTTATCGTCACTGTTAGTCACTCTTGACAAAAGCGTCTGCTCTATGACTAAATGTAAATATAATGTAAAGTTGTGAATATTTCATTTTATTTCAGTTAGCGAAAAGGTTTTTGGACCAACATATATATATTTTGTTTGTTTACTTGATTGAACTAGAATCATAGCAAGAAATACAAAATTGCATTCTTGTGTTTTTCTAGAAAAAGGTTAATAGTCTACATGAGAAATACAAAGAGGTGGTGTCCCAGCTGCAGATGGCGGAGGATGATGTGACTCAAGTCAACGACCTGCTCTCCATGCTCCAGGACTCCAAAGAGGTACACGCTGACATGCATGCAGAATCAAAAATAACATGCTTGTGTGCTATAAATGAACTCCACTGAGCTCACACTCAGACTCGTGCATGCTCTCGTCTCTGTCAGGATTA[T/A]GAGCATCTGGCCGCTCAGCTGGACGGAGCGAGACAGCCCCTAGCTGAAAAGGTGCAGAAGTACGCCCCTGCTGCTAATAAAATACCCCTGGTGGAGGCTGCAGAGAAACACGCAGAAATGCTGGAGCAGCTCGCCAACAATCTGTCCAGGTGTGTGTCATACCTGTCAACCCTCCCGTTTTTTCCGGGATTCTCCTGTATTTCACAGTTCTATCCCGTTATCATCCCGTAAAGGTATTTTTTCATGTTTCTCCCGTATTTTTAGTCTTTCTCTGAAGGGTGGCAAACAAACATTATAGAGCTGAGCCTTTGTATACGCAACCCATACCGCCGAACCTCCAGGGGCCGCCGCTTGCTCTTAAATGCGAGTCTGTTCTGTGCTTTCGCTTTGTTTAGGCATGAAAACACTGAAATAAACATAAAAATGGATTCCCTTCCTTTTCATTACAGGTGCCGTCTCCCTTTCGTATGCAATCCTCAAACAGTCATATTGCAGTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18231
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 2563 | 3664 | 57 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9711304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9669445 |
GRCz11 | 23 | 9604415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCACTGAGCTTTTGAAGTCAGCGGAAGAAYTCAACAACAGCAGTCAGA[G/A]TAAGAAGAGCCAACWCTGGATCTGACTGCCTTATTTTGAATGCTATCATG
Long Flanking Sequence:
CATTTACAAGAAAAGAGGTCTGGTGGATTTAGAGGTTTTTGCATCTGAACTCTTAATTTGTCAAAATACCTCACTATATATTGTTTCTATACTTTCTCTATATATTACCCACATATTACCCTCCTCTGATATGATGACTACTTTTAATATGCCTTTGTGTTTGTCGGACAGTCTGATATCTGGCTCCAACCAGGACAATTTTATACAGCGTGCTCTGAACGCGTCCCGCGCATACACTAACATTATCAACAGTGTGCTGGAAGCTGAGACTACAGCTCTGAAAGCCAATGAAACCGCTTCTATGGCCCTTGAGGTACAGTCAAACACATAAAAATCAGTCATTTTAACATGCTTATTAATGCACATTTATTAATACATGTCTATGTTTTTTCTTCATTAGAACATACGGGACAAAGACCTGCCAGCACAAGCGGCTGCGCTGAAGAATCAGAGCACTGAGCTTTTGAAGTCAGCGGAAGAACTCAACAACAGCAGTCAGA[G/A]TAAGAAGAGCCAACTCTGGATCTGACTGCCTTATTTTGAATGCTATCATGCAAAAAATGCTATTTTTATGGCTATTTTTTTTCTAAAGAGACTTTAAATATAATATTTAAAAAAATGTGAATCCATCCAAAATTGTACAATTGTTGTCAAAAGTAAACCTTAAACTGTGTTAGGTTTTTATCTTATATAGTATTATTTATGTATTTTGTCTTATGCGTTATTTATTCATTATGTTAATGTATTTTTATTGTTATCGTTTTTGTATTATTATATAAAAAATACATGTATAAAATGTTGTAAATTTGATCTGGGTTTGCCATGAAATAGCCTTGAAACTGTTATGGCAATAAATTAAAAACTGTCTTTCTGCTTTTCTTAACCTCCTTCTAATGTTGGCCACTATTATATCTTTGCCAGGTCTAAAGCCACGTGTGGACACCATAAAGATGAGTTTACTTGATGCTGAAAAGAAGAAAGAAAAGATGCTTCAAGACCTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43918
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 2700 | 3664 | 60 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9708899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9667040 |
GRCz11 | 23 | 9602010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCACGTTTCAGCCGTCCAACATCTCCGACAGCATCCAGAGGATTCGT[C/T]AACTCATTGAGCAAGCACGCAATGCTGCCAACAAGGTGCCAACTAAGCGT
Long Flanking Sequence:
TTTTTTTTTGTAATTACTTTTTTACTAGCTGCCAGAAGAATAAAAAACAGTTTCTTGTCTTTATTAATCTATCTAAATTATGTTACCTAAATGTAAAGATTCTAAACATTATCTGTTTACTTTGATACAGACGACATAGTGAACAGCATCTCAGCAGCTAAGAGTGCGGTGGAGCAGGCTAACAACACGGTGGCTAACGTTAGCGGTGTGCTGGCTCCAATTCAGAAGCAGCTGGAGGAATGGCAGAAGCAGTACGGAGACTCCAACGCCACTAGTGAGGATATCAACAAAGCCCTCAATGACGCCAACACATCAGGTGCGTGCAGTGAGCCCTTACGCATGAACATGCTTGATCTTGTTTTCACACTGATTCCAATGTGTTTGTGTTGGCAGTGGCTGCACTGAGCGACACTCTTCCTAAGCTGATAAAGAAGTTGGATCGCCTGCACAACACCACGTTTCAGCCGTCCAACATCTCCGACAGCATCCAGAGGATTCGT[C/T]AACTCATTGAGCAAGCACGCAATGCTGCCAACAAGGTGCCAACTAAGCGTTTTCCCGTCTAATCTGTTATAGAGTTAGTTCACGATAAAATGAGCATTCTGTTATTATTGTTTATCTTCAAATCACAAATGAAGATATTTTAGATTAAATTTGAGAGCTCCCTCATCCTCCATATACAGCAGTGGTTCCAAGATGTTCAAAGTCCAGAAAAGGAACAAAAACATTGTCAAAACATGATCTGACATGTAAGATATAGGTGAACAAAACCAATCTTTCAGATTTTTTTCCCACACAAAAAGTGTTTTTTGAATTACCTAATAACAGATTTTTATTTTATTTTTGAGTGACCTAATCCTCTACGATACTCAAGTTGTTTTCTGAATTGTTTTGCAATTCATCATAAAGGAATGGACTATGTCAGCCACAATATTCACATGGCATTTAAAGGGTGCTCATTTGCTACAGTGTGTCGGCGGGGTCTTAAAAAGTATTGATAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43917
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 2905 | 3664 | 64 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9699890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9658031 |
GRCz11 | 23 | 9593001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCTGCTCAGTATAAATGAAGAGCTAATCAGCCTCTATAACTTTGAG[C/T]AAACTTTCGACATGAACACCACAACTGATGCACCATGTTCACGGTCAGAG
Long Flanking Sequence:
TCAAGCAAAATTTTGAGCAAAAACCCTACAGACTACAAACTGTAAACTAAATTTAGATATTTTTGTTTTTCTTGATTTTACCTATTTTTCTTCACATTTCTATTTCATTTTTTGGAAAAACATGTACATTTGGATGTACTACATTTGGTTTCAATACTGACTAATCTTATGTTTATGCAAAAATTTAGTATTGTACAGCGTCTTATAGAAAATCTAAATTAAAAAAAATAGATCTGTGAGGTGTGTACTCATATATGCTGTGCATTGTATGTATCTCTGTATATGTCATATTTTTAAATAGAGAATAGAACATTTTTGTCTCTTTCTAGAATTATCTTTTTAAAAAACATCCCTCAATCTCAATCTTTCTTCTCTCTCTTTCTCTCAAACACACACAGCCTCCAGGGACTCTGAACCTGTCGTCGCCTTTAGACTTCTTCAAGGGCTACGTGGAGCTGCTCAGTATAAATGAAGAGCTAATCAGCCTCTATAACTTTGAG[C/T]AAACTTTCGACATGAACACCACAACTGATGCACCATGTTCACGGTCAGAGGGCTTTCATTTATTATAGATCACATAGCATTACCTGTGTTTAAACTTTTGTGTAACCTCATGTGTTAAAACAGGAAGAGGCCAGCAAACACGCCTGAATGGGTGGTTGACGGAGTGTATTTTGACGGTACTGGCTATGTTGAGGTTTTGTTCGAAACTCAGAAGGGCGACCGCACCTTTGACCAGACCATCAGACTCATCTCGCAAAACGGCATTCTGCTGTCCTTCCAGAGAGAGGTGAGATTCAGCTTTTTATTTGGAGGAAAGTTCTTACCCCAGGTGGAGGAGTTTAGGTATCTTGGGGTTTTGTTCACAAGTGAGGGAAGGATGGAACGTGGGATCGACAGGCGGATTGATGCAGCGGCAGCAGTAATGCGGTCGATGTACCGGTCTGTTGTGGTGAAGAAGGAGCTGAGCCAAAAGGCAAAGCTCTCGATTAACCGGTCAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24259
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 2975 | 3664 | 66 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9697861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9656002 |
GRCz11 | 23 | 9590972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACACGTTATCGTTTATTAATGTCATTTTTTTCTCTGTCTCTTAGGAT[A/T]AATACGTGACCATCGCTGTTCTTGATGGCTTTCTGAGGGTCTTTTATAAC
Long Flanking Sequence:
ATTTTTTTTTTACTGATATAGCAAGCCATTTTTGCATGTTCAGTTTCACGCTTAAGCATTATATTTTTTATCAATATGGCAAGGCATTTTTACATAAAGTCCAAGTCCATTTTTTGACTGTCAGAGACATCGAGGTTGATTTAAATCAGTAATATCAGCAAGAGGCTTTGATGTATCATAAAACACACACATATATATATAGCAATTTGTCTCACAGATACTATAAAAAATTATCTTATTAATATCCAAACAGGTTACCGAACAAAAAACAAGCATACACACTTTAATTTAATAATAATGATTCCTAAACATAATGACAAAAAAGATTAGTTGAAAAAACAAGACAGCTCAAAATCTTAATTTAATCATGAAGGCAACACGCCCTGTAAATAATACATCCAGGCTGCTAGAATTTTCCAGATTAAAATAGAGAATTTTTTGTGAAATGTAGATACACGTTATCGTTTATTAATGTCATTTTTTTCTCTGTCTCTTAGGAT[A/T]AATACGTGACCATCGCTGTTCTTGATGGCTTTCTGAGGGTCTTTTATAACGTTGAGGGAAGTTTGATGCCTGGACCAGGCAACCCAACAAAAATCAGCAATGCTGACAAAAAAACTGTAAGTGATACATACTATTTATTCAATATATTCTTGCCAGCATCAGCACCATCTTTTTAAGTTCAATTGATTTTATGGAATTATTCATTGTGTTTTTTTTTTTCAGTTGCAAGTCATCCTTCAACTTAACAACATGAAAATGCTTGTGAGGCTGGATCGTGAGACGTTATATACACTTTACAGCGAAGAACTCAATTTCACAGGAAGATACTTCTTAGGGGGAGTGCCAGAAGCTGAGATGCCTAATGAGTGAGCGTGCAGATATTTACATTCAATAGCGGCACTGTAAAAGGCGATTAGTTGACTTTACTTAAAAAAGAGAGTACACTTGTGGCCTTGTATTATATTATTAAATAAACAAACTGTGCATAGTTATAAAAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29878
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Essential Splice Site | 3014 | 3664 | 67 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9697640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9655781 |
GRCz11 | 23 | 9590751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAAGTTCAATTGATTTTATGGAATTATTCATTGTGTTTTTTTTTTTC[A/G]GTTGCAAGTCATCCTTCAACTTAACAACATGAAAATGCTTGTGAGGCTGG
Long Flanking Sequence:
TATAAAAAATTATCTTATTAATATCCAAACAGGTTACCGAACAAAAAACAAGCATACACACTTTAATTTAATAATAATGATTCCTAAACATAATGACAAAAAAGATTAGTTGAAAAAACAAGACAGCTCAAAATCTTAATTTAATCATGAAGGCAACACGCCCTGTAAATAATACATCCAGGCTGCTAGAATTTTCCAGATTAAAATAGAGAATTTTTTGTGAAATGTAGATACACGTTATCGTTTATTAATGTCATTTTTTTCTCTGTCTCTTAGGATAAATACGTGACCATCGCTGTTCTTGATGGCTTTCTGAGGGTCTTTTATAACGTTGAGGGAAGTTTGATGCCTGGACCAGGCAACCCAACAAAAATCAGCAATGCTGACAAAAAAACTGTAAGTGATACATACTATTTATTCAATATATTCTTGCCAGCATCAGCACCATCTTTTTAAGTTCAATTGATTTTATGGAATTATTCATTGTGTTTTTTTTTTTC[A/G]GTTGCAAGTCATCCTTCAACTTAACAACATGAAAATGCTTGTGAGGCTGGATCGTGAGACGTTATATACACTTTACAGCGAAGAACTCAATTTCACAGGAAGATACTTCTTAGGGGGAGTGCCAGAAGCTGAGATGCCTAATGAGTGAGCGTGCAGATATTTACATTCAATAGCGGCACTGTAAAAGGCGATTAGTTGACTTTACTTAAAAAAGAGAGTACACTTGTGGCCTTGTATTATATTATTAAATAAACAAACTGTGCATAGTTATAAAAGTTAAGTCAATGGGTTTTGTAATTCAGTTTTTATTTCCAAAATGAACATAACATTTTGCAATCAGACTGAAAAGTACCTTTAACAGCTACTACCTCATATATTTACCCCATCCCATCATATGCACATCAGGGATCACATGATAACTGTAGTTTAGACCAAGGATTAAAAGAAATTACATTAAGTTTGACATTCACAGTGTCAGATGAGGGTTAAGTGTCGCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6725
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 3019 | 3664 | 67 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9697623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9655764 |
GRCz11 | 23 | 9590734 |
KASP Assay ID:
554-4602.1 (used for ordering genotyping assays)
KASP Sequence:
TTTATGGAMTTATTCATTGTGTTTTTTTTTTTCAGTTGCAAGTCATCCTT[C/T]AACTTAAYAACATGAAAATGCTTGTGAGGCTGGATCGTGAGACGTTATAT
Long Flanking Sequence:
TTAATATCCAAACAGGTTACCGAACAAAAAACAAGCATACACACTTTAATTTAATAATAATGATTCCTAAACATAATGACAAAAAAGATTAGTTGAAAAAACAAGACAGCTCAAAATCTTAATTTAATCATGAAGGCAACACGCCCTGTAAATAATACATCCAGGCTGCTAGAATTTTCCAGATTAAAATAGAGAATTTTTTGTGAAATGTAGATACACGTTATCGTTTATTAATGTCATTTTTTTCTCTGTCTCTTAGGATAAATACGTGACCATCGCTGTTCTTGATGGCTTTCTGAGGGTCTTTTATAACGTTGAGGGAAGTTTGATGCCTGGACCAGGCAACCCAACAAAAATCAGCAATGCTGACAAAAAAACTGTAAGTGATACATACTATTTATTCAATATATTCTTGCCAGCATCAGCACCATCTTTTTAAGTTCAATTGATTTTATGGAATTATTCATTGTGTTTTTTTTTTTCAGTTGCAAGTCATCCTT[C/T]AACTTAACAACATGAAAATGCTTGTGAGGCTGGATCGTGAGACGTTATATACACTTTACAGCGAAGAACTCAATTTCACAGGAAGATACTTCTTAGGGGGAGTGCCAGAAGCTGAGATGCCTAATGAGTGAGCGTGCAGATATTTACATTCAATAGCGGCACTGTAAAAGGCGATTAGTTGACTTTACTTAAAAAAGAGAGTACACTTGTGGCCTTGTATTATATTATTAAATAAACAAACTGTGCATAGTTATAAAAGTTAAGTCAATGGGTTTTGTAATTCAGTTTTTATTTCCAAAATGAACATAACATTTTGCAATCAGACTGAAAAGTACCTTTAACAGCTACTACCTCATATATTTACCCCATCCCATCATATGCACATCAGGGATCACATGATAACTGTAGTTTAGACCAAGGATTAAAAGAAATTACATTAAGTTTGACATTCACAGTGTCAGATGAGGGTTAAGTGTCGCAGATTTCCTTGATTTCGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16872
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 3100 | 3664 | 68 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9694958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9653099 |
GRCz11 | 23 | 9588069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTTGTTCAGATAAAGACCATGAAGAGTTCAGGCATCAGCTTTGGCTG[T/A]CCAGATGACCTGCTGGTGAGAGATTACACTTTNATTCACTTGTGCTGATKC
Long Flanking Sequence:
CCACAGGTGCATCAATAAAGTATTGAGCAAAGATAATAATAAATTAATTAATAAATAAATTAATAAATTTGCAACAATTTCAAAAACTCTTTTTTTCACATTGTCATTATGGGGTATTGTGTGTAGAATTTAAAGGAAATAAAGGAAATTAATCCATTTTGGAATAAGGCTGTAACATTAAATACTTCCATATGCACTGTGTGTAAAAAGGTTTCTGGATAGATAAATCTATGATAATACTTACTTTTTAAAATTAAAATCACCTTGTTGCTTTTAATCCAATGAGTTTACTAACTTTTTTTAACTCATCGCTTTTTACAGTGTGTGTGCGTGTGCAGTTGTCAACAGGTTGTGTAATTAACCATCTGTTTGTGGCATTGCAGTTTGAAGAGCATCTATCTCAAGCATGGCTCCATCAGGGGCTGCTTCAGGATCATTAAGTCCATGGGGAGCTTTGTTCAGATAAAGACCATGAAGAGTTCAGGCATCAGCTTTGGCTG[T/A]CCAGATGACCTGCTGGTGAGAGATTACACTTTATTCACTTGTGCTGATGCTTCAGGAACATTCACATTCTTCTGGGATGAGGGGAACATACTAGTGTTTGCTTAGTTACAAGTGTCCTGTCATGACAAGATGAGATTACAGACACTAGTAATTTAGGTGTTCATAGCAAATGCTTTCTAACAGAAGCATTTAAATACCACAGACATTAAGAAGCACCGAATAGTGCACTGACTAAACTCCTAAACAAATGGACTGGTTTGTCATTCATTGTAAATAAAATGCTGGGTTCCACACCATTTCTTCATGTTGTCCCAACACAAATCGATCAAGTTAACCTAATACTTTTTTATACATTTAGGGGGATAGAATCTATAACAATTTAATTGTCCCAACAAAAACCTTAAAAATTCTGTCGTTTCAACTTTTAAATGAGTAGTTTGAACAAGCAGCGAGTAACTTCAATAAACATAACCAATGTATTTTAGAACAGATTTTAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13881
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045126 | Nonsense | 3200 | 3664 | 71 | 80 |
Genomic Location (Zv9):
Chromosome 23 (position 9690131)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9648272 |
GRCz11 | 23 | 9583242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCTKTGAGTTTCTAWACARTTTTGTCTTTGTTTAGGTTGAGCATTTA[T/A]ATAGAYGATGTGCTCGAGAGTTCTGGAGAAACTGGTAATGTAACCACKAG
Long Flanking Sequence:
TTAAACACACCTGAACCAGCTAATCAAGCTCTTGCTAGGTATACTAAAAAACATCCAGGGAGGTGTGTTGAAGGAAGTTGGAGCTAAACTATGCAAGACACCAGCCCTCCAGGACCGAATTTGGACACCCCTGTGCTAGGGTGTTCTGAGTCTTTGTTAGTAATTATATTATACATGGTTAATTGTATTCAAGTCATTAAATATATATTATATATTACTATAGTATACTATAATATACTATATTAATATAGTATATTAAATGTAGTGTTCTTTACTTGTGGATGTCTGATGACTAGCACACTTCCACTGAGCCAGCTGTGGTCATTTGGCAACAGAGCCGCGACGTCAACACACAGAATCTGTCGGCACAGTTCAGCACGGTTGTCTAGAACAGTTCGGCACGATAGTGGAAAAGCAGCTTTTGTCTTCAACTGTATACTATAATTGTGTTTGTCTTTGAGTTTCTAAACAGTTTTGTCTTTGTTTAGGTTGAGCATTTA[T/A]ATAGACGATGTGCTCGAGAGTTCTGGAGAAACTGGTAATGTAACCACTAGAAGAAACGCACTGCAGGAAGGCTTTACCTATGTTGGCGGGACACCGGAGTCAAACGGTCCGACCAACCTCACCGGCTGCATCAGCAACTTCTTCATCAAGAGGTTTGTACTGCCGAGAAGACTTTAAGAATTAGACTGATGGAGCTAGCGCTAGTGAACGCTACATCTTATACAAATTAAATGAAAGGTTGTCTTTAGATCTGCTGTCAGCATTTCTACTTGTGTGTTTTTAGAGCGAACGAACCACAGATTGTAGAAGATCTGAAAACAGCTCTAGAGGGACGCAAATACACATTCACCTGCCCTGATGCTTCAGCCCCACTGCAGATGTTAAATTCTCCACGGCCAAAGAAGGTGCTGCTGAAAAGATTTAACTTATTTTATTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTTATTT
Associated Phenotype:
Not determined