ZMP
speg
Ensembl ID:
ZFIN ID:
Description:
Striated muscle preferentially expressed protein kinase [Source:UniProtKB/Swiss-Prot;Acc:Q696W0]
Human Orthologue:
SPEG
Human Description:
SPEG complex locus [Source:HGNC Symbol;Acc:16901]
Mouse Orthologue:
Speg
Mouse Description:
SPEG complex locus Gene [Source:MGI Symbol;Acc:MGI:109282]
Alleles
There are 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25334 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14081 | Nonsense | Available for shipment | Available now |
sa13872 | Nonsense | Available for shipment | Available now |
sa26736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40677 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40678 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40679 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12597 | Nonsense | Available for shipment | Available now |
sa14625 | Essential Splice Site | Available for shipment | Available now |
sa40680 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7040 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40681 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40682 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7581 | Missense | Mutation detected in F1 DNA | Not yet available |
sa9635 | Essential Splice Site | Available for shipment | Available now |
sa45251 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25334
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 278 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 278 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22803963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059409 |
GRCz11 | 6 | 21119631 |
KASP Assay ID:
554-7839.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATCCTCTATCCAAACTCCCAAAGTGTCACAGGCAAGTTCCAAAATTT[T/A]AGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAA
Long Flanking Sequence:
GCTTTAGGTGTGACTTATTTTGTTTTCTGATTGCAATCTTTTTGATTTATTCAGCTCCCACATTTTAAATATTTCACCATTTGATGTTTTTTAATGCATGATTTGTTTGGTTTCTATTACTTAAATATGCTTTCACTCAAAAAAACATGCATGAGTAGCAAATCTGTGCACCCATTTTTTCCATTTTTATTTTCTGTCATAACACAACATCTTCCACAATCACCCTCATTTCAGGGGCCAATTGGATTTTAAAACAAGTGAAGCCTCACCATTTGTCCAAACCCAGCCACCTCACAAAGCTCAAGCCTCCATTACCAAAAGTGATGTAGATGCAACAATAGACTCAACAGCAACAAAGATTAAAGGCACCAAAACAGCCATGAATGGAGCTGAGGTCTCTATTAAATCTTCAAAAATCACAGGTTCACATCAGAGCGGTGGTTCACAAGATCCATCCTCTATCCAAACTCCCAAAGTGTCACAGGCAAGTTCCAAAATTT[T/A]AGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAAAGGTGTCTTCAAGATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCCCGATTACCAAAAATTAACCTGGCAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14081
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22804436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059882 |
GRCz11 | 6 | 21120104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCAGATGCAAAGGAAAGRTGGACARCCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACWGCCTSAAAATGAA
Long Flanking Sequence:
AAGTGTCACAGGCAAGTTCCAAAATTTTAGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAAAGGTGTCTTCAAGATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACAGCCTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCTAAGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTCATACCAGGGCAATGTTCACCAATGTTGCCTAGGACAAATGTTTCCAGAAAATGGCCAAAATCACCTGCCCAACCTATGGTGAAAGATGGTTTGGTGAAAGCCCCACAAAAGCCTCCAAGATTATTAGAATCAATTTCCACACTACCAACACCATTTAAAATGACCATACCTACTATTGTGGTTGAAAATAAGCCCGTGGATGAAGAGTTGGACCAAAAGGAAGGACAAATAATGAGACAAAACAGAGGTAAAAGTTTTTCCTGAACTTCTACCAGCTTCTTTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGCCAGATAGGGTAAAATATGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13872
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22804436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059882 |
GRCz11 | 6 | 21120104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCAGATGCAAAGGAAAGRTGGACARCCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACWGCCTSAAAATGAA
Long Flanking Sequence:
AAGTGTCACAGGCAAGTTCCAAAATTTTAGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAAAGGTGTCTTCAAGATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACAGCCTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCTAAGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTCATACCAGGGCAATGTTCACCAATGTTGCCTAGGACAAATGTTTCCAGAAAATGGCCAAAATCACCTGCCCAACCTATGGTGAAAGATGGTTTGGTGAAAGCCCCACAAAAGCCTCCAAGATTATTAGAATCAATTTCCACACTACCAACACCATTTAAAATGACCATACCTACTATTGTGGTTGAAAATAAGCCCGTGGATGAAGAGTTGGACCAAAAGGAAGGACAAATAATGAGACAAAACAGAGGTAAAAGTTTTTCCTGAACTTCTACCAGCTTCTTTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGCCAGATAGGGTAAAATATGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26736
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 466 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 466 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22804526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059972 |
GRCz11 | 6 | 21120194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCT[A/T]AGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTC
Long Flanking Sequence:
GATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCCCGATTACCAAAAATTAACCTGGCAGATAAAACAAAACAGCCTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCT[A/T]AGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTCATACCAGGGCAATGTTCACCAATGTTGCCTAGGACAAATGTTTCCAGAAAATGGCCAAAATCACCTGCCCAACCTATGGTGAAAGATGGTTTGGTGAAAGCCCCACAAAAGCCTCCAAGATTATTAGAATCAATTTCCACACTACCAACACCATTTAAAATGACCATACCTACTATTGTGGTTGAAAATAAGCCCGTGGATGAAGAGTTGGACCAAAAGGAAGGACAAATAATGAGACAAAACAGAGGTAAAAGTTTTTCCTGAACTTCTACCAGCTTCTTTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGCCAGATAGGGTAAAATATGAATTAACTAATGCTTAGCAAATGTTGTATGTCTTAAGCTTTTCAGTTTGTTAGATGAACATCTGTAAATTAATTTAAAAAATATTTAAAATAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40677
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 698 | 2995 | 8 | 38 |
ENSDART00000133507 | Essential Splice Site | 698 | 2995 | 8 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22815170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19070616 |
GRCz11 | 6 | 21130838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGTTTGATTATTATTTACTGTGCATCTTGTTCCTGCTTGTATGGTAC[A/G]GAAGAGCTCATTTGCACAGCTAATCTTCTGGTGATTCCATCTAAGGAGCC
Long Flanking Sequence:
TTGAACCCAACTGCATTTGCTCTTGACATTGTACACGAATGTTGATGTTAAATAGTTCTATTTTGAGCTACAGCATGAACTTTACATGATATACAGGCCTGTAACTGTTATTGTCTGCCTGGCAGCTCCTGCTGAGTCATTGCTGATAATCACCAGACCAATGCAGGATGTGAAGGTCAAGGCAGGAGAGACAGCCTTGCTTGAATGTTTCATCGCTGGGTCACAAGCTGTGGATGTTGATTGGTTAGCCAATGGGAAGTTGATACAGCCAGCACTGTTTGATTGCAAGATGCAGTTTGATGGACACCGATGCCGTCTTCTGTTCAAATCAGCACACGAAAATGACAGTGGATGCTATACTTGCAAACTTAGCACAGCAAAAGGTAGGAGTCAGCACAGCGGGCATCATTTGTGCATAGCATTGTTTGCAAGTAATAGTTTTTATTTCTAATATGTTTGATTATTATTTACTGTGCATCTTGTTCCTGCTTGTATGGTAC[A/G]GAAGAGCTCATTTGCACAGCTAATCTTCTGGTGATTCCATCTAAGGAGCCACTCTTTACACGAAAACTAGAAGTACTAGAGGCGATTGAGGGCCGATCTGCACAATTTGATTGTAAAGTCAGTGGATGTCCTCCTCCTGAAGTCACCTGGACTCACTGTGGTAAAAAAATTATTGAATCAATAAATAAATCAAATCTATTATTTAAGACAATAAATAAAATCAATAAAGTTCAAGAGTAATTTTTTAAGATACCTATTTTGTGTCATAGAAAAACCTCTGGTGGAAAGTGATAATATTCACATACTTAATGTGAATGGGCATCACTCTCTGCTAATCACTCATGTTAACAAGGAGAGTGAGGGACTTTACACAGCAATTGCTCAAAATGTTCATGGAAAAGCAGCGAGCTCAGCTGAACTCTACGTACAAGAACCACGACCGGCCATTTCTACACACATGTAAGAAGACAAGCCCTTGTATTATTGTCAAATTCATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40678
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 807 | 2995 | 9 | 38 |
ENSDART00000133507 | Nonsense | 807 | 2995 | 9 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22815607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19071053 |
GRCz11 | 6 | 21131275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCATGGAAAAGCAGCGAGCTCAGCTGAACTCTACGTACAAGAACCA[C/T]GACCGGCCATTTCTACACACATGTAAGAAGACAAGCCCTTGTATTATTGT
Long Flanking Sequence:
GTTTTTATTTCTAATATGTTTGATTATTATTTACTGTGCATCTTGTTCCTGCTTGTATGGTACAGAAGAGCTCATTTGCACAGCTAATCTTCTGGTGATTCCATCTAAGGAGCCACTCTTTACACGAAAACTAGAAGTACTAGAGGCGATTGAGGGCCGATCTGCACAATTTGATTGTAAAGTCAGTGGATGTCCTCCTCCTGAAGTCACCTGGACTCACTGTGGTAAAAAAATTATTGAATCAATAAATAAATCAAATCTATTATTTAAGACAATAAATAAAATCAATAAAGTTCAAGAGTAATTTTTTAAGATACCTATTTTGTGTCATAGAAAAACCTCTGGTGGAAAGTGATAATATTCACATACTTAATGTGAATGGGCATCACTCTCTGCTAATCACTCATGTTAACAAGGAGAGTGAGGGACTTTACACAGCAATTGCTCAAAATGTTCATGGAAAAGCAGCGAGCTCAGCTGAACTCTACGTACAAGAACCA[C/T]GACCGGCCATTTCTACACACATGTAAGAAGACAAGCCCTTGTATTATTGTCAAATTCATTAAACATTGTTTGTCTTTCACTCATTTCTTTGTAATTTGTACTCTTCAGGTCAAGGTTAGAGAAGATGCCATCAATCCCCGAGGAGCCTGAGGTCCCTGAGGGAGAGGTGGAACGCAGGACAATGCCAGACTTCATAAAACCTCTCAGTGACCTGGAGGTGATAGAAGGGAAAGAAGCAGTTTTGAAGTGCAGGGTGACTGGTCTGCCTTACCCAAAAATCACCTGGTACCACAATGGCAAGAAAATAGAGAGCACTAATGACAGAAAGATGACACAATGTAAGTCCACCAAAATATTGCTAGAAGCATTTTAAAGGGTGTTTGCAGTCCATCTTTGCTCTACAGGTGTGGTCTCGTTAACACTTTAAATTACAGTCCACAAATCACACATTAAGTAAAATTAACAATATAACACAGTTAGCACTGCTAGTCATTGTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40679
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 910 | 2995 | 11 | 38 |
ENSDART00000133507 | Nonsense | 910 | 2995 | 11 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22819826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19075272 |
GRCz11 | 6 | 21135494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCACAGTCTGGTCATTCAATCTGTTTGCCATGACCACAGTGGTGTGTA[T/G]AAATGTGTCATCTCCAACAAGGTGGGGAAGGCTGCCTGCTATGCTCATTT
Long Flanking Sequence:
GCCCCTTTAAGCTATAAATTGTTTCGATAGTCTACAGAACAAACCCTCGTTTTATGATAACATCCCTAATTACCCCAACCTGCTTAGTTAACCTAATTAACCTAGTTAAGCCTGTAACTTTCAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTAAAATATTATTTACTGTCATCATGTCAAATATAAAATAAACCAACTTAAAAATTCTACTGTAATCCATGTGAGATAATTGCATGCACTGCTTAAATTTGCACCCATCTAACTTTGCGTGGATTGTGTGGATTAATGTTGAAAGACCTGGATTTCTCAAAGAAACAGGAAATTTAATCACACTTTCTTGGGATTTCTTGGGATTCTAAATATGAGATTTGTGTACTTCATATTTTGTCTTGTAAATACATATTGTTGTCAGTCATATGCTACCAAGTATCTCTTTTAGACAGGGATGTTCACAGTCTGGTCATTCAATCTGTTTGCCATGACCACAGTGGTGTGTA[T/G]AAATGTGTCATCTCCAACAAGGTGGGGAAGGCTGCCTGCTATGCTCATTTATATGTTGCAGGTAAGATGGAACCTTCTATTATATTTGGGGGTGGTGTATTCGATGCATGTGCCTTACTCACATTATACCTACTTGACAGTTAGCCTTCCTGAGCCACCTGATGGTCCTCCAGTTATTGAGTCTGTAACTGGGAGAATGATCTTATTGAGTTGGAAAAAGCCAAAAAACCTGGACCCATCCATAGGTAATATTTTCTCTGTCTTTTTTTAACTGCCTGTGCATTATATGTCCTGATATTTTATTAGATTATCAGGAATTGACATCTTGGGAAGAGTTGCCATTTTACCATCAAATCTTTTTTGTTTTATTTGTATTTTCAGTCATGATTAATTGCATTAAGATATTGGTAACACTGCATCAGGCATGTACAAACATAGATTAATTTATGTCAATAGCACATGTACAAATTGCTTATTACACACACAGGGATCAGCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12597
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 1003 | 2995 | 13 | 38 |
ENSDART00000133507 | Nonsense | 1003 | 2995 | 13 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22822536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19077982 |
GRCz11 | 6 | 21138204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATTGCCTCCAGCCTCACAGACACCTCTTATACAGTCACCTCACTGTCT[A/T]AAGGAGTGTGCTATTCCTTCAGAGTCCTTAGTACAACTGGAAAAACACTA
Long Flanking Sequence:
GGTTGCTGCTTCTCCTGGTTTTCAGGTGGATTTTCTCTGGGTGCTCTCGTTTTTCCCCAGTCCAAAGACATGTGGAGGTTAATTGGGTAAACAAAATTGGCTGAAGTATGTGTGAATAAGGGAGTGTATGGGCTGATTTTTCAGTGCTGGGTTGCAACTGGATGGGCATACGTCACATAAAACTAATGAAAAAAACTTATGATAGAATAATTGGTGGTGTGTTCTGCTGTTGCAAACCTCATAAACTGGGTGTACTAAGGCAAAGAATAGACAGTGTGTGGTATTATTATACATGTTTGGCCATATTAATTTTTTTTAAATTTAAGCTTTTTTAAAAGGTTCTACTGTTTAGACTGTTTCACTCTTTAGCATCTTCTTTGTTAATTTCAGATCCCGCTTCACTGATGTATGTTGTTCAACAGCAAGTTCTGGGCTCCACCCAGTGGACAACCATTGCCTCCAGCCTCACAGACACCTCTTATACAGTCACCTCACTGTCT[A/T]AAGGAGTGTGCTATTCCTTCAGAGTCCTTAGTACAACTGGAAAAACACTAAGCAAACCATCACAACCAACTGATCTGGTCCAGCTCGTTGACAGAGGTATAGATTTGTGGGTAAAAAAATAGATATGTTACATTTTGATGAAACATCTTCTAATATATTGCAGAATTATTAATTAATGAATGCAGTTTTAATTAATGCAGTTCTCTTAGATATAGCTTTACTTAATTTTGGATTATTTTAGTGAAAATGTAACTTGCTTGTGAAATGCTGTATTTGTCATTGCCTGATAAATATATATTTTTTCCTTTATCACAGGAGAGTATTTTCGCAAAGCTCCAGTCATCATTGATAAGCCTGATATCGTGTACGCAGTTGAGAACCAGCCTGTAACCATTACAATTACAATTAATCATGTTCAAGCAACATGTACATGGAAAAGGTTAGTGGTAAAACAAGCCAGACATTGAAAGTACAATATGAATTATAAATATTAAGGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14625
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 1134 | 2995 | 16 | 38 |
ENSDART00000133507 | Essential Splice Site | 1134 | 2995 | 16 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22824843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19080289 |
GRCz11 | 6 | 21140511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAGAGAGCATTATTTTTGGTAGTAAAGNTTTTTCTGTTGGCCATTTC[A/C]GTGCCCCCTATATTTGAAACCATCATGGAGGACTTGGATGTGTGTGTTGG
Long Flanking Sequence:
GCCCAGATATTAGCACTCTTGCCTCACAGCAAGAATGTCACTGGTTCTAGTCCTTACCAAGTCAGCAGACATTTCTGTGCAGAGTTTATACGCTCTCCCCATGCTCACGTGGGTTATCCCCACATAAGTTAATTGACTAATCCAAATCGACACCATAGACATGCTCCTAGTAAGTAGTTATCTCTTAAAAGCAATCTCTATATGTTCATTAGCTACTACAGCAGGAGAGTTCTCGAGATCTACCTGAGCTCAAACTCCCCTCTCGCCTTTCAAACGGGAGCGAGCCCGTGCTCGAGGATCTTAAAGCCAAACAAGCTTTATAATGAATCATCAGCTAAGTGTGAACTCTTGAAATATATTGTAAATAACTATATAACCATTGATTTCTGGAGGCAGCTGTTCCTTACTTTCCATTCTTTATATTGAGTTTTTCTTTTTCATTAAATGTGCTTAAAGAGAGCATTATTTTTGGTAGTAAAGTTTTTTCTGTTGGCCATTTC[A/C]GTGCCCCCTATATTTGAAACCATCATGGAGGACTTGGATGTGTGTGTTGGGGAAACATGTCATTTTGCTGTGGTTGTGGATGGAAAACCCGACCCTGATATCCTCTGGTACAAGGTCAGTATTCACTGACACACAGATTTTTTAAAGAACTGATTTAAAGATTATCATGCTACTGTAATTGACCTCATCCATGTGGGGCCCAGATGAGTTACCCTTGGACTGATATCTGGGGCTCTCCTGGGCTAGCCAACTGGGACAAATTTTGTTCTCGGTTTCATGATGGCCCCACGTGTCAGCCTAAGTGAATAATCATGGGTCTTTAATAGGCTCCATATGAGATGCCCACCTTAATTTACCCATGTGGGTTCTAACGGGGCTACCAAGGTGGGCCCCACATTGTCAGGGTTCTGCCACTCGGGCCTTGTGAATTCTTGTTTTGGTGGCAGAGTCCGAAGACTAGCTATGTCTTGTCCTTTTTCTGTCATTGTGTGTGTCTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40680
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 1171 | 2995 | 16 | 38 |
ENSDART00000133507 | Essential Splice Site | 1171 | 2995 | 16 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22824959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19080405 |
GRCz11 | 6 | 21140627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGTGGTTGTGGATGGAAAACCCGACCCTGATATCCTCTGGTACAAGG[T/G]CAGTATTCACTGACACACAGATTTTTTAAAGAACTGATTTAAAGATTATC
Long Flanking Sequence:
TCCCCACATAAGTTAATTGACTAATCCAAATCGACACCATAGACATGCTCCTAGTAAGTAGTTATCTCTTAAAAGCAATCTCTATATGTTCATTAGCTACTACAGCAGGAGAGTTCTCGAGATCTACCTGAGCTCAAACTCCCCTCTCGCCTTTCAAACGGGAGCGAGCCCGTGCTCGAGGATCTTAAAGCCAAACAAGCTTTATAATGAATCATCAGCTAAGTGTGAACTCTTGAAATATATTGTAAATAACTATATAACCATTGATTTCTGGAGGCAGCTGTTCCTTACTTTCCATTCTTTATATTGAGTTTTTCTTTTTCATTAAATGTGCTTAAAGAGAGCATTATTTTTGGTAGTAAAGTTTTTTCTGTTGGCCATTTCAGTGCCCCCTATATTTGAAACCATCATGGAGGACTTGGATGTGTGTGTTGGGGAAACATGTCATTTTGCTGTGGTTGTGGATGGAAAACCCGACCCTGATATCCTCTGGTACAAGG[T/G]CAGTATTCACTGACACACAGATTTTTTAAAGAACTGATTTAAAGATTATCATGCTACTGTAATTGACCTCATCCATGTGGGGCCCAGATGAGTTACCCTTGGACTGATATCTGGGGCTCTCCTGGGCTAGCCAACTGGGACAAATTTTGTTCTCGGTTTCATGATGGCCCCACGTGTCAGCCTAAGTGAATAATCATGGGTCTTTAATAGGCTCCATATGAGATGCCCACCTTAATTTACCCATGTGGGTTCTAACGGGGCTACCAAGGTGGGCCCCACATTGTCAGGGTTCTGCCACTCGGGCCTTGTGAATTCTTGTTTTGGTGGCAGAGTCCGAAGACTAGCTATGTCTTGTCCTTTTTCTGTCATTGTGTGTGTCTCTGTGTGTGCCGTCGGGGGTGTGCGCAGGGCTTGATGCGGCCGCACAGGCTCTGCGTGTCTCGGACGCGCGCGCTCTTGTACTCGTGTTTGTGTTTTCATCTGTCTGCAGCGTGGCGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7040
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 1441 | 2995 | 23 | 38 |
ENSDART00000133507 | Essential Splice Site | 1441 | 2995 | 23 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22828751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19084197 |
GRCz11 | 6 | 21144419 |
KASP Assay ID:
554-4687.1 (used for ordering genotyping assays)
KASP Sequence:
AAAACTATCCTTCTCTTTGCAGGCCAGTTGGTGTCATAACRTATTTATGG[T/C]ATGTTTATAATGTCCACTAGCAAATTTGAAATTAGTGCTACATTTAAATK
Long Flanking Sequence:
CAGAGAACTACTGGCTAATCAAATAATCCACTGAATTGTATGTGCAGGTTCAGTCTATTATACGGCAGCTACTTGAGGGAATCGAGTATCTTCACCAGAATTACATAATTCACCTTGATTTAAAGGTCAGTCATGAACTAGCTGATTCACAAAATCAAAACAAATGGCTGTTTTTGACTTTTAAGAAACAAGTAATTATAACATGTGTGTATTTCAGCCTGAAAACATCTTAATGGCAGACCAAAAAACTGATCAGATTCGTATTTGTGATTTCGGCAATGCTCTGAAAGTCAAACCAAATGAAGAACTGTACTGCAAATATGGTACACCAGAATTTATTGCTCCAGAGATTGTAAACCAGTCACCTATCTCTAAATCTACAGACATTTGGTAATAGAGCACACATTTATCTACCATTTGATAAATATTGTTTCATTCTCTGTATTTTCTAAAACTATCCTTCTCTTTGCAGGCCAGTTGGTGTCATAACATATTTATGG[T/C]ATGTTTATAATGTCCACTAGCAAATTTGAAATTAGTGCTACATTTAAATTAATTTACCATGACTTTATAATGTGTTCAATTTACAGCCTCACTGGAGTGTCTCCGTTTGCTGGGGAAAATGACCGTGACACTCTGCTGAACATCAGGAACTATAATGTTGCATTTGAAGAAAGCATGTTCAAAGATCTTTGCAGAGAAGCAAAAGGATTCATTATAAAGGTTCTTGTTTCAAACAAACTGTAAGTGTTTATCATGCCATATTCTTTGAGTTATTGACTATCAATCCGATTGGTTGGCATAGAGTATTAAATTATGGTCAAACATTTGTACAGGAGACCCGATGCCACAGAGTGTCTTCTTCATCCATGGTTCAAGGTACAATAAAAAATACAGGCTGTTTATGATGTTTAAAACAGTAACATATTCACAAATATTCACACAAATGAAGGTGCAGTCTGTAAGTTTGACAACCAGAGGTTGAACTAAGTATTGCATTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40681
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 1506 | 2995 | None | 38 |
ENSDART00000133507 | Essential Splice Site | 1505 | 2995 | None | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22829128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19084574 |
GRCz11 | 6 | 21144796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACAGGAGACCCGATGCCACAGAGTGTCTTCTTCATCCATGGTTCAAGG[T/C]ACAATAAAAAATACAGGCTGTTTATGATGTTTAAAACAGTAACATATTCA
Long Flanking Sequence:
CTACAGACATTTGGTAATAGAGCACACATTTATCTACCATTTGATAAATATTGTTTCATTCTCTGTATTTTCTAAAACTATCCTTCTCTTTGCAGGCCAGTTGGTGTCATAACATATTTATGGTATGTTTATAATGTCCACTAGCAAATTTGAAATTAGTGCTACATTTAAATTAATTTACCATGACTTTATAATGTGTTCAATTTACAGCCTCACTGGAGTGTCTCCGTTTGCTGGGGAAAATGACCGTGACACTCTGCTGAACATCAGGAACTATAATGTTGCATTTGAAGAAAGCATGTTCAAAGATCTTTGCAGAGAAGCAAAAGGATTCATTATAAAGGTTCTTGTTTCAAACAAACTGTAAGTGTTTATCATGCCATATTCTTTGAGTTATTGACTATCAATCCGATTGGTTGGCATAGAGTATTAAATTATGGTCAAACATTTGTACAGGAGACCCGATGCCACAGAGTGTCTTCTTCATCCATGGTTCAAGG[T/C]ACAATAAAAAATACAGGCTGTTTATGATGTTTAAAACAGTAACATATTCACAAATATTCACACAAATGAAGGTGCAGTCTGTAAGTTTGACAACCAGAGGTTGAACTAAGTATTGCATTCCTGGATCAAAACAAATGCAAGCACAGGTTGCCAGATTGAGAACCAACAGGAGCGAGTCTGACGATTAAACCTAAAGGCTGATTTAAATCATGTTCTAAATAAAAGCAACAGTGTGCAATAGAAGGAATCTTCTCCATATTAAAATGAGTTTTTGTTCTAACCAACAACTTAAATTCACATATTAGAAACAGCTTCTATTTCTTGTATGAACCCAAAAAAACTGACAATGATCACCTCAGGTACATCTCATGTGCTTTAAATGCTAATAATGTGAGTTTGAATATGATTTTACATGACATTTATTGCCATACTACTGAAAGCAGCAGCAGTTTACCTCAGATCTTGAAAATAAAACAAACCATTTGAAATTGATCTTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40682
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 1546 | 2995 | 27 | 38 |
ENSDART00000133507 | Nonsense | 1545 | 2995 | 27 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22830585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19086031 |
GRCz11 | 6 | 21146253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTTCACTCATTAGATATGGGTCTAAAATGGTTATGAGGTCCATATCC[G/T]AACTGCTGGATGACTCCTCTAGCCATGTATCTCTTGCTGTGCCTAGAAAC
Long Flanking Sequence:
GTTCCGGACATAAAGACATTTTTAAAAGCAGAATAACTGACTTTAGCATTGTATTTTTAAGCAATAAAAGAATGTTCACCTGGCATGTTTCTTAAATATCAGCAAACAAATTCTGTTTTTTTTTAATTAGAAGAGTCAAAAACTTACATATAGTACATTTAAGTTTAAGTTCAATCTATGTGTGTAAAATACACAGTATGGCTAGAGTGAAACACAACACAATTATGAGCACCGAGATGTTTCTGTTTTACAACACAATATTCTTACTTTTTTTTTTTCCATTTCAGTCATTAACAAAGGGGAAGTCTATCAACACAACACTGCATAAGCAAGTGCTAGCCAGACGGAAGTGGCAGGTAAACCATTTATTAAGTATAATAAATAAATATTAATCAAAGATAAATAAAAGGACATTGATTACTAATAAAATGTGTTTATTTTGTCTATTTCAGTGTTCACTCATTAGATATGGGTCTAAAATGGTTATGAGGTCCATATCC[G/T]AACTGCTGGATGACTCCTCTAGCCATGTATCTCTTGCTGTGCCTAGAAACCTTAAAGATGGCTCGCCACCTCCATCATCATCTTCTGACTCAGATGAAGACATTGATGAACTTCCTTTCATCCCTATGCCCCACACAATGATGTTCTCTGGTTCCCGGATGTCTCTGACTGAGATCCATGAGGATGATGATAAAGTCATTAGAGGATCCAATGAATCCTACAAAAAGAACTTGAATCAACTTGATGACATCCCAGAATCCCAAATAATCGCTGGACAGAAGAATGAAGACTACCTGAAAAATCCAAAAAGGACTGATAACTGTTTGCAAAGAGGTTCCAGTGTAGAAGTTGATCAGGTTGCAAGCAAGACCAGAAGAGGGCTAATGCGAAGAGGGAGTTCTGCTGATAGTGCACTTCTTCTGCAAATAACACCTGAAGATAATGAAATAAAGGATACTACAGAGGATAGCCAAAAGCACATGAAAAAGGCAGTTTCCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7581
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Missense | 1894 | 2995 | 27 | 38 |
ENSDART00000133507 | Missense | 1893 | 2995 | 27 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22831630)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19087076 |
GRCz11 | 6 | 21147298 |
KASP Assay ID:
554-4105.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGGTGTCTAAGGAAGAGGCTAATAGTGATGTCTTGATTATGMATAGCT[C/T]TCGGTCTGCATTTAATTTAGAARACACTGAAATTATGGTAGAAGAGATGA
Long Flanking Sequence:
CAAGGAAGATTATGCTTTGAAACTGGATCTTATGAGGCAGAGGTTGCTAAAAGGAGGCACTGTTAACAAGAATATGAGTGGTCTTCGTGGTCCCCTACTGGAGACACTGGGTGTAGACGATGAGAGGAGAACTTCCTCTTTGGATCGTAACTTCAGAAATGCAAGGTTGAATGCTTCAGGAGATTCTGGGACATTTAACAATGACAGCTCTGAAGAAACTTACCAAAAACCTGCATTCAGGAAGAGGTCTTCTTTAAGAGACGAAAACTCAGAGTCAATTTCTCTTCATAGGAGATCTGGAGCCCCACTTGAGATTCCCTCAAGTTCTACTGGAGATCATAATGTGCTGAAAATTAAATCGACCATCCTGGATGAAAACAAGGCTAACCTGCCACCTTTGTTTCCAAGAGACATTTCTTCGAAGCCACCAACTCCAGTTTTAAAAAATAAACAGGTGTCTAAGGAAGAGGCTAATAGTGATGTCTTGATTATGCATAGCT[C/T]TCGGTCTGCATTTAATTTAGAAGACACTGAAATTATGGTAGAAGAGATGAAAGAACAAGACAGTGTTCCGGAAAATATGAATAAAAGTACTGAATTTCCTCTTGATATACTCCCACATGATATATCATCAAATTATTGCAGTAAATTGCAAGCAAATGGTAAAAAGGCATCATTTCTCACACCATTACCGACACCAGTTTTAAAAATCTCCCAGCCCAATATTCAACCTACCGCTGGGCGACCAGGTGTTTTTGCTTCTGCTTTTTCTGCACACCAGCCAAATCTTAGAAGTGATATCAAAAATATTGATTCAGAGGAAATTTTTGAAGCTAGATTTAAGAAAAGGGAATCATCTTTGGCACATGGTCTAAAACGATTGACAAGGACAAAGTCTGAAGAAAGCTCACCGGTTCCCCAACGGAAATCAGATGAAGTGGTCTATCGACCTGGACCTGTAGGTTCCCCATTGGAGTTTGGATCAACAGGATTAAAGGAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9635
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 2844 | 2995 | 35 | 38 |
ENSDART00000133507 | Essential Splice Site | 2843 | 2995 | 35 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22836190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19091636 |
GRCz11 | 6 | 21151858 |
KASP Assay ID:
2259-7493.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTCCCTCCAACAATGCAGCAGATATCTGGGAACTCTGGAATACATGG[G/A]TATGCACATACAATTTCTATGTTTTTCTASTAAAATTATTTAAAACATAT
Long Flanking Sequence:
AAGATAATACCCTATGATCAGAAAACCAAGCAAACCATTATAAAGGAATATGAGATTTTGAAGTCCCTTCGATGTGAAAGAATCATGGCCCTACATGAAGCTTATATCACACCACGCTACCTTGTACTCATAACAGAATATTGCTCAGGCAAGGAAATCCTGCAAAATCTAATTGACAGGTGTGTATGAGCCTTTCTTTGTGTGTGTGTGTTCAAGGACTTTGATAGCTGAACTGTGAAATTTAAGTCTTGACATCAATGGTATTTTCTCTTACAGATTCTGTTATTCTGAAGATGATGTAGTGGGTTTTATAGTCCAGATCCTTCAAGGTTTGGAATATCTCCACAACTGCAAAATTCTTCATCTGGACATTAAACCAGACAACATCATGGTCACCAACCTCAATGTAATTAAGATAATAGATTTTGGCAGTGCTCAAAGGTTTAACCCTCTGTCCCTCCAACAATGCAGCAGATATCTGGGAACTCTGGAATACATGG[G/A]TATGCACATACAATTTCTATGTTTTTCTACTAAAATTATTTAAAACATATTCATGCCATGCTGGTGTTAATGTTTTTTTCTGTCCTTTTTAAGCTCCTGAAATGCTGAAAGGAGATCTTGTTGGACCCCCAGCAGACATCTGGAGCTTGGGAGTTCTATCTTATATTATGTTAGTTTAGTCTATTTACAATTAAACACAACAGGACAGATTATGTTGATCCTAGAGCATAAGTCATGTTTAAAAATGTAATCCACATTCCAAATCCCCACCACTAAACCTAACTCTAACTGCCAATTATTCCCAAAATTACAAGGTGTTAATTGTTGGATAACAATGATGTAGAAGCACATAACCCTAAAGGCTGATTTATACTTCTGCATCAAACGGCGGCGTATGCTACGGCGTTGACGCATAGCTCTTCGCCGTGGCCGTCGGCGTCACTGACGTGCACCTCACAAAAAATGTAACTACACGTCGCAACAACGTGTAGCGCAAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45251
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 2944 | 2995 | 38 | 38 |
ENSDART00000133507 | Nonsense | 2944 | 2995 | 38 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22839369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19094815 |
GRCz11 | 6 | 21155037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCCTCATTCATTCATGGCTTCATGACTCATATCTGAAAAAGCTGCGT[C/T]GACAGACCTTGACTTTTACTACCACTCGTCTCAAAGAATTCATGGGTGAG
Long Flanking Sequence:
TATACAACAGCATGCATTTTAAAATTCCTAAATGTTTTGTTAGTATTTATGAGTATTTAAATGGCAAGCACACCATGCCTCTTTTTATGCTCCACAGCGGAGTATAAGATTTGAATTAAGCAGTGATTACGTGTGTTGAGGACATTCAAATCACACCGGTGTGATTATTTTTACAAAGGCTTAAAACTCAGCTGGAAGTTTTTTTTCAGTCAGAGCTACACACTGCATGAAAGGTCATTTTGAAAAATCAACAATGCAGACACTTTAAGCAATATTATTTTAATATTATTTCAAGCACAGAGTTTTAGCTATATGAAAATAAAGGTGAACTGAACATTTATATAGAATAAGTTTGATTTCTTTACAGAGAGTAATGAGGTGAACACTTTGAACCCAATAACTTGATTGATTTCATGTACTTTTTCTTCAGGTGCCGGCCTACTATTAAGGACTGCCTCATTCATTCATGGCTTCATGACTCATATCTGAAAAAGCTGCGT[C/T]GACAGACCTTGACTTTTACTACCACTCGTCTCAAAGAATTCATGGGTGAGCACCAGCGCAGATGTGCAGAGTCTGCTACTAAACATAAGGTTATTCTTCGAGTCTACCAGGGTGGACCTTCATCTCCAGCCTCACCTACCAAGTACACCACTCAGTGAACAGATAAAAGGACTTTCAATAGAATTGGGACATGGACTCTATATATATATAAACTCTTTCAGAGTGGGAAAAAAATCTGGAAAGTCTTGTTGACATTAATAATATGAGTATTTTCGACTTGACACTTTCTCACAAAAAAAGTAGTTGATGGTTGATAACAGTTTTTCCAGGGTGTGAGACATTACATTAAGAGCAATAAAGGATTAAAATAACTTTGGAACAGTGTTTTTAGATGACAATGATGATGATGATGATGATTTTAATGAAAGAGGTATGATATTATTTTGTGCACATTTGTGCAGTTACTGCTAATGAATCAACTTGAACACAGAAGATGTTAT
Associated Phenotype:
Not determined