ZMP
SDK2 (2 of 2)
Ensembl ID:
Description:
sidekick homolog 2 (chicken) [Source:HGNC Symbol;Acc:19308]
Human Orthologue:
SDK2
Human Description:
sidekick homolog 2 (chicken) [Source:HGNC Symbol;Acc:19308]
Mouse Orthologue:
Sdk2
Mouse Description:
sidekick homolog 2 (chicken) Gene [Source:MGI Symbol;Acc:MGI:2443847]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20127 | Nonsense | Available for shipment | Available now |
sa14658 | Nonsense | Available for shipment | Available now |
sa9046 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25259 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15654 | Nonsense | Available for shipment | Available now |
sa2127 | Essential Splice Site | F2 line generated | Not yet available |
sa14263 | Essential Splice Site | Available for shipment | Available now |
sa26140 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9315 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20127
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 |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 6 | 2106 | 1 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47784154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50099131 |
GRCz11 | 3 | 51139120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTAGTTGATGGGATTGTCATTTTCTTTCACCAGGTATGTAATTCCAT[C/A]GCTGGACCGCTCTCATGCAGGCTTCTACAGATGTATTGTCAGGAACAGAG
Long Flanking Sequence:
CTGGTCAGCATACACCATTGGCTCCATACTTTCTGATGTTCAGCTTCCTTTGATGGTCTTGCAGACTGATGCTTTTGCTGGTCTCTGTTAGTCCAAGGCTCCAGGGCACTGGCCTCGTCCATAATCCAACCCACATCCACATAAATATTTCTCTGCTTTGTTCTATCTGAAGTGTTAATGGTCTCTCCAGTGTTTTGTTACGATCACAGCATCAGGGCTGCCTGAGGACTCCTATCTATTGTTGATGAGGGTTCTTGCTTCAACAGGTTTCTCACGGACGTCCTGAGCGGGCTGAGTGTTGCAGTCTGATCTGCACTCGAGCAGACGCTGACAATGTATGATTAATTATGGACTGATAAATAGTCTTTTTCTGGATCAAAGGCCATTTGTTTTTGTCTGTGTTTTTTCGGGCCTGCTGGAAGCTCCCCTGCTAAGTATGGAAAGTAGCAAACAGTAGTTGATGGGATTGTCATTTTCTTTCACCAGGTATGTAATTCCAT[C/A]GCTGGACCGCTCTCATGCAGGCTTCTACAGATGTATTGTCAGGAACAGAGTGGGAGCATTGATGCAGAGGAGTTCACAACTCCAGGTCGCCTGTAAGTTTCACATCAATAACAAACATTTCATATCGCAATAGTTTAAATGACTATAGATACCGGCTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTAATTACTGCTAGTTTGCAGTCTCCTGTAGTCCTTTCTATCACTGCTAATTATTTTTAGCCATTTTGGTTGATTGCATGAGCGAAACTTGGAGAATAAAGTCATTATTAGTTGTTTATAGTCAGACCTGGATAGATTACTTATGAGTTGTAATTAGTTATTGAATACAAATTACATGACAATATTTGTAGTCAGTAATAATAATTTAAAATATTTCATTGCATTAGTAACCTAACCACTTTTAGATTACATTTTTGTTAGCACAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14658
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 |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 841 | 2106 | 18 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47848469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50034816 |
GRCz11 | 3 | 51074805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGTCCTGTAGGTCACCTGAGCTTTACAGAAATCCTGGACACATCTCTC[A/T]AAGTGAGCTGGAAAGACCCGCCTGAGAAGAATGGCATCCTCAYAGGTACC
Long Flanking Sequence:
GTACATTATTTCTGTTAAATAACAAGACTTTTGTCTATGCAAAGTCAGACCTTACTGTTCTAAATAAAACATTAAAATTCAAGGCCTGATCATATTTAATTTGTTACTTTGCCTTTTATACAAGCCACTTCTGATACCAACTGACCAACTAGAAGTGAAGCTATTATTTGTTGATGCTAAAACTTGGATTGACTTGGACCAAGACTTTGTCGGGTAGTGTAGATCTCAATGACTACTGGTTACTAGAATTCAGGTAACTATTCCTTTAAAAACACCATCTAGACAAAAAAAAAAAAAAGGTTTTATAGCTTTACTAGTGAAAGTCTTGTTTATAGAAATGAAAGTATCAAAAAACTCTGTGAATCACAGCCTGTAAAAAGGATCCATGACTATATTAGGGTGTCTGTTTGAAGAGACTTTGAAAAGTGTGGTTGTCTGTGTTCTCAGCTCCAGGTCCTGTAGGTCACCTGAGCTTTACAGAAATCCTGGACACATCTCTC[A/T]AAGTGAGCTGGAAAGACCCGCCTGAGAAGAATGGCATCCTCACAGGTACCTACATCACCCCCATTCAAAGATTTAGTCTGATATTTTGACTATTCGCTCAACTGCTTCCCATCTCAACTCTGTAGGGTATCGCATTTCTTGGGAGGAATTCAACCGGACAAACACTCGTGTCACGCATTACCTGCCGAACATGACGCAGGAATACCGGGTCACCGGTCTGACCGCACTCACTACCTACACTATTCAGGTGGCTGGAATGACCAACAAAGGTCAAGGTCAGCTCTCGTCCTCCACCATTTCCTCCGGCGTGCCACCAGGTCAGTTTTTACTCATGTTTTGTCTTACTCCGACATTGCATTGATACCGTCATCTATTTCATCATTTTTATGAAAGGACTAATTGCTGTCTTCAGGTATCAGAGACTATAGTAGAAAACTGGGCGATCTGAAAAAAAAAAAAATTACTTGAGGCCTGCTGTGAATCCAAGGTTGTACATTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9046
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 874 | 2106 | 19 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47848650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50034635 |
GRCz11 | 3 | 51074624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCATTTCTTGGGAGGAATTCAACCGGACAAACACTCGTGTCACGCATTA[C/A]CTGCCGAACATGACGCAGGAATACCGGGTCACCGGTCTGACMGCACTCAC
Long Flanking Sequence:
ACTTGGATTGACTTGGACCAAGACTTTGTCGGGTAGTGTAGATCTCAATGACTACTGGTTACTAGAATTCAGGTAACTATTCCTTTAAAAACACCATCTAGACAAAAAAAAAAAAAAGGTTTTATAGCTTTACTAGTGAAAGTCTTGTTTATAGAAATGAAAGTATCAAAAAACTCTGTGAATCACAGCCTGTAAAAAGGATCCATGACTATATTAGGGTGTCTGTTTGAAGAGACTTTGAAAAGTGTGGTTGTCTGTGTTCTCAGCTCCAGGTCCTGTAGGTCACCTGAGCTTTACAGAAATCCTGGACACATCTCTCAAAGTGAGCTGGAAAGACCCGCCTGAGAAGAATGGCATCCTCACAGGTACCTACATCACCCCCATTCAAAGATTTAGTCTGATATTTTGACTATTCGCTCAACTGCTTCCCATCTCAACTCTGTAGGGTATCGCATTTCTTGGGAGGAATTCAACCGGACAAACACTCGTGTCACGCATTA[C/A]CTGCCGAACATGACGCAGGAATACCGGGTCACCGGTCTGACCGCACTCACTACCTACACTATTCAGGTGGCTGGAATGACCAACAAAGGTCAAGGTCAGCTCTCGTCCTCCACCATTTCCTCCGGCGTGCCACCAGGTCAGTTTTTACTCATGTTTTGTCTTACTCCGACATTGCATTGATACCGTCATCTATTTCATCATTTTTATGAAAGGACTAATTGCTGTCTTCAGGTATCAGAGACTATAGTAGAAAACTGGGCGATCTGAAAAAAAAAAAAATTACTTGAGGCCTGCTGTGAATCCAAGGTTGTACATTTCTTGTTATTACTGTGTGGCCCTATTAACCTCAGTCTTGATATCTAAGTTAATGAAGGTACGCTGAATATGATGGCTTTGTGCATTAATATTCATAATCTTCAGCCACCCCTTAGACACAAGCTGAGACTAAACAAGGCACAGTGAGACACAGTGGATAGAAACGTTTGAAGTTTTCTTCGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25259
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 |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 1016 | 2106 | 22 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47853196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50030089 |
GRCz11 | 3 | 51070078 |
KASP Assay ID:
554-7813.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGAGACAAGTAAATATAGTGGGCACAAGCCCACCCAGTCAACCATCC[A/T]GAAAGATCCAGACCCTACAGGCTCCTCCAGACATCGCCCCAGCCAACATC
Long Flanking Sequence:
AGAAAAATAAATAACTGACTTAAAGGGATAGTTCAAACAAAACTGAAAATTTTGTAAACATTTACTCACACTTGTACCAAACCTGTTTTAATTTCACTAATTTCAATTTCAATAAACACAAAATATTAAAAAAAAAAATGTTTGATACCAGTAGCTACTGACTTTCATAGTATTCCTTTTTTTTTTTTTTTCTACTATGGAAGTCACGCGATACAGATTTCTAACATTTCTCAAATATCATCTCTTGTGCTCAACAGTAAAAAGGAAGCCCATACAAATTTGCAAACACTTAAGGGACAGTAAATAGCATGTATATTTCAATCTTTGTGTGAACTATTCCTTCAAAATCATTTTTAGCTTGCGAAAATGCTAGTGTTCAAAAACTTTTTGGCCTCCACTGTATTGAACGTTTACAGGCTGCTCTGTAACTTGGTGTCTAATTTAGGTTTCGGATGAGACAAGTAAATATAGTGGGCACAAGCCCACCCAGTCAACCATCC[A/T]GAAAGATCCAGACCCTACAGGCTCCTCCAGACATCGCCCCAGCCAACATCACTCTCCGCACAGCCAGTGAGACCAGCCTGTGGCTTAGATGGGTGGTACGTACTGTCTGTGTCCATTACTTTGACCGATACAATTAAAAGGAAAAACATGTGACAGCAGCTATGTTTGCTAATTAAAAGTATGCACTAAAAAAGTTTTATTGTATAAAAAAAAAGTTAATTGCTTAAAACATTTGCAAATAAAGCTCTATATGTTTCCATACAATAAGTCTCCAAGTTTTCAAACAAGTCTTCTTAAACAACTGGCGCTTGATATCAAAAACTTGCAGAGCCTACTGTGGGCATTTTTCTTTTTATAAATTACTTAAGCTTCAGAAGAGAAAACCAATGAATGCATGCTGGGGATTTTAGAATGATCAAAACAACATTTCAGATGTTGTGCAATGTGGTCAGTCTGCTGGTTTAGTAATACGATCCCATCACACCGCTTTTGTTATCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15654
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 1100 | 2106 | 23 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47856288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50026997 |
GRCz11 | 3 | 51066986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACAGGAGAGAGAGTTTRCCATCGAGGACTTGGAAGAGTGGACAGAATA[T/G]GAAGTTAAARTCCAGGCGTTCAACGGYATCGGACCAGGACCATGGAGCCA
Long Flanking Sequence:
TTTTGATAGTATGCTTTTAGAGAACAGTGACCTTTTTATGTCCCTAAATATCTAGGGATTTTAGAGTCCTCAGGTCATTACTCTTTTGAAAAAAAAAACATTTGTGGCTCATTAGGTCTTTCTCTCTGGAGATAAAGTTCAATTTGAAAAAAAAAAAAAAAGTGTAGACTTAATATTGAAAGAAAAGTTTCCATTTATTATTTTTGGGGGTATTAGGAATATTCCAGTTATAAATGTATTTTCATAACAAGGATAGGACCTGGTCATTTGATGCTGAATATTTAAAAATGCTACAGTAGGATTTTTTTTTTAAATATAATTTAAAGTGTGTCTATTTTCCAGCCTCTGCCAGAGTGGGAATACAATGGCAACCCTGAGCTGGTGGGTTACAGGGTGCAGTACTCTCGCTTGGGCTCAAAAGTTGGCTTCCTCTCCCACATCATTCCTGACAGACAGGAGAGAGAGTTTACCATCGAGGACTTGGAAGAGTGGACAGAATA[T/G]GAAGTTAAAGTCCAGGCGTTCAACGGCATCGGACCAGGACCATGGAGCCAACCAGTTCACGGCAGAACAAGAGAGTCAGGTGAACAAATCTGCTGTTTTTTCTGTCTACCTTCTGTTTTGTACTTTTACAAAAAAAAAATAATAATAATAATAAAATAAAATAAAACCTTTCCAAAATGCTTTTACAACACCACTGACCTTTAAATTAATTATGATGGCGGGCTATGAGAACGCTTTATTGCTTAAAGGTTGTCCTTTTATTGCCTGGGAGTCTTAATGGAGTTTGCTGTTATGATTCAACTGCCTTTGTATCTCCTAAAACTGCTTTGGAGTAATACAAATAGATATAAATGACACAATTGCTGGCATGCAATATGATTATATGCAGGTTATGTAACTTAGGTAAGTGATGAGATATATGTGAGTTCACATCAAGTTTTAATTGCAAACTTTAGTACCCTAGGAATCAAAGTTTGTTTGATTGTTGAGATCTCGTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2127
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113318 | Essential Splice Site | 1229 | 2106 | 26 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47857638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50025647 |
GRCz11 | 3 | 51065636 |
KASP Assay ID:
554-3357.1 (used for ordering genotyping assays)
KASP Sequence:
ATTGAGTCCTACCTRTAGTACATTTACTTTTTTATTATTATTATTTAAAC[A/T]GTACCTGGGCCTCCAGTTGGGATCCTTTTCCCTGAAGTCAGGACCTCATC
Long Flanking Sequence:
CCCTCTAGCGGCCCTGCGAATGTTTCGGCTTTTGCTACCACCTCCAGCAGCATCCTTGTCCGCTGGGGCGACGTGCCAGAGACTGACCGCAATGGATTAATTCTAGGCTATAAGGTACTTTGTAAACAGGATTCTGACCAGATTTATTGACCTTTAGTCCACTTTAGTGGCTAAGAGATGCATCTGTTCCTCCTCATGGCTTTCAGGTGGTGTATAAGGAGAAGGATGCAGAGTCAGTCTTGCATTTCTGGACGGTCGAGGGAAACACCACTTATAGTGTCCAGCTCACTGGTCTTGGGAAATATGTGCTTTACGAGATCCAGGTTCTATCCTTTACTCGGATAGGAGATGGCATGCCTAGTTCTCCTCCCATCTTTGAGCGCACACTTGATGATGGTGAGCGTCTGAAATGCTTTTAAGTTAGTGATGCTCTAGTTAGTGATCTAGCTTATTGAGTCCTACCTGTAGTACATTTACTTTTTTATTATTATTATTTAAAC[A/T]GTACCTGGGCCTCCAGTTGGGATCCTTTTCCCTGAAGTCAGGACCTCATCAGTGAGACTGATCTGGCAGCCCCCTGCCCAGCCAAATGGCATAATCCTTGGTAGGTCAAGTAAAGGCTACATAAAAACTATTGTTTCTAGTGGTGGGTCAGACATGGAAAACCATGGTTTGATTTAGTTTACAATCCTCTATTGTAAAACTTATACCATTTGGAAATACTATGCAGCAACATAAAATGCATATCTTTTAATCTACCATTTACAATATTTAAATACAAAAAGTTAAGCTGAAGATCATATATTCTAATGTATCTATATATTTTAGCAGCATAATAACATGTTCGAATAAAAATAATAAAAACACTCCCCGTCAAAAATAAATAAATAAATAAATAATTGTTTATTAATCCTTGGCAAGAGAACCACATGGTCTGGTATTTTTGCATGAATCGTTCCATCCCTAATTGTTACTTGTCACACTGCACCATTTAATCCTAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14263
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 |
---|---|---|---|---|---|
ENSDART00000113318 | Essential Splice Site | 1429 | 2106 | 29 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47859911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50023374 |
GRCz11 | 3 | 51063363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGCGAGTACAGTGAGGAGAGTGAGGCAATCACCACTCTACAGGAYGG[T/C]AGGTTCAATTGTGRAATGCTATTGGGGAACAAGTTCCTGAGGCCTGAGGK
Long Flanking Sequence:
AAGAGAGGTACTGCATCTTATCTTTTTCACAAGGTAAGATGTTGTTTACTACATTCTATTGATTAAAACGACTCATTTGATCTCCCCACAGCACGGCCACAACCCACAAGTCGCCCCGTTGTGCCTCAGGAAGAGGTCCAGGCCCGCAGTGTGCTGTTGTCATGGGAACCAGGCAGTGATGGTCTGTCACCTATTCGGTACTACACCATTCAATACAGAGAGCTGCCCGACAGCAATTGGACCGTCCACTCTGCATCAGTCAACCATGAGGCCACCTCTTACGTCATCGACAGGTGTGTCTCAACTGGTCCTGCACCAAACTTTCTAGAGGTCATAGAGGACAAAACCCTTAACACTCCAGCAGTCCCACTGAGCTTCTTTTTCCCTATTCACAGGCTCAAGCCTTTCACTTCCTACCAGTTCAGAGTGAAAGCCACTAATGATATTGGGGACAGCGAGTACAGTGAGGAGAGTGAGGCAATCACCACTCTACAGGATGG[T/C]AGGTTCAATTGTGGAATGCTATTGGGGAACAAGTTCCTGAGGCCTGAGGTGAATCATAATGTGGCCGAAATAGGACACAGTCAGCAAAGGGGAAAAACTGCGGGGTTACCTTATTCTTAACTTTTGGCGTCTAACTAGAAAGCTTAGCCTGATCTTACGAAAAAATCCATTTATTTTATGTGTTCTCAGAAAAGTGGATCTTTTGTAAAGATTTCATTCTTTAAAAACAATATTAGGGAGGTCTGCTTTTGTAAGTATGATGTATCATTTGGATGCCTCATTGAGCCAAACTTATATGTTTCATTTAATGATCTCATTTAGTAGTCAAACCTATTTAATTTTTCAGTTATTTAAGCATAGTCATTGGATTTTGACTTGCACAGTAACTGATGGACAATTTCAGCAGACGTTAGATGTAAGAAGACTGACTTTTTTTTTGGACATAACACAGTCAATTTAGTCAAACTGTGACCAAGAAATGGATGATCATAAAGCATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26140
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113318 | Essential Splice Site | 1589 | 2106 | 34 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47867018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50016267 |
GRCz11 | 3 | 51056256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATCCTCCTCCAGTGGAGGCCCAGAATGGGGATATTCAAGGCTATAAG[G/A]TACAACAAACCGGTTCTGTCCTTCAAATGATTCTGTTGTGACTCAAAATG
Long Flanking Sequence:
ACGTCTGGTCTTTCCTGTGCCCATTTCTCTCCACACTGTCATTGACTTTTCATCACAGCATCTCACTTCATTGGAATGGGATCATTATGTTTTAGCACCACTTAAGCTTTTATCAGGCTATATTGAAAAGAGTGTGTATGTGTGCGCATTTTCTCTATTGTTCAGATCTGAATAAACACAAGCGCTACGAGATCCGGCTGAGCGTTTATAATGCGGTAGGGGAAGGGCCCACCAGTTCGCCGCAGGAAGTGTTTGTCGGAGAGGCGGGTGAGGACTAAAACTTTTACTAAGTCAATATCATTGATTTCACGATCTAATAAAACGTGCACCGGCATCGTCACTTAGTATAAGTCTAATAAATCAGTTCCTCTCTGTCCTTATTAGTGCCAACCGCCGCCCCTCAGAATGTCGCTATCCAGTCCTCGACGGCCACTCAGCTTGATGTGACGTGGGATCCTCCTCCAGTGGAGGCCCAGAATGGGGATATTCAAGGCTATAAG[G/A]TACAACAAACCGGTTCTGTCCTTCAAATGATTCTGTTGTGACTCAAAATGCAACACATAGTTCTGTATATGGTGTCAGCTGCCAAGAAAGTCCTGGGTTTGGAAAAAACAGTCTTGGTTAGTGAACATTGTGACTGTGCTTGCAACCAGTGTTTGGGCTGATAAATGCAGTAGTCACTAGGGCTGCACAATATTGGAAAAATCTGATATTGCAATATTTTGTATTTCTTCGATATATATATATTGCAATATACAGTATATACAATTTCACCAGATGACTTAAGCATTCATAATTATTATTATTTTTTTTTTTATAGATGAATTTTTTAGGATCATTCTGTTGGCGAGTAAATCAGGTGCTTTAATTGACAAATTGCAAGATTATAAATACAATAGAGCAAGTATAAAAGTGAAATAAGCAGCACTTTATCATTTTCAAGGTAGCCAAATCATATTCAGGTACAGAAATTGACAAATCAAATATAAAAGAACACTGCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9315
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 |
---|---|---|---|---|---|
ENSDART00000113318 | Nonsense | 1737 | 2106 | 37 | 44 |
Genomic Location (Zv9):
Chromosome 3 (position 47879325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50003960 |
GRCz11 | 3 | 51043949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGACGGCGTAACCTACAACTTCCGCATCCGCGCTAAAACTCTTACCTA[T/A]GGAYCAGAGATTGAGGCCAACATCACCACTGGCCCTGGAGAGGGTACTTT
Long Flanking Sequence:
TACATATTACTATATATTAATATTACACAAACACACACACACACACACACACACACACACACGCACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACAGTACATATGTGTGCGCGTGCGTGTGTATTTATATGGTGGGGGGGCTCCAATGTTTGTATATGTTCATGGGGGGGGGCCCCAAAGAAAAAGGTTGGGAACCACTGATTTAACCCATCCTTGCTGGAAGCACAGAGTAAATAATGAGTGTTTCTATGTGTCATTGTTAGTGTTTCGTTTTAGCGTGGTATCTAGAGTTTGAGTGTTTCTTCTACAGACTCCTCTCCTCACACTTCAGGTGTCAGTAAGATTGTCACTGTGGATGTGAAGGGCAGTGCCCCCTTGTGGATGAAAATCAAAGATCTGGCAGACGGCGTAACCTACAACTTCCGCATCCGCGCTAAAACTCTTACCTA[T/A]GGACCAGAGATTGAGGCCAACATCACCACTGGCCCTGGAGAGGGTACTTTCACCTCACATTCAGCTCAACATTTACTATTACCTTGAACTGTATAATTTCTGATTTAACTGTATAATTTCTGTTTTATAAATATAGGTGCTCCAGGGCCTCCCGGAGAGCCATTTATCTCTCGATATGGCTCTGCGCTCACGCTCCACTGGTCCAATGGGGATCCTGGACGTGCCCCCATCACTCGATATGTTATAGAGGCAAGACCATCTGGTGAGTTAAAGAGAGAGAAATCTATTAACATGTTTCTATCAAAAAATATAAATTAGAATTATGCGCAAAACTGGAATACCACGTAAAACTTTTGCGAACGAAGCACCATTTCCAACCAATGAGTCAAAGAGAACAAAATCGTCACTTTTCTGGCGACAGATATCAAAATTGCTTTATTAGGAAAAGCCATAATGAGCCTTTTTTCTTATATAATAAATTACTTGCACCTCAATATCGA
Associated Phenotype:
Not determined