ZMP
si:dkey-49h9.6
Ensembl ID:
ZFIN ID:
Description:
Si:dkey-49h9.6 protein [Source:UniProtKB/TrEMBL;Acc:Q58EE5]
Human Orthologue:
IGSF9
Human Description:
immunoglobulin superfamily, member 9 [Source:HGNC Symbol;Acc:18132]
Mouse Orthologue:
Igsf9
Mouse Description:
immunoglobulin superfamily, member 9 Gene [Source:MGI Symbol;Acc:MGI:2135283]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16569 | Essential Splice Site | Available for shipment | Available now |
sa34288 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41110 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34287 | Nonsense | Available for shipment | Available now |
sa31628 | Essential Splice Site | Available for shipment | Available now |
sa17849 | Nonsense | Available for shipment | Available now |
sa21186 | Nonsense | Available for shipment | Available now |
sa21185 | Nonsense | Available for shipment | Available now |
sa38664 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13287 | Nonsense | Available for shipment | Available now |
sa1149 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16569
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004986 | Essential Splice Site | 276 | 2021 | 6 | 21 |
ENSDART00000126808 | Essential Splice Site | 187 | 1919 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5091566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4826758 |
GRCz11 | 8 | 4883025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTCACGTATGAGTGGTGGAAACAAGGACAAAACGTGYATCACATTGAG[T/A]AAGTGACCTACGAYTACTAACACAAGGCATATACAACATYATCACACAGA
Long Flanking Sequence:
AAAATATCTTCATAGAACATGATAATTATGGAAATTGTTTTTGCCATAAAAGAAAAATCCTACATTTTGATCCATTCAATATATTTTAAGCTATTGCTAAACATATATCCGCGAAACATAAGACTAGTTTTGTGGTCTATGTTTGAAAATCATCAATAATAAAGATTTAAACTTCACTTTCAACTCTGGAAAACTGTTTAGTGTAATTAAACAAGCAAACACTGCCCTCTATTGGTGGAAGTGCTTAAGTACAATACATTTTGGCACCAAAGCCACTCCAATACAAACAAAACAACCCCCTTCATTACGGATTCCCATTAAAGCTGATCACACACATGCTCCTATGCTTTCAAACAGGTCCTCCTATCATCATTATTGCCCCAGAGGACACCACCATGAACATGTCCCAGGATGCAGTTCTTCAGTGCCAGGCAGAAGCGTATCCTTCTAACCTCACGTATGAGTGGTGGAAACAAGGACAAAACGTGTATCACATTGAG[T/A]AAGTGACCTACGATTACTAACACAAGGCATATACAACATTATCACACAGAATGAGTCTTATTCAATTGCTGCAAATAGAAATATGTGACCCTGGACCACAAAACCAGGGTCATAAGGGTCCATTTTTGGGAACTTAGAGTTATACACCACATTAAAATCAAATTAAGTAAGCTTTACGTTGATGTATGGTTTGTTAGGATCACTTCAGCATTGATATAGCAATGTGTGTGTGCGCAATAGTCACATTACTAGATATGCAATGTTGTAGTTGAACAACCCAACAATTGACAATATATGAGATTTAAGGGTCATTGCAAAGTATAACCATAAGAAAGTGAAATGTCATCATTTGCATGTTTTAAAGGCATTTCAAAAGAGTTTAAAGCAAAAAAGGTACATTTGTAACTTTAATGAAGATTATTTTTACTGAATTATTAATACAATAAAGTATATGCAGTGTTATCTAACATTTCATTATTCATTTTCTGTCCCTGAGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34288
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Essential Splice Site | 373 | 2021 | 9 | 21 |
ENSDART00000126808 | Essential Splice Site | 271 | 1919 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5086169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4821361 |
GRCz11 | 8 | 4877628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATCATCAGGCATGTCATGATTTTTTTATTCCTCATCTTGATTGGACA[G/A]TATCCAGGATGGATGGTCAACTCGGAGGGATCTGTGTTCATTACTGCTGC
Long Flanking Sequence:
TTTTATTTTTGGTATCTTCCTCTCTTTTTTTTTTTTTTTTTTTTTTTGTTTGTTTAAGAAACATCAGCATGTCCACATTTTCTGTTACAAGTTAATGTTTCAGCTCATTTACAATTTCCTCTGCTGATGGAAAAAACCCTACAACTATAAAATAAACGAAATATAAGTCCTATACAAACTTTTGAAATGCTCATCCAAATAAAAAAATAAAAAAAGAGACTTTTGGACAAACGGAACATTTGCTAAATGTTCAAATTGCTTTACACGTCATTGTCAATTGGAGATTTTTTTAGTCCTTGTCATATTTACTATCACTGATTCAATAATATGATTGAACTGGTAAAAAGTGTAATAATTACATCCCTAAATACTAGTAAACTCTGCAAAACAAGGCCCTCTAGCAGCAGGTTTTGACTTACTTCATCATCAAGCATGACATCATTTACTTTCTTAATCATCAGGCATGTCATGATTTTTTTATTCCTCATCTTGATTGGACA[G/A]TATCCAGGATGGATGGTCAACTCGGAGGGATCTGTGTTCATTACTGCTGCCAATGATGATGCAGTAGGCATGTACACCTGTACAGCCTATAACAGTTACGGGACTATGGGCCAATCAGAACCTACCAAAGTCATCCTGAAGGTGAACCATACTGTACATCTGTAGTGGAAAAAAAGGTCCCACTTGCTTGCTTTACTACTGAGTATTATAAATGAATTGCATCAATTCAATTAAAGTTTATTTGTATAGTGCTTTTACAATAATCATACATGATATATATACTTACTGTATGGTTAGAAGAAGGGTTAGAGTTACCCACAAGAAAAATACTCTTCTAATTTACAGTAAATAATAAGTAGTTGAATTAATCAGTTGTGGTAATCCTATAGAAAACTATATATATATATATATATATATATATATATAAAAAACTATAGTAATATTGTAGTTTTCTACAACTATAAGATATATTATTTATACAATAGTAAACTTCGATATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41110
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 614 | 2021 | 14 | 21 |
ENSDART00000126808 | Nonsense | 512 | 1919 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5077611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4812803 |
GRCz11 | 8 | 4869070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGATATTTTTTGCATTTCAGCACCTCCAACAGAATCTCCTACTGTGT[T/G]AACCACCATGGCAGTGTTGTCTCCTCCCACATTGCTGTCAGCCAACCGTA
Long Flanking Sequence:
ACGGGGAGAACATACAAACTCCTCACAGAAACACCGGTCCTGTGGAACCAGGGCTGGCAGTGTTCTTGCTGTGGGGCTCACAGTGCTAACCACTGGGCCGCCGTGCCGCCCAATCAGAGGTAAAGGAGGAGAATAGGGGAGGAGGGGGGTTTCTTCCAAACGAAGATAAAGTGAACAGAAAACTCTGGCTATTTATAGTAGCTTAGGGTTTATATGATTGGAAGATAGTGATTAGCAAATGCGAGACCTGCCGTGATAAATCATAAGCACGTGATCCTCTCGAAATTAGTTTATGAATAAGCTTCACTTCAGCAAATAGGGTTGTAAAAAAATATTTTTGTACTCTCCCATTCACTACGCTCTACGTTTTCCCAACTATGACAACTACTGAGAAACCTGGAAATGTGAAAAGTGTCCATATGTATGATGGTCCATGCTAAGGTTTTGTAAACTTGATATTTTTTGCATTTCAGCACCTCCAACAGAATCTCCTACTGTGT[T/G]AACCACCATGGCAGTGTTGTCTCCTCCCACATTGCTGTCAGCCAACCGTACATCACTGGGTGTGTTGCTGCAGTGGGTCCCACCTCTAGAAGAGTCGTTAACTTCCTTTGCACTTCAAGCAAAGAGGGGAAAGGGGGAATGGGTCACTATAGACCGAGAGATCGCTGTCAACATGACGGAACTGATTGTACAAGGACTTGTAAAGGTAAAATGTTAAAGATCATGAGAATAGACTATTTTTCCAATTCATTGTCATATGAAGGGTCAAATTTCCTTTGTTTATTTCTAACACAGGACTCAAAGTATGAGTTGCGTCTTCTGTCTTGTCAAGACAAGCTGGTCAGCGTCCCAAGTGACTCGGTTCTCATCTCTACTGAAGGTGAAGCAAAAATAAGTAATATGGATTTGGACTTAGAGCTGGGCGATATGACAAAAATCTCATATCACGATATACCTAACCTAGTCCACTTTACAAAAGGGTTTCATTAATATGTTTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34287
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 638 | 2021 | 14 | 21 |
ENSDART00000126808 | Nonsense | 536 | 1919 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5077540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4812732 |
GRCz11 | 8 | 4868999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCCCACATTGCTGTCAGCCAACCGTACATCACTGGGTGTGTTGCTG[C/T]AGTGGGTCCCACCTCTAGAAGAGTCGTTAACTTCCTTTGCACTTCAAGCA
Long Flanking Sequence:
TGGGGCTCACAGTGCTAACCACTGGGCCGCCGTGCCGCCCAATCAGAGGTAAAGGAGGAGAATAGGGGAGGAGGGGGGTTTCTTCCAAACGAAGATAAAGTGAACAGAAAACTCTGGCTATTTATAGTAGCTTAGGGTTTATATGATTGGAAGATAGTGATTAGCAAATGCGAGACCTGCCGTGATAAATCATAAGCACGTGATCCTCTCGAAATTAGTTTATGAATAAGCTTCACTTCAGCAAATAGGGTTGTAAAAAAATATTTTTGTACTCTCCCATTCACTACGCTCTACGTTTTCCCAACTATGACAACTACTGAGAAACCTGGAAATGTGAAAAGTGTCCATATGTATGATGGTCCATGCTAAGGTTTTGTAAACTTGATATTTTTTGCATTTCAGCACCTCCAACAGAATCTCCTACTGTGTTAACCACCATGGCAGTGTTGTCTCCTCCCACATTGCTGTCAGCCAACCGTACATCACTGGGTGTGTTGCTG[C/T]AGTGGGTCCCACCTCTAGAAGAGTCGTTAACTTCCTTTGCACTTCAAGCAAAGAGGGGAAAGGGGGAATGGGTCACTATAGACCGAGAGATCGCTGTCAACATGACGGAACTGATTGTACAAGGACTTGTAAAGGTAAAATGTTAAAGATCATGAGAATAGACTATTTTTCCAATTCATTGTCATATGAAGGGTCAAATTTCCTTTGTTTATTTCTAACACAGGACTCAAAGTATGAGTTGCGTCTTCTGTCTTGTCAAGACAAGCTGGTCAGCGTCCCAAGTGACTCGGTTCTCATCTCTACTGAAGGTGAAGCAAAAATAAGTAATATGGATTTGGACTTAGAGCTGGGCGATATGACAAAAATCTCATATCACGATATACCTAACCTAGTCCACTTTACAAAAGGGTTTCATTAATATGTTTACTAAAATGAACTAATGATCAACACTATTGTACAGCATTTATTGATCATAGTTCAACATTTACTGAAGCATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31628
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004986 | Essential Splice Site | 780 | 2021 | 17 | 21 |
ENSDART00000126808 | Essential Splice Site | 678 | 1919 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5071773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4806965 |
GRCz11 | 8 | 4863232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACCTTTCAGATATCCCCTCTGCCTTCCAGAAGAGTTCAGCTCCACAG[T/G]AAGTGTCCATCCTTGCTATGCATGCATCATTACTATGCTTCTCTATCTTT
Long Flanking Sequence:
CTGAAAACCTGTAACCATTGACTTTCATAGTATTTGCATTTCTTACTGTGGAAATCAGGTTTTTAACCTTTTTCAATGTATCTTGTTTTGTGTTTAACAAAAGAAATAAACTTAAACAGATGTTGGAGCAACTTATGGGAGAGTAAATATTGAATAATTTAAAATTTTGGGGTGAACTATCCCATTAACCCTTAGATAAACAGGTATTTATGTATTGAGCAATGTTCTGACTCTTCATTAAGTCCATTCCTTTAAAGCTGTTGATGCATTATCAGTCTCTAAAACTGTATAAGCATTCAACGCCTCACAGATTGATGCATGATATATTTTAAATGCTGTTTATGGTATTGTCAGTCATGCATGGCATCTCTATTGTTTCTGTGGTGTTTGCGTTTGTTTTTGTCATCGTATGACTCATTACCTGTGGCATGATATGAACTTTGCATCCTCCCCACCTTTCAGATATCCCCTCTGCCTTCCAGAAGAGTTCAGCTCCACAG[T/G]AAGTGTCCATCCTTGCTATGCATGCATCATTACTATGCTTCTCTATCTTTGTCACTGTGCTACAGTATGCTTTTTTCCAGCCTTAAAGGCATAGTTCACCCAAAAGTCTTTTTAAAACACGAAAGCAAGGCTGCAGTGGGAAGAAACCCGGAAGTATAGGAGCAGCACTGTAAACATTTTCAATAACATGCTGTGGACTAGCAACCTCCAGCTGTTGCTGCAATTTCAAAATGTAGATGTGATGTAAACATGATTTTAATATCATTCAGTTCAGTTTAATTTAAACAATTAAAAGCATATTGGGCATCAAACAAACTCACAATCTCTATAGGAGTAATACACTTAAGTGTCCTCCTAGGCTTCAGTTCATGGCACCAGTTAAACACTGTAGGGATGCGTTCCTGCTTCAACCTATGTATCTTGGTGAGCGATTGTCTGATCGTGCTGTCTGTAACAGTGTTGTCCCGGTACTGAATTTTTAAAAGTTCCACTTACCGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17849
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 976 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 874 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5069117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4804309 |
GRCz11 | 8 | 4860576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGATGAGMAYGGTGGCTCTGAGGCCTTATTGGAAAGGGCCAGCTTTTA[T/A]TCTGACTGTAGTGAAAAGAAAGCAAGTGACTCGCWAAAAAAATACCGGGG
Long Flanking Sequence:
GACCGCTCAGACCGTTCCTCGTTCGATAAAGCCAGTCGTAGTGAGTACCAGGATCAAAAGAAGCAGCTGCTGTCCTCTTCATCTCCACCTCCACACTACACCCAATTTGAGAGCCACTTTGGAGGAACTCCATCGCCCACCCCTGCTATTGAATCTATATCGAGAAGTCCTGATGGCCGCTTCATTATCCAACCCGACCTGGAAAACTTCAAAAAGAACCTTAAGAAAGAGTTCCCACAGTCGCCTAGTAGAGGCAGTGGTAGAGGCAGCAGCAATGGATCTTTTAAAGAATCCAACCAATCAAATTCTGCAAGATCAGAAACAAACGCACAAACGGAGATGCCCTCAGCATTAACTGTGGATCATCCACACTTAGAAAGACCCCCTCACTCTCCTGGAAGGGTGAGAGCAATGGCTAGAAATTTCTCCCGTCATGGGTGTTTCTACTCTGATGATGAGCACGGTGGCTCTGAGGCCTTATTGGAAAGGGCCAGCTTTTA[T/A]TCTGACTGTAGTGAAAAGAAAGCAAGTGACTCGCTAAAAAAATACCGGGGTGCCATACATAGAGAGGAAATATTCCCAAGCTTAACCAGGAGAACCAGAGAGAGAGATAGGATGCTCCAGCAGGCACATTACCAACCTATCAATGGAGATAGTCAGCTGACAGAACCCAGCACTATGATAACTCAACTGGATGGAGAAAGAGAGAGGGACAACTTAAGCAAATGTTTAAAGCTGGCAAAGGAACGTGAGCAAATGGAGAAGGAGCTAGAGCACTACACAGCAAGTCGAAGAGTACAGGCACATGAGCGAGAACAGAGGCGGGCTAAATCTGCAAGTCCTTTACGAAAATGGACTGGTGTTGAATCTCAAGACCCAATTTGGAAGCCTCAAGACATCCAATTACGACAAAAATCCCGACCCAGCAGCTTGGCTCAGCATGTATCAGATAATAGGAGAGGCTGTTATTTTGGCAATACCAGTAGTCCCATGGAAAGACATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21186
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 1177 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 1075 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5068515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4803707 |
GRCz11 | 8 | 4859974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCAGCCTGGTGCCAGTGCAAAGCCTTTCTGAAGGAAACACACCTCACT[C/A]ACTTTACCCAAACATGCGTCAACAAGCCATTCCCAATGTAGAAGGTTCAT
Long Flanking Sequence:
GAGAGATAGGATGCTCCAGCAGGCACATTACCAACCTATCAATGGAGATAGTCAGCTGACAGAACCCAGCACTATGATAACTCAACTGGATGGAGAAAGAGAGAGGGACAACTTAAGCAAATGTTTAAAGCTGGCAAAGGAACGTGAGCAAATGGAGAAGGAGCTAGAGCACTACACAGCAAGTCGAAGAGTACAGGCACATGAGCGAGAACAGAGGCGGGCTAAATCTGCAAGTCCTTTACGAAAATGGACTGGTGTTGAATCTCAAGACCCAATTTGGAAGCCTCAAGACATCCAATTACGACAAAAATCCCGACCCAGCAGCTTGGCTCAGCATGTATCAGATAATAGGAGAGGCTGTTATTTTGGCAATACCAGTAGTCCCATGGAAAGACATCCTTCCTCTTCTTCATCATATATCCAGTGGGATATAAGCCCTGTGACGTCCCCTACCAGCCTGGTGCCAGTGCAAAGCCTTTCTGAAGGAAACACACCTCACT[C/A]ACTTTACCCAAACATGCGTCAACAAGCCATTCCCAATGTAGAAGGTTCATCAGCAACAGGCATATCTCATTCACCAGCTACACAGTATACCTCTCTTTCAATTTTCACTCCACATAGGGAATCATCTCCCAGTAGATCCAGCCTACACGGGGCACAAGCTAGATACTCGGAGAGTCAGCTGGAGGAGGAGCTGCCCAATAGGACTTTAGTTGAGGAAAGTTGGTTGGCGGAAAGGAAAATAGAAAAAGAGAGTCCACCATTTAGATCCAAATCCCCTGCTCACTTGAGTCCTCAACCATCTGAGCTGCACCAAGTGTTGGAAGGAGCTGACAGGGATGCTAATTCACATTACCTTGATCCCAGGTCCCAAGACGTTACAGATAAAGAGGAAGAAGGAATTGTTCAAAAAGATAGACTACTGAGCCGTAATCCATCAGGCTGCTCTACGTTACCCTACGACCATAAGAGGGGAGCAAAGGAAAAAGTCATTGATGATTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21185
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 1502 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 1400 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5067540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4802732 |
GRCz11 | 8 | 4858999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACGGCACACAGAATGTTCCCATGGAAAAACCTAAACCTGAGGACATCT[C/A]AGAACCACTTCCGCAATTAGAAGCAAGAGATAGATGTGTTAAATCAGGAA
Long Flanking Sequence:
AAAGGAAAAAGTCATTGATGATTCCCTCTCCATATTGCCTTATAATGAACAAGAAAAAGAAGGTATCAGGGCCCGATCCCGAAAGAGTGACAAATGTGTCTTGACTGAAAGTCCTAGTCGAATATCACCTCTAACCCTGTTGGAAAATGAGGCAGAAAGCGATCAGTCCAATTTCTCGAGAATGTCCGAATCAATGAAAGTTAAGCTTGCTTCCCAACCAGCAAGAATGTCCCCACTGCAGACCAGCACTATCCTGGAGTACCTGAGTCTTCCAGGTTTCATTGAAATGAGTGTAGATGATCCAGTAGAAGTGACTGAGCCTTCAGAATCTGTTGAACCCAATGTTGAGCTAGAAAGTGGGACAATGTTGAGAGTTGAGCCTGACGTTGTACCCAAAAGTTGGGAAAAACATAGTCAGGATCTCTCTGGAACCAATGGAGTGGTCCATGACCACGGCACACAGAATGTTCCCATGGAAAAACCTAAACCTGAGGACATCT[C/A]AGAACCACTTCCGCAATTAGAAGCAAGAGATAGATGTGTTAAATCAGGAACCTCAGACAAAAGCAATAAACGTTTTCCACCATTAAAAGAAAAGAACAAGAGTTCTGAGCCTTTGCTTTCTCAGAGTTCAGGATCTCAAAGAGAACAATTTATTCAGCATGGTCCAGCACAGACATTAATTAACACAGCTAAAAGCATGGCAGCGATAGTTTCCAAATGCCCAGACTTTATATCTCAACAATATCAAAGACCTCAGATTCACAGTGACAGTACCAACATGATATCCTCACGAATCAATCAGGCTCCTGTTCCTTTCATGAAGAAATCAGTCAGTATTGGTCCTTGTAGGACTCTCTCTGGAGCTGGGCAGCCTCGTCCTTTTCTTAGGAAGTCCATTAGTTTAGGATCAAGATATGAACATTCAGAACTTCCGAGACCTTATTTCTCTGAGACGTGCTACAGAGATCAGTTTCCCAACCCAGATATAAGGCTCAAATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38664
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 1584 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 1482 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5067295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4802487 |
GRCz11 | 8 | 4858754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGGCAGCGATAGTTTCCAAATGCCCAGACTTTATATCTCAACAATAT[C/T]AAAGACCTCAGATTCACAGTGACAGTACCAACATGATATCCTCACGAATC
Long Flanking Sequence:
GCACTATCCTGGAGTACCTGAGTCTTCCAGGTTTCATTGAAATGAGTGTAGATGATCCAGTAGAAGTGACTGAGCCTTCAGAATCTGTTGAACCCAATGTTGAGCTAGAAAGTGGGACAATGTTGAGAGTTGAGCCTGACGTTGTACCCAAAAGTTGGGAAAAACATAGTCAGGATCTCTCTGGAACCAATGGAGTGGTCCATGACCACGGCACACAGAATGTTCCCATGGAAAAACCTAAACCTGAGGACATCTCAGAACCACTTCCGCAATTAGAAGCAAGAGATAGATGTGTTAAATCAGGAACCTCAGACAAAAGCAATAAACGTTTTCCACCATTAAAAGAAAAGAACAAGAGTTCTGAGCCTTTGCTTTCTCAGAGTTCAGGATCTCAAAGAGAACAATTTATTCAGCATGGTCCAGCACAGACATTAATTAACACAGCTAAAAGCATGGCAGCGATAGTTTCCAAATGCCCAGACTTTATATCTCAACAATAT[C/T]AAAGACCTCAGATTCACAGTGACAGTACCAACATGATATCCTCACGAATCAATCAGGCTCCTGTTCCTTTCATGAAGAAATCAGTCAGTATTGGTCCTTGTAGGACTCTCTCTGGAGCTGGGCAGCCTCGTCCTTTTCTTAGGAAGTCCATTAGTTTAGGATCAAGATATGAACATTCAGAACTTCCGAGACCTTATTTCTCTGAGACGTGCTACAGAGATCAGTTTCCCAACCCAGATATAAGGCTCAAATCATATAGTTTGGGTCGTACTCCTTCACATTACTATCCCATATCTGGCCCATCGTGGCGAGGTTCAGTGCCCTATCAACCTCCTCACAGCTACAGTCTTGAAAGGCATCATATTGAGAGATCTGGAATGACACCACCTTACCAAACAACCTTTGTCCCAAATCCTTCACGACAGATGGAACCATCCCTTCCTTCTAGGCGGGAATCAGATCCACGTCGACAGGCAGCAGTCTTTCCAGATTCCTCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13287
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 1649 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 1547 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5067098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4802290 |
GRCz11 | 8 | 4858557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCATTAGTTTAGGATCAAGATATGAACATTCAGAACTTCCRAGACCTTA[T/A]TTCTCTGAGACGTGCTACAGAGATCARTTTCCCAACCCAGATATAAGGCT
Long Flanking Sequence:
GTCCATGACCACGGCACACAGAATGTTCCCATGGAAAAACCTAAACCTGAGGACATCTCAGAACCACTTCCGCAATTAGAAGCAAGAGATAGATGTGTTAAATCAGGAACCTCAGACAAAAGCAATAAACGTTTTCCACCATTAAAAGAAAAGAACAAGAGTTCTGAGCCTTTGCTTTCTCAGAGTTCAGGATCTCAAAGAGAACAATTTATTCAGCATGGTCCAGCACAGACATTAATTAACACAGCTAAAAGCATGGCAGCGATAGTTTCCAAATGCCCAGACTTTATATCTCAACAATATCAAAGACCTCAGATTCACAGTGACAGTACCAACATGATATCCTCACGAATCAATCAGGCTCCTGTTCCTTTCATGAAGAAATCAGTCAGTATTGGTCCTTGTAGGACTCTCTCTGGAGCTGGGCAGCCTCGTCCTTTTCTTAGGAAGTCCATTAGTTTAGGATCAAGATATGAACATTCAGAACTTCCGAGACCTTA[T/A]TTCTCTGAGACGTGCTACAGAGATCAGTTTCCCAACCCAGATATAAGGCTCAAATCATATAGTTTGGGTCGTACTCCTTCACATTACTATCCCATATCTGGCCCATCGTGGCGAGGTTCAGTGCCCTATCAACCTCCTCACAGCTACAGTCTTGAAAGGCATCATATTGAGAGATCTGGAATGACACCACCTTACCAAACAACCTTTGTCCCAAATCCTTCACGACAGATGGAACCATCCCTTCCTTCTAGGCGGGAATCAGATCCACGTCGACAGGCAGCAGTCTTTCCAGATTCCTCCAGGTGGCCTCTGTCTTATCAGGAAACACTCAGGTCAGTTCAGCACAAGTATGTACCACAAGATCCTCCTCGACCTTTTGGTCCAAACAGATCACTGGCCAGAGTGGACTACATGCATCCCGCGGAGCCCAGAAGATGCCCACCAAGACCTTTCCTTCCCAGAGGCTACAGCTGGCCATCACCACATCATCCAAGCTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1149
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 |
---|---|---|---|---|---|
ENSDART00000004986 | Nonsense | 1724 | 2021 | 18 | 21 |
ENSDART00000126808 | Nonsense | 1622 | 1919 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 5066875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 4802067 |
GRCz11 | 8 | 4858334 |
KASP Assay ID:
554-1060.1 (used for ordering genotyping assays)
KASP Sequence:
GATCTGGAATGACACCACCTTACCAAACAACCTTTGTCCCAAATCCTTCA[C/T]GACAGATGGAACCATCCCTTCCTTCTAGGCGGGAATCAGATCCACGTCGA
Long Flanking Sequence:
CAGCACAGACATTAATTAACACAGCTAAAAGCATGGCAGCGATAGTTTCCAAATGCCCAGACTTTATATCTCAACAATATCAAAGACCTCAGATTCACAGTGACAGTACCAACATGATATCCTCACGAATCAATCAGGCTCCTGTTCCTTTCATGAAGAAATCAGTCAGTATTGGTCCTTGTAGGACTCTCTCTGGAGCTGGGCAGCCTCGTCCTTTTCTTAGGAAGTCCATTAGTTTAGGATCAAGATATGAACATTCAGAACTTCCGAGACCTTATTTCTCTGAGACGTGCTACAGAGATCAGTTTCCCAACCCAGATATAAGGCTCAAATCATATAGTTTGGGTCGTACTCCTTCACATTACTATCCCATATCTGGCCCATCGTGGCGAGGTTCAGTGCCCTATCAACCTCCTCACAGCTACAGTCTTGAAAGGCATCATATTGAGAGATCTGGAATGACACCACCTTACCAAACAACCTTTGTCCCAAATCCTTCA[C/T]GACAGATGGAACCATCCCTTCCTTCTAGGCGGGAATCAGATCCACGTCGACAGGCAGCAGTCTTTCCAGATTCCTCCAGGTGGCCTCTGTCTTATCAGGAAACACTCAGGTCAGTTCAGCACAAGTATGTACCACAAGATCCTCCTCGACCTTTTGGTCCAAACAGATCACTGGCCAGAGTGGACTACATGCATCCCGCGGAGCCCAGAAGATGCCCACCAAGACCTTTCCTTCCCAGAGGCTACAGCTGGCCATCACCACATCATCCAAGCTTTCCCTTAAGAGAGCATGACTTTCCGAGGGAGCTCGACAAAGGGATGGGTGCAGTACGTGGCTGTGCAGAGACTGAGAGGGATGGGGGAAGAGCCAGTTATGCCAGCCAGAGCAGTGGAAGGGGTAGTGTAGGACCCTATGGACATCTTCGTCAGTCTCTGTCTATCACCCCAACCTTACTCAGCTCGCCAGAAACCACAGAGGAGAGCGAGAGGCACAGGGCAGAT
Associated Phenotype:
Not determined