ZMP
LOC572386
Ensembl ID:
Human Orthologue:
DOCK10
Human Description:
dedicator of cytokinesis 10 [Source:HGNC Symbol;Acc:23479]
Mouse Orthologue:
Dock10
Mouse Description:
dedicator of cytokinesis 10 Gene [Source:MGI Symbol;Acc:MGI:2146320]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30681 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28389 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22573 | Nonsense | Available for shipment | Available now |
sa10579 | Essential Splice Site | Available for shipment | Available now |
sa22572 | Essential Splice Site | Available for shipment | Available now |
sa15724 | Essential Splice Site | Available for shipment | Available now |
sa11003 | Nonsense | Available for shipment | Available now |
sa28388 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11297 | Essential Splice Site | Available for shipment | Available now |
sa1133 | Nonsense | F2 line generated | Not yet available |
sa45526 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35788 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30681
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 22 | 1969 | 1 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1975118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 2022240 |
GRCz11 | 15 | 1985812 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCCCAGAGGGAGCTGATGAACATGCTGAATGTCTGCTGGTCAGACAG[G/A]TAAGTGCATGTGTGCGTGCGTGTGTGCGCATGTGTGTGTGTGTCAAAAAT
Long Flanking Sequence:
GTGATCAGAAGCATGTGAGCACTGTCCTATAGCTGCTGAATTCTGAATGAACTGTGCTCGATGAAGCTGCTTATCAGGGATGCCAGATAGGAGAGAGTTACAGTAATCAATTCGTGATGCAACTAAAGCACGAACAAGTACTTCAGTACTTTGCTGAGGTCACATGACACTCACATTCATGAATTCGGTTGTGTTGCATTATGGGATAGCGTAGTGTACATCGGATGTGCACTGCAGAATCTCATCGGAAGTAGTAGATAATCAGGATACTTTTCATCTGTTTTTTTTTCCATACCACGAATTTGGACAAAGTACTACTCTGCTCTCATGCTGTTTCTAAGATATTAAATAGCAGGGAAGTATGTGATTTCAGACGCAGCCTTTGATTCTCTGTTTTTTTTTTTTTTTAGGTGTCCACACTTCCTGTAGAAAGGAGAACAGTGAAGTCTACTGTCCCAGAGGGAGCTGATGAACATGCTGAATGTCTGCTGGTCAGACAG[G/A]TAAGTGCATGTGTGCGTGCGTGTGTGCGCATGTGTGTGTGTGTCAAAAATCATACTTACAGCATCAGGACCTTTTGACGTTCAAATTTCAAAATTCAAATTTGACATTCAAAGTTTCCTAAAAGGGTTTGGGTTAGGGCTGGGGTAAGGCCACATAAAAAGCAGTTTTTACAATATAAATTATATTGCGCCTATAGAGTATAGAATATAGAGTCCTCTTAACCATATATTCAAGTGTGTATGTGTGTGGGTGTGGATTTGTTTGAGGTTTACGACAACATTATATTGTTTGACGTGTGTGATCTAGTCAAAATGCTTAAAAATCATACTTGCAGTAACAGGACCTTTGGACATTCAAATTTTGAAACCTGTTTCTTAATAGGGTTTGGGTTAGGGCTAGGGCAAGGCCATATAATGATCAGTTTTACTATATAAATTATATTATGCATATACAGTATAGAATACAGAGTCCTCGTAAACCATACAGTATTTACAAGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28389
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 167 | 1969 | 6 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1966745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 2013867 |
GRCz11 | 15 | 1977439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGAACTACCCCTTTAATGGCTAATAATTCTTGTTGGTGTGCGTAAC[A/T]GAATAATCGACTGAGGAAACATGCGTTTGAGCTGAAAATGAACGAAGTGA
Long Flanking Sequence:
TCTAAATTTAGTGCTAACGGTAGGCTCTTGTAGAAAATTATTCTAAGCTGGCAGCAGGTGAACAAAGGCTGAATATACAGCAGGAGCAGTCAGGTGCGGAATAAAACCTTGCGGGAGAGGGTGGGAGCGATACTAAAAAAAACAGTCCCGTGCAGACCTCTACTGTAAAACACTATAAAAGAGTGAAAATCTCAGCAGATAGTCTCACTCTGATTGGCTGTCGTTATTTTCCCACCATTAGTGTCTATCTTCAGCTCTGGGTTCAGCTTTGAGCTCCAGCTTGTGTTTCTTTCTTCTGTAGTTAAACACGATATTTCGAAAAAGCCTGTTACCATTGACATCCATACGGCAGTATATGTTATGGAAGTCAGTGGTAACATTTTTCTGACTAACTTATTTTGCGTTCAACAGAAACCACTTGAGATTGAGTAAATAGTAAATGTTCATTTTTGGGTGAACTACCCCTTTAATGGCTAATAATTCTTGTTGGTGTGCGTAAC[A/T]GAATAATCGACTGAGGAAACATGCGTTTGAGCTGAAAATGAACGAAGTGACATATTTTGTCCTGGCTGCCGAGAATGAGCAAGACATGGACGACTGGATCAACACTTTAAATCGCATCCTGCAGATCAGCCCTCCAGACGGCCCGGCTCAGGACCGCAAGAGTACGGACATGAGCGACTCTAAAAACGGTGGGTATTTGTCTAGCATCAAGCACTGAAGTATAGAATGAAATGATTGTTATTTATGTACATCCATTGAATTTTGCTTTACCAATTAAAAAGGAATATTGAAGGTGCAGTATGTAAGTTTGACGCCCAGTGGTTGAACTAGGTATTGCACTCCTGATTCAAAACAAACGCAAGAGCAGGTTGCCAGATTGATGACACCAACAAAGGTGTATTCTAACTAAAAGCAACAGCATATGATAGAAAGAAAATTTCCCATATTAAAAGGGTTTTTTGTCCTAACCAACACCTGAAATTTATATTTTAGAAACAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22573
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Nonsense | 636 | 1969 | 21 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1952269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1999391 |
GRCz11 | 15 | 1962963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAAGCTATCTGTTCATTAATGTTTGTTGTGCTCTGTTTGATCAGGTC[A/T]AGATTGAGTTGCCCACACATCTTCATGAGAAACACCATATACTCTTCTCC
Long Flanking Sequence:
AAAACTCTCGCTTATACAGAAATTGGGGGAAAATATACAGGGGGCGAATAATTCAGACTTCAACTGTACAGATTTTTCAGTAATCAAAACTGGAATTAATCTAACAATAAACTGAAGATCACAGGCCAAACATGAGTAGACCTAAATTAATATGTTGGTGAAAAATATTAAATAAAATGTCAATAAACAGGAAAAATCTAAAGACACACATAAAAATACATAATTTAGTTGAAGTCTTATAGTTTTTGTTGTTGTTTCAATAGCTTGTTTGACTTTAAGTGTATTATCTTTTTATTCCTAAAGATGTCTCTTATTTTAATTTATATAATCGTTTAATAAAACTCTTTTGTTTAAATGCACCAACAATTATGGCTAAATACATTGAAAAACTTGTAAAACTATTCATTTTCACTAGGGTTAGGGTTTATGCTAAGCCCTGTATATTTCAGTTGAAAAGCTATCTGTTCATTAATGTTTGTTGTGCTCTGTTTGATCAGGTC[A/T]AGATTGAGTTGCCCACACATCTTCATGAGAAACACCATATACTCTTCTCCTTCTATCATGTGACCTGTGACATCAATGCCAAGACCAGCTCTAAGAAGAAAGAGGCTCTTGAATTGCCAGGTATCACCCGTTCAGCACAAAACCTGTCTTCTGCATATGTAAATTGAACTTAAAGGGGTCTTATTATACCCCTCTTTACAAGATGTAAAATAAGTATCTAGGGTGAATGTGAAGATGTGAAGACCTAGATGTGAAGTTTCAACTCAAAATACCACTCAAATATTGTTTATAACTCTACGAAACGGACCCTTTTAGGCTTTGATCCTAATTTTGGTGACTGTCGCTTTAAATTCAAATGAGATTGTGCTCTTTTCAGAAGTGGGCGGAGCTACAAATGCCTGTGTGTCAGTATAGTGGCAGATTCAAAAACAAGACTAACGCCCTATGCTAATGAGGGGTCACTAGTGGGCGGGGTTTTCCCCCTCTGATGACACATACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10579
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 676 | 1969 | 21 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1952147)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1999269 |
GRCz11 | 15 | 1962841 |
KASP Assay ID:
2260-8048.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAATGCCAAGRCCAGCTCTAAGAAGAAAGAGGCTCTTGAATTGCCAGG[T/C]ATCRCCCGTTCAGCACAAAACCTGTSTTCYGCATATGTAAATTGAACTTA
Long Flanking Sequence:
AGGCCAAACATGAGTAGACCTAAATTAATATGTTGGTGAAAAATATTAAATAAAATGTCAATAAACAGGAAAAATCTAAAGACACACATAAAAATACATAATTTAGTTGAAGTCTTATAGTTTTTGTTGTTGTTTCAATAGCTTGTTTGACTTTAAGTGTATTATCTTTTTATTCCTAAAGATGTCTCTTATTTTAATTTATATAATCGTTTAATAAAACTCTTTTGTTTAAATGCACCAACAATTATGGCTAAATACATTGAAAAACTTGTAAAACTATTCATTTTCACTAGGGTTAGGGTTTATGCTAAGCCCTGTATATTTCAGTTGAAAAGCTATCTGTTCATTAATGTTTGTTGTGCTCTGTTTGATCAGGTCAAGATTGAGTTGCCCACACATCTTCATGAGAAACACCATATACTCTTCTCCTTCTATCATGTGACCTGTGACATCAATGCCAAGACCAGCTCTAAGAAGAAAGAGGCTCTTGAATTGCCAGG[T/C]ATCACCCGTTCAGCACAAAACCTGTCTTCTGCATATGTAAATTGAACTTAAAGGGGTCTTATTATACCCCTCTTTACAAGATGTAAAATAAGTATCTAGGGTGAATGTGAAGATGTGAAGACCTAGATGTGAAGTTTCAACTCAAAATACCACTCAAATATTGTTTATAACTCTACGAAACGGACCCTTTTAGGCTTTGATCCTAATTTTGGTGACTGTCGCTTTAAATTCAAATGAGATTGTGCTCTTTTCAGAAGTGGGCGGAGCTACAAATGCCTGTGTGTCAGTATAGTGGCAGATTCAAAAACAAGACTAACGCCCTATGCTAATGAGGGGTCACTAGTGGGCGGGGTTTTCCCCCTCTGATGACACATACAAAGGGGAATGTCAATCAAAGTGTTTCTGCAGACTGTTTCTATCAAGTCTGATTATAAAAACATACAATTAATTCATTTGTAACATTCAATCTACCATTAGATTGGCCATTTATCGTGTGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22572
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 745 | 1969 | 24 | 58 |
ENSDART00000112946 | Essential Splice Site | 745 | 1969 | 24 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1948374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1995496 |
GRCz11 | 15 | 1959068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATCTTCAAATTGTCCACTTTGGTGCTTTCTACAGTGTATACTCAGG[T/C]TTGGAGAAAAGACACAATTTCAGATAAATATTATATTGTTACGCTGCAGA
Long Flanking Sequence:
GGGCAAAAAAAAATGTTCCACTGATCTAATGTGGCAATAAGATCGTAACTGTACTGTGTATTTGCACAGTGGCCATATTCATCCAAACACACAAAAACAGCATTAACATTATAGCAGACACTATAAAAAGCTCATTTCCAGCCACTAGACTGTTCTGACAGGGGATTCCAGTGTCAGATGTGAAAGTATGTTGTTAGACTAGTGATCAGGAGTTTTTATTATGGATTATAGACTGCCAGATTTAGAAATGTAAAGGTGATTATAATGGAAGTCAATGGAGCAAAAACAGCCACCAGCAAAATGAAAGGGGAGTCCATTTGAAGAGTACACAAGGGTTAAGACAGATAATTATTTGCATGTAACATGTTGTAGTAACAGATTTATTTAGGGGTTTTTTTTTCTTGGTTGTTTGCAGAATGGCTCTGATGTGAAGTGGGTCGATGGAGGGAAGCAGATCTTCAAATTGTCCACTTTGGTGCTTTCTACAGTGTATACTCAGG[T/C]TTGGAGAAAAGACACAATTTCAGATAAATATTATATTGTTACGCTGCAGATAAATGCTCTTCTCACTCAGAATTCACATCTCATTTCTAGTCCAAATAAACTCTTAAATCTTTTTTGAGACAAGTAAAATATATTGGCTTGTTCTCAGAACTAAGCAACCCAGGCTCATTCTGAAATTGTAGCCCTGTATACATTTCTGGAGATCGCGAATTATGTAGCCAGAGGTACGTATGGCTGCATTTCATCTTTAAAACGAACACTACAGGGCGGTATGACTGCATTAATATTCGTGCTAGCCGCTGACTGCTTACTTCTATGTGGACGGCTTTCCCCGCTGTTACCAGTTTGTCCAGTGACTCGCCACGTACATTGGCGGACTTGAGACGCAGAGTGGAGTTAACTGCGATGACAGGGTTTGAGTCCAGCAAAGAACTGTTCCAGAAGGCGTTTAACACAAAAGCAAAAAATAAAATATTTTCAATCCTTGTGAGAATGTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15724
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 745 | 1969 | 24 | 58 |
ENSDART00000112946 | Essential Splice Site | 745 | 1969 | 24 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1948374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1995496 |
GRCz11 | 15 | 1959068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGATCTTCAAATTGTCCACTTTGGTGCTTTCTACAGTKTATACTCAGG[T/G]TTGGAGAAAAGANCACAATTTCAGATAAATATTATATTGTTACGCTGCARA
Long Flanking Sequence:
GGGCAAAAAAAAATGTTCCACTGATCTAATGTGGCAATAAGATCGTAACTGTACTGTGTATTTGCACAGTGGCCATATTCATCCAAACACACAAAAACAGCATTAACATTATAGCAGACACTATAAAAAGCTCATTTCCAGCCACTAGACTGTTCTGACAGGGGATTCCAGTGTCAGATGTGAAAGTATGTTGTTAGACTAGTGATCAGGAGTTTTTATTATGGATTATAGACTGCCAGATTTAGAAATGTAAAGGTGATTATAATGGAAGTCAATGGAGCAAAAACAGCCACCAGCAAAATGAAAGGGGAGTCCATTTGAAGAGTACACAAGGGTTAAGACAGATAATTATTTGCATGTAACATGTTGTAGTAACAGATTTATTTAGGGGTTTTTTTTTCTTGGTTGTTTGCAGAATGGCTCTGATGTGAAGTGGGTCGATGGAGGGAAGCAGATCTTCAAATTGTCCACTTTGGTGCTTTCTACAGTGTATACTCAGG[T/G]TTGGAGAAAAGACACAATTTCAGATAAATATTATATTGTTACGCTGCAGATAAATGCTCTTCTCACTCAGAATTCACATCTCATTTCTAGTCCAAATAAACTCTTAAATCTTTTTTGAGACAAGTAAAATATATTGGCTTGTTCTCAGAACTAAGCAACCCAGGCTCATTCTGAAATTGTAGCCCTGTATACATTTCTGGAGATCGCGAATTATGTAGCCAGAGGTACGTATGGCTGCATTTCATCTTTAAAACGAACACTACAGGGCGGTATGACTGCATTAATATTCGTGCTAGCCGCTGACTGCTTACTTCTATGTGGACGGCTTTCCCCGCTGTTACCAGTTTGTCCAGTGACTCGCCACGTACATTGGCGGACTTGAGACGCAGAGTGGAGTTAACTGCGATGACAGGGTTTGAGTCCAGCAAAGAACTGTTCCAGAAGGCGTTTAACACAAAAGCAAAAAATAAAATATTTTCAATCCTTGTGAGAATGTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11003
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Nonsense | 776 | 1969 | 25 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1946446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1993568 |
GRCz11 | 15 | 1957140 |
KASP Assay ID:
2260-8046.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAGGCRGAAATCTCTCAACCTCCTACCTCAAACTTCCTCAACTGCCTT[A/T]AAGTAAGTGTACTGACCAAATCMGTGAGGTCTGGATKGTYTTTTTGTAGG
Long Flanking Sequence:
CGCCATTCGCGCGTATCGCACCGCAGGAAGTCTATTCGCGCATTTGCATTGACTTAACATGTAAATCACTCACGCTTGACGCACGTGCCGCGTCTGGTGTGAACGCAGCATTAGAAGAGAGCAAAATAATCTGCCAGTGGGGTGAGCAAAATAATTAGATTTCAAATTGAAAACAAGATTATTTTGCTTAGCCAACTGGCAGATTTTTTTTTGCTTGTTTTAAGAAAAAAGGCACTTCATTTTGACTCATTTCTGAAACCAAGACTAAATATTTTACTTGTAAAAAAAATGGTTCTTGATTTAAGAACTTTTAAATATTTGGACTAGAAACGAGACAAGAAAAGCATTTATTCCAGTGTATATTGCTCATATATCCAATGATCTCATAAATCCTATCATCATTTTTGCAGGATCCCCATCTAAACCGCTTCTTCCAGCAGTGCCAAAAACGAGAGGCAGAAATCTCTCAACCTCCTACCTCAAACTTCCTCAACTGCCTT[A/T]AAGTAAGTGTACTGACCAAATCAGTGAGGTCTGGATTGTCTTTTTGTAGGTGCGTTAATGGTGTATATGCACACACACTTTTCATGGGTCAGCCAGCCCAAGCACTTCTGGTGAACTGTTGCACCATTACAAAATCTCCACGTTTAAGGTCTGATTTCTTTAAAAATGAGTGATGTGCACTACCTGATTGATTTACAATATAAAGTGGGTCCCACACAGAACAAGAAACCCTGCATTAAAATACATTTTCCCCTGCCATGCCTTTAAAATATGAATATTTTACTAAAGTATTTTCAATGGAGTTTCTGTGCTAGCCTGATGCTACTGATGGTACTAATGTTTACACAGTCTTTCATCTGGTTTTACACTTGAACAACTAAATGAATGCTTAAGTCTATTTAACTGCATGTATTTTAATTACATTACAAAATTGATGCTGTAAAAGAAACTTATGAAACTGAAAATAGTCACTATAACCTTTCACTAGAAGTTTATCGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28388
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 902 | 1969 | 29 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1940569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1987691 |
GRCz11 | 15 | 1951263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATAGTGAAGTCAATGGCTCAGCATCTGCTGGACTCAAACAAGCTCAAGG[T/A]AAATCTAGTCGCTTTGCTAAATGACTAAACTGTGAGTCTGTTCAACTTGT
Long Flanking Sequence:
CTTCTTTTGACAAGGTTTAGATATTTACTGTTTGACAAGGTAATTTGAAGTGTTAAGTTATGGATTATGATTACAGTCGAAACAACTGTACATATTGCTATAAAGAGACTACACAAAAGCCTTAACATTTTGTGTGATGCAGTGTGCAGTATTACCCCTTTGCTTCTGTGCACAATAAGCATCATGGTGAATTTGTAATCTTTTTTTAATGTTAATTTTTTTTGCTTTTTTCCGCATTTTTTCCGGCGGTCATTTTTGACCACAAAGACCACAAGTGTGACTTAGCCAGCTTAAATCATGGCCTAATTTTTTTTGTGTGTTCACATTCTGAAACCACTTGAGGGTGAGTCAATAGTGAGTAAATAGTTCATCTTCGGGTGAACTATCTCTTTAAGTGTTTACTTTAATATCTGTTTTATTTTTGCAGTTCTCGTGGTTCTTTCTCGAGATCATAGTGAAGTCAATGGCTCAGCATCTGCTGGACTCAAACAAGCTCAAGG[T/A]AAATCTAGTCGCTTTGCTAAATGACTAAACTGTGAGTCTGTTCAACTTGTTTACACTGTAAAATAGGCAGGGTTTCACACAATTCATTCAAGTTGTCTCAACACAAATCAGTTAACTTAACTGTTTAATGTTCAGTCCACTTAAATTAGTTAAGTTGTCCCCCCAAAAAATCATAAGAATTATTGTGTTGTTTCAGCTCATTTTGTATAAGTAGTTTGAACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGAAAATGGAAAGCAAGCTAATAATAATAACAATAATAATAATAAAATACATATCATTCCAGATTTTCAGAGTTAATAAATAAATAAATAAACATATTTTTTATTAATTAATTATTTAATTTTTTATTAATTTGTTTGTTTGTTTATTTATTTATTAACTTTGAAAGTCTGGAATGATATGTATTTTATTATTATTATTATTATTGTTCTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11297
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 1112 | 1969 | 35 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1933887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1981009 |
GRCz11 | 15 | 1944581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTTTTCCTCAGAGAWCTGTTTCCAAKCTGCCTGACRGCGAGTGACCAG[G/A]TACACACACTTTAAACTATACTGTAGCCAGGTATGAGCTTTCKGACGCAG
Long Flanking Sequence:
TCGCTTTGCAGGATGAGCAAGATCTGAGACACATCGCTCTGGCCTGCCTGAAGAACCTGATGGCCAAACACTCGCTGGACGCTCGATACGCCACAAAGGTTACCTTTCGCTCACTGCTACCAACTCACAACTCTGAATTTACTGTCACTCTGCATTAAAAGAACACCTTGCACAAGGTTGTTTATTGTAATTTGATAAAAAATACATCTTACAAATTTTGTAAGATGATACAACACAAGGTATAGCTTTATTAAAAAATCAAGATGTTAAAAACTTTTAAGGAATTAAGATGCTGATGACCGTTAAACATGTTATCACTAACTTGTGAAAAGGCTGCATAATAATAATAGTAACCCATTGTTTACTGTATTGTGTTTGTGCAGGAGAAACAGGCTCGGATAGCTTCTCTTTACCTGCCGCTTTATGGCCTGATCCTGGACAACATGCCTCGGTTTTTCCTCAGAGATCTGTTTCCAATCTGCCTGACAGCGAGTGACCAG[G/A]TACACACACTTTAAACTATACTGTAGCCAGGTATGAGCTTTCGGACGCAGCATGATAGTGTTACTTCAACATATTTCCTTCACAGGGATCCAGAGATGATCTCAGTGTTGGAGTAGGTTTGGGTGGTCAGGTGACCCATGTTTTACGCCATGGAAACTCAATGGACGCGTCCTTCTCCAAGGAAGTGCTCAACTCCATTACAGGTATTTATGATGGTAGATCGACTGTCTCCTTGTGTGGATGTGTTTCATTGACTTCCGCCTTATTAGTATACTTAAAGGGACAGTTCACCCAAACACTTTAGGTCACAATTCACGGTATCAAACTAACACTAGCTTAATAAACTACTAATTAGCTGTTTATTAATAGCTAGTAATATAGAAGTTGGGTTTAGGAAAAACCTGCAACAACTGACTTCCATAGCATTTGTTTTTCCTAGTATGGAAGGCAATGGTCACATGTGTCCAGCATTTTTCAAATTATCTTCAACTGTGTTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1133
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112946 | Nonsense | 1637 | 1969 | 52 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1904106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1951228 |
GRCz11 | 15 | 1914800 |
KASP Assay ID:
554-1044.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGCTCTGTAGGACACGCTGGTGGAGCAGCTGGAGATGTGTGTTGATTA[T/G]CTCTGGAAGTCTGAGAGATATGAACTTATTGCCGAGATCAACAAACCTGT
Long Flanking Sequence:
AGCGTGGTAAAAATCTGGCAAGAGGTTTTCTTTTTTCTGGATTGCTTTTGAAAACACTGTTGGATGGGTTTAGGGAAGTGGTTGGGCGCTGGTCAATCTTTTTTTATAACACTGTCATTTGGTTTTAGGAAAGTAGGTGGGAGGGGTTATCGGTCGATCATTTAGTCAGTCATTCAGTCGACAACGACCTCTAGTGGATTTACATGAGAACAGCAGGCACGAATAGCACTTGCAGGAGAAATTTGAGATCAGAAAAAACATACACAACGGCCTCTGGTGGATTTGTTAAAACATAAACCGCAAAAAAACGTAGCTCCTGGGCCGTATTTGGTGCTCTCCAGAAATGTATGTGGGGGCACGTATTCAGAATGAGCCTGGGTTGTTATTTCTGCACACTTTTTAGAGGAATATGAGCTTTAAATGTGTTTCACAGACAATGAATGATAAATGTCTGCTCTGTAGGACACGCTGGTGGAGCAGCTGGAGATGTGTGTTGATTA[T/G]CTCTGGAAGTCTGAGAGATATGAACTTATTGCCGAGATCAACAAACCTGTTATTGTCGTCTTTGAGAAGAGAAGAGATTTCAAGGTACTACGAATGTTGAATGGTGGACTATAATATACAGTCGAAAGTAATTGTATTAGCAGCCCTGTGATACTTAATAAAAAATTATATATATATATATATTTATTATATAAATAAATTATATAATTATATAATTATTAAAAAAAATATTATATAAATTTATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTTTATAAATTTTTTTTTCTGATTTTAATGGAGAGAAGAAATTTTTAAACATCATTTTAATAGCTGATTTCTTTTGTCTTTTCCATGGTATTCAATTCAGTCCATGTTACGACTCCAAATCAGAAAAAGTTGGGAGAATATGTAAACACAAATAATAAAAAGAAGTGATTTCTAAATTAACTTCGACATCATTGCAAACATTACAACAAACATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45526
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 1823 | 1969 | 56 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1892469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1939591 |
GRCz11 | 15 | 1903163 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCTCTAGACATTTACATATTTATATTGTGTGTGTGTGTGTGTGTGTT[G/A]CAGCGAGCTCTAGTTTCCCTTTCTTGAAGAAGCGTATAGAGGTGGTGGAG
Long Flanking Sequence:
ATTTAAAGGCTCCTCAACTGAATTTTTTGCTTTCATTGAACAAACCGTTCCAAACATGCAGTTCAATCATTTTTATGAGTAAATCAACTCTGAGCTCAAAAATAAGTCCACCTAACTTACAAAACTGAGTTAACAATTTGTAAGTTAGATTTTTTTTACAGTGTACTTTAAAAAGCGAGTAAACTCACATTGCTTTAAAAGTTATTAGTTAACTTTGAGAAATTAGTTGACTTTAAAAAGTGAGTAAAATTGTTGAAAATACTTCTTGAAATAAGACTTTTTAGATATTTGGACTAGAAACAAGACAAAAAAAAAACTAAACAAATAGAAAAAAAAAATTTAACAGGAGGGCTAATAATGCTGACTTTAACTGTATATAATATATAGAAACACTCTGACATATATATTTTATTCATATTGTGTGTATGTATGTGTGTGTGTGTGCTGCAGTAAGCTCTAGACATTTACATATTTATATTGTGTGTGTGTGTGTGTGTGTT[G/A]CAGCGAGCTCTAGTTTCCCTTTCTTGAAGAAGCGTATAGAGGTGGTGGAGCAACAGAGTACCGAGATGAACCCTATTGAGGTGGCGATAGACGAGATGAGCCGAAAAGTGTCTGAACTCAAACAGCTGTGCAATATGGAGGAGGTGGACATGATCCGTCTGCAGCTCAAACTACAGGGCAGCGTCAGCGTCAAGGTAAATGCAGGATATATATGAGCAATATATGAGGGCCTTAGAGTCTCACCAGTGCTGATATACAGCCATATCGCACTGCAACTCGTGCAATATTGCATATATACAACAGTTCGATGGCACAATTGTGTAAATTAAAAATGAAAATCAAACACGGAGAGTCTCCTTTTGTAAGAGGAACTACTTTCTTCGGCCATTCATTTGAATGAATAGTGTTTGAATGACTCTCTAGCGTAATGTCTGAAGTGAAGACAAAACAGCTGATTTTGCTCGCATTGTAAGATTATAAGGCTGAACAGCATGAAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35788
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 |
---|---|---|---|---|---|
ENSDART00000112946 | Essential Splice Site | 1922 | 1969 | 57 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 1891516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1938638 |
GRCz11 | 15 | 1902210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAGAAATACCCAGACAACCAGGTCAAACTGCTGAAAGAGATCTTCAGG[T/C]ACTGCTTCACTCACTGATCCTATCATTAATACATCCATTTTGTTTTTAAC
Long Flanking Sequence:
TGATTTTGCTCGCATTGTAAGATTATAAGGCTGAACAGCATGAAATGCCATCAGTCTGCAGAGATTTCCCAGTATTTCCCTGTTGCAATCAGGAGATCACAATAATTAACCCTGAAAAAGCCGAAGCAAAGTAAACACTACTAGATTACTGTGGTGTAAATACAGCACTACATCATACAAAAGACAGAGATTGACTTAAGATTGTCACTTACCTGATTTATAATGATTTTTTCAGCTGTAGTTTGAAACAGAGTTTATCATGCGGCCTCTATTGCTATCTTCAATAATAATAATAATATGAATAATTACACAAATAAATAGCTAATTACCTATATTTAATAAGATTGCAAAATTCCAACGTATTCCATGATTTATTTTAATTTGTTTTATTTTTTCAGGTAAATGCAGGACCCATGGCCTACGCCCGAGCCTTCCTAGAGGAGAAAAATGCTAAGAAATACCCAGACAACCAGGTCAAACTGCTGAAAGAGATCTTCAGG[T/C]ACTGCTTCACTCACTGATCCTATCATTAATACATCCATTTTGTTTTTAACAGAAGTATTATTGACAGCTGTAATTTGTTCATGTTCTTGTCCTGCAGACAGTTTGCAGAAGCGTGTGGACAGGCTCTGAGTGTGAACGAGCGGCTAATAAAAGAGGATCAGTTTGAGTATCAGAGCGAGATGAAAGCTCACTATAAAGACATGCTCACGGAGCTCTCCGCCATTATGAATGAGCAGGTCAGCACACACACACACACACATGAAAGTCTTCATTAAAGTATCTCGAGTGTTTAGTAAATTTTCAGCTCAAAATACCACACATAACCTTTTCTAACTCTCTGAAATGGACCCTTTTAGCCTTTGAACCTAATTGTGGAGTATTAGTGACTGTCGCTTTAAATGCAAATGAGATTGTGCTCTTAAGAAATAGGCGGAGCTGCAAACACCTGTGTCTCAGCATAGTGGCAAATTTAAAAACAAGACTAACGTCCTATGCTAATG
Associated Phenotype:
Not determined