ZMP
stab1
Ensembl ID:
ZFIN ID:
Human Orthologue:
DOCK9
Human Description:
dedicator of cytokinesis 9 [Source:HGNC Symbol;Acc:14132]
Mouse Orthologue:
Dock9
Mouse Description:
dedicator of cytokinesis 9 Gene [Source:MGI Symbol;Acc:MGI:106321]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33829 | Essential Splice Site | Available for shipment | Available now |
sa26704 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20666 | Nonsense | Available for shipment | Available now |
sa33828 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10789 | Nonsense | Available for shipment | Available now |
sa20665 | Nonsense | Available for shipment | Available now |
sa15473 | Essential Splice Site | Available for shipment | Available now |
sa26700 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13975 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33829
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Essential Splice Site | 38 | 2074 | 1 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12634165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12487387 |
GRCz11 | 6 | 12722245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCTTGGGGAGATGGAGGTGGATGGGGACACAGCAATGCCTGTTGGGG[T/G]GAGTCTCTTATGTGGACATAAAAAAAAACAAAAAAACATGTTTAGTATGT
Long Flanking Sequence:
GGTGAAACAGACAGTTAAGATCTCTGTTTCAGCGCAGAGGGAGGACAGATGAGCGTGACATAACACAATAGTGGACACACACACACACACACACACACATACACATGCACTCCCCCATACCAGAACAGCTGTGTGAAGGAGTGGTCTCTGCTTCTCCCATGCAGGGAAAAAAAAGAGAGCGAGGGAGGGACTGAAGTGATAGAGGAAAACACTCTTGAAAACTCCACATGGTAAAGTTCAGCTTCAGAGAGAGAGAAAAGTGGAAGAACAGAAGGAGTGCAGGAGAAGTGTGCAGTGCTGTTTGTTCAGTCCTAGCCTGGGTTTTATTTCTGTGCCTGTCGTTGATTTGAGTTGGGTTTTCTGGAGGGATTGTGTGTGGTGGATCATGCAGGGCAAGGCTGGACGAGCCGCCCGTAAGGATGCAGTGTGTGAAACACCTCAGCAGGGCAGGACTCTTGGGGAGATGGAGGTGGATGGGGACACAGCAATGCCTGTTGGGG[T/G]GAGTCTCTTATGTGGACATAAAAAAAAACAAAAAAACATGTTTAGTATGTCTGTGGTTGTTGAGGCTAGACTTAAAAGTTAGACTGTCAGAAAAATAACAATTTGTATTGTTAGGCAGTGCCTGTACTTTTGTCTTAAAAAGTGCATTTTAGTAGCTTGGAGAAGTAATATGTAGCCTTAAGGTACTGTTGCAAACTTTTATGGGCAAATAAGGTACAAAGATCATCAATTCTGACATTTTTTTCAAGGATTACTAAACTTCTTCTTTATGACAGTTACACAGAATAGTCAATTCAATTTAAATATGAAATGTAAGACTAAAACTACACAAAGAAAAAAAAGAAATGATATATTAACAGAATAAAGTTTAGATTCAAATTAAGATTAAATGCAACAGGTTTATTTTACTGCCTTAGTAATATTTTAGTTTTATTAATTGTTTAAATTAGTTGTATTTTTCTCTTAATATATCTCTTTTTTCTCTTTTATATATTTTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26704
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Essential Splice Site | 77 | 2074 | 2 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12625822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12479044 |
GRCz11 | 6 | 12713902 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCGATGTCCTCAGAGACATGCTTCAGTTTCCCATCGATGACTTCCAG[G/A]TAGGAACGTCAGTTCATCTCTCAAACCATCTGCTCTCCCATCAGTCTTCA
Long Flanking Sequence:
TGGAAGGATTCAGCCTTTAACTAAGCAGTAGATCTGCATAAATTATAATTACTTACAAGCAAAAATAAATTAATAAACAGCGCTTATTGGTTTTCTGCAGACTCTAACAGTATTTAAGAAGAGAAATTGAACAATCAAACGTTAAATAACATGGTCATCATTGTATAAATAATTTTTTAAAATAATATATTTAATTGTATCTTTATCTTTTAATCTTTAATATACAATTTAATAATGCGATGTGACTTTTGCAGACCCACACATTGCAATATCGATGCTTAAATCATATATTGTCCTAATTTAAAGTCCTGAAAATATCATTATTTCTTCTAGTTTGCTCTTGTTAAACTTAAGCACATGTATGCTTGTGTGTTTGTCTCCAGGTGAAACCCAAAGTGATTGAGCCGCTGGACTACGAGAATGTTCTCGTCCAGAGGAAAACTCAGATACTCAGCGATGTCCTCAGAGACATGCTTCAGTTTCCCATCGATGACTTCCAG[G/A]TAGGAACGTCAGTTCATCTCTCAAACCATCTGCTCTCCCATCAGTCTTCATTCCTCCATTCCTCCTTCTCATTCCTGTCATTGTTTTCTGTTCTCTTCTTGTCACACCCACACTGCGATTTCCTCTAAAGTGTTATTTTTTCAGCGTGATTCTGAGAGCTGAATGATGAGTAACCTGTGCAGATGTGAGTTTTCTCAGTCTCTCAGTGGCTCGTCTTAGGTTTGCTTCCTCCCTGGGCTCACTAGTCAAACATCTCTCGTCTTCCCTCAAATAGCATTAGAGTAACAGTGTCTCAGGGGATCTCTCGAACTGCTTCCCTGAATGAAACCGTCTCGTTGTTTTCCTTTAGAAATGGGTGTGTATGCTGGAGATTATTGTTATGGGATGTGGTTTATGGGGAACAGAAACATGAAAACTGTGTTGTGCAAACAGCTGCCTGCTTAGCCGAAACCAAACATTCGTAACTCAATTATAAGATTAGTGTTCGGAAATTAGACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20666
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Nonsense | 675 | 2074 | 19 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12590138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12443360 |
GRCz11 | 6 | 12678218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTCTTTATATAAATTATGTTGTGTTTGTGTGTTTTTGCTGAATAGTG[T/A]ATCTATGGTCGTCCAGGAGGGCCTGTCTTTACCAAACATGCCTATGCAGC
Long Flanking Sequence:
CCAATGATGGTGTCCTGTTGGAGGTGGAGGAGTTTGTTCCTTGTATCGCCAAGTGCTCTCAGCCTTTTACCACCTACAACAATCATCTCTACGTCTATCCCAAACACCTCAAATATGACAACCAGAAGTCCTTCGCCAAGGTACATTAGCATTATCTATATCTATATAGCTCGTCAAAACTGCACTTACAGATTCACCAGTATATGTTTTTTTCTGGCTCATATTTTCTTCTCTCTCATGTGACTCAGGCGAGGAATATTGCAGTATGTGTGGAATTCAGAGAGTCGGATGAAGAGGATGCTCAAGCCTTAAAGGTATATTGTTTATTCCAGATATACAGTAGAAGCTATATTTAATATACAAAGTGCTTCTGGCAAGTTCTATTGGAAAACAGAAAACATTTCCCAATATTTTCTGTTCTTTCATATTCTCTACCGTTGAAATCAGAGTAATTTCTTTATATAAATTATGTTGTGTTTGTGTGTTTTTGCTGAATAGTG[T/A]ATCTATGGTCGTCCAGGAGGGCCTGTCTTTACCAAACATGCCTATGCAGCTGTACTGCACCACCAGCAGAACCCAGAGTTCTATGATGAGGTGATCAAGGGGACACTGGCATACATTTTATATGGGGTGCAGCAGAAAATAATCATAAGATAAGAAAATGTATACAATATGTATACAGTATACAGTTCGTGACCCTGGACCACAAAACCAGTTTGCATGGGTATATTTTTGGCAAAAGCCAATATTAAATTGTTTTGGTCAAAATCATTGATTTTTATTTAATGCTAAAAAAATGTGAGTAATATGTAAAGGTGTTCCTTGAAGATTTTTCAGAGTACCCGCGGGGTCTTAAAAGCATTGAAAAAGTCTTACATTTGATGATCTCAAATTAAGGCCTTAATAGCCTTGAATTTGGTATACAAAGTCTTGGATTTTGTTACAAAGGTCTTATTTTATTCATTTATTTTTGCTTTCCCTAGGATTAAGTTCATTGTTACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33828
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Essential Splice Site | 782 | 2074 | 21 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12587809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12441031 |
GRCz11 | 6 | 12675889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAACCTACCAAATGGTTACCTCAGCTGCCAGGAGGGAGTAAGCAAGG[T/C]AAACCTTCTCTGCAGTCATAACAGAAACTTTTTTTGAGATTACAGGCATT
Long Flanking Sequence:
TCCTACATATATTTCGAATGTATTGCTCATGTTTTAGGTATATTTAAGTTCATAAAAAAATGTTATATGTCTTTGTGTATGACCTACAGATAAAAATTGAGTTGCCCACACAGCTACATGAAAAGCATCACCTGCTGTTCACTTTTTACCACATCAGCTGTGACAGTAGCACAAAGAAACGGGACATAGTGGAGACCCCAGGTACGGCATGCTGCATAATTGACTTAATGAACAATAATGAACAATACACAATTGCGGTATGCACTGTGGTTCCAGAAATGCACTTATTTAGAAATTTTATCTGATTATGACTAACGTTTTTGTTGTATAATTAATGAGTGCCATTGGATGAGTTGTGTTTGCATCTGTGTCTCTGTTAGTGGGCTCTGCCTGGCTTCCTCTGCTTAAAGATGGTCGTGTTGTTATGAGTGAGCAGCACATTTCTGTGGCTTCCAACCTACCAAATGGTTACCTCAGCTGCCAGGAGGGAGTAAGCAAGG[T/C]AAACCTTCTCTGCAGTCATAACAGAAACTTTTTTTGAGATTACAGGCATTTGCTGGCCAAATGTGAACCTGCAGTGCACTCTGTCCAGTATTTGGAACCTTATTTCTCTTTGTGTTGCTATTTGGACATCTACAACTTTATGCTAATTTATGCTAGCAACATGTTATTAGCATTCTAATTCTTTCTATCAGCATGTTAATAATGATAAAATATGCTAGCAGAGTGGTAATTCATACTAGAAATAGAGTAATCACATTTATTTGGTATATGGAAACACTGTGCTAATTACATACTCAGAACTTGCTACCAACATGTTAGTAAATGGTAAAACATGTTAGCAACATGATAATTCATACTAGCATCCTGCTAGCAGCATGTCAATTTATGCTAAAACATGTCATAAAGTAAGAAACATAACAGCAAAATCTTTTGCTAGCAAAATGCTAATTTATGGTAAAATATGTTCATTAAAACCTTGCTGAAAAAACAGCTTAAACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10789
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Nonsense | 1040 | 2074 | 29 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12580321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12433543 |
GRCz11 | 6 | 12668401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TKCATGGACAGAGGATTTGTCTTCAAGCAGATAAACAATTACATMACCWG[T/A]TTTGTTCCTGGAGATCCTAAGGTACACATRGTGAACTATTTATATTATAG
Long Flanking Sequence:
GATGCTTTTGGGAAACGCAGCCCTTGAAAGTTCCAGCAAAGTATATTGGAGCTAAAATCTACTGTATAATGGCCTTTTAGCAAGAGGATTGAGCACCGCTGTTATTATCTCTTTTGTGTTTTGTAGGAGGTGTTGAATTACTGTAGTACTTTTTAAAGTTCCTTGTGTAATTTGTTCTTGCATGTTTAGCTGTCCAGAAACCAGCGATTCACAGCTTCATTCCATCATGCTGTGGAGACGCTGGTGAACATGCTGATGCCTCACATCACCCAGAAGTACAAGGACAATTTGGACGCTGCCCGCAATGCCAACCACAGCCTGGCTGTCTTCATAAAGGTACATACATAAAGCAGCTGTGAAGTGTCTTGATTTGACTTTCATGCATTTCTTGACCATTTGAATTCATCATTAACAGTGTTTTCTCTCACTGTCTCACAGCGCTGTTTTACCTTCATGGACAGAGGATTTGTCTTCAAGCAGATAAACAATTACATAACCTG[T/A]TTTGTTCCTGGAGATCCTAAGGTACACATGGTGAACTATTTATATTATAGCTATATGAACTGCTTAAATCTTTATCTGTAATTCAGAATCAAGAGCTGTTGTTATTAGCTGTCTCATGCTCAAAAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAAAATATTAATATAATGAATGAGTGTGAATGAGTGTGAATGGATGATTCCCAGAGATGAGTTGCAGCTGAAAGGGCATCCGCTGAGTGGAACATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCTGATTAATAAAAGAGAATAAGCCGAAAAGAAAATGAATAAATGAATCCTATTAATTAATAATATTCTTTATTTTGTGATTTTTTTTTTTTTTTTTTTGTAAATTTTTTTTGAGTTGATGGAATTTAAAAATGTAAATAAACACCCATGAAACTTCAGAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20665
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Nonsense | 1160 | 2074 | 32 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12568408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12421630 |
GRCz11 | 6 | 12656488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGTCAGCAGGCCAGGTTGGCGACGCTTTATCTACCCTTGTTTGGCT[T/A]ACTACAAGAGAACGTTCACAGACTAAATGTGAGAGACGCATCTAATTTTA
Long Flanking Sequence:
TTTCTTTGTTTCTAAAGCTATTGCCTTATACTAAATCTTATACTCTTAATGGATGTAACTATTTAACAAAACCAAATTAATATTATTTAATTTAATAAAACTGCACCAAAATATATTAGTCTATATTCTCTGAGAAATGGATAAAAATATTACTACTGCCAGTACTCATTTAAGCTGAGCACTGTAGCTGTAAAAAAAATAATTTAAATAAGCTCAAGATACAGTGCATTTTAAGTCAACGTAACCTAGTTAAATTTGTATATATTTTGGGTTTGTAGAATCATTTCAAAAACAAAAAACATGTTAAATGACCAGGTAAACAGCACCTATAGTTTTTTTTAGGGAAGAGACTCAAGTTCCCAATCACAGCACAACACAACACAAACAAGCAAAAAAAAGGTGTCATGACAGCAGGTAAATCACTTAATTGTTCTATATGTGCGTGTTTGTGCAGAGTCAGCAGGCCAGGTTGGCGACGCTTTATCTACCCTTGTTTGGCT[T/A]ACTACAAGAGAACGTTCACAGACTAAATGTGAGAGACGCATCTAATTTTAACACCAACCAGGTGAATCGTCTTTATAAACTTTGTTTTCTTCACCAGTGTATCATTCAGACCTTTCACCACACATGCCATCTGAAATGTTAGGTTGAACTCTATTTTTGTTTTCCTCAGAATGGTCGAGATGAACATCTTGCCAGCATCCCTAGCGCTACGCCCCAAAAGCCTGTTGGTAATCTCGACAACAGCCTACATAAAGATGTATTTGGGGTCATCTCAGGAACTGGTGAGTGTTGACGGAATCATAAACACACAGCTCAAGCCTTTCAACCGCTGTTGAGATCTTCAGAAGATGTTTGTGTAAATGATATAGCTTTACTGTGTGTGTAGCCTCTCCTCACACCTCCACGCCAAACATCGGCTCTGTGCGTCACGCAGACTCTCGAGGTTCTCTGATTAGCACAGACTCTGGAAACAGCCTCCCTGACAAGACCAATGAGAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15473
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 |
---|---|---|---|---|---|
ENSDART00000090174 | Essential Splice Site | 1338 | 2074 | 37 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12560442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12413664 |
GRCz11 | 6 | 12648522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTTTGTCTACATCAGTTCAGGTATATGGGGAAGAGGTTCATTGCCAGG[T/G]AAAAAATAAAWGTTTCACYCCTAAYAGCATACATTTTTCATTGCTTTTCW
Long Flanking Sequence:
GTGAATGATTCTCTGCGTAAAGCTTTTAGATGTCCTGGTATATGATATTTTGATGTGTTTTCCATATTATACTTAATGTATGTGTGTGTGGCAGACTCAGTCAGCCTCTGCTCTGGGTAGCTCTATGCTGCGCTGTGATAAATTGGACAGAGAAGAAATCAAAAACCTGCTCATGTGTTTCCTCCATGTCTTAAAGAGCATGTCAGAAGGTAAGAATATAGACACAAGACTCTAATTGTTAGATTCTCCATACCTTCTCATAGAAATTTGCTCTTTTTTTCCTCCTAGATGCCTTATTTACATACTGGAATAAAGCTACGACCTCTGAGCTGATGGACTTTTTCACTTTAGTAGAGTAAGTCATCTGGACTGGCACTAATTAGATCAGTACTGAGCTCCTGTAACTTAATACTGAGCACTCAGTTCATCTCTCTCTCTTTCTCATGCACAGAGTTTGTCTACATCAGTTCAGGTATATGGGGAAGAGGTTCATTGCCAGG[T/G]AAAAAATAAATGTTTCACTCCTAACAGCATACATTTTTCATTGCTTTTCATCCTGAATCATGCATATTTCTGTGGGAAATCCAGGATTTTTTAAGACAGTAATCATAATCATATTTTTGTTAAATAGATAATAATAACATAAATAACATAAATAACATTAAATACATAATTATATCTCAACAGATAAGGTGCACCTTCTACATTTTTAAATGACAAACTTTTAAAGTCTGCTTTTGAATATTTAGTTTTTTATTTAAAATTGTACTTTTTTTAAACAATATTTTAGTCTAAAGGCCTGAAGAGTTCCCAGTTACAGGCATACTTCTATACGTACACATACATACATACTAGGGCTGCACGATATATCATATCAGCATTGATATCGCAATGTGAACATGCACAATAGTCACATCGTAAGATATGCAATGATAAGTCTGAATTAAAGTTGACCAGGAGCTACAGAACATGTGATTTGTAGAGTCACTGCTAAGTTCAATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26700
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090174 | Nonsense | 1706 | 2074 | 46 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12529451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12382673 |
GRCz11 | 6 | 12617531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGGAGGTGCTGATGGAGTTGTTGGAAGCGTGTGCTGATGGTTTATG[G/A]AAAGCAGAGCGCTATGAATTAATTTCAGATATCTACAAGCTCATCATCCC
Long Flanking Sequence:
TTTATTTTGCGTTTTTTATAAATGTCACATTTTTTTTTGAGTTGGAGTTGTAAAACAGGTGTATGTAAACTGTATATAACCAAAACCCGGTAAACACACTGAGATTAACCAAATCAGTAAGGAATGGCCTTCATTGCTGCGTAGTGATTGTTAACACATTAACCAACAGCTCACAGGAACAAGAAATTGGTCCCAAATGGGATATAAATAGTTATTATAGACAAAAGTTTGAATTGTAAAGCCTCACAAGGCACTTTATAAACTATCAACACTGCACACTTTAGCAAATCACTCCAATTAGAATCAATGTTGGATTATTGACATTTCTTAGATCAGCAGAAGCTTTTTGTGAGAAGATGATTTAGTTGTTCGGGGAGGTGTCATGATGGGATTGCATTAATTATGAGATACTGAGCATATAAATTTGTGCACATTTATATTGATGTCTCTCTGCAGGAGGTGCTGATGGAGTTGTTGGAAGCGTGTGCTGATGGTTTATG[G/A]AAAGCAGAGCGCTATGAATTAATTTCAGATATCTACAAGCTCATCATCCCCATTTACGAACAACGCAGAGACTTTGAGGTACGCAGAAACACACACACACATATTTATGTGAATCCAGTTTTCAAATTTTCTAGAAATACATATGCAGATGTACTGTATTAATGTAGTTTTGTGCTATTATGTAGAAACTGGCCCACCTGTATGACACATTACATCGGGCCTACACTAAAGTGATGGAGGTGATGCATTCTGGAAAGAGGCTACTCGGTACCTTTTTCAGAGTGGCATTTTTTGGTCAGGTAAGAAAATACAGCGCTTTCTAACAGTACAGCTAACACAGGCTGTTTGAATTAAATGCACTATGACAACAATATAACTGCATTTTTTAAAGGGGTCATATCATGAGGTATCAAATTTGATCTTGTTCTGTGAAAACATGTTTTGAATTTCATGCCTCTGGAGCTTCCTCCCTATTTGTCAAAAAAAAAAAAACTCGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13975
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090174 | Nonsense | 1879 | 2074 | 49 | 53 |
Genomic Location (Zv9):
Chromosome 6 (position 12515212)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 12368434 |
GRCz11 | 6 | 12603292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTATTTGAAACACCGTTCACAGAGTCGGGCAAGAGGCATGGTGGAGTC[G/T]AGGAACAGTGTAAAYGCAGGAYGGTTCTMACTAGTGAGTGATCACTATCC
Long Flanking Sequence:
ACTATAAACTATCAGCTCTTCTTGCTATCTGCTATCTATTATTCTTGGTTTGATTTACTACACAGTATACAATGTTCAGCAGTCATCAAAATGCACTCTATGTTGAAATTATTTACTTAATCCTAGGCTCATTTAAACGTGTGTATAAACAAACACACACATACAAGACGAGTATTACATTATACAAATGATTTGACAACATGCCTGCTGATATGCAGTCCACTTTAACCAGTCTCACTTTAACCCCAGTCCACAGACAACAGTTTTGTTTATTCATTTTTTATCAGCAGTTTTTGTACATCTCATTTTTACATCTTTCCCAGGTGAATCCTAAAGATCTGGAGGCAAAGTTCGCCTACATCCAAGTCACGCATGTGACGCCATATCTGGAGGAAAAGGAGCTCGAAGAGAGGAAGACTGACTTTGAGAGAAGCCACAACATTCGCCGATTTGTATTTGAAACACCGTTCACAGAGTCGGGCAAGAGGCATGGTGGAGTC[G/T]AGGAACAGTGTAAACGCAGGACGGTTCTAACTAGTGAGTGATCACTATCCCTGACTTTACAACTGTTGCATAAAAAGTGTAGCACACGCATAATGTGTAGGAAATTGATGCTTTATTCTACTACATTTAATTGACTAAAAAACCCTTACGCCACCACTTATCTACCGTCAACCCAATCAATCATAGTTCCACTTGTTTACTTTCGATTATTACAATATGTTTTCCTGTGAAGTGGACCTGTCCCTCCTGCAGCAAAACAGCCCCACAACATGATGCTGCCGCCCCCATACTTCACAGTTGGGATGGTGTTCCTAGGCTTGTAAGCTTTCCCCTTTGTCCTCCAACTGTAACACTGGTCATTATGGCCAAACAGTTCAATCTTAGTTCCATCAGACCACAGGACATGTCTCCAAAAATTATTATTTTTCCCAGATTAATTTAGCAAATTGTAATCTGGCTTTTTTGTTGATTCTGGCTTGTTTGTTGATTTTGCCATGTTG
Associated Phenotype:
Not determined