ZMP
wu:fa96e12
Ensembl ID:
ZFIN ID:
Human Orthologue:
AC103686.1
Human Description:
DNA-dependent protein kinase catalytic subunit [Source:UniProtKB/Swiss-Prot;Acc:P78527]
Mouse Orthologue:
Prkdc
Mouse Description:
protein kinase, DNA activated, catalytic polypeptide Gene [Source:MGI Symbol;Acc:MGI:104779]
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa978 | Essential Splice Site | Available for shipment | Available now |
sa13311 | Nonsense | Available for shipment | Available now |
sa21046 | Nonsense | Available for shipment | Available now |
sa903 | Essential Splice Site | Available for shipment | Available now |
sa12418 | Nonsense | Available for shipment | Available now |
sa17162 | Nonsense | Available for shipment | Available now |
sa13548 | Essential Splice Site | Available for shipment | Available now |
sa16262 | Nonsense | Available for shipment | Available now |
sa34148 | Nonsense | Available for shipment | Available now |
sa21045 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa978
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051679 | Essential Splice Site | 148 | 4119 | 4 | 86 |
ENSDART00000051679 | Essential Splice Site | 148 | 4119 | 4 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44124381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41114681 |
GRCz11 | 7 | 41394754 |
KASP Assay ID:
554-0883.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACAAATCTGCAAAGTGCAGAAATCCTGCTTTAGATCTTCTAATCAAA[G/T]TGAGTTCTTTTGTTTATATATTGTATGAATCTGACTCGAGACTTTGATGT
Long Flanking Sequence:
ATCTTTGCTCTTTGCAAAGGAAGAGGGATTGCTTAGCTTTCTTCGCAGGTCTCTGTCTACTGAAAAGGTAGGAGGAATTTAACTAATAAATGACATTTATATTATTTCAGAAGGATTTACCAGATTGCAATCTAATTTTATTAATATGAAATTGCTTAAATGGATTTTCTGCAGCTGGGGACTACAGGAGTGGAGATTCTGCGGGAAACGAGAGTGGAGATTATGAATTTCTTAGGGGCATTTCTACAGAGAATGTCAGCCACTGTCCGAGGATGGGAAAAGAACTATGCTGTCGAGCTTAAGGTACCTTTATCCTATCGTTTAATTAATGTGAATTAATGTGACTGCCAGCACTGACATGTCATCTTTGTTGCACTAGTTTAATTTGCTTGATTTTTTTTTTTTGTTTCTCTCTGCGTGAATAGGACACGTGCATTGTCGTTTACACAAAGGACAAATCTGCAAAGTGCAGAAATCCTGCTTTAGATCTTCTAATCAAA[G/T]TGAGTTCTTTTGTTTATATATTGTATGAATCTGACTCGAGACTTTGATGTTTATCCAACTGAGGTATGTCAGGATAGTTCTCTACATATCATAATAAAAGGTAGTCAGATAATTGTAAGCATGTCTGCTGATGCTGTTATTTCTATACATATATTGATAGTTAGGGCTGTGAAATATGGCAATATATATTAAAAAGTCTATACTGTAGTATCATATTATGCTCTACGCCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCTACCTATATCAAACACACCTGAACCAATTAAGGCCCCGTTTACACTAGTGCGTTTTAGTTTGAAAACGTATAAGTTTTGCTACGGTTACGCCATCCGTCCACACTATGCCGGAGTTCTCGAGCGCCGAAAACGGAGCTTTTTGAAAACGCTGGAGAGGCCGTTTTCATTCTAAAACGCTGCTGCTCCGTCTCAGTGTGGATGGGGAAAGACGGAGACA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13311
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 1035 | 4119 | 27 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44112872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41103172 |
GRCz11 | 7 | 41383245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCGTAATKATGTACTTTTTKGWTACATAGGATGGGATTGTGGATCCAT[T/A]GGACAGCACCCTCAGAGACTTCAGTGGCACCTGCATCCAGGAATTTGTCA
Long Flanking Sequence:
TTATAATATGGATGTCAATGCTTATTGGTTTTCAATAATCTTCTGTATATATTCCTTTGTGTTCAACAGAAGAAAGAAACTTGAACAGTTTTAGAAACAATTAAATTTACAATGAAATGCATATAATATTTTAAATTATTGATTTATTACCTAACACTTTACTGTTTAGCTCAGTGTTTTTGTGATAATTAAGTTGTTTATGTTTTGTTTTTTGAAATAATGTTTGCTTTAAGTTGCACATACTAACATTAATAGAAATGTAAGTAAGAAGTCGGTCATTTGAATGTTTCTTTAGGTGACGCGGCAACTCTTTGAGCCTCTGGTGATGCAGCTTATCCACTGGTTCACCAACAATCGAAAGTTTGAGAGCCAAGACACAGTGGCAGTGCTGGAGGCCATCCTGGTAAGCAGGCATGTGCAATTGCACTTTTTGTTTGCTGTGGAAACATTTGCCGTAATGATGTACTTTTTTGTTACATAGGATGGGATTGTGGATCCAT[T/A]GGACAGCACCCTCAGAGACTTCAGTGGCACCTGCATCCAGGAATTTGTCAAATGGTCTATCAAACAGACCACCCCCAAACAGCAGGAAAAGAGCCCGGCCAACATGAAATCCCTCTTCAAGCGTATCTACAGCTTGGCTTTACACCCCAGTGTCTTCAAGAGGCTTGGAGCTGCGCTGGCCTTTAACAGCATGTACAGGCAGTTCAGGTCTGTGTATGATGAGGACGAGATCTCATTATGGGCTTCTCAACATTTAAATAAATATGTCTTGAGTGGATGTTGGTAACAAATTTAAATCTCATGTGTTTTTCCTCAGGGAAGAGAGCTCTTTGGTTGAGCAGTTTGTCTTCGAGGTGCTGGTGGTGTTTGTTGAGAGTTTGGCTTTGGCCCACTTTGATGAAAAGTCTGTGGGTAAGAAACTGGACCACTATCAAGATATCCTTTCAGATGGTTATGACCGTGATCTTTACATGATATTTGGCTTCTGTTTATACAGGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21046
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 1063 | 4119 | 27 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44112789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41103089 |
GRCz11 | 7 | 41383162 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCCAGGAATTTGTCAAATGGTCTATCAAACAGACCACCCCCAAACAG[C/T]AGGAAAAGAGCCCGGCCAACATGAAATCCCTCTTCAAGCGTATCTACAGC
Long Flanking Sequence:
AACAGTTTTAGAAACAATTAAATTTACAATGAAATGCATATAATATTTTAAATTATTGATTTATTACCTAACACTTTACTGTTTAGCTCAGTGTTTTTGTGATAATTAAGTTGTTTATGTTTTGTTTTTTGAAATAATGTTTGCTTTAAGTTGCACATACTAACATTAATAGAAATGTAAGTAAGAAGTCGGTCATTTGAATGTTTCTTTAGGTGACGCGGCAACTCTTTGAGCCTCTGGTGATGCAGCTTATCCACTGGTTCACCAACAATCGAAAGTTTGAGAGCCAAGACACAGTGGCAGTGCTGGAGGCCATCCTGGTAAGCAGGCATGTGCAATTGCACTTTTTGTTTGCTGTGGAAACATTTGCCGTAATGATGTACTTTTTTGTTACATAGGATGGGATTGTGGATCCATTGGACAGCACCCTCAGAGACTTCAGTGGCACCTGCATCCAGGAATTTGTCAAATGGTCTATCAAACAGACCACCCCCAAACAG[C/T]AGGAAAAGAGCCCGGCCAACATGAAATCCCTCTTCAAGCGTATCTACAGCTTGGCTTTACACCCCAGTGTCTTCAAGAGGCTTGGAGCTGCGCTGGCCTTTAACAGCATGTACAGGCAGTTCAGGTCTGTGTATGATGAGGACGAGATCTCATTATGGGCTTCTCAACATTTAAATAAATATGTCTTGAGTGGATGTTGGTAACAAATTTAAATCTCATGTGTTTTTCCTCAGGGAAGAGAGCTCTTTGGTTGAGCAGTTTGTCTTCGAGGTGCTGGTGGTGTTTGTTGAGAGTTTGGCTTTGGCCCACTTTGATGAAAAGTCTGTGGGTAAGAAACTGGACCACTATCAAGATATCCTTTCAGATGGTTATGACCGTGATCTTTACATGATATTTGGCTTCTGTTTATACAGGAACTGTCCAGCAGTGTTGTAGTTCACTGGATCATTTGAAGAGAATCATCAAACACAAGGCAGACTCACTAAATATAAACTCCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa903
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Essential Splice Site | 1136 | 4119 | 28 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44112459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41102759 |
GRCz11 | 7 | 41382832 |
KASP Assay ID:
554-0810.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTTTGTTGAGAGTTTGGCTTTGGCCCACTTTGATGAAAAGTCTGTGGG[T/G]AAGAAACTGGACCACTATCAAGATATCCTTTCAGATGGTTATGACCGTGA
Long Flanking Sequence:
ATGTGCAATTGCACTTTTTGTTTGCTGTGGAAACATTTGCCGTAATGATGTACTTTTTTGTTACATAGGATGGGATTGTGGATCCATTGGACAGCACCCTCAGAGACTTCAGTGGCACCTGCATCCAGGAATTTGTCAAATGGTCTATCAAACAGACCACCCCCAAACAGCAGGAAAAGAGCCCGGCCAACATGAAATCCCTCTTCAAGCGTATCTACAGCTTGGCTTTACACCCCAGTGTCTTCAAGAGGCTTGGAGCTGCGCTGGCCTTTAACAGCATGTACAGGCAGTTCAGGTCTGTGTATGATGAGGACGAGATCTCATTATGGGCTTCTCAACATTTAAATAAATATGTCTTGAGTGGATGTTGGTAACAAATTTAAATCTCATGTGTTTTTCCTCAGGGAAGAGAGCTCTTTGGTTGAGCAGTTTGTCTTCGAGGTGCTGGTGGTGTTTGTTGAGAGTTTGGCTTTGGCCCACTTTGATGAAAAGTCTGTGGG[T/G]AAGAAACTGGACCACTATCAAGATATCCTTTCAGATGGTTATGACCGTGATCTTTACATGATATTTGGCTTCTGTTTATACAGGAACTGTCCAGCAGTGTTGTAGTTCACTGGATCATTTGAAGAGAATCATCAAACACAAGGCAGACTCACTAAATATAAACTCCAAGAGACGGATACCCAGGTGCACATGCATATATATATTTTTAATTTAATTAAGTTTTATTAAAAATAATAAAAATAAACTTTTTTTGTAACTGTTAATCTTCCAACCCACAACAATTCCTTGATTGCAGACATATATACATTTAGGTTATATTAGGGAAAATGTATATTTAAGTTATATTATGGGAAATAATATTTATGTATTTAATATAAAGGATATTATTGATATAATTATTTATTTATTTTTATTTGTTTTGTTTTTTTTACTTGTGAGTAATGAAAAGAATTTGTGTGGTTTTGTGGCGAGCTGACAGAGCTGTGTTTTCTCCTCTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12418
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 2015 | 4119 | 45 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44103793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41094093 |
GRCz11 | 7 | 41374166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTGTCTTTAATTTTGTTAACAGGTCCCTATTGAGAGGAAAAAGAARTA[T/A]GTCATGATYAGGAAAGAAGTGAGTGGAGAAAACGGAGGTGAGTTGTCYGA
Long Flanking Sequence:
ATTATGTGTCAGATCATGTTTTGAGGCCTTCACGGAGAACATGACAGGAGAGATGGTACTGCTGGAGTTGAGGAGACAGTTTCACTGCGCTGCTTACAACTGTGCCATAGCCCTTATCAGCTGCAGCTTCAACGAAACCAAGTTCTACCAGGGCTTCCTTTTCACTGAAAAACCTGACAAGGTCTGTTACTGCGCATGCAACAAGATTTTGTACAAGCAGGGTTTACAGTTTAGTGCTTATTTTTTCCCTGTCTTATTGCTGACTCATAACATTTAGTTTGTTCTGCATTCTTTGATATTTACAATTAATATGTGGCTTGATGTTTTGCAGAATCAGTTCATATTTGACAATCTTATTGATTCGCAAAGGGTGTACAACTTTCCTATAGAGATTGATGTAAGTATAGCTTTAAAATGATCAAATAATCAATTTGTACTTGTGCTGTTTAGTATTGTCTTTAATTTTGTTAACAGGTCCCTATTGAGAGGAAAAAGAAGTA[T/A]GTCATGATTAGGAAAGAAGTGAGTGGAGAAAACGGAGGTGAGTTGTCTGAGGCTCCAACTTATTAATAACTATTGCTATGTAGTAGAAATGCAAAGATTAACCGATTTTATTAATCATGATTTAATTCGTCACAGTTAATCGATCTTAAAGTATTCTCAACACTTTGTTTCTGCACGGAACAAAACTGCTGCAACTAAACAAAGTTATGTTTAAGTTTGTGCGCTAGTTTGAAGTTTCAAGCTTGTACTCTGAGGCTAATACGCACACAATGGCTGAGCCTATTAAGTAAGGGCCATGTCTTTTTTGCGCTCAAGTTTGTTATTTCTTTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCCAAGCGACTTACAAATTAGGACAAGGAAGCAATTTACACAACTATACGAGCAACAATGAATAAGTGCTATAGGCAAGTTTCAGGTAAGTAAAGTGTAAGACGCAGAACATTAGTAGTTTTTTTTTCTTCTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17162
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 2804 | 4119 | 61 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44092827)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41083127 |
GRCz11 | 7 | 41363200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATCTTCCTGATATTCAGATTCAGTTCAGCAGCCTCATTGCGCCACTA[C/T]AGGCCCTGGCACAGGTTWAATTCAGAGTTATTTTCAACACTGTGTGTGTW
Long Flanking Sequence:
AACTCTTTAGATGATGGGGAAAAATAGTAAAAGAGCATTTTGCTGAGTGTGCGGTATATTACTGTCCCAACTGTCTGTCTTGAATTTTTCACTGGGGAATGAATGAATAAAGCATGAATAAATTCTTGTGATAAAATGTTGCGACTTTCACAGTAGTGAACCTGATATTTGTGTTCCAAATAGCTGAGCGGGAGCGGCGTGCAGACATTCTGAGACTCAGAAGGAGATTTCTGAAGGATAAAGAGAAAGAGAGCATAAAATTCGCCAAGAAAGAAATCCATTCTCAAAGAACTGAGAGGGTAGATCTTTTTTAAATTGTAGACAAACTTTTGAGTGGTTTCCGATTATGCTTTGGATATAATACTCTTTTCTGTATTCTGCAGGAGAGAAGAGCAGATCTAAAGATCCGCCAGGATGCTCAGGTCACGCTTTACCGCAGCTACAGAGTTGGAGATCTTCCTGATATTCAGATTCAGTTCAGCAGCCTCATTGCGCCACTA[C/T]AGGCCCTGGCACAGGTTTAATTCAGAGTTATTTTCAACACTGTGTGTGTACTGCATGTTTGATGGTACTTGAGTAAATATCAGAAATGGACAACAAAGTCAGTTCTTACTTGTTTTACAGAGGGATGCCACACTAGCCAAGCAGCTGTTCAGCTCTCTGTTTGCTGGTGTGCTGGTTGAAATGGAGAGATTGAAATCAAATAAAGAAACAGCCGACATTCTGAAGGAGCTAGTGCAGACTCTAAACGCTTTCCTTAACAAGAGCACAGTCTACTTTCCGCCCTTCATTTCTTGCATCCAGGTGTGTGTGTATGTGAACGTGTGATGAGATTTAATACCAAATTGCTCTGTTTCTAAGCTAGTCTGTCAGCAAACTGTCTGCAAACCAGCTCATTAGCTATTAATCCCAGAATTTGAATATGGAAATCACCAGAAATTGCACAGGCCAAAATTTACCCATTGCTGTTTTTATCTATAAATGAATATAGCAGATTTTCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13548
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Essential Splice Site | 3048 | 4119 | 65 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44089879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41080179 |
GRCz11 | 7 | 41360252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCTCCCCTATCAGACTAGACAGAATGTGGACAGAGACATTTTATGTG[G/A]TACTWATTCTAATTTTGAGCTATTTTGCWGTGGATTTATCACCATGAGAA
Long Flanking Sequence:
TATGTAAGTAAAGTTTTGTGTATTTTTCAATTAAAGTCATTAAACCATCCAGACACTAAAAAACAGATTGAGAATGTACACAGATGTCAAATGATTTTAAATGTGTGAGAGAATAACACTCGCAATACATCGGGGTTGAGAATAAGAGTGAAAGCTGTAATCTTAAGCAGTTTATTATTTTTTTTTTTACGTATATGAGAGCATGCTTGTGTATTTCTGTGAATGCAAATTCACAAAGAGTTTAAAAAAATAGGACTTTATGCAAAGTGATTCCCAGCTGAACTTATCAATCCAACTGTGCTTTGATTCAGGCTCTAAACAAAGAGGACTGGGATGATGGAGAGCCCACAATCACAGAGAAAGATTTCTGGGAGATTGCAGCGCTGGAGGCCTACAATCACTTGACAGAGTGGAAATCTCTTGAGTACTGTGCCACGGTCAACATTGACGACAGCTCCCCTATCAGACTAGACAGAATGTGGACAGAGACATTTTATGTG[G/A]TACTAATTCTAATTTTGAGCTATTTTGCAGTGGATTTATCACCATGAGAATTAAACTGGGTGAAGTATATTTTTACAGTTATAGCACATAATTGCATCAAAATCAAAATGAATTATTACCATTAGCAAATATTTCCATCAACTTCAGTCTTAGCCTCTGCTTTTGGCTGTAATAGGAAACATACCTGCAGTACATGATGCGCAGTATGTTGAAGCAGTTGCAGATGGGTGAAACAAATCAGGATCTACTGAGCTTTGTCGATGCTGCCATGAAGACAGAGGAGCACAAGATCATCATGGAGACTCACTACAGTCAAGAGCTGAGTCTGCTGTACATCCTCCAAGAAGACTATGACAGAGCTAAATACTACGCCAACAACTGCATGCAAGTCTTCATGCAGGTCAGTTTCACTACACACCTAAACAACTTGAGATGTTTTACTTTGAGTTGTTTACAACTTTAAGTTGTCAAAATGTATTTTCAGATGATATGTTGGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16262
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 3104 | 4119 | 66 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44089538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41079838 |
GRCz11 | 7 | 41359911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATCATGGAGACTCACTACAGTCAAGAGCTSAGTCTGCTGTACATCCTC[C/T]AAGAAGACTATGACAGAGCTAAATACTACGCCAACAACTGCATGCAAGTC
Long Flanking Sequence:
GAGCCCACAATCACAGAGAAAGATTTCTGGGAGATTGCAGCGCTGGAGGCCTACAATCACTTGACAGAGTGGAAATCTCTTGAGTACTGTGCCACGGTCAACATTGACGACAGCTCCCCTATCAGACTAGACAGAATGTGGACAGAGACATTTTATGTGGTACTAATTCTAATTTTGAGCTATTTTGCAGTGGATTTATCACCATGAGAATTAAACTGGGTGAAGTATATTTTTACAGTTATAGCACATAATTGCATCAAAATCAAAATGAATTATTACCATTAGCAAATATTTCCATCAACTTCAGTCTTAGCCTCTGCTTTTGGCTGTAATAGGAAACATACCTGCAGTACATGATGCGCAGTATGTTGAAGCAGTTGCAGATGGGTGAAACAAATCAGGATCTACTGAGCTTTGTCGATGCTGCCATGAAGACAGAGGAGCACAAGATCATCATGGAGACTCACTACAGTCAAGAGCTGAGTCTGCTGTACATCCTC[C/T]AAGAAGACTATGACAGAGCTAAATACTACGCCAACAACTGCATGCAAGTCTTCATGCAGGTCAGTTTCACTACACACCTAAACAACTTGAGATGTTTTACTTTGAGTTGTTTACAACTTTAAGTTGTCAAAATGTATTTTCAGATGATATGTTGGAAATTTTATAGTCTACTAGACAAGAATTTTGTACTGAGAGCACTTTGATGTATGTTTTGTTAGTTTGTTTATCTGTGTTACCCTCTTTCAATTTTTTGAAAATTAGATTTATGCCATTTCTGAAATTTGAATAAATAAGCTTTCTATTCATGTACAATACAAATGTAAAAGAAGGGAACATTTTTGGCAGAGACTATTTGAATATCTGGAATCTGGAATGTTTTCTGAAGAGCATTTCACATTAAAGGTGCTCTCAATTGAAGCATGAAGAAAGGGTGGGACATAGAGTAACCCCTCATCTTTTTGAAAACAGCCAATAGCGTTTTGTTGTTATTACAGCTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34148
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 3155 | 4119 | 67 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44088477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41078777 |
GRCz11 | 7 | 41358850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTGCAGTCTGTCCAAGCTCTGACCGAGATCCAAGACTTCTTGAATTA[T/A]ATCACAGGAGATGGTGGGTTTTTGTGCTCAGTGGAGTTGGATTAATGTTT
Long Flanking Sequence:
TGTCAGATGCCACAGAGGATTTGATTGGTTAGAATATTTGAGGAGAAACTGAAGTATGAGGTGGCTTGAATAAACTGACAAACTACAAGCTTTACATGTTTATATCAACGTTAGACCTTCTAGATGCAGATTTTGTCAATGTTTTGGTGCACACTAGCTTATAGATATTCTAAAAACTAACAATGCTGGAACTGATACCTTCTAAACTTTAGTTTAATTTTAGGGAACCCTTAAAGGTATCTTTCCATTCTTTTAAGATTATAGGCATGCAAACACACACACACACACACTACACATATTTCTAAAATAGTTTGTGCCCTTTAAAGAAGGGTTTTTTGTCTATCAACAAATAATAGGAAGTGTTTAAATACCTGCTTTTTTTCAACATGATATAATATCCTGTAGAACTACTCCAGCATCGACCCCTTGCTGAACCGCAGCCGGCTGACTGTGCTGCAGTCTGTCCAAGCTCTGACCGAGATCCAAGACTTCTTGAATTA[T/A]ATCACAGGAGATGGTGGGTTTTTGTGCTCAGTGGAGTTGGATTAATGTTTGTTTATTAATAATATTTATGAGTCTGAATTATCACTGTTTGCTCTATCGGCTTTTAGTCTCAGTGAATTCTCTCAAGTTCATGATCAGACGGTGGACCAGCCACTATCCAGATGCTAAACTGGACCCCATGAATGTGTGGGATGACATCATCACTTCTCGGTGAGTCTGCTGATTTACACAGAAAGTACAGATTTCACAGTGCTTGCCTTGAAAAATCTGAGGAGGTATAAAGCTTATTTGTGTAGACCTAAGAATGTCATCTTTGTTTTCAGTTGTTTCTTCTTGGATAAGATTCTGAAGAGACTGAAGTCCACCCCTGAAAACAGCATGGAGGTGGACGGTGCAGACCAGGGCAGTGGAGAGGAGCTCGGAGTGCTGGTCAAAACCTGCAAGTTCAACATGAAACTCCAAATGGCTGACAGCGCATGGAAACAGGTGCTCAAATGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21045
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 |
---|---|---|---|---|---|
ENSDART00000051679 | Nonsense | 3389 | 4119 | 72 | 86 |
Genomic Location (Zv9):
Chromosome 7 (position 44086154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 41076454 |
GRCz11 | 7 | 41356527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGCAGATTCAGGCTCTGGAGTTGTTGAGGAGTGCTGCATGTAAAGCA[G/T]AAGAGGAAGAGCAGTCTTTCAGCCAACAGCATGTGAACACGCATGGTATT
Long Flanking Sequence:
AATTTAATCAATTTAAAATATTTTAAATAATAAAACTTTTGTTTAAAAGTTTTAAATCAATATTTCAGCAGTTATTATTTCTTCAGTTTTTTACATGATATTTACAAGATCATTCTGATTTCTTATTCGTGATCAGGATATTATTTTATTATCAGGATTTTAGTAGTTTACCTGTTTGCACTATTTAAATGAGCTAAAATACAATTTCTGCATCCTAAACATACTTTTTAAAACATTATGCATGAGATAGGGTCTGGTCTAATGGATTGAAACACAAATTATTGCTGCTCATTATTTTGTAGTGAATAAATTAGATTTGCCATTTGATTCTAGCGTTTAGTGACTTTTTGACATACTTGTGACTTCTTGTGTGCTTTTTGCACTTTAATATTAACTGTTGTTAACATTTCCACATTTGATGAGTGTCATTTATTGCTCAGGTGGTGGAGGGTCTGCAGATTCAGGCTCTGGAGTTGTTGAGGAGTGCTGCATGTAAAGCA[G/T]AAGAGGAAGAGCAGTCTTTCAGCCAACAGCATGTGAACACGCATGGTATTGTGGAAGCCTACATGACCATGGCCAACTTCTGTGACCGAAGACTACGAGAGAGTGAACAGAAAGAAGAGGGTGAGAAAACCTGAGCACCTGTACAGCACACAAGTGCTCTCTTAAATATTAGAAATTTACACAGGCTCTCTCAGAGTCTGAAAGGACACTTTTTGTGATTTTGTGTGCAGGATGAAGTGCATATAATGACACTTTAAATGTTTGATTTTAGCAATCAGTTCCAAGCTTCAGTCCTTGCCTGAACATGTCGTGAAGATGATGCTGAAGGCGCTGAAGCTTAGCTCTGAGGAGGCCAGGCTCAAGTTTCCTCGTCTGCTGCAGCTAGTAGAAGTGTACCCTGCTGAAACCCTTGACCTGATGGTCAGAGAGGTGCGTCAACATCCTTTGATGCACTACATTCATAGATTTTAGGAATCATGTTCATACTGTCATTATATGAA
Associated Phenotype:
Not determined