ZMP
si:ch211-259k10.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate WD repeat and FYVE domain containing 3 (WDFY3) [Source:UniProtKB
Mouse Orthologue:
Wdfy3
Mouse Description:
WD repeat and FYVE domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1096875]
Alleles
There are 14 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33670 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17802 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa20498 | Nonsense | Available for shipment | Available now |
| sa9941 | Essential Splice Site | Available for shipment | Available now |
| sa33669 | Nonsense | Available for shipment | Available now |
| sa2247 | Nonsense | F2 line generated | Not yet available |
| sa20497 | Nonsense | Available for shipment | Available now |
| sa10584 | Nonsense | Available for shipment | Available now |
| sa2246 | Essential Splice Site | F2 line generated | Not yet available |
| sa6996 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14824 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33670
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 339 | 3522 | 7 | 65 |
| ENSDART00000146664 | Essential Splice Site | 319 | 375 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41781605)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39556322 |
| GRCz11 | 5 | 40156475 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCCGCATGTGTCAGGGCTACACCTTCCTCATAGATCTTATGATCAG[G/T]TGACTTATTTGTAATTGTTTATTGCATGTTTAAATGTTTAGTGTTTTATA
Long Flanking Sequence:
ATTTACTCAACGTCCAGTTGCTCCAAACTATATGAGTTTCTTTGTTCTGTTCAACACAAAGGAAGATATTCTAAATAAAAAACAGTGATTGACTTCTGAAGATCAATGGCTGTTTTTTCCCCAACGTTTTTCAGAATATCTTATTTTGTTTTTAACAGAACAAAGAATTTAAAAATATTTAGATAAACGGTAAATGAGGAAATTTTCATTTTTGGGTGAACAAACCCTTAAAGTGACCCTTGTAGATTTTACCTAAAATTTTATATTATGACTAAAATTCATAACCGACATGAAACAATTTTTGTTTTGGCAGAGAAAGAGTGCTTATCAACATGCATCCAGAACATGCAGCAGTCAGATGACCTTTCTCCTCTGGAGATTGTGGAGATGTTCGCTGGGCTCTCCTGTTTCCTGAAGGACTCGAGTGATGTCTCTCAGACACTGCTGGATGACTTCCGCATGTGTCAGGGCTACACCTTCCTCATAGATCTTATGATCAG[G/T]TGACTTATTTGTAATTGTTTATTGCATGTTTAAATGTTTAGTGTTTTATATTGTTTTGAGCTCTGGTTATCAGCGCGGCATTGTTCTGTTTTTATTTTAAAACATGGCTTTAACAAAACATGGCTTAACGGATAAAACTTTTATTTTGGAATTCATTGAGCACAACCATTCAAAAACTTGGGTTGGAAAGATGAAAAAATTACATCTTTTAATTTGATTAAAATACAGTAATCTTATTAAAGTTTATAATAATTGTAAGAATCAAGTGTCACATTATCCTTCAGAAATCATTCTATTAAGCTGATTCGGCAACATCTGCTAATGATTGTGTTTTGAAATCACTTGTGCTGAATAATCATTTTGTAAAAATCTAGACATTTATGGATTAATTGATAAATATCAACTTGTTTTTTATGTAATAGCTTCTAGCAAGATAATAAAGCAATCTCTTTCAATTACATTTCTTCTTTCTATTGTTTGGGATCAGTTAAAAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17802
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, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 394 | 3522 | 8 | 65 |
| ENSDART00000146664 | Missense | 375 | 375 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41780305)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39555022 |
| GRCz11 | 5 | 40155175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCACCCTTCCTGCTTCCAGGTTTTGTGGTTCCACAGCCTTCTGGGAAAG[G/A]TCAGCCCTCTATAAAATAGCATACACTGGAGTCTTGACTTGTGTCATTGC
Long Flanking Sequence:
CAAACCAGTTTAAGTTTTTTTTTCTTCTCTTGAACACATAAGATATATTAAATAATATTGGAAACCTGTTATTATAGACTTATATATTTCCTTAATGCTTCCAACATTCTTCAAAATAACTTCTTTTTTGTTCAACACAATAGCAAAGCTCAAACAGGTTTGGAACAAGTCAAGGATGAGTAAATGATTTTTGGGTGAACTATCCTTTTACATTATGTAAAAAGATCACTTACCCCTAAATATTTGTCTTTTAAATGTGCTAATAAAAGTTTTTTTGCAATCCTGATACGATCGATTAGTGATATTCTCTGTTGTACTTGCTCTACTTCTTAGGTTGGAGCAGGCCAAAGAGGATGAATCCAAAGATGCTCTAAAGGACCTGGTGAACCTGGTGACCGCTCTGACCACATATGGTGTCAGTGAGCTGAAGCCAGCTGGACTTACCACCGGAGCACCCTTCCTGCTTCCAGGTTTTGTGGTTCCACAGCCTTCTGGGAAAG[G/A]TCAGCCCTCTATAAAATAGCATACACTGGAGTCTTGACTTGTGTCATTGCACAGCTGGGTGTGAAAGCTGGTGATGTGAAATTCCGGGTGTGTTGAACTTCAGCCAGGAAACACTAAGAAATCGAGGCATTCACAGGATTCAGATGGCAAGTTTGCAGTGTTAGGGCTTAAGTAGGGATTTAGTGTGCTTTTATGTTTGCGATTATTCTTTTTTTTTTTTTTTTCAATTGTTTTGCTTTTAGGACTTTTCGTAGTCAACATAAAATTTAAATAATGATTTAATCTCTTCTGGACAATTGGAAATTTTTGTACTGAAAATTTAGACTGATGTTCACCTCAGATGCGGATAAAGTGTCAAGTGTGAGTGATTTACATGTTAAGTCAATGTATAGATGTGATCAGACATCATGCGGCACTATTTGCGCAAATTAGGCGGCGCGAATGATGAGATGACATGGTGCGAATTGAGCATTTGACGTGCTTAATGCATGATTCCCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20498
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Nonsense | 585 | 3522 | 11 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41770387)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39545104 |
| GRCz11 | 5 | 40145257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGACATGGAGATGAGTTAATAATACAGATATGTCAATCTCTCAGGGT[T/A]GTTCCGGGAGTTTGGGGGAGCGCGGTGTGTGCACAACATTGTGAAGTATC
Long Flanking Sequence:
ACATTGCTTTGTTTTAAAACAGTACAGCACACCCCTAAGGCTTTCATTATAATTACATTATCGTTGTCCAAGTTTGCCTTTTGTTTCCAAGCACTCAGGGACGAGGAAGAATTCATTTCCATGCTCTCAGACCCCGCAGTTGTCTCAGTCTCAGTGCTGAGTCAGGTCTCTGCTAGAGAAACTCTCTGGACTTCAGCTCTCTAATCATTTCTCCTTTCTGTCATGACTGCTGATAGTCTCACAGATGCGCTCGTACTTCATTAATTGTCAGCCAATCAGAATGGCTTTGCTGCAGAAATTGAGTCATTTAAAATGCTTTGCTTCCTTTGAGGTGATCAGTCATTCCTAAATCTCATTATTACCAGCTCTTGATTGTTCTAATGTTTACATAAACAGAACATTAAACTTGTTGCCGAGCTGTAATGTTGAACATTAAACTGAACATTGCTTATTTGACATGGAGATGAGTTAATAATACAGATATGTCAATCTCTCAGGGT[T/A]GTTCCGGGAGTTTGGGGGAGCGCGGTGTGTGCACAACATTGTGAAGTATCGTCAGTGTCGTGAGCACGCTCTGATGATCATCCAGCAGCTGGTCTTGTCGCCGTCTGGAGATGATGACATGGGCACTCTGCTCGGCCTCATGCACTCCGCTCCAACAGCAGAACTACAGCTCAAAACTGACATCCTGCGGGTGAGGCACATTAACAAATCTGCCATGCTTTATTTAAATAGATGGGAAATAGAAGCAGAATTCACTACATTTTTTTCCATATTTGCATGAATACATTGGCCTTCTAAAATTTGAGGTTTGGAAGTGTTTACTTTTGTTTTATTTTATTTTTTATCATTTCAAAGTTTTATCATTACAAATGTTTGTATTATCGGTTTAATGCATCCTTGCTGAATAAAATAATTTGATTCTATATATAGCTATATATAACTGACAGTTATATAAAAAATTTAACCTATAAATTCATAAAATAAAAATTTGTGTTAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9941
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 829 | 3522 | 13 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41767565)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39542282 |
| GRCz11 | 5 | 40142435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACCTCGCTGCCCTCCCCTTGGGGCACGCCAGCAATCACCAGGAAGAG[G/A]TACTGCTTTCTGCCACCTCTTCCTTTTTCTCCCTCTGTCTTTTCCTTCTT
Long Flanking Sequence:
CAAACAATTGTTTGCATGACTAAATAGACCAAGTAGAATAATATAATAAGAAAATATTAGTTTGCAATTTAAGTCTCAAAGGAAACCCATTTTATCTTATTCAAATAGTGTTTTGTAACTTTACTAGTTGAGTAGTGTGCAAAACAATTACTCAACTATTTTCTATCTGACAAGATGCAAATGTCCTCACATGCTATCTGAATGTGTCTGTGCTTTAAGCTTGTGTTCGTGGTAGATTTGCATGATCTGTAGTTCCTCTAAGCTGTATATTCAACAAGAACTAACTGCCTCCCTCTGTTGCTCTTTGTCATTTCTCTGTCTCTGGTAACCTCTGGCATTGCCTGGCTGCACACGCGGGGTATGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGGATGTGTGTTTAAATGGTTGTAGTCGTGCCGAGCAGGTGCCCCCCTGCTTGACTCACGAGACCTCGCTGCCCTCCCCTTGGGGCACGCCAGCAATCACCAGGAAGAG[G/A]TACTGCTTTCTGCCACCTCTTCCTTTTTCTCCCTCTGTCTTTTCCTTCTTATTTTCTTTTTCTGTTCTCTGCTTGTTGAGTGATCAGACTTTTGTCCTCCCAGTCTGTTTCCTTTTCCTTCTTTTATTCTCCTTTTTTTCTACTAACAACTTAAATGCTTAGGTTGTGTTATAGTGTTTTTCTCTTCACTTTTTTAAATATATAACTTTACAACTCCCCTAGATGTAAACATTTGTTTTATCATTTTTTAATCCATTCAGATTTAGGCTGAACAACAATATACTGTTTGAGCATCGATATCGCAGTGTGTGTGTCTGCAATAGTCACATTTCAGGATTAGATAATTTATTAAATATTATTAATTTTTTTTTTATTATGTATGCAATGACAGTGTTGCGCTAGTTACTGAAAATAGTAACTAGTTATAGTTACTAGTTACTTCGTTCAAAAAGTAACTCAATTACTTTATCGATTACTTACAGTAAAAAGTAATGTGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33669
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Nonsense | 1397 | 3522 | 23 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41733778)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39508495 |
| GRCz11 | 5 | 40108648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCACACCAGTCAAGCTTGTTCATAATGCAGTAGGCCATCTCAACGGAT[C/A]AGCCAGGACCGTTGGAGCTGCAGTCATTGGTTACCTGGGTGAGTGCATTT
Long Flanking Sequence:
AAATTAGGTGTTTATTTAATAACCATGACAGGCCTAAATATTAATGATGAAACAATGATTTAAATAATACAAAATGTTTCAGTGGATTTTTGCATTCATTTTTTAAAATGTTTTCCTAATCTAAATAACTAATGGATAAGACTTCCTAATTAAAATTAAACTCACCAACCACCGAATGGCAATGCCCTAAAATCTCAATACTTTTCTAAAGTTTGGATTCAGTGAGATATTTGTAATGATTTTAAAAAAGATCTCCTGCTCCTACAGTATAAATATTTGTATGTTTTTAGGAATACTGCAATGGATTTTTAACATTTTGGAAAAAAATAACCCCCAACAACTTTTGCAACAATTGTTCGAAAGGATCAGACTTTTTTTGGTCATATATTTAAAGGCTGCTCAGAGTGATGTTTTCATCCCGTTTCAGCTGGGGGTTTCCTCTCATGAAAGTGCCACACCAGTCAAGCTTGTTCATAATGCAGTAGGCCATCTCAACGGAT[C/A]AGCCAGGACCGTTGGAGCTGCAGTCATTGGTTACCTGGGTGAGTGCATTTTCATTAGGAGCGTGGACATGGGTGAAGTTTGTTTTTGGACAATAAAGCATTAAATACATGGATGATGAAAATAAGAGAAGCTGCTCCAGCTCTTTCTCTCCACCTATTTATAACTGCAATCTTTTTCCATGTAGGTGTGCGGGCCTTTGTAACCAAACCAGTGGCCACCAACCTCCAGTACATCGGAGGAGCAGCTGCCATTCTGGGCCTGGTTGCCATGGCATCAGACGTGGAGGGTCTATATGCCGCAGTAAAAGCATTAGTGTGTGTTGTCAAGAGCAACCCACTTGCGAGCAAGGAGATGGAGCGTATCAAAGGCTACCAGGTGGGCTGCATAGACAATTACCCGGTGAACTTTGAACCCAGGATGTCCTCTGTTCTCCGCAGCTGTAGCTGTAGGATGTTATGAGCCAATGAGGTGGCAAATGAAATGATAACATTGATGCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2247
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114481 | Nonsense | 2452 | 3522 | 43 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41706026)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39480743 |
| GRCz11 | 5 | 40080896 |
KASP Assay ID:
554-3279.1 (used for ordering genotyping assays)
KASP Sequence:
CGGGAATGTACCAGCACTCCATAGAGCAGAACACAGAGGGAGAAACCACA[C/T]AACAAGAACCCGAACATGGAGAGGACACCATCGCAAGGGTCAAAGGTCAG
Long Flanking Sequence:
AAACCAGATTTCTTATTAAATGTATTTAATTTTTAAGAGTAAATGTATATATTTATGTCTTGTGTTTCCTTCAAATGATTCATTACAAATTATTGTACCAAATGTTTGAACACTTTTTGTTTGTGTTGTCTTAAAAAATTAATCTAAAAATGTGTAGAAATGCCTAAAAGTGCTTTATAGGTCAATTTAAACGTAACATTCATTTGAGCTGTCAGTGTGGGCTTTTCTTAAGGAGTGATGTACATGTGGTTTGCATGGCTCTGGATTCTTCTTTCACTGTCATTCAAGATGATATTTTGCATTATAAAATGAAAGATGAGCTAATCAGAACTAAATACATCATATAAACAGTTTTTATTATATTTCAATTGTTTCAGAAGCCAGCCCGATACCGGCGAGCAATCAGCTATGACAGTAAGGAGTATTACATGAGGCTATTGTCTGGAAACCCGGGAATGTACCAGCACTCCATAGAGCAGAACACAGAGGGAGAAACCACA[C/T]AACAAGAACCCGAACATGGAGAGGACACCATCGCAAGGGTCAAAGGTCAGCAATCTTTATTTGATATTCTGAAATGATTACAGAAATTTCCATGGTTACGTTTTCATTTACAGTCCTGTTTCACATGCACATGCTGTGTACTTATTATAGTAATTACAATAACTGGATAATAACTAGGTGCTAACTCTGAACCTAAATTTATCCCACATACGTATCTGTTAGCTATTACTTTCATAAAGAGAGTGGCTGCACTTTATTTTACAGTACAGTACATGAGTTACACAGTACATTTTTCTCACAGATGTATGATAAATGATTGGTTGATTAATCCAATGTGATTTTTTGTGTGTTTTGTCAATAGAGATGTCTATTACGGATCTAGTAAATATCCAGCCTGTTCTTTCAGATGGAGCAGCATTTAATACAAAGAGTTGTAATTCACAGCTATCAATAGCTATATAAAAAAAATGGTTTCAACATCGAAATGGATTTAATCAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20497
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Nonsense | 2504 | 3522 | 44 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41703741)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39478458 |
| GRCz11 | 5 | 40078611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAAGACCAGCTGCAGGAGCTGCTGGAGTCAGGAGCAATGGATGAAGAG[C/T]AGAAAACAGACAACACCACACTGCTCCGTCTGCTGGAGGAGGGAGAGAAG
Long Flanking Sequence:
AGTAAACGAACACCACTAACAGTACAGTGAGTTTGGTAGAACTTTATTCTACAGTCCTGATTTTATGTGTTACATGAACTGGGATAATACATATTATTCTCAAACCTACTAGACCTAAGGTTACTCTGAACGTTAACCCACCTAGTTATCCTATGTAGTCTAAGCTTCCAAGGAGAAAAGTCAGACTTTACTGATTTTAACTAGACTATGAGTTTATAACTCAAAATTGTAAGATATACTGTAAACTCAGTTCCTTAATTCCATAGAACCTGTATAAATTGAATGAGATAACTGGTGTGCTGAATTACTGTTTTATTTAAACTACTGAGCATGTAATGATAGGAGTGCGTTGTGTGGACTGAATGAATGTGCTGTGTGTATGTGTTTTAGGTCTGGTAAAGGCCCCTTTGAAACGATCACGCTCTACAGCAGATGGGGCTGATGAGGAGAGTCAAGACCAGCTGCAGGAGCTGCTGGAGTCAGGAGCAATGGATGAAGAG[C/T]AGAAAACAGACAACACCACACTGCTCCGTCTGCTGGAGGAGGGAGAGAAGGTCTGCAGCATTACATAATAGAAATGAAACAAAACAGTTTGCTCATGGTTCAGTTCTTATCATGGATTTAGGGTCACGGATTTGGTACAGCTTGGTATGTGATATGTTCAGTAAAAAACGTAAAGCAATTTAGCAAAGAGATCACTAAAATAAACAGGCTTTTCAGGTATCTGATGGTAGATTTTAGGTACAAAAACTAAATGATATAATCAAATATAAAACTGCATACTATATATAAACGTCACTGTATTAAATAAAGGTTAAACATTATTTAAGTTACCTACAACAACTATTCAGTCACGAGCGTAGAGAGTGAATCCATTGTCATTTGTTGGTTGATTAATGTTAAAAACAGAGAGCAGAAATAAAATGTTTTCACTTTGACACACTCCACAGAGCTAGCACATTGAACAAGTTACAGATAACACAGTTTCTCAAATATTTAGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10584
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Nonsense | 2769 | 3522 | 52 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41697530)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39472247 |
| GRCz11 | 5 | 40072400 |
KASP Assay ID:
2259-6288.1 (used for ordering genotyping assays)
KASP Sequence:
CAAACTTTTAAAACAAGGTTTTRTTTCTGTACAGGCGAGACTCCGGCATA[T/G]CATTACGGCACTCATTACTCTTCTGCAATGATTGTTGCCTCATATCTGGT
Long Flanking Sequence:
AATTCACCTTCAACTCCAGTAGATCCTACTTTTGAATTTGAATTTATCATTATCACGTGACCTACATTAGTCAGTTGTGTCGCTTCACTCGCATTCATTTGTTTTTCATCAAGCGCCATCTAATGTCAGCGTGTGATTTTGCACACAAACTCATCACCAGTGAAAATGGCTTGGGCATGAATGGTAAAAAATGTTGGTGATTAAGAACTAGTGTTAAACATTTGAGGATGCATAAGACTTGAGCTTGAATCTTCTCTCAGCAAGTGAAATATTGTTGAATTACTCCTCAGGAACTGGACCTCAACAATCCAAAGACATTCCGAAATCTGTCCAAACCAATGGGAGCTCAAACAGATGACAGACTGATCCAGTACAAGAAAAGATTCAAAGATTGGGAGGATCCTAATGGTGAGTCGAAGTTGATGATATGCAGGTTCTTTGTGTTATGGGCAAACTTTTAAAACAAGGTTTTGTTTCTGTACAGGCGAGACTCCGGCATA[T/G]CATTACGGCACTCATTACTCTTCTGCAATGATTGTTGCCTCATATCTGGTCAGAATGGAGCCATTCACACAGATCTTCCTTAGGCTTCAGGTTAGTCCATGGCCTGTTTTTAGTTTTGTTTTTTAACTTTCTTCTTTTCCTTGTTTTTTTATTTTATTCTTGAGAGAGTTGTGAAGAAAAAAAATCTCTAAATAGAGTGTATATTCATATATATATTTAAACCATTTTTTTCATGTCTCTACATTGAAAGACAATCCTAAACATAACAGGATTTGTTGCTCGTCTTCGGTTGCTAAACTTTACCCATTCTTATTCAAATGTAAATACTTTATAATAAATTATGTAAAATTAGACATCTATAGCTTCAAAAACACAGTTAGATATAAAGCCTGGAGATGAGCTGTCTCCAAATAAGCAAAGCATCTTCCATAGTTGCACAAATATTTGCAGTATTTATTCCTATTTTTAAAATTATTATTATTAATTCTGATTATTTCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2246
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 2952 | 3522 | 55 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
| ENSDART00000114481 | Essential Splice Site | 2952 | 3522 | 55 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41694785)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39469502 |
| GRCz11 | 5 | 40069655 |
KASP Assay ID:
554-3250.1 (used for ordering genotyping assays)
KASP Sequence:
AACCGCCACAATTGGATTCATTAACAACTTTGGYCAGATCCCGAAACAGG[T/C]TTGYGATTTCATTTTCCAAAATCTYATAAACATTTTCCAGTGAATWGCGT
Long Flanking Sequence:
GGTATGTGATCTTTTGTGGCTGCAAAAAACCCATATTTAAAAGTAAAGGAATTTTCTAGAAGTTGAATACAACCTCAAAACATTTTAGACATTTACACCTGTTTTTACTGTCAAACACTTGTGACTCAATAGATGAAATTCACATCTTTGTAATTTAAGGCACCATTTACAGCTGATATTTATTTCCGAAGATTCCAAGAACCACAGCAAAGGCCTCCAGAAACATGTTAATAATAAACATTTTGTTTCTTTTTTAATTTTTGTTTTGTTTTTTGTTTGTTTTCAGGCTCTGGAGTGTGATTATGTCAGTGCCCATCTGCATGAATGGATCGACTTGATCTTTGGTTATAAGCAGCAGGGTCCTCCAGCAGTGGAGGCGGTGAATGTCTTCCATCATCTTTTCTATGAGGGCCAGGTGGACATCTACAACATCAATGACCCACTGAAGGAAACCGCCACAATTGGATTCATTAACAACTTTGGCCAGATCCCGAAACAGG[T/C]TTGTGATTTCATTTTCCAAAATCTTATAAACATTTTCCAGTGAATAGCGTCTTCATAAATCTATTTAAAGTCACAGTGACATCAGTTGAGTAAAGTAATGGAAAGGAAAGTTGTAATTTGTCTCATTTAATCTAATTATGTTCATGCAATATGTGTGACTTGTGACTTGTGTGAATATGTGGGTGTTCAAATAAATTTTCCGAGCTCTTTGCAGTAATTTGTTTTATATGTGGAGCAGTAGCCTGAATAAACATGTGTGTCCTTTCTTTTAGCTGTTCAAGAAGCCTCATCCTCCAAAGCGTGTGCGCAGTAAGTCAAACGGAGAGGCGCCTGGAGGGCCTGTTACACTCAATTCCACATTAGACAAAATCTTCTTCCATCATCTGGACAATCTGCGGCCCTCTCTCACCCCTGTCAAAGGTAATACAGGTTATGTAGTCTATGAGTTATGAGTTTTACATTGGTACTTCATACTGGGTGTTTTGTCTTTTGGTTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6996
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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 3417 | 3522 | 63 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41679720)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39454437 |
| GRCz11 | 5 | 40054590 |
KASP Assay ID:
554-5050.1 (used for ordering genotyping assays)
KASP Sequence:
GCAAGGACAACGCTCATCCTGCCGAAATCACCGCTCTTGCCATTTCAAAG[T/C]AGGCGCTTTGTGTGTTCTGTGGGGAAATGAGAATAAAAGAGAAGAWGTTT
Long Flanking Sequence:
AGAGATGGTGGGGAACAGTGGAATTAAGTAAAGTGCTTGTCTGGTCTGAGAACCACTTTATATCATATATCTACAGTATCAGGCAGTGAAGATCACTGATTTTTAAAGAAAGCACATCTTAATTGTGGTGATTTTTGTAAGGGAAAGTTCATTGGAAGCCATTGGGCTGGCTGGTTGAAAAATTAGAAGTCTGTGTGGATGTATGATATTGTGCATTGTGAAAGTTTGCTGAGGGCCACTGAGAAGCACTGAGAAGATCAGTAAATCCTAAAATTAAAAACACATTGGTGTATTCATTTAATAATCATTCAAAGGCTGTTCTCTTATGGTGTAGGAATCTTCTGATATTGTTTATGCAACTGGCAGTTTGCTTTGTGTCCTGTGCAGGCTACAGATGGGAGAGACAGCTGGTGTTTCGGAGCAAACTCACCATGCACACCGCGTTTGACCGCAAGGACAACGCTCATCCTGCCGAAATCACCGCTCTTGCCATTTCAAAG[T/C]AGGCGCTTTGTGTGTTCTGTGGGGAAATGAGAATAAAAGAGAAGATGTTTTCTGCTGTGCTTTTTATTGTTACTTAATAATAACACTGTTTGCACAGAGGATATCTAATGAATTTTGTGCAAACAAGGAAGAGGGCTGACGGCAAGCTGTTGTTGTGTTTTCAGAGACCACAGTAAGATTCTGGTAGGTGACGGTCGAGGGCGAGTGTTCAGCTGGTCAGTGAGTGATCAGCCGGGTCGCTCTACTGCAGATCACTGGGTGAAGGACGAGCAGGTGGACAGTTGTTCTGGGTGCACCGTCCGCTTCTCCCTCACCGAAAGACGCCACCACTGCAGGAACTGTGGACAGGTCTTCTGCCAGAAGTAAGGTTATGTGCAGTAAAATGTATCATGTGCAAACAACACAATTTAATTAATGAATGAATTGGTTTATTTAAATTTTATTAGTTTATATAATTAATATTTTAGAATAAAAGGACTACTTCTGTTGCTGTTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14824
Status:
Mutation detected in F1 DNA
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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 |
|---|---|---|---|---|---|
| ENSDART00000114481 | Essential Splice Site | 3417 | 3522 | 63 | 65 |
| ENSDART00000146664 | None | None | 375 | None | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 41679720)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39454437 |
| GRCz11 | 5 | 40054590 |
KASP Assay ID:
554-5050.1 (used for ordering genotyping assays)
KASP Sequence:
GCAAGGACAACGCTCATCCTGCCGAAATCACCGCTCTTGCCATTTCAAAG[T/C]AGGCGCTTTGTGTGTTCTGTGGGGAAATGAGAATAAAAGAGAAGAWGTTT
Long Flanking Sequence:
AGAGATGGTGGGGAACAGTGGAATTAAGTAAAGTGCTTGTCTGGTCTGAGAACCACTTTATATCATATATCTACAGTATCAGGCAGTGAAGATCACTGATTTTTAAAGAAAGCACATCTTAATTGTGGTGATTTTTGTAAGGGAAAGTTCATTGGAAGCCATTGGGCTGGCTGGTTGAAAAATTAGAAGTCTGTGTGGATGTATGATATTGTGCATTGTGAAAGTTTGCTGAGGGCCACTGAGAAGCACTGAGAAGATCAGTAAATCCTAAAATTAAAAACACATTGGTGTATTCATTTAATAATCATTCAAAGGCTGTTCTCTTATGGTGTAGGAATCTTCTGATATTGTTTATGCAACTGGCAGTTTGCTTTGTGTCCTGTGCAGGCTACAGATGGGAGAGACAGCTGGTGTTTCGGAGCAAACTCACCATGCACACCGCGTTTGACCGCAAGGACAACGCTCATCCTGCCGAAATCACCGCTCTTGCCATTTCAAAG[T/C]AGGCGCTTTGTGTGTTCTGTGGGGAAATGAGAATAAAAGAGAAGATGTTTTCTGCTGTGCTTTTTATTGTTACTTAATAATAACACTGTTTGCACAGAGGATATCTAATGAATTTTGTGCAAACAAGGAAGAGGGCTGACGGCAAGCTGTTGTTGTGTTTTCAGAGACCACAGTAAGATTCTGGTAGGTGACGGTCGAGGGCGAGTGTTCAGCTGGTCAGTGAGTGATCAGCCGGGTCGCTCTACTGCAGATCACTGGGTGAAGGACGAGCAGGTGGACAGTTGTTCTGGGTGCACCGTCCGCTTCTCCCTCACCGAAAGACGCCACCACTGCAGGAACTGTGGACAGGTCTTCTGCCAGAAGTAAGGTTATGTGCAGTAAAATGTATCATGTGCAAACAACACAATTTAATTAATGAATGAATTGGTTTATTTAAATTTTATTAGTTTATATAATTAATATTTTAGAATAAAAGGACTACTTCTGTTGCTGTTTTTTTT
Associated Phenotype:
Not determined