ZMP
ush2a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Usher syndrome 2A (Autosomal recessive, mild) (USH2A) [Source:Un
Human Orthologue:
USH2A
Human Description:
Usher syndrome 2A (autosomal recessive, mild) [Source:HGNC Symbol;Acc:12601]
Mouse Orthologue:
Ush2a
Mouse Description:
Usher syndrome 2A (autosomal recessive, mild) homolog (human) Gene [Source:MGI Symbol;Acc:MGI:134129
Alleles
There are 26 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16626 | Nonsense | Available for shipment | Available now |
sa14011 | Nonsense | Available for shipment | Available now |
sa23107 | Essential Splice Site | Available for shipment | Available now |
sa23106 | Nonsense | Available for shipment | Available now |
sa13155 | Nonsense | Available for shipment | Available now |
sa23105 | Nonsense | Available for shipment | Available now |
sa11300 | Nonsense | Available for shipment | Available now |
sa1881 | Nonsense | Available for shipment | Available now |
sa13319 | Essential Splice Site | Available for shipment | Available now |
sa14237 | Nonsense | Available for shipment | Available now |
sa18585 | Nonsense | Available for shipment | Available now |
sa23104 | Nonsense | Available for shipment | Available now |
sa14514 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16626
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 81 | 5236 | 1 | 72 |
ENSDART00000086201 | Nonsense | 81 | 5236 | 1 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29830507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29754434 |
GRCz11 | 17 | 29771397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCWCACCAGCGAGAGCSACGTGCGGGATTCCCGAAAGGAGTACTTTCTG[T/A]CAAGCTGSCCAGGTTCAGGAAGATCTCCTYACTTGCATCCAGAAGTTCTG
Long Flanking Sequence:
CAAAAGTAATTGTTAAGCTTTTCTTGCATCAACTGGAATTCTTAGAGCCTCAGGGAAGATGTCAGGGTATAATATTTTTCCTAAATAGGTTTTCACAAATGATTTTGCTCTTCCTTTTCTCCTTTGGTTTTCTACAGGACTTTGACGGAGCCCAAATCCTAGCTATCATGTGAAGGCTTTGGCCTCCTCTTTGACATTGTGCCATTAAGCTGCGCTGCCTTACCCAAGGCACTGGACTGTAAAAATGTCACCACCGGCATGACCATCATTACTTATTTAAGATCACTACATCAGGAGGCAACCTCGCCACCAACAACGAATTGGCTCCTTGGGCACAAAGGTGCTATGTTATTACTGTACACCTTGGGCTTTTATGCCTCCCTCAGCCTGGTTGCCCCTCAGGGCAACTTCCCCAGGCTCGAGAACATAGGGGCACATAAATCTGTCAGCACCACACCAGCGAGAGCCACGTGCGGGATTCCCGAAAGGAGTACTTTCTG[T/A]CAAGCTGGCCAGGTTCAGGAAGATCTCCTCACTTGCATCCAGAAGTTCTGCATCCAAGAGTGTCCTCGCAGGCCTTCTACACCCGAATACATTGATGTTCTCACCGTAAACGTGGCCACGTGCTGGAAGGGCGATGCACGGGACCTTCGGCCAGGCGCAGAGGCCAATTCCAGCAGCTTCGTCTTTCCCACTTCAAAAGGTTGTCCGGCTTCCCCCTCGACTCTAGGCTACAGCCCAGCGAGCTCATTTACTTTAACGGTGTGGCTGAAACTCGAGCAAGACACTGTAATGTAAGTAGACACACGTCCAGAATTTTCCCTTAAGAAGATCAGAGAGGTAGTGCAAGTGTTTCTGTCACTTAGAGAGTGAATATTTTACTTAATCAACGGGATCAGTTTCAATACCTGCTCAGTTCCAGGAAAAGAATGACTTGTTAGAGCAACTAAAGTTGTATTATCTAAACCCGATATGGATTAGCTCAGCCGCTCGCCTTGTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14011
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 81 | 5236 | 1 | 72 |
ENSDART00000086201 | Nonsense | 81 | 5236 | 1 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29830507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29754434 |
GRCz11 | 17 | 29771397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCWCACCAGCGAGAGCCACGTGCGGGATTCCCGAAAGGAGTACTTTCTG[T/A]CAAGCTGSCCAGGTTCAGGAAGATCTCCTYACTTGCATCCAGAAGTTCTG
Long Flanking Sequence:
CAAAAGTAATTGTTAAGCTTTTCTTGCATCAACTGGAATTCTTAGAGCCTCAGGGAAGATGTCAGGGTATAATATTTTTCCTAAATAGGTTTTCACAAATGATTTTGCTCTTCCTTTTCTCCTTTGGTTTTCTACAGGACTTTGACGGAGCCCAAATCCTAGCTATCATGTGAAGGCTTTGGCCTCCTCTTTGACATTGTGCCATTAAGCTGCGCTGCCTTACCCAAGGCACTGGACTGTAAAAATGTCACCACCGGCATGACCATCATTACTTATTTAAGATCACTACATCAGGAGGCAACCTCGCCACCAACAACGAATTGGCTCCTTGGGCACAAAGGTGCTATGTTATTACTGTACACCTTGGGCTTTTATGCCTCCCTCAGCCTGGTTGCCCCTCAGGGCAACTTCCCCAGGCTCGAGAACATAGGGGCACATAAATCTGTCAGCACCACACCAGCGAGAGCCACGTGCGGGATTCCCGAAAGGAGTACTTTCTG[T/A]CAAGCTGGCCAGGTTCAGGAAGATCTCCTCACTTGCATCCAGAAGTTCTGCATCCAAGAGTGTCCTCGCAGGCCTTCTACACCCGAATACATTGATGTTCTCACCGTAAACGTGGCCACGTGCTGGAAGGGCGATGCACGGGACCTTCGGCCAGGCGCAGAGGCCAATTCCAGCAGCTTCGTCTTTCCCACTTCAAAAGGTTGTCCGGCTTCCCCCTCGACTCTAGGCTACAGCCCAGCGAGCTCATTTACTTTAACGGTGTGGCTGAAACTCGAGCAAGACACTGTAATGTAAGTAGACACACGTCCAGAATTTTCCCTTAAGAAGATCAGAGAGGTAGTGCAAGTGTTTCTGTCACTTAGAGAGTGAATATTTTACTTAATCAACGGGATCAGTTTCAATACCTGCTCAGTTCCAGGAAAAGAATGACTTGTTAGAGCAACTAAAGTTGTATTATCTAAACCCGATATGGATTAGCTCAGCCGCTCGCCTTGTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23107
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Essential Splice Site | 295 | 5236 | 4 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29794992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29718919 |
GRCz11 | 17 | 29735882 |
KASP Assay ID:
2261-1203.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAAGGATGCAGGATTTTAGATTTTATCCGAAGACATTAACCAACAGG[T/C]AAGCATAAGGTCGTACAGCATTAACATCAGGCATAGCTTTAGAGTTTTCA
Long Flanking Sequence:
TTTGCAGAGTTCCTGTAAACCATCAATACCAATGTGTGTGTGTGTGTGTGCATGTGTGAATGATAGGAGCAAAATAAATACAGCAAAATGCTATCTCCTATAAAAGAGAGACTCTGCACACAAAGATGAAAAGATTTCAGGGCAAACATCCATATATGACGTCTCAATCAGAGCCGGTTATTAGAACAGAAGTGATTATATCTTATCTGCTGATGTAGATGGACCCGCACGTTTAGACTCGGATCTATGCCGCCCATCCATTCTGTGGGATTAATGCTCACAGAGAACTGTAAATAAGCATAATAGATCCCACCATGCAGCAAGTGTCTCTTTAACTCAAATAAAGACATAGATAAGGTAATCCACTAGTTGTTATGGATTCTGCACACCGTCTTCAATAGCGCCCATTGACTTTCCTTTCTTTTTTCTCCCCAGGGTCAAATCAATTCATTGGAAGGATGCAGGATTTTAGATTTTATCCGAAGACATTAACCAACAGG[T/C]AAGCATAAGGTCGTACAGCATTAACATCAGGCATAGCTTTAGAGTTTTCAGAGAAAAACATGCTACACTGTAAACAAAACATTAATTTACAGTTGCTGTACCTCATTTCTGTTTATTTGCACTTTAATTGCATTATGAGACCTTGATCTCTGCATCGCTGCAATTACTTTTACTGACATGCTTAGATATTGTTTTATATTATAACATCTAAAATAAAGCAATATAAATAAAATATTAATAATATAATATAAAACAATTGAAAAAGTATATATATGTATGTACACTCACCGGCCACTTTATTAGGTTTACCTGTCTAACTGCTCATTAATGCAAATTTCTAATTACATGGCAGCAACTCAATACATTTAGGCATGTAGACATGGTCAAGACGATCTGCTGCAGTTTAAACCAGACATCAGAATGGGTAAGAAAGATGATTTAAGTGACTTTGAATGCGACATGGTTGTTGATGATAGACGGGCTGGTCTGAGTATTTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23106
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 730 | 5236 | 11 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29757283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29681210 |
GRCz11 | 17 | 29698173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTGCAGCCAGATATTACCTGTCACCAGGACTCAGGTCAATGCCAGTGC[A/T]AGGCAAACGTAATCGGTACGTATCAAGCAGCATTGCGGCCTCCATCGCTC
Long Flanking Sequence:
TCTTTCTGGCCAGCAGTATTAAATATTTCCTCCCATACATCCAAACACAACAGCTGCTATATTCAACCTCACCCAAAGAAGAGACCCATTCTGTTAAAGCACCCGACCCTCAGCACAAAGGCAGCTTTTGAGCTCAGGTGTTGTGACCCCTCTGCGCCCCCCCATCCCAAACCATTCAGTTCTCTGTAATGGAGATAAAAAGCATCCCAGCGGCCTGCTGGTGGATCAGTATAGAGACAGAGCAGAGCTTGGCCATCCATGACTCCCGCTCAACTTGACTAATTGGAGCGCGGTCACGTGCTGCTCTCTTTCCTCCGCAGATCGGGGGCCAGTGTAAGTGCAAGCGACATGTGTCTGGCAGACAGTGCAATCAGTGCCAACACGGATTCTACAAGCTGCAGTCGGCGCTGGCTGACGGCTGCCGTGCCTGTAACTGCAATACCGCCGGGACCGTGCAGCCAGATATTACCTGTCACCAGGACTCAGGTCAATGCCAGTGC[A/T]AGGCAAACGTAATCGGTACGTATCAAGCAGCATTGCGGCCTCCATCGCTCTTACGCTCTCTGCTCCCATCCTTCTCTTTCTTTACAACTTTTCTTTGCTTGTCTCTCAAGCTTTATTTTTGTTAATTGCCACTAGGGCTGCTCGATAAATCATTTTTTGCAATGTGCAAATCTGCAATATTCACATTGCAGGATCTGCAATGCCAAACTGGGATTATAATTAACCAGAAAACAGTTCAGAACATGCATGGAGAACATGGAGTTGTTGCTAAGTTTATCTTTAATCTAATAATATGAAGTACTTTTATTTGGATGTTTTTTGTTTTTTTTGGTGAATTTAACCCGTTTAGGCACAAGCAATTGTAAAGTTTGTCGGTTTAGTAAAGAATAGTTGTTTGATTATTTCATGCAATACAATAAAGACTATTCAGTGTTATTTTACATTAGAGTACTGAATTTCTGTTATTCAGTGCTGGTAATGTCCAACCGAAAACCATAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13155
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 2140 | 5236 | 32 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29664186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29588113 |
GRCz11 | 17 | 29605076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NCCCTCTCTCTATCCAGACGTTGGTGTGTTCACTCCWCATAAGYTGCTGT[T/A]GAGTGCCTGTACTGAGGCAGGATGTACCAACAGTRCCCAGGTTACCCTGT
Long Flanking Sequence:
TTAATATAGAAACTATTCATAAAATCACTTTGCCTTTCCAGTCATATTTATTTTTATAGGTTTTGTAATAACGCAGGGGTTGGAACACTTTTGTACCTTTTAAATGAGAACAATTGCATACCTTCATTTCAGTGGTACCATAAAAGGCACAGAACAGTACCATAAGAGGTCTCTTCTGTACCATATTTAATTGTCATACACAATTTTTACAAAGGTAAAGAACTGTTCCTTGTTGAACATTATTTGGACCATAGCGTACCTTGTATTCTGAGACTGTACTGTAGTAAGCTGTAATACAGACTCAACATTGCACATCCTCCAATGTGACTATTAAAGATGCACACAATGAAATGTCGATGCTGAAACGATAAACCATGTTGTAAGCCCTATTCCAAACTGTATTTGACAAGGTTTCATAGTATTTTTCATATTTTATTCATGTTTTTTTTTTCCCTCTCTCTATCCAGACGTTGGTGTGTTCACTCCTCATAAGCTGCTGT[T/A]GAGTGCCTGTACTGAGGCAGGATGTACCAACAGTACCCAGGTTACCCTGTTTACAGGCCAGTTGCCTCCTACTTATGTTGAGCCCCCCATCCTGACCGTGTTGGATGCCCGCAGTATCCACATACAGTGAGTATGACCAAAAAAAAATAAATTAATGTCACAAATTATACAGTACGTGGATTTTTTATGGAGTTTTTTTTATGTATTTAAACTGGTTTTATGTAAAAAATGTTGTCCCTAGAAAAGGAGAAAACACATTTAACCCTCCCTAGGTCTCGTCCTTGAACAGCTCACACAAGCACATGAACACTAACAAGGCATGAACAGAAGTGAAGATGGCCGTTCTCACCTTTTATAAGGCAATGTTTTATCAGAGAGATACGCTAATGAGGTGACAGACATTTGCTCTCTGCAAGAGGACAAAACGCATCTCAGGTCTCGTTATTCCTCACCATTATACAAAAAATAGCCTGCACATGTCAAAGCCATAACCCCTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23105
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 2378 | 5236 | 36 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29647621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29571548 |
GRCz11 | 17 | 29588511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACGAGCCAAGTGGGAGGCTCCCGCTGAACCCAACGGCAATCTAACCTA[C/A]ACAGTCCTCTTCGCAGGGCCAGGTAAATCAAACTTAACTGCTCCCCATCG
Long Flanking Sequence:
TGTTTTGCTTTGCTTGGCTTTGCTTTTTTTGCGAAATTATTTTAGACATATAACAAATGGTTACATTTTGATTGATAGTCCTAGTTCCAAGCAGAAAATAGGTGCATACCAGTTATGCAGTAATCTATTCAGATAGATAGATTGTTAGATGGATGGATAGATGGATAGATAGATAGATAGATAGAGAGATAGATAGAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATCATTATAGTGTATAGTGCTTTATTTGGGACACCACTAATATATTTATCTCGGTTCTTAGGTGGAAAGCAGGACTTTAGAGATGCCCCCCGTTGGCCATGTGACCCTTGTTGTCTTCAGCGAGACGCCACATTCAGTACGAGCCAAGTGGGAGGCTCCCGCTGAACCCAACGGCAATCTAACCTA[C/A]ACAGTCCTCTTCGCAGGGCCAGGTAAATCAAACTTAACTGCTCCCCATCGCTTCTCCACATCCCCCTCAGTTCCTCCGAGTGAACGCAACACTGCCTCCCTGCATGCTACCCCTGCTCCTCATATTGACTTCTGCTGTTTTCCCTTTGTTTGTTTACAAACAAAAATGCTGAAAGGTCAGTGAACCTTAGCACACCCTGCCTGCGCGGTAATAGGCTTAAATGAATTGTTGTCGGCCTCCATTTTGCTCAGGCTGACTATAGCAGGCCGGAAGGGCTTCAAGAGGACACCCGTACTCATCACACGCTCTTCTCCTCTCATTCTTCACGGGATGAAAGTGGACAGGTTTGTTAAAAAGCGTAATGGCACGTTCAAAAGGAATCTCCCGATGCTCGGTTGGAGCTTCCCCTATGCTGGTTAGAGGATAAACGCTTGCTGTAATGAGAGGGTGAGGGGTGCAAACACGCGTTCTTTATGTGAGTCTGTCAAGATCATGAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11300
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 3256 | 5236 | 49 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29569538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29493465 |
GRCz11 | 17 | 29510428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATAATATTACAACATATATKTATGCATGTGTTTTGTAGGAGAGRTCTG[T/A]TGTCTGGACTCTGTGGAGYAGCGTGTATCAGTGGGTCTCGGGGACTCGTG
Long Flanking Sequence:
CGCTGGAGAGAATCTATCCTGCCCTGATTTCTCGCCAAAGTAGGCAGTGGAGTCCGGCTAAATATAGCCCGCCGCTGTGGAGCGAAGAGGTGGGCTGGATTTCTACCTGCGCCTCTGTGGGCCCTCAGGACCGGAGCGTTGCCACCTCTTAACTTCTTAATTGCCTCGAGGAGTGCAAAACTTTGTTGATAATGTATTTGAATTGCATATATTTTGTGCGTGTGCTCTATTGTTTCAGATTTGCTGCTCAGGGACCGTTCACAACTTAATTCAGTCTCATCAGTGCTGTGAAGAGCGATATATTCCTGCTTCAGAGGATTCAGGGAGTGTGTGTTGTGGAGGTCAGTTTGTCCAGCCTCTGTCTCAACACCAGTGCTGTGGTGGATATCACGTACTTGTTTCACCAGGTATCTACTGCATTCAGTTCTTATCTCATTTATATTTGTTATTGTATAATATTACAACATATATTTATGCATGTGTTTTGTAGGAGAGGTCTG[T/A]TGTCTGGACTCTGTGGAGCAGCGTGTATCAGTGGGTCTCGGGGACTCGTGTTGTGCTGGGCGTCCTTTCGTCTCAGGAGTGGGACAGATCTGCTGTGGGGGTCGTCTGTATGATGGCTTCAAGTCCCAGTGCTGTGGAGGACAACTAGTCCCTAGAGAAACAGAGTGTTGTGGGGATGAAGAAGAAGGGATATCCTATGAACATGTGTCAGGTGAGCTTTTAGAAACATTCTTGCTGAAAAATGGTTCTGTTTTAAGTAGGGATGAACTGAATTTTTGACTGACAAAAATTAACGGTCGAAAATATAATTTGCTGTTTTCATCTAAGAGAGCAAAAAAGATAAAAGTATGAGGGGGGAAAAGACTCCTCCACAGTGTTCAACTCGCAGGTCTCATAGACTGATTTCACGCGGCCGCCATTTAAAAAGTGAAATTGAGGCTGTGGTGGGAAGAAATTCTGAAGTATCGCCTGAGTCACGCAGTAATGTTGTGTACCTAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1881
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 3263 | 5236 | 49 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29569519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29493446 |
GRCz11 | 17 | 29510409 |
KASP Assay ID:
554-1871.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTATGCATGTGTTTTGTAGGAGAGRTCTGTTGTCTGGACTCTGTGGAG[C/T]AGCGTGTATCAGTGGGTCTCGGGGACTCGTGTTGTGCTGGGCRTCCTTTC
Long Flanking Sequence:
TGCCCTGATTTCTCGCCAAAGTAGGCAGTGGAGTCCGGCTAAATATAGCCCGCCGCTGTGGAGCGAAGAGGTGGGCTGGATTTCTACCTGCGCCTCTGTGGGCCCTCAGGACCGGAGCGTTGCCACCTCTTAACTTCTTAATTGCCTCGAGGAGTGCAAAACTTTGTTGATAATGTATTTGAATTGCATATATTTTGTGCGTGTGCTCTATTGTTTCAGATTTGCTGCTCAGGGACCGTTCACAACTTAATTCAGTCTCATCAGTGCTGTGAAGAGCGATATATTCCTGCTTCAGAGGATTCAGGGAGTGTGTGTTGTGGAGGTCAGTTTGTCCAGCCTCTGTCTCAACACCAGTGCTGTGGTGGATATCACGTACTTGTTTCACCAGGTATCTACTGCATTCAGTTCTTATCTCATTTATATTTGTTATTGTATAATATTACAACATATATTTATGCATGTGTTTTGTAGGAGAGGTCTGTTGTCTGGACTCTGTGGAG[C/T]AGCGTGTATCAGTGGGTCTCGGGGACTCGTGTTGTGCTGGGCGTCCTTTCGTCTCAGGAGTGGGACAGATCTGCTGTGGGGGTCGTCTGTATGATGGCTTCAAGTCCCAGTGCTGTGGAGGACAACTAGTCCCTAGAGAAACAGAGTGTTGTGGGGATGAAGAAGAAGGGATATCCTATGAACATGTGTCAGGTGAGCTTTTAGAAACATTCTTGCTGAAAAATGGTTCTGTTTTAAGTAGGGATGAACTGAATTTTTGACTGACAAAAATTAACGGTCGAAAATATAATTTGCTGTTTTCATCTAAGAGAGCAAAAAAGATAAAAGTATGAGGGGGGAAAAGACTCCTCCACAGTGTTCAACTCGCAGGTCTCATAGACTGATTTCACGCGGCCGCCATTTAAAAAGTGAAATTGAGGCTGTGGTGGGAAGAAATTCTGAAGTATCGCCTGAGTCACGCAGTAATGTTGTGTACCTAGCTGTATATCTTGTTAGCGAAG
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:
sa13319
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Essential Splice Site | 3548 | 5236 | 52 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29539182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29463109 |
GRCz11 | 17 | 29480072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGAKGACATCATCCAGCTGGAATGGTCTGCCCCAATCAAACCCAATGG[T/C]AATGACCTCCAAATATATAATTACYTCCAAATATATRATTACCTCCAAAT
Long Flanking Sequence:
AAAATAATAAATAAGTTTTCTTGGTTACCTTTGTTGATCTGCTATGAAACAGTGTCCTCTGGGAAGGATATTTTATCATCCTGTCACTTTTAGAAGTGCTTCTGTCTGTCTGATGAAACCCATCACAAAGATTTACACTCATAACTTCCTGCACATGCGTTTACAACAAACCACTGTATTTCTGATAACAAAGAGCATTACAGTAAGCGCAGGTCTCCTGCTGCCCTTTAAACTGTACTTTTGTTTTAATGTGAAGCCTGGGATGCTTTAGAGACTAGTTGTTTTTGTGACTGTGTTTCAGACACTGAGCTGGAGCCGTACAGCAGTTATGAGTATAGGGTTGGTGTGTGGAACAGTTTTGGCCGTGGGTTCAGTGTCTGGACTCGTGTCAGGACAGATGAAGATGTGCCCTACAGTGTGTCTCCTCCGAACTGGAGTCATGTGGGTCTGCGTGATGACATCATCCAGCTGGAATGGTCTGCCCCAATCAAACCCAATGG[T/C]AATGACCTCCAAATATATAATTACCTCCAAATATATAATTACCTCCAAATGTTGAAGTCAGAATTATCAGCCCCCCTGAATTATTAGACCGCTTGTTTATTTTTTCCCCAATTTGTGTTTTTACAGCAGATTTTAACTAGGCAGGTTAGGGTAATAAGGCAAGTTATTGTATAACAATGAATTGTTCTGTAGATTATCGAGAAAAAAATTTAGCTTAAAGGGGCTGATAATTTTTTCCTTAAAATGGTGTTTAAAAACTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGATTTTTTTCCAGTAGGAAAAACATTATCAGGCAACCTGTGAAAATTTTCTTGCTCTGTTAAACATCATTTTGGAAATATTTAATATTAACTCATTTCTAATCAGCCAATCACAGGGAAGCAACCTTAATGCATTTAGGCATGTAGACACAAACCAAGCATCAAAATGGGGCTGAACGGTGATTTAAGTGATTTTGAACGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14237
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 3824 | 5236 | 58 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29500079)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29424006 |
GRCz11 | 17 | 29440969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTTTCTGTTTCCGTTTGCTTRTAGGTGTGTATAATTTAAGTTTCCCTT[T/A]GGAATATAACAYCCTGCTCAACGCAGGCACTGAGCGGCCACTCATTCGTT
Long Flanking Sequence:
TTGGCTCTCATAAATGTTGAATAACCTATCAGCCTCCAGTTGCCGTAAATTATGAAAGGCGCTAGTGATGGGAATATTAACAAAGCGTGGGTGCCAGGACTCTACATTCTTTAGTTCAAATGCATTACAGAAGAGCATGAGCGTGTCTGTGTGTTTCGGACAGCGCTGGGATAGACGGATCAGGGGAAGTGCCTGCTTGCCCAGATGGATGTTGGATCAAGGGCAAAGCTTCCAAAAGTGTCATATCCACTGTGTGTCAGTTCTTGCGCTGTAGTATAAGTACATACTGCGATTGTGGAAAGGATTGCGTGTTTGTTTTGTCACTAATAATTTTGTTTAGTGATTGGTGATTGTATTTATGTCGGGTTTCTACAATTTAAACCTGCTTTGACAAGCCTGTAATGCTAATTTCCTTGGATATACAGTAAGTGAGTTAAAACAATTGAATGTGACTTTCTGTTTCCGTTTGCTTATAGGTGTGTATAATTTAAGTTTCCCTT[T/A]GGAATATAACATCCTGCTCAACGCAGGCACTGAGCGGCCACTCATTCGTTCTGCTGGACTAGAGCAATTCCTGCTACTGCAAGGACTGGACCCCTATACCATCTACCATGTCCAAGTACAAGCCTGTCAGCCAGGTACTCTGGAAGCTGAAATGTGCTCAACATTAAGAGACAGTCAAAACATGATATGATTAGGGGGATATTTCAGCTTAGGAGGAGACATCAGCAATTATAATTCTGGAAATATATATGTATTTTTTTACTTTTTTATATACATTTAAACATTTTACAGAACTGAACAGTCAGTGACAGCAGCAGCTATTTTTAAAAAAATAGTTAAATAATAATAATAACACTACCAGTAAAGAAAAACAAATTACAAAAAAACACATTCATAATTTTCCAATTTTAAAGGGTACACCTGGGAATATTATGTCCTGTTGCCATGTTCAGATACATAGTAACAAGTGCCCATCTTTGTCTAAAAATATCAATTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18585
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 3826 | 5236 | 58 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29500072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29423999 |
GRCz11 | 17 | 29440962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTCCGTTTGCTTRTAGGTGTGTATAATTTAAGTTTCCCTTWGGAATA[T/G]AACAYCCTGCTCAACGCAGGCACTGAGCGGCCACTCATTCGTTCTGCTGG
Long Flanking Sequence:
TCATAAATGTTGAATAACCTATCAGCCTCCAGTTGCCGTAAATTATGAAAGGCGCTAGTGATGGGAATATTAACAAAGCGTGGGTGCCAGGACTCTACATTCTTTAGTTCAAATGCATTACAGAAGAGCATGAGCGTGTCTGTGTGTTTCGGACAGCGCTGGGATAGACGGATCAGGGGAAGTGCCTGCTTGCCCAGATGGATGTTGGATCAAGGGCAAAGCTTCCAAAAGTGTCATATCCACTGTGTGTCAGTTCTTGCGCTGTAGTATAAGTACATACTGCGATTGTGGAAAGGATTGCGTGTTTGTTTTGTCACTAATAATTTTGTTTAGTGATTGGTGATTGTATTTATGTCGGGTTTCTACAATTTAAACCTGCTTTGACAAGCCTGTAATGCTAATTTCCTTGGATATACAGTAAGTGAGTTAAAACAATTGAATGTGACTTTCTGTTTCCGTTTGCTTATAGGTGTGTATAATTTAAGTTTCCCTTTGGAATA[T/G]AACATCCTGCTCAACGCAGGCACTGAGCGGCCACTCATTCGTTCTGCTGGACTAGAGCAATTCCTGCTACTGCAAGGACTGGACCCCTATACCATCTACCATGTCCAAGTACAAGCCTGTCAGCCAGGTACTCTGGAAGCTGAAATGTGCTCAACATTAAGAGACAGTCAAAACATGATATGATTAGGGGGATATTTCAGCTTAGGAGGAGACATCAGCAATTATAATTCTGGAAATATATATGTATTTTTTTACTTTTTTATATACATTTAAACATTTTACAGAACTGAACAGTCAGTGACAGCAGCAGCTATTTTTAAAAAAATAGTTAAATAATAATAATAACACTACCAGTAAAGAAAAACAAATTACAAAAAAACACATTCATAATTTTCCAATTTTAAAGGGTACACCTGGGAATATTATGTCCTGTTGCCATGTTCAGATACATAGTAACAAGTGCCCATCTTTGTCTAAAAATATCAATTTTAGTAGAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23104
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Nonsense | 4183 | 5236 | 62 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29467720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29391647 |
GRCz11 | 17 | 29408610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCACCACAGAAGAGGCCATCCCATCCTCTCAACCAGCCCCCACAGTCTA[T/G]CAGGTACATTCCCGCAGTGTGGAGCTCTTCTGGTCTCCACCAGCCCAGCC
Long Flanking Sequence:
GGGTAATGTTTTTCAGGCTTATGTGTTTGGTTTAGAGCCTTACACCACATATAATATTCGTGTGGAGGCAGTAAATGGAGCAGGTCAGGTGTCAAGTCCCTGGACCACCATTCGAACCCTAGAAGCCTCTCCGAGTGGCCTGGCCAACTTCAGCGTTGAGAGAAGAGAACATGGCCGAGCTCTGCTGCTGCAGTGGGCAGAACCTGCTTCTCCTAATGGAGTCATCAAAGTATGTAATCCTTGGTTACATCATAACAGTCACGCTTCAGAATCACCCCTCATTTAACACATTCTTCTCCACAGATGTACAACATCTTCAATGAGGACAACTTGGAGTTTAGCGGCCTCGCACGCCAATTCCTCTTCCGCCGTCTGGAGCCCTACACAGTGTACACACTCATTTTGGAAGCTTGCACTGAAGCAGGCTGCACCAGATCTGCTCCTCAACGGGTCACCACAGAAGAGGCCATCCCATCCTCTCAACCAGCCCCCACAGTCTA[T/G]CAGGTACATTCCCGCAGTGTGGAGCTCTTCTGGTCTCCACCAGCCCAGCCCAATGGCAGGATCCTGCAGTACCAGCTTCTGGCTGTACGTCTGGAGGACGGCAGGGTGCGCAGTGATGAAGATGACTCCTTGAGAGCCAAGATCGTCTTTATCCAGAACAACACCCAGGCTAACAGCTTCTCCTATAATATGTCTGGCCTCCTGCCCTGGAGCAGGTACAAGTTTCGTGTGCGTGTCTCAAATGCGGCAGGGTTTACTGATAGCCCCTGGCTCACGGTTCAAACCAAACAAGCTCCTCCAAGAGGACTGGCTCCTCCGTCTGTCAGTCACATAGAGGGCAAGCCTAATGAAGTCTTCGTAGCTTGGACGCCTCCATTGGAGCCCAATGGGGTTCTTCTCACCTACAGGATTCAGAGGGATAACATTGGCTTTCATTTCAGCTTTGATTCGAGTGTGTTCAACTACACAGATGTGGATTTAAACGCATACACTCTCTACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14514
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 |
---|---|---|---|---|---|
ENSDART00000086201 | Essential Splice Site | 5012 | 5236 | 67 | 72 |
Genomic Location (Zv9):
Chromosome 17 (position 29447478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29371405 |
GRCz11 | 17 | 29388368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAGYGGCTTCCACAGYTTTCTACACATCCCACGCACCTCGGATAAAAG[T/A]ATGAACAMTGTGTGCCTCMGGCAGGACTCCATTTGACTCACAGGCYAGAS
Long Flanking Sequence:
AATTTTGACTACATTAATTAGTAGGACATAGTTTTTAATTTTTATCGTGGAATTTTGACTTTTTAATGCATTTTTTTTTTTACCTGGCAGAAATGGGCTTACATAGCTTTAGGTGTATTATTTGGGTTTTTCTTATATTGCATATATCTGTTTACTTCATTTTGCATATATATTTGTGTATTTTATTTTGCATATTTGGTGTGAATACGTTTAGTTTTGACTAGATAACCTTAAGACTAACATAAAAAATGATTTCAGTGGGACTTTATAAAAAATAGTTATGGCACATAAATCAATCCCCTCTGTCACTGTTTCCCTGTAGCTCCTCAGTATATGGAGGCATTTGTGGTGCACAGTAACCTGACCTCAGTGTTTGTGGACTGGAGTGGCTCTTTCTCTCTGAACGGGCCTCTGACAGAATACAGTCTAACCGAAAGCAGCCTGCGCGTCTACAGCGGCTTCCACAGTTTTCTACACATCCCACGCACCTCGGATAAAAG[T/A]ATGAACACTGTGTGCCTCAGGCAGGACTCCATTTGACTCACAGGCCAGACTTTTTTAGTTCCCTTTCAGTATCCTTGTCTCTCATCATCTGTCCGGTCTCTTTTCTCTTCAGCCTTTGCATTCCAAGTGACCTGCACCACTGACAGTGGCAGCGCCAGTTCTCCTGTCATTAAATACAACACGGCCACTGGTATAGGTATGTTTCTTCAGGTCTGCCAAGTGAAGGTGACTGGAGAAAAAAAGCAGTGTCTCCATCCTGACTGTCTGAGTAGAGCTGTTCCCCTGCCAGTATCACTGTTGCAGACTTTATCAGAGTTATCACTGAAAAGCCTGTTCACTTTTTGGTTTTGACAAGGAAATTGATGTTTAAACTTCTTTTCAGAATTGCTATATACAGTAGCAGATGGCTGCAGTCAAACTGGATGAGCGAAAACTGTGAATTTTACCACCCTTATTGTTTTACTTATTATACAGTCAAATGGCCATAAATATAGTTGGTG
Associated Phenotype:
Not determined