ZMP
si:dkey-76b14.4
Ensembl ID:
ZFIN IDs:
Description:
Novel protein (Sb:cb26) [Source:UniProtKB/TrEMBL;Acc:B8JKW4]
Human Orthologue:
C3
Human Description:
complement component 3 [Source:HGNC Symbol;Acc:1318]
Mouse Orthologue:
C3
Mouse Description:
complement component 3 Gene [Source:MGI Symbol;Acc:MGI:88227]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32790 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10419 | Essential Splice Site | Available for shipment | Available now |
| sa18656 | Nonsense | Available for shipment | Available now |
| sa19621 | Nonsense | Available for shipment | Available now |
| sa31242 | Essential Splice Site | Available for shipment | Available now |
| sa8557 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39715 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31241 | Nonsense | Available for shipment | Available now |
| sa1745 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32790
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Essential Splice Site | 24 | 1635 | 2 | 42 |
| ENSDART00000052688 | Essential Splice Site | 23 | 1643 | 2 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56720563)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55504496 |
| GRCz11 | 1 | 56173792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTATTATTAAATACGCAAGTTTTCAAGCGCTCTGATTTGATCTCCTC[A/T]GATATGTGCTGTCGGCTCCTAATCTGCTGAGAGTGGGTTCATCAGAGAAC
Long Flanking Sequence:
TAAGGGAGAAATGGTTAGTAGTGGGCGGGGCTTTCCCCCTTGGATGACACGTACAAAGGGACAATGTCAATCAAAGTGTTTCTGCAGACTGTTTCATATCATGTGTGATTATAACAAATATAATTAATTTATCGTTACCATTAGCAGCTGACTATATTCACTGATTGTTGCCACACATCTATGCTTAACCCCTAATAAAAGTGATTTTTGCATAATAGGTTCCCTTTAAATGACTTATGAATATAAAAGTTTAAATTGAATACTAAATTAAAAGTTTCAAATATAGACAAATAAAGCCACCTAACCCAACAACAATAATTTAACAGCTAAAAAACATTCAACTTCCTCAAATTTCAGCATTTTGTCTGGCAAAATGAGACATTTGCCATATTAAATGAGACACTGCTGCAGTTTTAGTACTAGCTGGTACTGTTTAATTTCTTCTTCTTCCTATTATTATTAAATACGCAAGTTTTCAAGCGCTCTGATTTGATCTCCTC[A/T]GATATGTGCTGTCGGCTCCTAATCTGCTGAGAGTGGGTTCATCAGAGAACGTGTTTGTGGAGGCGCAGGATTACTCTAAAAATGCTTTTGAAGTGAAAATCACAGTAAAAAACCACCCGAAGAAAGACAAGCAGATCCTGACCAAATCAGTGAATCTGAATGCACAAAACAATTTCCAGATCCTCACAGATATAAAGGTGAGCGCTCCTAAATCACAATGCAGTGATGCCATCTTTGCATTTCATTTTGGATGTAGCTAATACATGAATCTTCTGATATTTAGATCCCTGATGATCAGAACTTGTTCTCCGATGATCCTCTGGAGAAGCAGTATGTGTATCTGCAAGCTATTTTCCCGGATCACACTCTGGAGAAAGTGGTCTTGCTGTCGTTCCAGTCTGGATATATATTTGTACAGACTGACAAGCCCATCTACACGCCTTCTAGCACAGGTACACTTGCAAAAATGAACAAGGTAACACTTTACAATAACAGTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10419
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Essential Splice Site | 89 | 1635 | 2 | 42 |
| ENSDART00000052688 | Essential Splice Site | 88 | 1643 | 2 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56720365)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55504298 |
| GRCz11 | 1 | 56173594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGAAWCTGAATGCACAAAACAATTTCCAGATCCTCACAGATATAAAG[G/A]TGAGCKCTCCTAAATCACAATGCASTGATGCCRTCTTTGCATTTCATTTT
Long Flanking Sequence:
AAGTGATTTTTGCATAATAGGTTCCCTTTAAATGACTTATGAATATAAAAGTTTAAATTGAATACTAAATTAAAAGTTTCAAATATAGACAAATAAAGCCACCTAACCCAACAACAATAATTTAACAGCTAAAAAACATTCAACTTCCTCAAATTTCAGCATTTTGTCTGGCAAAATGAGACATTTGCCATATTAAATGAGACACTGCTGCAGTTTTAGTACTAGCTGGTACTGTTTAATTTCTTCTTCTTCCTATTATTATTAAATACGCAAGTTTTCAAGCGCTCTGATTTGATCTCCTCAGATATGTGCTGTCGGCTCCTAATCTGCTGAGAGTGGGTTCATCAGAGAACGTGTTTGTGGAGGCGCAGGATTACTCTAAAAATGCTTTTGAAGTGAAAATCACAGTAAAAAACCACCCGAAGAAAGACAAGCAGATCCTGACCAAATCAGTGAATCTGAATGCACAAAACAATTTCCAGATCCTCACAGATATAAAG[G/A]TGAGCGCTCCTAAATCACAATGCAGTGATGCCATCTTTGCATTTCATTTTGGATGTAGCTAATACATGAATCTTCTGATATTTAGATCCCTGATGATCAGAACTTGTTCTCCGATGATCCTCTGGAGAAGCAGTATGTGTATCTGCAAGCTATTTTCCCGGATCACACTCTGGAGAAAGTGGTCTTGCTGTCGTTCCAGTCTGGATATATATTTGTACAGACTGACAAGCCCATCTACACGCCTTCTAGCACAGGTACACTTGCAAAAATGAACAAGGTAACACTTTACAATAACAGTACATGAATAATGATGTATTAATATGTAAACTAAACATTACTTTATTATGAATTAATGATGAGTTAAGGTATGCACTAAATATGAATTAACTTTAAGTTCAACATGAGTCACATGAGTTCATGTGTAAATGACGACTACCTTAATTACTTGTTAGTACATGTTGTTAATTAATGTATTAATTAACATTTAAGTTTAGGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18656
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Nonsense | 241 | 1635 | 7 | 42 |
| ENSDART00000052688 | Nonsense | 240 | 1643 | 7 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56716807)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55500740 |
| GRCz11 | 1 | 56170036 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGGTTTCAGTGCTTCCAACATTTGAGGTGAAATTACAACCCAGTAAAT[T/A]ATTCTACTATGTGGGCGAYGAAAGTCTGACAGTCGACATCGAAGCCAAGT
Long Flanking Sequence:
AATGCTAAAGCACAGTTCTGTGATGATAATACAGCAACTTCTCTTAGCCTGAAGTTCACTAAAAGACAAGTGAAATATTATTAGTTAAAATAATAACGAATGCAAATTCTTTACGGTGGGGGATGGTGGATATTTTCTGTGTATTATTGAAAGACTTTGGCCCTTAATGGCAGTCAGTTGGTTTATAGTGTCTACTTTAGGACAATATTCATGTTCCGTGCCTGTTACAATCAGTTTTAATGTTGTGAGATCAGACAAGTGTGTGTTTATGGATGTGTTCTGCATGTTTCAGTCTGGGCATCTGGAAGGTCGTCACACGATTCGCAAACACTCCCCAGAAGACGTTTACTGCAGAGTTTGAGGTCAAAGAATACGGTGAGATGAGTGTCAACACCATGTTGTGTAATAGTCTGATAAGAGTGTGTTTGCTTATTTGTGTGTTTGGTTGGATTTGGTTTCAGTGCTTCCAACATTTGAGGTGAAATTACAACCCAGTAAAT[T/A]ATTCTACTATGTGGGCGATGAAAGTCTGACAGTCGACATCGAAGCCAAGTAAGATAAAATGAGTTTAAAAAGTTGTGGAAATTCTCTGTTTTCCTTGTGGTATGACTATTATTTCAACTGAGATCATCTAAAAGACTAAGAAACAACATTAAGAGTTGTCCACAGTTTGTGTTTTCGCTGTATTTTATGCCGAGTTCAGACTGCATGATTTTCAAAGTAGTCGTGTCACAGATGTTTTCACACTGCATGACTATCTGGGCTTGCGTTTCGTCGCTGTTTTGTTTACACTGCAAGATGGATCGGCGACAGGGACATTCACATTGCATGACTTTACTATAGAAAGAATCGCCGACAACTTCGTCCAAACTACGTCTCACAGCCAAAAACACGTCGTATATCTTTTGTTGTTGACTACATGATGAGAAAGAAGCCTTTAATGGGACATGTACATGTTTGCTCACCTGGGTTTAAAGGGAATTCGCCATTTCTCCTCAACATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19621
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Nonsense | 361 | 1635 | 10 | 42 |
| ENSDART00000052688 | Nonsense | 360 | 1643 | 10 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56713979)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55497912 |
| GRCz11 | 1 | 56167208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGACGTCTCCATACACTATCAACTTCAAGAAAACAGCTCAATTCTTC[A/T]AACCTGGAATGCCCTTCGATGTCTCGGTATGAATTTGTTCACTATAAAGT
Long Flanking Sequence:
CCTGTTTGGAAAGCAGGTGGAAGGAAATGCGTTTGTGATGTTTGGTGTGATGGACGGGGAGACGAAAACAGGCATTACTGGCTCTCTGCAAAAAATTCAGGTAAGAGATGTTTTCATCAACCTCAATGTTCTTCAACAACACGAGGTTGATTTTAAAAATGTAAGAGTTTTTACTGTCCTGTAGACTGATGTTGCTATGTTTCACCAATTTGATTAGATTTTGAAAGGAGTAGGAACTGCAGAACTGACCAAGCAAATGATCGAGACCTATAAAAGTATTGACAAGCTGGTTGGACAATCAATCTATGTTTCAGTCAGTCTTTTAACCGAAAGTGGTAAGACTCAACAGATGCTGTATGTGATTGTGCATGTGTGTGCGAACGGCTAATGGAGAGTATTTGTGTGTCTCAGGCAGTGAAATGGTGGAAGCAGAAAGGAGAGGAATTCGTATTGTGACGTCTCCATACACTATCAACTTCAAGAAAACAGCTCAATTCTTC[A/T]AACCTGGAATGCCCTTCGATGTCTCGGTATGAATTTGTTCACTATAAAGTTACAAACATAAGCTGAAGAACACGTTGATCAAAACACAAACAGAGATCACTGAGGTTGTTATTTCCGTCTGCTTTAATAAAAGATCTACGTAACGAATCCTGATGAGACGCCTGCTCAAAATGTGATAGTGGAGGTCAATCCTGGAGGAGTCAGAGGTCAAACAAAAGCCAATGGCATTGCTAAAGTGACGGTCAACACTCAAGGAAACGTTTTAACACAAGAGATCACTGTAAGACATCACTTAAATGATGTGGAACAAGCTGCGATTATCTGTCGTCTGGGTAAAAACCCAGTGATATTTCTATATTTATTACAGGCACAAACCAAAGATCCAGACATAACAGACGAAGAGCAAGCAGTGAAGAAGATGACGGCTCATGCTTACGTTCCCAAAGGTGGCTCCAAAAACTACCTGCACATCGGCATTGATGCTGCGGAGCTTGAGATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31242
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Essential Splice Site | 369 | 1635 | 10 | 42 |
| ENSDART00000052688 | Essential Splice Site | 368 | 1643 | 10 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56713951)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55497884 |
| GRCz11 | 1 | 56167180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAAAACAGCTCAATTCTTCAAACCTGGAATGCCCTTCGATGTCTCGG[T/A]ATGAATTTGTTCACTATAAAGTTACAAACATAAGCTGAAGAACACGTTGA
Long Flanking Sequence:
GCGTTTGTGATGTTTGGTGTGATGGACGGGGAGACGAAAACAGGCATTACTGGCTCTCTGCAAAAAATTCAGGTAAGAGATGTTTTCATCAACCTCAATGTTCTTCAACAACACGAGGTTGATTTTAAAAATGTAAGAGTTTTTACTGTCCTGTAGACTGATGTTGCTATGTTTCACCAATTTGATTAGATTTTGAAAGGAGTAGGAACTGCAGAACTGACCAAGCAAATGATCGAGACCTATAAAAGTATTGACAAGCTGGTTGGACAATCAATCTATGTTTCAGTCAGTCTTTTAACCGAAAGTGGTAAGACTCAACAGATGCTGTATGTGATTGTGCATGTGTGTGCGAACGGCTAATGGAGAGTATTTGTGTGTCTCAGGCAGTGAAATGGTGGAAGCAGAAAGGAGAGGAATTCGTATTGTGACGTCTCCATACACTATCAACTTCAAGAAAACAGCTCAATTCTTCAAACCTGGAATGCCCTTCGATGTCTCGG[T/A]ATGAATTTGTTCACTATAAAGTTACAAACATAAGCTGAAGAACACGTTGATCAAAACACAAACAGAGATCACTGAGGTTGTTATTTCCGTCTGCTTTAATAAAAGATCTACGTAACGAATCCTGATGAGACGCCTGCTCAAAATGTGATAGTGGAGGTCAATCCTGGAGGAGTCAGAGGTCAAACAAAAGCCAATGGCATTGCTAAAGTGACGGTCAACACTCAAGGAAACGTTTTAACACAAGAGATCACTGTAAGACATCACTTAAATGATGTGGAACAAGCTGCGATTATCTGTCGTCTGGGTAAAAACCCAGTGATATTTCTATATTTATTACAGGCACAAACCAAAGATCCAGACATAACAGACGAAGAGCAAGCAGTGAAGAAGATGACGGCTCATGCTTACGTTCCCAAAGGTGGCTCCAAAAACTACCTGCACATCGGCATTGATGCTGCGGAGCTTGAGATCGGTGATCAAATGAAAGTCAATCTGAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8557
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024624 | Nonsense | 465 | 1635 | 12 | 42 |
| ENSDART00000052688 | Nonsense | 464 | 1643 | 12 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56713473)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55497406 |
| GRCz11 | 1 | 56166702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAACTACCTGCACATCGGCATTGATGYTGCGGAGCTTGAGATCGGTGAT[C/T]AAATGAAAGTCAATCTGAACACTGGGCAAAGTCCAGGAGTCAAAGATCAA
Long Flanking Sequence:
GGAATGCCCTTCGATGTCTCGGTATGAATTTGTTCACTATAAAGTTACAAACATAAGCTGAAGAACACGTTGATCAAAACACAAACAGAGATCACTGAGGTTGTTATTTCCGTCTGCTTTAATAAAAGATCTACGTAACGAATCCTGATGAGACGCCTGCTCAAAATGTGATAGTGGAGGTCAATCCTGGAGGAGTCAGAGGTCAAACAAAAGCCAATGGCATTGCTAAAGTGACGGTCAACACTCAAGGAAACGTTTTAACACAAGAGATCACTGTAAGACATCACTTAAATGATGTGGAACAAGCTGCGATTATCTGTCGTCTGGGTAAAAACCCAGTGATATTTCTATATTTATTACAGGCACAAACCAAAGATCCAGACATAACAGACGAAGAGCAAGCAGTGAAGAAGATGACGGCTCATGCTTACGTTCCCAAAGGTGGCTCCAAAAACTACCTGCACATCGGCATTGATGCTGCGGAGCTTGAGATCGGTGAT[C/T]AAATGAAAGTCAATCTGAACACTGGGCAAAGTCCAGGAGTCAAAGATCAAGATTACACATTTATGGTAATGATCGTTTGATATTCAGCTACACCACCAATGTACCATTTACACCAGTCATTTATTTCTACCACAGCTTGTGTTTGGAAATGTGCAAAAAGCTTAAAGGTCCAATTACACCAAGAACTATAACAATAAATGTATATGCATCCACACTCATGAACATCAGGGCTGCGTCCGAAACTGCATACTTATATACTATATAGTACACTAAAATCAGTATGCGAGCCGAGTTGTATGTCCGAATTCATAGAATTCGAAAATCAGTATGCGAGATGTACCCGGATGATTTACTACTTCCGGCGAGATTCTGGAGTGCGCATCCCATGCATGCTGCGCTATCCCATAATGCCCCATGAGAGAATTCATGAATAGAAGTGAAGCGACGCAACTGACGCAGGTAAGTCACGTGACCATGACAAAATGGCGAATGTAGTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39715
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Essential Splice Site | 486 | 1635 | 12 | 42 |
| ENSDART00000052688 | Essential Splice Site | 485 | 1643 | 12 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56713406)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55497339 |
| GRCz11 | 1 | 56166635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACACTGGGCAAAGTCCAGGAGTCAAAGATCAAGATTACACATTTATGG[T/C]AATGATCGTTTGATATTCAGCTACACCACCAATGTACCATTTACACCAGT
Long Flanking Sequence:
CGTTGATCAAAACACAAACAGAGATCACTGAGGTTGTTATTTCCGTCTGCTTTAATAAAAGATCTACGTAACGAATCCTGATGAGACGCCTGCTCAAAATGTGATAGTGGAGGTCAATCCTGGAGGAGTCAGAGGTCAAACAAAAGCCAATGGCATTGCTAAAGTGACGGTCAACACTCAAGGAAACGTTTTAACACAAGAGATCACTGTAAGACATCACTTAAATGATGTGGAACAAGCTGCGATTATCTGTCGTCTGGGTAAAAACCCAGTGATATTTCTATATTTATTACAGGCACAAACCAAAGATCCAGACATAACAGACGAAGAGCAAGCAGTGAAGAAGATGACGGCTCATGCTTACGTTCCCAAAGGTGGCTCCAAAAACTACCTGCACATCGGCATTGATGCTGCGGAGCTTGAGATCGGTGATCAAATGAAAGTCAATCTGAACACTGGGCAAAGTCCAGGAGTCAAAGATCAAGATTACACATTTATGG[T/C]AATGATCGTTTGATATTCAGCTACACCACCAATGTACCATTTACACCAGTCATTTATTTCTACCACAGCTTGTGTTTGGAAATGTGCAAAAAGCTTAAAGGTCCAATTACACCAAGAACTATAACAATAAATGTATATGCATCCACACTCATGAACATCAGGGCTGCGTCCGAAACTGCATACTTATATACTATATAGTACACTAAAATCAGTATGCGAGCCGAGTTGTATGTCCGAATTCATAGAATTCGAAAATCAGTATGCGAGATGTACCCGGATGATTTACTACTTCCGGCGAGATTCTGGAGTGCGCATCCCATGCATGCTGCGCTATCCCATAATGCCCCATGAGAGAATTCATGAATAGAAGTGAAGCGACGCAACTGACGCAGGTAAGTCACGTGACCATGACAAAATGGCGAATGTAGTAAATCCGTATTCCATTCATACTTTTCACATTCATACTATATAGAACGCACTTTCCTAACGGCCGAGTAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31241
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Nonsense | 929 | 1635 | 23 | 42 |
| ENSDART00000052688 | Nonsense | 937 | 1643 | 22 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56701458)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55485391 |
| GRCz11 | 1 | 56154687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGTGTGCTGTTTCCACTGCAGAGGCCAAATGTAGAGCTCAATCCTGTT[A/T]AAAACGGTGAGATTTAATGTCAACCATGGAAACGAAGATGGATTATTATA
Long Flanking Sequence:
ATTACCATATTTTATCAAACTACTGAAGAGAAAAATTGTTGTTTATATTTAATATATAATATATAGTTACTACAGTAGCTTATAGTTACTAGTTCTATTGGATTGCGACCCCTGGTGTAATTACATCATTTCAAAGACACACCAATGGCGTCAGATGCAGCAGATTGATTTTATAACATCAGGTTAAACTTTCTGGCACATTTACAGCTCTGATTTACATTAAAAAAAGATTAAACTAAGAATAAACTTGGGTCTATTGGTGTGTGTGCGCTATTGCATGCAAGGTTTCTGTATATATAACCACCTCAGAGGATATTGGGGGTCGCGAGTCACTAGCATTGTTATTTTGGGGGTCGCAAGCTAATAAGTTTGGGAACCCCTGAACTAGAGCACAACTTTTAGTTCTCATGGTAGAGGCTCACTCACGCTCTGTCTCTCTCTTTCAGTCTGAGGGTGTGCTGTTTCCACTGCAGAGGCCAAATGTAGAGCTCAATCCTGTT[A/T]AAAACGGTGAGATTTAATGTCAACCATGGAAACGAAGATGGATTATTATAATTTTTCTTCTCTGCTATTTATGTCAGAAACATCTCTGAAACACTGTAGTTCCAGTCAGTAGCTATGTTTCCATTCACCTATTTTTATGCACATTTTGCATATGCGCATTAAAAAAAATGGTTTATGAAAACATCATGATGCGCATAAATTTTGAAAATGCGCATTAAAAAAACTTGTGCGCATAACTGAGTAGGATAAACTTTTAGTTTGATAAGGAAAGATGCGCATAAACTACGATGGAAACACTTTTACCGCACAAACTCTAGCATGTGCATTTAAAAAAGGTCATGTGATTTTGATAAAAGAGATCATGTAATGATAAAAATGTGTGTGAATGGACAAACCAGCAGGCTGAGCACACTGTAAAACATCAGTAATGTTGTTTTGGTCATTATAAAACGCCTTACCGTTTCAGTATTAGTGTTATTATATTATTAATGACCTCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1745
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 |
|---|---|---|---|---|---|
| ENSDART00000024624 | Nonsense | 1287 | 1635 | 31 | 42 |
| ENSDART00000052688 | Nonsense | 1295 | 1643 | 30 | 41 |
Genomic Location (Zv9):
Chromosome 1 (position 56692179)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55476112 |
| GRCz11 | 1 | 56145408 |
KASP Assay ID:
554-1738.1 (used for ordering genotyping assays)
KASP Sequence:
TTGAGCTGGCTGTAGAAGGAAGAAGCAAACCTAGCAGATATACTATCAAA[A/T]GAGATAATCGGCATGTTTCACGATCAGACAAGGTGAGGAGGGGCTCTGTT
Long Flanking Sequence:
AACTTGTACATGTGTCATATAAAAAAATATGAAAATGAACCAATGTAAAATACCTAGCTCGGGTATCCAAAAAACTGTGTATTTAAGTGTAAATAACTTTTATGCAGTAGAATAAAAACCAAAGTGATGCATATGTGCATAAAATATAGATTCTACACTTTCAAACGACACCACTTACGGGGGTCTGGTGCAACGCTAGCCCTTTAAATCTGAAAGCGAAAGTCGATGAGGTCACAGACCCGGTACCGGGTCCGCAGAGTTTAAGTGGTTAAACAAATTGCAAAAAGGATGATAAAAGCACTGTACTGTACAATATGCAACACTTTACACTAGAGTCTCATTAGTAATGCACTAAAATCTTTCTTGCTTTCTAGGCAACCATCATGGTGTTCCAGGCCGTGGCGGAGTACCGTACACAGGTGAAGGACAGCCAAAACTTCAACCTGGAAGTTGAGCTGGCTGTAGAAGGAAGAAGCAAACCTAGCAGATATACTATCAAA[A/T]GAGATAATCGGCATGTTTCACGATCAGACAAGGTGAGGAGGGGCTCTGTTTACTAATGCCAGGCGGGTTTTGTTACTTCGTAAAATTAATTGCATCATTACAACTGTATTCAGATCACTTGTTAAGAACTATGTTTGAAAAGTAATTTAATTACTGAATGAGAAACTCAATAGGAATGAGATTACTTGAGTCAATATTACACTATTTAGTTGAATCAAATAAACTTTTTTTAGTCATTTGAACTTACATTAATCAAACTGACTAAAATATGAAGGTAAACTTCGCATAACTTGTAGTTGAAACCTGATAAACTTGTTAAAATAAGTGAAAGGAACTTTTTAAGTCGAGTGAAAGACATTTGTCATATCATTTATTAATGTCTAATTAAAATCGTAATGGAAAGACAATATAAATTAAACGTAAACATAACATTCATTAGTAAGCAAATATAATTAATCTAAAAAAAAGAAAAGTTAAATAATATATGTATCAAAGCATCA
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |