ZMP
zgc:158748
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC791173 [Source:RefSeq peptide;Acc:NP_001074124]
Human Orthologue:
PNPLA7
Human Description:
patatin-like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:24768]
Mouse Orthologue:
Pnpla7
Mouse Description:
patatin-like phospholipase domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2385325]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17879 | Nonsense | Available for shipment | Available now |
sa15605 | Nonsense | Available for shipment | Available now |
sa12736 | Nonsense | Available for shipment | Available now |
sa17327 | Nonsense | Available for shipment | Available now |
sa23884 | Nonsense | Available for shipment | Available now |
sa13939 | Nonsense | Available for shipment | Available now |
sa11634 | Nonsense | Available for shipment | Available now |
sa37254 | Essential Splice Site | Available for shipment | Available now |
sa463 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17879
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 83 | 1354 | 4 | 35 |
ENSDART00000091647 | Nonsense | 83 | 328 | 5 | 10 |
ENSDART00000142983 | Nonsense | 83 | 329 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11859591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13560765 |
GRCz11 | 21 | 13657494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGGGTTCCTCGCTATCGCTTCAGAAAAAGAGATAAAGTGCTCTTTTA[C/A]GGCAGGAAAATCATGAGAAAGGTGAGTCCATTCTCACTTAATTCTATTTG
Long Flanking Sequence:
TGCATATATGGATTTATTTGGTTGTTACCAACATCTGGTGAAAACTCAAGTCAACAGCACCTTTACAAATATGTTTTCTGAGAAAAGTGGAGGCATGTTGAATACTTATTTCCCCCTTTGTTTTTGGGTCCAAAATGACCCAAACACTAAATGCTGAATCCTTAAAAAAAGTTGTATATTTTGAGGGTCATAAAGCATTTGTTCCACTAAAAATTTGCTGATAAATCTCCTCAGGGTCAACAAAGATTAAATTGTATTACGAGGGCCAACACTTGATTCTTAGTCATTGTAATGCAGATTTTTTGTTCATGTACATGCTATGAGTGTATTTAAAGCATCCTTGTTGAATTATAACTATTATTTTTAACATTTAACTGATAGTGTATGTTTACAGTAAGTCAGTGGAACGCCATTATGCATCTGCTTGTGTGTGTGTTTTAAGGTCAGGAGGCTGGGGTTCCTCGCTATCGCTTCAGAAAAAGAGATAAAGTGCTCTTTTA[C/A]GGCAGGAAAATCATGAGAAAGGTGAGTCCATTCTCACTTAATTCTATTTGCTCGCTTGTGATTTGCACTGTTTAGCTGCTGATTAATAGTCACTTTTCCAGTACAGAAGACAAATAGCCGAGGGGTCATACTCTGACTCTGCTGAGACTTGCACCGCAAATAGTCATTTATAGGTGTAATTAAAATGTACATAATCACCTTCAACCTCAGACTTCCTCCACTGGGGGGCAGCATAGAGTGTGGCAAGTGTCAAATGACTATCCTGTATGTGTGGCACTGTATGACTAACAACCTGATGTATGTGTGTATGTATGTATATATATATATATATATACTCTCCATCCTCCTCTGGTTTTCTTCCATTTGCTATCTCTCAGGTCCAGACCTTGTCCTCCACACCAACCTCCACTTTGGTGTCTAAGCAGCGCTCTCGGAAAAGACCTAAAGTTCTAAGTATAGCTCGCAGGTATGTTTAGGTTCACATATTTTACAGAGCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15605
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 472 | 1354 | 14 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11844739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13545913 |
GRCz11 | 21 | 13642642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCCATTTTYCAAGCCGCCAAGAAGGATCTACTAGGGATTATTCCACTG[C/T]AGGTTAAAATTTGTGAGATATGGGCTCATGGTTTATGTATGTTCAGATGG
Long Flanking Sequence:
TAGTTGTCTTAATAACTATCTAATACATTGTATATGTCAGCATATGAAATATAAACTTTTAGTTGTGAGGAAAAAAGTTACAATTGTTAATAGAAAATCATATTTACCTTTTTTATCTATTGACCATTAATAGAAGAAACTTCCAATCTGAACTAAACATACAATCTGGTTTTTGTGTTTGTATAGGAGTGACAGGGAATGACCTAAACATGGCCTACGAAAGAGCCCGTGTCACCATAGATGATCCTCCATCCACTTCTGTCATTCACAAGGTGTTTTTTTTTTCCCTTAATCTGTTTCTCATTCTTAATAACTCCTCATATTAAGACATTTGTTTTTGCGATCTACAGTCTATTTTGAAGAAGAGTGTGACCATGCAGCACGCTCCGTCCGCTGTGATTCACTACACAGACAATGCACCACACTCTGACGTTCCTCCTAGTAAAGTGGGTGCCATTTTTCAAGCCGCCAAGAAGGATCTACTAGGGATTATTCCACTG[C/T]AGGTTAAAATTTGTGAGATATGGGCTCATGGTTTATGTATGTTCAGATGGATTTATTGCGTGTGTTGGATGTTTTTTTTTTATTATTGGTGCTGTGTGTCCAGGACCCCAGTTTGCTGGAGGGCAGAGTGACACTCCATCAAGTTAAAGCTGGATCTGTCGTAGCTCGCCAAGGAGATCAGGTCAGACAACATGCAGCATGTGCATATGAAACAGATATGAATCAGAATCTAGTCAGGTGAATGACGGTCTGATGACTACATGGGCGGCAACTTCATTAATGTAGAATTAAATAGGGATGCATGCAAAATGAGCTGGCTTTCAAGGAGGCATCATTTTACTATTTTAAGTGCTTTTTGTCATGCAGTCTCTTATCATAAATCACGCCATGTTCATTTATTTAGCCCAAGAAGAACTGGGCCATCGAGTCTGGTTTCACCCCAGGATTTATTCTTACATTCTGTCACCTAATGGAGATTGAGTTGGGTTTAAAGGCTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12736
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 472 | 1354 | 14 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11844739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13545913 |
GRCz11 | 21 | 13642642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCCATTTTYCAAGCCGCCAAGAAGGATCTACTAGGGATTATTCCACTG[C/T]AGGTTAAAATTTGTGAGATATGGGCTCATGGTTTATGTATGTTCAGATGG
Long Flanking Sequence:
TAGTTGTCTTAATAACTATCTAATACATTGTATATGTCAGCATATGAAATATAAACTTTTAGTTGTGAGGAAAAAAGTTACAATTGTTAATAGAAAATCATATTTACCTTTTTTATCTATTGACCATTAATAGAAGAAACTTCCAATCTGAACTAAACATACAATCTGGTTTTTGTGTTTGTATAGGAGTGACAGGGAATGACCTAAACATGGCCTACGAAAGAGCCCGTGTCACCATAGATGATCCTCCATCCACTTCTGTCATTCACAAGGTGTTTTTTTTTTCCCTTAATCTGTTTCTCATTCTTAATAACTCCTCATATTAAGACATTTGTTTTTGCGATCTACAGTCTATTTTGAAGAAGAGTGTGACCATGCAGCACGCTCCGTCCGCTGTGATTCACTACACAGACAATGCACCACACTCTGACGTTCCTCCTAGTAAAGTGGGTGCCATTTTTCAAGCCGCCAAGAAGGATCTACTAGGGATTATTCCACTG[C/T]AGGTTAAAATTTGTGAGATATGGGCTCATGGTTTATGTATGTTCAGATGGATTTATTGCGTGTGTTGGATGTTTTTTTTTTATTATTGGTGCTGTGTGTCCAGGACCCCAGTTTGCTGGAGGGCAGAGTGACACTCCATCAAGTTAAAGCTGGATCTGTCGTAGCTCGCCAAGGAGATCAGGTCAGACAACATGCAGCATGTGCATATGAAACAGATATGAATCAGAATCTAGTCAGGTGAATGACGGTCTGATGACTACATGGGCGGCAACTTCATTAATGTAGAATTAAATAGGGATGCATGCAAAATGAGCTGGCTTTCAAGGAGGCATCATTTTACTATTTTAAGTGCTTTTTGTCATGCAGTCTCTTATCATAAATCACGCCATGTTCATTTATTTAGCCCAAGAAGAACTGGGCCATCGAGTCTGGTTTCACCCCAGGATTTATTCTTACATTCTGTCACCTAATGGAGATTGAGTTGGGTTTAAAGGCTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17327
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 519 | 1354 | 16 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11843886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13545060 |
GRCz11 | 21 | 13641789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGTTTGTGATCTCGGGCACGTTGCATGTATACCAGCGGATGATTGAC[C/T]GAGAGGAGGACACATGTCTGTTCGTGGCTCACCCAGGAGAGCTGGTGGGW
Long Flanking Sequence:
TTTTTGTCATGCAGTCTCTTATCATAAATCACGCCATGTTCATTTATTTAGCCCAAGAAGAACTGGGCCATCGAGTCTGGTTTCACCCCAGGATTTATTCTTACATTCTGTCACCTAATGGAGATTGAGTTGGGTTTAAAGGCTATGTGAGGCAGAGTTTGCTGTGATTTTTATTTCAGTATGTTGATGTACTTACAGCTGAAACAGAATGTTAAGTAGGGGCGGTGCTTCATTTTTGTGCATCATTCTCTTGTAGCAAATTAAAAATAAGGGCTGATTCAAAGCGAATGGATCTTTGCTTCTAAAAACGCTTGACGTGACGTGCAAAGAGTTCTGAAAAATGATACTTGTGTAAAAGTGCAAGTAGAGTAAAACTATCTTGTACATATTACTCAAAATTATGACATTTGTGTGTGTGTGTGTGTGTGTGTTTCTTTTAGGAAGTGAGTGTTCAGTTTGTGATCTCGGGCACGTTGCATGTATACCAGCGGATGATTGAC[C/T]GAGAGGAGGACACATGTCTGTTCGTGGCTCACCCAGGAGAGCTGGTGGGTCAGTTGGCAGTACTGACTGGAGAACCTCTTATCTTCTCTGTACGGGCACATCGTGACTGCAGCTTCCTATCCATCTCTAAAACACACTTCTATGAGTAGGTTTGCAGTCCATTTCTAATGTTAGTGCAGGTTTTGTGCTGCGTTCATTCTCAGCTGTCCGACATCACCATTGCCATTACTCTCCTGCCTGCCCGAATTACTGGAATGTACCACTATTTAAAATATTATGTCAATATTAACATCTATGTTAAGCTGCGTTGACGCAATCTACATTGTAAAAAGTCTCTCCAAGTATCACCATAATGATGAGGCAGATTAATTTCAATTATTAAAAATGTATTTTTTTATTGTCAGCCACTTTAAACATTTTAAATAGTTTTAATATCAACATTGTACTGTGCTTATAGGTAAAAAAAATCTATAAATAAAAAGTCATCATTTAAAATGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23884
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 775 | 1354 | 22 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11830745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13531919 |
GRCz11 | 21 | 13628648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCATGTCTTCCAGGTCCCACTCTTCTTTTAAATAGTGACATCATCAAA[C/T]AACGCCTTGGTTCTGCTGCTTTAGACAGGTAGGAAACAAAGCGTCATTAG
Long Flanking Sequence:
TGGGAGTTTGCCTGGCCCCGCTGTGCCTGTATAATGTCAGTTTTGTTCTGTCCATTTGATCTCATCAGGTAGTCACAAGGCTTATCCACCTGCTCGGGCAGAAGATCCTTCAGCAAGTTAATGGTCCTCTGACAGGTGTGTGTGTAAAACTACCCGTGTTTCATCAAACATTTGCTTTGATGCATAACTGCTTTGTGTCTTCATTTTAACATCCAGCTCGCAGTCTAGCTTTACACACACCCAGCAGTAAATGGGACGCAGGGAATCCAGCGTCAAACCTGTCCACTGTCGCTGTGCTCCCGGTTTCAGAGGAAGTTCCTCTCACCGCATTCACTTTGGAACTTCAGCATGCGCTTTTAGCTATCGGTGAGGACAGCGAAGTTATGTAGATTTTATACAGTATTTAAAAGATGTGAAGGTTTACATTTGGGAAAAGAAGTCATAAGTCATATTCATGTCTTCCAGGTCCCACTCTTCTTTTAAATAGTGACATCATCAAA[C/T]AACGCCTTGGTTCTGCTGCTTTAGACAGGTAGGAAACAAAGCGTCATTAGATGATGGCTTTTTATGGCATCAAATATTAGTCCATAATGTGTGTGCACTTCATCCTTCAGAATATGCAAATTCACTGTTAATACATGCAGATTGTCAGGACGAGTGTGTTACATCTGCCTAAAAAACAACAACAAATTAATCCTTTTTTTATTTTCTCACATTATAGTAACTGTCGTTTGATGAGTGAGATGAAAGCAGTTTTATAATATGTAAATGAACAACTCGGTTAACCCCAGAAATAAACAGTCCACGTCAGTCTTTTCCCTCTAAACCAGCATGAGGTCTTCCTCTCTTCTTGTAGTTGGCTGATGTTTGTGTGCGTTATGAGGTTTTTTCTGTTTAGGTTTAATTTAGAGCAACTTGTGCTAAAGTGCCAATGGTGGCCTGGTTTCTGTCACGATTATTGACAAGCTTTCATCCGTCATGTGTTTATTGGACAGTTTAACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13939
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 822 | 1354 | 23 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11828468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13529642 |
GRCz11 | 21 | 13626371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATCAGACAGATGTGTCACTCACCCCGTGGACTCAGCGCTGCAYCAGA[C/T]AGGCTGATTGCATCATCATCGTGGGACTAGGAGAGCAGGACCCAGCCGTG
Long Flanking Sequence:
CCTTTCCGAAAGGGTCCCCAAAAAGTGGTACAGTACTGTACGCTTTTTAGCACCTTTTGACAATGCAAACAGTCATAAAAGCATACCGAACTGTATCGTGCCACTCAGTGGAAATGGGCCATCAGATATTAGCTCTCATGTAGGTTATTCAGGCTGTCTTGGAGGTGGGAAATTTCCAGATCTCGTCATCTAGCTACTGGGGTACCTCAGGGCTCAGTATTTGGACCACTTCTCTTTTCCATTTACATGGCATCACTTCAATCTATAATTTAGAAATTTTGCTTTTCCCAACACTTGTATTTTAATGACACTCAACTCTACTTCTCATTAATTCAACCAGTCAAACAACTCAAGCTATTTGTAACTGAAAATATTCTCTCTACCTTAGTGTACATGAGTACAGGTTATCAAGTTGGCTGGGTCAACAGGAAGACATTCACCGCATAGTCCTGTATCAGACAGATGTGTCACTCACCCCGTGGACTCAGCGCTGCATCAGA[C/T]AGGCTGATTGCATCATCATCGTGGGACTAGGAGAGCAGGACCCAGCCGTGGGAGAGGTATGACGCTATTACATCATCACAAGGTGAAAACACTTACATAAAATTTCATTCCAAGATTCAGAGCTATAACACTTGCTACATCCACTGCAAATTGAAGAGTCTTTAATATAAAAACCCTTCAGTTTAACAGACTCAAATGAAATGGGGCTTCAAGGCCTGCAATTTATCATTTGCTGAGGATGGCAGGTACTTTTATAGGTTGAGCTCGAATAACATTAAGTTGTTTGAACCATAACACACTGTGTTGAAAATGGCTACTACTCATCCAGGTGCTGTTTTACCCTTCCACACTTTAAGTCACTACTCGACTACCATGATCAGGCAATAATGAACCTTCCTAGCAGGACTCCAGTTGAACTGCAGGCTTACTTGGTTCTTTTCCTGGAGAGCAAGAGATCAATCATTTATTTGTGGCAGGGAGAGAGCGGTTTTAGACATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11634
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 859 | 1354 | 24 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11827531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13528705 |
GRCz11 | 21 | 13625434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCATGTTAGAGGGGAGTGCRGTGAGAGYGCAGAAACAGCTGGTGTTGT[T/A]GCACYGTGAGGACGGTCCTCCTCCCAAAGGAACTGCTGAATGGCTGAACA
Long Flanking Sequence:
TTTCCTGGAGAGCAAGAGATCAATCATTTATTTGTGGCAGGGAGAGAGCGGTTTTAGACATCCAGGGGTTTGGATGGCCAGAACTGTGCTTTTGAAGTAGGATCATAGGTCTGGGGTAGAGCAACATCTCTATTGATCGTGTATATCCTGCAGTCTTTAAAGGGCACTGCCACTTGTAGTGCTGCTCTTTGAATCAGAGATTGTTTTAAATGAGTCTGCAATAGGTAATTGTATTTATATGGAAAGAATAGATAGAGGATGTGATTGTTCTTTTAAATGCACGTCCCATCCTGATTAATGATTATTCTTCTAAATGAGACGACCTTGGAAATGATACATATGTATTCATTGTGTTCCAATCAAGGAAATGGTTTTATTATTGTAATGCATTTGGACAGAGTGTTGTCTAGTTTTTAAATGCTCTGTCGGTCTCTTTGTCTCTCAGCTGGAGCGCATGTTAGAGGGGAGTGCAGTGAGAGCGCAGAAACAGCTGGTGTTGT[T/A]GCACTGTGAGGACGGTCCTCCTCCCAAAGGAACTGCTGAATGGCTGAACATGCGAAGCTGGATCTCAAGGCACCTTCACCTGTCCTGCCCCCGCAGAGTCTTCTCCAAGAGGAGCCTGCCAAAATTGGTACAGCACTCAATATTACATTACAGATTTAGTAAAATAATGACAACATTTTCAAAGTCATGCATATAGTACAGGGGGTCTTCATACTTTTGATCCCACACAAAATAAATATAATGCCTGTTAAAAAAATCTTCTTAAAAAAAAAAAAAAAAAAACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATGTATGTATGTATGTATGTATATATGTATGTATATATATATATATATATATATATATATATATATATGTATATGTATATGTATATATATGTATGTATGTATGTATGTATGTATGTATGTATATATATATGTATGTATATATATATATATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37254
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Essential Splice Site | 901 | 1354 | 24 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11827402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13528576 |
GRCz11 | 21 | 13625305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTCCTGCCCCCGCAGAGTCTTCTCCAAGAGGAGCCTGCCAAAATTGG[T/G]ACAGCACTCAATATTACATTACAGATTTAGTAAAATAATGACAACATTTT
Long Flanking Sequence:
CTATTGATCGTGTATATCCTGCAGTCTTTAAAGGGCACTGCCACTTGTAGTGCTGCTCTTTGAATCAGAGATTGTTTTAAATGAGTCTGCAATAGGTAATTGTATTTATATGGAAAGAATAGATAGAGGATGTGATTGTTCTTTTAAATGCACGTCCCATCCTGATTAATGATTATTCTTCTAAATGAGACGACCTTGGAAATGATACATATGTATTCATTGTGTTCCAATCAAGGAAATGGTTTTATTATTGTAATGCATTTGGACAGAGTGTTGTCTAGTTTTTAAATGCTCTGTCGGTCTCTTTGTCTCTCAGCTGGAGCGCATGTTAGAGGGGAGTGCAGTGAGAGCGCAGAAACAGCTGGTGTTGTTGCACTGTGAGGACGGTCCTCCTCCCAAAGGAACTGCTGAATGGCTGAACATGCGAAGCTGGATCTCAAGGCACCTTCACCTGTCCTGCCCCCGCAGAGTCTTCTCCAAGAGGAGCCTGCCAAAATTGG[T/G]ACAGCACTCAATATTACATTACAGATTTAGTAAAATAATGACAACATTTTCAAAGTCATGCATATAGTACAGGGGGTCTTCATACTTTTGATCCCACACAAAATAAATATAATGCCTGTTAAAAAAATCTTCTTAAAAAAAAAAAAAAAAAAACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATGTATGTATGTATGTATGTATATATGTATGTATATATATATATATATATATATATATATATATATATGTATATGTATATGTATATATATGTATGTATGTATGTATGTATGTATGTATGTATATATATATGTATGTATATATATATATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTGGTCCTTCGCTATAACGTGATTTACTTTTCGCGGCCTCGTATTTTCACAAATTTTTGTTTTCGTGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa463
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 |
---|---|---|---|---|---|
ENSDART00000023504 | Nonsense | 1199 | 1354 | 32 | 35 |
ENSDART00000091647 | None | None | 328 | None | 10 |
ENSDART00000142983 | None | None | 329 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 11817329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13518503 |
GRCz11 | 21 | 13615232 |
KASP Assay ID:
554-0168.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTTATTTTATCAATCAATTGATTCTGTGCATGTATAGGAAGTTGGATA[C/A]CAGCATGGGAAGACAGTGTTCGATGTGTGGTGCAGAAGTGGAGTGGTGGA
Long Flanking Sequence:
CTATAGTTCTGTCTATTGTTCTATTGTTTCATCTGTCTATCATTCTATTTATCTATCGTTCTCATTCTATCTATCGTTTTATCGTTCTATTTATCGTTGTTTTCTTTCATTCTATCATTCTATTTTTCATTTTATTTTTTATCTCTCTTTCTGTCTATCGTTCTATCTGACTATCATTCTAATTATCTGTCTATTATTCTATCTATCGTTCTTTCTATTGTTCACCTTTCTATCTATCGTTCTATCTATCTTTCCTTCTATCATTCTCTTTAATTCTATTGTTTTATCTATTGTACTATCTATCTGTCTATCTTTCTTTCTGTCTATTGTGACAGTCTATTCTGATCTATCTGTCAACATCATACTGTTAAATTATTACATTTTAGTTATGCACAATTTTGTGACGTCACTTTTAATGGGTATGGGTAAAGTGAACATGATTACTTGTATATTTTATTTTATCAATCAATTGATTCTGTGCATGTATAGGAAGTTGGATA[C/A]CAGCATGGGAAGACAGTGTTCGATGTGTGGTGCAGAAGTGGAGTGGTGGAGAAGATGATGAAGGACAGACATCAGGAAGAATTTCACAAAACACAGAGCAACAATGTGAGCCATACGTCACCTAAAAGCGAGACCTTTTGAGATGTAACGTGTGCTGAAACTCTTATTTGTTGTGCATCTGCAGGTGGTGACATGTCCAAATGCTTCCTTCACTGATCTGGCTGAAATAGTCTCACGCATTGAGCCAGTAAAACCAGCCCTTGTGGATGGTAAATCAATGTTAAACCTCTTAAATTTACCTTTTAAGAGCACATTTGGCAGACTTGAACTTCTTGGCTTACATTCACAGCATATTGATCCGTCTTTGGCCGCTATTAAGTTATATGTCATTTAGTGTTTAGTGTACAAATATCATTAAGCTAATGGGTTGAATATGTTTCCATCTCTCCTACAGAGGAATCAGACTACCACACGGATTATGAAGAGGAGATGGCAGAGAG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |