ZMP
piwil1
Ensembl ID:
ZFIN ID:
Description:
Piwi-like protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q8UVX0]
Human Orthologues:
PIWIL1, PIWIL3
Human Descriptions:
piwi-like 1 (Drosophila) [Source:HGNC Symbol;Acc:9007]
piwi-like 3 (Drosophila) [Source:HGNC Symbol;Acc:18443]
piwi-like 3 (Drosophila) [Source:HGNC Symbol;Acc:18443]
Mouse Orthologue:
Piwil1
Mouse Description:
piwi-like homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1928897]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8531 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7619 | Missense | Mutation detected in F1 DNA | Not yet available |
hu4333 | Nonsense | Confirmed mutation in F2 line | Not yet available |
hu2479 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa30904 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45333 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8531
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061115 | Nonsense | 128 | 858 | 4 | 20 |
ENSDART00000133021 | None | None | 231 | None | 7 |
ENSDART00000138019 | Nonsense | 128 | 858 | 5 | 21 |
ENSDART00000139249 | None | None | 180 | None | 5 |
ENSDART00000145076 | Nonsense | 128 | 373 | 6 | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45902300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44241189 |
GRCz11 | 8 | 44234608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGGGCCAATTTYATGCGTCTGCTTTCACGTCCTATGTGGGCTTTRTA[T/A]CAGTATCATGTGGACTAMAAGCCACCAATGGAGTCCAGACGACTGCGTTC
Long Flanking Sequence:
ATTAAAAATGTGTACATACACCGTCAATGCACCGTGATGCACCGAGATATCGAATTGAACCGAATCGATGGCATGATAATCGTAACCGAACCGAACTGTGAGACTAGTGTAGGTTCACACCCCTAAATAATAAATAATTGACTTTTTCTCTATCTTTATTAGTTTCAAAAACAGATTTATTTACAAAACATAAAAAAACACACACACATGAAAAAAACCTTACTATATAACAGAAAAAGTTATCCTTTTTTAAACCCTTTGTTTCTATACCGTGGTAAAAAATGCCGAACTTCTGTTAAAAAACTTAATACAAAAATAACGAAACCTCTAACAGACCCCAGAACTTTTTCACATACCTGTTCAGGTTGTCTACCTCAGTTGTTGAAATATAGTGTAATGCTATATTTGACACTTTCTTTGACTACAGGTGTTTCTGGGACTGCCATTGAGCTGAGGGCCAATTTTATGCGTCTGCTTTCACGTCCTATGTGGGCTTTGTA[T/A]CAGTATCATGTGGACTACAAGCCACCAATGGAGTCCAGACGACTGCGTTCGGCTTTGCTTTTCCAGCACGAGGAGACTCTGGGGAAAGCACACACCTTTGATGGAGCCATTCTCTTTCTCCCCAACAAACTGCGCAACGCTGTATGTTTGTAGAGTCTTAACATTTTATTTAACCTCTTACAGTGCTTTCACACCAGATACAGATGAAGTGTAAAGGGCAAATAATTTACATGTTAAGTCTATGCAAAGACTTAGATATCCTGCAGCATGGTTTGTTAGAATGGGGTGGCATGAATGACCAACTTGAGGGAATGACACATTGCAAACTGCATTCGGGGCAATTGAAGCACTTTAAAAATTGGAACTTTGGCATAAATTCATGCCATGTTAAAGGAATACTCCACTTTTTTTGAAAGGCTCTTAAAAGTTTTCCAGAGTTAAACAGTTGACTTTTTGAAACCATTTAGTTGGATGATTGTTTTGGCTTGGTCACGTTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7619
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 > A
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061115 | Missense | 155 | 858 | 4 | 20 |
ENSDART00000133021 | None | None | 231 | None | 7 |
ENSDART00000138019 | Missense | 155 | 858 | 5 | 21 |
ENSDART00000139249 | None | None | 180 | None | 5 |
ENSDART00000145076 | Missense | 155 | 373 | 6 | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45902380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44241109 |
GRCz11 | 8 | 44234528 |
KASP Assay ID:
554-4021.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGTCCAGACGACTGCGTTCGGCTTTGCTTTTCCAGCACGAGGAGACTC[T/A]GGGGAAAGCACACACCTTTGATGGAGCCATTCTCTTTCTCCCCAACAAAC
Long Flanking Sequence:
CGTAACCGAACCGAACTGTGAGACTAGTGTAGGTTCACACCCCTAAATAATAAATAATTGACTTTTTCTCTATCTTTATTAGTTTCAAAAACAGATTTATTTACAAAACATAAAAAAACACACACACATGAAAAAAACCTTACTATATAACAGAAAAAGTTATCCTTTTTTAAACCCTTTGTTTCTATACCGTGGTAAAAAATGCCGAACTTCTGTTAAAAAACTTAATACAAAAATAACGAAACCTCTAACAGACCCCAGAACTTTTTCACATACCTGTTCAGGTTGTCTACCTCAGTTGTTGAAATATAGTGTAATGCTATATTTGACACTTTCTTTGACTACAGGTGTTTCTGGGACTGCCATTGAGCTGAGGGCCAATTTTATGCGTCTGCTTTCACGTCCTATGTGGGCTTTGTATCAGTATCATGTGGACTACAAGCCACCAATGGAGTCCAGACGACTGCGTTCGGCTTTGCTTTTCCAGCACGAGGAGACTC[T/A]GGGGAAAGCACACACCTTTGATGGAGCCATTCTCTTTCTCCCCAACAAACTGCGCAACGCTGTATGTTTGTAGAGTCTTAACATTTTATTTAACCTCTTACAGTGCTTTCACACCAGATACAGATGAAGTGTAAAGGGCAAATAATTTACATGTTAAGTCTATGCAAAGACTTAGATATCCTGCAGCATGGTTTGTTAGAATGGGGTGGCATGAATGACCAACTTGAGGGAATGACACATTGCAAACTGCATTCGGGGCAATTGAAGCACTTTAAAAATTGGAACTTTGGCATAAATTCATGCCATGTTAAAGGAATACTCCACTTTTTTTGAAAGGCTCTTAAAAGTTTTCCAGAGTTAAACAGTTGACTTTTTGAAACCATTTAGTTGGATGATTGTTTTGGCTTGGTCACGTTTAGCTTAGCATAATTCATTGAATCAGATTTGACCATTGGCCTTTCGTTTAAATGTATTTTTATTTTAAATTTATTTATTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu4333
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000061115 | Nonsense | 544 | 858 | 13 | 20 |
ENSDART00000133021 | Nonsense | 222 | 231 | 7 | 7 |
ENSDART00000138019 | Nonsense | 544 | 858 | 14 | 21 |
ENSDART00000139249 | Nonsense | 135 | 180 | 4 | 5 |
ENSDART00000145076 | None | None | 373 | None | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45906712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44236777 |
GRCz11 | 8 | 44230196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGATTGAGTATGAAGATCGTCAGGAATCTCTCCTTAGAGCTTTGCAA[C/T]AAAACGTAGCACGTGAAACTCAGATGGTAAGTCGAGTATTCATGTAATAT
Long Flanking Sequence:
TAATTAGAAAAATGTCTTTTTTAAATTGCTCCATGGAAACGCAGTGTCCCTGAGTCAGATTAACACTGCATTTTTATCAAAAAAGTACAGTATTTTAGTTGTATAAATGAGGAGAGACAACTTGACCTCCAGCATGCATTCATAACACTTATCCTGAAACCTCAATTACTCTTGTCTTTCATCTCATAGTTTGAGTATAACCCATGGACAGCAGACTGGTCTAAAGAGATGAGAGGTCTCCCTCTGATTAGCTGCATGTCTCTGGACAACTGGCTCATGTTCTACACGCGCAGAAATGCAGATGTTGCCCAATCTCTGCTTCAGACTCTCAACAAAGTGTCTGGACCCATGGGGATCCGCATGCAGAGGGCTGTCATGTGAGTTGTGGTCGACTTTAAATGTGAACTACTTTTCAGTCTGTTCTCATGTTAATAAGCATTTCCTGACCAAGCAGGATTGAGTATGAAGATCGTCAGGAATCTCTCCTTAGAGCTTTGCAA[C/T]AAAACGTAGCACGTGAAACTCAGATGGTAAGTCGAGTATTCATGTAATATTGATTGTCCAGCAACTTTTTTTTTATTATTGCTTTTGTGCCTCTGTAGGTGGTGGTGATCTTGCCTACCAATCGAAAAGACAAGTACGACTGTGTAAAGAAGTACCTGTGTGTGGACTGCCCTACTCCTAGTCAGTGTGTGGTGTCTCGCACCATCAGCAAACCTCAAGCACTTATGACTGTGGCCACCAAGATTGCTTTGCAGATGAACTGCAAAATGGGAGGAGAGCTGTGGAGTGTAGAAATTCCAGTAAGGGTTTAAGACAATACACTATAATGCATCCTTCAACAACATCCTCAGTTCTTTCCTCAATAATCAACCTTTGTCTTTCAGCTCCGGCAGCTCATGATTGTAGGTATAGACTGCTACCATGATACCGCTGCTGGAAAAAGGTCCATCGGCGCAATGGTGGCCAGTCTAAATCAGGGCATGTCAAGGTAAGTCATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2479
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000061115 | Nonsense | 544 | 858 | 13 | 20 |
ENSDART00000133021 | Nonsense | 222 | 231 | 7 | 7 |
ENSDART00000138019 | Nonsense | 544 | 858 | 14 | 21 |
ENSDART00000139249 | Nonsense | 135 | 180 | 4 | 5 |
ENSDART00000145076 | None | None | 373 | None | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45906712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44236777 |
GRCz11 | 8 | 44230196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGATTGAGTATGAAGATCGTCAGGAATCTCTCCTTAGAGCTTTGCAA[C/T]AAAACGTAGCACGTGAAACTCAGATGGTAAGTCGAGTATTCATGTAATAT
Long Flanking Sequence:
TAATTAGAAAAATGTCTTTTTTAAATTGCTCCATGGAAACGCAGTGTCCCTGAGTCAGATTAACACTGCATTTTTATCAAAAAAGTACAGTATTTTAGTTGTATAAATGAGGAGAGACAACTTGACCTCCAGCATGCATTCATAACACTTATCCTGAAACCTCAATTACTCTTGTCTTTCATCTCATAGTTTGAGTATAACCCATGGACAGCAGACTGGTCTAAAGAGATGAGAGGTCTCCCTCTGATTAGCTGCATGTCTCTGGACAACTGGCTCATGTTCTACACGCGCAGAAATGCAGATGTTGCCCAATCTCTGCTTCAGACTCTCAACAAAGTGTCTGGACCCATGGGGATCCGCATGCAGAGGGCTGTCATGTGAGTTGTGGTCGACTTTAAATGTGAACTACTTTTCAGTCTGTTCTCATGTTAATAAGCATTTCCTGACCAAGCAGGATTGAGTATGAAGATCGTCAGGAATCTCTCCTTAGAGCTTTGCAA[C/T]AAAACGTAGCACGTGAAACTCAGATGGTAAGTCGAGTATTCATGTAATATTGATTGTCCAGCAACTTTTTTTTTATTATTGCTTTTGTGCCTCTGTAGGTGGTGGTGATCTTGCCTACCAATCGAAAAGACAAGTACGACTGTGTAAAGAAGTACCTGTGTGTGGACTGCCCTACTCCTAGTCAGTGTGTGGTGTCTCGCACCATCAGCAAACCTCAAGCACTTATGACTGTGGCCACCAAGATTGCTTTGCAGATGAACTGCAAAATGGGAGGAGAGCTGTGGAGTGTAGAAATTCCAGTAAGGGTTTAAGACAATACACTATAATGCATCCTTCAACAACATCCTCAGTTCTTTCCTCAATAATCAACCTTTGTCTTTCAGCTCCGGCAGCTCATGATTGTAGGTATAGACTGCTACCATGATACCGCTGCTGGAAAAAGGTCCATCGGCGCAATGGTGGCCAGTCTAAATCAGGGCATGTCAAGGTAAGTCATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30904
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061115 | Nonsense | 565 | 858 | 14 | 20 |
ENSDART00000133021 | None | None | 231 | None | 7 |
ENSDART00000138019 | Nonsense | 565 | 858 | 15 | 21 |
ENSDART00000139249 | Nonsense | 156 | 180 | 5 | 5 |
ENSDART00000145076 | None | None | 373 | None | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45906849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44236640 |
GRCz11 | 8 | 44230059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCTCTGTAGGTGGTGGTGATCTTGCCTACCAATCGAAAAGACAAGTA[C/A]GACTGTGTAAAGAAGTACCTGTGTGTGGACTGCCCTACTCCTAGTCAGTG
Long Flanking Sequence:
ATTCATAACACTTATCCTGAAACCTCAATTACTCTTGTCTTTCATCTCATAGTTTGAGTATAACCCATGGACAGCAGACTGGTCTAAAGAGATGAGAGGTCTCCCTCTGATTAGCTGCATGTCTCTGGACAACTGGCTCATGTTCTACACGCGCAGAAATGCAGATGTTGCCCAATCTCTGCTTCAGACTCTCAACAAAGTGTCTGGACCCATGGGGATCCGCATGCAGAGGGCTGTCATGTGAGTTGTGGTCGACTTTAAATGTGAACTACTTTTCAGTCTGTTCTCATGTTAATAAGCATTTCCTGACCAAGCAGGATTGAGTATGAAGATCGTCAGGAATCTCTCCTTAGAGCTTTGCAACAAAACGTAGCACGTGAAACTCAGATGGTAAGTCGAGTATTCATGTAATATTGATTGTCCAGCAACTTTTTTTTTATTATTGCTTTTGTGCCTCTGTAGGTGGTGGTGATCTTGCCTACCAATCGAAAAGACAAGTA[C/A]GACTGTGTAAAGAAGTACCTGTGTGTGGACTGCCCTACTCCTAGTCAGTGTGTGGTGTCTCGCACCATCAGCAAACCTCAAGCACTTATGACTGTGGCCACCAAGATTGCTTTGCAGATGAACTGCAAAATGGGAGGAGAGCTGTGGAGTGTAGAAATTCCAGTAAGGGTTTAAGACAATACACTATAATGCATCCTTCAACAACATCCTCAGTTCTTTCCTCAATAATCAACCTTTGTCTTTCAGCTCCGGCAGCTCATGATTGTAGGTATAGACTGCTACCATGATACCGCTGCTGGAAAAAGGTCCATCGGCGCAATGGTGGCCAGTCTAAATCAGGGCATGTCAAGGTAAGTCATTTAAACATGGTATTGTTAAATTAATGCTAGATTATTAGTTGAATATTAGACTGGTATGAATATCTTGGACTGGTTAGAGCAGGTCCTAGAGCTTAACTTAGAGCCTCTTTGGTGAATGCATCTAATTGAATTTACAGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45333
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 |
---|---|---|---|---|---|
ENSDART00000061115 | Nonsense | 698 | 858 | 17 | 20 |
ENSDART00000133021 | None | None | 230 | None | 7 |
ENSDART00000138019 | Nonsense | 698 | 858 | 18 | 21 |
ENSDART00000139249 | None | None | 180 | None | 5 |
ENSDART00000145076 | None | None | 373 | None | 12 |
The following transcripts of ENSDARG00000041699 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 45908516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44234973 |
GRCz11 | 8 | 44228392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCTATCTGAAATACAACAATTCTCTGCCCTCGCGCATCATTGTTTAC[C/T]GAGATGGAGTTGGAGATGGCATGCTGCAGAGCGTTGTGGACTATGAAGTT
Long Flanking Sequence:
GCACACACAGTATGTTTATCTGCTTTAAGAACAGCGATATTACTACCACAATTTTCAGAAACTTCTTGTGCTCATCAGGTTTGTAACATTTATGAATAAATTCAGTGTTGTGTATATGTAACTATTTGTATGGATGATCTGTGCAATTTTAGAAACAGTGTTTTTATTTTTCTTAAAAAATGTCAATTTTGATTGTTTATGTAAAGTGAGCCAGTAAAAACAGATACACAGTTTGGGCAATTCATTTGTGATTAACAGTAGCTCAATTAAATAATTTAGTCTGGTTACATTCACATCAGAAATTACCTGTGGTTTTGCATGAACTGTTCTCAGACCACCCTTTTTGGGTGGAATCCAGCATGTTTCACAGGTGCACACCTCAGTCCAGAAAATATCTTTTACATGAACTAAAACATACTTGATATCCAACTGTCTTTTTAGGTGCTCTGAAGGCCTATCTGAAATACAACAATTCTCTGCCCTCGCGCATCATTGTTTAC[C/T]GAGATGGAGTTGGAGATGGCATGCTGCAGAGCGTTGTGGACTATGAAGTTCCTCAGATCATGCAGTCTATCAAGACCATGGGGCAAGATTATGAGTAAGCCAGCCTTCATGCAGACACACTCACACTATAGGAATGATACATTTTCTTCATTGTTTTAATGTTTTTCTTTACAGGCCCAAGCTCTCAGTAGTGGTGGTGAAAAAGCGCATCAGCTCCCGATTCTTTGCTCGGATTGATGGCAAAATTGCCAATCCCCCTCCTGGGACAGTCATTGACACTGAAGTCACTCGTCCAGAGTGGTGCGTGTAGAGTACCCTGAAGGAACACTGCTCATTCTCAAACAAGCATTGCCCGATTAGTACATTTTTCTTTCACTTGGCCATCCAAAACATTCAGTTGTCCCGGTCAAGCATTAATACTGAACTTTGAATTCCTACTAATTGTTCATGGTACCGCTTACTTTTTTTTATGCATAAACTGGATTTTGTTGATACAGTAG
Associated Phenotype:
Not determined