ZMP
zgc:55413
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC406830 [Source:RefSeq peptide;Acc:NP_998674]
Human Orthologue:
PPT2
Human Description:
palmitoyl-protein thioesterase 2 [Source:HGNC Symbol;Acc:9326]
Mouse Orthologue:
Ppt2
Mouse Description:
palmitoyl-protein thioesterase 2 Gene [Source:MGI Symbol;Acc:MGI:1860075]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35960 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14512 | Essential Splice Site | Available for shipment | Available now |
| sa19122 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44829 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35960
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 |
|---|---|---|---|---|---|
| ENSDART00000037389 | Nonsense | 12 | 291 | 2 | 9 |
| ENSDART00000099658 | Nonsense | 12 | 177 | 2 | 8 |
| ENSDART00000128235 | Nonsense | 12 | 246 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 34409009)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35254785 |
| GRCz11 | 15 | 35112754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAGCAGTTGTGGCGATGGCTGATGGCTGCAGACCATGTGTTTTTATTT[T/A]GGTTGTTTTACTGCTGCTGCCCTCAGCCATCATGGCGTACAGACCAGTGA
Long Flanking Sequence:
ATTTAATACTTTCAAAAACCACGATCGTAATATATAACGTTATGTCCAGTAATGGCCAGAAAGTCATTCATTTTTTAATTAACTCTTAAAATTTTGGTATTTGTGATGCAGGAAACCCAGAGATTGTTGTCTACACTATGACTTTATATACAATTAACTTTAATGTGTGATATGAATTGAAAGTGATCATAAACAAATAATTTCTCAACTCAAATGAGTGGCGGCTTGGACCCGGTGGTAACAGTATTACATACGTCACCAACACGTCATCACTTAAGCGGATACTATAAAAGCGTCACCTCAAGCGACAGAACATCACGCTCCAAACAATTTACCAGCTGTTTTATCGTGGAGCGTCCTGCTAAGGTTAGTCATGCCTACTTGGGTGTCTAATTTAAGTTTGGCTTGTTATAATTATGAAATGATTATATACATGTTTGATTTCAGATTATAAGCAGTTGTGGCGATGGCTGATGGCTGCAGACCATGTGTTTTTATTT[T/A]GGTTGTTTTACTGCTGCTGCCCTCAGCCATCATGGCGTACAGACCAGTGATTATTATTCATGGGCTATTTGGTGGACCTAAAGAGTTGACACCCTTTGTGAACTTCATTAAAGAGGTAAGGAATCTAATGTATGTATTTTGTTTCACGCATGTTATCGTTTATACGGTCACTTGTATTGGTTGTTGTTGTTGTTGTTGTTTCACGTGCAGTACTTGCAAATCTAAGTATGGTAACTCCCTGCTCACACAGAAATGTATGGAAGCTCTTTCCCGCTAATGAAAAAAAAAATTCTCAAGATTGTGACTTGATGCAATTGTAACTCCTTTATATTTCAGAATTCCGACTTCATATTTAAAGTCATAATCTTTGTTTTATTCTTTGGTGGGATTTTAAAAAAAATGTCTTTAGTTCATTGGGGAGAGGATAGTTTTATTTATTTTTTTATTATTATTATTATTATTTTGCAGTCTAATTTTAAAAGATAATTAATTTAGCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14512
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 |
|---|---|---|---|---|---|
| ENSDART00000037389 | Essential Splice Site | 50 | 291 | 2 | 9 |
| ENSDART00000099658 | Essential Splice Site | 50 | 177 | 2 | 8 |
| ENSDART00000128235 | Essential Splice Site | 50 | 246 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 34408892)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35254668 |
| GRCz11 | 15 | 35112637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGGTGGACCTAAAGAGTTGACACCCTTTGTGAACTTCATTAAAGAGG[T/A]AAGGAATCTAATGTANNNNNNTGTATTTTGTTTCACGCATGTTATCGTNNATACGG
Long Flanking Sequence:
CAGAGATTGTTGTCTACACTATGACTTTATATACAATTAACTTTAATGTGTGATATGAATTGAAAGTGATCATAAACAAATAATTTCTCAACTCAAATGAGTGGCGGCTTGGACCCGGTGGTAACAGTATTACATACGTCACCAACACGTCATCACTTAAGCGGATACTATAAAAGCGTCACCTCAAGCGACAGAACATCACGCTCCAAACAATTTACCAGCTGTTTTATCGTGGAGCGTCCTGCTAAGGTTAGTCATGCCTACTTGGGTGTCTAATTTAAGTTTGGCTTGTTATAATTATGAAATGATTATATACATGTTTGATTTCAGATTATAAGCAGTTGTGGCGATGGCTGATGGCTGCAGACCATGTGTTTTTATTTTGGTTGTTTTACTGCTGCTGCCCTCAGCCATCATGGCGTACAGACCAGTGATTATTATTCATGGGCTATTTGGTGGACCTAAAGAGTTGACACCCTTTGTGAACTTCATTAAAGAGG[T/A]AAGGAATCTAATGTATGTATTTTGTTTCACGCATGTTATCGTTTATACGGTCACTTGTATTGGTTGTTGTTGTTGTTGTTGTTTCACGTGCAGTACTTGCAAATCTAAGTATGGTAACTCCCTGCTCACACAGAAATGTATGGAAGCTCTTTCCCGCTAATGAAAAAAAAAATTCTCAAGATTGTGACTTGATGCAATTGTAACTCCTTTATATTTCAGAATTCCGACTTCATATTTAAAGTCATAATCTTTGTTTTATTCTTTGGTGGGATTTTAAAAAAAATGTCTTTAGTTCATTGGGGAGAGGATAGTTTTATTTATTTTTTTATTATTATTATTATTATTTTGCAGTCTAATTTTAAAAGATAATTAATTTAGCAGAAATATATTTTTGCTGTGGTTAATAACTCGCAAGATTGCTCTATCAAAATCATTTGTCATTTTATATCAGTGTAGGGAAAACTCCAATACAACTTTTAAATCACGGGTGACCAAACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19122
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 |
|---|---|---|---|---|---|
| ENSDART00000037389 | Essential Splice Site | 198 | 291 | None | 9 |
| ENSDART00000099658 | Essential Splice Site | None | 177 | None | 8 |
| ENSDART00000128235 | Essential Splice Site | 198 | 246 | None | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 34400850)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35246626 |
| GRCz11 | 15 | 35104595 |
KASP Assay ID:
2260-8822.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTCTGGCCCCGCTGAATGGAGAAGTTGAACATGTCAACTCAACAGG[T/C]AACTAAGCTATTAATTTGCCTAAAATTATTCTGTTATTCATCAATTGCTC
Long Flanking Sequence:
CCTCAGTTTCACTTGTCATATAATTTGTGTAACAGGTGGTTTGATATGTCGAGGAGTTCTTGCTACTCTTCCTCAACACAATGCTCACTCTGTGATATTCCTGTCTTCACCACTAGCTGGCCAGTATGGAGGTCAGTGACGTTCACACCACAATATTTATTCTCATTCAAGAAACAAGACCGTGTACACATGCATAAGTGCTTTCTCCATGTTCTTTCAGTTACAAGGGCCATCAGCGGTGTGTTCCCTAAACTGCCCAAGTCCTCACTGCACAATGTTTGTTATACTGAACTTGGACAAAAAACATCCTTCTGCAGCTACTGGAATGGTAAGATGTGCTACTTTCATGCATCAGTTTAACCCCCGGCTCTGTCTGTGACTCATTATGTTTCATCTGCTGCTGCTTGCACTGTAGATCCACATCATAGAGAGAAATACTTGAATTCCAGTGTCTTTCTGGCCCCGCTGAATGGAGAAGTTGAACATGTCAACTCAACAGG[T/C]AACTAAGCTATTAATTTGCCTAAAATTATTCTGTTATTCATCAATTGCTCATGTCTTTCCAATGCCCTGATACCTTTTTATCTTTAGAACACTTTGTATTTTACTTATGTATTTATATTTATTTGTTTCTGTTTATTTAAAAACTATATATTTAATAAATTTATTTGATTTATATTTAATTTTAATTATTTTATTTTCATTCAATCGCTATCCAAACGATTTATGCAACCAAATATCTTTTAGTTGAAGTCAGAGAGCTCTCTCATCCGCCATACATGCAGCAATTATCTGGAGATGTTCCAGAAAGTCCAGAAACTTGGGTTTCATCTTTAATATCTTAATTTGTGTTCTGAAGATGAATGAAGGTCTCAGGAGAATTGTAATGACAAAATAGTGAGTAAATAATTTTGGGATGAACGTACCCATTAAAGACATGGCTGTTTAACTGGTGTTTATGTGCTGCTCAGATGTCCGTGTGTGTGCTCTTTCAGTTCTCCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44829
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000037389 | Essential Splice Site | 226 | 291 | 7 | 9 |
| ENSDART00000099658 | None | None | 177 | 8 | 8 |
| ENSDART00000128235 | None | 226 | 246 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 34400229)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35246005 |
| GRCz11 | 15 | 35103974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGATTGGCGGACCAAATGATGGTGTTATCTTACCGTGGCAATCAAG[G/A]TCTCCACAAAAGCTCCCAAAATTAACCCGAGCCTCGTTCACACATTTAAC
Long Flanking Sequence:
ATTTGTTTCTGTTTATTTAAAAACTATATATTTAATAAATTTATTTGATTTATATTTAATTTTAATTATTTTATTTTCATTCAATCGCTATCCAAACGATTTATGCAACCAAATATCTTTTAGTTGAAGTCAGAGAGCTCTCTCATCCGCCATACATGCAGCAATTATCTGGAGATGTTCCAGAAAGTCCAGAAACTTGGGTTTCATCTTTAATATCTTAATTTGTGTTCTGAAGATGAATGAAGGTCTCAGGAGAATTGTAATGACAAAATAGTGAGTAAATAATTTTGGGATGAACGTACCCATTAAAGACATGGCTGTTTAACTGGTGTTTATGTGCTGCTCAGATGTCCGTGTGTGTGCTCTTTCAGTTCTCCATCCTTGACTTGTACTGTTTGCTTCTGTTTTCCTGCAGAGTGGCGAAACAATTTTCTGCGCATAAAAACCATGGTGTTGATTGGCGGACCAAATGATGGTGTTATCTTACCGTGGCAATCAAG[G/A]TCTCCACAAAAGCTCCCAAAATTAACCCGAGCCTCGTTCACACATTTAACCTGCATTTCTTAATTCCAGCCCAGCACAATTTCCCCCCTCCCACATCAGTTTTTAATTGCAATTCTACAAGTTCCCTGCAAAGCAAACTCCACAGGAAAGTCCACCATGAATTTGAATGGAGTGTTTTATTCAAATGGCATTTAGTGGATGAGCTTTTGCCTCTCAAGGGTTGCTAACTGTTGGCTGTAAAAATCTAAAACTGTATTTTAAGTGCAATAATTAAATGACACTAACAGCAATCGTTGCATTTGAAATTGTCCTGACAATCAGCTAAGGTTTGCCACTCGACTGTATTGTGTGCTCCTAAGGCACAGGTGTCCACTCCAGTTTTTGGAGGGCCACAGCTCTGCACAATTAGTTTGATCAGGTGTGTTTAACTAGGGTTGGAACTAAACTGAGTCCCTCAGTTTTGTTTAAAACCTTCCAAGTAAAGCTGCAGTCACACTACA
Associated Phenotype:
Not determined