ZMP
pnpla7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate patatin-like phospholipase domain containing 7 (PNPLA7) [Source:
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 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14870 | Nonsense | Available for shipment | Available now |
| sa17088 | Nonsense | Available for shipment | Available now |
| sa20413 | Nonsense | Available for shipment | Available now |
| sa40422 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14870
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 |
|---|---|---|---|---|---|
| ENSDART00000002118 | Nonsense | 6 | 1275 | 1 | 36 |
| ENSDART00000128179 | None | None | 316 | None | 9 |
| ENSDART00000145061 | Nonsense | 31 | 1293 | 3 | 35 |
Genomic Location (Zv9):
Chromosome 5 (position 26739050)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 24566315 |
| GRCz11 | 5 | 25070115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCATCTGGTCAKGAAATCAAGGCTCGTGTGCAACACTTYATCGAGGAT[C/T]AGTTACACACCACCATGGTATATTACTGTAATTTATTCCCATGTGWATCA
Long Flanking Sequence:
GTTGTATTTTATTTTAACTAGACATTATGGAAAATGAAGAACAAGATGATACATGCAGATCTTTGGTAAGTTATTTCAATGTGGAGTTTTTGATTTTAAACTAATGGCTAACGACAGTGCAAATGTGTATCAGTGAGTCTTTTTTAAATTAAAATAAATAAATGCATGCTATTTATTCGCAATAAATCTGCTTTCGAACTTAGCTAACTTGACATAAGCTTAATTGAAAAAACAACTCCATTAGAGTAAGCTGGACTTTGTCCAAAAGCATGTACCCACTGAAGTGATTGGGCAAGGCTGTGATTAGAAAGATTGTCCATTTCCTTGATGAAATCAGAAGAGATTGAGACCAGAGATTGAACCAGTGACCTTTATTTTAGCTGTTGTCAATTGCTCTATTGTGTACAATTATGATTTTGATTTTGTTATATTTTTATCTCTTCTTCTAGGTGCCATCTGGTCATGAAATCAAGGCTCGTGTGCAACACTTCATCGAGGAT[C/T]AGTTACACACCACCATGGTATATTACTGTAATTTATTCCCATGTGAATCAATTTTCCATACTGATAGTTTTGCAGAGGTATTACGCTATTTATTTGTTCTCATTTCACAATGCAGTGGACTGGTGTGCTGATCGGAGCTGCAGTTGCAGTTTCAATTCTAAGTATTTTTGCCTTATTCTTTTACAGAAGACACAAGGCTGGTAAGTGTGTAATGATTATCATTTACAGCAGGGGTGTCCAAACTTTTTGGGCCGAGGGCCAGATGCAAAAAAACAAACGTTGTCGCGGGCCAAATTTTACATACATCACACAGACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATACAGTTGAAGTCAGAATTGTTAGCCCCCCTAAATTATTAGCCCCCGTTTATTTTTTCCCCAATTTCTGTTTAACGGAGAGAAGATTTTTTTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17088
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 |
|---|---|---|---|---|---|
| ENSDART00000002118 | Nonsense | 138 | 1275 | 5 | 36 |
| ENSDART00000128179 | None | None | 316 | None | 9 |
| ENSDART00000145061 | None | None | 1293 | None | 35 |
Genomic Location (Zv9):
Chromosome 5 (position 26735592)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 24562857 |
| GRCz11 | 5 | 25066657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGACYGAATTTGATATGCAAAACTCTCATCTGCCCTCTGAAGTCCTRTA[C/A]ATGCTGAAAAATGTGAGGTTGGTACTTTGCCATGTCATCAACAAAGAGCA
Long Flanking Sequence:
TTCAGGAAAAAACAATGTGTTATTTTTCCAGCTGTAAATACACTATAAAAGGAATATTGTTAAATCTGGAAGTGTTCAAATGTTTTAGTCTCACTTGTATTTACTGCTGTCTGCTTGTGATCAGATTGACAAAAACAAATCTTAAAACCAGGAGTAAACAAAGCCTCTAAAAGTCATGTGAAGGTATGCCCTTTTGTTATTTGTGGCTATTCAGGTCCAGACCTTGTCCTCGCCTCCCACCTCGGGTCCAGTATCTCAAAAGCGAACCAGGAAAAGAACAAAGGTGCTATCAATAGCTCGCAAGTATGTCACAGCTACAGAAAAAACACACATCAGAAAGAAAACCTGTTTAGATATCCTGTCCATCTCTTAATCAGAATCCTGCGTATCCGAAGAGAGCCACCAACCCTGCAGCCCAAAGAGCCTCCGCCTTCACTCCTGGAAGCAGATCTGACTGAATTTGATATGCAAAACTCTCATCTGCCCTCTGAAGTCCTGTA[C/A]ATGCTGAAAAATGTGAGGTTGGTACTTTGCCATGTCATCAACAAAGAGCAATTCATTCTTTATTCATAATGTGCAAAGCACAAAACCTGGTTTGGCAAGGAAGTTTGAATGTCTGTGGTCTGTGTGCCTCTCAGGGTTCTGGGTCATTTTGAGAAGCCTCTGTTCCTGGAACTGTGTCGGCATATGGTGTTTGTTCAGCTGCAGCAAGGAGAAGGGTTGTTTCGCCCAGGTGATACTGATGACAGCATCTTTGTGGTGCAGGATGGCCGTCTCGATCTGTGTATTCATGAGAATGTGAGCGCCAAACATTCTCCTGCAACTGTCCTACTAAATAAATAGTTATTTTTAATATGTTATTACTGAGCATCTAAATGTATTTGTATTTTTCTGTCTCAGGATGGGACTGATGTTGTGGTGAAGCATGTTTTACCTGGAGACAGTGTTCACAGTCTTCTCAGCATCCTCGACGTCATCACTGTAAAACCCATCTGTTCTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20413
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002118 | Nonsense | 639 | 1275 | 20 | 36 |
| ENSDART00000128179 | None | None | 316 | None | 9 |
| ENSDART00000145061 | Nonsense | 603 | 1293 | 18 | 35 |
Genomic Location (Zv9):
Chromosome 5 (position 26728306)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 24555571 |
| GRCz11 | 5 | 25059371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGATTGCGTTCTGTCATCATGAAGGATGATGGGAAGAAAGAGCTGGCT[G/T]GAGAGTATGGACGGGGAGACCTCATCGGTGTGGTGAGTGCTTATAAATAT
Long Flanking Sequence:
AACTAAAGTGTTACTAAAATAATAAAGACATTTCTTTTCTTTGGTCATAACCCACTTGTAATATAAATAATAAATACAGAATTAAATGACAGCTATTAGAAACACTTTGTTAAAAATGTCAGAATGCTGTTTAATGTGAACTGTGTGACTTGGATGCTAGGATAATGCGTGCCGAACCTCGAATGGTGTTGAATGTAGCTCACACAGTGGTGCGGAGGGTCTCCTCATTTGTCAGACAGATCGACTTTGCTCTGGATTGGATGGCACTGGAGGCTGGACGAGCTGTCTACAGGTCAGCACACTTTCCCATGCAGTCTTTCAGTGTCAGATCTCTCTGACTTTGAAATAACTTGAGATGGCATGTAATTATTGCATGTATTGCTTAGATTTTTTTTTTTGTCTTTCTCAGACAAGGTGATAAGTCAGACAGCACTTTCATTGTTCTGAGTGGGCGATTGCGTTCTGTCATCATGAAGGATGATGGGAAGAAAGAGCTGGCT[G/T]GAGAGTATGGACGGGGAGACCTCATCGGTGTGGTGAGTGCTTATAAATATATGTATGTTTCTAATATTCTAGGACTTGGAACTAGTACTAATTGTATTAATTTATACTTTCACTTGAGTTTCTTGTTACTTAGTCTGATATGCTAATATACTTTTAAAAGTTGAAACTTTTACATGGTAGTTTTAAATTGTGTGTTATTTCTTTACAGGGTAAAATTACCCATATTGATGAAACTATCTCGTTTTATGGGATGTACACATAAATTAACTGACTTGTGCAACTAAATGTTCTCTAAAATTAGCATTTCTTCATTTCTCCGCTTGCTAATGAGTTGCATTAGCTAGTACCAGCTTTTTTAGCTTGTAACTTACACTTAATATAAAATGATTTTAATAAGTATTTAATCACAGGAAAGACAATAATTTCACATCAGTTTCAGGGTTTTTGAACAAATTCTGCTGTAGTTTTTATCTGTTTTCATCAGTGTTTGTTGGTGTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40422
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 |
|---|---|---|---|---|---|
| ENSDART00000002118 | Nonsense | 975 | 1275 | 28 | 36 |
| ENSDART00000128179 | None | None | 316 | None | 9 |
| ENSDART00000145061 | Nonsense | 939 | 1293 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 5 (position 26719266)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 24546531 |
| GRCz11 | 5 | 25050331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGATCTGATCGGCGGCACTTCCATTGGTTCATTGATAGGAGCTCTATA[T/A]GCTGAAGAGCGTAGCGTCAGTCGCATGACGGTTAGGGCACGCCAGTGGGC
Long Flanking Sequence:
ATAATAACAAGTAATAAATGTATAGGTAGTAATCATACTACAGTTACTGTTATCTTTAATAGATTCTAGTATATAACAAATAAGTGGCTGTACAGGTATATAATAAGTAGTATTATGCAATCAATAATGAAAAAATGTATTTAAAAAATGTACAAGCTACTAAATAAGTACTAGAACGTAATGTAATAAACACTTGTATCTCTAAAGTAAGTACACACTTGTTAAGGAAGTCATATTATGTATGACTGAATTTTAGCTATTTTATGTATAAGACAGGTATGACAATAATAAATGACTCTCTTCACCTTTAAAAATGCTTTATAAACATACTAATATCACATAATGCATAAGTATTGTCTAAGCTCATGTATGAATATGTAAACACACTATACCCACAGAGGCTGCTCACAGGTGGGCATCATTCGTGCAATGAGCGAGGCAGGAATCCCTGTGGATCTGATCGGCGGCACTTCCATTGGTTCATTGATAGGAGCTCTATA[T/A]GCTGAAGAGCGTAGCGTCAGTCGCATGACGGTTAGGGCACGCCAGTGGGCAATGGTGAGACCTTTATGTACCGAACACCAGCATTCATACGTGTCAAGACTATCAAGAAGATTTCTTTCTTTGTTTTTGCTACAGGATTTTGGATCCATATTTAAGAAGATCACCGATTTGACCTACCCGGTGACCTCCATGTTCACTGGAGCATCATTTAACTCCAGCATTGGCACACTCTTCCAGGACAAACAGATTGAGGTTGAGTGGAATGATGATTCATACTACACAAAAACAAGCTATTACAGACTTAATTATATCAAGTCATAATCTTAAAGGGATAGTTCACCCAAAAATTTTAATTCTGTCATCATTTACCCAATGGCTATTTCAGATAAAATGATGGAAAAAGCAGCCATTGACTTCCATAGTGTCTTTATTCCTATTATAAATGATAATGGCCGATTTTCTCCAGCATTCTCTGTAATCTTCTTTTGTGTTTACCAAAA
Associated Phenotype:
Not determined