ZMP
pnpla6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PNPLA6, patatin-like phospholipase domain containing 6 (PNPLA6) [
Human Orthologue:
PNPLA6
Human Description:
patatin-like phospholipase domain containing 6 [Source:HGNC Symbol;Acc:16268]
Mouse Orthologue:
Pnpla6
Mouse Description:
patatin-like phospholipase domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:1354723]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32741 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14069 | Nonsense | Available for shipment | Available now |
sa17978 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32741
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 |
---|---|---|---|---|---|
ENSDART00000049716 | Nonsense | 454 | 1342 | 13 | 34 |
ENSDART00000139219 | None | None | 820 | None | 19 |
ENSDART00000140890 | None | None | 355 | None | 11 |
ENSDART00000144735 | None | None | 213 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 46368367)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45205879 |
GRCz11 | 1 | 45897674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATCCTGAGGAGGAATCAGGGATGGACATTTTTAGCTCATTTCAAGGA[C/T]GACCAAACGCTACAGTGTTCGAGGAGGCCCAGAAGGAGATCCTCAGACTC
Long Flanking Sequence:
AAATCATGTGATAACAACGAGTGTAATGAACTGGCATTAGTGGACAAAACACACTGTCCACTGTTTCAGCTTATGCTGTTGTCTTGCTGTGATGTTGTTGCTGATCTTTTCATCATCTCATTTTGTCGTGTACTGTGTGTGTGGTACAGGAATGCAGAAGAGTCTGCGTTCAGATTTCGACATGGCGTATGAAAGAGGTCGTATCTCTGTATCTGCAGAGGATGGAGTGCCTGCTTTCACAAAGGTGGTGGTTTATTTGTAAATTTTGAACTGAAGTGAACAGCATTTAGTTACAGTAATTACAGTCTAATGGAAAACATTACTGAGATTAAGAGTCCCCAAAAAAGGATGATTAAATATCTGTCTTGAACAAGATGTTTCTGTTTGTTGTGTTTCAGGAGCAGCGGGAGAGGAAAGTGACCGTGGATGAGGTTCCTTCAGGTGTGTATTTGTATCCTGAGGAGGAATCAGGGATGGACATTTTTAGCTCATTTCAAGGA[C/T]GACCAAACGCTACAGTGTTCGAGGAGGCCCAGAAGGAGATCCTCAGACTCATGAAGATCGAGGTATCTGTGTTTGAATTAAGGTTCATTACCCAGTAAAAGTAAGCCATTTTAGATGTATTTTAAAGCCAAACTGCAAAAAATGATTTTCTTACTTTTTTTGTCTTCTTTCTAGGTCAAATATCTAAACAATCTTATATCAAGAAGCATTTTCTAGGCAAGCAAAACATATTGCCGTTTTCAGAAATAATATGCCAATATTAAGTGAGTTTTTCCTTAAAACAAGCTAAATAATCTGCTAATGGGGTAAACAAAATAATCTTGTCAAAAGGGAAGTTTTAAGGAAAAACTCACTTAATGATGGCATATTATTTCTTAAAACAAGACGATATGTTTTGCTTGTCTAGACAATTCTTCTTGATTTAAGAATTTTTAGATATTTTAAATAGAAACAACAACAAAAAAATAATTTAAGTAAGAAAGTAATTTTTTGCAGGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14069
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 |
---|---|---|---|---|---|
ENSDART00000049716 | Nonsense | 901 | 1342 | 22 | 34 |
ENSDART00000139219 | Nonsense | 427 | 820 | 9 | 19 |
ENSDART00000140890 | None | None | 355 | None | 11 |
ENSDART00000144735 | Nonsense | 38 | 213 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 46360402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45197914 |
GRCz11 | 1 | 45889709 |
KASP Assay ID:
2259-0982.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGCTCTGGACACCTTCACCYGAAGTGTCCTCGTAGAGTCTTCTCACGA[A/T]GAAGCCCYACCAAACTGGTAAGAAAAATCACACAAATCCATCAGTGTTAA
Long Flanking Sequence:
CCATATCCCTATCAGGCACAGATTGTAATTTATCAGCATTTGAATAGCTACAAGTTTGGCTTGTGCAAACAGAATCAAGATGTGAACTTAGGGAAAAGTGGACATCTAATTGCACTTCCCACAAGTGAGTGGTCTTGTTAAGCCACCTGTAGGACACACTCCTTTAGGTATGACCGGAGGGAGGAAAAACGAACAAACTAAGACTTGTCATAGCTTTTATATACTACTGCTCTCTGACGATTTGAAGTCCTTTTATCCATACAAGTTATGTCTCCTAAATAAGTACATGTAATTCAAAGGTTTTGTTGTAATTTCGCATTTTCGTATCTTCTCAGTTGGAGCAGATGTTGGAGAACACAGCAGTGCGGGCTCTGAAACAGCTTATTTTGCTGCACCGTGAGGATGGTCCGGGCCCGTCAAGAACAGTCGAATGGCTGAACATGCGAAGCTGGTGCTCTGGACACCTTCACCTGAAGTGTCCTCGTAGAGTCTTCTCACGA[A/T]GAAGCCCTACCAAACTGGTAAGAAAAATCACACAAATCCATCAGTGTTAAAATAAAATAATAAAAAAAAAATAATAAATTATATTTGTTGTAATGTCTGGTATTTGCTGTGAATTTGTTTGTTTTGTCGAACAGAGAGAGGTATATGAAAAAGTGTTTGAGAAGACTGCAGACAGACACAGCGATTTCTCACGGCTGGCCAGAGTACTCACAGGAAACAGCATTGCCCTTGTGCTCGGAGGAGGCGGAGCCAGGTGAGTGACACCTAACAATTTGATTACTGTTGTTTAAACGTAAACCTTAATCATTTGAACTGAATGGACAGATAGAATGAACCTTTTATTTTAGAATTTCCACCTTTCAAGTGAATTATTTTTTTCTTTTGTTTTTATTTTTGTAATACTATTTAGAGTTCAGTTAGGAGTTCAGATTTAGTGCTTGTTGATTTATATTCGTTTTTATGCGTTTAGCTATTTTTCAGTTAAAATGAATGATTTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17978
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 |
---|---|---|---|---|---|
ENSDART00000049716 | Nonsense | 1005 | 1342 | 25 | 34 |
ENSDART00000139219 | Nonsense | 531 | 820 | 12 | 19 |
ENSDART00000140890 | None | None | 355 | None | 11 |
ENSDART00000144735 | Nonsense | 142 | 213 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 46359549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 45197061 |
GRCz11 | 1 | 45888856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAGTTATYAAAGCTATTTCTCTTGCCTGCAGGCTATGAACTCGGTGTTY[A/T]AAACAGTTCTGGATCTTACTTATCCAATCACRTCCATGTTCTCGGGCTCT
Long Flanking Sequence:
CCACCTTTCAAGTGAATTATTTTTTTCTTTTGTTTTTATTTTTGTAATACTATTTAGAGTTCAGTTAGGAGTTCAGATTTAGTGCTTGTTGATTTATATTCGTTTTTATGCGTTTAGCTATTTTTCAGTTAAAATGAATGATTTGCAAAAATAGTTTTAGTTATAGTTAACAGTAAGTACCCTAGTTAATTGTATGTTTAATCTTGCAGGGGTTGCTCTCATGTTGGTGTAATCAAAGCCATGGAGGATACAGGAATTCCCATCGATATAGTGGGAGGAACCTCCATTGGCTCATTCATTGGTGCTCTGTATGCAGAGGAGAGAAGTGCAGTTCGGGTCAAGCAGAGAGCAAGAGAGTGGTCCAAGGTAACATTGACTCTTATCATCCCATTAAAACCTTTACCTTTCCTTGGCCAACATCTTGAGTACTAATCCCTGAAATCTGGTCATTTAGTTATCAAAGCTATTTCTCTTGCCTGCAGGCTATGAACTCGGTGTTC[A/T]AAACAGTTCTGGATCTTACTTATCCAATCACGTCCATGTTCTCGGGCTCTGCCTTCAACACCAGCATCTCCAAAGTCTTTGAGGACAAACAAATTGAGGTGAGAGTGCAGCTAGCGTCTTAAAATGAACCCAATGATTCGGAAGCGTTCCCAATGTTTTTAATTCCTCAGTAATAATCAAATGTTTCATTCTGGATGATGATTATCATATGCATGACAAATGTAACATTTCCTGCTTGTGTTTGTAGGACTTGTGGCTGCCTTACTTCAACGTGACCACAGATATCACAGCTTCTGCTATGCGTGTTCATAAAGATGGTGAGTGATCACTGAACTGCTTTCTGTTTCAGCTCTAATGTGGAGTTCCACAGGGTTCTCTGGTAGGGGCATTTTATTTAGGAAAATAACATTTTATTAAATGTAAATACAATAGTAATTGTATAAAATAATACATTAATAGAAATAAATAATTTGACCAATTTTAAATGTAAAATACTGATA
Associated Phenotype:
Not determined