ZMP
ppl
Ensembl ID:
ZFIN ID:
Description:
periplakin [Source:RefSeq peptide;Acc:NP_001131138]
Human Orthologue:
PPL
Human Description:
periplakin [Source:HGNC Symbol;Acc:9273]
Mouse Orthologue:
Ppl
Mouse Description:
periplakin Gene [Source:MGI Symbol;Acc:MGI:1194898]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25257 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33247 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17491 | Nonsense | Available for shipment | Available now |
sa20080 | Nonsense | Available for shipment | Available now |
sa16489 | Nonsense | Available for shipment | Available now |
sa16429 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25257
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 |
---|---|---|---|---|---|
ENSDART00000055241 | Essential Splice Site | 459 | 1754 | 12 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | None | None | 1076 | None | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | Essential Splice Site | 263 | 474 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36721335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36327769 |
GRCz11 | 3 | 36469627 |
KASP Assay ID:
554-7475.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCATAATCCCTCCAACCGACCCTGAAGCTGTGGCCAGTGCTGACAA[G/A]TGGGTATTCCTCCATATCAGGATATACAGCTAGGAGAAATAAAGTGAACC
Long Flanking Sequence:
GACTCCTCAAAAACTGCTCCCTATCGAGGCTCTGTGTGAATACGATGCAGAAGAGGTACGCAGTCTGAGCTCTACATGCACACAGCTTATAGCTCCTCTAATACCAGTCAGTGAAACATCATGAGTAAGCGAAGAAGAAAAAAATGTTATGCTCTCTCTCTCTGTTCGGGTTTTGGATTCTCCCATTTAATGTATTTAAATCCTTAAGACGGCCTTCACCCAAACGATTCATCTCATATAAACCTCCAGAGACGTGCGCGGGGGGATTTTGTGCGGATTTCTCATTTATTTTGCAGCAGCAATATCAAGTTGAAACAGAGCTTACTTTGCTTATTTTGTTCAACACAGGGTTCAATTTTGCGAGGGGAGCGATACACCCTGCTCAGGAACAATGGGCCCAAATGGGACGTGAAGGACGCTAATGGACGCACCATGAGCGCTCCAGGAGTTTGCTTCATAATCCCTCCAACCGACCCTGAAGCTGTGGCCAGTGCTGACAA[G/A]TGGGTATTCCTCCATATCAGGATATACAGCTAGGAGAAATAAAGTGAACCCCTTTTGGACTAAAATTTTTTAGTTATGTGTTTGAATAAAATATAATAAGCTTTGTTTCATTCTGTAAACTACTGATGACATTGCTTCAGAATTAAAAAAATATATACAGTTGAAGTCAGAATTATTAAACCCCCTGAATAATTAGCTCCCCTGATTATTTTTTCCCCAATTTCAGTTTAATGGAGAGATTTTTTTAACACATGACTAAACATAACAGTTTTAATAACTCATTTCTGGTTTAAACATTTTTATTAATTTTCAGTTTTTCAAATGAGAAAGAACAACAATACAAACCCCTGACCCTTACCAATCCAACAGCAGGATAGCGCTCACATTAGCCAAAAATTAACAGATGTATGTATGTATATATATATATATATAATGTTTAAAAAATACCAACATATAACCATACATACCATATACAGCAAAATCAGATTATTTGAGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33247
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055241 | Nonsense | 735 | 1754 | 18 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 57 | 1076 | 2 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36726538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36322566 |
GRCz11 | 3 | 36464424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCATCTGCAAAGAGCTAAAACAGCCTACTCCAACTACCACAATGACTA[T/G]GAAAACCTCAATAGCTGGCTTTCCCGGATACCAAACTATGAGCCACGTGA
Long Flanking Sequence:
CTCGGGATTGAAACAACATGAGAGTGAGTAGTTACATGAGGTGATTATATAACATAATTTTAATTTTGGGGTGAACTAACACTTTTATGTCATGGTGACTCTTTATTATAATTAAATATAGTTCATTAATCATTATTTTTTCAATATATAAATTTACTATTGTTACTGTTAATTTATGGTTGGTCCAAAAACTTAATTTTGTGTTGATCTTGAACAAAACAACTACATAAAAACATACCATTACCTAAATTATTTAGTAAGATACAGTATAGATATGAAACTGTTGTTTATTGTTAGTTAAGCATATTGCAACAAATGGAAACAATCTAACCTGATTGTAAAGTGTTACCATGCTTATTTTACATAAAAATATAATTATTTTTGTCAATTATATCCTAAATTGTTTCATAGATTTTACTTTTAATTATTTTAAATCCATTTTTCAGATCACAGCATCTGCAAAGAGCTAAAACAGCCTACTCCAACTACCACAATGACTA[T/G]GAAAACCTCAATAGCTGGCTTTCCCGGATACCAAACTATGAGCCACGTGAAACTGATGACGTTAGACAGATTGACTCAAAACTGAAAAATCAAAGAGTGAGTCTTGAGTTTTTCCTGCCACTACTGACTTCATTATGAAATCATGATTTATATTTATTAACCAAAACTATGTATTAAATTGACAGAATCTGCTCTCTGACATCGCGAGGAAGGAATCAGACCTAAACAATGTGTCAAGAAATGCGCAGCTTTATCAGCAAGCAGTAAAGGTATGAAAAAATCACAATATAGTACTTGCAGAGCATTATTCTACAAACTTGTTTATGCAAAGCCACATGGACGCCATTGTGTTTTGGCTTTCAGGACTATGAAAATGAAGCAGAGCGGTTTAAATCCATCCTCGACCTTGAAGACGGCTTGGTTCCCCAGACATACAAAAGGAGCAGACTTGAATCTCCTGCCATGAAAGTGAATAGAGAGGTGAGCATTTTTGCATCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17491
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 |
---|---|---|---|---|---|
ENSDART00000055241 | Nonsense | 852 | 1754 | 21 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 174 | 1076 | 5 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36727912)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36321192 |
GRCz11 | 3 | 36463050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCTGCAATTGAGGCAAAATTCACCGAAGTAAATGCTGTGAACRAGCAG[A/T]GACTGCAGAACCTAGAATTTGCCCAAAGCCTTCTTAACCAGGTAAAACAT
Long Flanking Sequence:
AATTTAGAGCAGTATTCACTTTAATAATCATTGCGATTGTCACTGTAATTTGTCACAGAAACTTTTCAGTGCACCCTCTATGTGTGTAAGCAAATGTACAGTATACTTAAATGCATTTTATTATCCAATGGTCACTACTGTTACCATCACTGTTTTTACTTATTCTATGACCACCACACTCAATACAAAAACACTTCATTTTAAGATCTTTATTATATATTTATTTATATTTAAGCAAACTTTATTAACCTTTTGATTCTCTGGTGTAAACGGAAGTTAAACTGCTCCAGTCGCATGAAAATGTGCATTAACCATGTGACACTTCACAAATTTGATTGAGATATTTTTTTCGTACGTGCAGGAAATGCTCAAGTCAGTACTATTTTTGAAGCTTTTTAGATTAGAAGGTCTCTTTACAGTCACTGAAACATTATTGTTGTGTTCTGAAGGAATCTGCAATTGAGGCAAAATTCACCGAAGTAAATGCTGTGAACAAGCAG[A/T]GACTGCAGAACCTAGAATTTGCCCAAAGCCTTCTTAACCAGGTAAAACATGTTATTGTTCTGTATTATGTATATTCCAAACCATAGAGTAGTCTAAGGATTGCTCATTTACTTTAACGCATGCGATATTTTATAATTCTTTACAGCAACCAGAGGTTACAATAGTCAGGCAAGATGTCCAAACTGTGAGATCGTCTGCCCCAGGAGAAGAGCCCTGGAGAATCAAAAATCAGCTCCAGGAAGAAATTCAGCGCAGAGACCAACTAGAAAGGGAAATTCAAAGTGTCCAAAGTGACATCTATTTCCTGGAGGGCCAGAAACCACAGGATACAATTGTCAAGAAAGAACTTGTCAAGAAGGTGCCGGACCCTCAACTGGATGAGGAGTACCACAGAGTTCAGCAGAAGCTCCTGGATGAAAGCAGGACCACTCGGATCTTAGAGAGTGAACTGGACACCCTCCGTGTGAAGCTGCGTGGGATTGAGACCGAAATGAAAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20080
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 |
---|---|---|---|---|---|
ENSDART00000055241 | Nonsense | 1461 | 1754 | 22 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 783 | 1076 | 6 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36729843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36319261 |
GRCz11 | 3 | 36461119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTCAGCAGGACCCTCAACAAGAAAAAGAGCACTCTATCCTGCGCCTT[C/T]AGGTTGAAGAGGAGAGGCACAAGCGCATGCTCTTGGAGAAAGAGTTCAAC
Long Flanking Sequence:
ACAGAGAAGATCCTAAAACCAAGGAGGAGATCGAAAGCCTCAAGCGGAAACTGGCTGAGGAACAGAGGAAACGTTTGGAGCTGGAAAATGAAAGGGCCCTCAGTGAAGAAAAGATCAGGATCAAGAAGATCGACTTGTCACAGGTGAGGGAGAAACTTGTCCAGCAGGAAGTCGTGAAGATGGAGCTGGATCCACTCTTGAAGTCTGAATGTGACACCTTTTCTCTAAATATCAGCAATGAGCAGAAACAGAGAGAGATCTTGAAAGAAGAGCTGATCAGGCTCCAGCGTCAAAAAACTGAACTGGATGTTCAGCTTGAGGAACTGGAGCGTGAACGTAGAGCCCGCAGGGATGCGGAGCTCGAAATTCAGAGGTTGAGAGTGCGGCTTAATGAACTTGAGATCAGGGACAAGGAAAACAGAGAAAAGGTGACAGTAAAGCAAAAGGTTGTCCTTCAGCAGGACCCTCAACAAGAAAAAGAGCACTCTATCCTGCGCCTT[C/T]AGGTTGAAGAGGAGAGGCACAAGCGCATGCTCTTGGAGAAAGAGTTCAACGCCTTGTTGCAACAGCAGGAGATACTTGAGAGAACAGAAGTGCGTGAGAAAGTTGTGCGAACTGAAAAAATCCAAGTTGAGCGAGATCCAGATGCTGAGATGGATATTATCAGGCTAAAGAAAAGCCTTGAAGAAGAGGAAAGACGACGTCGTGAGCTGGACCAAGAGATTGTCACCCTAAACACAAAGCTTTCAGAAATGGAATTCACCAATACGAAATCATCAAAAGAACTCGACTACATTCGTGACGAAAGCAACAGGTTACAGCAGGAGAACCAGCGCCTACAAAACGAATTACGGAAGCTTCAATCTGAAATCGAAATCACAACAACAGAAACCAGACACATCACTGAGTCATCTCCGGTTGAGAGTAGCAGGAACTTGGAAATTCGAATGGAATCCTTGCAACGGGAACTTGCCGAGCTTAGACGCATCCGAATGGAGAAGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16489
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 |
---|---|---|---|---|---|
ENSDART00000055241 | Nonsense | 1502 | 1754 | 22 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 824 | 1076 | 6 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
ENSDART00000055241 | Nonsense | 1502 | 1754 | 22 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 824 | 1076 | 6 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36729966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36319138 |
GRCz11 | 3 | 36460996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTTGAGAGAACAGAAGTGCGTRARAAAGKTGTGCGAACTGARAAAATC[C/T]AAGTTGAGCGAGATCCAGATGCTGAGATGGATAWTATCAGGCTAAAGAAA
Long Flanking Sequence:
AGAAGATCGACTTGTCACAGGTGAGGGAGAAACTTGTCCAGCAGGAAGTCGTGAAGATGGAGCTGGATCCACTCTTGAAGTCTGAATGTGACACCTTTTCTCTAAATATCAGCAATGAGCAGAAACAGAGAGAGATCTTGAAAGAAGAGCTGATCAGGCTCCAGCGTCAAAAAACTGAACTGGATGTTCAGCTTGAGGAACTGGAGCGTGAACGTAGAGCCCGCAGGGATGCGGAGCTCGAAATTCAGAGGTTGAGAGTGCGGCTTAATGAACTTGAGATCAGGGACAAGGAAAACAGAGAAAAGGTGACAGTAAAGCAAAAGGTTGTCCTTCAGCAGGACCCTCAACAAGAAAAAGAGCACTCTATCCTGCGCCTTCAGGTTGAAGAGGAGAGGCACAAGCGCATGCTCTTGGAGAAAGAGTTCAACGCCTTGTTGCAACAGCAGGAGATACTTGAGAGAACAGAAGTGCGTGAGAAAGTTGTGCGAACTGAAAAAATC[C/T]AAGTTGAGCGAGATCCAGATGCTGAGATGGATATTATCAGGCTAAAGAAAAGCCTTGAAGAAGAGGAAAGACGACGTCGTGAGCTGGACCAAGAGATTGTCACCCTAAACACAAAGCTTTCAGAAATGGAATTCACCAATACGAAATCATCAAAAGAACTCGACTACATTCGTGACGAAAGCAACAGGTTACAGCAGGAGAACCAGCGCCTACAAAACGAATTACGGAAGCTTCAATCTGAAATCGAAATCACAACAACAGAAACCAGACACATCACTGAGTCATCTCCGGTTGAGAGTAGCAGGAACTTGGAAATTCGAATGGAATCCTTGCAACGGGAACTTGCCGAGCTTAGACGCATCCGAATGGAGAAGGACGATGAAATCGAAAAGCTTCAGAAGAGTCTGGCTGCAATGCGAGTGAAGAGGGAACAGCGAGAAAGTCACCTCCGCCGTTCAATCGTCGTCATTGATCCAGACACCGGAAAGGAGATGAAGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16429
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 |
---|---|---|---|---|---|
ENSDART00000055241 | Nonsense | 1502 | 1754 | 22 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 824 | 1076 | 6 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
ENSDART00000055241 | Nonsense | 1502 | 1754 | 22 | 22 |
ENSDART00000128929 | None | None | 531 | None | 2 |
ENSDART00000131845 | Nonsense | 824 | 1076 | 6 | 6 |
ENSDART00000136407 | None | None | 179 | None | 5 |
ENSDART00000137607 | None | None | 474 | None | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 36729966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36319138 |
GRCz11 | 3 | 36460996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTTGAGAGAACAGAAGTGCGTRARAAAGKTGTGCGAACTGARAAAATC[C/T]AAGTTGAGCGAGATCCAGATGCTGAGATGGATAWTATCAGGCTAAAGAAA
Long Flanking Sequence:
AGAAGATCGACTTGTCACAGGTGAGGGAGAAACTTGTCCAGCAGGAAGTCGTGAAGATGGAGCTGGATCCACTCTTGAAGTCTGAATGTGACACCTTTTCTCTAAATATCAGCAATGAGCAGAAACAGAGAGAGATCTTGAAAGAAGAGCTGATCAGGCTCCAGCGTCAAAAAACTGAACTGGATGTTCAGCTTGAGGAACTGGAGCGTGAACGTAGAGCCCGCAGGGATGCGGAGCTCGAAATTCAGAGGTTGAGAGTGCGGCTTAATGAACTTGAGATCAGGGACAAGGAAAACAGAGAAAAGGTGACAGTAAAGCAAAAGGTTGTCCTTCAGCAGGACCCTCAACAAGAAAAAGAGCACTCTATCCTGCGCCTTCAGGTTGAAGAGGAGAGGCACAAGCGCATGCTCTTGGAGAAAGAGTTCAACGCCTTGTTGCAACAGCAGGAGATACTTGAGAGAACAGAAGTGCGTGAGAAAGTTGTGCGAACTGAAAAAATC[C/T]AAGTTGAGCGAGATCCAGATGCTGAGATGGATATTATCAGGCTAAAGAAAAGCCTTGAAGAAGAGGAAAGACGACGTCGTGAGCTGGACCAAGAGATTGTCACCCTAAACACAAAGCTTTCAGAAATGGAATTCACCAATACGAAATCATCAAAAGAACTCGACTACATTCGTGACGAAAGCAACAGGTTACAGCAGGAGAACCAGCGCCTACAAAACGAATTACGGAAGCTTCAATCTGAAATCGAAATCACAACAACAGAAACCAGACACATCACTGAGTCATCTCCGGTTGAGAGTAGCAGGAACTTGGAAATTCGAATGGAATCCTTGCAACGGGAACTTGCCGAGCTTAGACGCATCCGAATGGAGAAGGACGATGAAATCGAAAAGCTTCAGAAGAGTCTGGCTGCAATGCGAGTGAAGAGGGAACAGCGAGAAAGTCACCTCCGCCGTTCAATCGTCGTCATTGATCCAGACACCGGAAAGGAGATGAAGCCC
Associated Phenotype:
Not determined