ZMP
pldn
Ensembl ID:
ZFIN ID:
Description:
pallidin homolog [Source:RefSeq peptide;Acc:NP_001074166]
Human Orthologue:
PLDN
Human Description:
pallidin homolog (mouse) [Source:HGNC Symbol;Acc:8549]
Mouse Orthologue:
Pldn
Mouse Description:
pallidin Gene [Source:MGI Symbol;Acc:MGI:1927580]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23209 | Essential Splice Site | Available for shipment | Available now |
sa36559 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43030 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23209
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 |
---|---|---|---|---|---|
ENSDART00000063024 | Essential Splice Site | 82 | 143 | 3 | 6 |
ENSDART00000142945 | Essential Splice Site | 86 | 156 | 3 | 5 |
ENSDART00000063024 | Essential Splice Site | 82 | 143 | 3 | 6 |
ENSDART00000142945 | Essential Splice Site | 86 | 156 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 4933251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 5653795 |
GRCz11 | 18 | 5506657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCACGAAATTCCGCGACTGCAACGCCATGATTGATCTGAACGCGCTGG[T/C]GAGTGTTTAACCGTGTGTTTTCTCATAAGATCCTCCTGTGTTGATCAAGC
Long Flanking Sequence:
TATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTAGAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACCCACGTATGTCATATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTAGAGGAACTCACGTTTTATATAAGAACACTGTTATAATGTTATTTTCTAGACAAAATCAAGTGATCTTGCTTGATACTCTGGAGCAGGAAGTCACGAAATTCCGCGACTGCAACGCCATGATTGATCTGAACGCGCTGG[T/A]GAGTGTTTAACCGTGTGTTTTCTCATAAGATCCTCCTGTGTTGATCAAGCTCACCGCTGATGTGTTTCAGTTCACAGAGGCCAAAGTTTATCACAGCAAACTGGTGAATATTCGCAAGGAAATGATCGTTCTGCACGACAAGACCAGCAGACTGAAGGTTTGAGCATTCAGCTGAGATGCGTACAGTTTACAGCTATCACACTCTGTGTTTGTGAGCGGAAAACACACTGAAACATTTACACGTGTGTGTTTTACTGTGTGTAGAAGCGAGCGCTGAAGCTGCAGCAGCACAAACAGAAGGAGGAGCTGGAGAGAGAACAGCAGAGAGAGAGAGAGATGGAGAGGGAGAGACGGCTGACCGCTAAACCGGCCAAACGCACCGACAACTGAACACACACACACACACACACACACACAGAAATGGAGAGAGAGAGATTGCTAAACACACACGCAGACATACAGAACTAGAGAGAGATCACCAAATGCAAACGTCTGAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36559
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 |
---|---|---|---|---|---|
ENSDART00000063024 | Essential Splice Site | 82 | 143 | 3 | 6 |
ENSDART00000142945 | Essential Splice Site | 86 | 156 | 3 | 5 |
ENSDART00000063024 | Essential Splice Site | 82 | 143 | 3 | 6 |
ENSDART00000142945 | Essential Splice Site | 86 | 156 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 4933251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 5653795 |
GRCz11 | 18 | 5506657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCACGAAATTCCGCGACTGCAACGCCATGATTGATCTGAACGCGCTGG[T/C]GAGTGTTTAACCGTGTGTTTTCTCATAAGATCCTCCTGTGTTGATCAAGC
Long Flanking Sequence:
TATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTAGAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTGCAGGAACCCACGTATGTCATATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTAGAGGAACTCACGTTTTATATAAGAACACTGTTATAATGTTATTTTCTAGACAAAATCAAGTGATCTTGCTTGATACTCTGGAGCAGGAAGTCACGAAATTCCGCGACTGCAACGCCATGATTGATCTGAACGCGCTGG[T/C]GAGTGTTTAACCGTGTGTTTTCTCATAAGATCCTCCTGTGTTGATCAAGCTCACCGCTGATGTGTTTCAGTTCACAGAGGCCAAAGTTTATCACAGCAAACTGGTGAATATTCGCAAGGAAATGATCGTTCTGCACGACAAGACCAGCAGACTGAAGGTTTGAGCATTCAGCTGAGATGCGTACAGTTTACAGCTATCACACTCTGTGTTTGTGAGCGGAAAACACACTGAAACATTTACACGTGTGTGTTTTACTGTGTGTAGAAGCGAGCGCTGAAGCTGCAGCAGCACAAACAGAAGGAGGAGCTGGAGAGAGAACAGCAGAGAGAGAGAGAGATGGAGAGGGAGAGACGGCTGACCGCTAAACCGGCCAAACGCACCGACAACTGAACACACACACACACACACACACACACAGAAATGGAGAGAGAGAGATTGCTAAACACACACGCAGACATACAGAACTAGAGAGAGATCACCAAATGCAAACGTCTGAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43030
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063024 | Essential Splice Site | 112 | 143 | None | 6 |
ENSDART00000142945 | Essential Splice Site | 116 | 156 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 4933514)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 5653532 |
GRCz11 | 18 | 5506394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCGGAAAACACACTGAAACATTTACACGTGTGTGTTTTACTGTGTGT[A/T]GAAGCGAGCGCTGAAGCTGCAGCAGCACAAACAGAAGGAGGAGCTGGAGA
Long Flanking Sequence:
ATATATAATATATAGTCACTGCAGGAACTCACGCATGTCATATATAATATATAGTCACTGCAGGAACCCACGTATGTCTTATATAATATATAGTCACTAGAGGAACTCACGTTTTATATAAGAACACTGTTATAATGTTATTTTCTAGACAAAATCAAGTGATCTTGCTTGATACTCTGGAGCAGGAAGTCACGAAATTCCGCGACTGCAACGCCATGATTGATCTGAACGCGCTGGTGAGTGTTTAACCGTGTGTTTTCTCATAAGATCCTCCTGTGTTGATCAAGCTCACCGCTGATGTGTTTCAGTTCACAGAGGCCAAAGTTTATCACAGCAAACTGGTGAATATTCGCAAGGAAATGATCGTTCTGCACGACAAGACCAGCAGACTGAAGGTTTGAGCATTCAGCTGAGATGCGTACAGTTTACAGCTATCACACTCTGTGTTTGTGAGCGGAAAACACACTGAAACATTTACACGTGTGTGTTTTACTGTGTGT[A/T]GAAGCGAGCGCTGAAGCTGCAGCAGCACAAACAGAAGGAGGAGCTGGAGAGAGAACAGCAGAGAGAGAGAGAGATGGAGAGGGAGAGACGGCTGACCGCTAAACCGGCCAAACGCACCGACAACTGAACACACACACACACACACACACACACAGAAATGGAGAGAGAGAGATTGCTAAACACACACGCAGACATACAGAACTAGAGAGAGATCACCAAATGCAAACGTCTGAACACACATCCACACCCATATGCAGGTGATTTTATCAGGATTAAACACACAGCTGCATCTCATATTTGGCTCTTATCATAAATCATCATCTGTGCGTTCTTCTCCAAATAAATAAATCTGATAATAATAATAATAAACCTGTAATAAAAGTGTTTGTCGTAACAATCTCCATACTATTAATCACCTTCATTACCAATGTTGTTAACTTAGACACAAATGTTATTTCAGCATAGTTTAGACATCATCATTATTAGTATTTTAATTGTTT
Associated Phenotype:
Not determined