Busch Lab

ZMP

pls1

Ensembl ID:
ENSDARG00000039272
ZFIN ID:
ZDB-GENE-030131-6205
Description:
plastin-1 [Source:RefSeq peptide;Acc:NP_956175]
Human Orthologue:
PLS1
Human Description:
plastin 1 [Source:HGNC Symbol;Acc:9090]
Mouse Orthologue:
Pls1
Mouse Description:
plastin 1 (I-isoform) Gene [Source:MGI Symbol;Acc:MGI:104809]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa19675 Essential Splice Site Available for shipment Available now
sa30813 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39771 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa19675
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057381 Essential Splice Site 77 628 3 17
ENSDART00000123103 Essential Splice Site 114 665 3 16
ENSDART00000131955 Essential Splice Site 77 616 3 16
Genomic Location (Zv9):
Chromosome 2 (position 7881031)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 8298685
GRCz11 2 8096690
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGTGACACCAACAAAGATGAGAAGATCAGTTTCGAAGAGTTTGTTGCC[G/A]TAAGCCTGACTATGAGTGTTGTGTTATTGGTCAGAGAATGTCTCAGCTGC
Long Flanking Sequence:
GACCAGCATGGAGAACAAAGTCACGCAGATCTCTCGAGAAGATCTGGAGGACCTGAGAGAAGCTTTCAACAAGATTGGTCAGTTCAAGTCATTGTGCATTGAAAAATATCAAAGGTTTGGAATCACATGACTGAGTCCGTCAAACATTACCAAAGATTACAATAACTGACTTCATGTAAATGTTTCTTTTTTTATTTTATGGATGATCATTGTCACGCTGGTTTTAGCAGTGTTTAGTTAGTGTTTTAAGTGGAAAACCAATGTATTTTGTCAACGGTTTGCTGCAGTGATGGATTCAGCTGCTCTAAAATGCAATATTGACACTGTACTTCATTCTAGATATCGATAACAGTGGCTACGTGAGTGATTTTGAGCTTCAAGAGCTCTTTCGTGAAGCCAGCTTTCACCTCCCGGGATACCAGATACGGGAGATTGTAGAGAAGTTCATTGCCGGTGACACCAACAAAGATGAGAAGATCAGTTTCGAAGAGTTTGTTGCC[G/A]TAAGCCTGACTATGAGTGTTGTGTTATTGGTCAGAGAATGTCTCAGCTGCTGATCGCGTGTTCTGATTTCAATAATGTCTTCAGATATCCCAAGAGCTGAGAAGTAAAGAAGTGAGAGAAACATTCCGCAAGTGTATCTCCAGGCGGGATGGGATTCGGTCGTTTGGTGGGACATCAGGTATCTCGAGTGAAGGAACGCAGCATTCCTACTCAGGTGGTGTTATACAAGTCTTATATTCTTTTTATATAAGTATATATGTAATGTAATACTGACAACATATATGATGTATATAAAATCTAATACTGTAACTTAAAATATCTGGCAAAAACAACAGGGTAATGAACATTTTAAGGATGTTCTTGCATGGTCAAATCCTATATTCTTAAAGGAACACTCCACTATTTTTTTGAACATAGGCTCATTTTAGAGTAAATTAAAAACATTTTTTTAAAATCCATTCAGTCTTTCTTTGTGGTTGTAGCAAGCACTTTTAGGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30813
Status:
Mutation detected in F1 DNA
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
ENSDART00000057381 Essential Splice Site 165 628 5 17
ENSDART00000123103 Essential Splice Site 202 665 5 16
ENSDART00000131955 Essential Splice Site 153 616 5 16
ENSDART00000057381 Essential Splice Site 165 628 5 17
ENSDART00000123103 Essential Splice Site 202 665 5 16
ENSDART00000131955 Essential Splice Site 153 616 5 16
Genomic Location (Zv9):
Chromosome 2 (position 7874161)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 8291815
GRCz11 2 8089820
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGACTGACAGTTTATTCAAATCTGTGAAAGATGGAATTTTGCTGTGG[T/C]AATATACCATTAACTGTGGTTTACTCTGGGCTGCTCTCTGTTTGTCATGC
Long Flanking Sequence:
GCTCAACCCTGTTAGACCAAAAAACATTTTCAAAAAATCTTTTTTCACATTTTCATTATGGGGTATTGTGTGTAGAATTTTGAGGAAATAAATAAATTAAATCCATTTTGGTATAAGGCTGTAGCATAAAAAAATGTGGGAAGTAAAGTAAAGCACTATTAAAAGTAAAAGTAAAGCACTATTAACAATTTCCGGATGGTCTGTAGATCTAATTGGAAAAGCTAAAACAAAATGACATGTAAGCTTTTTGTGCTGTAATTCTGAAGAGTGTGAACAGTTTGAAAAGAGATGTGTCTATTAATGACCCCTGACACAGATGGACCAAATGTCATTCTGCTAATGTTTTGTTTTTCCATCTCCTCTCAGATGAAGAAAAGGTGGCCTTTGTGAACTGGGTCAATAAAGCTTTGGCAAACGATCCCGACTGCAAACATCTGATCCCGATGGACCCTGGGACTGACAGTTTATTCAAATCTGTGAAAGATGGAATTTTGCTGTGG[T/C]AATATACCATTAACTGTGGTTTACTCTGGGCTGCTCTCTGTTTGTCATGCCGTTAAATATGCTGGGGTATCATTTTTTTTCATGTTTAATTTTCGCTTTGGCGTCTCTCTTTACAGTAAAATGATTAACCTGTCACAGCCAGACACCATCGATGAGCGGGTCATCAACAAGAAATGCACTCCATTCACAATGACTGTAAGCACTTTTACTTTTTAAATCATAGAGGTCTACTTCATGGGATCTATAAATCAAAATAATTAAAAAATAATAATAATAAACTAAAAAGTAAATTGGCATTTAAATCTACAGCTCAACTTAATTAATGATTAATTCTTACATTATACTATTGAAGGTATTATTAAATGCCCTGTGAATTTTGTTTTCCTTTTCAAATATTTCGCAAATGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTGAATTTTTTTCATCTGGAGAAATTCTTATTTGTTTAATTTCGGCTAGAATAAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39771
Status:
Mutation detected in F1 DNA
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
ENSDART00000057381 Essential Splice Site 165 628 5 17
ENSDART00000123103 Essential Splice Site 202 665 5 16
ENSDART00000131955 Essential Splice Site 153 616 5 16
ENSDART00000057381 Essential Splice Site 165 628 5 17
ENSDART00000123103 Essential Splice Site 202 665 5 16
ENSDART00000131955 Essential Splice Site 153 616 5 16
Genomic Location (Zv9):
Chromosome 2 (position 7874161)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 8291815
GRCz11 2 8089820
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGACTGACAGTTTATTCAAATCTGTGAAAGATGGAATTTTGCTGTGG[T/C]AATATACCATTAACTGTGGTTTACTCTGGGCTGCTCTCTGTTTGTCATGC
Long Flanking Sequence:
GCTCAACCCTGTTAGACCAAAAAACATTTTCAAAAAATCTTTTTTCACATTTTCATTATGGGGTATTGTGTGTAGAATTTTGAGGAAATAAATAAATTAAATCCATTTTGGTATAAGGCTGTAGCATAAAAAAATGTGGGAAGTAAAGTAAAGCACTATTAAAAGTAAAAGTAAAGCACTATTAACAATTTCCGGATGGTCTGTAGATCTAATTGGAAAAGCTAAAACAAAATGACATGTAAGCTTTTTGTGCTGTAATTCTGAAGAGTGTGAACAGTTTGAAAAGAGATGTGTCTATTAATGACCCCTGACACAGATGGACCAAATGTCATTCTGCTAATGTTTTGTTTTTCCATCTCCTCTCAGATGAAGAAAAGGTGGCCTTTGTGAACTGGGTCAATAAAGCTTTGGCAAACGATCCCGACTGCAAACATCTGATCCCGATGGACCCTGGGACTGACAGTTTATTCAAATCTGTGAAAGATGGAATTTTGCTGTGG[T/C]AATATACCATTAACTGTGGTTTACTCTGGGCTGCTCTCTGTTTGTCATGCCGTTAAATATGCTGGGGTATCATTTTTTTTCATGTTTAATTTTCGCTTTGGCGTCTCTCTTTACAGTAAAATGATTAACCTGTCACAGCCAGACACCATCGATGAGCGGGTCATCAACAAGAAATGCACTCCATTCACAATGACTGTAAGCACTTTTACTTTTTAAATCATAGAGGTCTACTTCATGGGATCTATAAATCAAAATAATTAAAAAATAATAATAATAAACTAAAAAGTAAATTGGCATTTAAATCTACAGCTCAACTTAATTAATGATTAATTCTTACATTATACTATTGAAGGTATTATTAAATGCCCTGTGAATTTTGTTTTCCTTTTCAAATATTTCGCAAATGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTGAATTTTTTTCATCTGGAGAAATTCTTATTTGTTTAATTTCGGCTAGAATAAAAGC
Associated Phenotype:
Not determined