Busch Lab

ZMP

D3HU68_DANRE

Ensembl ID:
ENSDARG00000059949
Description:
Protein tyrosine phosphatase lambda B [Source:UniProtKB/TrEMBL;Acc:D3HU68]
Human Orthologue:
PTPRU
Human Description:
protein tyrosine phosphatase, receptor type, U [Source:HGNC Symbol;Acc:9683]
Mouse Orthologue:
Ptpru
Mouse Description:
protein tyrosine phosphatase, receptor type, U Gene [Source:MGI Symbol;Acc:MGI:1321151]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa9765 Nonsense Available for shipment Available now
sa42777 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9765
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
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036656 Nonsense 147 898 3 18
ENSDART00000083939 Nonsense 147 888 3 17
Genomic Location (Zv9):
Chromosome 16 (position 37828386)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 35115732
GRCz11 16 35069762
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGGAGGTCAATGCTGGACAAAACGCCACTTTCCAGTGTGTGGCAGCT[G/T]GACGTCCCTCWGAAGCTGAGAAGTTCCTTTTGGAGGTGAGTATTTGAGGC
Long Flanking Sequence:
AGAATATGTGGCAAATGTTAGTGAGAGCTGACCAAGGATCAGAAGACTTAAGACCCAGAAATGAAAATTGCTCTGTAATTTACTTACCCTCAAGCCATCCTCTCTATATATGAGGGTTTTCTGTCAGATGAACACAGTCAGAGTAGTTTTAAATTTTATCCTCACTCTTCTTCCATGCTGTAAATGGTGTTGGATTGTGGCTTTTATTTTGAAGCTTATGACACAATTATTTAATATTTTTTAAATATGTGTGTTGTCTTACAAATCTATTTCTGAAAACTGCACTGTATATCATAAAAACAAACAAACACAAAATCTTTCTGATCTCAAACTTTTCAGTAGTAGTATGTTAAAACAAATCTTTGTTCTCACTCTGTGTGCTTTCTGTTATTCTGAACCCTTTTATGTCTCTGTGTCCAGATAAAGCCCCTCATTTCTCTCGTCTGGGGGATGTGGAGGTCAATGCTGGACAAAACGCCACTTTCCAGTGTGTGGCAGCT[G/T]GACGTCCCTCTGAAGCTGAGAAGTTCCTTTTGGAGGTGAGTATTTGAGGCAGATTTTTCTATTTTTGTGTGGAGATAATTTTTAACGCATTCATCAGCTAGAGGCTGAGATTGCCGTGGGATTGTGACTTGATGAATGTCAACTAAATTAGCATCAACAGGCTCAAAGCACCTACTGTAAGAGAAAGGCAGCTTTCTTAAAGCGAGACACTGCAGGTGATTAGGGTAAAAAATGAACTAATAGCAATCACCTTGCTATTCCAGGTGAATTATTACATTAACAATTCCAAGCATTCTTTATATTACAAACTTTTTAAAATCTTGTCTAAAATGTTTCAGTATGCAAATCAGGCATTTTTTAAATAAATTATGCTCTAATTTGTACACATTTCTAGCCCAAAAATCTAAATAGGGATCACTGCAGCATAAAGACCTCCAAATGGGAGGGATTACACCACAAGTAGGCTGGGTTTAGGGTTGGTGTAGGTGTTGTAGATATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42777
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036656 Essential Splice Site 217 898 5 18
ENSDART00000083939 Essential Splice Site 217 888 5 17
Genomic Location (Zv9):
Chromosome 16 (position 37844059)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 35100059
GRCz11 16 35054089
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATAGAGTTTTACTATAATCTCCTTTCTTTCTGTCTATTTCTGTCACA[G/A]TTCCCCCATCGCCCATTGCTCCACCACAGCTGTTGAGAGCGGGTTCCACG
Long Flanking Sequence:
AGTAATATGAATATAAAACTTTTTTACCTTGCGAATCAAATTTGATATATTTTTTCCAATCTTATCATGGCTACTGTGTAGCTGCACGCTGAGTTCCTCAGGGGGCCCAATATGAAAATCACACATTAAATAGCGTGACCTTGCATCTGACGTTCTTCCACAGTTTTTCCACATCTGTCGGCTTACTTATAGCTCTCTCTTGAGGACCTGAAAGAATCTGCTATTGGAGGTTTAATGTGTATGGCCAGATTGGTATTTTAACCTTTGAACCTAGCAATTTTTTAGTTGTACCGGTTTGAACTGCAAATGTTCTTTGACCTCACGTCTGGTCAAGATAAGCTTAAATAACTGGGTAGAAGAGATTAGACAGTTTCAGGTTAGAGAACATACTTTCCCTCTTGGGGGTTGCTTGAAAAAAGGATAATGTAAGAGCTCACTTTATTCATTCCCTGAATAGAGTTTTACTATAATCTCCTTTCTTTCTGTCTATTTCTGTCACA[G/A]TTCCCCCATCGCCCATTGCTCCACCACAGCTGTTGAGAGCGGGTTCCACGTATTTGATTATTCAGCTAAACACCAACTCCATTCTGGGTGATGGCCCCATCATCCGGAGGGAAATTGAATATCGGGCCAGCCTAGCGCCTTGGTCGGAGATCCTTGGGGTTAACATGGTTACCTATAAGCTGTGGCACCTGGATCCAGACACGGAGTACCATATAAGTGTGCTGCTCACCCGGCCAGGCGAGGGTGGCACTGGGCCACCTGGACCTCCACTCATCAGCAGAACCAAGTGTGCAGGTGAGTGACTAGAGAAGTTCGATTACGAAGTCTATTCTAATGCAGAAGTTTTATATTTTAAGTTCTAAACTCTGCAAAGTTGTTGCTTAACACAAATATATAATTAGCCAATCACATGCAAGCAATTTAAAGCAGTTAAGCATGACATGGTCAAGACAATCTGATGAAGTTCAAACCAAGCATCAATATAGGCATGAAATGTGATG
Associated Phenotype:
Not determined