Busch Lab

ZMP

LOC567443

Ensembl ID:
ENSDARG00000015891
Human Orthologue:
PTPRE
Human Description:
protein tyrosine phosphatase, receptor type, E [Source:HGNC Symbol;Acc:9669]
Mouse Orthologue:
Ptpre
Mouse Description:
protein tyrosine phosphatase, receptor type, E Gene [Source:MGI Symbol;Acc:MGI:97813]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa9616 Nonsense Available for shipment Available now
sa9880 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9616
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004122 Nonsense 359 681 11 19
ENSDART00000004122 Nonsense 359 681 11 19
Genomic Location (Zv9):
Chromosome 12 (position 45256279)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 43332535
GRCz11 12 43395936
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACGGAGCAGAAGGTGGACGTGTTCGGGTTYGTGTCCCGCATCCGTGAA[C/T]AGAGATCTCAGCTCATCCAGACAGACGTGAGGGCGCTTCTCTGTTCTTCA
Long Flanking Sequence:
AATTCCTAATTATGATGACTTAACGTAAAGAATATAATTATTAAAATACATTATACATGAACATATTACTATTATGATGCATAAAACATTTTTGAATATCATTAATTTATTTTGTCTCTGAATGGGAAAATTCAGTCAAAATTAGTGACAGTTTTACTGTAATAAACTAGTAAATTGGTCAAAGTATTAAACATAATAAATATGATGAATTAAATATATTGTTTTACATTTGTATGTTCAGTATATAATGCAGTATGTTATTACTTTATATTTTAGAAATTACAATTCTAGTAAATCTACATTTGAATTTCTTTACATTAAAAGAGGATTGGGTTGAAAATGCATGTAAGAGAATTCACAGAGAGTGAAAATGTTTGTGTCTCTCCATCAGTGCTGGCGTGGGCCGGACAGGAACCTTCATCGTCATTGATGCCATGATTGATATGATGCACACGGAGCAGAAGGTGGACGTGTTCGGGTTTGTGTCCCGCATCCGTGAA[C/T]AGAGATCTCAGCTCATCCAGACAGACGTGAGGGCGCTTCTCTGTTCTTCAGCACACACTCACTCTATTTATTACAGGCAGACTTAAGAATACTGAATACAGTATATGAAATGTGTGTGTTTATGTGTGCATGTGTGTGTGTACGTGTGTGTTTGTGTGTGTACATGTGTTTGCGTGTTGCTGTGTGTGTGTTTGTCTGTGTTTGTTTGTGTGTGTCTATGTGTTCTTGTGATTGTGTGTTTTTGTGTAATTGTGTGTTTCTTTGTGTGTGTAGTTGCAGTACTCGTTCGTCTATCAGGCTCTGCTGGAGTATTTTCTGTATGGAGACACAGAGCTGGACGTCTCTTCTCTTGAAGGACACCTGCAGAAACTGCACAACACCAATGCTCCGCTGGACCGCGTCGGCCTCGAGGAGGAGTTTAAGGTCAGCTTCTTCACTCACACCCATCCCTCAAACAGCACCTTTACATACACACACTGATGTTTCTAGACACCTGCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9880
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004122 Nonsense 359 681 11 19
ENSDART00000004122 Nonsense 359 681 11 19
Genomic Location (Zv9):
Chromosome 12 (position 45256279)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 43332535
GRCz11 12 43395936
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACGGAGCAGAAGGTGGACGTGTTCGGGTTYGTGTCCCGCATCCGTGAA[C/T]AGAGATCTCAGCTCATCCAGACAGACGTGAGGGCGCTTCTCTGTTCTTCA
Long Flanking Sequence:
AATTCCTAATTATGATGACTTAACGTAAAGAATATAATTATTAAAATACATTATACATGAACATATTACTATTATGATGCATAAAACATTTTTGAATATCATTAATTTATTTTGTCTCTGAATGGGAAAATTCAGTCAAAATTAGTGACAGTTTTACTGTAATAAACTAGTAAATTGGTCAAAGTATTAAACATAATAAATATGATGAATTAAATATATTGTTTTACATTTGTATGTTCAGTATATAATGCAGTATGTTATTACTTTATATTTTAGAAATTACAATTCTAGTAAATCTACATTTGAATTTCTTTACATTAAAAGAGGATTGGGTTGAAAATGCATGTAAGAGAATTCACAGAGAGTGAAAATGTTTGTGTCTCTCCATCAGTGCTGGCGTGGGCCGGACAGGAACCTTCATCGTCATTGATGCCATGATTGATATGATGCACACGGAGCAGAAGGTGGACGTGTTCGGGTTTGTGTCCCGCATCCGTGAA[C/T]AGAGATCTCAGCTCATCCAGACAGACGTGAGGGCGCTTCTCTGTTCTTCAGCACACACTCACTCTATTTATTACAGGCAGACTTAAGAATACTGAATACAGTATATGAAATGTGTGTGTTTATGTGTGCATGTGTGTGTGTACGTGTGTGTTTGTGTGTGTACATGTGTTTGCGTGTTGCTGTGTGTGTGTTTGTCTGTGTTTGTTTGTGTGTGTCTATGTGTTCTTGTGATTGTGTGTTTTTGTGTAATTGTGTGTTTCTTTGTGTGTGTAGTTGCAGTACTCGTTCGTCTATCAGGCTCTGCTGGAGTATTTTCTGTATGGAGACACAGAGCTGGACGTCTCTTCTCTTGAAGGACACCTGCAGAAACTGCACAACACCAATGCTCCGCTGGACCGCGTCGGCCTCGAGGAGGAGTTTAAGGTCAGCTTCTTCACTCACACCCATCCCTCAAACAGCACCTTTACATACACACACTGATGTTTCTAGACACCTGCTTT
Associated Phenotype:
Not determined