Busch Lab

ZMP

PTPRJ (3 of 3)

Ensembl ID:
ENSDARG00000086511
Description:
protein tyrosine phosphatase, receptor type, J [Source:HGNC Symbol;Acc:9673]
Human Orthologue:
PTPRJ
Human Description:
protein tyrosine phosphatase, receptor type, J [Source:HGNC Symbol;Acc:9673]
Mouse Orthologue:
Ptprj
Mouse Description:
protein tyrosine phosphatase, receptor type, J Gene [Source:MGI Symbol;Acc:MGI:104574]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa30262 Nonsense Mutation detected in F1 DNA Not yet available
sa38078 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44309 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30262
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124237 Nonsense 22 1271 1 24
Genomic Location (Zv9):
Chromosome 25 (position 24042658)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23221771
GRCz11 25 23319319
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAATCTTACTGTGGCCAACATCACAACATCATCTGCTTTTCTGAAAT[G/A]GGATGAACCTCAGGGGAATAGATCTTTCTTTAAAATTCAGTGGAGTGATA
Long Flanking Sequence:
CAGTGTTACATTTGGAGGACAATGGGGAAAGGTTACAAGCCTAGGAACACCATCCCAACTGTGAAGTATGGGGGCAACAGCTTCATGTTGTGAGGCTGTTTTGCTGCAGGAGGGACTGGTCCACTTCACAGTATAGATGGCATCATGAAGAAAGAACATTATGTAGAAATACTGTAGCAATATCTCAAGATGTTGCCAGGAAATTAAAACTTGGCCACAAATAGGTCTTTCAAACAGACCAAGACCCTAAGCATACTGCCAAATTAGTTAAAATGTGCTTTAAGGACAACAGTGAATATTTTGGAGTGTCCATTACAAAGCCCTCTATCTATCTATCTACATTGCAGCATATTCATTTATAATTGCATCATTTATATATGTGGTTTTTATCGCTGTTACACTAGCAGTTATGATTTCATTTTCTGTCCCTCACACAGAGCCAGATGTAATCAGAAATCTTACTGTGGCCAACATCACAACATCATCTGCTTTTCTGAAAT[G/A]GGATGAACCTCAGGGGAATAGATCTTTCTTTAAAATTCAGTGGAGTGATAATAATAGCGTCAACAATATAACAACTAATGACACATGGTATAACATCACTGATCTGACCGCTGGTGTCAGTTACACTTTTAACATCACTGCTGTTGCAACTGATAAATCAACACAGGGAGAACCTGTAGTTGCCATAAAATACACAAGTATGTTTCCATATTTCCAGATAAAGTTTTAAAATGTATCAATTTACACTTGTTAATTTTTTTTTCTTTTTATTAAGAGTTATAATCTCCAAATGTCTTTTATCATTCATTCACAGAGCCTGGTGTTATAATGAACCTCAAAGCTGATAATATCACCACATCATCTGTTTTACTTAGCTGGACCAAACCAAATGGCCAAAGCTCCTATTATAATATAGAATATGGAAATAACAACGTGACTACAGAGAACACTTCCATGGAAATACATTTTCTGGTTCCTGGAGCAAAATACACATTCAGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38078
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124237 Essential Splice Site 88 1271 2 24
Genomic Location (Zv9):
Chromosome 25 (position 24042970)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23222083
GRCz11 25 23319631
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTTATTAAGAGTTATAATCTCCAAATGTCTTTTATCATTCATTCAC[A/T]GAGCCTGGTGTTATAATGAACCTCAAAGCTGATAATATCACCACATCATC
Long Flanking Sequence:
TTACAAAGCCCTCTATCTATCTATCTACATTGCAGCATATTCATTTATAATTGCATCATTTATATATGTGGTTTTTATCGCTGTTACACTAGCAGTTATGATTTCATTTTCTGTCCCTCACACAGAGCCAGATGTAATCAGAAATCTTACTGTGGCCAACATCACAACATCATCTGCTTTTCTGAAATGGGATGAACCTCAGGGGAATAGATCTTTCTTTAAAATTCAGTGGAGTGATAATAATAGCGTCAACAATATAACAACTAATGACACATGGTATAACATCACTGATCTGACCGCTGGTGTCAGTTACACTTTTAACATCACTGCTGTTGCAACTGATAAATCAACACAGGGAGAACCTGTAGTTGCCATAAAATACACAAGTATGTTTCCATATTTCCAGATAAAGTTTTAAAATGTATCAATTTACACTTGTTAATTTTTTTTTCTTTTTATTAAGAGTTATAATCTCCAAATGTCTTTTATCATTCATTCAC[A/T]GAGCCTGGTGTTATAATGAACCTCAAAGCTGATAATATCACCACATCATCTGTTTTACTTAGCTGGACCAAACCAAATGGCCAAAGCTCCTATTATAATATAGAATATGGAAATAACAACGTGACTACAGAGAACACTTCCATGGAAATACATTTTCTGGTTCCTGGAGCAAAATACACATTCAGAGTGTTTGCAGTTGCAGCTGATCGAGTGACCGAGGGGGACTCTAATCAGATTTTACTATTTGCAAGTAAGATCTCATTTTAGAGTTTTAGCCCCAATCCTACACTTTCCAGCTGAAAATTAATAGTGTTTGTACAAATACAGCAAATAACAAATATGCGAGCCAGTAGTCTGTTAAATGTGCTTGCATCTTGTGGATTGACTTCAACGTAATCTATTGTCTAGTGATACCATATATGATGATGTACGTATGTAGTAGGAGTAGTGTCCTGTTTAAGGGAATATTTCCATGACTATCCCTTTACACTTTGATTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44309
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124237 Nonsense 1011 1271 17 24
Genomic Location (Zv9):
Chromosome 25 (position 24060657)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23239770
GRCz11 25 23337318
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCGCCCTGGCTCTTGAAAACAAGGAGAAGAATCGTTACTTAAATGTTT[T/A]ACCTTGTGAGTATCTTCACTGTTGTGTATTGTAAAAAAAAAGTGTCAGTA
Long Flanking Sequence:
ACCCGATTTCTAGAACTGTTGTTCACTGGACTTGAACCCCGTCGTCAGGGTCAACTCCTCTCTGTGCCTTTAGTCTGCCGATGTACATAGTGAGCTAACTGCAAAAACTGCTAACAGCGGGAAAGGCATCTATACGGAGGTAAGCAGTCAGCTAGTAAGCGCGAAAATGAACGTCATACAATATCGTCACACCGCCCCGTAGCATTCATTTTTAAAAATGAAATCCCGCCATACGTACGTACGTAAAGTAGGGCTATGTTTTCATAATGAGCCTGTGTTGCATGCAGTGACTTTCTGTGGTTATATCATCAAACTGTTGTGGCCATAACTTGTTGCACAGCAATTGATACATTCTAATAATAAAACATGCTAATTCTAGTTTTTCAAAGTCTAAAGATCTTCTGTGTTGTTGCAGGAGTTAAGATTTGTTGGAACAGCACAGGCAAATACCGCCGCCCTGGCTCTTGAAAACAAGGAGAAGAATCGTTACTTAAATGTTT[T/A]ACCTTGTGAGTATCTTCACTGTTGTGTATTGTAAAAAAAAAGTGTCAGTAGCTTATCAAAATCACAAGCTTCAATTTGATAGGCTGGCTGCTTTGAAATTTCCTGGAAAATTGACACACTGATAATGCAGTGAAAACACCATAAAAAAGCCAGTCGCTGCTTGTTCGAACTACTTATTTAATATTAGCTGAAACAACACAATTCTTTAGGTTTTTTTTCTCATTTAGGTCTCGTTTGTTTTATGTTCAATCCACTTAAATTTGAAATAACAACTTAATCAATTTCGGTTGGGAAAACCGTGCAGTTCTTTATGGATTTATTATTATTTATTTATTTATTTTTTGTGGACAAAGAAGCATAAGTTGACATGTGGCTCTAATTGCGACCAATTTAATATTTAATAAAATAATCAGACACTGGAGATAACAATAAGAAGCCAAAGAAATCCATGTGTTGTAATAATTTTTAAAACTAAAAAATGACATTTGCTGTTTGTTTAA
Associated Phenotype:
Not determined