ZMP
ptprja
Ensembl ID:
ZFIN IDs:
Description:
receptor-type tyrosine-protein phosphatase eta [Source:RefSeq peptide;Acc:NP_001129714]
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 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10152 | Essential Splice Site | Available for shipment | Available now |
| sa9428 | Nonsense | Available for shipment | Available now |
| sa12577 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10152
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016087 | Essential Splice Site | 360 | 1653 | 6 | 29 |
| ENSDART00000047942 | None | None | 124 | None | 7 |
| ENSDART00000016087 | Essential Splice Site | 360 | 1653 | 6 | 29 |
| ENSDART00000047942 | None | None | 124 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 40981508)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39317765 |
| GRCz11 | 7 | 39588782 |
KASP Assay ID:
554-6146.1 (used for ordering genotyping assays)
KASP Sequence:
AGTAGCCGGCNNNAACATATCTGGACCCTCACARTTCATACAGTGTAATACAA[G/A]TGAGTCTACATGCTACACATGTAAATGTAAATGGKTACACTGGCGTACAT
Long Flanking Sequence:
CCAGCCAGGGGTCAACCTACCTCTAACTCAAACCACCTCTTCAAATATGACAAATATTACAAATTTATTATCAGGCACCCAGTACACCATAACTGTGGTCACAAATGGAGTAAACAATCTCAGCAGCTCCTTTATAAACCTCATTGGGTATACAGGTAATGCACAGCACAGCATTTAATCTGAGCTGTCGATCGAGTCTTTTTACATGGTGAATTGTTGTATAATTTGTGTTTCCCCAGTTCCGAAAATCGTGCAAAATCTGGCAGTTTCTAATGTCAGCACTAATTCTGTCAGTCTGACCTGGCTTCCTCCTAATGGGACGTCCAGCCTGTTCTCCTACAATATCAACATCTCTTCACTCGGTCAGACTTTTTATACCACTTCCAACAGTTATCAGATCACGCAGCTGCAGCCTGGGACGCAGTATAATTGCTATGTCACAACACTCATAGTAGCCGGCAACATATCTGGACCCTCACAGTTCATACAGTGTAATACAA[G/A]TGAGTCTACATGCTACACATGTAAATGTAAATGGGTACACTGGCGTACATTTGTGTAATGTTTTGTTTAATTATGCATTTAAAATAGTTTTTTAAACATTCAAGCACAATGAATTACAAATTTGGTCCAACAAACATTTACACAATAATTAACAATAAAACAAGGGGGTCACGGTGGCACAGTGGGTGGCATGATCGCCTCACAGCAAGAAGGTCACTGGTTCAAGCCCTGGCAGAGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGATCGCGTGGGTTTCCTCAGGGTGCTCCTGTTTCCCCCACAGTCAAAAGACAATGTGTTATGGGTAAATTGATAAGCTAAATTGGCCGTACTGTATGAGTGTGTGCAAGAGTATATGGGTGTTTCCCAGTGTTGGGTTGCAGCTGGAAGGGCATCTGCTGTGTAAAACATATGCTGGATAAGTTGGCGGCTCATTCCGCTGTGGGGACCCCTGACTAATAAAAGGACTAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9428
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016087 | Nonsense | 768 | 1653 | 11 | 29 |
| ENSDART00000047942 | None | None | 124 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 40966448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39302705 |
| GRCz11 | 7 | 39573722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTCCACTGAAATGATCACTGTGACAAACTTGCAGCCTGGCACAYTGTG[T/A]CAGATCAGTATATATAGTGTGGCATGTGGCCTTCTGGGACAACCAGTGAA
Long Flanking Sequence:
TTAGGATCATGAGCAGTTCCTTTCCTTCTCCATACTCCTCTCTTCCCATCACGCTGGTACAAGTTGATCTTGGTCTCATCTATCCATAGGATGTTGTTCCAGCACTGAAGGCCTTTTTGATGTTCAAATTGATTTTCATTTCAAATCAGTTGTGTTTTTGTATAGAGCCAAAATTGTTAAAATTGTGTTGATGTCCAAATATTTATAGACCTAACTGTATTAATACAACTTACTGTTAACCAATTACAGTTTTTAACCATTGAAATCACAGACATTTTTTTACAGTCTTTGTTTTTTTTTTCAGGGCCAAATCGTGTTAACAACGTGAGTTCTGTGGCTTTGAATGTTTCCACTGTGAGGTTGAGCTGGGCTCGTCCTTTGCAATACAACCAGTTAGTTTCCTACCAAGTGTTAGTTTCCAACTGCACAAAAAACAGCATGAACATGTCTACTTCCACTGAAATGATCACTGTGACAAACTTGCAGCCTGGCACACTGTG[T/A]CAGATCAGTATATATAGTGTGGCATGTGGCCTTCTGGGACAACCAGTGAACACCTCTGTCCTCACAAGTATGTAATCAACCACACACACACACAGAGTCAATCAAACACAAAAATGTCTTTAGTATGGGCAGAAAGAATTATTTTGCTCTCTCTATCTCTTTCAACAGTGCCATCTACAGTGCAACCAGTTGTTAATAGTCAAGGCTCTAATAACTCTCTTCTGGTGTTGTGGAGTCACCCTGATGGTGGTCTTGATATGTATATTTTGAACATCAGCAGTGATGGATGGAGCGACTTTAGTTTCCTCAACAGCACTGAAAACAATTACACCTTCACTCAATTAAAAGCAGCAACACTCTACACAGTCACTCTCACGACTGTCAAAGGATCCTTTCAGGAAACATCAGGGGCAGTAGTTAGCGCTACCTGTGAGTATGAAACCCTTAAACACAGCAGATATTTATAGGTCTGCGTTATTTATAGGTGCTGATTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12577
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 |
|---|---|---|---|---|---|
| ENSDART00000016087 | Essential Splice Site | 967 | 1653 | 13 | 29 |
| ENSDART00000047942 | None | None | 124 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 40965672)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39301929 |
| GRCz11 | 7 | 39572946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCCATTGAATTTGCAGAGTGAATCTATGAGATACAATGTAACTACAAG[T/A]AAGTTWACAAWTATAATTATAGTKTATAATTRTATTGTGCTGTATTTTGC
Long Flanking Sequence:
AGCAGTGATGGATGGAGCGACTTTAGTTTCCTCAACAGCACTGAAAACAATTACACCTTCACTCAATTAAAAGCAGCAACACTCTACACAGTCACTCTCACGACTGTCAAAGGATCCTTTCAGGAAACATCAGGGGCAGTAGTTAGCGCTACCTGTGAGTATGAAACCCTTAAACACAGCAGATATTTATAGGTCTGCGTTATTTATAGGTGCTGATTGTGTGTGTTTTCAGATCCAAACAGCCCAGGGATGATTACGGTTTTGTTTAAGAACACCCATTCAGTGCTTTTACATTGGGATATCGCTCAGAACATGACGCCTGGCAGCTTCAACTACAGCCTGTCCTTCTGGTCAAGCAAAAACAACAGTCTGTATCTCACTCCCAATAACACTTTGCTTTTGGATGGACTACAATCTGGAACGCCCTATAACGTTTCTTTGGCTACTGTGGGGCCATTGAATTTGCAGAGTGAATCTATGAGATACAATGTAACTACAAG[T/A]AAGTTTACAATTATAATTATAGTGTATAATTATATTGTGCTGTATTTTGCTAAACCGCCATGAAAAACAGAACACAATAAGGTCAATAAGATTATTTATTATTTCAATTTCAGCACTATTCAGGAAAATGTTAAAATACTTTGATTTGGATAACATTTAAAGACCAAATTAATAGATCAACACATTTCTAATTAAAAAAACTAATTTATATAATAATTAATATTCAGGGTCACACAGAATCTGCAAACATTTTGTAACTATTTTTGCGCAGAACTTAAAAAAAGTGCAGCTTAAAACTTATGCAGAATGATTTTAGGAGTATCGTAACTTAAAACTTAATATATTAATTAAAAAAGGTATTATTTTTTATTTAATTTATTATTTAATTATTATTTGTATTAATTATTTTATTTAATGTTTACAATGCAAATCCAATTAGATGCACTTATTTGATAATCAAAGCAAGTCTCCCATATAATATGTCTATTAAAAGACAGAAA
Associated Phenotype:
Not determined