ZMP
ptpn2b
Ensembl ID:
ZFIN ID:
Description:
tyrosine-protein phosphatase non-receptor type 2 [Source:RefSeq peptide;Acc:NP_997819]
Human Orthologue:
PTPN2
Human Description:
protein tyrosine phosphatase, non-receptor type 2 [Source:HGNC Symbol;Acc:9650]
Mouse Orthologue:
Ptpn2
Mouse Description:
protein tyrosine phosphatase, non-receptor type 2 Gene [Source:MGI Symbol;Acc:MGI:97806]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32239 | Missense | Available for shipment | Available now |
sa8418 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32239
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052239 | Missense | 47 | 393 | 2 | 10 |
ENSDART00000125910 | Missense | 47 | 360 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 13013337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12471683 |
GRCz11 | 19 | 12391211 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGTGGCCAAGTATCCAGAGAATCGCATTCGAAACCGATACAGAGAC[G/A]TGAGTCCATGTAAGTAGCCTCAGATTTGAGTTTATATTTTGTTATTTAAT
Long Flanking Sequence:
CGTTTTCGTGTGATCAGTGACTAAATTTATAAGCATTACAGGCAACTCTACTGACATATTAATGAAGTTGTTTACTTAAAAATCAGTATTTTATTCATAGAACAAGGCTAAAACCTTATATAGTCTTAAAGTGCTAGATAAACAAACATAGGCCTCATATAGTTGTGTTGTGTTGTGCTGAGTGAGAGTGTGTATGTGACTAAACAAACAACAGTGTAGCTTCCCTGATTAATATTTCCAGTAATATTATGTAACTATTTCTGGGAGCTGTTCAGTCCTGATTGACGTGAGCTAATTTGTTTTATTATTTTTCCTGTCCGCTGTTTGCTGACTTGGACAATTAATTTAAACGCAACCTAATGAATCAGTAATGGCCTGATTAAGCTTGTTTTGAAGCTCTGCGTGCATTTCTTTCCCAGGAGATACGCAACCAGTCGCATGAATGTGCATTCAAAGTGGCCAAGTATCCAGAGAATCGCATTCGAAACCGATACAGAGAC[G/A]TGAGTCCATGTAAGTAGCCTCAGATTTGAGTTTATATTTTGTTATTTAATGAATGTTTTGTTTCATTTAACATTGTTTAACGTTATTTCCTCAAATAATCAGTTGATCACAGTCGAGTGAAATTGGAAAATACAGAAAATGACTACATCAATGCCAGCCTGGTGGTAATGGAAGAAGCCCAGAGGAGGTACATACTTACCCAGGTGAGTGAACACCACCCAGGACAAGGACACTATGTGTGTGTATACGATTACACAACACTGTTTCATATAAAAAAATAAGGCCATGTTTTGACCATTTTTTATTTGTATTGCATTAGTTATTTGAGGCTCTGAAAAATAACTTTTCAAACTTATTCATACAGCTCATTTTCAGCCTATAATTGTATGTGTAAGGACTTGGCAACCAACTAATGAGAGCGTTACAGCTAAATATACGCTATTTGTGTTTATTAATGAGCTCTTCAATACAAACCACAAATGAAACTAGCTGAAAGACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8418
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052239 | Nonsense | 278 | 393 | 7 | 10 |
ENSDART00000125910 | Nonsense | 245 | 360 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 13005644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12463990 |
GRCz11 | 19 | 12383518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGATCAGCTGCGTTTYTCATATATGGCTGTGCTGGAGGGTKCCAAGTA[C/A]ATTATGGGAGACTCGTCTGTGCAGGCATGTGATCTAGACAGTWTTTTCAA
Long Flanking Sequence:
GCACTAATATTGATTACTTTATTCATTTTGGTTTGAGAAAGCAAAATTTTCCTGTGTAATTGTGATTATACTAATGGCAGGTATTATTTGGTAGTTTGGTCATTTATTTCACTAACTTGGCAGCCGTCAAACGTCATCAAGGAAACAGTTTGAATTTCCGCTTCCTAAAAAAACGTTAGTAATCCATTTGGCACGACATTACATTTATATACTATGCTGTTCAATGTGTAAATGTATGAGTGTGTAGTGTGCCATTTGGGACGCAGCAAGTATAATATCTCGTTCTCCCTTCTTCCTGTTTGTCCTTCATTAAAGCTTATTTACTACTGTTTTTTCTTTTCTTCCGACACTGATATATCACAGATGGACAAAAGAAAAGACCCATTATTGGTGGACATCAAAAAGATTCTTCTAGACATGAGAAAGTACCGGATGGGTTTGATTCAGACCCCTGATCAGCTGCGTTTTTCATATATGGCTGTGCTGGAGGGTGCCAAGTA[C/A]ATTATGGGAGACTCGTCTGTGCAGGCATGTGATCTAGACAGTATTTTCAACTGAGTCACCATTAACCCAATCCTGTATCCTGTGTTTGTGAAAAAAACTGATTTGGTTTTTTATGTCCGTGTGCAGAAACAATGGCGAGAGCTTTCCAGAGAGGACCAAGAGCCCCTGTCTGAGTCTCCCCCTCCACCGCAGCCCCCTAAATGCACAGAACGCTACAATGGCAGCAAACCAGCTCATCTGGAGGATGGGATCGACTCAAAGACGGGAAAGAAAACAGGGCCAGAGGCCCCCAATAAAGAACCAGACAGGGATGCTGGAACACAGTATGTAAAAAAAGACTTTTTATGTTTCTTAGACTTGTTCCAAAACTTGAATGTGGCTGATAAGGAATCAGCATTCATCAAGCATGAATTCAAATGCCAAATTTGCCAAATGAATTCTGAAATTCTCGAATCTTCTGTGTGTGTTCAGTGTTTCCTCTAGGAATTTTTTCAGCTGTG
Associated Phenotype:
Not determined