ZMP
ptpn11b
Ensembl ID:
ZFIN ID:
Description:
protein tyrosine phosphatase, non-receptor type 11, b [Source:RefSeq peptide;Acc:NP_956748]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11510 | Nonsense | Available for shipment | Available now |
sa11037 | Essential Splice Site | Available for shipment | Available now |
sa7505 | Missense | Mutation detected in F1 DNA | Not yet available |
sa37695 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45799 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11510
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046951 | Nonsense | 84 | 592 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 24257882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24044448 |
GRCz11 | 23 | 23970999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGGGAGAAGTTCGCCACGCTGRCTGAGCTGGTCCAGTATTACACCGAG[C/T]AGCACGACCTCCTKAGGGAACGCAATGGAGATGTTATTGAGCTCAAAWAC
Long Flanking Sequence:
ATATGATGTCACAAGATGTGACCATAAAAATGACAGAATTAAAAAAATAATAATTGAAAAGTAAACATGATGTTTGCCTATATTGGATATGCTTTATGTTGTTGCTCAAATATTCAAATGTAATTTTTATGTTTGCTATCAATGTATAAAATCATTAACTAGACAGTTATTTCACTTTATTTATTTATAATTCTTAGCTTCACCTCATATACAGTATTTACCTTATTATTATGTAACTCAGCATTTTCCCTGTTTAATATGTCAGTTTTCAACAACATCCTCCTAACTGTTGTCTGTCTTTTCCATCTTTTCCATTCTGTCTGTCATCCCTCATTTCCAAACCCCCTGCTCTTTCCCCGTTGCGACTCCATCTGTTTGTTCTGGGCAGGAGGAATGATGAGGTCACCCACATTAAAATCCAGAACTCGGGGGACTATTATGACCTGTACGGAGGGGAGAAGTTCGCCACGCTGGCTGAGCTGGTCCAGTATTACACCGAG[C/T]AGCACGACCTCCTGAGGGAACGCAATGGAGATGTTATTGAGCTCAAATACCCACTCAACTGCAAAGACCCCACATCTGAGAGGTACAGTCTTTCCAAATCTCTACCTAGACTTAATATTGAGTGGACAGAATAAATCCTGCCCCCTAGTGTTCAAACATCAGTGCAAAGGAAGAGCTGTGGTTTGTTTGGCAGAACTTGTTTGTGCTTATGTTAGGGGGGTGGGGGGCTAACAGTTTGTGTTTCTTCTTTCTGTTTTGACATTTATGTTTTTGAGGTCCAGAATCGTTTTTTGGGTCCAGTATACTTTATAACTTCCTTCACCTATGTAAATAATTACGTTTGATGTTTCTGTGGTGTGTATGGTGCAACATCCTGTAGGCTGTGAAATCTAAGTGTTTATAAATGGGTCAAAGATGCCTTTTAAACATCAAGGCAATAAACATGTCATTTAGATTTACATTTAGTTGTTGTTGTTGTTTAAACTTATTTACTTAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11037
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046951 | Essential Splice Site | 111 | 592 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 24257966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24044532 |
GRCz11 | 23 | 23971083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTGAGCTCAAAWACCCACTCAACTGCAAAGACCCCACATCTGAGAGG[T/C]ACAGTCTTTCCAAATCTCTACCTAGACTTAATATTGAGTGGACAGAATAA
Long Flanking Sequence:
GGATATGCTTTATGTTGTTGCTCAAATATTCAAATGTAATTTTTATGTTTGCTATCAATGTATAAAATCATTAACTAGACAGTTATTTCACTTTATTTATTTATAATTCTTAGCTTCACCTCATATACAGTATTTACCTTATTATTATGTAACTCAGCATTTTCCCTGTTTAATATGTCAGTTTTCAACAACATCCTCCTAACTGTTGTCTGTCTTTTCCATCTTTTCCATTCTGTCTGTCATCCCTCATTTCCAAACCCCCTGCTCTTTCCCCGTTGCGACTCCATCTGTTTGTTCTGGGCAGGAGGAATGATGAGGTCACCCACATTAAAATCCAGAACTCGGGGGACTATTATGACCTGTACGGAGGGGAGAAGTTCGCCACGCTGGCTGAGCTGGTCCAGTATTACACCGAGCAGCACGACCTCCTGAGGGAACGCAATGGAGATGTTATTGAGCTCAAATACCCACTCAACTGCAAAGACCCCACATCTGAGAGG[T/C]ACAGTCTTTCCAAATCTCTACCTAGACTTAATATTGAGTGGACAGAATAAATCCTGCCCCCTAGTGTTCAAACATCAGTGCAAAGGAAGAGCTGTGGTTTGTTTGGCAGAACTTGTTTGTGCTTATGTTAGGGGGGTGGGGGGCTAACAGTTTGTGTTTCTTCTTTCTGTTTTGACATTTATGTTTTTGAGGTCCAGAATCGTTTTTTGGGTCCAGTATACTTTATAACTTCCTTCACCTATGTAAATAATTACGTTTGATGTTTCTGTGGTGTGTATGGTGCAACATCCTGTAGGCTGTGAAATCTAAGTGTTTATAAATGGGTCAAAGATGCCTTTTAAACATCAAGGCAATAAACATGTCATTTAGATTTACATTTAGTTGTTGTTGTTGTTTAAACTTATTTACTTAGGACACCCATTGTCATGTACATTTAGAAAAATCATTTAAATATTAAAAGACTCAAATTCAAAATACTATTTAATTTTCTTTTGAAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7505
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:
T > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046951 | Missense | 304 | 592 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 24267930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24054496 |
GRCz11 | 23 | 23981047 |
KASP Assay ID:
554-4142.1 (used for ordering genotyping assays)
KASP Sequence:
CCAYTCGAGTGCAGATCAAGGAAGMGGATCCTGATGTTCCCGGATCCGAT[T/C]ACATCAACGCTAACTATATCCGAGTAAGACCCCGCTTCGCTCGTAATGAT
Long Flanking Sequence:
AAAAGTCAATTTGATGAACTGCACAGTTGAATTTTTAATATCAAAGGTTCACGGGCGAAAGATAAAGGTCCCATAATGCAAATTCATAGTCGCAAATAAGCAGAGAACGCTTGTGAATTGCAAAATACAGAATCTGTTAATTAACAGACATTTTATAACTAAACATTAAATCTAAACATGGATCCACATTTCATCCTGACTGTCTTTTATTTTGTCTCCTGTGGTTCTGCAGGTTTTACAGCAACAAGAATGTAAACTCCTTTACCCCAGGAAAGAGGGGCAGAGACCAGAAAATAAAAACAAGAACAGATATAAGAATATACTACCATGTGAGTAACGTGCTGTATTTTTCTGGTTTCTTAATGGGAGAGGCATGTTTCATAATGCAACGGTTAATCTCCAGGGCTCTTGTTCATGCTTTGATCATCATTTTCTGGGTTGCAGTTGACACCACTCGAGTGCAGATCAAGGAAGCGGATCCTGATGTTCCCGGATCCGAT[T/C]ACATCAACGCTAACTATATCCGAGTAAGACCCCGCTTCGCTCGTAATGATTACACGTCAATCTGAATGTCAAGCTTTTGCTGGGTTGTTGAGCTGTGATCAATAAGTTTAGAGATTGCATGTTCTTTTTATCCTTATTGATTTTGTTCTTTTTTCATTTAGAGCGTGAATGAAGAAGGACGTCATATGGATGAAGGTAAAGTGTTCATCGCTACTCAGGGCTGCCTTCAGAACACAGTCCTGGACTTCTGGAAAATGGTTTATCAGGAAAATACACATGTTATTGTCATGACAACCAAGGAGATGGAGAGAGGACGGGTAAGGTCCAGGATGAAAATATTGTACATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCGATCGTTCATTAATACATTTATATTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATATTATATTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37695
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046951 | Nonsense | 362 | 592 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 24268242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24054808 |
GRCz11 | 23 | 23981359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGGAAAATACACATGTTATTGTCATGACAACCAAGGAGATGGAGAGA[G/T]GACGGGTAAGGTCCAGGATGAAAATATTGTACATTCATTCATTCATTCAT
Long Flanking Sequence:
TAAGAATATACTACCATGTGAGTAACGTGCTGTATTTTTCTGGTTTCTTAATGGGAGAGGCATGTTTCATAATGCAACGGTTAATCTCCAGGGCTCTTGTTCATGCTTTGATCATCATTTTCTGGGTTGCAGTTGACACCACTCGAGTGCAGATCAAGGAAGCGGATCCTGATGTTCCCGGATCCGATTACATCAACGCTAACTATATCCGAGTAAGACCCCGCTTCGCTCGTAATGATTACACGTCAATCTGAATGTCAAGCTTTTGCTGGGTTGTTGAGCTGTGATCAATAAGTTTAGAGATTGCATGTTCTTTTTATCCTTATTGATTTTGTTCTTTTTTCATTTAGAGCGTGAATGAAGAAGGACGTCATATGGATGAAGGTAAAGTGTTCATCGCTACTCAGGGCTGCCTTCAGAACACAGTCCTGGACTTCTGGAAAATGGTTTATCAGGAAAATACACATGTTATTGTCATGACAACCAAGGAGATGGAGAGA[G/T]GACGGGTAAGGTCCAGGATGAAAATATTGTACATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCGATCGTTCATTAATACATTTATATTTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATTTTATTTTTTGTCATATTATGTTATATTGTTTGTCATGGGATACATAGAATATAAGAAAATAAACAATTTGTTATAAAAAAAAATATTTTTTATGCTCTTAATTATATTTCCTTAATTATTTGTGATAATAAAAGTAATTTATATTTTTGGGGGGAGAAATTCATTCAGAATTCATATCAGTTTTAAATACACTGACCATAAAACTGCTAAATGATGACAATCTTGATTCAATTACCCATACAATTATATATTCCAGCCACAATGATTTGGTTTTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45799
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046951 | Nonsense | 480 | 592 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 24274294)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24060860 |
GRCz11 | 23 | 23987411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAACAGGCACAATTATCGTGATTGACATTCTTATCGACATCATAAAT[A/T]GACAAGGTAAGCATTTCATACAGAATTATCCCAGTGGTGTCTTTTTTGTC
Long Flanking Sequence:
GTTAGTACAAAAGTAAAAAAAATGGAACTAATCTAAAAAAGGAAGGTCACAGTCCAAAAATTAGTACACCCAAATTAATATGTTGGGGAAAATGTTAAGCAAATTTTTATTTAAAAAGGAAAAATCAAGAGAAACTTAAAAATATATGTAATGTAGTTTTTGTTTTCTAATTTGTAAATTCTTTTTATTTTATTATTATTATTATTTTATTTGAATTTAAATGTATTATCTTTCTATTCGTGAAGATGTAAGGTGACCCCCCCCCCCCCATTTTTTAACAGGTATAACTGTATAATTAAACTGTTTTGTTTAAATGCAACAAAATTATTAGCTTTATTCACTAAGAAATGGACAAAAATATAAATTTTCAAAGAGGGGTGTACTGAATTTAAAAGCTGTGCTCCACAATGTAAATGTCCCACTGTTGCTGTCATTCTAGTGCAGGGATTGGAAGAACAGGCACAATTATCGTGATTGACATTCTTATCGACATCATAAAT[A/T]GACAAGGTAAGCATTTCATACAGAATTATCCCAGTGGTGTCTTTTTTGTCTGTCATTGATTACATTTAACACAGCTGAACTGCTTCTCTAAGGGCTGGACTGTGACATTGACATCCCAAAAACGATTCAGAGAGTGCGACAGCAGCGGTCCGGTATGGTTCAGACTGAAGCCCAGTACAAGTTCATCTACATGGCTGTTCAGCAATACATTGATACTGCTCAGAAGAGACTAGAAGAGGAGCAGGTGCTTGAACACTACATTTTCAATCAAAATAATGTGATGGAGATACATATATATATAAATTACATGCTACAGTACAGTCAAAGTCAAACAGAAACACTTTACAATAAGGATGTATTAGCTAGTGTTAGATAATGCATTTGCTAAAATGGTCAAACAATGAACAATACATTTATTGCAGTATTTATTCATCTTTGTTAACATTAGTTTCCCAGTCTTGGGTTGCAGCTGGAAGCCCATCCGCTGCATAAAAAATATG
Associated Phenotype:
Not determined