ZMP
ptpn23b
Ensembl ID:
ZFIN ID:
Description:
protein tyrosine phosphatase-like [Source:RefSeq peptide;Acc:NP_001038393]
Human Orthologue:
PTPN23
Human Description:
protein tyrosine phosphatase, non-receptor type 23 [Source:HGNC Symbol;Acc:14406]
Mouse Orthologue:
Ptpn23
Mouse Description:
protein tyrosine phosphatase, non-receptor type 23 Gene [Source:MGI Symbol;Acc:MGI:2144837]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45667 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32240 | Essential Splice Site | Available for shipment | Available now |
sa43256 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16423 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45667
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104395 | Essential Splice Site | 96 | 1229 | 3 | 20 |
ENSDART00000122588 | None | None | 166 | None | 7 |
ENSDART00000127876 | Essential Splice Site | 96 | 1229 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 18826137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19671372 |
GRCz11 | 19 | 19244325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGTGTTCCCATGGCAACTGGGCAGGAGGCTGCTCTGCCTGTGACATGG[T/C]AAAGATCATACTTGTTACAGTCAATGTGCATCATTTAAGTTTTTTTTTTT
Long Flanking Sequence:
AACAATAAATTATTTATTGTTAAATTACTTGAAATAAAATGATATAAAATACTGTTAGTACTACTAGCATCTTGCTTGACTTTGCCATTATTTGACTGTATGTCAGAAATACTGGTTTCAGAAAAATATGACAGTGTCTTTTCTTCCTCGTATGTCCTAGTACATTGAAATAAACTATGGTGAGAACCCGGAGAACTACAGCGAGGCACTGAAAAGACTGGAGCAGCTTAGACAAGTGGGTATATCAGTGGAATTATAGGAAATATAGTTACACACTTGCATATGGCTGCAGTTAATGAGTAATAGATAAAGGTTGATGATGATGAAGATGATGATGATAATAACTGCTTTGAAATCTCTCTCATTCTCAGAGTGTAGTAAACATCCCAAGGGATTTTGAGGGCTGCAACACTCTTAGAAAGTACTGTGGTCAGCTGCACTTTCTGCAGAGTCGTGTTCCCATGGCAACTGGGCAGGAGGCTGCTCTGCCTGTGACATGG[T/C]AAAGATCATACTTGTTACAGTCAATGTGCATCATTTAAGTTTTTTTTTTTTTTTTTTTATATTTTCTGCATTTCATCTTCTTTCAGGACAGATATCTTCACAGGGAGGAATATCACACATGAGGATATTAACTATGAGCATGCTTGTGTCCTTTATAACCTGGGTAATATAAATACAATCAAAGCATCAGCATAAAAAATCTAATCAAAACTTTGTCTCTGTTTTGCATAACAAACTGCAATTAAATTTGCTCTAATCTCTAATCTGTTTTAGGTGCTTTGCACTCGCTGCTGGGAGCTGTGGATAACCGCCTATCTGAAGAGGTGAACATGGGATTTATTCTAACTTATACTTAAAATACAACAAACAGTAACTGAAATAAAGTAAAATGTTCAATGTACAGAAGGTCAAATAATGAAAAATTAAACACGTCACCATTTTTCTCAGAAAATATAACATAAGATAACATAAATCAGGTATTAGAAATTAGTTATTAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32240
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 |
---|---|---|---|---|---|
ENSDART00000104395 | Essential Splice Site | 300 | 1229 | 10 | 20 |
ENSDART00000122588 | None | None | 166 | None | 7 |
ENSDART00000127876 | Essential Splice Site | 300 | 1229 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 18828681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19673916 |
GRCz11 | 19 | 19246869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCAGTTCTCTCTTGACAAACTTAATGAGGCAATTAAACAGAGCAAG[G/A]TAACTGTTCCTAATCATCCACACACACAGCCCAGCCATTTCAACTTTTTA
Long Flanking Sequence:
ATTAATGTCAAGTCTCGTTTCAGGTGTGTGACTATTATAAGGATTGTCTCAGGGTGTTGGAGAATTCTGAATGTGTGCCAGGGAGGATTCAGAAAGAGTGGAGGAAACTCATTAACATGAAGATCAGCTACTTCAGTGCCATCACACATGTAAGACCATAACATTAACCATGCAGTGCTGTATACATTATACATTTCCTAAGACACATTATTTTAATAAATGTATTGTTTTATTTCCATTAGTTGCACATGGGAAAGCAGTCAGAGGAACAGCAGAAATACGGAGAAGCAGTAAGTGTATGCTTGTGTGCGTTTAGTGCACTTTTTGACTTGGCAGTTTGGTTCGCCAACTATGAAGTGAAAACATTATTAGGTGTACATTTTAAAACGTCCAACAGCTCTGTGGAATGTGAGCCCTCTGATGATAGTGTTGTTTGTCTGCAGGTTGCATATTTTCAGTTCTCTCTTGACAAACTTAATGAGGCAATTAAACAGAGCAAG[G/A]TAACTGTTCCTAATCATCCACACACACAGCCCAGCCATTTCAACTTTTTACAGACACCTTGATGATAAAATTGCCTTTGCTTGTATAGTGTTTTATTTAATCTCAACCAGTCAAATGCATGCATGTAAATACAGTATATAGATACATACATATATATAGTCAGTTATGTTATGATTAGAAATGTGTTGAAAAAAAACTTCTCTCCATTAAACAGAAATTGGGCAAAAAAGATAAACGGGGGCTAATAATTCTGACTTCAACTGTATGTGGTCTTGAATATTGGTTTTGAATATTAATCACCTTGTCTCAATCACAATATTCCCAATTGCTACCAAAGAAACTGGTGGTGTGGTGTATATTAAGCATATTTACATGTGCTTCACAGGGCCAACCAGAAACTATACAGGAAGCATTGAAATTCACAATGGATGTAATTGGTGGAAAGTAAGCCACTTCAATTGTGCATTTACATTTGTGGGGTCTAATATTTAAATCACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43256
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104395 | Essential Splice Site | 658 | 1229 | 19 | 20 |
ENSDART00000122588 | None | None | 166 | None | 7 |
ENSDART00000127876 | Essential Splice Site | 658 | 1229 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 18847469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19692704 |
GRCz11 | 19 | 19265657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTAACAGATTAGTTAATTTATTTATTAATCACCTTACTTTGTCCTGAA[G/A]ATGGAACACCACTGTGCAGGCTCTGATTGCCTCATTCGAGGCATATGAAG
Long Flanking Sequence:
TAGTACTCTTTCAGTTTTTGAAAACATTACTTAGTGAAATGATTGTTGCTAAGCTGTTTACAGTAATATTACTACAATATTATGGACTGAAAATGCTTTGTTCAGTGTCTTTTTAAACGGTTGTACAGTTAGTTATATCCGTCTAATGGGGGCATTAATGGCCCTTTAAAAACCACAGGATGTACTTTAAAAAGAGTAGGGGTTTGTCTCCGACATACTGACCAAACTTGCCCACTGGCCTTTGTCCGTCATGGCTTCCTAACCATCCCCATATCCTCTAATTGGCTTCATCACTCTTGTCTTCTCTCAGTCATTAAGCATGTTTGTGGCGTTTTGGTCTGGCACAGAAAAGCCTCTGTAGCATAATTCAGATTGAGGCACACTGATGGTGGTTGCGGAGATTCCCTGCATCTGTAAAATGCTTTGTGTATCCACAAAAGCACTATGTTAATGTAACAGATTAGTTAATTTATTTATTAATCACCTTACTTTGTCCTGAA[G/A]ATGGAACACCACTGTGCAGGCTCTGATTGCCTCATTCGAGGCATATGAAGAATTGATGAAGAAGGCTGAGGAGGGAAGAGATTTCTACCAGGATCTGGACAAGAAGACCTCTGGCTTGTTGGATCAAACAAAGTCCTATTGTCAAACCAGAGAGGCAGAGCGAGTTGCCTTGCTGGAGAGGTAAGATGTCTTGTGTAAAAAGATTTCGGTATGTGCATATGTGACTTTCAGAGTTGCTTTGAGGAAAGCCTGTACAATATAAGAAAATCATTTGCATATGCAACTAAATTTTATGGGGTGACTAAATGATTTCTAATGTTAGCCATTAGCTTACATTTCAGAATTTTTTTCACCAGTGATTGATTTGAATGTGTAGAATAAGTTTTTAGCAGATACATCTTCAAGTTCATGCTCTTGAACACACTTTCTATGTGTCTTGACAGTGCAGTAAGACCATTATGGGTATTATTACAGACTGTCTGTAATAATAGTACACTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16423
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 |
---|---|---|---|---|---|
ENSDART00000104395 | Nonsense | 1066 | 1229 | 20 | 20 |
ENSDART00000122588 | None | None | 166 | None | 7 |
ENSDART00000127876 | Nonsense | 1066 | 1229 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 18851951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19697186 |
GRCz11 | 19 | 19270139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCACCACAGCAAGTACATTCCAGATCTCAACTCTTTTCACAAGCACCCT[T/A]GAACCAAAATTCCCAAGTTCCATATGGTCCTCGTCAACTCGGTCAGCCCC
Long Flanking Sequence:
ATCCTTGCCAAATTCCCAAATTGGGCAGCCAATACTAACTGGTCAACCTCAGTCTTCCTCTGCCCAACAAATAGTACAAGGCCAAAGCTTTACTCCCCAACCTATACAAAGCATCCATTCAACCTCACAAAGAGGTGCATTTTCTGGGCAAATCCTGCCACCCTTCTCACCTTTACAGGTTCAGCCCATCATGCCAGGTCAAACACAGCAACAATCTGGCCTCCCCTCAGGTTACCAACCAATGTTACTTCCACAAACCCAGCCCCAGCTTGGACCATCAGGCCAACTAACAGCATCCCAACCTCAGGGAGCCCTTATTCCAGGGCAAACTCAGCCTCACTTCAATCTTTCAAATCAGGCCCATCCTGGACAACTTCCACAAAACAGGCCCCAGCAATATATGGGTTACGCCACCACATCTTTTCCATCCTCACAACCTCTGCATATCTCTGCACCACAGCAAGTACATTCCAGATCTCAACTCTTTTCACAAGCACCCT[T/A]GAACCAAAATTCCCAAGTTCCATATGGTCCTCGTCAACTCGGTCAGCCCCAAATGCCACCAGGACCTATACCACCCCAGAACAACATGTATCCATTTGCACCAACACACATGGGCCAGCAACCTATGGGACAACAGCCAATTCCACCCCAATTCAATGCAATGTTTAATGGATCTGGGAGACAACCCATGCACCCTCCTGGTCAAAGCCAACTACTTGGTCCCCAACAACTGGCTTACCCGTCATCAGGACCAACAGTTGCGGCAGTGATGGACAATCCAGTTCCACCATCACTGGCCAACACACTCATACCTACTCCATCACCTCTTCAGGTTTCATCCCAGAGCCAGACCACTACTCCCACATCATCTTTTGCAACCCAGAATTTCAAGCCACAAACCACAAATGCTGCTCCAATCAACACGAACAATTTAGACTCTGCTACAGTTCTGGATTCTGTTCAAAGCAAGGTGGATAATCTCAGTATTGGCTGATTGTGGA
Associated Phenotype:
Not determined