ZMP
ptpn23a
Ensembl ID:
ZFIN ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25027 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32106 | Nonsense | Available for shipment | Available now |
sa36225 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1072 | Nonsense | F2 line generated | Not yet available |
sa36224 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25027
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 |
---|---|---|---|---|---|
ENSDART00000102649 | Essential Splice Site | 42 | 1893 | 1 | 26 |
ENSDART00000145956 | Essential Splice Site | 28 | 2003 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 43796960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41181353 |
GRCz11 | 16 | 41131385 |
KASP Assay ID:
554-7340.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATCTAAAGGAGGCAGGAGAGTTTCAATTCAGCCCGACTGTCAAACAG[G/A]TGAGGGACCAGACAGGCCTGATCGAGCCGTTCATTTATGTCACTGCTCCT
Long Flanking Sequence:
ACTAAATATTTTGATGTGTACATTTTGACAAACCTTTGTTCTTTAAAGTTAAAAAAAAGGTAAAGCTATAATTATAATATTTTTTAGCATTATTATTTTGTATAAATTCTTACTATTAATCTTTGTAGATACATTTCACTATAATAAAGCACAGCGCGTGTGAAAAGTCATTAAATAACAGACACACTAGCTCGCAACACACTGCAAAAGAACCACATTTCCCATAGTCGAGATTCAGATCCCATGACGTCACTTCCGAAAACCGCAATCGCTTCCTGTATGGGTGTAAATGGGGACATGACACAGTCGTTTAGAGCTGTAAAATTGAAAATAAACCTTCCGCGGGTACTTTTCCAAGCGCTTGAACTCTTCAAAACGTTTCTGCTTTAGTCGGCTCAGCGAAATCGGCCGCTGCGATGGAAGCCGTGCCGCGAATGCCGATGATCTGGCTGGATCTAAAGGAGGCAGGAGAGTTTCAATTCAGCCCGACTGTCAAACAG[G/A]TGAGGGACCAGACAGGCCTGATCGAGCCGTTCATTTATGTCACTGCTCCTGTACACTCGGAAAATAAACAGAACGGCGTGTTTTGTGTAGGTGATGTGGTCCAAACTGAAGTAGTAAACATGGGCCTTGTTTTTCTCTTTATATGCTCAACCTACAGGCTGCCTGCCTTTAACAAAAAAAGTATGCCATTGTTTATTTACCCTGACATCATTGGAAATCCTTGAGCGTTTACTTCTTCAGCTAACAACACAAAATTAGCTCTTTTAAGGAATTTAGCAACAGAGATACACCATAGAAATGTAAATTATTATTATACTGTTTTAAAATATACATGTATACTTTTCTGAAATTGTGTTATTAAGGAGAAAGTCTGAATCTGTGATCACAAAAGTAATAATAATACTGTATAATAGCTTTTCCTGAGGTAAAGTTGGTTTATATCAGCACATTCAGACTTTCACCTACTTAATATAATTTCAGAAAAGCATTCCTTGCAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32106
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102649 | Nonsense | 126 | 1893 | 4 | 26 |
ENSDART00000145956 | Nonsense | 112 | 2003 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 43790832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41175225 |
GRCz11 | 16 | 41125257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACGGAGATATTTTCTGGGAAGACGGTGACCCATGAGGACATCTGCTA[T/G]GAGCAGGCCTGCATCCTTTATAATTTGGGTGAGTTAGCATGAGACCGATA
Long Flanking Sequence:
TATATATATATATATACATATACACATATACATTTTATATATGTTACTCAAAGCTACTGTTAGATACCTGAAAAACACTTTATCTTTGCTATATTGTATTCATTTTGTTTTGTATTTTGCTTATAGACTTTTCTTGATTTTTATTTGACTGTCCTGTTTTTTACTGAACATATATTCTATACCATACTGACCCTAAAAGCAAAAGAAAACCATAAACATTTAAAGTCTGTATTGTTGCCCCTAATTTCAACATTTTTAATCAAATATTTGCCCTCAAGTGAGAAATATGATCACAGGAATGAGTACGTTTCTCAGTATGTGAATAGTTCTTTTCATGTGGTCAGTATAATAAATCTATTGATTGATTGATTGAAATGATCTTATATTATGATATTTATCATTATCAGGATATGAGATTATGTATATGATGTGATAATTTTGTTATATCTTAGGACGGAGATATTTTCTGGGAAGACGGTGACCCATGAGGACATCTGCTA[T/G]GAGCAGGCCTGCATCCTTTATAATTTGGGTGAGTTAGCATGAGACCGATACGTCAATGAGCGCATTGTCTGAGAGTGAAATAAATCCTGTGAGGTTGAGAAAAGGGTATTGTTGAAAATCAGGCTTGTTTTGCTGATTCAAGTCATGTTTTCACGCCTCTAGGAGCACTTCATTCAATGCTGGGAGCCATGGACAACAGGGTGTCCGAAGAGGTGAGCTGAACTACAGAAGACACAGCATGGACTAATTTAAATGTCATGTGATTTACTGTCGCAACCGACCGTAAGTCACACTGTGTTGAGAGGAAAGTGGTACATGTAACAATTCTTGCAATTCAGAAGTCATTTAAAGTCATTTTATCTCACTAAAAAAATCTATAACATGTAATTTTATTAATATATGGATAAAAATAATGAATAACTACAAATAGTTTGGCATTATATGAGGTATGGCCATGCAATGGCGCAGTTGGTAGTGCTGTTGCCTCACAGCAAGAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36225
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 |
---|---|---|---|---|---|
ENSDART00000102649 | Nonsense | 242 | 1893 | 8 | 26 |
ENSDART00000145956 | Nonsense | 228 | 2003 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 43787165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41171558 |
GRCz11 | 16 | 41121590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTATTACAAAGAGGCATGCAGGGCTTTGGAGAACTCTGAAACCGCTT[C/A]GATGTTGGGAAAGATCCAAAAAGACTGGAAGAAATTAGTGCAAATGAAAA
Long Flanking Sequence:
ACTAAATTGAAACTTTATTTTTTTTACATGGTTTTATAGTTTTTTGTTATTAAAATTGAAAAATTGAAGTTCCTGTTTCAAAACTTACAGATAGATGGCTAATTTGTATGTCATTGATATGTTCAGTGCTAAGGTAAATAAGTACTTTTGGCACTTTTTTCGAGTCTTTTCATTAGTTTTGTTTTCCTGTAAATTACTCAATAAATACCATGCCGTGCCATTCATACTGAGGTATTACCGTACAGTGAAATTCTGATACCGTTACATCCCTATAATAAACCGCTAATTAGCTGTTTATTAATAGTTCATTGGGTAGAAGTTAGTTTTAGGTTTTGGGTAGGATTAGTGATGTAGAATAAGGTCATAGTTTATAACTACTAATGAACATTTTACATTTCATCTCAAAATTACAGTCTCAAAATTATAATATGTCTTTTTGTTTTAGGTGGTAGATTATTACAAAGAGGCATGCAGGGCTTTGGAGAACTCTGAAACCGCTT[C/A]GATGTTGGGAAAGATCCAAAAAGACTGGAAGAAATTAGTGCAAATGAAAATTTACTACTTTGCTGCCATTGCTCATGTGAGTCTCTTGTTTGAAACTGAGCTTGGATGAACTACAAAGCAGGCCGGCCAAATGTGTATGTGGATGTTTCTAAGAAAGTCACACTAAATCCTATTTCTTTCAACAGTTGCATATGGGGAAACAGGCTGAAGAGCAGCAGAAGTATGGAGAGAGGGTATAAATGCCTGTTTTTCTGTCTTCATTTTCATTTAGTCACCATCTTTGCTGTTTGTCTAGGAGAACTTCATCTCTTTGTTTAAAGATCTATTTCTTAAAGGACAAACAGAGATGCTTCTTGTAGTTAACGTCTAAAGTTATACAAATCATTTAACTTCACATTTTTGCTTACAAATGTATTTTTTCCAATAGGTGGCTTACCTTCAGAGCTCACTAGACAAACTCGGTGAGGCAATTAAACTAGCTAAGGGTCAGCCAGACAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1072
Status:
F2 line generated
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102649 | Nonsense | 1095 | 1893 | 21 | 26 |
ENSDART00000145956 | Nonsense | 1203 | 2003 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 43781400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41165793 |
GRCz11 | 16 | 41115825 |
KASP Assay ID:
554-0974.1 (used for ordering genotyping assays)
KASP Sequence:
CTCCTCATCCACAGATGCCCTCAGTCTCTCAGCCACCACCTCACTGCCCC[C/T]AATCCCATATAATTCCTGCTCATCAACCAAATCAACAACCACCATACCCA
Long Flanking Sequence:
AGGCCCCACTTCCACAAGTTAACACTATCAACCCAGGCCAGATGTCCCATTCTGGCGTTAGTCCACAAATGCCACTATCTTCCCATCCAGTTCCCCCTGTGTCAATGCCACACTTGGCTCATGTTAATCAGCATATTCCTCCATCCTCCCAGCCAGTGCCCTCAATGTCAATGCCACATTTAGCACGTGTTAATCTGCAAATTGCCCCATCCTCCCAACCAGTGTCCTCTGCCTCAATGCCACACTTAGCACATGTCAGTCAACAGATTCCTCCTGCTTCACAGCCCCAACCACCTCCTGTTAATCATTTGTCTCATCCTCCTCACCGTCAGATACACCCATCCTCTCATCATTTAGGCCCCACGCCTCATATGCAGATACCTGCTGCCCCAACACAGATGCCTCCTCCCCAACAGCCTCAAATGCATGCATCATCCACTCACATGTCTCCTCCTCATCCACAGATGCCCTCAGTCTCTCAGCCACCACCTCACTGCCCC[C/T]AATCCCATATAATTCCTGCTCATCAACCAAATCAACAACCACCATACCCAGCAGTTCCAATGCAGGCTACTGTTCCTATTCAACCTCAGGCACCCCATGGCTCACTCCCTTCACAAGTGCAAATACACCCTAACACTCCTTCACAGCATCAAAACCACCCTCATCCTCAAATCATTCCCCAGTCCTGTCCTCCAGCTCTCCCTCACAATATGTACAAACCTCAGCCAACTATTACACCTATCTCTGCACCTATGAGTTTTCCAGGAGGTGTCCCTATGGTTCCCCATCAGTCTGTGCCCTCTCTGCAACCTCAGTCTCAGCCACCCTCTTCAAAGCCTTTAGTCCCACAACAGCTTCCCCCAGGAGGACCAATATCTTATGCTGTTCCACAAGTTGGGAATATTCCCCCTGGAGCAATGCAACATCCCGTTGCAACTGCTTCCCCTGGGCCACAAAGCATGATACCTCCATCCTCAGGAGCACCAGGGGCACCACAGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36224
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 |
---|---|---|---|---|---|
ENSDART00000102649 | Essential Splice Site | 1517 | 1893 | 21 | 26 |
ENSDART00000145956 | Essential Splice Site | 1625 | 2003 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 43780131)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 41164524 |
GRCz11 | 16 | 41114556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGGTTTCTGTAATCGTCATGCTAGTGTCTGAGCAAGAACTAGAGAAG[G/A]TAAATGTTTAATGTTAATGGATTTTTTGGTAATTTCTACAATCTCGTTGG
Long Flanking Sequence:
TACCAACCAAAGCTGATCCCCAAGAGGAACATCACAGAAAAAAAGCAGAGGGTGTGAGACTTATTCAGGGTGACCCTTATCAAGCACCAGAGAGGGTTTCAAAACTCAGCGCACAGCTTGAGAGATTTCGTTCAACCGTCCAATCCTTAGAGCGCCCAACAGGGGAGGGTGGTCTGTCCGAACTTGATGCTCAATGGAAAGAATTGCAGGAGCAGCAGGAAAAGGATACTCGGCAGCTCTCCATTGCTATTGCTCGTTGCTACACTATGAAGAACCGCCATCAGGATGTGATGCCTTATGACTGCAATCGCGTTGTCTTGCATTCTGGTAAAGACGATTATATAAATGCCAGTTTCACTGAGGACCTATCTCCATATTGCCCCCGGCTCATTGCAACACAGGCTCCCCTCACCGGCACTGCAGCTGACTTCTGGCTAATGGTTTATGAGCAGAAGGTTTCTGTAATCGTCATGCTAGTGTCTGAGCAAGAACTAGAGAAG[G/A]TAAATGTTTAATGTTAATGGATTTTTTGGTAATTTCTACAATCTCGTTGGCTTTTCAAGCAATTTCAAATAATGTGCAATGTTTCTTTTTATCCCCAGCAAAAAGTATTGCGCTACTTTCCATCAGAGAGAGGCCAGCAACTTGCTCAGGGGCCAATCACCCTTACACTGACCACCCAGAAGAGCACTCCTACACACATTGAACGCATGATAGGACTGCAGTATCGGGACCAAAGTCTAAGACGCACCGTTGTGCACCTTCAGTTTACATCATGGCCTGAACTGTAAGGGACTTTTTTTATACATGATAAGAGTATACCAACATATTAGAAGTTCTATTTTTCATTAAAAAATCATATTTATTTTTAAAAGGGGCCTTCCAGAGAGTAAAAGCAACCTTATCCGCTTCATTCAAGAAGTGCATGGACATTATCTGCTTCAGCGTCCATTACACACTCCTGTTGTGGTGCACTGCAGGTACCACACATCAAGCATATTTTA
Associated Phenotype:
Not determined