ZMP
ptpn4a
Ensembl ID:
ZFIN ID:
Description:
tyrosine-protein phosphatase non-receptor type 4 [Source:RefSeq peptide;Acc:NP_001007201]
Human Orthologue:
PTPN4
Human Description:
protein tyrosine phosphatase, non-receptor type 4 (megakaryocyte) [Source:HGNC Symbol;Acc:9656]
Mouse Orthologue:
Ptpn4
Mouse Description:
protein tyrosine phosphatase, non-receptor type 4 Gene [Source:MGI Symbol;Acc:MGI:1099792]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10967 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38744
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 |
---|---|---|---|---|---|
ENSDART00000000670 | Nonsense | 120 | 928 | 4 | 26 |
ENSDART00000078823 | Nonsense | 74 | 882 | 3 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 30022821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 29178767 |
GRCz11 | 9 | 28989513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGGGTGAAATTCTTTGTGAGTGACCCCAACAAACTTCAGGAAGAATA[C/A]ACACGGTGAGTTTGTCAATTTGGACTTTGCGTTTTTATTTGGTGTGAGAA
Long Flanking Sequence:
TCAATTATATTGATTGCTAAAGTAAAATCGAAGTTCAAGAGTTTGCTTTGTTTGTAACTTTAAAACAGTCAGTTTGTCTCTTTGTGTTGTAACTGCAGATAAGTACATCTCCACCTCTCCACAGAACAAAACACAAGACTATTGAATTATTGAGTGGCATTAGGTTGTGTTGGACTGTTGCCATGTTATTAAGGTTTTTCTTCCTCTCTTTATCCCTGTCTCTCTCTCTTTCTTTCTCTCCATCAATAATTTATAGAGGTGGCTGGATCCAAATAAACCCATAAGGAAGCAATTAAAAAGTAAGTAATTTTTATTGAAAGCACTGGACTGAGCTGTTGCTTGCCACCAGACGTTAATTATTCTTCCTTTTGCTTTATATTTGCACATCTTTGTATCTACATTCATGTTGTGCTGACTTAAATGACAGGGGGCTCCCCACATCATCTGAACTTCCGGGTGAAATTCTTTGTGAGTGACCCCAACAAACTTCAGGAAGAATA[C/A]ACACGGTGAGTTTGTCAATTTGGACTTTGCGTTTTTATTTGGTGTGAGAAGTCAAATTGTGGTCGCACTTTAAATTTGGGGACTCATGCAAAACCTCATCTCGCATATCCAGACTGAATAACTGACCTCATCACAGATTTTATTTGGTACCAACCTAGTGGACGTTTGACTGGCATGAAATCAACCAGGAACAGTTTGTTTTGTTCAGAGTATTGTTTAGGGACATGTAAATATCCTTACAATAACAGACCAGCATGCGGCCATAAAAGACTCTATGAACTTTCTGCTTTGTTTAACGGTTCCTTTATGGTGCTTTTTCACTGCATGGTATACCCTAAATCGGTTCAGCTCACTTTTTGCGCCTTTTGCATTGCATCCCCTTCCAAATAACTGGCACTTTTGTTAGGTTACAAGGAAGCTGTACCATTACCAAAACAGCAAACTAATCACTGATTGAAATTTGCTGATCACTGATTGCTCCAAATCATCACTACCAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10967
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 |
---|---|---|---|---|---|
ENSDART00000000670 | Essential Splice Site | 711 | 928 | 21 | 26 |
ENSDART00000078823 | Essential Splice Site | 665 | 882 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 29982134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 29138080 |
GRCz11 | 9 | 28948826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTCATTCTGAAAGGCACAGAAGACTACATCAATGCAAATTACATCAAC[G/A]TGAGTGACTCATAATTATTCTATTATCTCACTAAAATCTCAAGTACCCCA
Long Flanking Sequence:
ATATTTGTGTTCTGGTAGTGCAAGTAAACGTCTTTTTGCAGTATTTGCACAGTTTGTGTTTTTTTTGGTGCACCTCACCGCTGTCATTTTACTCTTGCTTGCCGCTGATGTGCAGGTAAAGCGAGTTTGCACACTGTTCAAAAATATATCACGATTTGTGAGGGAAATGTTTAATGTGTGACATTTCTGAAATGATACGAAAGGTCAGACTTAAAGATTTAGTCTATTATTTAACATTACTTTTTTTCTTTTCTTTTAAAAGCAATTGTATCGTAAAAGGCCTGGAATGACAATGTCATGTGCCAAATTACCTCAGAATATTTCCAAAAACCGCTACAGAGACATCTCACCTTGTGAGTATACCTGCACTCCTTTCCTTTGTACTAATAACAAGTGTCATTGATAAAACATGAGTCTGTTTTGTTGTTTTTCTGTCAGATGATGCAACTCGAGTCATTCTGAAAGGCACAGAAGACTACATCAATGCAAATTACATCAAC[G/A]TGAGTGACTCATAATTATTCTATTATCTCACTAAAATCTCAAGTACCCCAGGAAAGATGCGCTGTGATAAATAGCCTTTCATAATGTGTTCTGTCATGTTCACAGATGGAAATCCCTGCCTGCAGTCTCATAAACCGCTATATCGCCTGCCAGGGGCCTCTGCCCAACACGTGCTCTGATTTTTGGCAGATGACGTGGGAGCAGGGCTCTTCTATGGTAGTCATGCTTACTACTCAGGTTGAGCGAGGACGTGTATGTATGCCTTTTGACCTTTGAGGATTATGTGATGGTCTTGTTGTTTGCTTTTCGAGCTTTCATAACTCATTTACTTTTTACTGCAGGTCAAGTGCCATCAGTACTGGCCGAACCCCTCAGGTAGCGCTACATACGGCGGCTTTCAGATTTCCTGCCAGACTGAAGAGGGAAACTCTGCTTTCTTGGTTCGGGAAATAACACTTACTCACATTGAGGTGAGCTTATCACAGACTTAGTCATTTTAT
Associated Phenotype:
Not determined