ZMP
si:ch211-251f6.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
PSTPIP2
Human Description:
proline-serine-threonine phosphatase interacting protein 2 [Source:HGNC Symbol;Acc:9581]
Mouse Orthologue:
Pstpip2
Mouse Description:
proline-serine-threonine phosphatase-interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1335088]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18976 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6160 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21656 | Essential Splice Site | Available for shipment | Available now |
| sa21655 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18976
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 |
|---|---|---|---|---|---|
| ENSDART00000075474 | Essential Splice Site | 117 | 206 | 5 | 8 |
| ENSDART00000138875 | Essential Splice Site | 129 | 198 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 7135475)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 8148275 |
| GRCz11 | 10 | 8106975 |
KASP Assay ID:
2261-7167.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAAAATTAGAAGACTTCAGAGAGAAACAGAAAGAGGCCCGGAAAAAGG[T/C]AAGAGCATTTCATACCTTTTTAATTGATTTAAAGTGTGTTATTTGTACTT
Long Flanking Sequence:
ACTGCAAGCATTTAAAGGGATAGTTCACCCAAAAATGAAAACTCTGTCATCATTTACTGTTTTTTAGACGTGTATGCATTTCATTTTTCTGTTGAACCTCAAATAATAAATGATAAATAATAAATTCTGTTGAACCTCAAATGATAAATGTTGGAAAAAACAGCCATTGGCTTCCATTGTGTTTATGTGTTCCTACTATGGATTTCAATGGCTGCCTTTCATAAACATTCTCCAGAATATTTTGTTTTGTGTTCAACAGAAGAAAGAAATGTATGAAAATGTAGAACCACTCGAGTGATTAAATGATGAGGAAACGTTTATTTTTGGATGTTAATGAATAATTGCAGTTTATTGTTCTGTTGCATTCCTGTAATTTTAATTTACATGTTTAGAAACCGAAAACATGAGTTTATCTCATCTGCATTTGGCCCAAACTATGAGGGAGGAAGCCAAAAAATTAGAAGACTTCAGAGAGAAACAGAAAGAGGCCCGGAAAAAGG[T/C]AAGAGCATTTCATACCTTTTTAATTGATTTAAAGTGTGTTATTTGTACTTCAGCAAATGGAAAGGCTTTTTATATCAGAAGAATATTGTCTGTTAGCAGTCTTGTTCATTAAATAGCCACACTTTTGGTCTTACTTGAAAGCTTGTGATTAAAACAGGAAATTGTTGGTAACATAGGCTCATTTTGAAAACGTACACCTCTATATATTTCTGGAGAGTGTGAATCATGTAGCTCGAGCTATGTATGACGTCTTAAAAGCGAACGCTATGGGGTGGTATGATGCTGCCTGTTTCTTCTTGCGCTACCAGCTGCCCACTTACCTCCGTGTGGACGGCATTTCATTTCTGGTAATGGTTTATTCAGTGGCTCGCCACGTACGTCGGCAGACTTAAGATGCAGAGAGGAGTTGACCGCAATGACAGGGTTCGAGTCTGGTGCAGATCAGTTCCAAAAAGCAGGTAAAACAAAAAATAAAATAGAACGTGGTAAGCTCTGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6160
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075474 | Nonsense | 145 | 206 | 7 | 8 |
| ENSDART00000138875 | Nonsense | 157 | 198 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 7155614)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 8168414 |
| GRCz11 | 10 | 8127114 |
KASP Assay ID:
554-4752.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTTTAAAATGTCAGTCATTGTCTTTTAAGGCAAAGAAGAGCTACGAT[C/T]AAAAATGCAGAGACAAAGAGGAAACAGAGCAGAACATGAACAGAAGTGCC
Long Flanking Sequence:
ATCATATTTTTTCTTATTTGTTTTATTATGTCTAGAATAAAAGCAGTTTTGAATTGTTTTCAACACCATTTTAAAGTCAATATTATTAGCCCCTTTAAGCTAATTTTATTTTGATAGTCTACAAAACAAACCATTGTTATAACTTGCCTAATTACCCTGGCCTGCCTAACTAACCTAATTAACCTAGTTAAACCTTTAAATGTCACTTTAAGCTGTACAGAAGTGTCTTGAAAAATATCTAGAAAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTGCTTTTCTCCATTAAACAGATATTGGGGAAAAAAATAAACAGGGAGACTAATAATTCAGGGGGACTAATAATTCTGACTTCAACTACTGTATATATACGATTTCATTTAGGTGCTTATACAATTTTGATTGTCGTATTACAGCTAAGATGCGATGAACAGCACTTTTTAAAATGTCAGTCATTGTCTTTTAAGGCAAAGAAGAGCTACGAT[C/T]AAAAATGCAGAGACAAAGAGGAAACAGAGCAGAACATGAACAGAAGTGCCACCACTTGCAGTGCCAAGCAGCAAGAAAAGGTACATAAATATAACTGTGAGAAAGAATCATGCTTTCTTTTAAATTTGCTTTGCTTTAGTGCATCGTTTTTATTTTTGATGGCTCGCATCTTGCTTTTACACACACTTTTTACAGTGTTTCGATGATTTATTGATATTACAGTTAAAAGTAATTTCACTTCCTAATCTGCAATTGCCTATCTGGATATCACACTAACTGTACACACACACACAAAAAATAAATAAATAAAATAAATAAATAAATATTATATTATATTTATAATATAAATTACTAATACTTTCCGTCTTAGACTTTACAGACCTGAAACTTGCCTATAGCACTTATTCATTGTTGCTCTTATAGTTGTGTAAGTTGCTTCCTTGTCATCATTTTTAAGTCGCTTTGGATAAAAGCGTCTACTAAATGACTAAATGTAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21656
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075474 | Essential Splice Site | 171 | 206 | 7 | 8 |
| ENSDART00000138875 | Essential Splice Site | 183 | 198 | 7 | 8 |
| ENSDART00000075474 | Essential Splice Site | 171 | 206 | 7 | 8 |
| ENSDART00000138875 | Essential Splice Site | 183 | 198 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 7155695)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 8168495 |
| GRCz11 | 10 | 8127195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACATGAACAGAAGTGCCACCACTTGCAGTGCCAAGCAGCAAGAAAAG[G/T]TACATAAATATAACTGTGAGAAAGAATCATGCTTTCTTTTAAATTTGCTT
Long Flanking Sequence:
ATTATTAGCCCCTTTAAGCTAATTTTATTTTGATAGTCTACAAAACAAACCATTGTTATAACTTGCCTAATTACCCTGGCCTGCCTAACTAACCTAATTAACCTAGTTAAACCTTTAAATGTCACTTTAAGCTGTACAGAAGTGTCTTGAAAAATATCTAGAAAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTGCTTTTCTCCATTAAACAGATATTGGGGAAAAAAATAAACAGGGAGACTAATAATTCAGGGGGACTAATAATTCTGACTTCAACTACTGTATATATACGATTTCATTTAGGTGCTTATACAATTTTGATTGTCGTATTACAGCTAAGATGCGATGAACAGCACTTTTTAAAATGTCAGTCATTGTCTTTTAAGGCAAAGAAGAGCTACGATCAAAAATGCAGAGACAAAGAGGAAACAGAGCAGAACATGAACAGAAGTGCCACCACTTGCAGTGCCAAGCAGCAAGAAAAG[G/T]TACATAAATATAACTGTGAGAAAGAATCATGCTTTCTTTTAAATTTGCTTTGCTTTAGTGCATCGTTTTTATTTTTGATGGCTCGCATCTTGCTTTTACACACACTTTTTACAGTGTTTCGATGATTTATTGATATTACAGTTAAAAGTAATTTCACTTCCTAATCTGCAATTGCCTATCTGGATATCACACTAACTGTACACACACACACAAAAAATAAATAAATAAAATAAATAAATAAATATTATATTATATTTATAATATAAATTACTAATACTTTCCGTCTTAGACTTTACAGACCTGAAACTTGCCTATAGCACTTATTCATTGTTGCTCTTATAGTTGTGTAAGTTGCTTCCTTGTCATCATTTTTAAGTCGCTTTGGATAAAAGCGTCTACTAAATGACTAAATGTAAATGTAAAAGTGAACCAACCTACGAAGTGACTCTAGCTGGTTACACCTAAAGTAATATTTTTTAAAAACTTAATTCATGACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21655
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 |
|---|---|---|---|---|---|
| ENSDART00000075474 | Essential Splice Site | 171 | 206 | 7 | 8 |
| ENSDART00000138875 | Essential Splice Site | 183 | 198 | 7 | 8 |
| ENSDART00000075474 | Essential Splice Site | 171 | 206 | 7 | 8 |
| ENSDART00000138875 | Essential Splice Site | 183 | 198 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 7155695)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 8168495 |
| GRCz11 | 10 | 8127195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACATGAACAGAAGTGCCACCACTTGCAGTGCCAAGCAGCAAGAAAAG[G/T]TACATAAATATAACTGTGAGAAAGAATCATGCTTTCTTTTAAATTTGCTT
Long Flanking Sequence:
ATTATTAGCCCCTTTAAGCTAATTTTATTTTGATAGTCTACAAAACAAACCATTGTTATAACTTGCCTAATTACCCTGGCCTGCCTAACTAACCTAATTAACCTAGTTAAACCTTTAAATGTCACTTTAAGCTGTACAGAAGTGTCTTGAAAAATATCTAGAAAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTGCTTTTCTCCATTAAACAGATATTGGGGAAAAAAATAAACAGGGAGACTAATAATTCAGGGGGACTAATAATTCTGACTTCAACTACTGTATATATACGATTTCATTTAGGTGCTTATACAATTTTGATTGTCGTATTACAGCTAAGATGCGATGAACAGCACTTTTTAAAATGTCAGTCATTGTCTTTTAAGGCAAAGAAGAGCTACGATCAAAAATGCAGAGACAAAGAGGAAACAGAGCAGAACATGAACAGAAGTGCCACCACTTGCAGTGCCAAGCAGCAAGAAAAG[G/A]TACATAAATATAACTGTGAGAAAGAATCATGCTTTCTTTTAAATTTGCTTTGCTTTAGTGCATCGTTTTTATTTTTGATGGCTCGCATCTTGCTTTTACACACACTTTTTACAGTGTTTCGATGATTTATTGATATTACAGTTAAAAGTAATTTCACTTCCTAATCTGCAATTGCCTATCTGGATATCACACTAACTGTACACACACACACAAAAAATAAATAAATAAAATAAATAAATAAATATTATATTATATTTATAATATAAATTACTAATACTTTCCGTCTTAGACTTTACAGACCTGAAACTTGCCTATAGCACTTATTCATTGTTGCTCTTATAGTTGTGTAAGTTGCTTCCTTGTCATCATTTTTAAGTCGCTTTGGATAAAAGCGTCTACTAAATGACTAAATGTAAATGTAAAAGTGAACCAACCTACGAAGTGACTCTAGCTGGTTACACCTAAAGTAATATTTTTTAAAAACTTAATTCATGACAAAA
Associated Phenotype:
Not determined