ZMP
tpst1
Ensembl ID:
ZFIN ID:
Description:
Protein-tyrosine sulfotransferase 1 [Source:UniProtKB/Swiss-Prot;Acc:Q9PTE6]
Human Orthologue:
TPST1
Human Description:
tyrosylprotein sulfotransferase 1 [Source:HGNC Symbol;Acc:12020]
Mouse Orthologue:
Tpst1
Mouse Description:
protein-tyrosine sulfotransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1298231]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22625 | Nonsense | Available for shipment | Available now |
| sa9716 | Nonsense | Available for shipment | Available now |
| sa18619 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22625
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 |
|---|---|---|---|---|---|
| ENSDART00000114464 | Nonsense | 23 | 355 | 2 | 5 |
| ENSDART00000128534 | Nonsense | 23 | 366 | 1 | 4 |
| ENSDART00000136767 | None | None | 28 | None | 3 |
| ENSDART00000143610 | None | None | 11 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 19671405)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20774031 |
| GRCz11 | 15 | 20709763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAACTTACTAGTGGCCTGTCTGGTCATTAGCTCGGTCACAGTCTTCTA[T/A]CTGTGTCGCCATGCCATGGACTGCCATCACCGGATAGAGGAGCGCAGCCA
Long Flanking Sequence:
TTTTCTGGGAAATTTTCTTCCCCCTTGGTTTTGAGTGTTTTCCTCAAAAATTCTCAGTTTCGAGGGGTATTTAGCCCTTCCTCTTAGCCCTACACCTTCAAGCTAAAGAGAATTCCGACAGCCTTACCCTTTCATGTAAATGCATAAAACGAGAATTAGGGGTAAGGGGAAGGGCGAAGGGGTAGAATTGGGATTGGGTCTCTGTCATCGTATGAGGAGTCTGATCTGGTGTTTTCTGTGTTTCAGGCCTGATGGGTTCAGGGACTCAACGAGAGCTGCGTACAGCAGATCCCAGCCTCCACTCGCTCCGCTACGGCCAGTCCTGAGTGTCGGGCATTCACCTGAACACACTCTGCCCGACCACACCTTCCCTTTATCTGCTTCTTCCTTGTCTGTGTCCTCCTCTGGCTCCTCCACCCGCACATCCCCGAGATGATTGGCAAGTTAAAGCAGAACTTACTAGTGGCCTGTCTGGTCATTAGCTCGGTCACAGTCTTCTA[T/A]CTGTGTCGCCATGCCATGGACTGCCATCACCGGATAGAGGAGCGCAGCCAGCCCCTGTTGAGCAGCTTGCACGCCACCCTCCGAACAGGCCAAAACCTTAGCACCCCCTTTATCTACAATAAAGACATGCCTCTAATATTTATCGGCGGTGTCCCTCGCAGCGGCACCACTCTAATGAGGGCTATGCTGGACGCTCATCCCGATGTGCGCTGTGGGGAAGAAACCCGCGTAATCCCTCGGATTCTGGCTATGAAGCAGATGTGGAGCCGCTCTGGCCGGGAGAAAATGCGTCTAGATGAAGCCGGAGTGACAGATGAGGTCTTGGACTCGGCCATGCAAGCTTTCCTACTAGAAATCATCGTAAAACACGGGGAACCTGCCAACTACCTGTGTAATAAAGACCCGTTTGCTCTTAAATCACTCACTTATCTGGCCAAGATCTTCCCGCATGCTAAGTTCATTCTTATGGTTCGTGACGGCAGGGCCTCCGTCCACTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9716
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 |
|---|---|---|---|---|---|
| ENSDART00000114464 | Nonsense | 40 | 355 | 2 | 5 |
| ENSDART00000128534 | Nonsense | 40 | 366 | 1 | 4 |
| ENSDART00000136767 | None | None | 28 | None | 3 |
| ENSDART00000143610 | None | None | 11 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 19671356)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20773982 |
| GRCz11 | 15 | 20709714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTGTGTCGCCATGCCATGGACTGCCATCACCGGATAGAGGAGCGCAGC[C/T]AGCCCCTGTTGAGCAGCTTGCACGCCACCCTCCGAACAGGCCAAAACCTY
Long Flanking Sequence:
ATTCTCAGTTTCGAGGGGTATTTAGCCCTTCCTCTTAGCCCTACACCTTCAAGCTAAAGAGAATTCCGACAGCCTTACCCTTTCATGTAAATGCATAAAACGAGAATTAGGGGTAAGGGGAAGGGCGAAGGGGTAGAATTGGGATTGGGTCTCTGTCATCGTATGAGGAGTCTGATCTGGTGTTTTCTGTGTTTCAGGCCTGATGGGTTCAGGGACTCAACGAGAGCTGCGTACAGCAGATCCCAGCCTCCACTCGCTCCGCTACGGCCAGTCCTGAGTGTCGGGCATTCACCTGAACACACTCTGCCCGACCACACCTTCCCTTTATCTGCTTCTTCCTTGTCTGTGTCCTCCTCTGGCTCCTCCACCCGCACATCCCCGAGATGATTGGCAAGTTAAAGCAGAACTTACTAGTGGCCTGTCTGGTCATTAGCTCGGTCACAGTCTTCTATCTGTGTCGCCATGCCATGGACTGCCATCACCGGATAGAGGAGCGCAGC[C/T]AGCCCCTGTTGAGCAGCTTGCACGCCACCCTCCGAACAGGCCAAAACCTTAGCACCCCCTTTATCTACAATAAAGACATGCCTCTAATATTTATCGGCGGTGTCCCTCGCAGCGGCACCACTCTAATGAGGGCTATGCTGGACGCTCATCCCGATGTGCGCTGTGGGGAAGAAACCCGCGTAATCCCTCGGATTCTGGCTATGAAGCAGATGTGGAGCCGCTCTGGCCGGGAGAAAATGCGTCTAGATGAAGCCGGAGTGACAGATGAGGTCTTGGACTCGGCCATGCAAGCTTTCCTACTAGAAATCATCGTAAAACACGGGGAACCTGCCAACTACCTGTGTAATAAAGACCCGTTTGCTCTTAAATCACTCACTTATCTGGCCAAGATCTTCCCGCATGCTAAGTTCATTCTTATGGTTCGTGACGGCAGGGCCTCCGTCCACTCCATGATCTCCCGCAAGGTCACCATCGCTGGATTTGACTTGAGCAGCTACCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18619
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 |
|---|---|---|---|---|---|
| ENSDART00000114464 | Nonsense | 166 | 355 | 2 | 5 |
| ENSDART00000128534 | Nonsense | 166 | 366 | 1 | 4 |
| ENSDART00000136767 | None | None | 28 | None | 3 |
| ENSDART00000143610 | None | None | 11 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 19670976)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20773602 |
| GRCz11 | 15 | 20709334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAACTACCTGTGTAATAAAGACCCGTTTGCTCTTAAATCACTSACTTA[T/A]CTGGCCAAGATCTWCCCGCATGCTAAGTTCATTCTTATGRTKCGTGACGG
Long Flanking Sequence:
GAGATGATTGGCAAGTTAAAGCAGAACTTACTAGTGGCCTGTCTGGTCATTAGCTCGGTCACAGTCTTCTATCTGTGTCGCCATGCCATGGACTGCCATCACCGGATAGAGGAGCGCAGCCAGCCCCTGTTGAGCAGCTTGCACGCCACCCTCCGAACAGGCCAAAACCTTAGCACCCCCTTTATCTACAATAAAGACATGCCTCTAATATTTATCGGCGGTGTCCCTCGCAGCGGCACCACTCTAATGAGGGCTATGCTGGACGCTCATCCCGATGTGCGCTGTGGGGAAGAAACCCGCGTAATCCCTCGGATTCTGGCTATGAAGCAGATGTGGAGCCGCTCTGGCCGGGAGAAAATGCGTCTAGATGAAGCCGGAGTGACAGATGAGGTCTTGGACTCGGCCATGCAAGCTTTCCTACTAGAAATCATCGTAAAACACGGGGAACCTGCCAACTACCTGTGTAATAAAGACCCGTTTGCTCTTAAATCACTCACTTA[T/A]CTGGCCAAGATCTTCCCGCATGCTAAGTTCATTCTTATGGTTCGTGACGGCAGGGCCTCCGTCCACTCCATGATCTCCCGCAAGGTCACCATCGCTGGATTTGACTTGAGCAGCTACCGGGACTGTCTTACAAAGTGGAACCGGGCCATAGAGACAATGTACACTCAGTGCCTGGAGGCAGCAGACAAGTGTCTGCCCGTGCACTACGAACAGCTCGTCCTGCACCCTGAAAAGTGGATGAGGACGCTTCTCAGATTCCTCAACATTCCTTGGAACGATGCAGTTCTGCACCACGAGGAGCTCATCGGGAAAGCAGGCGGCGTTTCGCTCTCCAAGTAAGTAATGGGGATTTGTGGATTAGTCAATTAATCAATAATAATTAGCAGAACCACCACAGGGGTCAAATTCACCCTTAGGTGTTTTTCCAATGTACATAACACATTTTCCAAGCCTCACAGTCATTGATTCCCTGTTGTTAAAGTTTGTTTAGATTAAATCTG
Associated Phenotype:
Not determined