ZMP
papss1
Ensembl ID:
ZFIN ID:
Description:
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 [Source:RefSeq peptide;Acc:NP_0011221
Human Orthologue:
PAPSS1
Human Description:
3'-phosphoadenosine 5'-phosphosulfate synthase 1 [Source:HGNC Symbol;Acc:8603]
Mouse Orthologue:
Papss1
Mouse Description:
3'-phosphoadenosine 5'-phosphosulfate synthase 1 Gene [Source:MGI Symbol;Acc:MGI:1330587]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32765 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19587 | Essential Splice Site | Available for shipment | Available now |
| sa39687 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19586 | Essential Splice Site | Available for shipment | Available now |
| sa39686 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32765
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024984 | None | None | 624 | None | 12 |
| ENSDART00000123274 | Essential Splice Site | 32 | 815 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 51038660)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49887751 |
| GRCz11 | 1 | 50531577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTGCAATATTATATTCTAAAGTCTTTTGTATTAATTTTTGTTTTTTC[A/G]GGCAGAAATATTAAGTGCCGTCAAGGTCAACACAGTAAGTACATTCTAAA
Long Flanking Sequence:
AACTCCACACAGAAATGCCAACTGAGCCGAGGTTCGAACCAGCAACACAGCGCCCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCTTCACCCCCACTTGTGAATGAGTTCATTAAAAGTTTTATACACATTCACAATTCTATTAGTTAATTTATTACTTAACCAATGGGCCTTGCTTTGATAACTTAATGCTTAATTTTATAGCAAGTCTACAATTTTGCGCTAAACGTAGATGCCAAAGTTGTAAATAAATACACTCAGAGAAATGTTTTTTACTGCTTGTTCAAACTACTTATTTAAAATAAGCAGAAACAACACAATTCTTGATATTTTTTTGGGCAACTTAATTGTTTTATGCTCAATCAACTTAAATGCATTACGTTAACTTAATCGATTTGTATTGGGATGACATAAATTAATTTTGTTGAACCCTGAATTTTTTGAAAGTACTTTGCAATATTATATTCTAAAGTCTTTTGTATTAATTTTTGTTTTTTC[A/G]GGCAGAAATATTAAGTGCCGTCAAGGTCAACACAGTAAGTACATTCTAAAATGTCATGCTAAATACTCTCATTATAATACATAAAAAATTTTATAAAAGTCCTACATCAGGCATGTCCTCAAGGTTTGTCTTCCTGGATTCAGATCTTCAGAAGCGTTCGGGTGAAGATGTTGTGATTCTGGAAGGTTATGAAGTGACTCCGCAGGATCAGGAGCGAGGTGTTGGGTGTGAGGAGCATGAAACCGCCGGTCTTTTCCCAACTCCTCCTTCTGAAGCAATCAGAGGCAATCAAGTACCACAAATGCCAGCCCCAACCTCTAAAATACCACCCAAAAAGCAGTTGTGTTGGATGTACTACGGTACGCCTGTGAGGCTGTATTTACCAATGAGGAATCTGCCCAATTCTCAAGGCAATAATAAACCGTATACGGGAGGAATGAGTGGAAACACTCAGGCGAGGGTGGTGTGTGGAAAACCTATGGGGAACTTCCCTAAGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19587
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 |
|---|---|---|---|---|---|
| ENSDART00000024984 | Essential Splice Site | 138 | 624 | 4 | 12 |
| ENSDART00000123274 | Essential Splice Site | 329 | 815 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 51031112)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49880203 |
| GRCz11 | 1 | 50524029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGATTTATATGGTCAAATTTGGTAACAGTTCTTTGCTATATTTCTCCA[G/A]GACCGCATGAATGCAAGAAAGATCCATGAAGCTGCTGGCCTGCCGTTCTT
Long Flanking Sequence:
CAGGGTGAGAAACATCATACTGAACACAGTGCATGTGTGTGTGACGTATTATATACAGCCGCAAGTATATTTTTCTTCAACCTCTGTTTAATGGAAAGATTTTTTTTAACACATTTCTAAATAATAGTTTAAATAACTCCTTTCTAAAAACTGATTTATTTTATCTTTGTCATGTTGACAGTAAATAATATTTGACTAGATATTTTTCAAGACACTAATATTCAGCTTAAACGGATATTTAAAGGCTTAACTAGGTTAATTAGGCAAGTTAGGGTAATTAGGTAAATCATTGTATAATGATGGTTTGTTCTGTAGTTAATTGGAAAAAGTACTGCTTAAGGGGCCTAATAATATTGGACCATTTAATATCTTAAAATGGTTTAAAAGAAAAAAAATTATTTTATTCTAGCCGAAATAAAACAAGCAATTTTAATATACAGTAAGACACGGTATGATTTATATGGTCAAATTTGGTAACAGTTCTTTGCTATATTTCTCCA[G/A]GACCGCATGAATGCAAGAAAGATCCATGAAGCTGCTGGCCTGCCGTTCTTTGAGGTGTTTGTAGATGCTCCTCTGGATGTGTGTGAGCAGAGAGATGTGAAGGGACTCTACAAGAGGGCCAGAGCTGGAGAAATCAGAGGTGAGGCCATCGGGAGACGTGCAAATACAATAAATGTGAACTGTTTTTTTTTTTTTTTTTTTGTAGTGTGTACAGCATAACTTAACAAAATACACGCTATCTATCCATCCATCTATCCATCTATCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCCGTCCGTCCGTCCGTTCGTCCATCTTTGGATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39687
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024984 | Essential Splice Site | 184 | 624 | 5 | 12 |
| ENSDART00000123274 | Essential Splice Site | 375 | 815 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 51028974)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49878065 |
| GRCz11 | 1 | 50521891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGTAAATGTAGTAGTTTTAACAGTAGCTGGTTACTTCCATTGTCCTCA[G/T]GGTTCACAGGGATAGACTCCGAGTATGAAAAACCTGAGGCTCCTGAACTG
Long Flanking Sequence:
ACGTGTGGTGATGAGAGTGATTGTGGTTTACACTGTTGCAGGAAATATCTTTATTCTTGTTCACTTATTAACTGATACATGAGCAGCACATTGTTCTGCAGTTACATAGTTCTGCACTGTTTTCAGGACAATTCTTTCATCATGCAATTCATGAATTTATGGTGACCCAATTAGGGCTGCATGATACTGGAAAAGTATGCAACGTTGTGTTGAGGTAATGATATTTGTTACGATATAATATTTCCCTAGAAAATTGCTATTAAATTAACTAAATTTTTCAGATCTACTTAATTCTAATTCAGACTAAACATTGTCCAACATTTGTTTTTTAATACACTATGAATGTGTAAACACTCAAGCAGATATTCTGACTCTGATTGGCTGTTGTCATTTTCCTCTCATCTCCACTCCCGCCACTAGTGTTTATTTTTTACCTTTAGGCTAAATAGTGAAGTAAATGTAGTAGTTTTAACAGTAGCTGGTTACTTCCATTGTCCTCA[G/T]GGTTCACAGGGATAGACTCCGAGTATGAAAAACCTGAGGCTCCTGAACTGGTGCTAAAGACCGACTCCTGCAGCGTGAACGAGTGCATCCAGCAGCTTCTAGACCTCCTGCAGGAGAGGGTAAATAACTGCACATTCATGTCAGACTTACTTATCATCCTCATTTGTTAGTTTTAAATTGTTAAACTCCAATAATGTCTAATTTCTGAACATTTGCAGGATATTGTGCCTGTGGATGCGTCCTATGAGGTGAAAGAGCTCTATGTGGCCGAGAACAAGCTGGATTTGGCCAAGGCCGATGCAGAGACTCTTCCAGCAGTGGAGATCACTAAAGTATGTTCACTTCTCATGTGCCACTCACAATTGAAGTCAAAATTATTCAACCTCCTGCCAATTTATTAATTTCTTTATATTTCCCAAACTATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTTCCATAATATTTTTTCTTTTGGAGAAAGTCTTATTTTTTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19586
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024984 | Essential Splice Site | 299 | 624 | 7 | 12 |
| ENSDART00000123274 | Essential Splice Site | 490 | 815 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 51026999)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49876090 |
| GRCz11 | 1 | 50519916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAAAGAGAGTTCCTGCAGTGTCTGCACTTCAACTGTCTGCTCGATGG[T/A]GAGAACTTGCTTTCATTTGAACGTTTTAGTCCTGCATATAATCTGGCACA
Long Flanking Sequence:
CCTGGAAATCCTTCCTTAGCTTGGTCAACCACAAACATCTTTAAATCCTCAAGCATTTTTCTCTTAGGCTTGATTTTGCAATAACTTTTGGCAGTCTACAAGACTCTAAAAGTTTATTTTTTTCTAGTTCAACCGATTGGTACAGCCCAAAACATGACAATAGTTGATAATTTCCATAATCAAAATATGCATGTTTCATTTGCTTCAGTGGTTTGTTTACATTCTGAGCCTCCAATATGGCTGATTGAAGACATGTCCTCTATAGATCGTTAGCAAATTAATTTTAGCATATTAACTCCTTACAGAACTAGCTTGAAGCAATGTCTGGTCTGTATTAGTGGAAAATGTACATTAAAAGCTAGCACCCATGTTGTGTTGATGGTTTAGGTGGACATGCAGTGGGTTCAGGTGCTTGCTGAAGGCTGGGCGACTCCTCTGAACGGCTTCATGAGGGAAAGAGAGTTCCTGCAGTGTCTGCACTTCAACTGTCTGCTCGATGG[T/A]GAGAACTTGCTTTCATTTGAACGTTTTAGTCCTGCATATAATCTGGCACAGGCGTTTTATATGGTTGTGCTGTCTCAGTCCAACGCTAGGTGGCGCCATCAGGCAGAGCAACGCCGTTTTTCCAACCGACCGCTGTTTCATTCAGAAGTGCTTTTAGATTTCCCGTTCGCAGCATTCACCCCGTTCAGCTTTTTTTGCTTCATCTTTTCTTTTAACTGACAAATAGAGTGAAAACACTTTCTTAGAAATGTGTTTTCTGTCAAATATGAAAAATATAGGTACCTGTTCAGGCCCTTAAAGGCATAGTTCACCTGAAAGCAAGTATAATTTATTAATCTATATATAATTTCACATTTAAAAGACTTTGGTTTGTTGTTGGATCTTAGATTTTGTATATCAGCACTTTTAGCAGAGGAACTGAAACTTCTCTGGGTTATTAATGTGTGTTTGAGGATTAACCCCCAAGTCTTATCGGTTTTGAATCAATATGAATGTGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39686
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 |
|---|---|---|---|---|---|
| ENSDART00000024984 | Nonsense | 419 | 624 | 10 | 12 |
| ENSDART00000123274 | Nonsense | 610 | 815 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 51009949)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49859040 |
| GRCz11 | 1 | 50502866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTATACAGTTAATTAGCTGTTCTTATTTTTAGATGCCGTCTTTGCCTTT[C/T]AACTGCGAAATCCGGTGCATAATGGCCACGCACTGCTCATGCAGGATACA
Long Flanking Sequence:
GTTTGTCCAACATTGGTTTTTGTTGCAGATGGTGATGGAGAGTGGTGATTGGCTGGTTGGAGGTGATCTCCAGGTGCTGGATCGTATCTACTGGAATGACGGGCTGGACAGTTACAGGCTTACACCAACCGAACTCAAGCAGAAGTTTAAAGAGATGAACGCAGGTATGCAACTACACTAAGGAGTCACTTTAACTTAGTTATGCCTAGTCTGTTGATTGTAATTAGCAGTATTCTCTTCTAACTGTTGCAGTCAACATAAAAACATGGATTATCTTTAAATGACTGCATTAGTTTTAATGCGAACTACTATAATAAGTCAATATAGAGGTTGTTTTTTATTGCTATAAGGAGGTCTGGTCTCATGCACTCCTGCAGATTTTAGCTCCAACCCCAACCAAACACACCTGGGCTGGTTAATCAAGCTCTTAGATCAAGTTTGAGAACCACTGCTATACAGTTAATTAGCTGTTCTTATTTTTAGATGCCGTCTTTGCCTTT[C/T]AACTGCGAAATCCGGTGCATAATGGCCACGCACTGCTCATGCAGGATACACAGCGGCGTCTAATTGAACGTGGCTACCGCCGACCCGTTCTTCTGCTTCACCCGCTGGGCGGATGGACCAAAGATGATGATGTGCCATTGGCCTGGCGCATGAAACAGCATGCAGCCGTGCTGGAGGAGGGTCTACTTGATCCCAACTCCACCATAGTTGCCATTTTCCCATCACCAATGATGTACGCCGGCCCCACAGAAGTAAGTGCGGAATGCAAAAAGACCTAGAATAGACACCGGAGGTTTCCCATTATAAGTAATAATGTTTTATCATTAGAATTATTAGCTATTTATTATATCTATTTTTTGTTTTCATACTTTAATTGGTTACTCTTTATCATGTACTAATCTATAAACAGTTTTATGGTCAGTAGCCCAATTTTTTTTTTTGCTCATTTAAAGTCTCGCCTACTTGTTTACTTACATGCTGCTTGACATGTGCAATGTTTC
Associated Phenotype:
Not determined