ZMP
spns3
Ensembl ID:
ZFIN ID:
Description:
Protein spinster homolog 3 [Source:UniProtKB/Swiss-Prot;Acc:A2CER7]
Human Orthologue:
SPNS3
Human Description:
spinster homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:28433]
Mouse Orthologue:
Spns3
Mouse Description:
spinster homolog 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1924827]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9844 | Nonsense | Available for shipment | Available now |
| sa18804 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40468 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40467 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9844
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051392 | Nonsense | 135 | 500 | 3 | 12 |
| ENSDART00000127787 | Nonsense | 135 | 498 | 3 | 12 |
| ENSDART00000051392 | Nonsense | 135 | 500 | 3 | 12 |
| ENSDART00000127787 | Nonsense | 135 | 498 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 32612753)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30373583 |
| GRCz11 | 5 | 30973736 |
KASP Assay ID:
2259-5995.1 (used for ordering genotyping assays)
KASP Sequence:
TCGTTGGGCTGGTTATGTGGATCGTCACAACACTGGSAAGCTCTTTCGTC[A/T]GAAAATCGGTACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGAT
Long Flanking Sequence:
TATACTATCCTATCCTATCCTAAAAATGTTTCTATGTTTCCTATGAATATATAAAAAATGAATGAATGTATTGAATTCATTGAATTAACGAATAAATAAATAAACAGGCTAATTGTTTTTCAATCAGATTCATTTCTAAAGGCTATGTGATTCTGTAGATTGGGGAAAATTTAGTTTTAAATTCAATTGATATATTTATGTATATTTTAAAATCTGTTAAAAGAAATCACTTATTTTAAAGCGTTTATAATAGTTCACAGCATTAATCTTGATCCTGACCAACATAAAACATGTCTTAAAAAATCATATTGATACTAAACATTTCAGAAGTAGAGTATCTTTGCCGTCCACCTTGCAATAACATATTTACAGTTTTTATCTGCAGCTTCATGTTCTTGGCACCAGTGTTCGGTTACCTTGGAGATCGCTATGATAGGAAGCTTATTATGATCGTTGGGCTGGTTATGTGGATCGTCACAACACTGGGAAGCTCTTTCGTC[A/T]GAAAATCGGTACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGATTTATATTTCACACCTACACCTTTAACTATACTGGATTTTTTTTATGGAGTTACATTTTTTAAGAGCACAATTTAAAGTCTTAATTCTCACCACAGCACTTCTGGGTTCTGGTTGCGACAAGGGCTTTGGTCGGGACAGGAGAGGCCAGTTACTCCACCATTGCTCCTACTATCATTGGTGACCTGTTCGCTGGCTCCAAGAGAACTCTTATGATCTCCTTCTTCTACATCTTCATACCAGTTGGAAGGTGAAAACCTCACTGCAAAATTAAATAAAAAGAATTGATTGCTGTCTACATCGATAGCCCAGTGGTTAGTCTTGTCATCAATCCCAGTTGTAAAGGCAACAATGAATAACTTAACTTCTTGTTGATCATTTGGACACTGCTTTTAGATTCTAAATGAAACTGTATAAAAATCCTCTATATCACAAATGCATTCCACAGCCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18804
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051392 | Nonsense | 135 | 500 | 3 | 12 |
| ENSDART00000127787 | Nonsense | 135 | 498 | 3 | 12 |
| ENSDART00000051392 | Nonsense | 135 | 500 | 3 | 12 |
| ENSDART00000127787 | Nonsense | 135 | 498 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 32612753)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30373583 |
| GRCz11 | 5 | 30973736 |
KASP Assay ID:
2259-5995.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTTGGGCTGGTTATGTGGATCGTCACAACACTGGGAAGCTCTTTCGTC[A/T]GAAAATCGGTACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGAT
Long Flanking Sequence:
TATACTATCCTATCCTATCCTAAAAATGTTTCTATGTTTCCTATGAATATATAAAAAATGAATGAATGTATTGAATTCATTGAATTAACGAATAAATAAATAAACAGGCTAATTGTTTTTCAATCAGATTCATTTCTAAAGGCTATGTGATTCTGTAGATTGGGGAAAATTTAGTTTTAAATTCAATTGATATATTTATGTATATTTTAAAATCTGTTAAAAGAAATCACTTATTTTAAAGCGTTTATAATAGTTCACAGCATTAATCTTGATCCTGACCAACATAAAACATGTCTTAAAAAATCATATTGATACTAAACATTTCAGAAGTAGAGTATCTTTGCCGTCCACCTTGCAATAACATATTTACAGTTTTTATCTGCAGCTTCATGTTCTTGGCACCAGTGTTCGGTTACCTTGGAGATCGCTATGATAGGAAGCTTATTATGATCGTTGGGCTGGTTATGTGGATCGTCACAACACTGGGAAGCTCTTTCGTC[A/T]GAAAATCGGTACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGATTTATATTTCACACCTACACCTTTAACTATACTGGATTTTTTTTATGGAGTTACATTTTTTAAGAGCACAATTTAAAGTCTTAATTCTCACCACAGCACTTCTGGGTTCTGGTTGCGACAAGGGCTTTGGTCGGGACAGGAGAGGCCAGTTACTCCACCATTGCTCCTACTATCATTGGTGACCTGTTCGCTGGCTCCAAGAGAACTCTTATGATCTCCTTCTTCTACATCTTCATACCAGTTGGAAGGTGAAAACCTCACTGCAAAATTAAATAAAAAGAATTGATTGCTGTCTACATCGATAGCCCAGTGGTTAGTCTTGTCATCAATCCCAGTTGTAAAGGCAACAATGAATAACTTAACTTCTTGTTGATCATTTGGACACTGCTTTTAGATTCTAAATGAAACTGTATAAAAATCCTCTATATCACAAATGCATTCCACAGCCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40468
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 |
|---|---|---|---|---|---|
| ENSDART00000051392 | Essential Splice Site | 137 | 500 | 3 | 12 |
| ENSDART00000127787 | Essential Splice Site | 137 | 498 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 32612744)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30373574 |
| GRCz11 | 5 | 30973727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTATGTGGATCGTCACAACACTGGGAAGCTCTTTCGTCAGAAAATCG[G/A]TACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGATTTATATTTC
Long Flanking Sequence:
CTATCCTATCCTAAAAATGTTTCTATGTTTCCTATGAATATATAAAAAATGAATGAATGTATTGAATTCATTGAATTAACGAATAAATAAATAAACAGGCTAATTGTTTTTCAATCAGATTCATTTCTAAAGGCTATGTGATTCTGTAGATTGGGGAAAATTTAGTTTTAAATTCAATTGATATATTTATGTATATTTTAAAATCTGTTAAAAGAAATCACTTATTTTAAAGCGTTTATAATAGTTCACAGCATTAATCTTGATCCTGACCAACATAAAACATGTCTTAAAAAATCATATTGATACTAAACATTTCAGAAGTAGAGTATCTTTGCCGTCCACCTTGCAATAACATATTTACAGTTTTTATCTGCAGCTTCATGTTCTTGGCACCAGTGTTCGGTTACCTTGGAGATCGCTATGATAGGAAGCTTATTATGATCGTTGGGCTGGTTATGTGGATCGTCACAACACTGGGAAGCTCTTTCGTCAGAAAATCG[G/A]TACAGTACAAAGTCTCACAGCTTCGATAACGTGTATATGATTTATATTTCACACCTACACCTTTAACTATACTGGATTTTTTTTATGGAGTTACATTTTTTAAGAGCACAATTTAAAGTCTTAATTCTCACCACAGCACTTCTGGGTTCTGGTTGCGACAAGGGCTTTGGTCGGGACAGGAGAGGCCAGTTACTCCACCATTGCTCCTACTATCATTGGTGACCTGTTCGCTGGCTCCAAGAGAACTCTTATGATCTCCTTCTTCTACATCTTCATACCAGTTGGAAGGTGAAAACCTCACTGCAAAATTAAATAAAAAGAATTGATTGCTGTCTACATCGATAGCCCAGTGGTTAGTCTTGTCATCAATCCCAGTTGTAAAGGCAACAATGAATAACTTAACTTCTTGTTGATCATTTGGACACTGCTTTTAGATTCTAAATGAAACTGTATAAAAATCCTCTATATCACAAATGCATTCCACAGCCGGGTCCAGTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40467
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, Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051392 | Essential Splice Site | 308 | 500 | 8 | 12 |
| ENSDART00000127787 | Splice Site | None | 498 | None | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 32604969)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30365799 |
| GRCz11 | 5 | 30965952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGTGGGGCTGAAATTGAATAACATCACATTGTTTCTTCTTTCTTTCA[T/C]GCGTAAGCTACATTTTTGGAGCAATCACAGTGGTGACAGGGGTTGTGGGG
Long Flanking Sequence:
TTGTGTTGTAACAATACAAATGTATGGTGATAAGAGTAGAAATTAATGCAACAACAAAACAAAATGGTAACACTAGTTTAGGTCACAATTCACACTAAACTAAAGTGATACCTAATTTACTGGCTTATTACCTGCCTATTATTAAGTTATTAACTGTCCATTAGTAGTTATAAAGTATGATCTTATTCTGCTTCCCTAATTAAAACCTAAACCCAACTTCTACCTAACTAATTAAAAAACAGCTAACCAGTAATTTATTATGCTAGTAGTGTTAGGTAATGGTTTATTAATACTGTAAGTGACCTAAACTAAAATGCTACCAAAAAATGTGATACAATCATATAGCTACCATTTGTACCTCCAAACTGTGCTGATCATCTTACAGAGAGAGTATTGTTCACTTTTTCTAGTCCAACTGGTCTAGTAGGGCCTGTGAGGAACAAAACACAGAGAAGTGGGGCTGAAATTGAATAACATCACATTGTTTCTTCTTTCTTTCA[T/C]GCGTAAGCTACATTTTTGGAGCAATCACAGTGGTGACAGGGGTTGTGGGGGTGTTTCTGGGCACCTGCATTTCCAAGAAGCTGAGAGACCGAGTGCCGAACGCAGACCCGCTCATCTGTGCCGTAGGAATGCTCAGTTCCTCACCTTGCTTCTTCATTGCTATAGTCCTGGCCTCCACCAGCATCCCGGCCACTTATGTAAGAACAGTTCAGCTATGCTGCTGGATTATTCTATGGCATTCAGAATTTCTGTTGATATTAAGGGAGTAATTCACCCAAAAAGAAACTTGTTTTCTTTTTTTTTTGCAAAGTCACCGAGCTCAATAACAATTTTAGACTCCAGTGACCAAAATATGACCTTTCCTGTAGAAAGTGATTTATTAGATAACATAATTGTAATTTTTGGTAAGCTATTCATTTAAAGATATAGATTATTTTTAACTAACACAATTGGGTTTTCAATGTTTTCGATGACATGGGCATCTATATAATTTGTTATGT
Associated Phenotype:
Not determined