ZMP
txndc9
Ensembl ID:
ZFIN ID:
Description:
thioredoxin domain-containing protein 9 [Source:RefSeq peptide;Acc:NP_956315]
Human Orthologue:
TXNDC9
Human Description:
thioredoxin domain containing 9 [Source:HGNC Symbol;Acc:24110]
Mouse Orthologue:
Txndc9
Mouse Description:
thioredoxin domain containing 9 Gene [Source:MGI Symbol;Acc:MGI:2138153]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13931 | Nonsense | Available for shipment | Available now |
| sa17131 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13931
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101991 | Nonsense | 71 | 226 | 2 | 4 |
| ENSDART00000136902 | Nonsense | 71 | 226 | 3 | 5 |
| ENSDART00000145431 | Nonsense | 71 | 101 | 2 | 2 |
| ENSDART00000146850 | Nonsense | 71 | 226 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 22854407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 22010193 |
| GRCz11 | 9 | 21821062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCTGTTTTATGCGTTTRTTCTTAGGAGTGGAWCTCTAAAGGGCATGGY[G/T]AATACAGAGAGATCCCAAGTGAGAAAGACTTCTTTCCAGAGGTGAAAGAA
Long Flanking Sequence:
AGGCTCTGGAGCAGCAGGTGCTTCAGTCAGCACGGATGGTGGAGGAGCAGCTGGATGCTGAGCTGGAGAAGCTGGAGCGCATGGATGAAGACGAGCTGGAGCTGCTGAAGGAGAGAAGACTCGAGGCCCTTAAGAAAGCTCAGAAACAGAAGCAGGTGACTTATGTGTGGTTTTGAATACATCTTTTAATGTTGCATCTAACAGTTATTCTGATAATCGATTCATTTGGTGAGTGTTTTCTTAGTTGAGCTGATGAAAATCCCTGTGTTATTAAAATGTACACACTGTAATGAAGTATAAAATGTAAACCTTTTATACAAATTTTCCTAATGTCCAAAAATGGTTAAATACACCCATTCTTAGGCTAAAGCCAGATGAGTGTATTAAGAGTTGTAAGTGTAAGAGTGACCTATATTAAGTGACATGTATATGTGTGATTAAACATTGTGAACTCTGTTTTATGCGTTTGTTCTTAGGAGTGGATCTCTAAAGGGCATGGT[G/T]AATACAGAGAGATCCCAAGTGAGAAAGACTTCTTTCCAGAGGTGAAAGAAAGCAAAAGTGTGGTCTGTCATTTCTACAGAGACTCCACCTTCAGGTATGTCAGGACACATTTGTTTTGCTTGACTGTCATATTATAAATCTGTAATTTTTTATGTTATTTTCCAAAGATGCAAGATTTTGGACAAGCACCTAGCTATTTTGGCTAAGAAGCATCTGGAAACGAAGTTCATCAAGCTGAATGTGGAGAAGGCTCCTTTCCTTACAGAGAGGCTGAGGATTAAAGTCATTCCAACATTGGCACTGGTGAAGGACGGCAAGACCAAAGATTATATTGTGGGTTTCAGCGATCTGGGCAACACCGATGAGTTTCCTACCGAAATGCTGGAGTGGAGACTGGGCTGTTCTGACATCATAAACTACAGGTCAGCGTAATATTGTAATATTGCAGATTAATGTTTAGAATATTTAACTTTTTCGTAATCTTTAATGAGCTTTTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17131
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 |
|---|---|---|---|---|---|
| ENSDART00000101991 | Essential Splice Site | 102 | 226 | 3 | 4 |
| ENSDART00000136902 | Essential Splice Site | 102 | 226 | 4 | 5 |
| ENSDART00000145431 | None | None | 101 | None | 2 |
| ENSDART00000146850 | Essential Splice Site | 102 | 226 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 22854574)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 22010360 |
| GRCz11 | 9 | 21821229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCWTGACTGTCATATTATAAATCWGTMATTTTTTATGTTATTTTYCAAA[G/T]ATGCAAGATTTTGGACAAGCACCTAGCTATTTTGGCTAAGAAGCATCTGG
Long Flanking Sequence:
TGGTTTTGAATACATCTTTTAATGTTGCATCTAACAGTTATTCTGATAATCGATTCATTTGGTGAGTGTTTTCTTAGTTGAGCTGATGAAAATCCCTGTGTTATTAAAATGTACACACTGTAATGAAGTATAAAATGTAAACCTTTTATACAAATTTTCCTAATGTCCAAAAATGGTTAAATACACCCATTCTTAGGCTAAAGCCAGATGAGTGTATTAAGAGTTGTAAGTGTAAGAGTGACCTATATTAAGTGACATGTATATGTGTGATTAAACATTGTGAACTCTGTTTTATGCGTTTGTTCTTAGGAGTGGATCTCTAAAGGGCATGGTGAATACAGAGAGATCCCAAGTGAGAAAGACTTCTTTCCAGAGGTGAAAGAAAGCAAAAGTGTGGTCTGTCATTTCTACAGAGACTCCACCTTCAGGTATGTCAGGACACATTTGTTTTGCTTGACTGTCATATTATAAATCTGTAATTTTTTATGTTATTTTCCAAA[G/T]ATGCAAGATTTTGGACAAGCACCTAGCTATTTTGGCTAAGAAGCATCTGGAAACGAAGTTCATCAAGCTGAATGTGGAGAAGGCTCCTTTCCTTACAGAGAGGCTGAGGATTAAAGTCATTCCAACATTGGCACTGGTGAAGGACGGCAAGACCAAAGATTATATTGTGGGTTTCAGCGATCTGGGCAACACCGATGAGTTTCCTACCGAAATGCTGGAGTGGAGACTGGGCTGTTCTGACATCATAAACTACAGGTCAGCGTAATATTGTAATATTGCAGATTAATGTTTAGAATATTTAACTTTTTCGTAATCTTTAATGAGCTTTTTCACACTTTTATAAATCATCACACACATCACACAAGTCATCACACAAGTTTCTATTAAATGCATCAGGGCATTGCATCTAGAATAGGTTTATTCCTGTACAATCTTCAGGTTTCCTCATAAATGAAAAATGGATGAAGGCATTTATATACACTGGCAATATTCCTTAGAGA
Associated Phenotype:
Not determined