ZMP
si:ch211-39i19.6
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate tensin family [Source:UniProtKB/TrEMBL;Acc:B8JKC7]
Human Orthologue:
TNS3
Human Description:
tensin 3 [Source:HGNC Symbol;Acc:21616]
Mouse Orthologue:
Tns3
Mouse Description:
tensin 3 Gene [Source:MGI Symbol;Acc:MGI:2443012]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17437 | Essential Splice Site | Available for shipment | Available now |
| sa7478 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17437
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 |
|---|---|---|---|---|---|
| ENSDART00000044368 | Essential Splice Site | 130 | 1182 | 5 | 26 |
| ENSDART00000135390 | None | None | 79 | None | 3 |
| ENSDART00000136567 | None | None | 856 | None | 16 |
| ENSDART00000138361 | None | None | 177 | None | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 6667093)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 6572167 |
| GRCz11 | 20 | 6562114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYATACCATGTTTTGTGTTTCTGACCTGTTTCTTGTTCTYTTGTTTCTCA[G/A]TGAGGAACATGCGTTAGATCTGTATTCCATGAAGAGRTTCTGCAGTGATC
Long Flanking Sequence:
ATGCAAAAATTACATATTGTGATTAAAAATGCATACATAAAGCAATTTAGATTAAATTTATCTTGTAATGGAAGTTAAGACTTCCCCTTTTTTTCCACTATCATGACGTACATCCACTTAACATGGTCCTAAAAAAAAAAAAAAAAAGGAAGGCAGGGCATGATTTTGTCCTTGGATGAAGGCAGAGCTGAAATTAGACACCCCTGATATCCTTGCCCTAAAGGCATTCCATGTGACCAGGAAGTAAAGAAAAGTTGTCTCGAGAGGGCAGGCCTAAGGTATTTGATTTAAGTTTATGAGCTCAAATGGATTTTTACAAAATAATGAAGGGCACTGATACACAGTTTCTAACAAGAGCTACAATACAGACATACAAATCAAAAGGGCACATTTTGATTTTATGGTGACTTAATTGTTTATTGATTTATACAGATTAAATGATCGTATTTGGTATACCATGTTTTGTGTTTCTGACCTGTTTCTTGTTCTCTTGTTTCTCA[G/A]TGAGGAACATGCGTTAGATCTGTATTCCATGAAGAGATTCTGCAGTGATCAAATGGTTAACCTCCTGACTCCATCTCAGAAAAGGCAAGGCTCAGTCTTTAATGCATTAACTTCTTTATTTTCACAATTGTTACTGTACTTACAGTTGAATGAACCTGTGGGTATTACAGAGAATTAATTAACAAGGTTACTTTGATATACTTTACCTCTATACCGAGGGAAGTCATTTATTTGACAGTTAACTAGCCATAACTAGCCAAATTATTTCCATTCTTTAATACATTGGCAGTCCACTTTGTTATATAATAAGTGGATGAGTTTCCATGGACTAAAAGCGAGACATTGTTTGAGATTTGACATTTTGAGATTTTTCAATTATTTGCTTTTCTTACTTACTTTTATATATATATATATATACAGTTGAAGACAAAATTATTAGCCCCCTATAAAATATTTCATTATTTTTCAAATAACTCCCAAGTGCTTTTTAATGGATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7478
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 > A
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044368 | Missense | 229 | 1182 | 8 | 26 |
| ENSDART00000135390 | None | None | 79 | None | 3 |
| ENSDART00000136567 | None | None | 856 | None | 16 |
| ENSDART00000138361 | None | None | 177 | None | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 6675152)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 6580226 |
| GRCz11 | 20 | 6570173 |
KASP Assay ID:
554-4136.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCTCAGTCAGGTTGATGTCGGTCTGATGGACAGAGTGTGTTTTGTTC[T/A]GGATCCTCCTCAGATGATCAAAGGTGATATCATGGTGAGAGACATCTTTY
Long Flanking Sequence:
TGCAATGTAACTTAAATTCAACAAGTAGACCATTAAAATAAAGTATGAGCTAAAAAATATAGGTATCACTTAAATTTAAGGTTTCCTTGTTGCACATGTTCCATGTACTTACTATAGTATTTACAATGATACATAACTGCATGCAATTAACCCCTAACCCGCAGTCTAACCCTAACCATATAGTAAGTACATGTACTTAATTAATATCCTCATGTAATGAGTAGTTACACTGTAACATTTACGCCTTAAAATGAAGTGCAACCAAAATGAATAAAGAAACGTAATATGTTTTTCATATGTGTTTTGTTTTCAGTGTGCCAGCTGTTTATCAGAGTAAATCAAGGCACGCAGACAGCATACACTTCAGGACTGCAGTAGGAACATAAAGATTTTTTAAAGCAATACAAAAGAGCAGAAATTCTGGATTATGTATATTAAGTGCTTGTGTGTAACTCTCAGTCAGGTTGATGTCGGTCTGATGGACAGAGTGTGTTTTGTTC[T/A]GGATCCTCCTCAGATGATCAAAGGTGATATCATGGTGAGAGACATCTTTTCCTGTCTCTTTCACACTGCACGCACATAGACTGCACTGATCTCATGAACGCTGCACAGTGGATCATCTTCTATTCCTCTGTCGCTGCAGATTGTGTGTTATCATAAAAATGTTTCCACGAGGACTCAGGAAACATTGTTTCGTGCTCAGTTTCACACTGCTGCTCTGAGTGCAAAACAATTTGCCTTGCAGAAAGAAGACCTGGATCTGGCCAACAAAGGTAAACCGAAGTGTTTTTAGTAAAGTCATTCACATTATTATAACATATATTAGAACCTTCTTAAGTATATCTAGTTGGCATAACTTATTTTTTTCTAGTTATATTAAACTTTATTTATTATTTATTATTTCTGCAACTTAATACTTTATAGTTACTGGAACTTATTTTTTTTAGGTACAGGAACCTAGTATTTATTGTTATGGCAGCTTATTTTTTCTAGTTCTTCAGCTT
Associated Phenotype:
Not determined