ZMP
sept3
Ensembl ID:
ZFIN ID:
Description:
Neuronal-specific septin-3 [Source:UniProtKB/Swiss-Prot;Acc:A2BGU8]
Human Orthologue:
SEPT3
Human Description:
septin 3 [Source:HGNC Symbol;Acc:10750]
Mouse Orthologue:
Sept3
Mouse Description:
septin 3 Gene [Source:MGI Symbol;Acc:MGI:1345148]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10682 | Essential Splice Site | Available for shipment | Available now |
| sa25647 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10682
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 |
|---|---|---|---|---|---|
| ENSDART00000044057 | Essential Splice Site | 196 | 361 | 5 | 10 |
| ENSDART00000128383 | Essential Splice Site | 196 | 361 | 4 | 9 |
| ENSDART00000044057 | Essential Splice Site | 196 | 361 | 5 | 10 |
| ENSDART00000128383 | Essential Splice Site | 196 | 361 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 46094816)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44932328 |
| GRCz11 | 1 | 45624123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAYACCAGAGTGCACTGCTGCTTGTATTTCATATCCCCTACTGGACATTC[G/A]TGAGTTTACATACCAACATTTTACTYATTACTCCATACCTACTAGATCAT
Long Flanking Sequence:
AAGCAGCAGAAATATGTACCTGCTACATAAAATTGTCCTGTCTGCACATTATTTGAGCAAAATTTGCTTTTCTGATTAGCGTGAGCGGTACATACATACTGCAGATAAGTATACAGGTACAAGAGTGAAATATCCACAAAGATGAATATTGAGTTGTTTTGAACTTTGAACATCTCTGTCGAAATCCTCAGACCTGTTTATTTAGTATTTTTTTTTAGTTTAGCTTTTTAAAATTACGGTTGAACCACTGATGACACATGGACTGTTTTTGAACTATCCATTTAAATAAAATACAAGGCCAGTCCAGTTATTCATTTGAATTTGAACACCACTCATTTTGTTTTATCCTTCTATGTTCTTAGCTGGGAGCCAATATCCAAACATATCAATGAACAGTATGAGAAATTTTTGAAGGAAGAAGTCAACATTGCCCGCAAGAAACGCATCCCAGATACCAGAGTGCACTGCTGCTTGTATTTCATATCCCCTACTGGACATTC[G/A]TGAGTTTACATACCAACATTTTACTCATTACTCCATACCTACTAGATCATATACTAGATAAAACAGCTCACATACTGACTACCAAATTTATTCATTTATACTAAATAGATATTTCTTCCCCCAAAAGACATACTAGACACATAAGAACACAGAGTATTTTCTCTTCTATTGAAGTTTCAAGTAAGCAATAAAGATATAAAGATGCCATGACACTACATGAATCAAGCATTTCCTTAATGCAAATCTTCACATCACGATATATGATTGTTTTTTGACAAACAGATTCATATAAATGCTTTATTGTACATATAAACTTACATGTAGAGCATATGGTTAACACAAAAAACTTGTGTACATGTGGAATTAAAATTTGTGCTTTGATGATTAACCAAATTTCTTATGGGTTTGAAGGTGATCTCACGTATTGCTGACTTACTGTGGATTAAACTGTAATTGAATGAATGTGACCCTGGACCACAAAGTTAGCCATTACAGTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25647
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 |
|---|---|---|---|---|---|
| ENSDART00000044057 | Essential Splice Site | 196 | 361 | 5 | 10 |
| ENSDART00000128383 | Essential Splice Site | 196 | 361 | 4 | 9 |
| ENSDART00000044057 | Essential Splice Site | 196 | 361 | 5 | 10 |
| ENSDART00000128383 | Essential Splice Site | 196 | 361 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 46094816)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 44932328 |
| GRCz11 | 1 | 45624123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACCAGAGTGCACTGCTGCTTGTATTTCATATCCCCTACTGGACATTC[G/T]TGAGTTTACATACCAACATTTTACTCATTACTCCATACCTACTAGATCAT
Long Flanking Sequence:
AAGCAGCAGAAATATGTACCTGCTACATAAAATTGTCCTGTCTGCACATTATTTGAGCAAAATTTGCTTTTCTGATTAGCGTGAGCGGTACATACATACTGCAGATAAGTATACAGGTACAAGAGTGAAATATCCACAAAGATGAATATTGAGTTGTTTTGAACTTTGAACATCTCTGTCGAAATCCTCAGACCTGTTTATTTAGTATTTTTTTTTAGTTTAGCTTTTTAAAATTACGGTTGAACCACTGATGACACATGGACTGTTTTTGAACTATCCATTTAAATAAAATACAAGGCCAGTCCAGTTATTCATTTGAATTTGAACACCACTCATTTTGTTTTATCCTTCTATGTTCTTAGCTGGGAGCCAATATCCAAACATATCAATGAACAGTATGAGAAATTTTTGAAGGAAGAAGTCAACATTGCCCGCAAGAAACGCATCCCAGATACCAGAGTGCACTGCTGCTTGTATTTCATATCCCCTACTGGACATTC[G/T]TGAGTTTACATACCAACATTTTACTCATTACTCCATACCTACTAGATCATATACTAGATAAAACAGCTCACATACTGACTACCAAATTTATTCATTTATACTAAATAGATATTTCTTCCCCCAAAAGACATACTAGACACATAAGAACACAGAGTATTTTCTCTTCTATTGAAGTTTCAAGTAAGCAATAAAGATATAAAGATGCCATGACACTACATGAATCAAGCATTTCCTTAATGCAAATCTTCACATCACGATATATGATTGTTTTTTGACAAACAGATTCATATAAATGCTTTATTGTACATATAAACTTACATGTAGAGCATATGGTTAACACAAAAAACTTGTGTACATGTGGAATTAAAATTTGTGCTTTGATGATTAACCAAATTTCTTATGGGTTTGAAGGTGATCTCACGTATTGCTGACTTACTGTGGATTAAACTGTAATTGAATGAATGTGACCCTGGACCACAAAGTTAGCCATTACAGTCCTT
Associated Phenotype:
Not determined