ZMP
neu3.3
Ensembl ID:
ZFIN IDs:
Description:
sialidase 3.3 [Source:RefSeq peptide;Acc:NP_001071006]
Human Orthologue:
NEU3
Human Description:
sialidase 3 (membrane sialidase) [Source:HGNC Symbol;Acc:7760]
Mouse Orthologue:
Neu3
Mouse Description:
neuraminidase 3 Gene [Source:MGI Symbol;Acc:MGI:1355305]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23919 | Essential Splice Site | Available for shipment | Available now |
| sa11219 | Essential Splice Site | Available for shipment | Available now |
| sa23920 | Nonsense | Available for shipment | Available now |
| sa37292 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23919
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 |
|---|---|---|---|---|---|
| ENSDART00000081184 | Essential Splice Site | None | 402 | 1 | 4 |
| ENSDART00000084600 | Essential Splice Site | None | 402 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20755280)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 21766773 |
| GRCz11 | 21 | 21803409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGCTCTTGTGGTGTGAATCATTTGTTTTTGCAGCAGGAGTTTTTTT[G/A]TAAGTATTGCTTCTGATTAGTAAAGAATTATTGATATAGACAGAATCCAT
Long Flanking Sequence:
ACTCTTAAGGTTAAGTTGATTCAGCTTAAAAATTTACCAGGCAGCCAGGATTTTTTACAGTGCATGAATAATTATGTTGTTTCATTTCAGCATATTTGTAACACTGGAAAATGTCTTCACAGATTTGACATCATTTTTGGAAATAGAATTGGTTGCTTGCACCAAAATAGGACAGTTCTGACCTTTTCTTGTTTCAGGTTTCTGTACAATTTAATTAAACAGTACTGTAAAATAAATAATTAAAATATAGTTTTTACATTTTTAAAAAATGTTTTTGCAAAATAATCACGTTAAATGAAATAATAAATAGTTAATATTTGACCACATTGTCTTTTACTTATCATCCTGCTCTTTAAGTTAGTAAATGTTCAACCTGGCTTCAGTCATTTCCTTTGTTGATATGGGATATTATAAATAAGGAGTGCCCAGCATGTGTTGGTTAGACCAGATGAGAGGCTCTTGTGGTGTGAATCATTTGTTTTTGCAGCAGGAGTTTTTTT[G/A]TAAGTATTGCTTCTGATTAGTAAAGAATTATTGATATAGACAGAATCCATTGGGTTTCCCCATAAAGATTATGCTGAACATATTTCATGGTATGGTAATGTCACTTTAAAATTACTGATATAAAATGATGAATTTTCAGTTAGAAGAACTAAAATCTAATGTTACTTTTGTTTAAAAAATGATTAGATACATTGTTTTGCTTTGGACAAAGCAAGGTGAAGTGTTACTTCATCCTGTGAAGGCCCGTCATTTTTTTCAATCCAGGGTGAGTTCTTCATGATTTTTGACTGAATAATACTGTGAATTTTATTTTATTTATATATTTTTTTACAGTTTTTGCAAACTTTTACTTCAGATATGCATCAGCAAAGACAGCATAACTGCAGCTGCACACTAAAAAGTATCATATAAGTGGCTGTAAAATTACTTTTTATAGCTCTACCTCTCATACAGTGGCATTAAAATATGTAAGTGTAAAGTTCTCAGTGTATAGTAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11219
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081184 | Essential Splice Site | None | 402 | None | 4 |
| ENSDART00000084600 | Essential Splice Site | None | 402 | None | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20755281)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 21766774 |
| GRCz11 | 21 | 21803410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGGCTCTTGTGGTGTGAATCATTTGTTTTTGCAGCAGGAGTTTTTTTG[T/C]AAGTATTGCTTCTGATTAGTAAAGAATTATTGATATARACAGAAWCCATT
Long Flanking Sequence:
CTCTTAAGGTTAAGTTGATTCAGCTTAAAAATTTACCAGGCAGCCAGGATTTTTTACAGTGCATGAATAATTATGTTGTTTCATTTCAGCATATTTGTAACACTGGAAAATGTCTTCACAGATTTGACATCATTTTTGGAAATAGAATTGGTTGCTTGCACCAAAATAGGACAGTTCTGACCTTTTCTTGTTTCAGGTTTCTGTACAATTTAATTAAACAGTACTGTAAAATAAATAATTAAAATATAGTTTTTACATTTTTAAAAAATGTTTTTGCAAAATAATCACGTTAAATGAAATAATAAATAGTTAATATTTGACCACATTGTCTTTTACTTATCATCCTGCTCTTTAAGTTAGTAAATGTTCAACCTGGCTTCAGTCATTTCCTTTGTTGATATGGGATATTATAAATAAGGAGTGCCCAGCATGTGTTGGTTAGACCAGATGAGAGGCTCTTGTGGTGTGAATCATTTGTTTTTGCAGCAGGAGTTTTTTTG[T/C]AAGTATTGCTTCTGATTAGTAAAGAATTATTGATATAGACAGAATCCATTGGGTTTCCCCATAAAGATTATGCTGAACATATTTCATGGTATGGTAATGTCACTTTAAAATTACTGATATAAAATGATGAATTTTCAGTTAGAAGAACTAAAATCTAATGTTACTTTTGTTTAAAAAATGATTAGATACATTGTTTTGCTTTGGACAAAGCAAGGTGAAGTGTTACTTCATCCTGTGAAGGCCCGTCATTTTTTTCAATCCAGGGTGAGTTCTTCATGATTTTTGACTGAATAATACTGTGAATTTTATTTTATTTATATATTTTTTTACAGTTTTTGCAAACTTTTACTTCAGATATGCATCAGCAAAGACAGCATAACTGCAGCTGCACACTAAAAAGTATCATATAAGTGGCTGTAAAATTACTTTTTATAGCTCTACCTCTCATACAGTGGCATTAAAATATGTAAGTGTAAAGTTCTCAGTGTATAGTAGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23920
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081184 | Nonsense | 13 | 402 | 3 | 4 |
| ENSDART00000084600 | Nonsense | 13 | 402 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20756007)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 21767500 |
| GRCz11 | 21 | 21804136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATTTTAAAAATGGGCAACAAGACACCGTCAAAAAGCAAATCAGGTTA[T/A]CCTAAAGAAATGAACACAACCACAGTATTCAAACAGGAGCAGCCTCAAAC
Long Flanking Sequence:
CTTCATCCTGTGAAGGCCCGTCATTTTTTTCAATCCAGGGTGAGTTCTTCATGATTTTTGACTGAATAATACTGTGAATTTTATTTTATTTATATATTTTTTTACAGTTTTTGCAAACTTTTACTTCAGATATGCATCAGCAAAGACAGCATAACTGCAGCTGCACACTAAAAAGTATCATATAAGTGGCTGTAAAATTACTTTTTATAGCTCTACCTCTCATACAGTGGCATTAAAATATGTAAGTGTAAAGTTCTCAGTGTATAGTAGGAAAAACAGTATGATGCTCAGCTTTTTAAAAATAATTAAATATTTTCCAAACTCCTTAAACTATCATAATGACTAAACAGAACAAATGCAGTAACTTTGCATTAAATAATTATTGAAACTATTTTGTTTAACACATGTCTACTGCTTTGTTATTAATTTAATGTGTTCTGTTTCTAGGCCTAAATTTTAAAAATGGGCAACAAGACACCGTCAAAAAGCAAATCAGGTTA[T/A]CCTAAAGAAATGAACACAACCACAGTATTCAAACAGGAGCAGCCTCAAACTTGGTGCTGCTGTTTTAAAAAACAAGTGTCTTATAGAATTCCAGCTCTCGTTTATGTCAGTGATGAGCAAACCTTCCTTGCCTTTGCTGAAAAGAGAAAAACATTAAATGACACAAATGCAGAAGTGCTTGTGATGAGAAGAGGAACATGGGTGGATGCCAAGACTAAAGAAGTTGAGGTATGTAAGAATTAAAAATTATTCTACATGAGTTATTCCAGGGTCATTAAGCCCTGGTCATTAAACCTTGTTCTGCTCATTCTTTACATGAGAGATAACGTACTTCCAGATGGTTGTTATGTCTGCATAAATCCCCAACAGGCCGGTCAGATTTTGAATTAGTCTCGAGCATGCAAAATGATAAGTCTAAATGTATTACAAGGAAAATGAACAGAAAGCTCCCATGAGGAAAATTCATTCATTCATTTTCCTTCCACTGAGTCCCTTTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37292
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 |
|---|---|---|---|---|---|
| ENSDART00000081184 | Nonsense | 95 | 402 | 4 | 4 |
| ENSDART00000084600 | Nonsense | 95 | 402 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 20758327)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 21769820 |
| GRCz11 | 21 | 21806456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATTGTTTTGTTTTGTTTCTTATTTATTCCAGTGGATCTGTGGTCAT[C/T]AGGTGCTAAGTTCAGCTAGTCTACCAAACCACCGCAGCATGAATCCATGT
Long Flanking Sequence:
GATAGACTTGGGATTGGGCATAAAAATGGGCTGTCAGTGAAAATTTAATGGACGTCTAAGAATAGGAATATCGTCAAATAAACTGAAATGAATGACACATATAACGTCTATCTTATTTGTCGATTTGACGACTAGTCTAGTTTTGGGCTATTCTCAGATTTTCACTGACAGCCCAAGTTGAGCTTTGTTTTAGCCAAACTGTCTACATTTAGATGTCTATTAGACGTGCTTACCCACATTTCAATTTGGCAATGCTTGACATCACTTCATTTCAAATACTATATGACACACTGTGCGTTTGGCATGCGAGCCTTTTGTAAAAAATCCCTATACTCAAAATTAATTTCTTGTTAGAACAAACTTTGTTGGAACATGTGAAAACTCCTTAAATTGTCTTTGTACCAACTTCACCATTTCATAGATGCTTTACACAATCTAATCTGAAGAGAGTCATATTGTTTTGTTTTGTTTCTTATTTATTCCAGTGGATCTGTGGTCAT[C/T]AGGTGCTAAGTTCAGCTAGTCTACCAAACCACCGCAGCATGAATCCATGTCCAGTCTACGAGAGAGACTCCAAGACCCTCTTCCTGTTCTTTGTCTGTGTTCCGACTCAGGTCTCTGAATTTGATCAAATACGAACAAATAAGAGCCAGGGGAGACTTTGTTATGTAACCAGTAAGGACGCTGGCAAAACCTGGAGCCAAACAATAGACTTGACAGCAGATGTGATCGGTGAGCAGGTGAACGAATGGGCTCCCTTTGCTGTTGGACCAGGACACGGTGTTCAAACAAAGAACGGAAGACTGATTATCCCAGCATATGCCTATCGCTACACAGGCAAAACTGACTGCACTTCATGCTGCTGCTTATCATTCTGCTGCTTCACACCGTATGCTTTAGCTTTCTACAGTGATGATCAAGGAATCACATGGAAGGCAGGACAACAAATGGACGTTGAGTCATGTGAGTGTCAGATGGCAGAGATTGTAGGTGAGAAAGGTGAC
Associated Phenotype:
Not determined