ZMP
snap29
Ensembl ID:
ZFIN ID:
Description:
Im:7145101 protein [Source:UniProtKB/TrEMBL;Acc:Q502H0]
Human Orthologue:
SNAP29
Human Description:
synaptosomal-associated protein, 29kDa [Source:HGNC Symbol;Acc:11133]
Mouse Orthologue:
Snap29
Mouse Description:
synaptosomal-associated protein 29 Gene [Source:MGI Symbol;Acc:MGI:1914724]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1919 | Essential Splice Site | F2 line generated | Not yet available |
| sa13359 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1919
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000056208 | Essential Splice Site | 20 | 288 | 1 | 7 |
| ENSDART00000141452 | None | None | 148 | None | 3 |
| ENSDART00000143473 | Essential Splice Site | None | 232 | 1 | 6 |
| ENSDART00000148254 | Essential Splice Site | None | 266 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 2022177)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 1834559 |
| GRCz11 | 8 | 1839765 |
KASP Assay ID:
554-1908.1 (used for ordering genotyping assays)
KASP Sequence:
TGATAACAGGAGAACAGAACAGAACACTTCACCTCTTCCAGCGACCAAAG[G/T]TACAAATTCAGCGATAAAACGTTCAAAATATAGTTTGAGAGTTATGTTAA
Long Flanking Sequence:
TAATATAATTTAGAAAAGTATATAAATATTAATAATAATTATTTAAAATAAATATAATAATTATATACTACTAATAATGACTTTTGTTTTGTTTTTTGCTGTTATTATTAATATTTTTATTATTTTTATTATTATTATTATTAATAATAATAATAAATGAATAATAATTTTTTTCAATATTTAGCCTTTTATTGTTATTCTGGAACAATTACAATTAATCTTTAATTGGACACCCAACAGTTTATTATCTGTCAAGGAAAAACAAAGAAAAGTACAAACGTGGGCTTAAACACTGATCTCTATATAGAATGACTATTTTCTAAGTTCTCTATCCATACGGATCGTCATCTGGCACACATTATTTATAGATCAGTGGTGTAGCGACAAAGGGGAGCCAATATATGACGTCACCGTGACACCACCGGAAGTCGTCCGAGCAAAAGCGTCAGCTGATAACAGGAGAACAGAACAGAACACTTCACCTCTTCCAGCGACCAAAG[G/T]TACAAATTCAGCGATAAAACGTTCAAAATATAGTTTGAGAGTTATGTTAAACACGCGATTTATGTTATTAAATATAACGTAGGTCATTTGTAGAGTCTGTGTTAGGTAATATAACGTACTATAGCCGAGAAAGAAAACAGTAACAGGCGACTTTCTACAGCATATTCACCTGAAATGTCGTTAAATGTTGAAGATTATATAGGATAATAACTGTTGTAAATGTTATTATGCTCAGTCTGTATATATGATTGTTTGTCGGTGAGCATTTGCCAGATATAATAGTTTATTCAGGACACACTTCGTCCATTTATCAAGATCTATTTAACTATTAACAGAAAGTACCGTCTTTTTAACGTTTACCATTAGCTATAGAGCTAAATCTGCCTTATAATTAATCTTTTACAGCAGAGCTAATTAAAATTTAGCATTGTACAACCTTTTGATCTTCCACAACCTTTTTATTTCAGCTTAAATATCTGTATTATTTGGTCCTTATGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13359
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 |
|---|---|---|---|---|---|
| ENSDART00000056208 | Nonsense | 187 | 288 | 4 | 7 |
| ENSDART00000141452 | Nonsense | 82 | 148 | 2 | 3 |
| ENSDART00000143473 | Nonsense | 165 | 232 | 4 | 6 |
| ENSDART00000148254 | Nonsense | 165 | 266 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 2031129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 1843511 |
| GRCz11 | 8 | 1848717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAGGCTACAGACGGCGCTTGCGGAGAGCAAACAGCAAGAAGACAAATA[T/A]CAGGCCAGTCAYCCAAACCTCAGGAAACTGGAAACATCTGGTAAACACAC
Long Flanking Sequence:
CCAGCTGAAAACATTTATTTAAACAAGGTAACTTTCAAATAAAATAGTTTTATTCAAGTTTAAACTTACAGAATTAGCATAGATGCATACATTAAAGCAAATAAATGGTTTTAAAATTTTGACATCCTCCTCTTGTTCCAAACCGGTTTGAGATTATTTCTTCTGTTGAACACAAAGGAAGATATCCTGAAGAATGCTGGAATAAACAGCCATTGACATCTACAGTATTTTTGTTCCTACTATGAATGTTAAAGGCTGCTTTCTCCCCAACATTCTTCAGAATATCTTCCTTTGTGTTCAGCAGAAGTAAGACACTCATAAAATGCTTAAAACTTTTACTTGAGTGCGAGTAAATGATCAGGAAATGTGAATTCGGGGTGAACTGACCCTAAGTGACTAAATGTAAATGTTACAATAAATTGCTTTGTCATTTTTTGAATGTCTGATGATTTTAGGCTACAGACGGCGCTTGCGGAGAGCAAACAGCAAGAAGACAAATA[T/A]CAGGCCAGTCATCCAAACCTCAGGAAACTGGAAACATCTGGTAAACACACACACCACCAACAACAACAACACACACACACTTTCTTCCCTTAAGAGCAAGTATCAGCTAGTGATAGGATTCAGTCTCTTAAAAATGCTGAGTGGTATTTTAGGCCAAATAAAACAAACTCAACATTTGGTGAAATATAAAATATTATTTCATTTAAATTGCACAGCAGATGGATTCGCTAATATTTGACCCAGTGTTTTTTTTTTCTTTTTTCAAAGCACATGAATTGACGTCTGCTGTTCAGAATAGTATAAATGCAGAGAAAACTACACGAGAACAATTTACAAACACCGATTAATTTTTTTTTTTTATCAGTGCATTGCATGCTACATATTGATGGTGTGCAGTGAGGGGTGTGTCAAGTGTTCCTCACAGTGTTCCTCATTTATGTTTTCTTAAATCTTACACAGTCACATGTCTTAAAAACGCATCCAAATGAAAATCTTTCAGT
Associated Phenotype:
Not determined