ZMP
sv2c
Ensembl ID:
ZFIN ID:
Description:
synaptic vesicle glycoprotein 2C [Source:RefSeq peptide;Acc:NP_001121811]
Human Orthologue:
SV2C
Human Description:
synaptic vesicle glycoprotein 2C [Source:HGNC Symbol;Acc:30670]
Mouse Orthologue:
Sv2c
Mouse Description:
synaptic vesicle glycoprotein 2c Gene [Source:MGI Symbol;Acc:MGI:1922459]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18001 | Nonsense | Available for shipment | Available now |
sa40545 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45226 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33695 | Nonsense | Available for shipment | Available now |
sa20517 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18001
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 |
---|---|---|---|---|---|
ENSDART00000084024 | Nonsense | 367 | 745 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 47667708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45456448 |
GRCz11 | 5 | 46056601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGCYGTCGTGGCCTTAACCTTCATGCCGGAGAGCCCACGCTTCTACT[T/A]GGAGGTGAGGAGCATCKCAARCCAGGKTAAAAGTTCTAATGAAAACTCCA
Long Flanking Sequence:
CATCAAATTGCTTAGTATTTTGGATGTGTTTTGACATCAAGGTGCCATGTTGGGTTCTCTTTTGTGAACTAAAATCATCAACCTCTTTGTTAAAGAAAACCTGTCATACTGTATTACATACATTAAACTTGCCGATCTTCAATTCCAGTGCCTAGAAAAGACAAAAACACTAGGCTTAACTCTTCTGTAATCAATCAATGTTGGACAAATGAAATGGATGCGTTCACTCAGCCTGTAACCACTATGACATGTCAGCAGTTATTGATAAATGTTAGCAGTTCAGATGCTACAGTCTCACAGTGAGTACTATCAGCCGACCCTTTGTCTGTTCAGGATCAATAACATGAGCAATTGTGTGATGTTTTCCTCAGGCTGGAGTTTCAGTATGGGCTCTGCTTATCAGTTCCACAGCTGGAGGGTGTTTGTGGTGGTTTGCGCTCTTCCATGCGTTTGTGCTGTCGTGGCCTTAACCTTCATGCCGGAGAGCCCACGCTTCTACT[T/A]GGAGGTGAGGAGCATCTCAAACCAGGTTAAAAGTTCTAATGAAAACTCCATTAGCAGATACGTAGTTTGCAGATACAGTGCATCCGGAAAGTATTCATATCATTCACCTTTTTTGTATGTAACAGCCTTATTCCAAAATAGTTAAAATTAATTTATTTCCTCAAAATTCTACACACACTACCCTATAATGACAGTCACTCCCACTAGCCACTTTGGCTGGTTGAAAATAAATTTTAAATTGTGGTTTGCTTAAAAGCAGGGTTTGACTATAAGGATGACCCAATATGTGTGCAAATGTGATCTTAGAATCGAGAAACAGCACGACTAACAAAAATAATTGCTTTCGCTTGAGCAATAGAAAGCAAGTGAATATTGAATGAGAGGATGATCACTCACGCAAACTGCTGATGTGATGCACACGACTGTTTAAAGCGCGTGCGCGCTCCTGTTTCCTTGCTTGAAGCAACCATCCCTTGAACGCAACTGTGATCGGTTCTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40545
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 |
---|---|---|---|---|---|
ENSDART00000084024 | Nonsense | 381 | 745 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 47669437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45458177 |
GRCz11 | 5 | 46058330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTCCTTTCAGGTGGGGAAGCACGACGAGGCCTGGATGATCCTCAAG[C/T]AGATTCATGACACAAACATGCGAGCGCGTGGACAGCCAGAGAAAGTCTTC
Long Flanking Sequence:
TAGTAACGTTGGAAATCTACTAGCCATTGTGGCTGGTTATCAAAAAAGTTGTCAAGCCCTGGTAATCAATATGCTAAGAAAAAAAAAGGATTACTACACCTCTAACATAGTAAATCCATGGTTAATTTATGCAAGAAATGTCCAAAAAACTCACAGAACTTTTATTTATTTATCATATATCAAATTGTATGATGTTACATTATTAAAATACATGGTTTATAGCTAACATAGTTTCTAGCTATCATGATTAGAAGAACATCCGTTTAGTTTACTGTAAATGACTAAACTCTGAGGAAACTGAGGAAACAGGCTGACTGCAGTGAACGTGACTGTCTTTGAAGCTAATGACGTGTGTTTGTCGTGACTCTTTCGTGGCAGTCGAGGTGGGCGTCTGTCATCCAGCGCTGCGGTTTCCACTTAATCCACTTAATCTCTCCGAAATGTTTTTGGTTCTCTCCTTTCAGGTGGGGAAGCACGACGAGGCCTGGATGATCCTCAAG[C/T]AGATTCATGACACAAACATGCGAGCGCGTGGACAGCCAGAGAAAGTCTTCACCGTGAGTCGATTCCCTAACTTTAAGCTGCTTAGAGCCCAGAGCATGCTTTAAAGTTGCTTCAATTCATGAATGATTGTCTCATCCTGCGCTCTATGTGTGCTTTTCTGATGTTTTTGGTGTCATTTACTGAGCCTCAGAATTAGAGGCAGATTGCAGCCTGCTTTAAGACTTTTCAGCAGCAGTAATGATGAAGATTAAGATGTCACCAAAATTGGTATAATATACAGTGGTCTTCAAAAGTATTTGCATATCCAAAGCGATAGTTCAACCAAAAATGAAAAATTACTCACCTCACACAAAGCTACTTTGTATCTGAAATACTTAAAAGAAACACTCAAACTAGATACATTTGAGGCCTTGAGACGAAGAACTCAAGTCCATATTTTCTAATTTTGAGTAATAAGATTTCATTTGGATTTGGAACATTATATTATACATTTTTATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45226
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084024 | Nonsense | 391 | 745 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 47669467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45458207 |
GRCz11 | 5 | 46058360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCTGGATGATCCTCAAGCAGATTCATGACACAAACATGCGAGCGCGT[G/T]GACAGCCAGAGAAAGTCTTCACCGTGAGTCGATTCCCTAACTTTAAGCTG
Long Flanking Sequence:
GGCTGGTTATCAAAAAAGTTGTCAAGCCCTGGTAATCAATATGCTAAGAAAAAAAAAGGATTACTACACCTCTAACATAGTAAATCCATGGTTAATTTATGCAAGAAATGTCCAAAAAACTCACAGAACTTTTATTTATTTATCATATATCAAATTGTATGATGTTACATTATTAAAATACATGGTTTATAGCTAACATAGTTTCTAGCTATCATGATTAGAAGAACATCCGTTTAGTTTACTGTAAATGACTAAACTCTGAGGAAACTGAGGAAACAGGCTGACTGCAGTGAACGTGACTGTCTTTGAAGCTAATGACGTGTGTTTGTCGTGACTCTTTCGTGGCAGTCGAGGTGGGCGTCTGTCATCCAGCGCTGCGGTTTCCACTTAATCCACTTAATCTCTCCGAAATGTTTTTGGTTCTCTCCTTTCAGGTGGGGAAGCACGACGAGGCCTGGATGATCCTCAAGCAGATTCATGACACAAACATGCGAGCGCGT[G/T]GACAGCCAGAGAAAGTCTTCACCGTGAGTCGATTCCCTAACTTTAAGCTGCTTAGAGCCCAGAGCATGCTTTAAAGTTGCTTCAATTCATGAATGATTGTCTCATCCTGCGCTCTATGTGTGCTTTTCTGATGTTTTTGGTGTCATTTACTGAGCCTCAGAATTAGAGGCAGATTGCAGCCTGCTTTAAGACTTTTCAGCAGCAGTAATGATGAAGATTAAGATGTCACCAAAATTGGTATAATATACAGTGGTCTTCAAAAGTATTTGCATATCCAAAGCGATAGTTCAACCAAAAATGAAAAATTACTCACCTCACACAAAGCTACTTTGTATCTGAAATACTTAAAAGAAACACTCAAACTAGATACATTTGAGGCCTTGAGACGAAGAACTCAAGTCCATATTTTCTAATTTTGAGTAATAAGATTTCATTTGGATTTGGAACATTATATTATACATTTTTATTCTATTTTATGTTATTATATACAATGGACAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33695
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084024 | Nonsense | 471 | 745 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 47675387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45464127 |
GRCz11 | 5 | 46064280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATTTAAAGAACTTAATATTTCTGCAGGTATTACGGTTTATCTGTGTG[G/A]TTTCCTGACGTCATCAAACACCTTCAGAACGATGAATATGCCTCTAAAGG
Long Flanking Sequence:
TTGACAATAAGTTCACTGTAGTCAAATGGCCTCCACAGTCAAAAGATCTCAATCTAATAGAGCACCTTTAAGATGTGGTGGAACGGGAGATTTACATCATGGATGTGCAGCCGACAAATTTGCAGCAACTGCGTGATGCTATCATGTCAATATGGACCAAAATCTCTGAGGAATTTTCCAGTACCTTGTTGAATCTATGCCACGATGGATTAAAAAAGTTCTGTTGGCAAAAGGGGGTCTAACCTGGTACTTGTAAGGTGTACCTGATAAAGTGGCCGGTGAGCATTTTAGATTCTGATGCGCTGTGAACCCTACGTGGTCATGAATGGCTGCCTGCTTCGCATGCATACCAAAGCAACGTTATTTGTGAAAATGTCCGATACCTACTGTACAGTATACACATACTGTATCATCACAGTGTCCATCCATTGATTTCTATCATCTCTACTGTGTATTTAAAGAACTTAATATTTCTGCAGGTATTACGGTTTATCTGTGTG[G/A]TTTCCTGACGTCATCAAACACCTTCAGAACGATGAATATGCCTCTAAAGGACAGCGGCATAACAACGAGCGCATTGAGGACTTCACCTTCAATTTCACCCTTGAAAACCAGATACACACTAATAGCTTATTCATCAACGACAGGTGACTTATTCCAAAGCTTAATCTTTTTATTAATGTCTGTATAAATTATCACATAAATCATTTCCTTTATTCTGTCCTCCAGGTTCATAAATATGAAATTCAAGTCTGTCACATTCATCAATTCCACCTTTCAAAGCTGCTTTTTTGAGGATGTGACATCCGTTGGATCTTTCTTTCGTAACTGCACATTTATAGAGGCTGTCTTCTACAACACTGGTAAAATCCTCATTTATTTTGGAACCCTTTCCACCACTTTGCTACGTATCTGTGTCTAATTATCACTTTCTGCTGTGCTTTAAACTTGACAGATATTGACGATTCCAAACTTAAGAACACAGATGTTATAAACAGTACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20517
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 |
---|---|---|---|---|---|
ENSDART00000084024 | Essential Splice Site | 519 | 745 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 5 (position 47675532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 45464272 |
GRCz11 | 5 | 46064425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCCTTGAAAACCAGATACACACTAATAGCTTATTCATCAACGACAGG[T/C]GACTTATTCCAAAGCTTAATCTTTTTATTAATGTCTGTATAAATTATCAC
Long Flanking Sequence:
GTCAATATGGACCAAAATCTCTGAGGAATTTTCCAGTACCTTGTTGAATCTATGCCACGATGGATTAAAAAAGTTCTGTTGGCAAAAGGGGGTCTAACCTGGTACTTGTAAGGTGTACCTGATAAAGTGGCCGGTGAGCATTTTAGATTCTGATGCGCTGTGAACCCTACGTGGTCATGAATGGCTGCCTGCTTCGCATGCATACCAAAGCAACGTTATTTGTGAAAATGTCCGATACCTACTGTACAGTATACACATACTGTATCATCACAGTGTCCATCCATTGATTTCTATCATCTCTACTGTGTATTTAAAGAACTTAATATTTCTGCAGGTATTACGGTTTATCTGTGTGGTTTCCTGACGTCATCAAACACCTTCAGAACGATGAATATGCCTCTAAAGGACAGCGGCATAACAACGAGCGCATTGAGGACTTCACCTTCAATTTCACCCTTGAAAACCAGATACACACTAATAGCTTATTCATCAACGACAGG[T/C]GACTTATTCCAAAGCTTAATCTTTTTATTAATGTCTGTATAAATTATCACATAAATCATTTCCTTTATTCTGTCCTCCAGGTTCATAAATATGAAATTCAAGTCTGTCACATTCATCAATTCCACCTTTCAAAGCTGCTTTTTTGAGGATGTGACATCCGTTGGATCTTTCTTTCGTAACTGCACATTTATAGAGGCTGTCTTCTACAACACTGGTAAAATCCTCATTTATTTTGGAACCCTTTCCACCACTTTGCTACGTATCTGTGTCTAATTATCACTTTCTGCTGTGCTTTAAACTTGACAGATATTGACGATTCCAAACTTAAGAACACAGATGTTATAAACAGTACATTTTACCACAACAAAACAGGCTGTCAAATGACTTTTGAGGATGATTACAGTGCATACTGGGTCTACTTTGTCAATTTCTTGGGAACACTAGCTGTTCTGCCTGGCAACATTGTTTCTGCACTGCTCATGGACAAAATTGGCCGCTTG
Associated Phenotype:
Not determined