ZMP
stx16
Ensembl ID:
ZFIN ID:
Human Orthologues:
RP11-261P9.5, STX16
Human Descriptions:
Syntaxin 16 isoform a variant [Source:UniProtKB/TrEMBL;Acc:Q59G13]
syntaxin 16 [Source:HGNC Symbol;Acc:11431]
syntaxin 16 [Source:HGNC Symbol;Acc:11431]
Mouse Orthologue:
Stx16
Mouse Description:
syntaxin 16 Gene [Source:MGI Symbol;Acc:MGI:1923396]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18854 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9414 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18854
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 |
---|---|---|---|---|---|
ENSDART00000002693 | Nonsense | 276 | 324 | 8 | 9 |
ENSDART00000002693 | Nonsense | 276 | 324 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 49688575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 49738256 |
GRCz11 | 6 | 49736909 |
KASP Assay ID:
2259-8128.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATTAAATCCAGGGTACAGTCCTTGACAGAATCGACTTCAATGTGGAA[C/T]AGTCTTGTGTGAAAACAGAGGAGGGACTCCAGCAGTTACAAAAGGTGAGG
Long Flanking Sequence:
CCACCCTAGCCTCGCAAGTCTGATATATTTAACTATATCAATTTCCTTATACAAGGCTGCAAGCTCATTGTTGTGACGTATCCTCCACTGATTATTGTCTTTAATTGGGCCATATATTCTCCTCAGAATTTTTCTTTCAAAAACGAAGAGCTTTTGTTCCATGGCTTTTGTGATTGTCCACGTTTCTGAACCAAAGGCCAGCGAATCATGACTTTATAGAGGGTTATCTTTGTCTGTCTAGGCAGTGAACGGTTCTTCATGTACTTCATGAGTCCGTAGTAGCTTAGAATAGAATATTTCCTGTACCTTGTTAAATCTATGCCTCGAAGGATTGAGAAAGTCCTGAAGGTAAAAGGGGGTCCAATCTGCTTCTAGTAAGGTGTACCTGATAAAGTGGCCGGTGAGTGTATATACTTCATACGTTTTTCAAAATATGCATTAACATCATGGCAAATTAAATCCAGGGTACAGTCCTTGACAGAATCGACTTCAATGTGGAA[C/T]AGTCTTGTGTGAAAACAGAGGAGGGACTCCAGCAGTTACAAAAGGTGAGGCTCTTATCAGCCCTGACAACGTGTTAAACAATAAATCAAGGGTTAAATGCTTACATTTACTTTGCTTGCAATATTAATTTACTCTGCAATATCCGTGTGTCATTTAAAAGTATTAATATGTAACAAAGAGCAAAAGCACACTCATCTTTTCTCCTTTCTTTGTCAGGCTGAACAGTATCAGAAGAAGAACCGCAAGATGTTGGTCATTTTAATTCTCTTCGTCATAGTTGTCGTTCTAATACTTATTCTGTTCGGGACCAAGTTTAGTTGAATCATTCCATGGCCTCTAGGAGGGATTTACCAGTATGGATGAGAAAACGGATGTATTTGTGTGCGCGAGTGTGTATGTTAGACCATTATTTAAGTGTGGAATATTCCTCAAACAGAAGGTGCTTCTATTTGAAACGCTACACCACAAGATGAAGCCTGTAAGGACTCCCCCTGCTGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9414
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002693 | Nonsense | 276 | 324 | 8 | 9 |
ENSDART00000002693 | Nonsense | 276 | 324 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 49688575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 49738256 |
GRCz11 | 6 | 49736909 |
KASP Assay ID:
2259-8128.1 (used for ordering genotyping assays)
KASP Sequence:
CAAATTAAATCCAGGGTACAGTCCTTGACAGAATCGACTTCAATGTGGAA[C/T]AGTCTTGTGTGAAAACAGAGGAGGGACTCCAGCAGTTACAAAAGGTGAGG
Long Flanking Sequence:
CCACCCTAGCCTCGCAAGTCTGATATATTTAACTATATCAATTTCCTTATACAAGGCTGCAAGCTCATTGTTGTGACGTATCCTCCACTGATTATTGTCTTTAATTGGGCCATATATTCTCCTCAGAATTTTTCTTTCAAAAACGAAGAGCTTTTGTTCCATGGCTTTTGTGATTGTCCACGTTTCTGAACCAAAGGCCAGCGAATCATGACTTTATAGAGGGTTATCTTTGTCTGTCTAGGCAGTGAACGGTTCTTCATGTACTTCATGAGTCCGTAGTAGCTTAGAATAGAATATTTCCTGTACCTTGTTAAATCTATGCCTCGAAGGATTGAGAAAGTCCTGAAGGTAAAAGGGGGTCCAATCTGCTTCTAGTAAGGTGTACCTGATAAAGTGGCCGGTGAGTGTATATACTTCATACGTTTTTCAAAATATGCATTAACATCATGGCAAATTAAATCCAGGGTACAGTCCTTGACAGAATCGACTTCAATGTGGAA[C/T]AGTCTTGTGTGAAAACAGAGGAGGGACTCCAGCAGTTACAAAAGGTGAGGCTCTTATCAGCCCTGACAACGTGTTAAACAATAAATCAAGGGTTAAATGCTTACATTTACTTTGCTTGCAATATTAATTTACTCTGCAATATCCGTGTGTCATTTAAAAGTATTAATATGTAACAAAGAGCAAAAGCACACTCATCTTTTCTCCTTTCTTTGTCAGGCTGAACAGTATCAGAAGAAGAACCGCAAGATGTTGGTCATTTTAATTCTCTTCGTCATAGTTGTCGTTCTAATACTTATTCTGTTCGGGACCAAGTTTAGTTGAATCATTCCATGGCCTCTAGGAGGGATTTACCAGTATGGATGAGAAAACGGATGTATTTGTGTGCGCGAGTGTGTATGTTAGACCATTATTTAAGTGTGGAATATTCCTCAAACAGAAGGTGCTTCTATTTGAAACGCTACACCACAAGATGAAGCCTGTAAGGACTCCCCCTGCTGGCC
Associated Phenotype:
Not determined