ZMP
stx5al
Ensembl ID:
ZFIN ID:
Description:
syntaxin 5A, like [Source:RefSeq peptide;Acc:NP_955924]
Human Orthologue:
STX5
Human Description:
syntaxin 5 [Source:HGNC Symbol;Acc:11440]
Mouse Orthologue:
Stx5a
Mouse Description:
syntaxin 5A Gene [Source:MGI Symbol;Acc:MGI:1928483]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13268 | Essential Splice Site | Available for shipment | Available now |
sa23950 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13268
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 |
---|---|---|---|---|---|
ENSDART00000021121 | Essential Splice Site | 126 | 298 | 6 | 11 |
ENSDART00000146315 | Essential Splice Site | 175 | 347 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 25939211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26509029 |
GRCz11 | 21 | 26545724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGCAGACATCTTCAGACACATTCCAACACCATCGTGGTCTCATTACAGG[T/C]ATTAACCTCTGGCTTTAGTATTCATTTAMAAAAYAGTGAWGTCTAGTGGA
Long Flanking Sequence:
TTTGACCTATAATTTATTCAGACCTACTTAAGCTTTAATGGTCTGTGTTATTTCATCGACTTGGCTTTATGACAGATATTGACCCGCATCTTATTAACAGGCGAATTGGAAGAGACCTCAGCAACACTTTTGCCAAGCTGGAGAAGCTCACAATTCGTAAGTATCTTGTCTCTCCTGTCATCGTTGCACATGTTTTTAGCATATAACTCAAACGGTTTACGTCTACAGTTGCCAAAAGAAAGTCCCTGTTCGATGACAAAGCCACTGAGATTGATGAACTCACTTATATCGTGAAACAGGTGAGGGTTTATTATTACCTGCCATTCAAAAAGGACACATTATTCTTTCTGTGCATTTCATACTCTTAACCATCCCTGTTCAGGACATCAACAGTCTGATTAAGCAGATTGCTGGCCTGCAGGAGCTGGTTCGGTCTCGAAGTGCACAGAACGGCAGACATCTTCAGACACATTCCAACACCATCGTGGTCTCATTACAGG[T/C]ATTAACCTCTGGCTTTAGTATTCATTTACAAAACAGTGATGTCTAGTGGATGTTCTCTTGAAATATAATATGTTTTCTGTTTGTAGTCCAAACTGGCATCGATGTCCAGTGACTTCAAGTCTGTCCTGGAAGTCAGAACAGAGGTAATTGATTTCCTTTTTTGCCTTAAATGCAGTATTTGGTAGGAGTGCTAACTTTGACCAAATATAGAGTTTGCAATCGGCTAATAATCACTTATTAGTTCTCAAGTTATTGATCTCATTAAATTGATCTGATCTGATATGCTTACAGCGGTGAGGTGAAAGTCATACATCTTGATCTATATTAACTAAATATACCTCAATGGCAGTTAGTCTTCAGCCTGCAAAAACACACAAAGATCTTCTTGATGTCTTCTGTGAATTTTTCATTCTCCATTATATTGGTTGGTGTTGCCAGATTTCACTAGAAAATCACACCAGCTGTTTTTATGCCTTAAGACAGAGGTGTCCAAAGTCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23950
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 |
---|---|---|---|---|---|
ENSDART00000021121 | Nonsense | 198 | 298 | 9 | 11 |
ENSDART00000146315 | Nonsense | 247 | 347 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 25943231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26513049 |
GRCz11 | 21 | 26549744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCAAGAAGACGGATATATCTATAGATATGGACCTGAATTCCAGTCAG[C/T]AGATGCAATTAGTCAATGAACGGGTATTGTTTGTTTATTGGTTGTTTTGT
Long Flanking Sequence:
AAAATAGGAGTTTGGTCACCTAACATCTATAGAAATAGGAAGATAATACATTTAAAAAATGTACAAACTATATTTGACATGTTTTGTGTTACTCTTAATTTTTCCTGTTTATTAAATTTTATTTCCTATTATTACCCCAACATAATAACTTGAGTATATTAATGTTTGAACGGATTCGCTTCTGTTTTGTCCTTGGTGCTGTCTAATCTACTGATAAGCATAAATATAGTATTTTTTTATTTCCTATAGAAAATATAATTTTAAAAGAGAGACTTGTGAGGTCCTAATGACTGTAATAAAGGTCAAATCTGAGACAAACAATTGACAAGACAGTGTATATTTTACATTTACTGTGTTTGTTTTATTATATAAAATTCTGGTAACAAACCCGGCACTCTTTTTCATCTTTTTCATGTTTATTCCCAGATAATTCAGTGCTTATGCAGGACGACTCCAAGAAGACGGATATATCTATAGATATGGACCTGAATTCCAGTCAG[C/T]AGATGCAATTAGTCAATGAACGGGTATTGTTTGTTTATTGGTTGTTTTGTAACAAAAGCTGCTTGTAAACTGGTTTAAATGTGTTTAAATCACTGCTGCCTTGTTTGTGTTTAGGATTCGTACATTCAGAACCGTGCAGACACTATGCAGAATATAGAGTCCACCATTGTTGAGCTCGGATCCATATTTCAGCAGCTGGCTCATATGGTGAAAGAACAGGAAGAGACTGTACACAGGTGAGGAAAGAAATGTTTGTGCTTTTCAATACATGTGGATTTGGTTATTGACCATTAGACACAATCCAGGATAGTTTGGTTCTTCAAAACTCATCCAAGTGTTTTTGTCATAGCAGCATGTCTGCAGCATGTGAGTTCAAACCTGCCCAGAAGCAGATTTTTTTATATAAAAAGTATTCAGTTGAGCTGTTTCAAGTAAAGGTGATTCTGAAAGCATGTACCGATAAATGATATTTCCTTACAAGTGTGTTTTGATTTCATTTC
Associated Phenotype:
Not determined