ZMP
st8sia6
Ensembl ID:
ZFIN ID:
Description:
Alpha-2,8-sialyltransferase ST8Sia VI [Source:UniProtKB/TrEMBL;Acc:Q6KBZ7]
Human Orthologue:
ST8SIA6
Human Description:
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 [Source:HGNC Symbol;Acc:23317]
Mouse Orthologue:
St8sia6
Mouse Description:
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6 Gene [Source:MGI Symbol;Acc:MGI:2386797
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33121 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18485 | Nonsense | Available for shipment | Available now |
sa40026 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33121
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122519 | Essential Splice Site | 32 | 359 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 15886080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 16116299 |
GRCz11 | 3 | 16266099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTGTGCTCTTTCTGCAGTGTGGCCTTCTGGATTTTCATCTCCAACAA[G/A]TGAGTATTTCAGTTTTAGCGTTTGTGTGTACCCTTTTATTTGGAGAGTAA
Long Flanking Sequence:
TGGAAAACAGGATGAGGTGAAGAAGAGCTGGGGATAAAATAAGAAGATGCCTTAAAGGAATGCACTGGACAGGAAAGAAGCGGAGAAATTTCTTCTTGTGCATGTGAGAAGAAAAGTAGGCTGATGGATTGAGTAATAAAAAGCCAGGCCTGTCAGTGGAGAAAAGAAGAGAAAGAGAGAGAGAGAGAGAGCGAGGGGCAGTTAAATTAAGCAGAGGGAGGGAGAGTGAGGAGATTAACAGTCTGAGAGAGAAACAGAGAGAGAGAGAGTAAAGAAAAGGGTGCAGTCGTTAAGAAACCGGCAGAGTTGTAAAATACAGAGAGAGCGGCAGCAGCATCTGCATTTGAATGAGAGCACACGCATGTCCGCGGATATGTGTGCCACCGAGACCGTGTGTAAGAGTGGATGCGCGTTATGAGGACTCTTATGCGCTGGCTGCTTCCTGTCATCCTTCTGTGCTCTTTCTGCAGTGTGGCCTTCTGGATTTTCATCTCCAACAA[G/A]TGAGTATTTCAGTTTTAGCGTTTGTGTGTACCCTTTTATTTGGAGAGTAAAGTTGAAAAGACCAGAGTGTTAACAGATATCAGACCACCATGACTGAAGGAAGTCTTTTTAAGTCAAGTTAGTTATCAATAAATCTTTATAAGACATTTCTAATCTTTGTGCTGTCAGGAAACCGTTTCACCGCAGGCATCTGATTAGCAAAAGAGTATATTGTGTCATCATTACAGGAGAATTTATGCAGAAGCATAAAGATGATGCATACTGAAATGTTTTTTTTTGTTGTTGTTAATGGTTCAATGTTTCAGGATGCTGGACAGGTCTAAAAGTTGGACTTTAGATGCTGATTGTTTGTTCTGTTTCAGAAGTTTAGAATCACATTTCACATGAGTAAATAATTGAAAGTTGCATATGTTTGCCTGAATCAGGGATGCTCTTATTGCAAGTAACCGTTAACCAAAAGAATGCATTTTTAACAATTAATGGTATCAATTAAACAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18485
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122519 | Nonsense | 117 | 359 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 15896250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 16126469 |
GRCz11 | 3 | 16276269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATAACACTCCTCTGGGGTCAAATGTTGTCTATGATGGCGAAMGAAGA[A/T]AGCCACTACAGGTGACCCAAGCCCTKTACAACATCTTGGCTARGGTAGCG
Long Flanking Sequence:
GGCAAAGCACTGGGAAACTATTCAAACAGCTGGAAAAAACACGAGGCAAACTATAAAAGATTCAGGTAAAACGATAACCCGTTTAAAAGTAAAAAGACTGTTTTGTTTGTTTCTACTGTTGAACACAAAAGAAGATATTTTGAAGAATGCTGAAAACCTGTAACCATTGACTTCCATACTAGAAAAGGAAATACTATAGAAATCAATGGTTACCTTTGCTTTTTTTCCAAATATATTTTATTTTGTGTTCAACAGAAGAAAGAACTTCATAAAGGTTTAAAACCACTCGAGGGAGTAAGTAGTGAGAAAAAGTTTTTTCTGGGTGAACTATCTTTTTAAAGTTAGATCTGATGTTTTTAATTAAGAGAATCATAAACGTAGCATTTCTGTTTCTCTCCAGGTTATTACTAAATGAGAAATGCCATGCTGTGTCTAAAGCTGTGGTCACACAGAATAACACTCCTCTGGGGTCAAATGTTGTCTATGATGGCGAAAGAAGA[A/T]AGCCACTACAGGTGACCCAAGCCCTGTACAACATCTTGGCTAAGGTAGCGTATACAAAGTTTAAAACTGATGACAGTTTTTCAGATGATTTTGTATTTTTTATATTTTGTGTGTGTGTGTGTTTTGTAGGAACAACCATTTGGAAATGCGACATGGGAGTCATGTGCTGTAGTGGGGAATGGAGGCGTTTTGGCCAATAGCAGTTGTGGAGAAGAAATCAATTCAGCCCAGTTTGTCATTAGGTATGTCTCATATCACCCCATGTGAACTATTGCTTACATTATTATCAAAATGATCATAATCCACTTCAGCATAAGTCATATAAATGCTAAAAGGTTTTAATGACAGTTACTCAGTTACTACATCAATCTCCTATCAGTAACCATGGACTAATCCTAATCAACCCCTGTATTTTAGATGCAACCTTCCACCACTTGATGACAGATATGAGAAAGATGTGGGAAACAAAACCAATCTTGTCACAGCAAATCCCAGCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40026
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122519 | Nonsense | 163 | 359 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 15896474)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 16126693 |
GRCz11 | 3 | 16276493 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGAATGGAGGCGTTTTGGCCAATAGCAGTTGTGGAGAAGAAATCAATT[C/A]AGCCCAGTTTGTCATTAGGTATGTCTCATATCACCCCATGTGAACTATTG
Long Flanking Sequence:
TTCCAAATATATTTTATTTTGTGTTCAACAGAAGAAAGAACTTCATAAAGGTTTAAAACCACTCGAGGGAGTAAGTAGTGAGAAAAAGTTTTTTCTGGGTGAACTATCTTTTTAAAGTTAGATCTGATGTTTTTAATTAAGAGAATCATAAACGTAGCATTTCTGTTTCTCTCCAGGTTATTACTAAATGAGAAATGCCATGCTGTGTCTAAAGCTGTGGTCACACAGAATAACACTCCTCTGGGGTCAAATGTTGTCTATGATGGCGAAAGAAGAAAGCCACTACAGGTGACCCAAGCCCTGTACAACATCTTGGCTAAGGTAGCGTATACAAAGTTTAAAACTGATGACAGTTTTTCAGATGATTTTGTATTTTTTATATTTTGTGTGTGTGTGTGTTTTGTAGGAACAACCATTTGGAAATGCGACATGGGAGTCATGTGCTGTAGTGGGGAATGGAGGCGTTTTGGCCAATAGCAGTTGTGGAGAAGAAATCAATT[C/A]AGCCCAGTTTGTCATTAGGTATGTCTCATATCACCCCATGTGAACTATTGCTTACATTATTATCAAAATGATCATAATCCACTTCAGCATAAGTCATATAAATGCTAAAAGGTTTTAATGACAGTTACTCAGTTACTACATCAATCTCCTATCAGTAACCATGGACTAATCCTAATCAACCCCTGTATTTTAGATGCAACCTTCCACCACTTGATGACAGATATGAGAAAGATGTGGGAAACAAAACCAATCTTGTCACAGCAAATCCCAGCATCCTACATGAGAAGTAAGTCTGTGATTGAGGTTCACCCCAAAATAAAAATGTACACACTATTTACTCACCCTCAACGGGTTATACACTTTATGAGTTTTTTTCTTCTGTCAAAAAGCAATTGAAGATATTTTGACAATAACCGTTTTTAGGGTTTACCACGGTTTAGAAAAGCCAAGGTTTTAAAACTGCCAAAATTTTCGGCTATTCTATTCCGAAGGTATATGTA
Associated Phenotype:
Not determined