ZMP
st6gal1
Ensembl ID:
ZFIN ID:
Description:
beta-galactoside alpha-2,6-sialyltransferase 1 [Source:RefSeq peptide;Acc:NP_001003853]
Human Orthologue:
ST6GAL1
Human Description:
ST6 beta-galactosamide alpha-2,6-sialyltranferase 1 [Source:HGNC Symbol;Acc:10860]
Mouse Orthologue:
St6gal1
Mouse Description:
beta galactoside alpha 2,6 sialyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:108470]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43676 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12294 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43676
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065366 | Nonsense | 318 | 484 | 6 | 8 |
ENSDART00000100911 | Nonsense | 318 | 404 | 6 | 9 |
ENSDART00000126205 | Nonsense | 329 | 495 | 6 | 8 |
ENSDART00000137728 | None | None | 265 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 29942759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31143010 |
GRCz11 | 21 | 31179705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTGCATAGTTAATGGCATCTGAAGACCACCATTTCCTCTCCAGCTCTT[T/A]GTACAGTGCAGGGATTTTAGTGAGCTGGGATCCTAGCCCTTATTCTTCAG
Long Flanking Sequence:
TTGGAAATTCACCAAATGACCCCCCACCCCCACCCCCACCCCATCAATTGATAATTCATAGTTTTGGGTGAACTATCCTTTTAGGTGTTTGTCACTATTCATTTATATACAATAGACAAAGCAATTTGCATTGAATTATCATGAAGAAATACCTGAATTTTGATACTCCATTAAAACATTGGAAATACTCCACCCCCACAATGTCTGCTATCTATTCTACAATCAAAATAATTCTGATTTTATACATGATGCAGTATTACTAATAAAGTTTCTGAATTGTAGATTCTCATGACGCAGTGATACGATTCAATGCCGCACCGACAGCTGGTTTTGAGACAGACGTGGGCTCCAAAACAACAGTGCGCCTTATTAATTCACAGGTAATTTCCTTCAACTAATGAAAAATGTAAACAGCATATGGTTACATGCTTATGAAATTCATTGCTTGTTTCTTGCATAGTTAATGGCATCTGAAGACCACCATTTCCTCTCCAGCTCTT[T/A]GTACAGTGCAGGGATTTTAGTGAGCTGGGATCCTAGCCCTTATTCTTCAGATCTATGGGAGGTAAGAATGGGCTTTGTGTACTTTCTAGCATTCTTCAAACACAAAAAAAGGCAAAAAACCCTGCTTTCTCACTGACTATTGCGTGTACCCGTAGTATGTACTTGTGCTGGTTGCACCATACAACCACTAAGCCACTCCTCGTTAGTATAGTGGTAAGTATCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGATGCTAATCTTTTTTTCTTGTTTTCCCAAGTATGCATCACTACATGGTGTTGGTATACAATACTTTAAACAAATTCTAATCAAAAACCTAATTGCAAACAGTTCTTTTAATTGTCTAAACAAGCTGTTTGTCTTTTCACATTAAATTACACAAGTAAAATGGGAAAATGAGAAAATGGCCAAAAATTGGAAAAATAATAAAAAATAATAAAAATAAATAAATAAATGTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12294
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065366 | Essential Splice Site | 338 | 484 | 6 | 8 |
ENSDART00000100911 | Essential Splice Site | 338 | 404 | 6 | 9 |
ENSDART00000126205 | Essential Splice Site | 349 | 495 | 6 | 8 |
ENSDART00000137728 | None | None | 265 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 29942821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31143072 |
GRCz11 | 21 | 31179767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATTTTAGTGAGCTGGGATCCTAGCCCTTATTCTTCAGATCTATGGGAG[G/A]TAAGAATGKGCTTTGTKTACTTTCTAGCATTCTTCAAACACAAAAAAAGG
Long Flanking Sequence:
TTTGGGTGAACTATCCTTTTAGGTGTTTGTCACTATTCATTTATATACAATAGACAAAGCAATTTGCATTGAATTATCATGAAGAAATACCTGAATTTTGATACTCCATTAAAACATTGGAAATACTCCACCCCCACAATGTCTGCTATCTATTCTACAATCAAAATAATTCTGATTTTATACATGATGCAGTATTACTAATAAAGTTTCTGAATTGTAGATTCTCATGACGCAGTGATACGATTCAATGCCGCACCGACAGCTGGTTTTGAGACAGACGTGGGCTCCAAAACAACAGTGCGCCTTATTAATTCACAGGTAATTTCCTTCAACTAATGAAAAATGTAAACAGCATATGGTTACATGCTTATGAAATTCATTGCTTGTTTCTTGCATAGTTAATGGCATCTGAAGACCACCATTTCCTCTCCAGCTCTTTGTACAGTGCAGGGATTTTAGTGAGCTGGGATCCTAGCCCTTATTCTTCAGATCTATGGGAG[G/A]TAAGAATGGGCTTTGTGTACTTTCTAGCATTCTTCAAACACAAAAAAAGGCAAAAAACCCTGCTTTCTCACTGACTATTGCGTGTACCCGTAGTATGTACTTGTGCTGGTTGCACCATACAACCACTAAGCCACTCCTCGTTAGTATAGTGGTAAGTATCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGATGCTAATCTTTTTTTCTTGTTTTCCCAAGTATGCATCACTACATGGTGTTGGTATACAATACTTTAAACAAATTCTAATCAAAAACCTAATTGCAAACAGTTCTTTTAATTGTCTAAACAAGCTGTTTGTCTTTTCACATTAAATTACACAAGTAAAATGGGAAAATGAGAAAATGGCCAAAAATTGGAAAAATAATAAAAAATAATAAAAATAAATAAATAAATGTGTATGTATGTATGTGTGTGTGTATATGTGTGTGTGAATATATATATATATGTATGTATGTATGTAT
Associated Phenotype:
Not determined