ZMP
si:ch211-51n14.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC799868 [Source:RefSeq peptide;Acc:NP_001076403]
Human Orthologue:
ST6GALNAC1
Human Description:
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran
Mouse Orthologues:
Gm11735, St6galnac1
Mouse Descriptions:
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran
predicted gene 11735 Gene [Source:MGI Symbol;Acc:MGI:3713525]
predicted gene 11735 Gene [Source:MGI Symbol;Acc:MGI:3713525]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14861 | Nonsense | Available for shipment | Available now |
sa22086 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14861
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 |
---|---|---|---|---|---|
ENSDART00000064335 | Nonsense | 108 | 427 | 2 | 9 |
ENSDART00000112847 | Nonsense | 108 | 270 | 2 | 10 |
The following transcripts of ENSDARG00000043816 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 22044532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20570113 |
GRCz11 | 12 | 20691987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAAACACAAATTCACTTCCTTGCCTCACTGGAAATTTGATGATCTGTAT[C/T]GATTGGACCCACATTTTAAACMGAGTGTAAGTACAGTCTACAATAACTAT
Long Flanking Sequence:
GAGGGGGAGCAGCGTAATGGTTCAAAAACGTCACCTAAAAGAGCTCTCTTGAGTCCTAATCAGTTTGTGGACGCGCAGGTGCGCGTGTGCGTTGCCAGATCATGTTTCTCCTGAGGATTTTCTTAGTCACAACTTTCATAGCTTCTCTTCCTTTGTTTATTTTTGTCACATTTTATAATGGAACTAGCACTTTACAGATAAAATGGAGGTAAGAAACTTTACCAAATCGAATCTGCATTAACGTGAAGTTACAGGCTAACAAGTATTGTCACTTTTACCTCTTAAGACAGTATTACTATTGGCTGAACCAAGGTCAAGTCGCAGGTTCTTTGCTGACAATTGTGGAGCCTGAGCCAACCAACAGTTCAGCTTTAACTGACATATTAGCCAACACCACTACAATGAGGCTTGATCCTTTTGAGACTCTATCAACTCCTCTGCCCATTATGGACAAACACAAATTCACTTCCTTGCCTCACTGGAAATTTGATGATCTGTAT[C/T]GATTGGACCCACATTTTAAACCGAGTGTAAGTACAGTCTACAATAACTATAGAAATGTCAATCTGTGTGTGGTTGCTTGTATATCAATTTAGCCTTCTGCTGAATGCTGCATTCTGATTGGCAGAAGAACATTGTGTAAGGCAGGGGCATCAAACTCAGCTCAACACAAAGGATCAACACAAATTCATTCGTTTAACACAAATCATCTAACTAATTGAGTCCTTCAGGCTTGTTTGACACCTGTGCTCTGAGGTGTACAATTATTTTAAGTAAACCGCACATATTTTGCCGCTGTTTGAGGAAAAAAAAAGTCTTGAAATACAACATCTGCAGAATGTTCAGGTCTACTGTAGAGCAGGGTGTCAAACTCATCTACTAGATGGCTGGAGCCCTGGAGAGTTTAATTCCAGCTCTGCTTCAACACACTTACCAGTAGGTTTCAAACAAGCCTGAAATAGTCAATTAGTTTGATCAAGTGTGTTTAATATAGCTAAACTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22086
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 |
---|---|---|---|---|---|
ENSDART00000064335 | Essential Splice Site | 336 | 427 | None | 9 |
ENSDART00000112847 | Essential Splice Site | None | 270 | None | 10 |
The following transcripts of ENSDARG00000043816 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 22050933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20576514 |
GRCz11 | 12 | 20698388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTACTACATCCTCCATCCAGATTTTCTCAGATATGTGCGAAACAGG[T/C]ACATCCTGAAAATGCATAATTTATTCCTCTTTATGTTTCTGTAAATTTAT
Long Flanking Sequence:
TTAGAAATTTGCGTTAACAAGCAGTTGGACAGGTGTACCTAATAAAGTGGCCGGTGAGTGTATATTTTCTTTATGAAAATAAAATTGTGTTAGTGATGCTTAATCTCCCTTTTAAAAACCTTTGACTAATGTCACAAGTTTCAGTTCAGTTTTTCTGTCTTATAAATGAATGCAAATTGGCAAATATTAAATTAAATTCTGCCTCATTTTCATATTTCAACATACCATTTTAGAAAACATACAGAATTGTTTTGCAGTTATTAATATATTTGAGTTAATTATTACCCAGATCATCTGAGGTGTTTTTCTTATCCGCCAAAAGATTAAGCTTGTTTTTGAGGATTGCTGCTTACATCTAATGTAGATTGGATTAAATATCCCGTTAGATGATTATTTATTATTTCATATTTTGAAGGCCAAGGAAATATTACAGCGGGCATTTTAATGAAAGTTCCTACTACATCCTCCATCCAGATTTTCTCAGATATGTGCGAAACAGG[T/C]ACATCCTGAAAATGCATAATTTATTCCTCTTTATGTTTCTGTAAATTTATATATTGTGTTTTTGTTTTGTTAATAGTCAAGTTTACTTTTTCATCTTAGATTTCTTAGGGCTAAACAACTAAAAACAAAGCGGTGGTGGGTGGTCAGACCCACTAATGGAGCATTCACTCTTCTGTTGGCTATGCACACCTGTGACATTGTAAGTGATCTTTCTCTTTTTTTTAAGATTTATTTATAACTTCCCTTTTAGATTGAAGTCTTGTTTATTACTTTAATAGAGATTTTATCTGATGAACTGACCGTCTATCAGATAAACCGACCTTTATTGATTTTTATCATGTGAGCAGTTATTTTTTCCATCTGTTGAGCTGACGAATATTTTTATAACAGTGTTTTGTTTTTCCTGTTCTTATAGGTTAGAGTCTATGGCTTTTGCACGGCTGACTACCGGAAATATCCAAGCTACTATTATGACACCAAACACACTAAACTAGTGTTTT
Associated Phenotype:
Not determined