Busch Lab

ZMP

zgc:86586

Ensembl ID:
ENSDARG00000043482
ZFIN ID:
ZDB-GENE-040625-129
Description:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3-like [Source:RefSeq peptide;Acc:NP_00
Human Orthologues:
B3GNT3, B3GNT6
Human Descriptions:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 [Source:HGNC Symbol;Acc:13528]
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 (core 3 synthase) [Source:HGNC Symbol;
Mouse Orthologues:
B3gnt3, B3gnt6
Mouse Descriptions:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3 Gene [Source:MGI Symbol;Acc:MGI:215253
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 (core 3 synthase) Gene [Source:MGI Sym

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa41142 Nonsense Mutation detected in F1 DNA Not yet available
sa13454 Nonsense Available for shipment Available now
sa7610 Missense Mutation detected in F1 DNA Not yet available
sa41141 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41142
Status:
Mutation detected in F1 DNA
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
ENSDART00000063834 Nonsense 148 390 2 2
Genomic Location (Zv9):
Chromosome 8 (position 14052231)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13497575
GRCz11 8 13535280
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGGAAAACATGGGCTGAAGAGAGATTGCACAAAGGTGTGTGGATCCGT[C/T]GAGTCTTTATAATCGGTACAAGTAGAAGTGGCTTTGAGAAACACAGGCTG
Long Flanking Sequence:
ATATGTTTTGATACTAACAACACTATGATTTGTGTTTTTGTTCTTAAACAGGTGCCAAGATGAAAAAGAAGAATGTGGTGATGATTGCATTATTTCTGACAGGTCTCATGTGCCTGCTCATAACCATTAACAAAATAGAGTCTAAAGAGGATGTGAGTCCAAAGTGCAGGCGAATAGAAGAAATGCTTCATAATCTTACTAATTTTCCCAGAACTCAAACTCCTGAGCCATCATCTGCACCTTGTTACCCAAATATGTCAGCTTATAAACTTCCTGAATTCTCTACTCTGCAAGATCATATTAAAGACTTTCTGCTTTACAGACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCATGATAAGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTTTTGCTGGTTATCAAGAGTTCTCCAGAGAATTACGATCGCAGAGAAGTTCTGCGGAAAACATGGGCTGAAGAGAGATTGCACAAAGGTGTGTGGATCCGT[C/T]GAGTCTTTATAATCGGTACAAGTAGAAGTGGCTTTGAGAAACACAGGCTGAATAGGCTACTGAAGCTAGAGAACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTACAGTGGATGGACAGAAGGTGCCCGAACGCCAGATTCCTTTTAGATGGAGATGATGACATTTTTGCCAATACGTTTAACATGATCGAGTATCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGCACCTTTTGCAGAAAGTAAAGCCTATAAGAAAGCTTTCAAGTAAATACTATGTCCCAGTTCAGATACACGAGTCTAACAGATATCCTCCATATTGTGGAGGGGGCGGCTTTCTACTGTCAGGCTTCACAGCCAGAACGATCTACAAGATGTCGCACTCTATAATTCTGCTGCCCATTGATGACGTCTACATGGGAATGTGTCTGGAAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13454
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063834 Nonsense 156 390 2 2
Genomic Location (Zv9):
Chromosome 8 (position 14052207)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13497551
GRCz11 8 13535256
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAYTGCACAAAGGKGTGTGGATCCRTCGAGTCTTTATAATCGGTACAAGT[A/T]RAAGTGGCTTTGAGAAWCRCAGGCTGAATAGGCTACTGAAGCTRGAGAAC
Long Flanking Sequence:
ATGATTTGTGTTTTTGTTCTTAAACAGGTGCCAAGATGAAAAAGAAGAATGTGGTGATGATTGCATTATTTCTGACAGGTCTCATGTGCCTGCTCATAACCATTAACAAAATAGAGTCTAAAGAGGATGTGAGTCCAAAGTGCAGGCGAATAGAAGAAATGCTTCATAATCTTACTAATTTTCCCAGAACTCAAACTCCTGAGCCATCATCTGCACCTTGTTACCCAAATATGTCAGCTTATAAACTTCCTGAATTCTCTACTCTGCAAGATCATATTAAAGACTTTCTGCTTTACAGACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCATGATAAGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTTTTGCTGGTTATCAAGAGTTCTCCAGAGAATTACGATCGCAGAGAAGTTCTGCGGAAAACATGGGCTGAAGAGAGATTGCACAAAGGTGTGTGGATCCGTCGAGTCTTTATAATCGGTACAAGT[A/T]GAAGTGGCTTTGAGAAACACAGGCTGAATAGGCTACTGAAGCTAGAGAACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTACAGTGGATGGACAGAAGGTGCCCGAACGCCAGATTCCTTTTAGATGGAGATGATGACATTTTTGCCAATACGTTTAACATGATCGAGTATCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGCACCTTTTGCAGAAAGTAAAGCCTATAAGAAAGCTTTCAAGTAAATACTATGTCCCAGTTCAGATACACGAGTCTAACAGATATCCTCCATATTGTGGAGGGGGCGGCTTTCTACTGTCAGGCTTCACAGCCAGAACGATCTACAAGATGTCGCACTCTATAATTCTGCTGCCCATTGATGACGTCTACATGGGAATGTGTCTGGAAAAGGCTGGCCTCCAACCAACATTCCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7610
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063834 Missense 228 390 2 2
Genomic Location (Zv9):
Chromosome 8 (position 14051990)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13497334
GRCz11 8 13535039
KASP Assay ID:
554-4163.1 (used for ordering genotyping assays)
KASP Sequence:
TTTAGATGGAGATGATGACATTTTTGCCAATACRTTTAACATGATCGAGT[A/G]TCTTCAGGGTCAAGAAGACAATKATGGAAGTAGACATCTCTTTACTGGGC
Long Flanking Sequence:
TTGTTACCCAAATATGTCAGCTTATAAACTTCCTGAATTCTCTACTCTGCAAGATCATATTAAAGACTTTCTGCTTTACAGACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCATGATAAGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTTTTGCTGGTTATCAAGAGTTCTCCAGAGAATTACGATCGCAGAGAAGTTCTGCGGAAAACATGGGCTGAAGAGAGATTGCACAAAGGTGTGTGGATCCGTCGAGTCTTTATAATCGGTACAAGTAGAAGTGGCTTTGAGAAACACAGGCTGAATAGGCTACTGAAGCTAGAGAACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTACAGTGGATGGACAGAAGGTGCCCGAACGCCAGATTCCTTTTAGATGGAGATGATGACATTTTTGCCAATACGTTTAACATGATCGAGT[A/G]TCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGCACCTTTTGCAGAAAGTAAAGCCTATAAGAAAGCTTTCAAGTAAATACTATGTCCCAGTTCAGATACACGAGTCTAACAGATATCCTCCATATTGTGGAGGGGGCGGCTTTCTACTGTCAGGCTTCACAGCCAGAACGATCTACAAGATGTCGCACTCTATAATTCTGCTGCCCATTGATGACGTCTACATGGGAATGTGTCTGGAAAAGGCTGGCCTCCAACCAACATTCCATTTTGGTGTAAGGACCTTTGGTATGAATGTCCCAATTAAAAACGCAGACAAACTTGACCCTTGCTATTACAGAGAAATCCTTGTAGTCCATAGATTTCAGCCGCACATGATTTTTGTGATGTGGAATGAAATACAAAATCCAGATTTGCAATGCTCAAAGACACATTATTCTCTTCAGACAAGCACCACTAGCTCAGTATTTATGTGAACTATTCCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41141
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063834 Nonsense 255 390 2 2
Genomic Location (Zv9):
Chromosome 8 (position 14051910)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13497254
GRCz11 8 13534959
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGACATCTCTTTACTGGGCACCTTTTGCAGAAAGTAAAGCCTATAAGA[A/T]AGCTTTCAAGTAAATACTATGTCCCAGTTCAGATACACGAGTCTAACAGA
Long Flanking Sequence:
GACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCATGATAAGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTTTTGCTGGTTATCAAGAGTTCTCCAGAGAATTACGATCGCAGAGAAGTTCTGCGGAAAACATGGGCTGAAGAGAGATTGCACAAAGGTGTGTGGATCCGTCGAGTCTTTATAATCGGTACAAGTAGAAGTGGCTTTGAGAAACACAGGCTGAATAGGCTACTGAAGCTAGAGAACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTACAGTGGATGGACAGAAGGTGCCCGAACGCCAGATTCCTTTTAGATGGAGATGATGACATTTTTGCCAATACGTTTAACATGATCGAGTATCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGCACCTTTTGCAGAAAGTAAAGCCTATAAGA[A/T]AGCTTTCAAGTAAATACTATGTCCCAGTTCAGATACACGAGTCTAACAGATATCCTCCATATTGTGGAGGGGGCGGCTTTCTACTGTCAGGCTTCACAGCCAGAACGATCTACAAGATGTCGCACTCTATAATTCTGCTGCCCATTGATGACGTCTACATGGGAATGTGTCTGGAAAAGGCTGGCCTCCAACCAACATTCCATTTTGGTGTAAGGACCTTTGGTATGAATGTCCCAATTAAAAACGCAGACAAACTTGACCCTTGCTATTACAGAGAAATCCTTGTAGTCCATAGATTTCAGCCGCACATGATTTTTGTGATGTGGAATGAAATACAAAATCCAGATTTGCAATGCTCAAAGACACATTATTCTCTTCAGACAAGCACCACTAGCTCAGTATTTATGTGAACTATTCCTACTCAGCAATTATTGTAATGACTTTCATGCTTAACATAAAATAAGCTATAAAGCTGTCACAGGGCAGAATTCTAATGGACT
Associated Phenotype:
Not determined