ZMP
b3gat3
Ensembl ID:
ZFIN ID:
Description:
beta-1,3-glucuronyltransferase 3 [Source:RefSeq peptide;Acc:NP_001015059]
Human Orthologue:
B3GAT3
Human Description:
beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I) [Source:HGNC Symbol;Acc:923]
Mouse Orthologue:
B3gat3
Mouse Description:
beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I) Gene [Source:MGI Symbol;Acc:MGI:1919977
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26951 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17161 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26951
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025582 | None | None | 326 | None | 7 |
| ENSDART00000109696 | Nonsense | 318 | 328 | 5 | 5 |
| ENSDART00000122164 | Nonsense | 320 | 368 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 26193918)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 24755670 |
| GRCz11 | 7 | 25026827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCCGGACTGAGAAGCCAAAGATGAAGAGAGAAGAAGCTTTGCTGAAG[C/T]AGGGGATGGGCTCTGATCCGGATGTGGAGGTGTGAGCAGAACATGCCCGA
Long Flanking Sequence:
CCCAAACTACGTTACACCTTTAAACCGGTTATTGTCCCATGCCTATCATTGACTTTATTTTATGAATCACCAAGTACTACCTTTTTACCTAAAATTCTTCTTTAATGCTGAAGAGAAAAAGTCACCATCTTGAATGAGTTCTGAAGGTAAATAAACTATCAGCAGAATTGTGTTTTAGGGCGAACAGCCACTTAAAGAATGCTTTATAAAGTCCACTTAAGTTACTGATTGCCATGACCTACTTCTACAAATAGTTGTTCAGCAATTTAAACTTGAAATTCCTGTGCGGACAATAAATTTGAAATTGCTCATGAACTAAAAGCCAGCCAGTTCCTAAACTCTGAGTGTTGCCCAACCCTTTTTGCAACGAGGGTGAGTAAAAAATGACTTTTTTTGCCGAAATGATGCTTTTTTTTGTTTTTCAATGCTCTTCTCAGGTGCTGGTTTGGCACACCCGGACTGAGAAGCCAAAGATGAAGAGAGAAGAAGCTTTGCTGAAG[C/T]AGGGGATGGGCTCTGATCCGGATGTGGAGGTGTGAGCAGAACATGCCCGAACTTCACCAAACATCCACACTTCCATTGTGCCAAACACATTCTCTTATTTATCTGGCAAGAGCTGAAGCTTGTAATGTAATGCAGACACTATAAATGTGAACTCTGGCCTACAAACCAAAGACATGAGGAATGAGGAAAGAAAATGATGAATGCATAGATAAGAAAAGCAGGAGATGCACACAGAACAACCCGTGACTTAAATGCAAATGGCTTGCTAGAAATCATTTTACATTTCAGAATCCATGCTTATCATCTGAATAGTATTTAAAGAATTTTACAGGCACGCAAGTTGAGCTTGTGTCGATGTTTTTAGAAATGTATAAAAGTTTGCCGGGATTATATTTATTACTCATTGTTATGTCTATGCTCTCCATGTCTCTATTACATTAGGTGTTCTTGTCCTATGTATTAAGTCTTAAAGGGATAGTTCACCCAAACATACCAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17161
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, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025582 | None | None | 326 | None | 7 |
| ENSDART00000109696 | Missense | 328 | 328 | 5 | 5 |
| ENSDART00000122164 | Essential Splice Site | 329 | 368 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 26193948)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 24755700 |
| GRCz11 | 7 | 25026857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAAGAAGCTTTGCTGAAGCAGGGGATGGGCTCTGATCCGGATGTGGAG[G/A]TGTGAGCAGAACRTGYCCGAACTTCACCAAACATCCACACTTCCATTGTG
Long Flanking Sequence:
ATTGTCCCATGCCTATCATTGACTTTATTTTATGAATCACCAAGTACTACCTTTTTACCTAAAATTCTTCTTTAATGCTGAAGAGAAAAAGTCACCATCTTGAATGAGTTCTGAAGGTAAATAAACTATCAGCAGAATTGTGTTTTAGGGCGAACAGCCACTTAAAGAATGCTTTATAAAGTCCACTTAAGTTACTGATTGCCATGACCTACTTCTACAAATAGTTGTTCAGCAATTTAAACTTGAAATTCCTGTGCGGACAATAAATTTGAAATTGCTCATGAACTAAAAGCCAGCCAGTTCCTAAACTCTGAGTGTTGCCCAACCCTTTTTGCAACGAGGGTGAGTAAAAAATGACTTTTTTTGCCGAAATGATGCTTTTTTTTGTTTTTCAATGCTCTTCTCAGGTGCTGGTTTGGCACACCCGGACTGAGAAGCCAAAGATGAAGAGAGAAGAAGCTTTGCTGAAGCAGGGGATGGGCTCTGATCCGGATGTGGAG[G/A]TGTGAGCAGAACATGCCCGAACTTCACCAAACATCCACACTTCCATTGTGCCAAACACATTCTCTTATTTATCTGGCAAGAGCTGAAGCTTGTAATGTAATGCAGACACTATAAATGTGAACTCTGGCCTACAAACCAAAGACATGAGGAATGAGGAAAGAAAATGATGAATGCATAGATAAGAAAAGCAGGAGATGCACACAGAACAACCCGTGACTTAAATGCAAATGGCTTGCTAGAAATCATTTTACATTTCAGAATCCATGCTTATCATCTGAATAGTATTTAAAGAATTTTACAGGCACGCAAGTTGAGCTTGTGTCGATGTTTTTAGAAATGTATAAAAGTTTGCCGGGATTATATTTATTACTCATTGTTATGTCTATGCTCTCCATGTCTCTATTACATTAGGTGTTCTTGTCCTATGTATTAAGTCTTAAAGGGATAGTTCACCCAAACATACCAATTTCCTGACAATTTACAAGTGATTCCAATCTTTT
Associated Phenotype:
Not determined