ZMP
b3gntl1
Ensembl ID:
ZFIN ID:
Description:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 [Source:RefSeq peptide;A
Human Orthologue:
B3GNTL1
Human Description:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 [Source:HGNC Symbol;Acc:21727]
Mouse Orthologue:
B3gntl1
Mouse Description:
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1 Gene [Source:MGI Symbol;Acc:MGI:2
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39723 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17799 | Nonsense | Available for shipment | Available now |
| sa1977 | Essential Splice Site | Available for shipment | Available now |
| sa39722 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39723
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 |
|---|---|---|---|---|---|
| ENSDART00000063750 | Nonsense | 84 | 338 | 4 | 12 |
| ENSDART00000104222 | Nonsense | 125 | 379 | 4 | 12 |
| ENSDART00000143018 | Nonsense | 125 | 143 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57663922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56639361 |
| GRCz11 | 1 | 57354448 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTGTAGTGGGATATGCCAAAAACCAGGCTGTGAGTCAGAGCTCGGGA[C/T]GATTCCTCTGCTTTCAGGATGCGGTGAGTGTGTGTGTGTGTGTGTGTGTG
Long Flanking Sequence:
ATCTGATCACTCAATTGATTCAGTAACCTGAGCGCTCACTTGATTCATTAATCTGAACACTCATTTGATTCATTAATCTAAACACTCAGTTGATTTATTAATCTGAACACTCATTTGATTCAGTAATCTGATTATTTAATTGATTTAGTAATCTGAGCGCTCACTTGATTTATTGATCTGAACACTCATTTGATTCATTAATCTGAACACTTTTTTGATTCAGTAATGTGAACACTCATTTGATTCAGTAATGTGAACACTCATTAGATTCAGTAATCTGAACACTCATTTGATTCAGTAATCTGATCACTCAATTGATTCAGTAATCTGATCACTCAATTGATTCAGTAATCTGATCACTCAATTGATTCAGTAACCTGAGCGCTCACTTGATTTATTGATCTGAACAATCATTTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTTGTTCCTGTAGTGGGATATGCCAAAAACCAGGCTGTGAGTCAGAGCTCGGGA[C/T]GATTCCTCTGCTTTCAGGATGCGGTGAGTGTGTGTGTGTGTGTGTGTGTGTAATGGGTTCCACCTATGAATGTTAATACACTCCTAAATGCAAAGTGTGTTGTTGTGCTGTTCAAAGTATTGTGTGTGTATGAGTATTTATGTGTGTACATGAGTGTGTGTGAGTGTGAATGTGTGTAAATGAGTGTGTGTGTGTATCTGCATGAGTGTGTGAATGAGTGTACATTAGTGTGTTTGTGCAGCAGTGTGTGTGTGTGTGTGTACGCACATGAGTGCATGTATATGTGTGTGTGCGCATGATTGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCCGCTGTGTTTCTGCTGGGCGAGAGCAGATTCCCAGCGTTCCTGCAAACCTCACTGAGAGCTGATTCTGTCCGTCTGGAAAAGCAGAGCAGGGAAAACCCCTCAGAAATCACTGAACTGTAAAGCAGACCAGAGGAAACACACAGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17799
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000063750 | Nonsense | 147 | 338 | 7 | 12 |
| ENSDART00000104222 | Nonsense | 188 | 379 | 7 | 12 |
| ENSDART00000143018 | None | None | 143 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57657437)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56645846 |
| GRCz11 | 1 | 57360933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGATCGTTTCTGNNNNNNNNTGTGTGTGTGTNNNNTGTGCAGGTCTA[C/A]ACGTCTCATGGGCCGACCGTCATCATGCCGTCCTGGTTCTGCTCGCGCAG
Long Flanking Sequence:
TGAAATATTTTATACATTTTTGTTGTGCAATGATGATAGCTCCTTGGCTTTTTAGCTAAAATTTTAACAGTTTGTTTATATATAACACAATAGTTTTAATGTTGTAATGTTCGTATGCGATCAGCTTGTAGCACAATAAGATAAATGAGGTAAAATCGTTGTATTCATATAAAGTTTAGCAGCAACCATAGGTAACTGATGCCTAATGTTTCTATAGATCAGAGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTCCTACCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCACGTGATAATTACAGGCAGGTGTGTTTGATATGGGTAGGAACTGAAATCTGTAGAAAGGTGGCTCTCCAGGAACGGGGTTGGCCACCCCTGCTTTAGATCCTCAGGACATCTGTTTTAAACACAGTGTCACTTTGATCGTTTCTGACCATGTGTGTGTGTGTGTGTGTTGTGCAGGTCTA[C/A]ACGTCTCATGGGCCGACCGTCATCATGCCGTCCTGGTTCTGCTCGCGCAGCTGGTTTGAGAAAGTGGGTCAGTTTCACGAGGGAGGCAAGGTGAAGCTCTGCTCAACACACAATAGCTCTTTTCACACAGTAAATATCTGGAAGATTTAAGGAACGACTTTACCGGCAAATTAAAAAAAAGTACTGTTCACACAGACGAGGACGTTACGGAATTTTTCCGGAAAAGATTGTTCACACATCCATTCCAAAACACCGGAAAATTCTGACATCATAAACCATGATGAGAAATGAGCTCTAAACAGCTGCGCTTGTGTTGGTAAACATTCGACTACATTACAAATACAATCGATTCATGTTGATCCTGAGAGGCTGCTGGAGAGATTCACACGCCGCTGACACACAGCTGGACTTAAACCCCTTATTAAAGTGATTTTTGCATAATAAAGCCTGTTTCATCTCTTCTGTTCAGGGCGTTCCTGAAGATCTGCTCTTCTTCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1977
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 |
|---|---|---|---|---|---|
| ENSDART00000063750 | Essential Splice Site | 312 | 338 | 11 | 12 |
| ENSDART00000104222 | Essential Splice Site | 353 | 379 | 11 | 12 |
| ENSDART00000143018 | None | None | 143 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57653994)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56649289 |
| GRCz11 | 1 | 57364376 |
KASP Assay ID:
554-2720.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTTCACTTCAGAAACGCCTCGCCACCATTTATTGTGTGTGTCAAACTG[G/A]TGAGTGTGTGTTTGTGTGTGTGNNNNTGTATGTGTTAGTGTGTCTGTATGTA
Long Flanking Sequence:
TACACTCACCGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGCAAATTCCTAATCAGCCAATCACACGGCAGCGACTCAATGCATTTAGGCATGTAGACATGGTCAAGAGGATCTGCTGCAGTTCAGAGCGAGCATCAGAGTGTAGATATTGATGAATAACATTATTAGAGGGGCTTTGAAAACATGTTTACCGGTTGATCAACACACAGACGGCCTATCGGCGTCCACCTGACTGTAGATGATTTAAAGAGACAGGCGCATGCGTTAGGTCTGGATGCGATTTAATATTTTTATTACAATGACTGCTCAATATTACAGTAATATACATTATAATGCTGTATGTACACTAGATTCTCACACGTCTGGTCTAAATGTGAGTGTGTGTTGTGTGTTTAACTCTTTCTGTTTCTCTCAGGAGCGGCCAAAGCCGAAGATTCCTGTCCTTCACTTCAGAAACGCCTCGCCACCATTTATTGTGTGTGTCAAACTG[G/A]TGAGTGTGTGTTTGTGTGTGTGTCTGTATGTGTTAGTGTGTCTGTATGTATCTGTGTTTATATATTTATATGTGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTATGCAGGACATGACAGATGGAGTTCTGGAGGGAAATCTTCATTCTCTGCAGCTCACAGAGGGAGTCCATTACTACCATTTCAACTGACGACAGTGTGTGTATGTGTGAGAGAGAGAGAGAGTGTGTGCATGCGACTGTGTGTAGGTGACAGAGTGTGTATGTGAGATAGCATGTGTTTGAGGGAGACAGTCAACAAGAATGAGAGCTCAGGTACCTCATATGAACTCAACAGCGTCTTCCTGAAATGCAGAGAATGCCAAACCTTCTGTCAGAGTCTGGGAAACAGCAAGAAGAGTGTGTGTGTGTGCGGGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTTTTCGGATACTAAAGATCTGGGAAAAGCTTCAGACTGTATTTCCCAGAG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa39722
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 |
|---|---|---|---|---|---|
| ENSDART00000063750 | Nonsense | 334 | 338 | 12 | 12 |
| ENSDART00000104222 | Nonsense | 375 | 379 | 12 | 12 |
| ENSDART00000143018 | None | None | 143 | None | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57653811)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56649472 |
| GRCz11 | 1 | 57364559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTGGAGGGAAATCTTCATTCTCTGCAGCTCACAGAGGGAGTCCATTA[C/A]TACCATTTCAACTGACGACAGTGTGTGTATGTGTGAGAGAGAGAGAGAGT
Long Flanking Sequence:
CTTTGAAAACATGTTTACCGGTTGATCAACACACAGACGGCCTATCGGCGTCCACCTGACTGTAGATGATTTAAAGAGACAGGCGCATGCGTTAGGTCTGGATGCGATTTAATATTTTTATTACAATGACTGCTCAATATTACAGTAATATACATTATAATGCTGTATGTACACTAGATTCTCACACGTCTGGTCTAAATGTGAGTGTGTGTTGTGTGTTTAACTCTTTCTGTTTCTCTCAGGAGCGGCCAAAGCCGAAGATTCCTGTCCTTCACTTCAGAAACGCCTCGCCACCATTTATTGTGTGTGTCAAACTGGTGAGTGTGTGTTTGTGTGTGTGTCTGTATGTGTTAGTGTGTCTGTATGTATCTGTGTTTATATATTTATATGTGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTATGCAGGACATGACAGATGGAGTTCTGGAGGGAAATCTTCATTCTCTGCAGCTCACAGAGGGAGTCCATTA[C/A]TACCATTTCAACTGACGACAGTGTGTGTATGTGTGAGAGAGAGAGAGAGTGTGTGCATGCGACTGTGTGTAGGTGACAGAGTGTGTATGTGAGATAGCATGTGTTTGAGGGAGACAGTCAACAAGAATGAGAGCTCAGGTACCTCATATGAACTCAACAGCGTCTTCCTGAAATGCAGAGAATGCCAAACCTTCTGTCAGAGTCTGGGAAACAGCAAGAAGAGTGTGTGTGTGTGCGGGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTTTTCGGATACTAAAGATCTGGGAAAAGCTTCAGACTGTATTTCCCAGAGTCCTCAGCTTGAGAAACATCTCACATCCCTCTCGCACCTAGATTCAAACACTCACACACTCACACACACACACACACACACACACACACACTGTTTGCATTCCTGCTGCAGCGTGTCGCTGCATTTCTCCGTCATTCCTGAGTGACGTCATTCTCAAAATAAAGCTCTTTCCCGCAGAGCTGT
Associated Phenotype:
Not determined