ZMP
si:ch211-126g16.11
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC561028 [Source:RefSeq peptide;Acc:NP_001121717]
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;
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
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 (core 3 synthase) Gene [Source:MGI Sym
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10924 | Nonsense | Available for shipment | Available now |
sa34343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10924
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000139285 | Nonsense | 103 | 392 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 14115228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13560572 |
GRCz11 | 8 | 13598277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTTTACCGACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCCTGAT[A/T]AGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTCCTGCTGGTCATC
Long Flanking Sequence:
AACCTATAAAGTCGGCCAATTTCAAACCTTATGACTTTTTTCTGCAGAGCACAAAACAATGTATTTCATGTCCACACAAAAATATAAAAGACATAAAAAAACATCACAAAAGTAGTTTTTTATATACTTGTTTAGTGAACTTGCATGACTAACAATAATGTAAATTGTGTCTCTGTTCTTAAACAGGTGAAAAGATGAGAAAGAAGAATGTGGAATCTGCACTATTATTTCTAACAGGTGTCGTGTGCCTGCTCATTATCACCAACAAAAATGACTCTAAAGAAGATGATGTGAATCTAAAGAGCAAAAAAACAGAAGAAATCCTTCATAATCAAGAAGATTTCTCTAGAACTGAAACTCTTCCGCCATCGACTTCATATTGTCAGCCGAATATGTCATTTTATAAACTTCCTGAATTCTCCACTCTGCCAGATCATATCAAAGACTTTCTGCTTTACCGACACTGTAAGAGTTTTCCCATGATTCTCGATGTGCCTGAT[A/T]AGTGTGGTGGAGCTCAAAACTCTGCAGATGTCTTCCTCCTGCTGGTCATCAAGAGTTCTCCGGAGAATTACGATCGCAGAGAAGTTCTGCGGAAAACATGGGCTGAGGAGAGATTGCACAAAGGGGTGTGGATCCGTCGAATCTTCATAATCGGTACAAGTAGTAGTGGCTTAGGGAAACGCAGGATGAATAGGCTACTGAAGCTGGAGAACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTAGAGTGGATGGACAGAAGGTGCCCACACGCCAGATTCCTTTTAAATGGAGACGATGACATTTTTGCCAATACGTTTAACATGATCGAGTATCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGAACATCATTCAGAACGTAGGCCCTATAAGAAAGCGTTCAAGTAAATACTATATCCCGGTTCAGATACAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34343
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000139285 | Nonsense | 340 | 392 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 14114517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13559861 |
GRCz11 | 8 | 13597566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTGGCGTAAGAACTGCTGGTTTGCGTGTCCCAGTTGGAATTGTCGAC[A/T]AATTTGACCCTTGCTATTACAGAGAAATCCTTTTAGTCCACAGATTTCTG
Long Flanking Sequence:
ACAATGAGAACAAGGACATTTTACAATGGGACTTCAATGATTCATTCTTCAACCTCACACTGAAGCAGATCCTTTTCTTAGAGTGGATGGACAGAAGGTGCCCACACGCCAGATTCCTTTTAAATGGAGACGATGACATTTTTGCCAATACGTTTAACATGATCGAGTATCTTCAGGGTCAAGAAGACAATGATGGAAGTAGACATCTCTTTACTGGGAACATCATTCAGAACGTAGGCCCTATAAGAAAGCGTTCAAGTAAATACTATATCCCGGTTCAGATACAGGAGTCTGACATTTATCCTCCATATTGTGGTGGAGGGGGATTTCTACTGTCCGGCTTCACAGCCAGAACGATCTACAACATGTCACACTCTGTAATTCTGCTGCCCATTGATGACGTTTACATGGGAATGTGTCTGAAGAAGGCCGGCATCAAACCTACGTCCCATTTTGGCGTAAGAACTGCTGGTTTGCGTGTCCCAGTTGGAATTGTCGAC[A/T]AATTTGACCCTTGCTATTACAGAGAAATCCTTTTAGTCCACAGATTTCTGCCACACATGATTTTTGTGATGTGGGATGAAATACAAAACCCAAATTTGCGATGTGCAAAGAACAATTTCAAAAGAACAAAAGAGCAGGGTGTGTTTCAAAGGGAGATATAATAGCTTGCTGGATTCATTATGATCAGGATTTTTTAATGAATGTTGGCTTTTGAAAATGAGGTTGACTTTTGCACTTTAACTGGGTGGTTGATTCTTTCACAGCAATATTTATTGTATTCTTCATAGGCCTTATGTTTGTTTTAAAAAATCAAAGAGTGCTTTCAGTATACCTCATAAGTTGTAAAGCTGTCACTCAAAAGCTGAGAGGTAAATCTTTCTGCCTTGTTTGTTTTTTACCTTTTTACTTTAAGAGAGAACAAGTATCAAAATATCTCTTGCCCCTTCAAATCAATTTTATCAGGGGAATTACTGAGTACAAATAACTGTGGGTTACTTAAG
Associated Phenotype:
Not determined