ZMP
zgc:66030
Ensembl ID:
ZFIN ID:
Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:RefSeq peptide;
Human Orthologue:
MGAT1
Human Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:
Mouse Orthologue:
Mgat1
Mouse Description:
mannoside acetylglucosaminyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:96973]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9475 | Nonsense | Available for shipment | Available now |
sa19121 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9475
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123182 | Nonsense | 411 | 502 | 2 | 2 |
ENSDART00000123182 | Nonsense | 411 | 502 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 34164627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 35010403 |
GRCz11 | 15 | 34868372 |
KASP Assay ID:
2260-8814.1 (used for ordering genotyping assays)
KASP Sequence:
TTTGTGCCTTTTAMAAAAATGGACCTGTCTTATTTAGAGAAGGAGAAATA[T/G]GATGAGAGCTTTGAGAAGGARGTTTACGCTGCTTCACTTGTCACATTGGA
Long Flanking Sequence:
ATGGAATGAACTGTTTCTTTGCTGGCATCACAAGCCCATTTTTATTTTGTTAACTCTACGTTGGATCTCTTTCACCAGGTGGCCCCTGATTTCTTCGAGTACTTCAGAGCGCTTCATCCTATGTTAAAATCCGACCCGACGCTGTGGTGCGTGTCTGCCTGGAATGACAACGGCCGGGATGGATTCGTAGACCCTGGAAAAGCGAGCCTCCTGTACAGGACTGATTTTTTCCCAGGCCTGGGCTGGATGCTCACAAAAGACCTCTGGGCAGAGCTTGAGCCAAAATGGCCGGCCTCCTTTTGGGATGACTGGATGCGCCACCCTGATCAGCGCAAAGACAGATCCTGTATCAGACCGGAAATATCCAGAACGTTAACCTTCGGTCGAAAGGGTGTGAGTTTGGGGCAGTTCTACGACAAGTACCTCCGCTTTATTAAGCTCAACACCGAATTTGTGCCTTTTACAAAAATGGACCTGTCTTATTTAGAGAAGGAGAAATA[T/G]GATGAGAGCTTTGAGAAGGAGGTTTACGCTGCTTCACTTGTCACATTGGAGGACTTAAAGAGTGGTAAACTGTCTGGATCTGGCCCATTTCGGGTGCAATATTCTAGTCCGGACAGTTTTAAAAGTTTGGCTCGCAATCTCGGCGTAATGGACGACCTGAAATCTGGAGTCCCAAGAGCTGGGTATAGAGGAGCAGTCAGCTTTCTTTTACGTGGGAAGAGGGTTTATTTAGCTCCACCTGCTGGTTGGAGTCGGTATGATCCAAGCTGGAGTTGAGGTGGGCTGTGCCTGCTTCACATTTAAGGTGCAAAGCACACTAAAAAAATAATAATATTGCATGTAAACATCATTCCCTTCACAGCATTGATGAGATTAATTATCATTGTGCTGCTTTATGATGGAAAACCTCATTGAAGGGGTTTCAGGATGAACGCGATACCAAAGATTATAAACAAACCAACTTGTTGCCTCAGGTTTCATTATCATGTCTCAATGGTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19121
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123182 | Nonsense | 411 | 502 | 2 | 2 |
ENSDART00000123182 | Nonsense | 411 | 502 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 34164627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 35010403 |
GRCz11 | 15 | 34868372 |
KASP Assay ID:
2260-8814.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGCCTTTTACAAAAATGGACCTGTCTTATTTAGAGAAGGAGAAATA[T/G]GATGAGAGCTTTGAGAAGGAGGTTTACGCTGCTTCACTTGTCACATTGGA
Long Flanking Sequence:
ATGGAATGAACTGTTTCTTTGCTGGCATCACAAGCCCATTTTTATTTTGTTAACTCTACGTTGGATCTCTTTCACCAGGTGGCCCCTGATTTCTTCGAGTACTTCAGAGCGCTTCATCCTATGTTAAAATCCGACCCGACGCTGTGGTGCGTGTCTGCCTGGAATGACAACGGCCGGGATGGATTCGTAGACCCTGGAAAAGCGAGCCTCCTGTACAGGACTGATTTTTTCCCAGGCCTGGGCTGGATGCTCACAAAAGACCTCTGGGCAGAGCTTGAGCCAAAATGGCCGGCCTCCTTTTGGGATGACTGGATGCGCCACCCTGATCAGCGCAAAGACAGATCCTGTATCAGACCGGAAATATCCAGAACGTTAACCTTCGGTCGAAAGGGTGTGAGTTTGGGGCAGTTCTACGACAAGTACCTCCGCTTTATTAAGCTCAACACCGAATTTGTGCCTTTTACAAAAATGGACCTGTCTTATTTAGAGAAGGAGAAATA[T/G]GATGAGAGCTTTGAGAAGGAGGTTTACGCTGCTTCACTTGTCACATTGGAGGACTTAAAGAGTGGTAAACTGTCTGGATCTGGCCCATTTCGGGTGCAATATTCTAGTCCGGACAGTTTTAAAAGTTTGGCTCGCAATCTCGGCGTAATGGACGACCTGAAATCTGGAGTCCCAAGAGCTGGGTATAGAGGAGCAGTCAGCTTTCTTTTACGTGGGAAGAGGGTTTATTTAGCTCCACCTGCTGGTTGGAGTCGGTATGATCCAAGCTGGAGTTGAGGTGGGCTGTGCCTGCTTCACATTTAAGGTGCAAAGCACACTAAAAAAATAATAATATTGCATGTAAACATCATTCCCTTCACAGCATTGATGAGATTAATTATCATTGTGCTGCTTTATGATGGAAAACCTCATTGAAGGGGTTTCAGGATGAACGCGATACCAAAGATTATAAACAAACCAACTTGTTGCCTCAGGTTTCATTATCATGTCTCAATGGTAGG
Associated Phenotype:
Not determined