ZMP
mgat5
Ensembl ID:
ZFIN ID:
Description:
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A [Source:RefSeq peptide;Acc:
Human Orthologue:
MGAT5
Human Description:
mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase [Source:HGNC Symbol;Acc
Mouse Orthologue:
Mgat5
Mouse Description:
mannoside acetylglucosaminyltransferase 5 Gene [Source:MGI Symbol;Acc:MGI:894701]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13731 | Nonsense | Available for shipment | Available now |
sa24101 | Essential Splice Site | Available for shipment | Available now |
sa17972 | Essential Splice Site | Available for shipment | Available now |
sa10529 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13731
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105788 | Nonsense | 47 | 742 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 12105976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 11966144 |
GRCz11 | 22 | 11995826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAKTTCACCATCCAGCAGAGGGCGACGCATGAAAGCAGCGYGCAGCTA[C/T]GAAWGCAGAYACTGGACCTTAGCAAGCGAWACATTAAAGCCCTTGCAGAG
Long Flanking Sequence:
CTTGTAAGGGTCATTTAAGTGGTTATTAGGGTTATTTTGTTTGTGTGATTAGCTAGAACCATTTGAGAAGTAGTTTATGTTTTTAGACAGTTTTCATTTGATCAGACATTTTAGGTTTATTAATTTGGTGAGTGCTTGTATCCTAACTCTGACTTTTTTCTTGTTCTTTCTAGTGTCTTCACTGTAATGGAGCTTCTGGTGGGCATGTCTCTTGTTTGATTGACATCTCACGCTAAAAGGAATGGACTACAGTGAAGAAAAGAGCGCGTAGAGACCACACCCTCAAAACACAATGAGGCTGAACTCGTCTTGAGTTGCCCAGACACACACTCCACACACTCACACCAACAAACTGTCTCACCATGGGCTCCGTGTACTTGTGGAAGTTGTCTTCCCAAAAGTTGGGTTTCTTCCTCGTGAGTTTCGGCTTCATTTGGGGGATGATGCTGCTTCATTTCACCATCCAGCAGAGGGCGACGCATGAAAGCAGCGCGCAGCTA[C/T]GAATGCAGATACTGGACCTTAGCAAGCGATACATTAAAGCCCTTGCAGAGGAGAACCAAAGCGTGATGGATGGACCCTACGTAGGCACCATGACAGCATATGGTAAGTCTTTAAATTGCGATTTGTTTGTTGAAAAATTGCTGTGTGGAAGTATGTACGTGTATAGTTTTACTTTCCTGCCGTGGACAAGTCCTCCAGCATGGCGAACTGAGAAATGTAATATTAAGATCGCAGTGTTTGCAGAAAGATTGTAAACATGTCAACTTTAACCACACAGCTGTAGTTGACGTCTCATTATTAATATTTGTTTAAGAACATCTTCAGACTTTCCTTTAGCACAATATCTGCAAATTGGTTCAAACACATTATTCGTATTTCAGTTTTTTGTTGTTGTTTTTTAACACAATTTTTGATAATAATAGTTTGTTTAAAGGTTACATAAATGTGTTGCATAGTTTAAAAGTTAATGTTTGTTTTAAAAAAATTTACTGTTTTTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24101
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 |
---|---|---|---|---|---|
ENSDART00000105788 | Essential Splice Site | 270 | 742 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 12160256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12020424 |
GRCz11 | 22 | 12050106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGCTCACTTGCCAACAAACAAAACCTCCACCACCGCAAACGCAAGAAG[G/A]TGAGGCTAAACATAAAACTGTGTAAAAAAAAAATCATCATCTATGGTAAT
Long Flanking Sequence:
ACAACTGAAGTCAGAATGATTAGCCCCCATTTATTTTTTCCCCCTAATTTCTGTTTAAAGGAGAGAACTTTTTCAGCACATTTCTAAACATAATAGTTTTAATAACTCATCTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTTTTCAAGACACTTCTCTACAGCTTAAAGTGACATTTAAAGGTTTATAATTCTGACTGTGGTTTCTTTAATCTAGGAGAAACTAAACAGGAATAGAAATCATCACCTTAGTCTCCATCTGTCTGTTCTCAACTCACTTTAAATGTGTGGATTATTTTTTTTCACAGTTGGAGGTCCGCACAAGTTTTGACGAGTTGTATCGCGTGATGTCGCGGCGTGAGGAGTTTCGCTGGATGATGCTGCGGATCAAGCGGATGGAGGAGCCGTGGGTCAGCGCCGTTCGCTCACTTGCCAACAAACAAAACCTCCACCACCGCAAACGCAAGAAG[G/A]TGAGGCTAAACATAAAACTGTGTAAAAAAAAAATCATCATCTATGGTAATGTTGCTGCTGTTGTAGTTTTTAAGGAATATTACACAGTTTTGGAAAATCTACTCATTTTTAACAGTTAAACAGTTTAGTTCAGCAGATCTCCAGGTCTGGCGGAATTTTAGCTTAGCTTAGCATAGATCATTGAATCTGATTAGACCATTAACATTTCAGAACATTCAAAAAAGTTTTTAGGTAATTTTTCTATTTAAAGCTTGACTCTTTTGTTAGATCATGTAATAAGACCAGCGGAAAATGAAAAGTTACTATTATTTTTTTTAGGCTGGCTACATACACTCATTTTGCCGTAATCCATACCTGTCAACTTTCTCATTTTTCCCGGGATTCTCTTGTATTTTACATGTCTATCCTGCTATCATCCTGTAAAGGATTTTTTCAGTATTTCTCATTTATTTTCAATCTTTCTATGAAGAGTGGCAATAAATATCAAAGAGCCGATCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17972
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105788 | Essential Splice Site | 372 | 742 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 12167875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12028043 |
GRCz11 | 22 | 12057725 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCATATTTCTCGTCCTCATCTGGTGTTGTCGGCCTCTGTTGCGTTTT[A/C]GGTGWATGCTGCGTGTGCTGGACTCATTCGGGACGGAGCCRGAGTTCAAT
Long Flanking Sequence:
AGTACAGCCAATCAACAACGGTTAATATCAAATTATCTTGTTTACTCAGTTATTTTAACAACAAATCACTTTTTTCTTTCTTTCTGATGCTACACTTAAAGCAAAATTGGCTGGTTTTTGAAACTACTTATTTAAAATGAGTTGAAACAACACAATACTTGAGTATTTTTTGAGAACAGCATAATTATTTAGTGTTTGATCTACTTAAATTTTTAAAACAATTAAATGGGGCAGCTTGAAGGAATTGTGTGCACTCAAAAAATAATGTTTGCTATTTGTTCAATCTACTTATTTAAAATGAGTTGAAATGACCCAATTCATTTGCGACAACTTAATTGTTTTATTTTCAAGTCACTTAAATTTGTAAAAACGAACAAGTTGTCTTAAATTCTTCATGTTGTCCCAACACAAAAAGCAATCGTGTGGAACCCAGCATTTTTGACAGTGCATCAGCCATATTTCTCGTCCTCATCTGGTGTTGTCGGCCTCTGTTGCGTTTT[A/C]GGTGTATGCTGCGTGTGCTGGACTCATTCGGGACGGAGCCGGAGTTCAATCACGCTCACTACGCCCAGTCCAAAGGCCACAAGACTCCGTGGGGCAAGTGGAACTTGAACCCGCAGCAGTTCAACACCATGTTTCGTAAGTGTGCTTGAGAGAGGCTTTTCATGCATGTGTGTATGTGTGTGTGTGTGTGTCCCCCTGCTTTACCCTTTGGACATGGAAACGTGATCAGGGGGTTTTGGGGTTTTTTCGGGTGGCGTCTCTGATCGTCTCAGCCTCTGAATGGCTCTTTTGTTTACTAACAGACTTTGACATTCTCATAAAACCCGCGGCTCTCCAAGCAGAACTGCTCTTATTTCCGATTCCAGAACAGAGATTGTTTTCACTGAGACACGAGTTCCACTGAACAACATGTTTGAGTATTTTCATCAACTTGAAATAATCAATGAAAAGTTTGGTGGAGAATAAAAAAAAAAAGCTGTAAATTAGCCGTTTTCCGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10529
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105788 | Nonsense | 373 | 742 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 12167880)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12028048 |
GRCz11 | 22 | 12057730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTTCTCGTCCTCATCTGGTGTTGTCGGCCTCTGTTGCGTTTTAGGTG[T/A]ATGCTGCGTGTGCTGGACTCATTCGGGACGGAGCCRGAGTTCAATCACGC
Long Flanking Sequence:
AGCCAATCAACAACGGTTAATATCAAATTATCTTGTTTACTCAGTTATTTTAACAACAAATCACTTTTTTCTTTCTTTCTGATGCTACACTTAAAGCAAAATTGGCTGGTTTTTGAAACTACTTATTTAAAATGAGTTGAAACAACACAATACTTGAGTATTTTTTGAGAACAGCATAATTATTTAGTGTTTGATCTACTTAAATTTTTAAAACAATTAAATGGGGCAGCTTGAAGGAATTGTGTGCACTCAAAAAATAATGTTTGCTATTTGTTCAATCTACTTATTTAAAATGAGTTGAAATGACCCAATTCATTTGCGACAACTTAATTGTTTTATTTTCAAGTCACTTAAATTTGTAAAAACGAACAAGTTGTCTTAAATTCTTCATGTTGTCCCAACACAAAAAGCAATCGTGTGGAACCCAGCATTTTTGACAGTGCATCAGCCATATTTCTCGTCCTCATCTGGTGTTGTCGGCCTCTGTTGCGTTTTAGGTG[T/A]ATGCTGCGTGTGCTGGACTCATTCGGGACGGAGCCGGAGTTCAATCACGCTCACTACGCCCAGTCCAAAGGCCACAAGACTCCGTGGGGCAAGTGGAACTTGAACCCGCAGCAGTTCAACACCATGTTTCGTAAGTGTGCTTGAGAGAGGCTTTTCATGCATGTGTGTATGTGTGTGTGTGTGTGTCCCCCTGCTTTACCCTTTGGACATGGAAACGTGATCAGGGGGTTTTGGGGTTTTTTCGGGTGGCGTCTCTGATCGTCTCAGCCTCTGAATGGCTCTTTTGTTTACTAACAGACTTTGACATTCTCATAAAACCCGCGGCTCTCCAAGCAGAACTGCTCTTATTTCCGATTCCAGAACAGAGATTGTTTTCACTGAGACACGAGTTCCACTGAACAACATGTTTGAGTATTTTCATCAACTTGAAATAATCAATGAAAAGTTTGGTGGAGAATAAAAAAAAAAAGCTGTAAATTAGCCGTTTTCCGTATTTTGTG
Associated Phenotype:
Not determined