ZMP
mgat4a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate mannosyl (Alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyl
Human Orthologue:
MGAT4A
Human Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A [Source:HGNC
Mouse Orthologue:
Mgat4a
Mouse Description:
mannoside acetylglucosaminyltransferase 4, isoenzyme A Gene [Source:MGI Symbol;Acc:MGI:2662992]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8425 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21431 | Nonsense | Available for shipment | Available now |
sa34553 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8425
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 > C
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092435 | Essential Splice Site | 32 | 533 | 1 | 15 |
ENSDART00000133638 | Splice Site | None | 537 | None | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 7254394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7234487 |
GRCz11 | 9 | 7212878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCGTTTCTCAGTCTGTCCTGGTACACGGCTTGGCAAAATGGCAAAGG[T/C]GAGTCTCATCTGTGAGATCAGCTGTCAAATTGGGGTAAAGYTGGTTTTAT
Long Flanking Sequence:
TTGTGAGTGTCCCTTAGTGATTCATTTTCTAAGTAATAAGGTTACATGCATATTTAAACAGCGATCTGTCTAACTCCGTCAGTCTCTGCGGTCTGCACAATAAAAGCTGAGCAATACCTGCTGCTCTATTACTGTTTCATTAATTTCATGTCTCTCCCAGTAACGGCAGGCATGAGGATTGCACGTCTTTCTCTTGAAATGCATCAGTTCCGCTGGGCTGCCTCGTGACTCCAGCAGCGACCGAGAGGAGGAGGAGGAGGTGGTGGTGGAGGAGGAGGACTGGACCGCGGTGAAGACAACAGATGATCCGGGCCCCCGTCACCTCCTGTCCGCTCCTCTGAAGCGCGTCTGCTCGCCGGGATCAGGAGCACTAGAGGCGGCCGCACGGAGAGGCGTTGAAATGAGATGAGGCTCAGACATGGAACTGTTGCCACTGCGATTGTTTTCTTCACATCGTTTCTCAGTCTGTCCTGGTACACGGCTTGGCAAAATGGCAAAGG[T/C]GAGTCTCATCTGTGAGATCAGCTGTCAAATTGGGGTAAAGTTGGTTTTATTTTTCCGACATTCAGACTTTCTCCTTAATTTACTTTCATACAAGTTTTTTTTGCTCATATAAATAGTGAAATCATATTAGCAGCCAGTGACTATCAAAGTACACCATTGTTCACACTAAAATAGTCAAATAGTATTGAGGTAAAGTTGGTTTTATTTTCTGACTTAAATTCATTTAAAAATATGTAATATGAAAATATATTGTTTACTTTACTTTTTGTATTTGGTCTGTAATAGCATGCAAAGTATGACTTCAAAACAACATTAGCACTACTTCATTCAATTCACCTTTATTTCTAAAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATGTTTACTATGATCTTCTATGTGAAGCTTCTTTGACACAATCTACATTGTAAAAGCATTTTAGAAATAAAGGTGAATTGAATTCAACATAGAAGATCATAGTAAACTGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21431
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 |
---|---|---|---|---|---|
ENSDART00000092435 | Nonsense | 256 | 533 | 7 | 15 |
ENSDART00000133638 | Nonsense | 255 | 537 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 7156758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7136851 |
GRCz11 | 9 | 7115242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGACTATTCTTTTCTTATGATGTATGCTGTCAACAAAGGGGTCTATTA[T/A]GTCCAGGTAAATCAAATGAGTGAGTTTAAAGGTGAAGCTGGTGATCTGTG
Long Flanking Sequence:
TTGTAAACCACCAATACCAACACATATATGTGATTTTTAGCTTGACTGCGCATTGTTTAACATCGCAGTTCTTATTCTGTGCCACAAACTCACCGCTCATCCTCTTTATCTGAGCCATTCTGATCAAAGGAAATGAGCGCCTTTGATGCCCATCGCATTTAATATTCTGCCTTTTTGAATATTTATATCTCTCTCTTTCGAAACCCTTACTGCAAAGGACAACTCGATAGAAAAGGTTACACTGAGTACATGTGGGTGAGTTTTGTTTGTACCTTTATGTGGCTGTAGGAGTGTGTGTGTGTTTTGTGTTTTTGGCAGTCACACACCTGTCCATCTAGAGTTTCAGTTCTCTGACTCATCGACAGGTCAACTTCCACATTTAACCTTGGCTTTTAAGGCTGCTGAACATGATGTGTTTGTGTTTCTTTCAGATGGAGGACCAAGCAGAACTTGGACTATTCTTTTCTTATGATGTATGCTGTCAACAAAGGGGTCTATTA[T/A]GTCCAGGTAAATCAAATGAGTGAGTTTAAAGGTGAAGCTGGTGATCTGTGCACCACTAATGTTAATGAATGGAATTGAAAACTATAAACCTATAAAAACAAAAAGTGTTCAATAGTGGTTGGCTAATGAATTGATTGTAACTGTAATCCTACATGGTTGGTCCTTGCCAATCAACACCTACATCAGTTTCAGCTAATAGGGGTCATTTACATGACAATGTTTTCAGCCAAAAGCAGAACACTATGTGTTTTGCCTGGTTTGGGGACGGAAAACGTTTAAAAACTGTCTCAAAGTTGAAGTTTTTGAAAATGCCACCATTATCTAACAAGATGATGACAGTGTCAAATCACTCAGTTCCCATGACAGAGAGCTACAGCCCCGGAAATGTTAAGGTCTGGATACGAGAGAATGAAAACAACACTGGCAGATTCAGTTTAAGAATCCAGCTAGAGTTAAAACGGTAACACTTTATAATAACTACACATTATGAATCATTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34553
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 |
---|---|---|---|---|---|
ENSDART00000092435 | Nonsense | 346 | 533 | 10 | 15 |
ENSDART00000133638 | Nonsense | 345 | 537 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 7150455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7130548 |
GRCz11 | 9 | 7108939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTCACACTTGCTGTATGTGTGTTCCTCTTCAGAAACACTGTGAGAGA[C/T]AGAAGTCGAGTCTGCGCATTCGTTTCAGGCCCTCTTTGTTTCAGCACGTA
Long Flanking Sequence:
TTTACTTTCATAATCGCATTATTGTTGTTTTTACAACCTTTTTAATCATGTCAATGCAGCTTTGGTTAACATAAAAGAAAGAACATTTATTTGGTCATCTTAATTGATGTTGGTGTCGTTTTATCTTTCTTTCTTTCAGGTAAGATGTTCCAAGCCCCAGATCTAAATCTCATCGTGGAGTTTATCTTCATGTTTTATAAAGAGAAGCCCATCGATTGGCTGCTGGATCACATACTCTGGGTCAAAGTGTGCAACCCAGAGAAAGATGCCGTAAGTTAATACTCCCCGACCGCTTGCGTGACCTTCAGCTCTCCTCCGCTGTGGTGCATCAAGCAGAGAGACTTTTCACAGCTCTGAATGCAGCAGAAGAGGAACCTGTTTTTCTGATTTCTCCATTTTATCACACACACATCGTCATGCCTCTATATTCACTCTTAACTCTTATTTACCTCATTCACACTTGCTGTATGTGTGTTCCTCTTCAGAAACACTGTGAGAGA[C/T]AGAAGTCGAGTCTGCGCATTCGTTTCAGGCCCTCTTTGTTTCAGCACGTAGGCCTGCACTCCTCTCTGGCTGGGAAAATACAGAAACTCACGGTAATTTATGTCATGACTCTTGTGTTTTTTTTTTTGTTTTTTTTTTTTAAGTTCTGTTTACAACCAAGATAAACATCCATCGTGGTGAGCTAACCAGGAAGTTAAAATCCTTGTTACGTGATTACTTCAGTTGATATCCAGGACACGTTGTTTACACAACATATAGGTTTGGTGTTTATTCCCCAAAACAGCCTTTGAAGCTAGCTAATTTTTATATTGCTGATCACCAAGGTTATTATAGGTAACGAAAATGAACAGAAAAAGAAAACTAGATTTGAAAAACATTTTCGTTAACTGAAACAAAAAATATAAACTAACTGAAACCTTATTGTGTACATTAATGATGCGCGGATGGCGGTTAAATCCGCGGGCGCTGCGGATAATCCGCGGGTTGGGTAGTAAAAAATA
Associated Phenotype:
Not determined