ZMP
mgat4b
Ensembl ID:
ZFIN IDs:
Description:
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B [Source:UniProtKB/Swiss-Pro
Human Orthologue:
MGAT4B
Human Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B [Source:HGNC
Mouse Orthologue:
Mgat4b
Mouse Description:
mannoside acetylglucosaminyltransferase 4, isoenzyme B Gene [Source:MGI Symbol;Acc:MGI:2143974]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35655 | Essential Splice Site | Available for shipment | Available now |
sa14606 | Essential Splice Site | Available for shipment | Available now |
sa22441 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35655
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001159 | Essential Splice Site | 33 | 547 | None | 15 |
ENSDART00000115340 | Essential Splice Site | 33 | 121 | None | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 14436421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16448371 |
GRCz11 | 14 | 16754024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGGCTTATATCGTTATCCTGGTACACCGCATTCAGCAATTCCAAAGG[T/C]AAGACCCACGGCTGGAAGCGCGTGTTTACGCTAAAGCAAACGCATCATGT
Long Flanking Sequence:
ATACAATAATGAGGAGATAAACAATGTCAAACCGTAGTTTTTGAGACATTAATTAAAATATAAGAAAACATAAATCCAATCCAAAACACCAATTGTTTTAAAACAGAATATGTGTGTTTCTCTTTTGACCGCACGGAGGAGCAACTGCACCTCTGCACGAGTCCAGCGTTCACCCAAAACACTCTCTCTCTCTCTTTCTCTCTCTCAAACACGCTCACACACACCCTCCTTATAAACGACATCTGTCTGTACACAGGATCTCGCATTCTCGCCCTCCCTCTCATCATCTCATGTGCGCGCGCTGTCATTAACGCACGCACGCACGCACCGCATCAGCAGCGCACGCCAGACGCGCTCGAGCACACGGTTCGGTTCGGACATGATACCGGCGCGGACCCGGAGATGAGGCTCAGAAATGGCACCTTCCTAACAGTCTTACTCTTCGGGTTATGTGGGCTTATATCGTTATCCTGGTACACCGCATTCAGCAATTCCAAAGG[T/C]AAGACCCACGGCTGGAAGCGCGTGTTTACGCTAAAGCAAACGCATCATGTGTGGAAATGAAATGCTCCTCTTGCGTTCTGTCATGCATTCAAATGCGCCACTGAAGCGCTTGAGCTGCAAAACACTGAACAGCTGTTCAACGCAACGCTGCTTCTGCTGCTTGGCGTGTTTGTGTTTGTGCACCGTATGCCTTCAACTGCTCCTCAAACTATTAAAGAGGCCTGCTGAGGTTTCCCAAAGCACCACATAACGTTATAATCGATGTTAACGGTTTATTTTGGAAGCGAATCTACTGTTGTCCAAAGAACCAATTTCTTCTGAGATGTTTGCTTGTTAGTTTGGTTGGGCTTTGATTGATCTGCACGTTTTCATACAAGGAACCTACGTTACGTTTTCTGTCAAGAGATTTTTTGCTTGGTTCTTGAGAGGTTGTATTGAGTTTTGAGGATTTTTAAAGGAGTCTTAAGCTGTTCAAGATGCATTTCATGAAGAACCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14606
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001159 | Essential Splice Site | 93 | 547 | 3 | 15 |
ENSDART00000115340 | None | None | 121 | None | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 14293948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16305898 |
GRCz11 | 14 | 16611551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGACCATGGCATGCATTTATGTGTATCCATGTCGTCTCTCTCTCTCNN[A/G]GAKGAGACCAAGCTGAAGTTGTGGAACGTGACCAGCAGTAAGAATGTTCT
Long Flanking Sequence:
ACAAAAGGGTTACCAAATAAATATTTAAACCAAGTTCTAAATTTCAAAGATATAAACTAATTCTAATAACAAAGGTTGTATGTTAGAGGATTGTTTAATTTATTAATTGTTTTGCTTTTGTTGATTAGAGGCCAAAGAAATGTTGATACTGTACATTTTTATGTAAATTATTATAATTACCTAAATTATGATATAGTATGAGCAAAAGCTTTTAATCACAGTCCAGGGCCACTTAATAGTTTAAAAAACTGTTCCAAACCTTTTTACTCGAGGTAAATTCACTTTCAATAGTAATACTGCATACTTGAGTTTTCAACATTTTTAAAAATATCTACTTTTGTCTTCAACATTTGAAAGAATCTCAAACAACTAAGGATGAGTAAATGACTGCAAAGTCAATGATAGCAGATAGCGGAATAATACTTTTTGCTGACCTGCCCCTTTAAGTCATTTGACCATGGCATGCATTTATGTGTATCCATGTCGTCTCTCTCTCTCTC[A/G]GATGAGACCAAGCTGAAGTTGTGGAACGTGACCAGCAGTAAGAATGTTCTTCAGCTGCCCAGCATCTTCCACCATCTGCCACATTTGCTGGCCAAGGAGAGCAGCCTTCAGCCGGCGGTGCACATCGGCCAGGGTCGCACCGGAGGTGAGGAAACTAGCCTCTCTGATGCATTTGATATGTTTCATTACATTCTCCTCCAGGCCTGTCCAGTTTGCATAAATGTGGGTTTAGCGCCTCCAGTGACCTGCAGCTGTCAGATGAGTTCATGCGATATTGTTGTGTTTTTGTATTCAGTGACTTTTAGGCGAGTGTTGTTGAATGCGCAAACAAGGCCCAGTTTTACTCTTTATATTAAGCTGTACTTCAGTTCATCCTTTCACAAGTGAATGACACTAAATAATTGTAAACAGGGTGTAAAACTTTAACTCAAGAGCTGCAGAGGCAGTCATTTTGACTGTTTTTAAATGTTGCATTTTGATAACATTAAAATAAAACCCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22441
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 |
---|---|---|---|---|---|
ENSDART00000001159 | Nonsense | 190 | 547 | 5 | 15 |
ENSDART00000115340 | None | None | 121 | None | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 14270098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16282048 |
GRCz11 | 14 | 16587701 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTAAACTATTGATTCTTGCTTTGTTTTTTTGCAGACGGATCAACAATA[T/A]GCAAATAGCGTTGCTGACAACCTTAAGCGCCTGTAAGTAGCCTGTTTTTA
Long Flanking Sequence:
GGTACACCAACAGTACATATTTTAAACATTTAGTTTGCATCAAAAAATAAAGCAGTTTTTAAGCAACCTTGAAAACAAAAATCTGATTGAGGAAAATAAAAGATGTTATTCAAATGTTTGCTATAGTGCCTCTTGTGGAAACTCAGAGTATTTTCGTACTTAAGTTGCATTTTGAACGAAGCGTGAAATTGAATCTGAACAGTTAAATCCATCTGCTGCTTTATAGTGGAAAGTGCTTCGGCAGCTCATGATCATTTGCTTCCATTATTGGACAGTTAAAGTTCCCCTCTTGACTACAGAGACCGTATAATCTCTTTAGCAGAAAAAGTCAGGAAATGAGAACCGACATTGAACTTACAACATCCTTCCAAAAAACTGATACAAACACTTGTCTAGCCCAAAGGTGAACATTTGTTTTTAGGGGGAGAACATTTGTGACGCATAAAAGTTAATTAAACTATTGATTCTTGCTTTGTTTTTTTGCAGACGGATCAACAATA[T/A]GCAAATAGCGTTGCTGACAACCTTAAGCGCCTGTAAGTAGCCTGTTTTTATTATCACTACACAATATGCTTTAGTTTTGCTGAGACATCTGTGTTTGTGTTTGAGTGAGAGATCAATCATGTGACTGTAGACTTTCCTCACATGCTTTTTGAGGACAATAGCAGAATAAAAAACATAAGGGTAAATTTGTCCTCTGGGTGTTTGAGATCTTCTGCTTCATTCTGCTCGTCCCACATTAGTCATGTGCTTGTGTTTACATTGATTTCTGCAGAGACTTACAATACAGGATCTTTGTGCAGGGGTTTTGATTAGATCTTTTGTTTGGATTATGTGTGTAATGTGGATGCAGAGTTATTGAAATTTACAAAAACTAACTAACTAACTAACTAACTAACTAACTAACTAACTAACTAACTGTTAATGATATGAAACAAAATAAACCATTAAAAAGGCAAAATTTTCATTTTAATCTAATTAGTTTATACACTCACTGGCCACTT
Associated Phenotype:
Not determined