Busch Lab

ZMP

zgc:101663

Ensembl ID:
ENSDARG00000037852
ZFIN ID:
ZDB-GENE-041114-149
Description:
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C [Source:UniProtKB/Swiss-Pro
Human Orthologue:
MGAT4C
Human Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme C (putative) [S
Mouse Orthologue:
Mgat4c
Mouse Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme C (putative) Ge

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa32418 Nonsense Available for shipment Available now
sa608 Nonsense F2 line generated Not yet available
sa32419 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa32418
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000055148 Nonsense 81 454 4 4
ENSDART00000114000 Nonsense 81 454 3 3
Genomic Location (Zv9):
Chromosome 23 (position 408707)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 379698
GRCz11 23 392491
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGTGTGTGATATGTTTATTCAGAGTACCTCACGGTGGGCTTGTCGT[C/A]GGTGAGAAGAGAGAAGGGGTTTTACCTCCATGACACCCTGCAATCCATCT
Long Flanking Sequence:
AAACACTGCCCTCTGGAGCTGATGACTTTACAATACAGTCCAATGATTCAATGAGAGAAAAGAGCAGAATAGTTTACATTCAACAAACTTAACACACTCAAATGAGTTTAACTGTGTTCAGTATTCAGGGGGAAATATTAAGGCAGACCTATTCTGCCCATATCTGCAGCATGCATCTATGGTGTGTCTACAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGCTGAGAACAGCACACAGATGATGTCCTCCTCCTCTCTGAAACTGACCCTTTCAGGCTTTGATCCTGATCGTGGTGTTTTGGTGACTGTCGCTTTAAATGCAAATGAGATGTTCAAGCCATGACTTTACTTAAGAGGCACTACTGTATTATTAAGCGAAACAAGTATCCCATAATCCCTCTGTGTGTGTGATATGTTTATTCAGAGTACCTCACGGTGGGCTTGTCGT[C/A]GGTGAGAAGAGAGAAGGGGTTTTACCTCCATGACACCCTGCAATCCATCTTCTCCGAGTCCTCAGAGGAAGAGCTGGATCAGATGGTGGTGGTGGTTCTCCTTGCAGACTTTGACTTACCCTGGATCCAGCAAACCGCGGACAAGATCAGCCGAGAATTCGCCGTTCAGCTCTCTAAAGGCCGTCTGCTGGTCATCCACGCAAATAAAGAGCATTATCCTCCGCTGACCGGATTAAAGAGGAATTTTAATGACGCTCCAGACCGCGTATCCTTCCGCTCCAAACAAAACGTGGATTATTCGTTCTTGCTACACTTCAGCAGCAACCTCTCGCAGTACTACATCATGCTGGAGGATGACGTGGGATGCTCCAGAAACTTTCTGTCAAGCATTCAGCAACACATTCGCTCCATGACGGACTCCAAATGGGTGACGTTGGAGTTTTCCAAACTGGGCTACATCGGGAAACTCTACCAATCCAAAGATCTGCCCACTCTGGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa608
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000055148 Nonsense 289 454 4 4
ENSDART00000114000 Nonsense 289 454 3 3
Genomic Location (Zv9):
Chromosome 23 (position 409332)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 380323
GRCz11 23 393116
KASP Assay ID:
554-0518.1 (used for ordering genotyping assays)
KASP Sequence:
GATAAAGTCATCCGCTTCCGGCCGTCTTTGTTCCAACACATGGGMACGTA[T/A]TCGTCATTTCGGGGAACGTACAATCGCTTAAAAGATGAGGACTTTGTTCA
Long Flanking Sequence:
ATCCAGCAAACCGCGGACAAGATCAGCCGAGAATTCGCCGTTCAGCTCTCTAAAGGCCGTCTGCTGGTCATCCACGCAAATAAAGAGCATTATCCTCCGCTGACCGGATTAAAGAGGAATTTTAATGACGCTCCAGACCGCGTATCCTTCCGCTCCAAACAAAACGTGGATTATTCGTTCTTGCTACACTTCAGCAGCAACCTCTCGCAGTACTACATCATGCTGGAGGATGACGTGGGATGCTCCAGAAACTTTCTGTCAAGCATTCAGCAACACATTCGCTCCATGACGGACTCCAAATGGGTGACGTTGGAGTTTTCCAAACTGGGCTACATCGGGAAACTCTACCAATCCAAAGATCTGCCCACTCTGGCTCGATTCCTGTACAACTTCTACCAGGAGATGCCCTGCGACTTTCTGCTGTCGCATTTCCGCAGATTGCTAATGCAGGATAAAGTCATCCGCTTCCGGCCGTCTTTGTTCCAACACATGGGAACGTA[T/A]TCGTCATTTCGGGGAACGTACAATCGCTTAAAAGATGAGGACTTTGTTCAGGAGCTTGCTGACAATCCTCCAGCGGATGTCAGAACTAACATTCAGGTATTTCAGACTTACGTCCCGGAGAAAGCGTACAGTCAGGATGTGGAGTACTTCTGGGGTGTTTCCCCGATCGGGACTGAAAGCTTCTTCTTGGTGGTGTTTCGGGAGGCGGTGCGCATCTCTCGAGTGCAGATACACACTGGATCGGATGGGAAAGACGAGCTGGCGTCTGCTGATGTGGAGTTGGGGAGGGTTTTGGTGACAGGAGAGCCTGCGGTGGATTGCTCTGGGTTTAAGACGCTGGGTTCTCTTCAGCACGGTCAGTTTAATGAAGAGGGGGTTCAGAAGCTGCTGCCGGACGCTGTGGTGTGTTTACGCATCAGAGTCACCGCTGCTCAACCTGAGTGGGTGATTATTAGCAGGATACAGGTCTGGACTGTTAAAGAAGACAAGACCATCTGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32419
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000055148 Nonsense 426 454 4 4
ENSDART00000114000 Nonsense 426 454 3 3
Genomic Location (Zv9):
Chromosome 23 (position 409742)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 380733
GRCz11 23 393526
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTAATGAAGAGGGGGTTCAGAAGCTGCTGCCGGACGCTGTGGTGTGTT[T/A]ACGCATCAGAGTCACCGCTGCTCAACCTGAGTGGGTGATTATTAGCAGGA
Long Flanking Sequence:
CGACTTTCTGCTGTCGCATTTCCGCAGATTGCTAATGCAGGATAAAGTCATCCGCTTCCGGCCGTCTTTGTTCCAACACATGGGAACGTATTCGTCATTTCGGGGAACGTACAATCGCTTAAAAGATGAGGACTTTGTTCAGGAGCTTGCTGACAATCCTCCAGCGGATGTCAGAACTAACATTCAGGTATTTCAGACTTACGTCCCGGAGAAAGCGTACAGTCAGGATGTGGAGTACTTCTGGGGTGTTTCCCCGATCGGGACTGAAAGCTTCTTCTTGGTGGTGTTTCGGGAGGCGGTGCGCATCTCTCGAGTGCAGATACACACTGGATCGGATGGGAAAGACGAGCTGGCGTCTGCTGATGTGGAGTTGGGGAGGGTTTTGGTGACAGGAGAGCCTGCGGTGGATTGCTCTGGGTTTAAGACGCTGGGTTCTCTTCAGCACGGTCAGTTTAATGAAGAGGGGGTTCAGAAGCTGCTGCCGGACGCTGTGGTGTGTT[T/A]ACGCATCAGAGTCACCGCTGCTCAACCTGAGTGGGTGATTATTAGCAGGATACAGGTCTGGACTGTTAAAGAAGACAAGACCATCTGAAATATTGCAGGAAAAAGTGAGTTTTTGGTCTTGTTTATGGTTTAAATATGTAAGATTTCTTACATCAAGAAGCGTTTTCTTGACAAGCACAAAATATCTGGTTTTATTTTCAGAAATAATGAGTTAAAATGAAGAGAGTTTCTCCTTAAAACAAGCAAAATAATCTGACAATGGAGGAAGAAACGATCTTGTTTTTATTTTGAGTTATGATTCTTCTTACAGCATTATTCTGCTTGTTTTAAGGACGAACTCTCTTCATTTTGACTCATTATTTCTGAAAACAACACTATATTTTTGTATTCGTCTAGAAAGTGCTTCCCGGTTTCAGAAATTTGAGATATTTGGACTTGAAACAAGACACAAACTCTAAGTAAGAATGGTTTAAATATCTAAGAATTCTTGCATCAAGATG
Associated Phenotype:
Not determined