zgc:152896

Ensembl ID:
ENSDARG00000054746
ZFIN ID:
ZDB-GENE-061103-619
Description:
UDP-glucose:glycoprotein glucosyltransferase 1 [Source:RefSeq peptide;Acc:NP_001071002]
Human Orthologue:
UGGT1
Human Description:
UDP-glucose glycoprotein glucosyltransferase 1 [Source:HGNC Symbol;Acc:15663]
Mouse Orthologue:
Uggt1
Mouse Description:
UDP-glucose glycoprotein glucosyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2443162]

Alleles

There are 5 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa39901 Nonsense Mutation detected in F1 DNA During 2018
sa10280 Nonsense Available for shipment Available now
sa6018 Nonsense Mutation detected in F1 DNA During 2018
sa39900 Nonsense Mutation detected in F1 DNA During 2018
sa25117 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa39901
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123886 Nonsense 230 1554 6 40
Genomic Location (Zv9):
Chromosome 2 (position 40638740)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 41031930
GRCz11 2 40886164
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGACTCCATCAACTGATGCTTTCAAAAGCCAACAAGGGCATGATCACTTA[T/A]GTTCTGCGGCACTTTCTTGCTGTAAGAAGTAAAACTGCTATTATTTTAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10280
Current 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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123886 Nonsense 700 1554 19 40
Genomic Location (Zv9):
Chromosome 2 (position 40629007)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 41022197
GRCz11 2 40876431
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GTGATCATGACGTGGTGGATTATATCATGAATCAGCCCAACGTGGTCCCT[C/T]GAADCAATTCCAGAATYCTGAGCACCAGCAGGAATTATCTGGACCTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6018
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123886 Nonsense 777 1554 21 40
Genomic Location (Zv9):
Chromosome 2 (position 40622272)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 41015462
GRCz11 2 40869696
KASP Assay ID:
554-3745.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTCTGGGTAGTGGGAGACTTTGACCAGCCATCGGGTCGACAGCTGCTGTA[T/A]GATGCCATACGTCACATGGTAGGCGAATGTCACTGARCAATTACTGTRAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39900
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123886 Nonsense 1170 1554 30 40
Genomic Location (Zv9):
Chromosome 2 (position 40603138)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 40996328
GRCz11 2 40850562
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCTGAAAGCAAACCCAGGAGCCTGGATGCTCAGGCTGAGGAAAGGCAGGT[C/A]GGATGATATCTACAAAATCTACAGGTACCCTATTACAGCCTGTCAGACGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25117
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123886 Nonsense 1304 1554 35 40
Genomic Location (Zv9):
Chromosome 2 (position 40592310)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 40985500
GRCz11 2 40839734
KASP Assay ID:
554-7817.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TGTAAATATGCATTATATCTTATATATTTGTTGCAGGAATTCATTCCATA[T/A]ATGGCAGAGAAGTATGGTTTCCAGTATGAGTTGGTGCAGTATAAATGGCC
Associated Phenotype:
Not determined

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