ZMP
zgc:152896
Ensembl ID:
ZFIN ID:
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39901 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10280 | Nonsense | Available for shipment | Available now |
sa6018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39900 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25117 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39901
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 > A
Consequence:
Nonsense
Transcripts:
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)
KASP Sequence:
None
Flanking Sequence:
AGACTCCATCAACTGATGCTTTCAAAAGCCAACAAGGGCATGATCACTTA[T/A]GTTCTGCGGCACTTTCTTGCTGTAAGAAGTAAAACTGCTATTATTTTAGT
Long Flanking Sequence:
CATAATAAGTAGCCTTTTATCCAGTATTATACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTCAGTATGTTTATTCTTCTAATTAGTAAGCCTGTTGGAATGATGTCTGACATCAAATGACATCTTTAAATGACTTGTCTCTTGGGTATGCTTGAAAATATTGTTAATTAGTGTAGACTTGTATAGAAAGTAGAGACCCAATTTACTGCAGTGATATAAAAAATGAACTGGTGTGATGTCATTTCAAACATAAAAAACATTTAATTTGGAGTTTATTTCAGGGAATAATATCCAAAATGCATTTTCGTTTCAGGCCAAAGCCAAACCTGTTCAAAGGTGATCACAGATACCATTCAGCCAATCCTGATGCACCAGTTGTGATTTTGTACGCTGAAATGGGCACCAAAGAATTCTCCAGACTCCATCAACTGATGCTTTCAAAAGCCAACAAGGGCATGATCACTTA[T/A]GTTCTGCGGCACTTTCTTGCTGTAAGAAGTAAAACTGCTATTATTTTAGTCAATATAAAAGTGTATTTTCATCTTAATACGAATCTCTTCCGCATATTCTGTCATCCATGCAGAGCCCAAGTAAAAGTAAAGTACACCTGTCTGGATATGGAGTGGAACTGGCCATCAAAAACCAGGAGTACAAAGCCAAAGACGACACACAAGTTCAGGGTATGATATCAGCCAGATTTCTTTTTTTATTGTGGCTTAAAATTACTGTTTTAAAGATATTCCTAAATGTAGCAAACTTATTAATGTTTTTTCTTTTGCTTTTTACAGCTGGAGCTGATGCAAATGCAACGGTAATAGGTGAAAATGATCTGGTGGATGAAGTGCAGGGCTTTCTTTTTGGCAAACTCAAGTAATTAAAAGGCTCATGCTTATTTAAGAGTACTCTCCACTGACTAACATGCACACTAATGTTTGAGATTATGTTTGACAGCAGCACATACTGTTGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10280
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 |
---|---|---|---|---|---|
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)
KASP Sequence:
GTGATCATGACGTGGTGGATTATATCATGAATCAGCCCAACGTGGTCCCT[C/T]GAADCAATTCCAGAATYCTGAGCACCAGCAGGAATTATCTGGACCTTTCC
Long Flanking Sequence:
TGTTGGCCCTCTGCCAGTGGTGTTGTATAATGGTATGCCTTTACAGCGTGAGCAGTTAGACCCTGATGAACTTGAAACGGTCGTCATGCACAAGATCTTGGAGACCACCAGCTTTTTTCAGCGCACTGTCTATCTGGTGAGAATGACACGTCTGTCACCAGGGGTGTCCTCTTTGGTCAACATTTTTGAGTGGCAATACATTATAAAATTTCACTGCAGCCAAAAAAGGCTAAATCCTACTGACAACTGGCTAGACTTATCTGAACGAATAAATGATTGAAAATAATATAGCATTTGGGATATTTGAAAAAAAAATGAATGAAAACTCTCACAAGTGTTTTTAGAATGTATTCATCTACCAGTGTGTTTATTTTCATTAGTTCAGTTTGGTCTTATTTTTTTGTCATCCAAAATGCTTCTTGTGCATTCTTTTTCAGGGTGAGCTGAACAGTGATCATGACGTGGTGGATTATATCATGAATCAGCCCAACGTGGTCCCT[C/T]GAATCAATTCCAGAATTCTGAGCACCAGCAGGAATTATCTGGACCTTTCCGCCACCAGTGAGTTTTTGAGTTCTGACTGTATTCATTAAGCAAAATGTCTCCTGAATATTTTGCCGCTCTCTGGCTCTTTTTCTGTTGAATCGTAAGCAGCCTTTCTTTCTGTAAACTAGCTAGTTTGAGATATACAACACGTATGTAGACTCTTGGGAATGAATATCTGCCTCATTGTGAATTCTGTGCTAAATGTCTTGTTTGTTCTTGAAAGCCCATTTATTTACAAAGACGTACAAATGAGACTGCGGCAATGATATTCATAAACTGCTTTATTTTTTTTACGAAAATACGAAACTGAATTTTAATAGCTTTTGAATAGCATATTTGCAGTCTTTCAGGAAGCTGAGCAAAAGGCCCATTTCATACTGAACTCAAATAGCAGTCAATGTTCAGAAATAGCTGTGTTCGAAATGACTTCGCTCAGATTCAATTATGAATGCGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6018
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 > A
Consequence:
Nonsense
Transcripts:
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)
KASP Sequence:
TTCTGGGTAGTGGGAGACTTTGACCAGCCATCGGGTCGACAGCTGCTGTA[T/A]GATGCCATACGTCACATGGTAGGCGAATGTCACTGARCAATTACTGTRAA
Long Flanking Sequence:
CAAGTTTTCAGATTAGTGTCTTGTTGTTCTTGTTCTTTTTTCCTTTTAACGTAGTGAAGAAGTTTTCTAAAGCTCGCTATTGATTTACGCGCAGCTGTGCATTTGTCATCTGTCAGAACTGTCAGTGAGTGATGGATGAAGGAGAATCTCTTTCTATCCTGTGGTCCCATGTAATATCTTTCTTTTACAAACGTTTACAGGTTTATATCTCAGTTGAAATTGCCTGTCTGTCTTTTGCGTGCCGCTTGGGCACTTCGGGAAACCTCTCGCTTTCTTGATTGCTAGCACCCGAGACAAGCGAGAGTCCGTTTCAGTTCCTCCCATCACTTTCACTCAACTTTTTTTCGATTGCATGAGGAAAAGCGCACATCTCGGCGGTGTAATTTCCTTTTAGCCCATGTGTCTGCTCTTCTGTGACTTGCAGATGATGGCATCATCCGTCCGGTGACTTTCTGGGTAGTGGGAGACTTTGACCAGCCATCGGGTCGACAGCTGCTGTA[T/A]GATGCCATACGTCACATGGTAGGCGAATGTCACTGAACAATTACTGTGAATAGATCCAAATTCTTTCACTTCAAGTAAATCGAGTGTCTATGTCAGATTAACCCTTATGTGTTGATCAAATTGACTACCCTTTGTTATGTTAATAGCTGTTTTTGCTCAATTGACTTCCACCATAATGCAATTATTATACCATATAAGCATGCATTCTTCATTTGTTGGTTAAAGAGGTAAAATTTGCCATTTTTACTGTTGATTGTAAAAAAAAAATGTCATTATGGTGGAAGTCAATGGTGCAACAGCCACAAACATTAAGAAAAGGTAGTACATTTGCCCAGAGTATATTGAGTTTAAAATAAATAAATAAATAAATCAAAGCATCTACCCAAAATATGTGTCAAAATTAGATTTGTCACGAAAAATCATTCCATTTCCTAAAACACGGACAAAGTTGTGACCAAATTAAGATTAAAAAAGACCGCAGAGTGCATGAAACAGCACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39900
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:
C > A
Consequence:
Nonsense
Transcripts:
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)
KASP Sequence:
None
Flanking Sequence:
GCTGAAAGCAAACCCAGGAGCCTGGATGCTCAGGCTGAGGAAAGGCAGGT[C/A]GGATGATATCTACAAAATCTACAGGTACCCTATTACAGCCTGTCAGACGC
Long Flanking Sequence:
CCAGTAATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAACATATGATGGATAAGTTGGCGGTCATTCCACTGTGGCAACCCCAGATTAATAAAGGAATTAAGCCAGGAAGTAAATGATGATATATTTGTGGTTATTAAAAATGTATAATAAAAAAACAAATGATTCTACAAAATTCATATTTTCTGTGCAGGTGGACAGTGTCGTGGCCGCCGAGTATGAGTTGGAGTATTTATTACTGGAGGGTCACTGTTTTGACGTGACCACAGGTCAGCCTCCCCGTGGTCTGCAGTTCACTCTGGGCACTGCCTCCGACCCTGTCATAGTGGACACCATCGTCATGGCCAACCTGGTGAAAAGTCATCATCATTATTCATCTATGAAATAATCACTAAGTCTCTTATTAAAGGTCATCTTACTCTGATCCGGCTTTAACAGGGTTATTTCCAGCTGAAAGCAAACCCAGGAGCCTGGATGCTCAGGCTGAGGAAAGGCAGGT[C/A]GGATGATATCTACAAAATCTACAGGTACCCTATTACAGCCTGTCAGACGCCTGTCTCTCTTAATGTCCTTCTGTCTCTTGGCTTTATTGGTCGTTTGACTTTTTTTAAATTCCCCTCTCGCAGTCACGATGGCACAGACTCTCCAGCCGAAGCTGATGATTTAATCGTCGTCCTTAACAACTTCAAGAGCAAGATCATTAAAGTGAAAGTAAGTAATGGAGGGCTGAATCGGGTGACGGGGTGAGGTCACATATAAGGGCTCTCTGTCTGTTCAGATTGAGGGTATCAGCTTTTAATCTGACGTCACAGTTTCAAGGTCCAAACACTTTATCAGATGCCAAATAGCAAATGCTACTAATAGAATCACAGTGTGATTTAATATTATGATCATAATGTTTATTATTCATGGCCAATCTCAGATGGTAGACAATGGTTCATCTTTTATAAATCATTCAAATATTGGTGTCTGGGACCCAGCAAGCCCAGAGATTTGTAGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25117
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 > A
Consequence:
Nonsense
Transcripts:
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)
KASP Sequence:
None
Flanking Sequence:
TGTAAATATGCATTATATCTTATATATTTGTTGCAGGAATTCATTCCATA[T/A]ATGGCAGAGAAGTATGGTTTCCAGTATGAGTTGGTGCAGTATAAATGGCC
Long Flanking Sequence:
ATAAATGGTAATTAATGGTTTGTTTATATTTTAAAAATAAATTATTTAGACCAAAAGTGTCCAAACTTGGTCCTTGAGGGCTGGTGTCCTGAAATGAGTTCCAACTTGCTTCAACACACCTGCAAGGATGCTTCTAGAAAGCCTAGAAAGAGCTTGATTAGTGTCTGATTGGGGTTGGAATTAAACTTTGCCGGACACCGGCCCTCCAGGACAGAGTTTGAACACCCCTGGTTTAAAACGTTTTAGTTAATAAATTATAAAGATTAGAAATCATATTTACAATTGCATTTTGATCCATAAACACTATTTAAAAAAAAAAATTAATCGTTTTGGTGCTAATGAGCCTGAAAAGATGTTTGCTGTATTAATTATTTTTATACTGAATGACATTTTAGTAGGCATCTTCTGTATATCGGAGTAAAAATGTGTGAAAGTCATTATCTATTTTTCTGTAAATATGCATTATATCTTATATATTTGTTGCAGGAATTCATTCCATA[T/A]ATGGCAGAGAAGTATGGTTTCCAGTATGAGTTGGTGCAGTATAAATGGCCACGTTGGCTTCACCAGCAGACAGAAAAGCAAAGGATCATTTGGGGCTATAAGATTCTGTTCCTCGACGTGCTCTTCCCGCTGGCTGTGGACAAGTTCCTCTTTGTGGATGCGGATCAGGTACAATAACTGAGCTGTGCAGTTGTGTGGCATGAACTCTTGTCTCCGGAGTGCAATAAGCACCAATCTGCCCGTGTGAGATTTATTTTCAGAAGTTGTATGTACAGACAAATCACCCCATTTGCAGTCACTGGAAGTGCACAGCAGTTGTTTGTTACACAAACCAGAGAAACATTATGCATAGAATGATACACTGCTGCCACCTTTGGGTAAAGGAAAATACAGTTTGAGGATAAACGTTGAAAGTATCAATAAATAAAAGTATTACCGACCTATCATATCTTGATCTATTAAATGAAGAACACAAAAGAAGCTATTTTGAATAATGTAAC
Associated Phenotype:
Not determined