ZMP
alg3
Ensembl ID:
ZFIN ID:
Description:
dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase [Source:RefSeq peptide;Acc:NP_001018
Human Orthologue:
ALG3
Human Description:
asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae) [Source:HG
Mouse Orthologue:
Alg3
Mouse Description:
asparagine-linked glycosylation 3 homolog (yeast, alpha-1,3-mannosyltransferase) Gene [Source:MGI Sy
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6860 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44547 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6860
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075146 | Essential Splice Site | 331 | 434 | 8 | 9 |
ENSDART00000144024 | Essential Splice Site | 95 | 151 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 45040114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 45125615 |
GRCz11 | 2 | 44978613 |
KASP Assay ID:
554-4421.1 (used for ordering genotyping assays)
KASP Sequence:
TTTWATTYTKARCTTATATGACTATAAACGGYTCCTTAACCCAGATTGTA[C/T]AGATGGTTCTTATTCTGTTTACATCWAACTTCATTGGCATGTGCTTCAGC
Long Flanking Sequence:
ACCTCAATTTTGTGCTATGCTTAGGGCTGGGCAATTTTTTTTAATTGGGGAGTGGGGGTGGGGGGTAGAGCTTTTTGTTAAATTATAGTTCTGAAAATATAATGTTTATATTTTACTGACCTTTGTCATTTTTTAATGTGTTTTTACAGGTCTGGGAGCAGTATTTGGACTATACTAAAAGATCCATCTGAGAGAAAGGAGACTGCACATAAAGTTAATGCCGATCATATCCTTTCTGTGGTAGTTAAAATCAAATTGGTTTAAAGTCTTTTATACATACATCCAGCAGTCAACATTTGAAGTGGATCAAACAATTTTCCAAAATTGTCCTGAGAAAACAATGGGTGTTAAATAGTTTTTGGGAAAACACTTTTGGGAAAACACTTTGTTTCCACTTCAAATGTTGACTACTGTATATTTCAGGCATGTATAAATATTCAATTCTTCTGATTTTATTCTGAACTTATATGACTATAAACGGTTCCTTAACCCAGATTGTA[C/T]AGATGGTTCTTATTCTGTTTACATCTAACTTCATTGGCATGTGCTTCAGCAGATCTCTGCATTATCAGTTTTATGTCTGGTATTTTCATACGCTGCCCTACCTGCTGTGGAGTGGAGGAGTGAAGAAGCTGGCACACCTACTCAGGTAAAACATATCTCAATATTTAGATAACACTGTAGTGTACAGTCAGTCTAATGCAGATATATAGATGATTAAAGTTCCCACACTTTATCTGGAAAAAGTGGAAATTTACAGGGTTGTTTTCCAGTCATGAATGTGATCTGTGGTCTTATTTTTAAAATGTTGCATAGAAACCTTAATAACGCTGAAAGCCAGAGTAAATTGTAATTTATTAGTTAATGATTATGGCTCATATGATGATTTAAAGTGGTTAAACTAAGTCCACATTTAAGGTATATGTTTATTTAGAGTTTACTTACATCTGCGTGGATTCTTCAGGATTTTTTTTTTTATAGATATCAATCTTTGTGTGGGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44547
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075146 | Essential Splice Site | 379 | 434 | 8 | 9 |
ENSDART00000144024 | Essential Splice Site | 143 | 151 | 3 | 4 |
ENSDART00000075146 | Essential Splice Site | 379 | 434 | 8 | 9 |
ENSDART00000144024 | Essential Splice Site | 143 | 151 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 45040261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 2 | 44978760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACCTGCTGTGGAGTGGAGGAGTGAAGAAGCTGGCACACCTACTCAGG[T/C]AAAACATATCTCAATATTTAGATAACACTGTAGTGTACAGTCAGTCTAAT
Long Flanking Sequence:
AGGTCTGGGAGCAGTATTTGGACTATACTAAAAGATCCATCTGAGAGAAAGGAGACTGCACATAAAGTTAATGCCGATCATATCCTTTCTGTGGTAGTTAAAATCAAATTGGTTTAAAGTCTTTTATACATACATCCAGCAGTCAACATTTGAAGTGGATCAAACAATTTTCCAAAATTGTCCTGAGAAAACAATGGGTGTTAAATAGTTTTTGGGAAAACACTTTTGGGAAAACACTTTGTTTCCACTTCAAATGTTGACTACTGTATATTTCAGGCATGTATAAATATTCAATTCTTCTGATTTTATTCTGAACTTATATGACTATAAACGGTTCCTTAACCCAGATTGTACAGATGGTTCTTATTCTGTTTACATCTAACTTCATTGGCATGTGCTTCAGCAGATCTCTGCATTATCAGTTTTATGTCTGGTATTTTCATACGCTGCCCTACCTGCTGTGGAGTGGAGGAGTGAAGAAGCTGGCACACCTACTCAGG[T/C]AAAACATATCTCAATATTTAGATAACACTGTAGTGTACAGTCAGTCTAATGCAGATATATAGATGATTAAAGTTCCCACACTTTATCTGGAAAAAGTGGAAATTTACAGGGTTGTTTTCCAGTCATGAATGTGATCTGTGGTCTTATTTTTAAAATGTTGCATAGAAACCTTAATAACGCTGAAAGCCAGAGTAAATTGTAATTTATTAGTTAATGATTATGGCTCATATGATGATTTAAAGTGGTTAAACTAAGTCCACATTTAAGGTATATGTTTATTTAGAGTTTACTTACATCTGCGTGGATTCTTCAGGATTTTTTTTTTTATAGATATCAATCTTTGTGTGGGAAGTGACATAAATGCATTCCCACCCCCATTTTGTGTGTTCACCCAACACGATCTCACAGCAGTTCATAAATTTTAGATTTAGTGCCTAATTCATATGAAATCATACGATCTTATACTAATAATTTTGTACAATCACGGTTGGGTTTAGGGG
Associated Phenotype:
Not determined