ZMP
si:dkey-1h24.5
Ensembl ID:
ZFIN ID:
Description:
Asparagine-linked glycosylation protein 11 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q7ZW24]
Human Orthologues:
AL139082.3, ALG11
Human Descriptions:
Asparagine-linked glycosylation protein 11 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q2TAA5]
asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog (yeast) [Source:HGNC Symbo
asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog (yeast) [Source:HGNC Symbo
Mouse Orthologue:
Alg11
Mouse Description:
asparagine-linked glycosylation 11 homolog (yeast, alpha-1,2-mannosyltransferase) Gene [Source:MGI S
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12399 | Nonsense | Available for shipment | Available now |
sa24848 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12399
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 |
---|---|---|---|---|---|
ENSDART00000049514 | Nonsense | 111 | 500 | 3 | 5 |
ENSDART00000136760 | Nonsense | 90 | 195 | 3 | 4 |
ENSDART00000140345 | Nonsense | 82 | 265 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 28702480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28953309 |
GRCz11 | 1 | 29757240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTCGTAGTCTACACGGGTGATCAGGGGGTGACGGCAGAAGAGATTT[T/A]GGATGGAGCACGGAGAYGMTTTAACATCAGACTCCCCCGAYCCGTTAAGT
Long Flanking Sequence:
TGACATAACTCACAAGCCATATTTTTTTTTAAACTTCTGAAAATGTGTAAAACAATTAAAAGTAAACATGGTTACGTGATATTTGTTAATAAAATATGGATTACCATGAAGTCACTCTTTGTCATGGGACCCCAGCAGCAACACCATGACTGAAGCTATTGACTTGAAATCAGAATTTACAAGGTTGATTTTGCTCGCTCACATTATTCTTAAGGTGAATAATTAATCCATCAAAGTTAATCCGCTGAAAAATCTGTTTGTTTTTATAATTTCCAATGTAATTCTGATGATGTGCAAAAGAAAGTATTCTCAGTATTCCATTTCAGTTGGAAACAAATCAACATACTGAAAAAAAAAGTGTCAGCCCAAAACGTGTGACATCAACAAAGCTGGCCTTCACCATATTGAGCAAATAAATTCTGTATGTTTGCACTGCAGGTACCAAGATGTTTCTTTCGTAGTCTACACGGGTGATCAGGGGGTGACGGCAGAAGAGATTT[T/A]GGATGGAGCACGGAGACGATTTAACATCAGACTCCCCCGACCCGTTAAGTTTGTGTTCCTGAAGCATCGTCTACTGGTGGAGGCAAAACTTTACCCACATTTCACCCTTCTGGGGCAGAGTGTGGGCTCCATCTTCTTGGGGTGGGAGGCATTGACCGAGTTTGTTCCAGATCTCTATATTGACTCAATGGGCTTCGCCTTCACCTTACCCGTGTTCCGCTATCTGGGTGGTTGTCAAGTGGGAAGCTATGTGCACTATCCAACCATCAGCACGGACATGCTGTCTGTGGTTCGAGAAAGAAACCCCAGGTTAGTCAAGAAAGTCATGTATTACTATTATTTAGTAAATTAAATGTGAATAATTTATTTCATATTTAATGTTAAATGATTACTTTACATTCCATAATGGGCTTCAATAACACCACAATGACTGTGTTAAATATTTGTGTTTAGTTAAATCTGTTCCAGTTTACTTATTAAATGTGCATGTATTTTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24848
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 |
---|---|---|---|---|---|
ENSDART00000049514 | Nonsense | 364 | 500 | 4 | 5 |
ENSDART00000136760 | None | None | 195 | None | 4 |
ENSDART00000140345 | None | None | 265 | None | 4 |
Genomic Location (Zv9):
Chromosome 1 (position 28699820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28950649 |
GRCz11 | 1 | 29754580 |
KASP Assay ID:
554-7820.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGTCGGAACCAGGAGGATGAAGATCGGGTTCTGATGCTGAGAGGAT[T/A]GTGCCAGGAGCTGGGCATAGCAGACAGGGTGGAGTTTAAGCTCAATATTC
Long Flanking Sequence:
TCAAGTAACATTATAAGTTTACATGCAGATGTTTGTAAATGTTCATTCCAGGTTCAACAATGCAGACTACATCTCCAGCAACCCTGTACTCAGTGCCATTAAAGTGATTTATTATTGCGTCTTCGCACTGCTGTATGGCCTGGCTGGCTCCTGTAGTGACGTCATCATGGTCAATTCCACCTGGACTTTGGGTCACATTCTGGCTCTGTGGCGCACTCCGAACCGCACCAGTGTGGTTTACCCACCATGCGATGTTCAGGCATTCCTGGATGTTCCAATTGGGGAAGACAATGAAGAGAAAGAGCAAAAGAAGTGTCACAGTCTGGTCTCTGTGGGTCAGTTCCGGCCAGAAAAAGACCATCAGCTGCAGATCAGGGCATTTAAAAAGCTTTTGGACAGAAAGGAGGTGGAGCCTGCGGGAAGAGAGGCTGTGAAGCTGGTGCTGATTGGTGGGTGTCGGAACCAGGAGGATGAAGATCGGGTTCTGATGCTGAGAGGAT[T/A]GTGCCAGGAGCTGGGCATAGCAGACAGGGTGGAGTTTAAGCTCAATATTCCATTCCAGGAGCTGAAGAAAGATTTAACAGATGCCACTATCGGGTTGCACACAATGTGGAATGAACATTTTGGCATTGGTAAGATGATGAATATCATGCTCTCAGCCAGTTTGATCGCAAAACACTAGATTTCCCTTTTCTCTTATTTTTTTTTGTAATAAATATACTTTTATGATTATGCCAAGCTGTAATATGTTGTATTGGTTAAACTCAAAGTAAAAAAAAATCTATTTATTTCAAGAATGACTTGACTGTCATCATCATCAAACAAAAAAAAAGTTTGTTGTAGAATAATAATCACCTAATAAATATTATGTTAAATATTTATTTTCTATTCAAAAACTTAATTAAATTGATCAATCAAAAAAAAGCTCCCTTAAATTAACATGAAATAATAACTAACATTAACAAATAATAAATAACTTATGTATTACTTTATACAGTCAAGTC
Associated Phenotype:
Not determined