ZMP
dyrk1aa
Ensembl ID:
ZFIN ID:
Description:
dual specificity tyrosine-phosphorylation-regulated kinase 1A [Source:RefSeq peptide;Acc:NP_0010741
Human Orthologue:
DYRK1A
Human Description:
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A [Source:HGNC Symbol;Acc:3091]
Mouse Orthologue:
Dyrk1a
Mouse Description:
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1a Gene [Source:MGI Symbol;Acc:MGI:13
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15575 | Nonsense | Available for shipment | Available now |
| sa21625 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15575
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 |
|---|---|---|---|---|---|
| ENSDART00000100073 | Nonsense | 621 | 734 | 11 | 11 |
| ENSDART00000141723 | None | None | 226 | None | 5 |
| ENSDART00000144722 | None | None | 222 | None | 7 |
The following transcripts of ENSDARG00000063570 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 220539)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 63550 |
| GRCz11 | 10 | 63550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCACCACCATCAYCACCACCACCCGCCGCCRCATGGACAGGGCCCTGCC[C/T]GACCTCGACCCCGGCTCTACTCTCCGTCCCACAGCGCCTCCACGCAGGAC
Long Flanking Sequence:
GTTTTGCTGTCGTGGCAATGACTGAACTGCCCTACAGTGGAGCATTAGAGAGTCAACAGCGCTGTTCATCAGGGATCAGGGGGTTCACTGAGGGAATCTGGGTTTGCTTCTAAACAAGCCACCATTTTCCCACACAGAGGAGGGAGAAGATCCACACATCTCTTTCCTAGCCTCCTTGTTGTGTTTTACATGACAGTGACACACTTTTATTGTGAAGTGCAGTGGTGACGTGCATGTTAATGTGTGTGTGTGTGTGTGTGTTAATGTGTGTGTGTGTGTGTGTGTTAATGTGTGTGTGTGTGTGTCCTTCTCAGGCAAGACAGGCGTTTGTGCCGGCGCTGGGCTGGGTTGGAGACGGACTCCAGCAGGCGTCAGGAGAGACTCACCCCGTACAGGAGACCACTTTCCACGTGCCCCCACACCAGCCCAAAGCCCTGCACCCCCACCAACACCACCACCATCATCACCACCACCCGCCGCCGCATGGACAGGGCCCTGCC[C/T]GACCTCGACCCCGGCTCTACTCTCCGTCCCACAGCGCCTCCACGCAGGACTCAATGGAGGTGACGCACGGACACCTGTCCATGACCTCGCTGTCTTCCTCCGCCTCGTCCTCCTCCACCTCCTCCTCCTCCACCGGCAACCATCACTACGCCTACCAGAGCCGCCCGCTGCCCCACGGCCTGGGCTTCGGCCACAGCGGCAGCATGACTCTGGGCCTGGGTGCCTTCTCCAACCCGCGACAGGAGACGGGCGTGGCAGGCGTAGGTCTGCGGCCGGGTCTGGAGCGCGAGGAGTCCCCGATGGCGGGTGTATGTGTGCAGCAGAGCTCCGTGGCCAGCTCCTGACCCGCCTGAGGAGGCCGATTCACGCGCCCGTCCATACTGGAGCTGAGCGGAGCTGGAGCCAAGCGGAGCCAGCACTCCTGCGGCCGTGGACGTTAACTTCGGTCTGCAGCTCTGACGCTGCCGGAGCCCAGCGCTCGCCCGCCGCCGCCACCGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21625
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 |
|---|---|---|---|---|---|
| ENSDART00000100073 | Nonsense | 623 | 734 | 11 | 11 |
| ENSDART00000141723 | None | None | 226 | None | 5 |
| ENSDART00000144722 | None | None | 222 | None | 7 |
The following transcripts of ENSDARG00000063570 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 220545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 63544 |
| GRCz11 | 10 | 63544 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCATCACCACCACCCGCCGCCGCATGGACAGGGCCCTGCCCGACCT[C/T]GACCCCGGCTCTACTCTCCGTCCCACAGCGCCTCCACGCAGGACTCAATG
Long Flanking Sequence:
CTGTCGTGGCAATGACTGAACTGCCCTACAGTGGAGCATTAGAGAGTCAACAGCGCTGTTCATCAGGGATCAGGGGGTTCACTGAGGGAATCTGGGTTTGCTTCTAAACAAGCCACCATTTTCCCACACAGAGGAGGGAGAAGATCCACACATCTCTTTCCTAGCCTCCTTGTTGTGTTTTACATGACAGTGACACACTTTTATTGTGAAGTGCAGTGGTGACGTGCATGTTAATGTGTGTGTGTGTGTGTGTGTTAATGTGTGTGTGTGTGTGTGTGTTAATGTGTGTGTGTGTGTGTCCTTCTCAGGCAAGACAGGCGTTTGTGCCGGCGCTGGGCTGGGTTGGAGACGGACTCCAGCAGGCGTCAGGAGAGACTCACCCCGTACAGGAGACCACTTTCCACGTGCCCCCACACCAGCCCAAAGCCCTGCACCCCCACCAACACCACCACCATCATCACCACCACCCGCCGCCGCATGGACAGGGCCCTGCCCGACCT[C/T]GACCCCGGCTCTACTCTCCGTCCCACAGCGCCTCCACGCAGGACTCAATGGAGGTGACGCACGGACACCTGTCCATGACCTCGCTGTCTTCCTCCGCCTCGTCCTCCTCCACCTCCTCCTCCTCCACCGGCAACCATCACTACGCCTACCAGAGCCGCCCGCTGCCCCACGGCCTGGGCTTCGGCCACAGCGGCAGCATGACTCTGGGCCTGGGTGCCTTCTCCAACCCGCGACAGGAGACGGGCGTGGCAGGCGTAGGTCTGCGGCCGGGTCTGGAGCGCGAGGAGTCCCCGATGGCGGGTGTATGTGTGCAGCAGAGCTCCGTGGCCAGCTCCTGACCCGCCTGAGGAGGCCGATTCACGCGCCCGTCCATACTGGAGCTGAGCGGAGCTGGAGCCAAGCGGAGCCAGCACTCCTGCGGCCGTGGACGTTAACTTCGGTCTGCAGCTCTGACGCTGCCGGAGCCCAGCGCTCGCCCGCCGCCGCCACCGCAGCGTTTC
Associated Phenotype:
Not determined