ZMP
dpysl5b
Ensembl ID:
ZFIN ID:
Description:
dihydropyrimidinase-related protein 5 [Source:RefSeq peptide;Acc:NP_001018351]
Human Orthologue:
DPYSL5
Human Description:
dihydropyrimidinase-like 5 [Source:HGNC Symbol;Acc:20637]
Mouse Orthologue:
Dpysl5
Mouse Description:
dihydropyrimidinase-like 5 Gene [Source:MGI Symbol;Acc:MGI:1929772]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20168 | Nonsense | Available for shipment | Available now |
| sa45162 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20168
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 |
|---|---|---|---|---|---|
| ENSDART00000067455 | Nonsense | 334 | 568 | 9 | 13 |
| ENSDART00000134323 | Nonsense | 334 | 568 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 575017)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 792933 |
| GRCz11 | 4 | 806381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGACATCATTAACGTGGTGGCGTCAGATCATCGCGCATTCAGCACCAAG[C/T]AGAAGGCCATGGGCAAAGAAGACTTCACGAAGATCCCTCACGGGGCGCCC
Long Flanking Sequence:
CGTATGCTGAATGCAGTAAGTGACTGTTATCATCAATAACGTTAAAAAAACAACAGAAAAAAAAACATAATATTACCTATGAAATGTTCTGCCTTTGTGCTTTGTTTTCTTTGTTTGCTCGTTACTACACCCGTAGACAGCGCTAAAGTCCCGCATCTTCACGTAATAACACTGTCTTGACTAGTGCGGTTAAATGACATTTGTCCTGGGAGCACTGTACCAATGTGGCGGCGCTATTGACGCATGCTCAGGGTCCCTATGCGATATCTAGTGTATATATCTATGATAGGATTGTAAAAGAATGATTTGTTGTGCTCTTCCATTCATTACGTTCTAAGTTTACCAACTATAACCACTACTGCTGCGGAGAAACAAGCAAATGTAAAAAAAGAGTCAGTTTGCGAAATTAGAGGATCGTTAACATGTGATGATGTGTTTCCTGTGTACGCAGCGACATCATTAACGTGGTGGCGTCAGATCATCGCGCATTCAGCACCAAG[C/T]AGAAGGCCATGGGCAAAGAAGACTTCACGAAGATCCCTCACGGGGCGCCCGGCGTCGAAGACCGCATGAGCGTCATCTGGGAGAGAGGAGTGGTGCGTTGATAACAACACGCTACACATGCTAACCGCAAACACAGTTACACAACAAGCTGGGTGGAATACTTATGAATTTTAATCACCAGTTACTGATTACACATTACATGACAAAAATTGTAGCCTGTTATATATTTCTTAGTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTCTTGCATATTTATGATTATGTAATCTGAATACTTTTGGATTACATTTAGATTACTTTTGCGCTAACACTTATTTGATGCCACGTATGTATGGTATAGAAACATATGGTAGTCATTTATGGTAATGTAAATCGACGAAAAGCGAAAAAGGTGCGTCAACGAAAGTGAAGGGTGGTGCTTCTCTCTATGGCGCCCCTAACAAGATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45162
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 |
|---|---|---|---|---|---|
| ENSDART00000067455 | Essential Splice Site | 412 | 568 | 10 | 13 |
| ENSDART00000134323 | Essential Splice Site | 412 | 568 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 4 (position 572774)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 790690 |
| GRCz11 | 4 | 804138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAGGAGCCGATGCGGATGTGGTTGTGTGGGATCCAGACGCCACACGG[T/C]ACAAGATGATAATAACCGTATTTGGAAAAGCACAGTTTAATGTAGTTTAC
Long Flanking Sequence:
AAAACAGAGAAAAATTAGGAGAATCCGTGAATTGTGAACAGTTTATCGCCACTGTGTAAATAATATTTAATCCATCAAAAAGTAACTGTAATCAGATTACAAGTATTTTAGAAAGTCGCTTTCTCTAGTTATAAGTATTTGATTTTTGTATCTGATTACATAATCCAGATTACATGTAATCCCCTACTACCCGGCTCTGCATACACACGCATGAAGGTTTTTGTGCCATTATCAAAGACTACACACATCGCTTTTGAATGGACATTCTGTTAACGTTACTGGGAGAACATTTAGAGAACATTTCCAGAATGTTTTCCCTGGCTCGTAGTCTGACAGATGTGTCTTTATGTTTTTAGGTCAGTGGGAAGATGGATGAGAATCGTTTTGTGGCGGTGACGAGCTCAAACGCTGCTAAAATCTATAACCTCTATCCACGCAAGGGCCGTATAATGCCAGGAGCCGATGCGGATGTGGTTGTGTGGGATCCAGACGCCACACGG[T/C]ACAAGATGATAATAACCGTATTTGGAAAAGCACAGTTTAATGTAGTTTACTTAATATCATTACATACTTAATAAAACTTAATAAAAGCAACAGCTTTGAATTAAACATGACTTGTAAAATGTGTAAAGACGTAAGTGTTTTCTCGTAAAATGCACTCCAGTACCTTTTAAAAGACTTTTATTGGGTATTTGTGTACTGAGACATATACAGTGCTCAACATATATGAGTGTCATATGTATTTATCAGCATACACATTTTAACAGGACGATTTCAGCAAGCACTCAGGCTCAGGGTGGAGACTTCAACCTGTTTGAGGGCCAGCGGTGTCACGGCGTCCCATTGGTGACCATCAGCCGCGGGCGTCTGGTGTGTGAAAACGGCGTCTTCATGTGTGCTCAGGGATCCGGAAAGTTCTACCCGATGAGAGCATTTCCAGATTTCCTCTATAAGAAGCTGATTCAGAGAGAAAAGGTGACTCCGTTAATGCACTAACCGTTAAG
Associated Phenotype:
Not determined