ZMP
zgc:152928
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC555848 [Source:RefSeq peptide;Acc:NP_001071008]
Human Orthologue:
CPD
Human Description:
carboxypeptidase D [Source:HGNC Symbol;Acc:2301]
Mouse Orthologue:
Cpd
Mouse Description:
carboxypeptidase D Gene [Source:MGI Symbol;Acc:MGI:107265]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15154 | Essential Splice Site | Available for shipment | Available now |
| sa15322 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15154
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076000 | Essential Splice Site | 712 | 1275 | 10 | 21 |
| ENSDART00000113607 | None | None | 389 | None | 12 |
| ENSDART00000076000 | Essential Splice Site | 712 | 1275 | 10 | 21 |
| ENSDART00000113607 | None | None | 389 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 38045083)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39165162 |
| GRCz11 | 21 | 39210220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATACTGGGAGAAGAATCATAAAGCRCTCTTACAGTTCATGCAGCAGG[T/C]GATTCATTCCTGGCCATRACATTGTCTATTTTTGGTTGAGCAATTCAATT
Long Flanking Sequence:
AAAACCATAATATTGTATTTTTTTACTTTTTTAAATAAACTAATAAGGAAAAAATTGCAAAACAAAATGAATACCAGTGTCTCCTAGTAATATATTGTGGTCTTATAAAGCAAGTGATCTGTGGAAGAAACACAACTATGTTCATTATCTCCAACCCAAAACTTTTGCAAATGCTTAAGAGTGGTTTCATTTTTAAGTGAAGCATGTCTTCAATATTATACTTTTTCTTGTTAACACCGAACATATGTACTTTCAAATAATTTCTTTCTGTTTAAATGCATTTCAGAAGTGTTTTTTTTATGTTGAGCATCCTGTTTCACACAAAAATAAGTGTTGTTTTTTGCCTTTTATAGGAACCGATATTCTGACCTGGGCGTATCGGGGATCAGACACTCTAGCTGTGAACATTGGTTTGAGTTGTGAGCTGCTTCCACCAGAGAAGTCACTCTCTGTATACTGGGAGAAGAATCATAAAGCACTCTTACAGTTCATGCAGCAGG[T/C]GATTCATTCCTGGCCATGACATTGTCTATTTTTGGTTGAGCAATTCAATTTAAGTTTATTTGTATAGTACTTTTTACTATAATTATTGCATCAAAGCAGCTTTAAAAAGCTGCACATTGTTGCATTAAACTCGGATACGTCAAGGTTATTAGTTGCATAACTTTATTAGTTACTAATAACCTTAGTTGACTAGTAACTTAATAGCTTTTAACAGGTAAAGTTATTTATATAAACATAATTAACTTGCAATTATACAGTATATATGTGATGTCTATGTGTACATGTTCAATGAAGTGTATGTGTTGTCCTTGAAGTCTTCGGATGAGCAATTACATATACATGATTTGTGTGCTTGTGGTCATCAGGTTCATTTGTCTGTGCGGGGTGTGGTGACTGATGGTAATTCTGGAAGAGGCATTGCTAATGCTACAGTCATGGTAGAGGGCTCAAAGCATCTAGTGCGCACCAGTGGCACAGGGCAATACTGGAGACCTCTGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15322
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076000 | Essential Splice Site | 712 | 1275 | 10 | 21 |
| ENSDART00000113607 | None | None | 389 | None | 12 |
| ENSDART00000076000 | Essential Splice Site | 712 | 1275 | 10 | 21 |
| ENSDART00000113607 | None | None | 389 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 38045083)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39165162 |
| GRCz11 | 21 | 39210220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATACTGGGAGAAGAATCATAAAGCRCTCTTACAGTTCATGCAGCAGG[T/C]GATTCATTCCTGGCCATRACATTGTCTATTTTTGGTTGAGCAATTCAATT
Long Flanking Sequence:
AAAACCATAATATTGTATTTTTTTACTTTTTTAAATAAACTAATAAGGAAAAAATTGCAAAACAAAATGAATACCAGTGTCTCCTAGTAATATATTGTGGTCTTATAAAGCAAGTGATCTGTGGAAGAAACACAACTATGTTCATTATCTCCAACCCAAAACTTTTGCAAATGCTTAAGAGTGGTTTCATTTTTAAGTGAAGCATGTCTTCAATATTATACTTTTTCTTGTTAACACCGAACATATGTACTTTCAAATAATTTCTTTCTGTTTAAATGCATTTCAGAAGTGTTTTTTTTATGTTGAGCATCCTGTTTCACACAAAAATAAGTGTTGTTTTTTGCCTTTTATAGGAACCGATATTCTGACCTGGGCGTATCGGGGATCAGACACTCTAGCTGTGAACATTGGTTTGAGTTGTGAGCTGCTTCCACCAGAGAAGTCACTCTCTGTATACTGGGAGAAGAATCATAAAGCACTCTTACAGTTCATGCAGCAGG[T/C]GATTCATTCCTGGCCATGACATTGTCTATTTTTGGTTGAGCAATTCAATTTAAGTTTATTTGTATAGTACTTTTTACTATAATTATTGCATCAAAGCAGCTTTAAAAAGCTGCACATTGTTGCATTAAACTCGGATACGTCAAGGTTATTAGTTGCATAACTTTATTAGTTACTAATAACCTTAGTTGACTAGTAACTTAATAGCTTTTAACAGGTAAAGTTATTTATATAAACATAATTAACTTGCAATTATACAGTATATATGTGATGTCTATGTGTACATGTTCAATGAAGTGTATGTGTTGTCCTTGAAGTCTTCGGATGAGCAATTACATATACATGATTTGTGTGCTTGTGGTCATCAGGTTCATTTGTCTGTGCGGGGTGTGGTGACTGATGGTAATTCTGGAAGAGGCATTGCTAATGCTACAGTCATGGTAGAGGGCTCAAAGCATCTAGTGCGCACCAGTGGCACAGGGCAATACTGGAGACCTCTGGCT
Associated Phenotype:
Not determined