ZMP
pepd
Ensembl ID:
ZFIN ID:
Description:
prolidase [Source:RefSeq peptide;Acc:NP_944594]
Human Orthologue:
PEPD
Human Description:
peptidase D [Source:HGNC Symbol;Acc:8840]
Mouse Orthologue:
Pepd
Mouse Description:
peptidase D Gene [Source:MGI Symbol;Acc:MGI:97542]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9779 | Nonsense | Available for shipment | Available now |
| sa5906 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9779
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 |
|---|---|---|---|---|---|
| ENSDART00000004023 | Nonsense | 149 | 496 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 1162999)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 1710509 |
| GRCz11 | 18 | 1363212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAATAATGAGATGGTTTAACGTGTTTCTCTGTGTTTCYTCGTGTGTAG[C/T]GAGGGCWGAACACTGATAGYGGYAGCACCTGTCGTGAAGCCTCCTTTRAA
Long Flanking Sequence:
GTGTGGTGTGTGTGGATTAGTGTTGAGCTCCTGCAGAAATGTGGATTTCTCAATGAAATCTACCCGCAGGTAAAACCGTCTGTGTTTGATTCGTCCTGTGGGTTTAAAACGCTTCTCATCCACTCCTGAGAGCACATAAAACAGCTCCGGTGTTCTTCCCACAATCCTTCGCTCACAGTACAGCGGCTGCAGATTATTGATGATTCAGTGTCTGATTGGTCCACGTGAAGATTGTTTGTCTACCTTGAGGAAATCTCTGCTCAAATCCGGTCTCGCTGATGTTCATTGTAGCTGTCAGAAATGTTGAGGGATTTGGATTTTCCTGGATATTTTGCTTAAATGATGTGCTTTTCTCCACAGATCGCTGATGTCCTGGCTAAGATGAAGCCAAGTGTGCTGCTCACATTGGTAAGATTGTTCATTAGATGATGGTTCAGTTCAATTCTTGCCTACAATAATGAGATGGTTTAACGTGTTTCTCTGTGTTTCTTCGTGTGTAG[C/T]GAGGGCTGAACACTGATAGCGGCAGCACCTGTCGTGAAGCCTCCTTTGAAGGCATCAGTCGGTGAGTTTCATCCTTTATTCAGAGTTCTGCTCCTGAAACTCACTCGGAGAAAGTGGCACACAAAACCCTCTGTGTGTTTGATGTAAGATCACACACAGGGTTTAGATATTCACTGTTATCTCTTACTGCAACATTTATGGACGAGGACGTTTTAATAGTGTCTGAATGTCATCGCATTAGATACAAAAGAGTCCATTCAGTTCAGCTCAATTCAAAAGAGTCAATTCAGCTCTGTTCAGTTCATAAGAGTCCGTTCAGTTCAATTCAAAAGAGTCAATTCAGCTCTGTTCAATTCAAAAGAGTCCATTCTGATCAGTTCAATTTAAAAGAGTCGATTGAGCTCTGTTCAATTAAAAAAGTCAGTTCAGTTCAATTCAAAAGAGTCAATTCAGCTCTGTTCAGTTCATAAGAGTCCGTTCAGTTCAATTCAAAAGAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5906
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 |
|---|---|---|---|---|---|
| ENSDART00000004023 | Essential Splice Site | 209 | 496 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 1153959)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN149820.1 | 234 |
| GRCz11 | 18 | 1354172 |
KASP Assay ID:
554-3645.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAGTTCTGCGCTACACAAACCGCATTTCCAGCGAAGCCCATAAAGAGG[T/C]AAAAACACCACCGTCTGTCAATTCATTTCMCTGTTAATAAGCTATWCTCT
Long Flanking Sequence:
TTAATTGAAATAATAAAATAAATAAATAGTTGAAATAAATAGTTAAATAAATAAACAAATAGTTTAAATAAATAGTTAAATGAAGTAAATGGATAAATAAACAATTGAAATAAATAGATAAATAAACAGCTAAATAAATAAATAAATAAGTAGTTGAAATAAATAGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATAGTTGAAATAAATAGTTAAATAAATAAATAAATAGTTGAAAAAAACAAATTAATAGTTGAAATAAATAATTAAATAAATAATCAGTTAAGTAAGTAATTAAGTAAGTAAATAAGTCGCAGATCATTAATGGTGTTTATTTCTCTCTGTCTGTAGTCGTCTGCTAAAGACCGACATGGAGCTGGAAGTTCTGCGCTACACAAACCGCATTTCCAGCGAAGCCCATAAAGAGG[T/C]AAAAACACCACCGTCTGTCAATTCATTTCCCTGTTAATAAGCTATACTCTTGGCAGAGTGTTTGCAGGATGATCCAGAGGGAGAATCACTCATAAACACACACAGATGCGCTGAAGTTGAGCTTGTGTTTTCTGCATTGTTAGTGTGTATCAGTACAGTAAACGCTTCCAGAATAATCACACAGATTCAGACCGTTTGATCAGAATCTAGGCCAGCCATGCATTTATTCTTCACAAGGCAATACCAGCATGCTAAACACTTGATAACTGAGCACAGAAAATAGTTTACATCTTGATTTAGATTCATTAATGATTTAATACTAAACAAAACATGCAAATAATAGAAAATAAAACAAACAAACTCTGCCCAATGTCTGCTATTTGTGAATAAGCTTGCATGATGTATATTATTAGTCTTCAGTCACTTTGCTGTAAATCATTCAGACTCTCAGCATAAGCGCTAGTATTTATAATGTGAACATGACGTTTGAGAGATGCATG
Associated Phenotype:
Not determined