ZMP
ppdpfa
Ensembl ID:
ZFIN ID:
Description:
Pancreatic progenitor cell differentiation and proliferation factor A [Source:UniProtKB/Swiss-Prot;A
Human Orthologue:
PPDPF
Human Description:
pancreatic progenitor cell differentiation and proliferation factor homolog (zebrafish) [Source:HGNC
Mouse Orthologue:
Ppdpf
Mouse Description:
pancreatic progenitor cell differentiation and proliferation factor homolog (zebrafish)RIKEN cDNA 27
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21282 | Essential Splice Site | Available for shipment | Available now |
| sa6098 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21282
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 |
|---|---|---|---|---|---|
| ENSDART00000032996 | Essential Splice Site | 45 | 117 | None | 5 |
| ENSDART00000137536 | Essential Splice Site | 45 | 90 | None | 5 |
The following transcripts of ENSDARG00000007682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 24068249)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23194067 |
| GRCz11 | 8 | 23215306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTAGCAGTTCGGAGTACACTGGGGAGGTCATTCCACACCCACCAGG[T/C]ACAAACAAAGCATCACATCAGTACCACAATGACTGCATTACAAATACACA
Long Flanking Sequence:
TCCATCTTCCACACGGTCGACCCTTTAGAGGACGGGGAAAATGGCAGCAATTCCATCCAGCGGTTCCCTCATCGCCACCCATGATTACTACCGAAGTGAGTTTAGTTTTATTTTATATCAAAATAATTCAACACAGTGGAATCCAATGCTAAATCCAACAAGAGTGGATTAAAAGTGGTAATATATACACTTAAAAAGTTTCACAATGATAAATGCGCTGCTTATTTTCTGTTAGTTACAGAAGAATATGGGGAAATCATTCTGCAGTTTTGAATTCATTTATTTAATCTGTCAAAAATATGTAATACATAATTCATTTGCAATAATAGAAGGCTGATGCTCCAGGAAGGAGCTTCAGTTATTATTATTTTATTAATATTAAGTAATATTTATTGATTACTAATATTTATTGATGTTTCAGGGCGCATTGGATCTACATCCAGTAACAGTTCCTGTAGCAGTTCGGAGTACACTGGGGAGGTCATTCCACACCCACCAGG[T/C]ACAAACAAAGCATCACATCAGTACCACAATGACTGCATTACAAATACACACAATACAGTCAGCTCTCACTGTGCCAAAAGCTCAAGGTGTTCTTGCACGGCAGGTCTGGCACGTCAGGACTCTGGCCACTGGTGGTCCAGTTTCTTCTTTGGGAAGCAGAATCAAATGGGAACACCCAACGGATTTGAGTCCCAGCAGAAGTGAGTTGAGCACCTGCTGTTGTTTATTTTGTCTTAACTTTTGGTGCTGGTTTTCACACAGTGTTTTTTGTTTTTTTTTGTGTGGCAGGACTGGCACCTACACAGTGACAAACGGTCAAGTGACCTGCGTCGCTCGCGAGATTGTAATGAAGAGGCATTTGAGTGAGAGCAGTGACTCTGGGAAGGAGCCGGGTTCACCCCTGCCCTCATAAAGCACACACCACCACGCACCCCACCCTCATCCAGGAGTCACCGTGGGCCGGCGCTGGCGACGGAGGCCCTGCTTTTTTTTTTTCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6098
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:
G > A
Consequence:
Missense, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000032996 | Missense | 47 | 117 | 4 | 5 |
| ENSDART00000137536 | Nonsense | 54 | 90 | 4 | 5 |
The following transcripts of ENSDARG00000007682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 24068358)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23194176 |
| GRCz11 | 8 | 23215415 |
KASP Assay ID:
554-3886.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCTCTCACTGTGCCAAAAGCTCAAGGTGTTCTTGCACGGCAGGTCTG[G/A]CACGTCWGGACTCTGGCCACTGGTGGTCCAGTTTCTTCTTTGGGAAGCAG
Long Flanking Sequence:
ATTTTATATCAAAATAATTCAACACAGTGGAATCCAATGCTAAATCCAACAAGAGTGGATTAAAAGTGGTAATATATACACTTAAAAAGTTTCACAATGATAAATGCGCTGCTTATTTTCTGTTAGTTACAGAAGAATATGGGGAAATCATTCTGCAGTTTTGAATTCATTTATTTAATCTGTCAAAAATATGTAATACATAATTCATTTGCAATAATAGAAGGCTGATGCTCCAGGAAGGAGCTTCAGTTATTATTATTTTATTAATATTAAGTAATATTTATTGATTACTAATATTTATTGATGTTTCAGGGCGCATTGGATCTACATCCAGTAACAGTTCCTGTAGCAGTTCGGAGTACACTGGGGAGGTCATTCCACACCCACCAGGTACAAACAAAGCATCACATCAGTACCACAATGACTGCATTACAAATACACACAATACAGTCAGCTCTCACTGTGCCAAAAGCTCAAGGTGTTCTTGCACGGCAGGTCTG[G/A]CACGTCAGGACTCTGGCCACTGGTGGTCCAGTTTCTTCTTTGGGAAGCAGAATCAAATGGGAACACCCAACGGATTTGAGTCCCAGCAGAAGTGAGTTGAGCACCTGCTGTTGTTTATTTTGTCTTAACTTTTGGTGCTGGTTTTCACACAGTGTTTTTTGTTTTTTTTTGTGTGGCAGGACTGGCACCTACACAGTGACAAACGGTCAAGTGACCTGCGTCGCTCGCGAGATTGTAATGAAGAGGCATTTGAGTGAGAGCAGTGACTCTGGGAAGGAGCCGGGTTCACCCCTGCCCTCATAAAGCACACACCACCACGCACCCCACCCTCATCCAGGAGTCACCGTGGGCCGGCGCTGGCGACGGAGGCCCTGCTTTTTTTTTTTCTCTCTTATTCTTATTCTTTTTTTAGTAAAATCCGGCTGCTTTTTACGTCATGCTATATAGTGCTCTTTTTTTTTTATTCCTGACCAAATAAACTTTGTAAAGCTTTAAAGTGC
Associated Phenotype:
Not determined