ZMP
pafah1b3
Ensembl ID:
ZFIN ID:
Description:
platelet-activating factor acetylhydrolase IB subunit gamma [Source:RefSeq peptide;Acc:NP_957352]
Human Orthologue:
PAFAH1B3
Human Description:
platelet-activating factor acetylhydrolase 1b, catalytic subunit 3 (29kDa) [Source:HGNC Symbol;Acc:8
Mouse Orthologue:
Pafah1b3
Mouse Description:
platelet-activating factor acetylhydrolase, isoform 1b, subunit 3 Gene [Source:MGI Symbol;Acc:MGI:10
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9090 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42671 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9090
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060145 | Nonsense | 35 | 221 | 3 | 6 |
| ENSDART00000134793 | Nonsense | 35 | 209 | 3 | 9 |
| ENSDART00000136329 | Nonsense | 35 | 78 | 3 | 4 |
| ENSDART00000141101 | Nonsense | 35 | 221 | 4 | 7 |
The following transcripts of ENSDARG00000058047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 13528563)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 11887654 |
| GRCz11 | 16 | 11778556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ANNNNNNNNNNTAATAACATTGTCTTGTCTTTGCAGCACAATCGATTTGTATCAGACAGT[A/T]AAGGAAAAGAGCCYGAWGTTCTGTTTGTTGGAGATTCACTCATCCAGCTT
Long Flanking Sequence:
TTACTCTATTCGTGCTTGCCACAGGACATGAAGAACACATAATCTAACCTCAGTACAACTTAAATTAGATATTTAACATATTTATAGTTTTTTTTACGTTTAGACACAAAAATTGCTTCAAGTATGCAACTTGGATTTAATATTTTTGCATTACTTAAAGCATTTTTGTGCTTAACTGTAAAACATCAGATGTTGTTTTGTTTAAAGCAAAGATCATGGAGGAAATGTGACCTGCCATGTCCCTCTGTCTTTCTTCAGGAAGTGATGAGTGGAGATTCAAACCCTGCAGCCACACCCACCCCCTGTCAGGACATACAGGGAGATGGACGATGGATGTCATTGGTGGTTCTTTTGAATAACATCAGAATTAAAAAGAGATTTATATGTTCCGTCCAGATAAGATATCTGTATTATGCTGCTAAAATGTGATTGTCTGCTTTTCTCATATGCATAATAACATTGTCTTGTCTTTGCAGCACAATCGATTTGTATCAGACAGT[A/T]AAGGAAAAGAGCCTGATGTTCTGTTTGTTGGAGATTCACTCATCCAGCTTCTGCATGAGTTTGAGGTATAGCAAAGTGTGCATACTTGATACACGCCCATATAGACAATGAGGATAAGGGTATTCAAGCCTCAAAACAATAAAAGTGTAATGCAACACTTAAATGTGACCTGCTGAGACACTCGCATACATGTATAAAATATCTTTTCTTGTTGGCAGGTTTGGAGAAAATTGTTTTCTCCTCTCCACGCTCTAAACTTTGGGATTGGTGGAGATGCTACGCAGCATGTGCTGTGGAGGCTCATCAATGGAGAACTGGATTACATCAGCCCAAAGGTACATTATTTAAGATTTAGCTTTTTTAGCTATTATTTTATTTTCAATGAAGGATTAACAAAGGAGAAAAAAATCCCTCAAATGTAATTAAATAAATGTACTAACAGAAACAAATGAAGGAGACCTTGTTGTAATAGAATAGAGGAATTTAATGGTTTTTTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42671
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060145 | Nonsense | 38 | 221 | 3 | 6 |
| ENSDART00000134793 | Nonsense | 38 | 209 | 3 | 9 |
| ENSDART00000136329 | Nonsense | 38 | 78 | 3 | 4 |
| ENSDART00000141101 | Nonsense | 38 | 221 | 4 | 7 |
The following transcripts of ENSDARG00000058047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 13528554)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 11887645 |
| GRCz11 | 16 | 11778547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTTGTCTTTGCAGCACAATCGATTTGTATCAGACAGTAAAGGAAAA[G/T]AGCCTGATGTTCTGTTTGTTGGAGATTCACTCATCCAGCTTCTGCATGAG
Long Flanking Sequence:
TCGTGCTTGCCACAGGACATGAAGAACACATAATCTAACCTCAGTACAACTTAAATTAGATATTTAACATATTTATAGTTTTTTTTACGTTTAGACACAAAAATTGCTTCAAGTATGCAACTTGGATTTAATATTTTTGCATTACTTAAAGCATTTTTGTGCTTAACTGTAAAACATCAGATGTTGTTTTGTTTAAAGCAAAGATCATGGAGGAAATGTGACCTGCCATGTCCCTCTGTCTTTCTTCAGGAAGTGATGAGTGGAGATTCAAACCCTGCAGCCACACCCACCCCCTGTCAGGACATACAGGGAGATGGACGATGGATGTCATTGGTGGTTCTTTTGAATAACATCAGAATTAAAAAGAGATTTATATGTTCCGTCCAGATAAGATATCTGTATTATGCTGCTAAAATGTGATTGTCTGCTTTTCTCATATGCATAATAACATTGTCTTGTCTTTGCAGCACAATCGATTTGTATCAGACAGTAAAGGAAAA[G/T]AGCCTGATGTTCTGTTTGTTGGAGATTCACTCATCCAGCTTCTGCATGAGTTTGAGGTATAGCAAAGTGTGCATACTTGATACACGCCCATATAGACAATGAGGATAAGGGTATTCAAGCCTCAAAACAATAAAAGTGTAATGCAACACTTAAATGTGACCTGCTGAGACACTCGCATACATGTATAAAATATCTTTTCTTGTTGGCAGGTTTGGAGAAAATTGTTTTCTCCTCTCCACGCTCTAAACTTTGGGATTGGTGGAGATGCTACGCAGCATGTGCTGTGGAGGCTCATCAATGGAGAACTGGATTACATCAGCCCAAAGGTACATTATTTAAGATTTAGCTTTTTTAGCTATTATTTTATTTTCAATGAAGGATTAACAAAGGAGAAAAAAATCCCTCAAATGTAATTAAATAAATGTACTAACAGAAACAAATGAAGGAGACCTTGTTGTAATAGAATAGAGGAATTTAATGGTTTTTTATGTCTGTTTGTG
Associated Phenotype:
Not determined