ZMP
ptgesl
Ensembl ID:
ZFIN ID:
Description:
Prostaglandin E synthase 2 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUC7]
Human Orthologue:
PTGES2
Human Description:
prostaglandin E synthase 2 [Source:HGNC Symbol;Acc:17822]
Mouse Orthologue:
Ptges2
Mouse Description:
prostaglandin E synthase 2 Gene [Source:MGI Symbol;Acc:MGI:1917592]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10731 | Nonsense | Available for shipment | Available now |
sa41245 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10731
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 |
---|---|---|---|---|---|
ENSDART00000098936 | Nonsense | 111 | 377 | 2 | 7 |
ENSDART00000129882 | Nonsense | 112 | 378 | 2 | 7 |
The following transcripts of ENSDARG00000068415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31856838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30999564 |
GRCz11 | 8 | 31008796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTGTTTCAGGCATCAGATCTGGACACAGACCTGAAATTGACTCTCTAT[C/T]AGTATAAGACCTGTCCGTTTTGCAGCAAAGTGCGAGCTTTCCTGGATTAT
Long Flanking Sequence:
TGTCATTGCGCTTGCCGTAGATTTGTGGGAGTTTATGTAAAATCATGATGGCGGCGGCCTGTACGAGAACGCTGGGTAAGGTCGGCCGGTTAGTTTTAGACACGCCGACGTGCCGTTTTACAAACACTGCGGCATTCGTGCCGAGAACCTCCATGAGATGCCAAGGGAGAGCTTACGGTACCGGTAGCTCGGGGTTTAAATCCAGACTTTTGCTCGCGGCGCCGGTGCGAGGCAGTGGCAGAGTCCTGGGATGCGCCTTCTTGCTCGGAGGTGGTTTCGGCTTGTACCAGACCATCAAACTCACACTTCAACATCACCTTGCAGAGAAAGAAGCTGACGTAAATATACACGAATGTGCAATGTCTGACACCCTTGAAATTTTCTCGTTGACGTGCAGCTGTTGAAAGTCCAATATGTGTAATTTTTAGTTTGCTGGCTTACCTTGATTTTTATTGTTTCAGGCATCAGATCTGGACACAGACCTGAAATTGACTCTCTAT[C/T]AGTATAAGACCTGTCCGTTTTGCAGCAAAGTGCGAGCTTTCCTGGATTATCATCGACTGCCATATGAAATCGTGGAGGTCAATCCCGTTATGCGGCAGGAGATCAAGTGGTCGACCTACAGAAAAGTCCCCATCCTGATGGTGAACGGGACGGTGGTATGTAGTCTTTCCTGATTATGGATAGTGAAGTATATGATGCTTCTGCTCACAAAGTCTCTTTCTTGATCGATTCCTCAACAGCAACTGAATGACTCTTCAGTAATTATTAGTGCTTTGAAGACATACATTAGCAGCAAGTGAGTATCTTCTGCTTGAATAGTTTTATTTTATTTGTATGGATGTTATTGTTAGACTATTTATAAGATATGTCTGCATAAAAACAAATTCTAATCTACAGAATATATTGATATACTTATTAAAATGGGAATTATAATTAAAACATCATTACAAATTTAGTTTTTTTGCCTGATAAATGGATAAATCAGTGACAACGTATAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41245
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098936 | Nonsense | 244 | 377 | 5 | 7 |
ENSDART00000129882 | Nonsense | 245 | 378 | 5 | 7 |
The following transcripts of ENSDARG00000068415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31858973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31001699 |
GRCz11 | 8 | 31010931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTATTTCTCAGAGAAGAGATTAAATGGCGGACATGGGCAGATGATTG[G/A]CTGGTGCATCTAATTTCCCCAAATGTTTACCGGACGCCAACTGAAGCCCT
Long Flanking Sequence:
GTTTGACGCAGAAGTATAAATCAGCCTTAAGGAGTCCATTTTTATTTTGGGTTAACTATCCCTTTAAGTACTGCATTCATTTTTGTGATTGCTTCTTCGCTATAAAAAAGTTGTGGTTCTGTTCATTCTGGCAAATGAATGTAAATTTAAATGCAAATTTGGATGGTCTGTTTTCTCCTCCTAGGGACAAAAAGATATCTGAGATTCTTGCTTGTTATCCTGAAATGAAGTCAAAGAACGACAGAGGGAAAGACGTGATAGAGTTTGGCAATAAGTACTGGGTCATGGTGCATGACGCGGATGCTGATCAACTATATCCTGGAAAAGACAGCAGAAAGTAAAGCAAATCAGTTATGTCTGAGAGTGATTGCATTCTCAACATTTCATTTTTTATTTACTGTGTCAAACAATAATTTAGCTTTATGGGGCTTCCTCTATGTTTCAATAACATTTTTATTTCTCAGAGAAGAGATTAAATGGCGGACATGGGCAGATGATTG[G/A]CTGGTGCATCTAATTTCCCCAAATGTTTACCGGACGCCAACTGAAGCCCTCGCATCTTTTGACTACATAGTACGGGAAGGGAAATTCGGTTCCTTCGAGGGCTTTTTTGCTAAGTATTTTGGAGCTGCTGCCATGTGGATCATCTCAAAGAGATTAAAATATAAGTATGCACCTGTTGGCAGTGTGTAAATAATATGTAAAAAAAATGATTTGATATTAAAGTTAAATTTGCTCGTTCTACAGACACAATCTGCAAGCTGATGTAAGGCAGGATCTTTACAAGGCTGTCAATGACTGGGTGGCAGCCATTGGAAAAAACAAGCAATTCATGGGAGGTGATGAACCCAACCTTGCAGATCTGGTATGTGTTTTTCTGATAGACAGAAATTATATTAATAGAAATACACTTTATTTCTGTAAACTGGGGTCTATGAAAGCTTTTTCCACCACTAAATGAAAAAAAGGTTATTGCTACTTTTTAGCTCAGAATTCAAAATCCT
Associated Phenotype:
Not determined