ZMP
PTGFRN (2 of 2)
Ensembl ID:
Description:
prostaglandin F2 receptor negative regulator [Source:HGNC Symbol;Acc:9601]
Human Orthologue:
PTGFRN
Human Description:
prostaglandin F2 receptor negative regulator [Source:HGNC Symbol;Acc:9601]
Mouse Orthologue:
Ptgfrn
Mouse Description:
prostaglandin F2 receptor negative regulator Gene [Source:MGI Symbol;Acc:MGI:1277114]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39530 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39530
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110331 | Nonsense | 36 | 867 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 1705916)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1801336 |
| GRCz11 | 1 | 1949130 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCCGGTCAGTTTCGGTGTCTGGGGGCCCTTTGCTCCGGGTGGAGGGC[C/T]AGCCACTGTCCATCCGCTGTGATGTGTCCGACTATGAGGGCCCCAGAGAG
Long Flanking Sequence:
GCAAGTTTTGCCCAGCAGTAATTATATTCTGTATATTTATTTATACCATTTTTAATGAATTAAATCTGAAAAAAAAATGGCTAGTTACCATATTTACATTGTCATAGTGCATAAAATCATAATAAATCATAACAACATTTCCATATTATATGCTGAACTGTTAAAAGACCTTGCAAATTAATTGGTTGTGTTTATAAAAGAGTCATTACTATTGTTTTTTAATTGTTTATACAGTTTTTAAATGATTTAAATTATGAAAATTGCAGGTTTTCATAATAATAAATCACAATAAAAGCCTCACCTTGTATCGATTGCACTGTATCATTTGGAATTATGCTCATTAAATGGTTTGCTAACACAGTTTCATGTTGACATAATTGAAAGTGTATTTGATATAAGGGCTGATCAATAACTCCCTGTTGTGTTGTTGGTGTTTTCCAGGTTTATGCAGCTGCCGGTCAGTTTCGGTGTCTGGGGGCCCTTTGCTCCGGGTGGAGGGC[C/T]AGCCACTGTCCATCCGCTGTGATGTGTCCGACTATGAGGGCCCCAGAGAGCAGGACTTTGAATGGACTGTAACACGAGAAACAAAAACCATCAACGTGATCTCCACATTCGATCCTGCATTCTCAGACCGCTCTCTACAGGACCGCATAAAGACCGGCGACATTAGCATAGCACGACTTGCGGACAATGTAGTGGAACTGAGGATTCAAGAGGCTCAAATTAGCGACAGCGCCACCTATCGATGCAGTACTCCAAGCACAGACTCGGTGATAAGCGGAAACTATGAAGCATCTGTTCAGCTGCAAGGTTAGTTGAAGATAAGGCTGTATGATACTGGAAAAATCCAAGTGGTGCTCGCTGCAGAGCCATTTGGGCGAGCTGAGCTCCAGCGAGGGGGAGCTTGAGCTTGAGCTCCACCTTTTTTGGACTTCTTCTACGAGTGATGTCACTGGGGGTAGGGTTAGGGGTGGGGTTGGTGTACGCATTAAAACAGCTGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38238
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110331 | Nonsense | 82 | 867 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 1706054)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 1801474 |
| GRCz11 | 1 | 1949268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAACGTGATCTCCACATTCGATCCTGCATTCTCAGACCGCTCTCTA[C/T]AGGACCGCATAAAGACCGGCGACATTAGCATAGCACGACTTGCGGACAAT
Long Flanking Sequence:
TTCCATATTATATGCTGAACTGTTAAAAGACCTTGCAAATTAATTGGTTGTGTTTATAAAAGAGTCATTACTATTGTTTTTTAATTGTTTATACAGTTTTTAAATGATTTAAATTATGAAAATTGCAGGTTTTCATAATAATAAATCACAATAAAAGCCTCACCTTGTATCGATTGCACTGTATCATTTGGAATTATGCTCATTAAATGGTTTGCTAACACAGTTTCATGTTGACATAATTGAAAGTGTATTTGATATAAGGGCTGATCAATAACTCCCTGTTGTGTTGTTGGTGTTTTCCAGGTTTATGCAGCTGCCGGTCAGTTTCGGTGTCTGGGGGCCCTTTGCTCCGGGTGGAGGGCCAGCCACTGTCCATCCGCTGTGATGTGTCCGACTATGAGGGCCCCAGAGAGCAGGACTTTGAATGGACTGTAACACGAGAAACAAAAACCATCAACGTGATCTCCACATTCGATCCTGCATTCTCAGACCGCTCTCTA[C/T]AGGACCGCATAAAGACCGGCGACATTAGCATAGCACGACTTGCGGACAATGTAGTGGAACTGAGGATTCAAGAGGCTCAAATTAGCGACAGCGCCACCTATCGATGCAGTACTCCAAGCACAGACTCGGTGATAAGCGGAAACTATGAAGCATCTGTTCAGCTGCAAGGTTAGTTGAAGATAAGGCTGTATGATACTGGAAAAATCCAAGTGGTGCTCGCTGCAGAGCCATTTGGGCGAGCTGAGCTCCAGCGAGGGGGAGCTTGAGCTTGAGCTCCACCTTTTTTGGACTTCTTCTACGAGTGATGTCACTGGGGGTAGGGTTAGGGGTGGGGTTGGTGTACGCATTAAAACAGCTGACAGGAGGCAGAGCGAGAGCTCATGCTCCCCCTCGCTGGAGCTCAGCTCTGCTCAAATGGCTCTGCAGCAAGCACCCTCTCGAAAAATCTGACATTGCGATGTTTTGTTTTGTCTAGGGCTGCACGATATTGGATATTGCAA
Associated Phenotype:
Not determined