ZMP
pgr
Ensembl ID:
ZFIN ID:
Description:
progesterone receptor [Source:RefSeq peptide;Acc:NP_001159807]
Human Orthologue:
PGR
Human Description:
progesterone receptor [Source:HGNC Symbol;Acc:8910]
Mouse Orthologue:
Pgr
Mouse Description:
progesterone receptor Gene [Source:MGI Symbol;Acc:MGI:97567]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23367 | Nonsense | Available for shipment | Available now |
sa23368 | Nonsense | Available for shipment | Available now |
sa32215 | Essential Splice Site | Available for shipment | Available now |
sa43163 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23367
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 |
---|---|---|---|---|---|
ENSDART00000052206 | Nonsense | 309 | 617 | 3 | 8 |
ENSDART00000128345 | Nonsense | 245 | 553 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 40225870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41835641 |
GRCz11 | 18 | 41825833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCATTGTTGATAAAATCAGGAGGAAAAATTGTCCCGCATGTCGTCTT[C/T]GAAAGTGCTACCAGGCAGGGATGATGCTTGGAGGTACTGTTCATATGTAT
Long Flanking Sequence:
TTTTAATATAACGTTTCAATGTGTATGAGTCAAGGTGTGTTACGGTGTCCCGGAAGACTTTAATTATCATTCGGACTGATGTTCCCAGTGTTCTTTCTTTGCCTTGTTTTTCTTGTTATCTCCAAGGAAAGATATGTAAGAGCCACTGTGTCTGACCATGGCCATGTCACTATGCCCTGTCAGCCTTGCTTCAAACCAATTCACTCTACGCCTCAATTTTTCTCTCTCTCTGTACTCTCCCAAATGATCTCACTTTAAAAATAACATGTTCCTACTATGATTTCAGGTGGAAGACTCGAATCATTTATGTGCATTGTGTTCATACTTTTTTCATCTTCTTCACACATTCATAAGTTGAATCATTTTCCTTGTAGTGTTGAGTCGAATGTTTTGTTTTTTGTTTTCTTCTTTGTCTAGGTCATCATAACTACCTGTGCGCCGGACGAAATGACTGCATTGTTGATAAAATCAGGAGGAAAAATTGTCCCGCATGTCGTCTT[C/T]GAAAGTGCTACCAGGCAGGGATGATGCTTGGAGGTACTGTTCATATGTATATATTTTAAATGTTTCTTACTTCTATTGAACTTATTGGTCAAAAGTGGGCAGTTTTTAAATTGTGAGACAGAATTTTTTCTGAAAATCAATTTTAAGTGCACTTGGTGACCAGTGTTGATGGTAAGGGATTACAAGTACATTGAAAAAAATTACACCTTAAACTAACTTATTTTTTTTCCTTCCTCAAACTTTTGTTAAATTCAACTAATAAAATTAGAAAATAAAATAAAAAATTTGGGCGGCTCAGTGGTTAGCACTGTCATCTCACATCAAGAAGGTTGCTGGTTCGAGTCCCAGCTGGGTCAGTTGGCATTTCTGTTTAGAAATTGCATGTTCTCTCCATGTTCGCATGGGTTTCCTTAAGGTGCTCCGGCTTCCCCCACAGTCTAAAGACATTCGCTATTGGTGAATTAACTATAGTGTATTAAGCCATAGTGTATGTTTGCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23368
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052206 | Nonsense | 412 | 617 | 4 | 8 |
ENSDART00000128345 | Nonsense | 348 | 553 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 40229968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41839739 |
GRCz11 | 18 | 41829931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCTCCTCCTCAACAGCCTCAACAGACTCTGTGAGCGTCAGCTGCTCT[G/A]GATTGTCAGATGGTCCAAATCTCTTCCAGGTAACAATTTGGCTAATCGAA
Long Flanking Sequence:
AGTGAGGGATTATAGAACTACTAAACTGTGTTTTATTTCTTTATTGCTGAGATCGCCTCGGTAATTCTAGTGTTAAAGACCATTAAATAAGACAGCGGCTCCCACCCAGAAGACTCCAAGACAACAAATAAATTATGTTTTCATCCATCAAATCACATCATAATCTATCATACAAGAGTGACCAGATGATCAAAATGTACAACATGTCCATTGGTGTGTTTCAGGCCGTAAGATGAAGCGGTTTGCGGGACTGAAGGTCATGGGTCTGAGTCCTTCGCTGATGTTCCAGAGTCCGTTATCTCTGCTGACTGACGGTCAGACTCTGTCCTCTTTGCCCTGCATGTCAGCCATGCGTGAGCTCCAGCTGTCTCCGCAGATGATCAGCATCCTGGAGAACATCGAGCCGCAGGTGGTTTACTCCGGATACGACAACACACAGCCAGAGGTTCCTCACCTCCTCCTCAACAGCCTCAACAGACTCTGTGAGCGTCAGCTGCTCT[G/A]GATTGTCAGATGGTCCAAATCTCTTCCAGGTAACAATTTGGCTAATCGAAGTCTTCATGAAACAAACATAGATCCTTGAAATAAAATATGGTTTTGTTTCAACAATTGTACTATATTGCCAAAAACAGAACGAAAAACAGAGAAATTCTTAGATTAAAAATCTTACATTTAAATCTTGTACAATTACACTGATAAATCCCAACAGGTACACAACGTCATAAGATGTTAATATTAGGTTAGATTTAGTTTATGATGTTGGGTGACCAAAATTCAATGTTGTGTTGGAAAGTGACCAAAATTTAACGTTGAGCCATCATTTTAAACCAATCCCATATTGATGTCGAATACTGAAATTTATTCAACCAAAATCCAACGTCCGCTAGACGTCATAGTGGTAACGTCCACACAACATCAAGCTGTAACATCATTAGGCGTAAATATTTAGTTATTTTTAGGTTGCGTTGGAAAGTGACCAAAATCCAACATCTCTTTGATGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32215
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052206 | Essential Splice Site | 470 | 617 | 5 | 8 |
ENSDART00000128345 | Essential Splice Site | 406 | 553 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 40232387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41842158 |
GRCz11 | 18 | 41832350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTCACCCCTGATTATCTGTATTTTGCACCCGATCTTGTCCTGAGCAA[G/A]TAAGTAAGAGTGAAAGAAATTCAATTAATTTCTGTTGTGGTTAAGACATG
Long Flanking Sequence:
TAACACCTCAGAAGGCAATTACACCAGGTGACTTTTGTTGCATCAGCTATGTGAAAAAAAAAAATCATAGTTATTATTCAAATGTCAGATACCCTTGTGGTCAAAGTGATTGACTTACTGTAGGAAACAAATAAGACGTTGACATTTTCCGAATCACCAAGGACCATGGTTTCATCTAGATTTATTTATCTTTATTAAAGTAACATCCCATTTGATTTAGGTGGCTTTTATTTTTGATCTGGGGTACTGAAATCTATCCAAAGCACCAAATAACTGAGATCTTTATAATCATACAATGCTACAGTAAGTTCAGATTCTTCAATAGATATTTCTTGTTCATCTGTGTTTAACAAAGGTTTTCGTAATTTGCACATCAATGACCAGATGACACTAATTCAGTATTCCTGGATGGGCTTGATGTTGTTCTCGCTGGGTTGGAGAACCTTTCAGAATGTCACCCCTGATTATCTGTATTTTGCACCCGATCTTGTCCTGAGCAA[G/A]TAAGTAAGAGTGAAAGAAATTCAATTAATTTCTGTTGTGGTTAAGACATGATATCCTTCAGCTTTTGTCATTTTTAACAAAATATGGTCAAAACTAACCCTAACCCTGACCCTAACAAAAAAAAAGTAGGTTTTAAGAATTTGAGTATTTTTTACGTTGAAAAAAAAAAACATCCTGCTGTTTAATTAAGGCGGCATTATTCCCGTCACTGTGAATGAGTAGCTTGATAAGAATAAAGGTCTCACATGAACACAGTGAATCTTCCTGAACTACTGAGTTCATGTGAGACATTTATTATTATTAGGTTACTTGGATGGCTTGGATGTCAGAGCTGGTGAAAACAGGGTAAATCTGTAGAAACAGACTGTTTTTCACGGAGCCAGATCAGTCTCAAAAATAATACATTTGCAAAATAAAATTCAAGCATGCACAGCACAGTTTATAATTCATGCACAACTCCAATTCGTAAATTTAAAATGCAGTTCATAAATGCACAACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43163
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052206 | Nonsense | 519 | 617 | 7 | 8 |
ENSDART00000128345 | Nonsense | 455 | 553 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 40236239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41846010 |
GRCz11 | 18 | 41836202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTAATGTTTCAACGCTGATGTGTTTGTGACAGTTCCTCTGGAGGGCT[T/A]GAAGAGTCAAACACAGTTTGATGAAATGAGGCAGAACTACATCTGCGAGC
Long Flanking Sequence:
TTGTTCGCAACCACCTCAGCAGCCAATGAGCTTGCTCCTCAGCATTTAAATACCTCAATGTCGTTTGAGCTAGCACGTTTTTGGATACCTGCCTTGACCTAAGCTTCACCAGTGAATAGATCTGCAACAGGGGGTTACATGTATCTCGGTGTTATGTTGTCAGGCAGCATGTTTGCGAATATACTGGCTTTACTTGCTTTGGACCAATAAACATAGCAGCAGCAGCGTAGCAGATTTATTCCTCCAAGACCAAATGTATTTTTTTATACTAAATAAAACTAAATTTAGATGATAAATCTAATTCTGTCAAACTGCTGAAGAGGCCACTGTCAGTCAAGATATGTTTACTGTCTAGAGAGGTGTCACCATTCCAGCATTTAAAAGAAGCTTTCTTTCATCTGAGACAGCAGTACTGTGGTAAACTCTATCATCACTGTGGGGAGATGCGTATCAGTAATGTTTCAACGCTGATGTGTTTGTGACAGTTCCTCTGGAGGGCT[T/A]GAAGAGTCAAACACAGTTTGATGAAATGAGGCAGAACTACATCTGCGAGCTGTCCAAAGCCATCCAGCTAAAGGAGAAAGGAGTGGTGGCCAGTTCACAGAGATTCTACCATCTGACCAAACTCATGGACAACATGCATGAGGTACAGTACAGCACACAGAACAAAATACACAGACCTTGTTCTTTATGTATGAAGCAGCCATTAGAATCTTTAAGGCTGGAGATTTCCGTTCTCATTCACTTTCATGGATTTTTCAACGATATCTCATGTCAATTCGTAACATTTTTATTTAGTGGTTAATTCGTATGAATTGATACAATCTAATTCTGACAATTTACTACGTTTAGCTCATCCCCCAATGACAGTTGGGGTTAGGTGCCACGCCTCCTTTTTAAAATCATACATACGACTGAACTCGTACGAATTAGCCACTAAACTGACGAAATGTAAAATACTTACGTTTCCTCATGAGATCAGGGTGGATTTTTAGACGTTAAAA
Associated Phenotype:
Not determined