Busch Lab

ZMP

paqr5a

Ensembl ID:
ENSDARG00000041145
ZFIN ID:
ZDB-GENE-040426-867
Description:
Membrane progestin receptor gamma-A [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVH1]
Human Orthologue:
PAQR6
Human Description:
progestin and adipoQ receptor family member VI [Source:HGNC Symbol;Acc:30132]
Mouse Orthologues:
Gm6821, Paqr6
Mouse Descriptions:
predicted gene 6821 Gene [Source:MGI Symbol;Acc:MGI:3779634]
progestin and adipoQ receptor family member VI Gene [Source:MGI Symbol;Acc:MGI:1916207]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa29024 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36635 Nonsense Mutation detected in F1 DNA Not yet available
sa30704 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29024
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060311 Essential Splice Site 61 345 3 9
Genomic Location (Zv9):
Chromosome 18 (position 20244548)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20474771
GRCz11 18 20463837
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAACAAATGAAACCCTCAATATTTGGACTCATTTTCTACCTACATGG[T/A]AAGTTCTTTTTCGAGATATTTTTTTAAATATGGCCACATTTAGTTAGTTT
Long Flanking Sequence:
TCCAAAAGTAAGTTTCATTAATGCAGACTGGTTTGCAAACAAAAGTGACTGTGTTACAGGTATTTACCTGACAAATTCAAATTGAATTGATCTCTTTTAATCAATTCAAGTTGTACAGCACTTTTCACAAAAGTTGTCTTTCAAAGGCAGCTTCACAAATGCTGCACATCATTACATTACAGTCAAAATTAGGAAAGTTGTGGAGTTGTTTAAAGGGTTGGCAGTATATAAACGTAGTTACCTGCAGTTATACAGTATGATAAATTTACATCTAATAATAATACATGTTCAGTGTTTAATGTCCTCGAATATCTCGAATGGTTGGCCTCATCTCTTCTATATTATTATATCTCATCTCTATCTCATCATAGGTCTTCCATGAAGATGGTATCATCTCAGGGTATCGCCACCCATGCAGCTCTGCCAAAGACTGCGTGCTAAGTCTTTTCCAGCTAACAAATGAAACCCTCAATATTTGGACTCATTTTCTACCTACATGG[T/A]AAGTTCTTTTTCGAGATATTTTTTTAAATATGGCCACATTTAGTTAGTTTTAAAATCAAGACTAAATTCTGCATAATAATAACAACAATTGCACGTGTTCAAGTATCTGCTTAATTGTTACCTCATTCCATTTTATTTTGAAATATACATGTTTTATGTATGATATATGCATTTTTTTTTTATTATTTAAAGAAAAACTAACCTCTAAAATGTTATTTAACAATAGATTAGGTACACCCAAGTAAGATGACAAGCCTATTTAGATATGAATCACTTCACAACATATTAAATCAGCCCCAAAATGTGAATCATTTGTGATTTTATTTTGCTAAAATCCTTTAAACCACTGGGTGTTTACTCATTTGTCAGGATTTTAATCATTTCAAAATAGAAAAATGAAGTATAATCACATGCTACACTTACACAAGGTTACACTTACTAGTTGAAATTATTTCACCCATATATAGATATTTTATTTGTATTTTTTATATAGACGTTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36635
Status:
Mutation detected in F1 DNA
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
ENSDART00000060311 Nonsense 153 345 5 9
Genomic Location (Zv9):
Chromosome 18 (position 20243190)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20473413
GRCz11 18 20462479
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTACTCGTTTCCAGATAAATGGGTTAATGGCACATTTCACTTAAACTA[T/A]GTTTCTATAGCTGTTGTCAACTCTATTATCTCCACTGCTCTTGCCTGCTA
Long Flanking Sequence:
TGCTGTGTGTATCCACTGGCTTCCAGCTGCGCCCACACCTTCAGCACCATGTCTGAACGGGCCAGGCACATCTGCTTCTTTTTTGATTATGGAGCACTCAGCTTCTACAGCCTTGGTTTGTATATGATGCAAACAAAACTACAGGGTAAAAAGTTTCCAATTATGTACGACTTTTGTATGTTAATGGGATGGTTCACTCAAAAATGGGCATTTTGCCATCATTTTTACCTGCTTGGGGTTCTGTCTTTGAACAAAAATGAAGATATTGTGAAGCATTTTTCTTTTCCTACAGTTTTCAAAATTGAGTCTTTTGCTTTTACAGAAAAAACTCTGTGTGACCACTTGAGAATGAGTAAATGGTCAACAAATGTACATGTTGGTGTTTGAACTGTCCATCTAACCTTTACATTGTGTGTTTGTTTACCAACAGGTTCTGCCATCATCTACTCCTCTTACTCGTTTCCAGATAAATGGGTTAATGGCACATTTCACTTAAACTA[T/A]GTTTCTATAGCTGTTGTCAACTCTATTATCTCCACTGCTCTTGCCTGCTACTCAAGGTAGGATAGGTGATCAATAAAACCTATAATTCCAGTATGACTATTTTAGATACAGATTTTGCTTTAACTGTACATATTATGCAAAAATGTCTTGATGAAGCTTTTGATTTGTTTGTTTTTAGACTTGGTTTACCATTTCTTGAGTATAATTGCCACAGCATTAAAAGGTATTTATTGTTTTGCATTTTAATCTTGATTGTAAAAATAATGTTCAAGTGAATAAACTATTGTTATTCTCTTTTAGGCCTTCTGGGAAATTGGATCAGAAGCTTTGTAAATGTCTCCGGATAATTGCATTTGTTTATCCATATCTCTTCGACAACATCCCCCTCTTTTACAGAGTAAGTGGCTCATATCTGATTTTGTTTTGCTGCGCATTGCTTTAGCTGTATTTAAACTGAATTTGCATATGAATAACAGTCATTATTTTAAAGTGCCTGTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30704
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060311 Essential Splice Site 187 345 6 9
Genomic Location (Zv9):
Chromosome 18 (position 20242966)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20473189
GRCz11 18 20462255
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGACTTGGTTTACCATTTCTTGAGTATAATTGCCACAGCATTAAAAG[G/T]TATTTATTGTTTTGCATTTTAATCTTGATTGTAAAAATAATGTTCAAGTG
Long Flanking Sequence:
TTACCTGCTTGGGGTTCTGTCTTTGAACAAAAATGAAGATATTGTGAAGCATTTTTCTTTTCCTACAGTTTTCAAAATTGAGTCTTTTGCTTTTACAGAAAAAACTCTGTGTGACCACTTGAGAATGAGTAAATGGTCAACAAATGTACATGTTGGTGTTTGAACTGTCCATCTAACCTTTACATTGTGTGTTTGTTTACCAACAGGTTCTGCCATCATCTACTCCTCTTACTCGTTTCCAGATAAATGGGTTAATGGCACATTTCACTTAAACTATGTTTCTATAGCTGTTGTCAACTCTATTATCTCCACTGCTCTTGCCTGCTACTCAAGGTAGGATAGGTGATCAATAAAACCTATAATTCCAGTATGACTATTTTAGATACAGATTTTGCTTTAACTGTACATATTATGCAAAAATGTCTTGATGAAGCTTTTGATTTGTTTGTTTTTAGACTTGGTTTACCATTTCTTGAGTATAATTGCCACAGCATTAAAAG[G/T]TATTTATTGTTTTGCATTTTAATCTTGATTGTAAAAATAATGTTCAAGTGAATAAACTATTGTTATTCTCTTTTAGGCCTTCTGGGAAATTGGATCAGAAGCTTTGTAAATGTCTCCGGATAATTGCATTTGTTTATCCATATCTCTTCGACAACATCCCCCTCTTTTACAGAGTAAGTGGCTCATATCTGATTTTGTTTTGCTGCGCATTGCTTTAGCTGTATTTAAACTGAATTTGCATATGAATAACAGTCATTATTTTAAAGTGCCTGTTATGACTTTTTTTAAAGTCTCTAACTTCGCTCCGGAGGTCTCCTGTTGCAGGTTTGGACCCATTCAAGATTGTAAAATAATTATTGTAAAATTCTAATTCAATTGATTAATTTAGTCCTGTTTCCTCTTTAATTGAACTTTACCACAAAAGCCACATTTGTGAGGCAAAGGCTCACTCCGTTCCCACGGCTCTCGGCCACGCCCCCTCGCCACAAAAGCCTTCAAGT
Associated Phenotype:
Not determined