Busch Lab

ZMP

LOC100148532

Ensembl ID:
ENSDARG00000074160
Human Orthologue:
PAQR4
Human Description:
progestin and adipoQ receptor family member IV [Source:HGNC Symbol;Acc:26386]
Mouse Orthologue:
Paqr4
Mouse Description:
progestin and adipoQ receptor family member IV Gene [Source:MGI Symbol;Acc:MGI:1923748]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa35228 Nonsense Mutation detected in F1 DNA Not yet available
sa41982 Nonsense Mutation detected in F1 DNA Not yet available
sa19031 Nonsense Mutation detected in F1 DNA Not yet available
sa9849 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa35228
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112565 Nonsense 20 272 1 3
Genomic Location (Zv9):
Chromosome 12 (position 14270807)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 13126460
GRCz11 12 13164763
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTACTGGACCAAAACTTCTGGATTTTAAGAGCTCACCACCACATCTT[C/T]AGTTCAACAAGTATGTCCATACAGGATACCGGCCTATATCCACTTGCAGA
Long Flanking Sequence:
CTTTCTCTGCACTAATAATCTCTTATATAGTAGAAAGCAAATGGGATTATCATATGAACAATTTTTGGAAATGTCTCCGATAAGAAATGAAACGCACGTGTGGAAGTCTGCCAGTAGGGTTGTACTTAAGGAACTCTAATCTTCCATGAGCCGACCTCTGCTGAGCCTGACTGCTGCCCACTGATTGGCTACGACACTAAGTAGGAGTAAATTGACCCACAGCTCCTCTGCAAGCAACAGGTTGCTGCAGTTCTACCTGCCGGTACTTCCAAGATGATGGGGCTCGGGTGGCATAAAGTCACAACTTTTGCTAACACTAGATAGCACTAGCTAACTGCACACTTTTAGCTTGATGTAAGCCATTTAAAGAGATTGTAGGCTGTCCGTGCGAAGGAAAGTTCGGAGAGTGGTTAAGGACACTTGAGCGCATTTCATATTCTGCTATGGGTTATTTTACTGGACCAAAACTTCTGGATTTTAAGAGCTCACCACCACATCTT[C/T]AGTTCAACAAGTATGTCCATACAGGATACCGGCCTATATCCACTTGCAGAGAGTGTCTACGAAGTTTATTCTATCTCCACAATGAATTTGGGAACATCTATACACATGGTATGGAAAATAAATTGCACAATTTGCATGTCTGAAATGTGTTCATTTGTAATGTATGCTTCATTCTACTGCACTGCAATAAAAATATCAGTTTTTATCTTTAGTTATTTATCTTTTGTTTTAGCAAAACATCTGGTTTCAAATGAAAAACGAGATTAATTTGCTCACCATTTGGCATCTTATTTGACTTGTTTTAAGGAAAAACTTATTTCTTAAAGGAAGACCTTTTTTGTTTTGTTTTTTTGCTTGTCTAGGAAATGGTTCTGGATTTAAGATTTTTTTTAGATGTTAAAAAAGCATTTTCACAGTGGATTGAAGATGTTACATTTACAAATATGGAACACACTTAACAAAAGTAACATGGATTACTTTCAAATGATTAATTTTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41982
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
ENSDART00000112565 Nonsense 152 272 3 3
Genomic Location (Zv9):
Chromosome 12 (position 14282543)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 13138196
GRCz11 12 13176499
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACATTGTTGTGTCACCCAATCACCCGTCAAGTGGCGATGTTAGCGTA[T/A]CTCCTCCTCTCTGGCTATGGTGTTCACTGCGCTCTCACTGCAGAGAGTAA
Long Flanking Sequence:
TGGAAGGTCATTTTCAAAAACCCATAACAGGGGCACTTTAATATGTGTCAACGACAAATTGTGCATTATAGATGTGCTGCTAAAAATCTGCATTGGTATATTTTAGTATGGATCTCCTTGTTGAACCTACAAGGCACAAAGAATTTTGGCAAAAAAGAGGTTCAACCTGATTCTAGTAATTAATACAATGAATCCACAATTGTTGTCAACCACTAATTTTTTTTAATTAAACAAAAGTTTTACATTCAGAATATTTCCATTTTAAATTTTATTTATTTATTTATTTTTTGTGGCCCTTAAAAAGTTAACCAGGTCAACAGGTTTAATCAGGGTGACATGGTCATAAAGTTGTCCATAAACAGTTAAATACCAGAATTTTTGCTGCTTCTTTTTATTCAAGGGCCAATAAAGTTCCCTTTTGGTTTTCCAGGTGCTCTGCCAATCATTCACATCACATTGTTGTGTCACCCAATCACCCGTCAAGTGGCGATGTTAGCGTA[T/A]CTCCTCCTCTCTGGCTATGGTGTTCACTGCGCTCTCACTGCAGAGAGTAACATTCACCGCCTGCAGTCCTTCATCTGGCAGGCAGGCTTCCGCTTTGTTCTCTTTATGTTTCGTCTGATTGGTCCAGGCAGAGGAAGCCCCTCCTCCCTTCAGCTCTACCTCACCATGGATGCTCTGGCAATGTTTGGAGGACTTGTCAATGTTTCCCGCTTTCCTGAGCGATTCAGTCCTGGACGGTTTGACTACTGGCTAAATAGTCATCAGATTATGCACATCATGGTCGTTCTGTCTATACTTTACTTACACTGGGGCATGCTGGAGGATTTACGATGGTTAAAGGGATATCACTGTCCTGATGAATATGGCATTTATGATATTTAAAACAATTAACAGTTGCCTGTAGCTTTTGATTCATAAATGCTTTCCATTTATATGCTTTCAAGATGCATTATAAGACACTGTCTGTGGTTGAATTTGACAATGGTTGATTCGGAAAGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19031
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112565 Nonsense 262 272 3 3
ENSDART00000112565 Nonsense 262 272 3 3
Genomic Location (Zv9):
Chromosome 12 (position 14282871)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 13138524
GRCz11 12 13176827
KASP Assay ID:
2260-5099.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCGTTCTGTCTATACTTTACTTACACTGGGGCATGCTGGAGGATTTA[C/T]GATGGTTAAAGGGATATCACTGTCCTGATGAATATGGCATTTATGATATT
Long Flanking Sequence:
AGGGTGACATGGTCATAAAGTTGTCCATAAACAGTTAAATACCAGAATTTTTGCTGCTTCTTTTTATTCAAGGGCCAATAAAGTTCCCTTTTGGTTTTCCAGGTGCTCTGCCAATCATTCACATCACATTGTTGTGTCACCCAATCACCCGTCAAGTGGCGATGTTAGCGTATCTCCTCCTCTCTGGCTATGGTGTTCACTGCGCTCTCACTGCAGAGAGTAACATTCACCGCCTGCAGTCCTTCATCTGGCAGGCAGGCTTCCGCTTTGTTCTCTTTATGTTTCGTCTGATTGGTCCAGGCAGAGGAAGCCCCTCCTCCCTTCAGCTCTACCTCACCATGGATGCTCTGGCAATGTTTGGAGGACTTGTCAATGTTTCCCGCTTTCCTGAGCGATTCAGTCCTGGACGGTTTGACTACTGGCTAAATAGTCATCAGATTATGCACATCATGGTCGTTCTGTCTATACTTTACTTACACTGGGGCATGCTGGAGGATTTA[C/T]GATGGTTAAAGGGATATCACTGTCCTGATGAATATGGCATTTATGATATTTAAAACAATTAACAGTTGCCTGTAGCTTTTGATTCATAAATGCTTTCCATTTATATGCTTTCAAGATGCATTATAAGACACTGTCTGTGGTTGAATTTGACAATGGTTGATTCGGAAAGTATTCACTGTGCTTCATGTTTCCACATTGTTTATGTTACAGCCTTATTAAAAAATTTCCCAAAAAATTCTACACACAATACACCATACGGACAATGGGAAATAAGATTTTTTTGAATTGTTGCAAATAAAAAAGTTTTTTTAAAAGCTCTAAATTGAGCTCAGGTCCTCTGATCATTCTTGAAATGTTTCAGCAGCTTAATTGGAGTTCACCTGTGGTAAATTCAGTTGATTGGACATGATTTGAAAAGGCATACACCTGTCTATATAAGGTCCCAGGGTTGACAGTGCATGTTAAAGCACAAACCAAGCATGAAGACAAAGGAATTGCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9849
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112565 Nonsense 262 272 3 3
ENSDART00000112565 Nonsense 262 272 3 3
Genomic Location (Zv9):
Chromosome 12 (position 14282871)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 13138524
GRCz11 12 13176827
KASP Assay ID:
2260-5099.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTSGTTCTGTCTAWACTKTACTTACACTGGGGCATGCTGGAGGATTTA[C/T]GATGGTTAAAGGGRTATCACTGTCCTGATGAATATGGYATTTATGATATT
Long Flanking Sequence:
AGGGTGACATGGTCATAAAGTTGTCCATAAACAGTTAAATACCAGAATTTTTGCTGCTTCTTTTTATTCAAGGGCCAATAAAGTTCCCTTTTGGTTTTCCAGGTGCTCTGCCAATCATTCACATCACATTGTTGTGTCACCCAATCACCCGTCAAGTGGCGATGTTAGCGTATCTCCTCCTCTCTGGCTATGGTGTTCACTGCGCTCTCACTGCAGAGAGTAACATTCACCGCCTGCAGTCCTTCATCTGGCAGGCAGGCTTCCGCTTTGTTCTCTTTATGTTTCGTCTGATTGGTCCAGGCAGAGGAAGCCCCTCCTCCCTTCAGCTCTACCTCACCATGGATGCTCTGGCAATGTTTGGAGGACTTGTCAATGTTTCCCGCTTTCCTGAGCGATTCAGTCCTGGACGGTTTGACTACTGGCTAAATAGTCATCAGATTATGCACATCATGGTCGTTCTGTCTATACTTTACTTACACTGGGGCATGCTGGAGGATTTA[C/T]GATGGTTAAAGGGATATCACTGTCCTGATGAATATGGCATTTATGATATTTAAAACAATTAACAGTTGCCTGTAGCTTTTGATTCATAAATGCTTTCCATTTATATGCTTTCAAGATGCATTATAAGACACTGTCTGTGGTTGAATTTGACAATGGTTGATTCGGAAAGTATTCACTGTGCTTCATGTTTCCACATTGTTTATGTTACAGCCTTATTAAAAAATTTCCCAAAAAATTCTACACACAATACACCATACGGACAATGGGAAATAAGATTTTTTTGAATTGTTGCAAATAAAAAAGTTTTTTTAAAAGCTCTAAATTGAGCTCAGGTCCTCTGATCATTCTTGAAATGTTTCAGCAGCTTAATTGGAGTTCACCTGTGGTAAATTCAGTTGATTGGACATGATTTGAAAAGGCATACACCTGTCTATATAAGGTCCCAGGGTTGACAGTGCATGTTAAAGCACAAACCAAGCATGAAGACAAAGGAATTGCCG
Associated Phenotype:
Not determined