ZMP

PLA2R1 (1 of 2)

Ensembl ID:

ENSDARG00000077474

Description:

phospholipase A2 receptor 1, 180kDa [Source:HGNC Symbol;Acc:9042]

Human Orthologue:

PLA2R1

Human Description:

phospholipase A2 receptor 1, 180kDa [Source:HGNC Symbol;Acc:9042]

Mouse Orthologue:

Pla2r1

Mouse Description:

phospholipase A2 receptor 1 Gene [Source:MGI Symbol;Acc:MGI:102468]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21855	Essential Splice Site	Available for shipment	Available now
sa35032	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21855

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

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111091	Essential Splice Site	827	1470	16	30

Genomic Location (Zv9):

Chromosome 11 (position 11140722)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	11091578
GRCz11	11	11075241

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGATTTCCACAGGTGTGGAGCTGGTCAAGCCATACTGGTACAGCGACC[G/A]TAAGTAGTAAATTACTGCTCTACCAAAAGTTATGTGCTCTCAAGTTTTAA

Long Flanking Sequence:

TCGTATTGGATTTTTTATTTTATTTTATTTTGAGCTGGTGAGCCAACTGACAAAAGCCCTTTTTTCCCCCCTGCTCTGCCGGCCACGCTCACTCCTCCCTATGCTTGCAGCGCTCCACGCCCATCATGAAGCATTTTTTTTTTTTAATTCTGAGGTAGACTTGAACTGATAGAGGGGGCTTTCATGACCCTTTAAGTAATTAACTTATTCATGCCATCCTGCAGGTGGTGACATCGTTCATTGAGGATATGAATGAAGCAGACTCTCACATGTGTGCTGCGTACAGTGACCTCACAAACACTCTCACTCCTCACTCCTGTGACTCCAAATATGAATGGATTTGCAAAGTGCCTCGAGGTTTGTGAAGTCTGTTTGTTTGTTAATAACTTGCTGGTCTTTTAAGCGAAAACAAATATCCATAGAAATGCACTGAAATGCAGCCGTATGATTTTTGATTTCCACAGGTGTGGAGCTGGTCAAGCCATACTGGTACAGCGACC[G/A]TAAGTAGTAAATTACTGCTCTACCAAAAGTTATGTGCTCTCAAGTTTTAAAAAAAGTTTGGAATTAGCTTTTCCTAGGATATAAAATACTGAAGAAAAAGACTCTCTCTAACGGTCAAAGCAAATTTAACAACATTTACTTACAATTTACAATTACAAGACTTTTTATAATAATACTACTAAATAAATGTACAAATTTTATACAGTGAAAGAAAAACGTAACTTTTTTCCAAGATGATTTATTACACTATTAGGTTGCTTTGTATATTTCAACATGCAGTCAGATATTTATTTATTTTTATGTTTGCACTATATCAGTTGACGTATAAATTACTCACACTGGTGGGTTGCTTTCCACTGCTTTTAGTCGCACCAGGCGGCTGACAGTTTTTCTCAGTCGCTTTGGTGCATTTCTCACAACACTATTTACATTTGCACAACAGGTAATGCATTTTTCAAAACAATTAGTCATTTGTGCACATCATAGAAGCAGTTTCTCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35032

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
ENSDART00000111091	Nonsense	1160	1470	24	30

Genomic Location (Zv9):

Chromosome 11 (position 11156106)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	11106962
GRCz11	11	11090625

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGAAGGGGGCAACACTCGTGAGCATCACAGACCCATTTCAGCAAGCTTA[T/A]CTGACCTTTCTGATCAACAGACTGGACGCCCCGCATTGGATCGGCTTATA

Long Flanking Sequence:

CATGTATATATAATATGCAAATATGTTTATTGACGTTAGAAATGTATCTATCTCAGATAATGTTTATCATATTCATTTATTTTATTAAATTTTTATTTAAAAAAAATTATGCTATATTAAAAAATAGTTATGTATTTGAGACAAGTGACCAGACAAATTCACACATGGCATTTTAAATAATTGATTTTACAGTAAAAGTTTTTGTTCACAATTTTAAAAAATATTATGAAAAAAATGCATTTTATTTTATTGCTCCTTGTCCATAATGTGGAACTAATTATCATGGTTTTATTTATTTGCTCCATTATCTTCATTATTTCAGACACCACCAAGCGTCCCACTCACTCCTATCACACTGCATCCTCTCTGGGCACATCTGAGTTCAGGAACCACACTTATCTGGTCGCCCATGGCAACATGAGCTGGTACGAGGCCCAGGAAAGGTGTTTGGTGAAGGGGGCAACACTCGTGAGCATCACAGACCCATTTCAGCAAGCTTA[T/A]CTGACCTTTCTGATCAACAGACTGGACGCCCCGCATTGGATCGGCTTATACAGCACAGACGTAAGGACACAGGGAAGTTCATGTGTTTTACAGGTGTATTGGTAATATATATTTGAAGTCAGAATTATTAGCCCCCCTTTTTACCTTTTTTAAATATTTCCCAAATGATGTTTAACAGAGCAAGGACATTTTCACAGTATGTCTGATAATATTATTCTTTTGGAGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTAATTTTTTTAAGAACCATTTGGACATCAAAATTATTAGCCCCTTTAAGCTAACTTTATTTTCGACAGTCTACAGAACAAACCATCGTTATACAACATCTTGCCTAATTTCCTTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATACCACTTTAAGCTGCAAGGTGTCTTGAAAAATATCTAGCCTAATAATATTTACTGTCATCATGAAAAAGGTAAAAT

Associated Phenotype:

Not determined