Busch Lab

ZMP

si:ch211-248g20.1

Ensembl ID:
ENSDARG00000063545
ZFIN ID:
ZDB-GENE-091204-455
Human Orthologue:
P2RY2
Human Description:
purinergic receptor P2Y, G-protein coupled, 2 [Source:HGNC Symbol;Acc:8541]
Mouse Orthologue:
P2ry2
Mouse Description:
purinergic receptor P2Y, G-protein coupled 2 Gene [Source:MGI Symbol;Acc:MGI:105107]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa15998 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15998
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092962 Nonsense 92 329 1 1
ENSDART00000133984 Nonsense 92 329 2 2
Genomic Location (Zv9):
Chromosome 18 (position 2070105)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 2595845
GRCz11 18 2564052
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCTCACTCTTCCGTTTYTMATCTACTACTACRCCGATGAGAAYGCATG[G/A]CCGTTTGGTGAACTGATGTGTAAATTAATCCGCTTTCTCTTCTACACAAA
Long Flanking Sequence:
GTCAATCAAAGTATTTCTTTACATCAAGTGTGATTATAAAAACATAAATGAATAATTTTTCTACCATTAGAAGCTGGTTATAATCACACACTGCTGCTGCACAACTGTGTTTCAACCCCTTATAAAAGTGATTTGTGCATAATAGATCCCGTTTAACTCATACCTCATTGCTTACATTGATATGACTGATTTGATTGCATTTGTCTTCTGCAGATCTGGATCACGATGGCCACATTCAACAACACTACCATCGCCAATGCCAGCGATCTGTACTCCTGTATATTCGATGAGACTTTCAAGTACATTCTCCTCCCGGTGAGCTACAGTCTGGTGTTCGTGTTCGGCCTGGGACTGAACATCACCGCCATGTACGTCATCTTATTTCGAACCAAACAGTGGAAGCCCAACACCATCTACATGATCAATCTCAACGCCTGTGACACGCTCTACATCCTCACTCTTCCGTTTCTCATCTACTACTACGCCGATGAGAACGCATG[G/A]CCGTTTGGTGAACTGATGTGTAAATTAATCCGCTTTCTCTTCTACACAAACCTCTACGGAAGCATCCTGTTCCTCAGCTGCATCAGCGTGCACAGATTCATAGGCGTCTGCCATCCGGTGCGGTCTTTGTCCTGGACGAATGCCCGTCGTGCTCGTTTCATCTCGTTGTGCATTTGGGCAACGATGCTCATCTTCCAAGCCCCGATCCTTTATTTCTCCAGGATGAAAAGCGATACGATGGTTTGCTATGACACGACAAGCAAGGAGCTCTTCAATGATTTTCTGGTCTACAGCTCGGTGGTGATGCTCCTGCTCTTTGTCCTGCCGTTTGGGGTCGTGTTAGTCTGCAACGCGATGATGGTTAAGAAACTTCGTGAGCCAGGTGTTGGCGATGGTCCAATGTCGCAGAAATCCAAGCAGAAGTCGGTGAAGATGATTATAATTGTGCTTGTGGCGTTCATGCTGTGCTTCTTGCCCTTCCATGTGAACCGCAGTATATA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa550
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092962 Nonsense 267 329 1 1
ENSDART00000133984 Nonsense 267 329 2 2
Genomic Location (Zv9):
Chromosome 18 (position 2070628)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 2596368
GRCz11 18 2564575
KASP Assay ID:
554-0460.1 (used for ordering genotyping assays)
KASP Sequence:
TGCCCTTCCATGTGAACCGCAGTATATACTACGGCTTTCGCTACCTSGAT[A/T]AACAGGTGAGCTGCTCGATGTTGGAGATCGCCAGCATGGCCTATAAGATC
Long Flanking Sequence:
AATTAATCCGCTTTCTCTTCTACACAAACCTCTACGGAAGCATCCTGTTCCTCAGCTGCATCAGCGTGCACAGATTCATAGGCGTCTGCCATCCGGTGCGGTCTTTGTCCTGGACGAATGCCCGTCGTGCTCGTTTCATCTCGTTGTGCATTTGGGCAACGATGCTCATCTTCCAAGCCCCGATCCTTTATTTCTCCAGGATGAAAAGCGATACGATGGTTTGCTATGACACGACAAGCAAGGAGCTCTTCAATGATTTTCTGGTCTACAGCTCGGTGGTGATGCTCCTGCTCTTTGTCCTGCCGTTTGGGGTCGTGTTAGTCTGCAACGCGATGATGGTTAAGAAACTTCGTGAGCCAGGTGTTGGCGATGGTCCAATGTCGCAGAAATCCAAGCAGAAGTCGGTGAAGATGATTATAATTGTGCTTGTGGCGTTCATGCTGTGCTTCTTGCCCTTCCATGTGAACCGCAGTATATACTACGGCTTTCGCTACCTCGAT[A/T]AACAGGTGAGCTGCTCGATGTTGGAGATCGCCAGCATGGCCTATAAGATCACTCGACCCCTGGCAAGCGCCAACAGCTGCATTGACCCCATCCTCTACTTCATGGCAGGACAGGGCTTCAAAAGCAGCATCAAGAGGAATAAATCACCAGTAGCAAGATCTGGAAAGAAACCACCTTCAACCTCTTTATAATAAGCAGAAAGTCAATTCGAAGACTACTTACTCAGGGATGTGACCCAAGGTCAAAGACTGCCGCTAAAGGAGAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATAATAAATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTTTTTAGCTTAGCTAGTTTTGGGGTGATTTTATTAATATTTGGACTTTTCGAACCATCATATATAAGATTTTAAAGGTGCGGTCACGTTTACCATTGCTTTCACAT
Associated Phenotype:
Not determined