ZMP

p2rx3a

Ensembl ID:

ENSDARG00000010477

ZFIN ID:

ZDB-GENE-000427-3

Description:

purinergic receptor P2X3 [Source:RefSeq peptide;Acc:NP_571698]

Human Orthologue:

P2RX3

Human Description:

purinergic receptor P2X, ligand-gated ion channel, 3 [Source:HGNC Symbol;Acc:8534]

Mouse Orthologue:

P2rx3

Mouse Description:

purinergic receptor P2X, ligand-gated ion channel, 3 Gene [Source:MGI Symbol;Acc:MGI:1097160]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22465	Nonsense	Available for shipment	Available now
sa45513	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22465

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000021417	Nonsense	10	410	1	12

Genomic Location (Zv9):

Chromosome 14 (position 22962871)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	21662359
GRCz11	14	21959604

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTAAGCTACACAAACTTCTACTATGGCTCCCAGAGTGCTGGGCTTCATC[A/T]AAGGGTTCTTCGTCTATGAAACCGCCAAGTCTGTAGTAGTGAAGAGCTGG

Long Flanking Sequence:

GTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTGTTAAAGACAATACATGTGCCTGAAAAAACTCAAATCAACTGCTATGTTTAGTAGTAATATGTTTATAATTGCTCAAGATTAGGTTTGTAAAATATATATGAATTAAAAGAGGAGGAGAGAAAGAGATATAAAATAAATCTGAGAGAGTTGATCAAATGAGCAGGCTATTAAGAAAATGGACACTGAAGGACTCTGGGGGGTTGATAGAGGAGAGGCTTGACCATGAAAAGGGGAGGGAAAATGTGGACTTTTTTTTTTTTTTTTTTTTATCTGTCAAGTAAAATAAGATCCCTTACTACAGATGTGCAGTAGTGAGGAGCGTGTTGGTTCATCAAGAAACATCTCAAGATTTTCTTCAGATTACACTTGTTAGCGTTAAGCTACACAAACTTCTACTATGGCTCCCAGAGTGCTGGGCTTCATC[A/T]AAGGGTTCTTCGTCTATGAAACCGCCAAGTCTGTAGTAGTGAAGAGCTGGTCTGTTGGAATAATCAACCGGGTCGTTCAGCTGTTAATTATTTTGTATTTCATCTGGTAAGCTTTAACTATATCTTCTTCTCACAAATGTTATTTTAAACTGTTTTTTTTTTACTTGAATCTACAGTTGAAGTCTTTATGTTTAGAGCTTGCTATTTTTCACAGTATCCTTTATATTCTTTTTCTTCAAGTGCAAATGATTTCAGCTAAAATAAAAAAAAACAGTTTTTTATTTTTAAAAAAGCTCTTTTAAGGTCAATATTATTAGTCCCTTTAAGCAAGTTTTTACTCAATAGTCTACAGAACAAACCATTGTCACACAATAACTTGCCTAATTACACTAACTTGCCTAGTTAACCTAATTAATCTAGCAAAGCCTTTCAAAGTGAATACTAATTTCTTGTAAAACAAACAGTAAAATATTAAGTACTGTCATCATCATGGAAAATTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45513

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000021417	Nonsense	384	410	12	12

Genomic Location (Zv9):

Chromosome 14 (position 22948003)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	21647491
GRCz11	14	21944736

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCTTCAGGTATCAGGCTTTGTGCCTGAGTCTGGAAGCAACATACTCTA[C/A]AAGGGCAGCCAGGTGTCGATCAAAGCACTGGAGAAGAACTCTAATGACTC

Long Flanking Sequence:

GTGGAGCAGTTCCTAGAGAAACGGAATATTCAATGAGAAAACAATAGGCGTGGCTTGTTTTTTCTACTGCGAGCTGATTGGATAAGTAGGCATTTCATTCAGAATGATTTGGAAAAGGGCTTTAGGAGAGTTACTACAACCTAACAGACTTCTTACTCTTTCTGTTTGCTGTTAAAACTGACAGTTGGAGGGGAGTAGTTAAGTTTGTTAGCCACACCAAATACCTTAGACAGACGAAATTTGACAATTTAACTAAAAACATACAGGAAGTGCATTTTCAGATTTCAATTAAACATTAGAAGGGTAAACTTTTTTCTAAATGACATACACGGACAAATTGTTCACCACAAAACTAGCATTGTGAGCTAACCAAATCATATGGTTAGTTTTGATTTCACATGTACTACGTTTACTGTTTTAAAGTGTGAGTAGTGATATCTTTCTGTCCCCTTTCTTCAGGTATCAGGCTTTGTGCCTGAGTCTGGAAGCAACATACTCTA[C/A]AAGGGCAGCCAGGTGTCGATCAAAGCACTGGAGAAGAACTCTAATGACTCGGGGACTTTTTCTATTGGGCGTCAGGAGTGAGTCATGTAGTCTGTCAAATCAATGAGACTTTCAAACAACATTACTGCTTATGGATTTTTATGCACTTGCAATTTCTTAAGGTGGAAGTTTCAAATGTTTTATTCTGATTTTAAGTTTGTCAAACATTTGAGCTGGATTTGTCAATAAGTAATGACATCATTCAGGTAATACCAAACAAGAAAGCACACATACAGTAGATATTTACATTATTAAGTCAAAGAGATAAAATCACTATACAAATATTGCACATGTAAAATCACATTTTATTTTCTGATGACATTCAGGGTAACACTTTATAACAGTCCTTTTTACATAAACTTAGTAATAACAATAGCTATGTATCATTACAAGAAAATAGAAACAATCCCTCAACAATCAAACAGAAACAATCCCTCATCATAGTGAACTCATGTTGTTCA

Associated Phenotype:

Not determined