ZMP

p2rx8

Ensembl ID:

ENSDARG00000024139

ZFIN ID:

ZDB-GENE-030319-7

Description:

purinergic receptor P2X8 [Source:RefSeq peptide;Acc:NP_945336]

Human Orthologue:

P2RX5

Human Description:

purinergic receptor P2X, ligand-gated ion channel, 5 [Source:HGNC Symbol;Acc:8536]

Mouse Orthologue:

P2rx5

Mouse Description:

purinergic receptor P2X, ligand-gated ion channel, 5 Gene [Source:MGI Symbol;Acc:MGI:2137026]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42512	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35838	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42512

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
ENSDART00000029063	Essential Splice Site	250	391	7	12
ENSDART00000143584	None	None	45	None	2

Genomic Location (Zv9):

Chromosome 15 (position 15367825)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	16412788
GRCz11	15	16348810

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGATATTGTGAGCAAAGCTGGATATAGGTTTGAAGAAGTGGCAGCAAAG[G/T]TGAGAAATTCGAGTGGATTTAATGTGTGGTGGAAGTACTAAACTTAATTT

Long Flanking Sequence:

GAAATATATGGCTGGTGTCCCACTGAAAAGTCCTCGCGGCCAGAGTAAGAAAGTTTTCTCTCACTTTTTAAAATTCACTTCCAATGCTATACCCAGAATAGGATAATAATAAAATGAGATAAAGTACAAAATGATAAAAGAAAAACCCTAAATGCTGTGAAATGTTTTAGGGCCGCAACTATGTTGAGAGAAGCTGAAAACTTTACTGTGTACATAAGGAACTTCATTAAATTTTCCCAGTTCAACCTCTCCAAGTAAGATAATCAGTGTGCTTTAAATATAAAAACCCTTGACTGAATAAAACAGTTGATTAACTATTATCAATAAATGATCTCAAATGTTATTTTGTTCCTCTCAGAACAAATATTCTAAAGGAAGGTTATCCGTCGTATATAAAAACCTGTTTGCATGACGAAATTCATCACCCATATTGTCCTGTATTTCGGCTGGGAGATATTGTGAGCAAAGCTGGATATAGGTTTGAAGAAGTGGCAGCAAAG[G/T]TGAGAAATTCGAGTGGATTTAATGTGTGGTGGAAGTACTAAACTTAATTTGATGTGCTTATTATGCTACATGTTATATTTATTTTTAATTCCAGGGTGGTTCAATTGGGATTGTGATTAAGTGGTCATGTGACTTTGATATGGATACTTCAGACTGTCATCCTCAGTACAGCTTTATGGCAATGGGGAGCAGCACGCCAGTCACAGCTGGATATAACTTCAGGTATTCACATGCTGATCAAAATTGTTCTCAGAGTTTTGATAATGACTTTTCAACAGACCAATATTAGAAGACAGATTATGCACACTTGATTGCTTCAGAAACAATGTAATGCTCATTGTCCAACATCTGCAGAAGTTTTAATTGTGGTTATACCATGTTACCCTTTAAAATTAGTCAACAACTATAGAACCTTTTTACAAGACTGTTATGACACATTTTACAGTCATCATAATCCTAAATCCTTGAAAGTTTTTAAAATTTAGATTTTTTAAAATGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35838

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029063	Essential Splice Site	371	391	11	12
ENSDART00000143584	Essential Splice Site	25	45	1	2

Genomic Location (Zv9):

Chromosome 15 (position 15389942)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	16434905
GRCz11	15	16370927

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGTTGTTTATGGTGAAGAAGAAATATGCAAAGTTTGAGAGCTTGATAAA[G/A]TATGTAATAGCAGCATGTTTCTGTGAAATACTAACGATATAGTTTGAGAA

Long Flanking Sequence:

CTGGACTCCGTTTTAAAAGATTAATCAAATTTATTATTAAAAAAAGCATTTCTAATTTATTGAAATCATGAAATGTACACAATATAAAACAATTTATAAATACTGCAAAAAAATGATGCTTTTTTCTTGATTTAATTTGATTGATTTCATTACATATAAAACTGATGTAAAGCTAAGGGAATGGCATAATTATTCAACCCTTCTTCAGCATTGTTGTTGTTAAGTCATTAATTTGTATTGTAATGATTAAAACTGTATAAAGACATAATAGTTTCTTTAACATTGAATTAGTTTTTTTTATTTTTAAATTGTAAGAGATATAGACAAATCAAAATAAGCCTATATGCATAATTTAACATCAACGTGCATAATTCACAAAACCTAAATTACAAATTCCTAATGTTGTGGTTTGTATACATTTTCCAGGGTTCTTACATTTGTGATGTCATACTGTTGTTTATGGTGAAGAAGAAATATGCAAAGTTTGAGAGCTTGATAAA[G/A]TATGTAATAGCAGCATGTTTCTGTGAAATACTAACGATATAGTTTGAGAAATATATTATCACTCATTCTGCCACAACACAACATTAATCACCTTTATTTCATATCTCCTCAGGGCTGACAAAGAAATCGCATTGCAAAAGATGCCAGATCATTCGAAAAGAAAGTTCAGTTACTGAATTTGGTGATGCATGTGCTGCGAAATATAAGAAAAGCAGCGATTCTAAAACATTTGAAAGGAAATCTCATTCATACACTGAAAAAATGATGTCTGTTGCAAACAATTTATGTGTTGAATTTAATCCAACAAATTAAATTTAATAACGTTCAACATAATTTGTTTGTTTAAATTCAACCCAAATAAATAGTTTACAACCACTTAACTCTTCAACAAAATTGTAAATCCAAGAATCTCTATCTGTGAGCTTAAATCTACTAAATGTTATTTCTATAATATATTGCATATAAATAAAATCGCAGAGATTTGTGTTTTATGTTGAGCT

Associated Phenotype:

Not determined