ZMP
p2rx3a
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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