ZMP
p2rx7
Ensembl ID:
ZFIN ID:
Description:
P2X purinoceptor 7 [Source:RefSeq peptide;Acc:NP_945335]
Human Orthologue:
P2RX7
Human Description:
purinergic receptor P2X, ligand-gated ion channel, 7 [Source:HGNC Symbol;Acc:8537]
Mouse Orthologue:
P2rx7
Mouse Description:
purinergic receptor P2X, ligand-gated ion channel, 7 Gene [Source:MGI Symbol;Acc:MGI:1339957]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17772 | Essential Splice Site | Available for shipment | Available now |
| sa21329 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17772
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062229 | Essential Splice Site | 40 | 596 | 1 | 14 |
| ENSDART00000122741 | Essential Splice Site | None | 302 | 1 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 31627005)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30769731 |
| GRCz11 | 8 | 30778963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGGCTCACTGAAMTGGACGTTAAACGGAGTGATCTTGATGTTYATTTG[G/A]TAAGTGTTTCTCCAWATGTCGCCCCCRCWTCGTCCAACAAGAGCTCATTC
Long Flanking Sequence:
TGTTTTATTTAAATTTGAGAAGAAAAGTTGAGACCGAACAAAATACTCCAGAGAAACAACGAATTTCAAGTGGACTCTTCATTTCCCCATAGCTGCCTGTAGCAGACAAATACAATCGCTAGAATAATTTTTCAATTCATTTCAATCACTTTTGCATCCTAACATGATCCCAAGATGAAGGTCTGCATGAATGCTAAGTCAATTTGAACACAACACACTCAGTGTATCTCGTTCTCCGCCCTAAGAACGAGTGTATTATTATGGCACTGTAACTGTCCTCCCTTGACCATGTGACCTTCTTCTTCTAGTGCTCGAGCTCTGCACAGCAGCACTCCGCAGTCATCGCTTCTGTCCTTCCCCTCTGTTTACAAAATCACCGCCATGCCTTGCGTTTTGCTGAACCTCTGTGAATACGACACGCAAAAACTCGTCAAAATCAAGAGTGTGAAACTTGGCTCACTGAAATGGACGTTAAACGGAGTGATCTTGATGTTCATTTG[G/A]TAAGTGTTTCTCCATATGTCGCCCCCACATCGTCCAACAAGAGCTCATTCATGTACATTCTTTGCCAATGTGCCTTTTTTCCACACATATTATGTTGTGTTTAAGTGTTGAACCCACAAAATTAACAATGGTTTTATTATAGTAAAAGTGTAGAAACAATGTTTTTTTTGTAAACAAACTAGCCTATTTGATTTACCACGGTGTTACTACAAAAATATGCTAAAAACTTAGTGTAACAAAAATATTGATGAATTTTGGTTACAATTGTACCATGTAATTACAATTTATATCATTGATATAACTTCCTCATTTGGTGTCTCAAGCCAGTCTTAAATGTCTTTACTTTCCAGTATCATGATGTTATGGAATAAAGAATACCAGGAGTATGATTTTGTAGTGAGTTCTGTCACCACAAAGGTTAAGGGAGTTGCAAAGATTACCTTACCAGAAGTTGGAGACGTTGTAGCAGACCCCATCCGAATGATGGCCGAAACTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21329
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062229 | Nonsense | 194 | 596 | 7 | 14 |
| ENSDART00000122741 | Nonsense | 159 | 302 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 31617600)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30760326 |
| GRCz11 | 8 | 30769558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTCACTGTGATGATCAAGAATAACATCAGATTTCCAGCATTTAACTA[C/A]ATAAGGTATTTTACTTTTAACACAGAAAACGTTATTTTAATTACTCTACA
Long Flanking Sequence:
GCCACAACCCAGTACTGGGGAATATATGAGAGATGTGGTATTAAATAATGTGGCATTTTACACACAAAAGCTATCAGTATAATTCACATCTGTTTTCATTAGCTCAATATTCCATAAATATATATATATATTATACAGTTCATTGTATGGAATATCTAAAGGTAAGGTATTAATATAGAAACAGTTACGTTATTTGTGCAAACAATTATAAATACACTGACATGGACATTTGCAAGTAAAGCTCTTTGTCAACAAAGACCAGTTCATCATCAGCTTTGCCCCAAAATAAGTAAATCTGCAGTGCTGCCAGAGACTTTTGAGGAACCCATTTGAGGAAGTTTCCCTTTAATGTGGCACTTTCATATAAACTGAGATTCTATATACAGATATGTTCTAATGTCACACTTTCATTTCTCTCTCCCCAGACCTGCTCTTTTGGCTGCAGCAGAAAATTTCACTGTGATGATCAAGAATAACATCAGATTTCCAGCATTTAACTA[C/A]ATAAGGTATTTTACTTTTAACACAGAAAACGTTATTTTAATTACTCTACAGATGTTTATACACTGATATAACTCATGAACTGTTATTCATATACACTTTCAAACACTAATAAGAAACTCATAAGCAGTATTTGAGGTTATTAACCTGAAGAAAGCCCAGGGTAATAATTTAAACTGATTATTTAATCATCTTTTTATATTAATCCCTACCACCACATAAATGCCTGTTGAAAGCACCTCAAAGCATTGTACATTGAAACACAGTTGAGTGGGCTTGACAAACCACTTGTATGAAACACTTTCCTCTTCATATGCACCAGACACTTTTTTATAAACACACCATGTTACAAAAACTCAGTAATAAAAATTAGTACAAAATTAGAAAAAAGTACATTATACTGTATAACTGCAGATTAGGCATGAGCCGGTATAAGATTCTGATGGTATAATAACCTTGGGTAAAAATATCACGGTTTTGCGATTTCACGGTATTGTGATTAC
Associated Phenotype:
Not determined