ZMP
p2rx4b
Ensembl ID:
ZFIN ID:
Description:
purinergic receptor P2X, ligand-gated ion channel, 4b [Source:RefSeq peptide;Acc:NP_001119914]
Human Orthologue:
P2RX4
Human Description:
purinergic receptor P2X, ligand-gated ion channel, 4 [Source:HGNC Symbol;Acc:8535]
Mouse Orthologue:
P2rx4
Mouse Description:
purinergic receptor P2X, ligand-gated ion channel 4 Gene [Source:MGI Symbol;Acc:MGI:1338859]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21328 | Essential Splice Site | Available for shipment | Available now |
sa2440 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa21328
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 |
---|---|---|---|---|---|
ENSDART00000098969 | Essential Splice Site | 149 | 401 | 6 | 13 |
ENSDART00000098975 | Essential Splice Site | 142 | 394 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 31600032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30742758 |
GRCz11 | 8 | 30751990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAAATGTAAAATGGTCATCAACATCCTTCTTGATGTGTGATCCACACA[G/A]GCGTTCAGACGGGCAAATGTGTCCAATACTCTGAAACCATCAAAACCTGC
Long Flanking Sequence:
CAACTGGTCTCTGAACGCAGTTGACACCATGTTGACGAGAAGTCTGTGTTCGGGGGAACCCAGCTGACCTGCGGGTACGTTTGCAGCTGGATACATGATGAACAGATGGGAGAAGTAACGTGTTGTGTGCCTGGCTGCTCTGTCCCTGGAGGATATTGAAGATATCTATCTATTCGGAACTTTGATAACTGGGTTTCTTCTAATGGGCTTCAACAGCAGTCTGAGAGGGTCTTTTTTCGCCTCCCTCTTCCCTAATGTATTTTATTTCCTCTTTCTAAAAGCTACCTCTCGTTGACCGGTCATTCCCTGATATGTTTGATGTTTGTGTATGGTCAAGGGGGTCCAATTTCACTGCATGTAAAAGTGTATGTGACAAAGGCTTTTCATCATCCTTTTTCCCATCATCAAAACATTTATGAAACGATTTGATGCCACAAAGCAAAAAAGTAAATTAAATGTAAAATGGTCATCAACATCCTTCTTGATGTGTGATCCACACA[G/A]GCGTTCAGACGGGCAAATGTGTCCAATACTCTGAAACCATCAAAACCTGCGAGGTCCTGTCATGGTGTCCTCTGGAAAACGACACTGTCATTCCAAAGTGAGTGTTCAGTAAAAGTGAACAAGTTTAATGCACAATTGAAACTGGGAATATTAATAAAGTTTGTGATTGTACAGGCCTGCTCTTTTGAGCGCAGCGGAGGATTTCACCGTGCTCATCAAAAACAACATTCAGTATCCAAAGTTCAAATTCAGAAAGTAAGTACACTAATTAGTAGTTCAGGCATTTTATTTTTACAAAAATACCTGTTGTTAGCATTTTGCTAAATGAGAGAGTTCAGCCAAAAGTTAATTTATACTGTGGTTCTTAACTATTTGGAATTTCTTTCTTTCCCTGATTTTCACTACTTTTAGTAGCAAGAAAAAATACTATTACAATCAATGGCTGTAATTTTGTCAATGGCTGTAATAATGAAACTTTGTCAGATTTTAAAACAAGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2440
Status:
F2 line generated
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098969 | Nonsense | 201 | 401 | 7 | 13 |
ENSDART00000098975 | Nonsense | 194 | 394 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 31600267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30742993 |
GRCz11 | 8 | 30752225 |
KASP Assay ID:
554-3003.1 (used for ordering genotyping assays)
KASP Sequence:
TTGAGCGCAGCGGARGATTTCACCGTGCTCATCAAAAACAACATTCAGTA[T/A]CCAAAGTTCAAATTCAGAAAGTAAGTACACTAATTAGTAGTTCAGGCATT
Long Flanking Sequence:
TTCGCCTCCCTCTTCCCTAATGTATTTTATTTCCTCTTTCTAAAAGCTACCTCTCGTTGACCGGTCATTCCCTGATATGTTTGATGTTTGTGTATGGTCAAGGGGGTCCAATTTCACTGCATGTAAAAGTGTATGTGACAAAGGCTTTTCATCATCCTTTTTCCCATCATCAAAACATTTATGAAACGATTTGATGCCACAAAGCAAAAAAGTAAATTAAATGTAAAATGGTCATCAACATCCTTCTTGATGTGTGATCCACACAGGCGTTCAGACGGGCAAATGTGTCCAATACTCTGAAACCATCAAAACCTGCGAGGTCCTGTCATGGTGTCCTCTGGAAAACGACACTGTCATTCCAAAGTGAGTGTTCAGTAAAAGTGAACAAGTTTAATGCACAATTGAAACTGGGAATATTAATAAAGTTTGTGATTGTACAGGCCTGCTCTTTTGAGCGCAGCGGAGGATTTCACCGTGCTCATCAAAAACAACATTCAGTA[T/A]CCAAAGTTCAAATTCAGAAAGTAAGTACACTAATTAGTAGTTCAGGCATTTTATTTTTACAAAAATACCTGTTGTTAGCATTTTGCTAAATGAGAGAGTTCAGCCAAAAGTTAATTTATACTGTGGTTCTTAACTATTTGGAATTTCTTTCTTTCCCTGATTTTCACTACTTTTAGTAGCAAGAAAAAATACTATTACAATCAATGGCTGTAATTTTGTCAATGGCTGTAATAATGAAACTTTGTCAGATTTTAAAACAAGTTTGGCACAAGTGGAGAAGTAAAGCATGGTAAATCAGTTTTCATTTTTGGGTGAACTATCCCTTTACCACTTGCATTTTTATATTACAATTTATATAGTTGTAATGTAGCTGTTTTTTAAAGGTCTGCAAAGTTTTAAGAGATCAAAAAAGTCTAAACTGATTCTAGTTTTATTTCTACAACCGATCTGTAACAATAGGCATATTTCCATTACATTTCTTTTCTTTTTTTATCTAAACA
Associated Phenotype:
Not determined