ZMP

pr2y4l

Ensembl ID:

ENSDARG00000053570

ZFIN ID:

ZDB-GENE-030616-77

Description:

pyrimidinergic receptor P2Y, G-protein coupled, 4-like [Source:RefSeq peptide;Acc:NP_001004501]

Human Orthologue:

P2RY4

Human Description:

pyrimidinergic receptor P2Y, G-protein coupled, 4 [Source:HGNC Symbol;Acc:8542]

Mouse Orthologue:

P2ry4

Mouse Description:

pyrimidinergic receptor P2Y, G-protein coupled, 4 Gene [Source:MGI Symbol;Acc:MGI:1926594]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7394	Missense	Mutation detected in F1 DNA	Not yet available
sa42415	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7394

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:

T > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045018	Missense	37	341	1	1

Genomic Location (Zv9):

Chromosome 14 (position 33661510)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	32443143
GRCz11	14	32783457

KASP Assay ID:

554-4174.1 (used for ordering genotyping assays)

KASP Sequence:

GGAAGYGAACTTCAGCTGTACTTTCGATGAGGAGTTCAAGTATATTCTTC[T/A]GCCCGTKTCATATTCCCTGGTGTGTTTCTTCGGACTAATCCTTAACTCTG

Long Flanking Sequence:

GAAAAAAAAGCGCGTGTATATTATACTAAGTAAACTAAGTGTGTTATTTCTTATGAAAATTGTTAAAAACACACTAAATAACTTACGTCTCACACAGAATTTCACTCGCTTCCCCTCAAAGACAGCGCAAAGAAAATGGCGGTTTCTCACGTTGATGTCCCTGCATGTTGACGTGACGTGCGTGCTCTCTTTCACGTCCGCGTTCCCAACCCAGCACTGCTGGGTTATAGATAAAGATCGATTTTCAACCCAAATTGGGTTGAATCAACCCAATTTTGTTACCCAGCAGTCTCAACCCAGCATTTGGGTTAAAAAACCAACCCAGCGTTTTTTAGAGTGTATGCTAAAACATTTTGTTATTTTTTTTAACAGAGAAATGAATTATTTAAGGAAAAATGTCTCAGGCAATTTTTCCCTTCCTTCCGACTCACTGATGCCGATGTCTTCGAAGGAAGTGAACTTCAGCTGTACTTTCGATGAGGAGTTCAAGTATATTCTTC[T/A]GCCCGTTTCATATTCCCTGGTGTGTTTCTTCGGACTAATCCTTAACTCTGTGGCTCTGTGGATGTTCATCACTAAGATGAGGCCTTGGAAACCCAGTACGGTGTACATGTTTCATCTGGCCCTGTCAGACACGCTGTATGTGCTCTCCTTGCCTATGCTCATATACTACTATGCAAACCGCAGCCACTGGCCTTTTGGCGTTGTCCTCTGTAAGATCGTACGGTTTCTTTTTTATGCCAACTTATACTGCAGCATCCTTTTTCTCACTTGCATCAGTGTGCATCGCTACCTTGGCATCTGTCACCCTATTCGTTCTCTGACTTTAATAAAGCCACGCCATGCACACATGGTCTGTGGTTTTGTCTGGACAGCGGTGATAGCCTGCCTGGTGCCCACGCTCATTTTAGTCAATACTTCTAGAAATGGAAATAGCACTTTGTGTCACGACACAAGTCGCCCTGAAGAATTTCACAACTTCGTAACCTACAACTCTGTGGTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42415

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000045018	Nonsense	238	341	1	1

Genomic Location (Zv9):

Chromosome 14 (position 33662112)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	32442541
GRCz11	14	32782855

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAATGGCACGGGCCCTTTGCCAACCCCGAAAGGGCCTGGCCCAAAATCAA[C/T]AAAGTTCATCCCGGAAGAAGTCCATTAAACTCATCATAGTGGTATTGGTT

Long Flanking Sequence:

TGTACATGTTTCATCTGGCCCTGTCAGACACGCTGTATGTGCTCTCCTTGCCTATGCTCATATACTACTATGCAAACCGCAGCCACTGGCCTTTTGGCGTTGTCCTCTGTAAGATCGTACGGTTTCTTTTTTATGCCAACTTATACTGCAGCATCCTTTTTCTCACTTGCATCAGTGTGCATCGCTACCTTGGCATCTGTCACCCTATTCGTTCTCTGACTTTAATAAAGCCACGCCATGCACACATGGTCTGTGGTTTTGTCTGGACAGCGGTGATAGCCTGCCTGGTGCCCACGCTCATTTTAGTCAATACTTCTAGAAATGGAAATAGCACTTTGTGTCACGACACAAGTCGCCCTGAAGAATTTCACAACTTCGTAACCTACAACTCTGTGGTAATGGTGTTGCTTTTTATTCTGCCATTTCTAGTCATCGTGGTTTGCTACTGTTTAATGGCACGGGCCCTTTGCCAACCCCGAAAGGGCCTGGCCCAAAATCAA[C/T]AAAGTTCATCCCGGAAGAAGTCCATTAAACTCATCATAGTGGTATTGGTTGTGTTTGCAATCTGCTTTGTTCCCTTCCACATCACTCGCACCCTCTACTACGCCTATCGTATTTTTGACGCAGATTGCAAGACTCTTAATATTGTCAACTTTTCATATAAAATCACTCGTCCGCTTGCTAGTGTCAACAGCTGTTTGGACCCTATCCTCTACTTCCTGGCAGGGGATCACTACCGCTCTAAACTCCTCCGAGTGCTCACTAGACAGACTCCGAACACTCGTTCTACTGCGTATGAGTACGCACCTAATGGCAAAAACATCGAACTGGCCTTTAAGAACCCAGATGCCCAAGCTGGCAGTGATTCGAGACTCTAGAGCAACATACCCAGACATTTTGGGTAATCGTTTTTAAAAACAGTTCTGGACGACTGCCTCAAATATTATTATAAATCCCAAGTGTACTCTATCAACAGCTGTGTCTTCAGAGCCAGGCATTCAGAA

Associated Phenotype:

Not determined