ZMP
ENSDARG00000075406
Ensembl ID:
Human Orthologues:
PVR, PVRL1, PVRL2
Human Descriptions:
poliovirus receptor [Source:HGNC Symbol;Acc:9705]
poliovirus receptor-related 1 (herpesvirus entry mediator C) [Source:HGNC Symbol;Acc:9706]
poliovirus receptor-related 2 (herpesvirus entry mediator B) [Source:HGNC Symbol;Acc:9707]
poliovirus receptor-related 1 (herpesvirus entry mediator C) [Source:HGNC Symbol;Acc:9706]
poliovirus receptor-related 2 (herpesvirus entry mediator B) [Source:HGNC Symbol;Acc:9707]
Mouse Orthologues:
Pvr, Pvrl1, Pvrl2
Mouse Descriptions:
poliovirus receptor Gene [Source:MGI Symbol;Acc:MGI:107741]
poliovirus receptor-related 1 Gene [Source:MGI Symbol;Acc:MGI:1926483]
poliovirus receptor-related 2 Gene [Source:MGI Symbol;Acc:MGI:97822]
poliovirus receptor-related 1 Gene [Source:MGI Symbol;Acc:MGI:1926483]
poliovirus receptor-related 2 Gene [Source:MGI Symbol;Acc:MGI:97822]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39956 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39956
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:
G > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113876 | Splice Site, Nonsense | 396 | 548 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 58182695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 57915958 |
GRCz11 | 2 | 58030721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCACTGAGTCGCATGGATAGCGGCATGAAGAACAGCGTTTTATCAGTG[G/T]AGGTGTGTGTGTGTGTGTGTGTGTGCGTGATATATGTGATAAAGTACTTG
Long Flanking Sequence:
CATCACTGGTTACTAGGCAAGTGAGGTACAGAACCAGATAGTCGCTAGCCCAGTTTGTCGGCTAAAAAGGGAAAGTGTTGGTTTAATCCGCTGTGGCCAAGGAATCCGAATTACTTTTATGCAAACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGGAGGAGATGATCAGTCTGTCGCGGCAGGTGTCCATGAGGAGACTGGACTCCATCAACTGTGACCCCAGAGCGCAGGTACATGCCTATATTAATACTGGACACAACATTAATATTACGTTATTTTCAATACAATGAAAACTAAAACTTGTAGAAAACTTTGGGTAATATTCGCAGATATGAAAATAATGTTCTGCATTATTATTAGTTTTGTTTTTCTGTGTTTTCATGTTCAAGTAAAGCATTAAGACTGTTGCTGATGTTTGCAGGCGGAGGACAGTTCACTGAGTCGCATGGATAGCGGCATGAAGAACAGCGTTTTATCAGTG[G/T]AGGTGTGTGTGTGTGTGTGTGTGTGCGTGATATATGTGATAAAGTACTTGTAGATTTGACTGAACACCGTCTGACCTGAGATGCAGCTTCTGCTGAAGTGAAGAGATAAGTGTGTTTGTGTATGCATGTGTGCGTGTACATGTGTTTGCGTGTGTGTGCAAACGTGCATGTGTTTGCTTCTGTGCATTTGCATGTGTGTGCGTGCATTCATGTGTATTTGTGTGTATGTGCGCGCGTGCGTGCATATGCATGTCTGTGTGTTTGCATGTACATGTATGTGTGCGTGCGTGCATGCATGTTGTGTGTGTGCATGTGTGTGAGTGTCTGTATGTGTATGCATGTGCATGCATGTGTGTGTGAGTGTCTGTATGTGTATGCATGTGCATGCATGTGTGTGTGAGTGTCTGTATGTGTATGCATGTGCATGCATGTGTGTGTGAGTGTCTGTATGTGTATGCATGTGCATGCATGTGTGTGTGTGAGTGTCTGTATGTGTATGC
Associated Phenotype:
Not determined