ZMP
v2rx3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3KQL8]
Mouse Orthologues:
AC139131.1, AC161211.1, AC161211.2, Vmn2r54
Mouse Descriptions:
vomeronasal 2, receptor 53 [Source:RefSeq peptide;Acc:NP_001098114]
vomeronasal 2, receptor 54 Gene [Source:MGI Symbol;Acc:MGI:3704110]
vomeronasal 2, receptor 55 [Source:RefSeq peptide;Acc:NP_001098115]
vomeronasal receptor Vmn2r56 [Source:RefSeq peptide;Acc:NP_001098118]
vomeronasal 2, receptor 54 Gene [Source:MGI Symbol;Acc:MGI:3704110]
vomeronasal 2, receptor 55 [Source:RefSeq peptide;Acc:NP_001098115]
vomeronasal receptor Vmn2r56 [Source:RefSeq peptide;Acc:NP_001098118]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18387 | Nonsense | Available for shipment | Available now |
sa18204 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18387
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078381 | Nonsense | 612 | 853 | 6 | 6 |
ENSDART00000137208 | Nonsense | 572 | 813 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31509084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33305943 |
GRCz11 | 18 | 33280538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTAGCAGGAGCCTGCCTCACATTAGCTGTGTTTTCCKTGTTTCTTTA[T/A]TACAAAAACACTCCTGTAGTACGCATAAATAACTCCGAACTCAGTTTCTT
Long Flanking Sequence:
GCTGCGTAAAACGTGCTGGATATATATATATTTTATTTTTTTTCAAAAAATTGTATTTTACACACACAAAAATACTGCTTTTGTATTTATGAACTAACCATATATGTATGGATCTGTTGTTTAAGCAGGTGCTGGTGTCTGTGTGCAGCAACAGCTGTGCTCCGGGATTCAGGAAGGCTGTTCGTCGTGGCCAGCCTCTGTGCTGCTTTGACTGTGTACCATGTGACAGTGGCAAAATCAGTAATGAGACAGGTCAGAGAACTTCAGTAATTTGTATATAAATTTGCAAAAAGTGACCTTCAACTTAATTTTCCCTCTTTCTCTTTAGATTCACTAGATTGTATTGCCTGCTCTGAAGATTACTGGTCAAATGCTGATGGAACAGTGTGCATTCCTAAAGTGGTTGAATTCCTGTCCCATGATGCAATGGGATTAACCCTGACAGTAATAGCTGTAGCAGGAGCCTGCCTCACATTAGCTGTGTTTTCCGTGTTTCTTTA[T/A]TACAAAAACACTCCTGTAGTACGCATAAATAACTCCGAACTCAGTTTCTTCATCTTGTTATCACTGACTCTTTGTTTTCTGTGTGCTTTGATATTCATCGGGGAACCCACATCTTGGTCCTGTATGCTTCGACACACTGCATTCAGCATCACCTTCTCGCTTTGCATCTCTTGCATCTTGGGAAAGACTTTAGTGGTGCTGGCTGCTTTCACAGCGACCCGACCTGGAAACAATTTAATGAAATGGTTGGGCCCTACACAGCAGAGAATCATCATTTTCTGCTGCACTCTCATTCAGGTGCTCATATGTACAGTCTGGCTTGTAGCATCCCCACCATTTCCCTATAGAAACACTAAATATCAACAGTCCAAGATCATTCTGGATTGCAGTGTGGGCTCTGATCTGGCATTTTGGTGTGTGCTGGGATATATCGGTCTTTTAGCTTGTGTCTGCTTTTTTCTGGCTTTTCTGGCACGGAAATTACCAGGTAATTTTAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18204
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078381 | Nonsense | 676 | 853 | 6 | 6 |
ENSDART00000137208 | Nonsense | 636 | 813 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31509275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33306134 |
GRCz11 | 18 | 33280729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WTTCAGCATCACCTTCTCGCTTTGCATYTCYTGCATCTTGGGAAAGACTT[T/A]AGTGGTGCTGGCTGCTTTCACAGCGACCCGACCTGGAAACAATWTAATGA
Long Flanking Sequence:
CAGCCTCTGTGCTGCTTTGACTGTGTACCATGTGACAGTGGCAAAATCAGTAATGAGACAGGTCAGAGAACTTCAGTAATTTGTATATAAATTTGCAAAAAGTGACCTTCAACTTAATTTTCCCTCTTTCTCTTTAGATTCACTAGATTGTATTGCCTGCTCTGAAGATTACTGGTCAAATGCTGATGGAACAGTGTGCATTCCTAAAGTGGTTGAATTCCTGTCCCATGATGCAATGGGATTAACCCTGACAGTAATAGCTGTAGCAGGAGCCTGCCTCACATTAGCTGTGTTTTCCGTGTTTCTTTATTACAAAAACACTCCTGTAGTACGCATAAATAACTCCGAACTCAGTTTCTTCATCTTGTTATCACTGACTCTTTGTTTTCTGTGTGCTTTGATATTCATCGGGGAACCCACATCTTGGTCCTGTATGCTTCGACACACTGCATTCAGCATCACCTTCTCGCTTTGCATCTCTTGCATCTTGGGAAAGACTT[T/A]AGTGGTGCTGGCTGCTTTCACAGCGACCCGACCTGGAAACAATTTAATGAAATGGTTGGGCCCTACACAGCAGAGAATCATCATTTTCTGCTGCACTCTCATTCAGGTGCTCATATGTACAGTCTGGCTTGTAGCATCCCCACCATTTCCCTATAGAAACACTAAATATCAACAGTCCAAGATCATTCTGGATTGCAGTGTGGGCTCTGATCTGGCATTTTGGTGTGTGCTGGGATATATCGGTCTTTTAGCTTGTGTCTGCTTTTTTCTGGCTTTTCTGGCACGGAAATTACCAGGTAATTTTAATGAGGCTAAATACATCACCTTCAGCATGATTATATTTTGCGCAGTATGGCTGGCTTTTGTGCCTGCATATGTCAGTTCACCTGGTAAATTTACAACTGCTGTGGAGATTTTTGCCATTTTAGCCTCTAGTTTTGGCCTGCTTCTTTGTTTATTTACCCCAAAGGTTTATATCATTTTAGTGAAGCCAGAGAAGA
Associated Phenotype:
Not determined