ZMP
v2rh13
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:Q1LV88]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23326 | Splice Site, Nonsense | Available for shipment | Available now |
sa43135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23326
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099142 | Splice Site | None | 820 | None | 7 |
ENSDART00000144160 | Nonsense | 311 | 766 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31583410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33380269 |
GRCz11 | 18 | 33354864 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACCATTAGAATCTTTTGGGAGACCATGTTTGGGTGCAAGTTTGAGGTT[G/T]GAGGTAAAAAAGTAGATGAACAGCAAGAAAGGGGGAGAAACAAATGTTCA
Long Flanking Sequence:
TGCGGGCTATGGTTCAGATCTTAAGACATTTTGGATGGACCTGGGTTGGTCTCCTCTACAGTAATGATGACTATGGCATCTACGCTGCTCAGTCCTTCCAGCAAGAAATGCAGATTTTGGGAGGTTGTGTGGCTTTTTCTGAAATGTTGCCTTATGATAACAACGGTAGAGACATTCAACGAATAGCAGGAGTTATTCAAAAGTCTACAGCCAAAGTAGTTGTAGCATTCTCAACTGATCTGGCATCCTTGATGGATGAGTTGTTACTGCAAAATGTGACAGGCAAGCAGTGGATTGCAAGTGAGGCTTGGACTACAACACCTGTCCTGCAAACTCCACAATATTTACCGCTACTGGGGGGCACACTGGGAATTGCCATCCGGCGTGGACAGATTCAGGGACTTTATGAATTTCTAAAAAATCTTCGACCTGACAAAAATCCAAAAAACAGCACCATTAGAATCTTTTGGGAGACCATGTTTGGGTGCAAGTTTGAGGTT[G/T]GAGGTAAAAAAGTAGATGAACAGCAAGAAAGGGGGAGAAACAAATGTTCAGGCCAAGAGGATCTTAACAACTCAGAAACAGCATACACGGATGTGTCAGAGCTGAGAGCCTCTTATAATGTTTATAAAGCTGTTTATGCCTTGGCACATGCACTTCATGACCTAGTAAAGTGTGAGGAAGGAAAAGGGCCATTCACTGGGAACAGCTGTGCTGACATATCCAATCTAAAACCATGGCAGGTAAGTCTTCTAAATAGCACATATTGTATGTACAATTTCTAATACTGTGCCACAGATTTTATATAACGTGTGTTCTATATACAAACTGAACAGCTGGTTCACTACATACAGAATGTAAAATTCACCACAGGCTTTGGGGATCATGTGTCATTTGATGAGAATGGAGATGCTCTGGCCATCTATGATGTAATGAATTGGCATCCAAGGTCTGATGGGTCGATCATTGTCCATGTGGTCGGTGTTTATGAAGAGGCAATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43135
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099142 | Nonsense | 471 | 820 | 5 | 7 |
ENSDART00000144160 | None | None | 766 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31583949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33380808 |
GRCz11 | 18 | 33355403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCAATATTAGGGAAAGTCTTAACACTGGATGAGGATGCATTATTCTG[G/A]AACTTTGAAACAAAAAAGGCAATTAGCATATAATATTCAAAATAAAATGA
Long Flanking Sequence:
AACAAATGTTCAGGCCAAGAGGATCTTAACAACTCAGAAACAGCATACACGGATGTGTCAGAGCTGAGAGCCTCTTATAATGTTTATAAAGCTGTTTATGCCTTGGCACATGCACTTCATGACCTAGTAAAGTGTGAGGAAGGAAAAGGGCCATTCACTGGGAACAGCTGTGCTGACATATCCAATCTAAAACCATGGCAGGTAAGTCTTCTAAATAGCACATATTGTATGTACAATTTCTAATACTGTGCCACAGATTTTATATAACGTGTGTTCTATATACAAACTGAACAGCTGGTTCACTACATACAGAATGTAAAATTCACCACAGGCTTTGGGGATCATGTGTCATTTGATGAGAATGGAGATGCTCTGGCCATCTATGATGTAATGAATTGGCATCCAAGGTCTGATGGGTCGATCATTGTCCATGTGGTCGGTGTTTATGAAGAGGCAATATTAGGGAAAGTCTTAACACTGGATGAGGATGCATTATTCTG[G/A]AACTTTGAAACAAAAAAGGCAATTAGCATATAATATTCAAAATAAAATGAATAATGCTGTGCAAAAATAAATTGTGTAAAAATAAACGTTTGTTTTGACATACTGTATAGTATATATGAATATATTAATACACATATGCATGCTATATTTGAGAAAATGTAAATTATACAAATTATTTAGAAATTTAAATAACTATTTATAGTTATTTAGTAAAACTAGTATTTAGTTTTTTTTTATAGTTTTGTGTGTGTGTGTGTGTGTGTGTATACACATATATTGTTAAAACAAGCTTTTATTTTGATGTGATTAATCATGATAAATCTTTCCCCAGCACTAAAAGTTATAGACTAATAATATTAATATTACTAATAATAATAATATATGAAAATATAACAAGACATTTAAATATTGATTATATTCAGCCCCCAGACTCTGTGTGTAGTGAGAGCTGCCCCCCAGGAACCAGGCGAGCCAGGAAGAAGGGTCTCCCTGTCTGCTGT
Associated Phenotype:
Not determined