ZMP
v2rh32
Ensembl ID:
ZFIN ID:
Description:
vomeronasal 2 receptor, h32 [Source:RefSeq peptide;Acc:NP_001076358]
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 |
---|---|---|---|
sa5912 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43136 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5912
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048182 | Nonsense | 45 | 855 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31602604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33399463 |
GRCz11 | 18 | 33374058 |
KASP Assay ID:
554-3776.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCAAGTTGAACAGAATGTATAAGGATGGAGATTATATCATTGGAGGCT[T/A]GTTTGAGGTTCAGCACCTCAAAGTATTTCCAGAACTGAGTTTCCGAATGG
Long Flanking Sequence:
GTAAAATAGTGCCATTGTTAATTGAATTTGCAGTGCATGACTGCCACCTAGATCAGATTCGGTGTAGCCTACTTAAAAAACAGTCCCAGCTCTTCCAGCCCATCTCAGTTACCCAAAATAATCTTAGTTTATTATACATGCAAGGGTAATTGAACAATACATTTTTTTTTCATTCTGTACTATCATTCATTAATGGTATTCAAAAGCATAAATAACCTCATAATTACATATAAATGTATGTAACTACATTACAGAACCACCTGTTCTATGGGGTGGGTGGGAGGTGGTGCTATGGCGCATGTCCATATGGCTAATAAATTCAGAAGCTGAAATGGTTTGTGGCTCATAAAAAGATTAATGGAGAGAGATGTGTATCACTCTAAACATCTGCCTGCATCTGTCCTTTATCTTTATTTCTGTCAATTCTGACTCCTGTCAAATCCAGGGACATTTCAAGTTGAACAGAATGTATAAGGATGGAGATTATATCATTGGAGGCT[T/A]GTTTGAGGTTCAGCACCTCAAAGTATTTCCAGAACTGAGTTTCCGAATGGAGCCAGAACAGCCAAAGTGTGAGGAGTAAGTGAACAAATTAAACAATAACAAATTATGTATACTGAAAAAAAAACATGTTTTTTTTTTTTATTTGATTGCATGTCAAATTTATTAAGTACTAAAATCAACTCCTACATAAATTAAATATTGTACAAACTGTACCATAATTCTCAAAGCTGTGATTTTGTTCTGTGTAGTTCCACTGATGTCATTTTGAAAATATTGTTTGCATTTTTACTCTTTATTATTTGTTTCATTCTATGCTTCAGATTCTACATGTCAAGCTTCCAGCAGGCACAGACCATGGTTTTTGCTATAGATGAGATCAATAAGAATCCAAACCTGTTGCCTAACATCACACTTGGTTACCATCTTTATGACAACTGTTTAAAGCTTGTGGTGGCATTTCGGGCTGCTACAACTCTTATTAGTGGGACGGAGGAAACGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43136
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048182 | Nonsense | 338 | 855 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31603816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33400675 |
GRCz11 | 18 | 33375270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCCATCGGGGAAAGATCAAAGGACTTCATGAATTTCTGCTACACATA[C/T]AACCTGACAATGATCCAACAAATAACATGGTGAGAATTTTTTGGGAGAAC
Long Flanking Sequence:
ATGCCACATGCTCATGTTTGAGTAACAGGAAAAAGTACCCCTCTTTCTTCAGAACAATCCCCAGTGATGCATTCCAGGTTCGGGCTATGGTTCAGATCTTAAAATATTTTGGATGGACCTGGGTTGGTGTTCTCTATAGTGATGATGACTATGGCATTTATGCTGCTCAGTCCTTCCAGCAGGAAATGCAGCGGTTCAAAGGCTGTGTGGCTTTTTCTGAAATAGTGCCCTATGATAATCATAGGGACATTCAACGCATAGTGGCAGTTATTAAGGCCTCTACAGCCAGAGTAGTCGTGGCTTTCTCAACTGATCTGTTACCCCTGATGGAAGAGCTGTTACAACAAAATGTGACAGGCAGGCAGTGGATTGCAAGTGAGGCATGGTCCACCTCCCCTGTCCTTCATCTTCCACGTTTTGTACCTCTCGTTAGGGGCACGCTTGGCATTGCTATCCATCGGGGAAAGATCAAAGGACTTCATGAATTTCTGCTACACATA[C/T]AACCTGACAATGATCCAACAAATAACATGGTGAGAATTTTTTGGGAGAACATGTTTGGGTGCAGTTTTGAGAAAGGCAACGGGTATGGAGAAAAAATGTGTACAGCACAAGAGGATCTAAACATCACAGTTAATGAATACAATGATGTATCAGAGCTGAGAGCCTCTTATAATGTCTATAAGGCAGTTTATGCACTGGCACATGCACTTCATGATCTTATGCAGTGTGAGGAGGGGAGAGGACCATTCAGTGGGAACAGCTGTGCTGACATAACAAAACTGAAACCTTGGCAGGTTAGACCTGGAGCTTACTGCTCCAAAAATCTACATAAATTACGGAAAACTAATTTGGGGAAAAAAGACAAGCATATGTATGTAAAATATATTTGTTGATATTTGCAGATGGTTCCCTACCTGCAAAAAGTGAACTTCACTACAGGCTTTGGGGATCATGTGTCATTTGATGAGAATGGAGATGCTCTGGCCATTTATGATGTGATG
Associated Phenotype:
Not determined