ZMP
si:dkey-47k20.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate pheromone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3QJY0]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23330 | Nonsense | Available for shipment | Available now |
sa25069 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23330
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 |
---|---|---|---|---|---|
ENSDART00000059457 | Nonsense | 111 | 864 | 4 | 8 |
ENSDART00000135254 | Nonsense | 109 | 864 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31786240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33583099 |
GRCz11 | 18 | 33557694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGAAATCAATAGGAATCCAAACCTGCTTCCGAACATCACTCTTGGTTA[T/A]TATCTTTATGACAACTGTGTCAAGTTGAGTGTGGCATTCAGGGCTGCTAT
Long Flanking Sequence:
TCAGATCAGGTCCCTGTCAGCTCCAGGGGCAATTCAGGCTGAACGGGATGTTCCAGGAAGGAGATCTCATCCTTGGAGGGCTATTTGAGGTTCACTTCCTCACAGTGTTCCCAGAGCAGAGCTTCAGAACAGAGCCAGAACCACCATACTGTGAGCAGTGAGTCTGGGGTCAGACTGGACCAAGATTTCTTATAAATACAAAATGAATATATTAAATCAAGACGCTACTTAAGAATTAACAGTTATATGTTTTACTTATCAGAATATGTAAACAATTAATGTTTACCATAAAAAGCAGCTCTTTAAGAATATAAGATTTTTTGTCAGGAATTGTCTTGTATCTGCAAAGATTTTCTGAAATATCAGTTCTGAAATAACATAATTTCTTCTGCTCTTTATAGATTTGATATGGCAAGTTTCCAGCAGGCACAGACTATGGTCTTTGCAATAGACGAAATCAATAGGAATCCAAACCTGCTTCCGAACATCACTCTTGGTTA[T/A]TATCTTTATGACAACTGTGTCAAGTTGAGTGTGGCATTCAGGGCTGCTATGGCTCTTGTTAGTGGCACAGAGGAATCATTCTCCAGCCTAAACTGCACTGGCCCTCCACCAGTGATTGCCATAGTGGGGGACCCTGGATCTACCCACTCAATTGCAATCTCTAGTATATTAGGGCTGTTTAGAGTGCCTATGGTAAGTGTGAATGTGAAATTTGTGGGGGAAAAAATCTAACTGTACAGACTGCATTTAAATTGCCAAATAAATAAGAGTAGAATTTACCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAGCAACAACAGAAATCTTATTTACAGCTCATCTGTGTCTCTTCTATAAGGTTAGCTACTTCGCAACCTGCTCCTGTTTAAGTGACAGGAAAACATACCCATCTTTCTTCAGAACAATACCCAGTGATGCTTTCCAGGTGCGGGCTATGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25069
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 |
---|---|---|---|---|---|
ENSDART00000059457 | Nonsense | 547 | 864 | 7 | 8 |
ENSDART00000135254 | Nonsense | 545 | 864 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31789252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33586111 |
GRCz11 | 18 | 33560706 |
KASP Assay ID:
554-7393.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCCCCAGGCACCAGACAAGTCAGGAGGAAGGGCCTTCCTGTCTGCTG[T/A]TTTGATTGCCTGCCATGCGCAGATGGAGAGATTTCTAACACAACTGGTAT
Long Flanking Sequence:
CTAACTCATTCTGAATTATTCTAAAAACCCTTAAATACTCTTAAATACAAATGGTTTGTAAATAATGCAATACTTAATTTAGTAATGAAAATAAATCATTAGCAAAGCATGAAAGTACAATTATTAAGCACATTATAAATGTTTGTAAGTCAAGAATAGAGCATATGTAGCTGCAGTTATAAACTGCTTACTAATGTAGAGTTAATGCTTAGAGTTAAAACAGATAATGAATTCACCATTTGATTATGCTTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCAAACTATCTTGTACTACATTCTTATACTTTGGTTTGTTACTATGAAATTGTATATGGTTTGAACCTATACTTAATGATGGATGAACATACATATTACAAAGATAAGTAATATTATATGCTGTACCCCTTAGCCCCCACAGTCTGTGTGTAGTGAGAGCTGCCCCCCAGGCACCAGACAAGTCAGGAGGAAGGGCCTTCCTGTCTGCTG[T/A]TTTGATTGCCTGCCATGCGCAGATGGAGAGATTTCTAACACAACTGGTATAAATTCTACTACAAAATTGTAATTAAATTGAAAAGGGAACCAAATAATTGTTTGTTTTTTTTCATACAGATGCTATTGAGTGCAAAATATGTCCTGATGAGTTATGGCCCAATCCAAATAAAGATCAGTGTGTCCCAAAAGAAGAAGATTTTTTGTCCTTTGAGGATCCTCTGGGCATCTCTCTGACCACTGCTTCCCTGCTTGGCACCTGCTTCTGTGCTCTTGTTATGGTCATCTTCTCTCATCATCGTAACACTCCTGTAGTTCGTGCCAACAATTCAGAGCTCAGCTTCCTGCTACTTTTGTCACTCAAACTGTGTTTTCTGTGTGTGTTGCTGTTCATTGGACGACCAAAGTTATGGACATGTCAGTTAAGGCATGCTGCATTTGGCATAAGTTTTGTTTTATGTGTCTCCAGTATCCTGGTCAAGACTATGGTGGTAATAGCCG
Associated Phenotype:
Not determined