ZMP
v2ra18
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3KQL4]
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 |
---|---|---|---|
sa44891 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36683 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44891
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064137 | None | None | 252 | None | 1 |
ENSDART00000136603 | Essential Splice Site | 499 | 844 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31553089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33349948 |
GRCz11 | 18 | 33324543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAATTCAGCCTGAGCAGAGCTATCATTTGGTATGATGGCACTGAAGAG[G/A]TATTAAATGTGTTCTATAATAACTCCTGAATGTTATGGAATACTCTAATA
Long Flanking Sequence:
AGTTGCGCATCTCTAACATGGTGTACAAAGCCACATACGCTATAGCTCATGCACTCCATGGCATTATCTGTAATGAAAAGAAGTGCAACAAAAACATCAAGATTGAGCCACGAGAGGTATTTATTTTGTGTTTTTTAATGTACCAAGTAATAGTTATAATTTGCTTTTAAACAGGGCTAAAAAATATCTGTGTAATCCAGTAGGCTAATGCATTTCTGATAGCAGATAACGCAATTTTCGCTTTAACACATTTAAATAATTTCATGTCTGTCATGCAGGTTCTTGATAAGCTCAAACAAGTGAAGTTTTCTAAAAATAATTATTCTGTTTCGTTTGATGCTTATGGAGACCCTGTGGCCGTGTATGAGCTTGTGAACTGGCAGCTTCAAAAAGATGGTTCAATTGATTTTGTAACAGTGGGTAAATATGATTCTTCCCAGCCCAAAGGCAAAGAATTCAGCCTGAGCAGAGCTATCATTTGGTATGATGGCACTGAAGAG[G/A]TATTAAATGTGTTCTATAATAACTCCTGAATGTTATGGAATACTCTAATACATTTGTGACTCTGATATTATACACGTCTGTCACCTGCAGGTGCCTGTGTCTGTGTGCAGTGAAAGCTGTCCACCGGGTACACGGAAAGCTGTCCAAAAAGGAAGACCTGTCTGCTGTTATGACTGCATTAATTGTGCCGATGGAGAAATCAGCAATGATACAGGTGCTTTGGGCATGTTCTGCTGGATAAATCACACATGGGCACTGACATACTATATACGACAGTACATGACAAAGAAAAATTACTGGGTAACACTTTCTATGAAGCTCATACTTGTAATGAATTATAACACTCTGTTTACAATTATTTATAATTAACCATAACAATTCTATACATTTATGTATAAAGACGCAACAAACCTTTATAAACTATATTAAAATGACAGTTATAGCTAGATGTATAACAACGTTATCAATACTTACTACAGATACATTTCAATTGTCAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36683
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064137 | None | None | 252 | None | 1 |
ENSDART00000136603 | Essential Splice Site | 541 | 844 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31559272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33356131 |
GRCz11 | 18 | 33330726 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTCTATTGTCCATGAATAACTTTTTAACACTGATTTCCTTACCTTCC[A/G]GATTGTTTGGATTGTCATGAATGTCTCTCAGACTACTGGCCCAATAATGA
Long Flanking Sequence:
ACATTACGTTCACACGCAGGCTGCGCCGGAGCATATGTGTGCACTTGACGCAGAAGTATAAATCTGCCTTTAGGCTTTGACAAGGTGGCAAGTTTTGTCACTCTAGTTAGCCCTGGCTCTTTCACTCCTCCACTGGCAAAAGTGATAAATGTCAATGAAAACAAACTATTAGTAGGAAACAGAACAAAAGACATTAAATGGGACAGAACTAAATACAAATTGAGACTTAAACTCACAGTAGACAATTAACTAAATGTATGTGAGGATAATGTAAAAAACAAATGGGAGAAATAGAACAAAGTAAACTAGGCTCAACTAATTCAATGAAAACAATAACATAAGGTCCACAACTGTGACATTTACTTAAATACATACGTTATACTGCTTATATGTAAACTGGTGTTAAGTGTATGTAAACATAACATCTAATATTCTGCATGCCAACGATGTCATTTCTATTGTCCATGAATAACTTTTTAACACTGATTTCCTTACCTTCC[A/G]GATTGTTTGGATTGTCATGAATGTCTCTCAGACTACTGGCCCAATAATGAGAAGAACAAGTGTCTCCGCAAACCAGTGGAGTTTCTGTCTTGGGATGAGATCCTTGGAATTATTCTGGCTGCTTTTTCTGTTGCTGGCTCTTTAGTGGCTTTAAGTATGGCTTTAGTGTTCTATAAAAACAGGGCTTCTCCAATAGTGAGAGCCAACAACTCTGAGCTGAGCTTCCTGCTGCTCTTCTCACTGACTCTGTGTTTCCTCTGTTCACTCACTTTCATCGGTCAGCCCACTGAGTGGTCCTGTATGTTGCGTCACACAGCTTTTGGGATCACTTTTGTCCTCTGCATCTCTTGCGTTCTGGGGAAAACAATAGTGGTGTTAATGGCCTTCAAAGCTACACTTCCAGGAAGTAATGTCATGAAATGGTTTGGGCCTTCTCAACAGAGACTCAGCGTTTTTGGTTTCACTCTTGTACAGATTATTATTTGTGTGCTTTGGTTAAC
Associated Phenotype:
Not determined