ZMP
v2rc1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3KQM4]
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 |
---|---|---|---|
sa8580 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
This allele has been removed from public view.
Allele Name:
sa4030
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000147225 | Nonsense | 235 | 815 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31415809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33212668 |
GRCz11 | 18 | 33187263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAATCATCTTMTGCTAGAGTCATACTAAATTTCTCTGTGGACTCTTA[T/A]CTTTATGGTGTTCTAAAAGAATGCAGACGGCAAAATGTCACAMATCTGCA
Long Flanking Sequence:
TCATGTTAGCCTTTTCCCCACACAGAATGTGTTATATACAGGGACATTTTGATTTGCTCTATTCATAGTGTTAATGCTATTAATATTACATTTATGTCTGGTACATGGTGTGACTTTTTATTACATATATTGCACTACTAATCTTATATATGTGCTTTAATTTTACAGGTGAGCTACTTTGCATCATGCTCTTGTCTCAGTAACAAAAGGGAGTTTCCAGCATTCATGCGCACAATGCCAAGTGACCTATTTCAGATTAAAGCTTTAGTAAAACTTGTTTATTATTTTAAGTGGACATGGCTTGGGGTTATCGGTGTGGATACAGACTATGCTCGATTTGCCATCCAGCTGTTCTTGAAAGAGTCAGAAAAATATAATATTTGTCCTGCCTATGTTCACATTTATCCTGTTGCGCTTACTCAAAATACAGTTGAGGAACTTGTTAAGATTTTAAAATCATCTTCTGCTAGAGTCATACTAAATTTCTCTGTGGACTCTTA[T/A]CTTTATGGTGTTCTAAAAGAATGCAGACGGCAAAATGTCACAAATCTGCAGTGGATCGCCAGTGAGGCTTGGGCCACATCAAAAGTCCTCTGGGATGACTTTGGTGATTTGTTAAAGGGAACACTGGGCTTTGCCATACGGAGAGCTGATATTCCGCATCTTGGCAGTTATCTCAGATCAGTAAGCAGTTCTGTTGCTCAGACCTCCCCTTTTTTTACTGAGTTTTGGGAAGAGACTTTCCATTGCAGACTAAATGGATCCTTAAACACTCATGTACATGAAGAAGCATCTTACAACTGGCCAGCCTGCAATGGTAATGAAACTCTGGATGATGTGTATACTCTTTATTCGGATGTGTCACAACTCAGAGTCTCCTACAATGTTTACAAAGCAGTGTATCTCATAGCACATGCACTGCATGACATGAGCACATGTGATCCTGGAAAGGGCCCATTTAAGAATGGTACATGTGGGAGTCTGTATCAAATTTTGCCATGGCA
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa29057
Status:
Less stringent filtering
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:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000147225 | Nonsense | 420 | 815 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31416496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33213355 |
GRCz11 | 18 | 33187950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTACTATATGAAACGAACCAACTTCACAACACTCGGAGAAGAGGTT[C/T]GATTTGATAAGAATGGGGATCCTATTGCATCCTATGATCTGATGAACTGG
Long Flanking Sequence:
AGTTCTGTTGCTCAGACCTCCCCTTTTTTTACTGAGTTTTGGGAAGAGACTTTCCATTGCAGACTAAATGGATCCTTAAACACTCATGTACATGAAGAAGCATCTTACAACTGGCCAGCCTGCAATGGTAATGAAACTCTGGATGATGTGTATACTCTTTATTCGGATGTGTCACAACTCAGAGTCTCCTACAATGTTTACAAAGCAGTGTATCTCATAGCACATGCACTGCATGACATGAGCACATGTGATCCTGGAAAGGGCCCATTTAAGAATGGTACATGTGGGAGTCTGTATCAAATTTTGCCATGGCAGGTGTGTATTGCTTCCCTTTTTTACATTATCTGCCAGTTTTATTCAATAATTATCAGATAGTATAAAAGTATTCAATTATTATAACTGGACTACATTCATATTTTTGTTTTGATTTTCTCCCAAATTCATCTAAGCTTTTGTACTATATGAAACGAACCAACTTCACAACACTCGGAGAAGAGGTT[C/T]GATTTGATAAGAATGGGGATCCTATTGCATCCTATGATCTGATGAACTGGCAACGAGAATCTGATGGCTCCCTTCAGCTTGTCAGGGTGGGAATCTATGATGCCTCCTTCAAAGATGACAAGGACCTAGTGATAGATGAGTCAGTAATTATGTGGCACAGAGGGGACAAGGTGTGTGCCATTCCACGAATCACCAGATATTGCTGGTTATGTTTACTTTTGCTTAAGCTTTACCTAACATTAATGATGGAACTAAAGAGAACTCTATTTAATAATATTAAATGGATATGTGACACTTGAACGCAACATTTTATAAAAAAATCATGTTCTAGTATACACTTTTTTGTACATTTACTACATTTGCGCCATTGATCATTTCATTCATTTACAAACCCAAAATATTTCTCTAATAAAGAGTTATATGCACAATCATATGTTTTACAGTGTAGTGTTTTTCTACTGCTTGTTCCATTGTGGTCATTAGGCGCCAGAATCTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8580
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000147225 | Nonsense | 541 | 815 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31417268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33214127 |
GRCz11 | 18 | 33188722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGTTCCAAGGACACGTGGCCTAACCAATCCCAAGACCAGTGCATCCCC[A/T]AAACTTTAGAGTTTTTGTCCTTTCAGGAGCCCTTGGGAATAATTCTTTGG
Long Flanking Sequence:
TAATATTAAATGGATATGTGACACTTGAACGCAACATTTTATAAAAAAATCATGTTCTAGTATACACTTTTTTGTACATTTACTACATTTGCGCCATTGATCATTTCATTCATTTACAAACCCAAAATATTTCTCTAATAAAGAGTTATATGCACAATCATATGTTTTACAGTGTAGTGTTTTTCTACTGCTTGTTCCATTGTGGTCATTAGGCGCCAGAATCTTTGTGCAGTAAAAGCTGTCTGCCAGGCTCCAGGAAGGCCAGGCAAAAAGGAAAGCCAGTCTGCTGCTTTGACTGTATATCATGTGCTGAAGGAGAGATCAGTAATCAGACAGGTGTGATTTTCCAGACAGCTTCTCTCTGAATGGCATTCTCAAAAAAGAAAGGAAAATTGCTATTTTATGGTCCAATTTTCTCCAATGTTTCCACAGACTCAATTGATTGCCTGACATGTTCCAAGGACACGTGGCCTAACCAATCCCAAGACCAGTGCATCCCC[A/T]AAACTTTAGAGTTTTTGTCCTTTCAGGAGCCCTTGGGAATAATTCTTTGGGTATTTTCAGCATTGGGGGCCTGTGCAGCATTAGCAGTGCTCTGTGTGTTTGTAATGTATAGGACGACTCCAGTCATACGAGGAAACAATATAGAGTTAAGTTTCCTTCTTCTGTTGTTCCTCTGTGCTTGTTTTTTGATTGGCCTAACATTTTTAGGGAAGCCCACTGACTGGTTGTGCCAAATTCGCTATCCAGCTTTTGGAATCAGCTTTACGCTCTGTATTTCCTGCATCTTGGCAAAAACTGTAGTCGTTTTAATGGCTTTCAGGGCCACCATCCCTGGCAATAATGTCATGAAGTGGTTTGGTCCTGTTAAACAAAGATCAAGTGTTATCCTGTGCACATGTGTGCAAGCACTTATTTGCATCATATGGTTAACAACTAAGCCCCCTCTTGCTTCATACAACAGCAAGTTCCTGAGCGCAACTATAATTGTTGAATGTTCTGTG
Associated Phenotype:
Not determined