ZMP
v2ra1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate pheremone receptor [Source:UniProtKB/TrEMBL;Acc:A3KQL3]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31618 | Nonsense | Available for shipment | Available now |
sa34237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41080 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21144 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31618
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059643 | Nonsense | 137 | 837 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71862299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32474730 |
GRCz11 | 18 | 32445186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCATTGATGAATGTTCAAGAATTTGCATCAAGAGGTAGCTGCAATGGA[C/T]AGTCTCCAGTACATGCTATCATAGGTGAAACAGAGTCTTCCAATACAGTG
Long Flanking Sequence:
CTTTCAGATGTCAGTCTTTTTTTGCACACTTCTAATTTTCTTTCAACTTTATGCAAAGGCAGAAAAGCCTATTTGCATCATGATGGGAGACCCTAAGTATCCGCTGCTATCCAAGGAGGGGGACATTTCTATTGGAGCAGTTTTTCCAGTCCACAGCATAGAGACATTACCCTTGTTTAAGTTTACGCAAAAACCTCAGCTTTTATCATGCTCAAGGTTTGTTACTGTGGAAAATATTTTAGAATCAGTACAGATCATGCAGAAAAAATTATTTGTTTAACCCTCTAATTTTTTTTTTTAGTGTGAGTATAAGAGACTTTCGAATGGCTCAAATTATGGCATTTGCCATTGAGGAGATTAACAGAAATGAAAGTTTGCTCCCAAATGTTTCACTTGGTTACCAAATTTATGACACCTGTGGTTCAGGATTGTCTTTGATGGGTGCAAACATGGCATTGATGAATGTTCAAGAATTTGCATCAAGAGGTAGCTGCAATGGA[C/T]AGTCTCCAGTACATGCTATCATAGGTGAAACAGAGTCTTCCAATACAGTGATTTTGTCAAGAACTACAGGACCTTTTAAAATTCCAGTGGTAAGAAGCTATAATACAGTTTGTTGACATAAATAATGCACTGACCAATCATTTTACATTTTCTTTTGTCTTTTTTTCAGATAAGTCCCTCTGCATCATGCGAGTGTCTCAGTAATAGAAAAGAATACCCCTATTTTTTTAGAACTATTGCTAGTGATTACCACCAGAGCAGAGCACTTGCTTACATAATCAAATATTTTGGCTGGTCTTGGGTGGGAGCTGTGAACAGTGACAATGACTATGGAAACCATGGAATGGCTATATTTCTAAGTACAGCAGAGAAAGAGGGGGTTTGCGTGGAGTACTCTGTGAAATTCCAGAGAACAGAGCCAGAGAAACTGAAAAAGGTGGTAGATACAATAAAAAAAGGCACTTCAAAAGTGATTGTTGCATTTCTTACTGAATTTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34237
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 |
---|---|---|---|---|---|
ENSDART00000059643 | Nonsense | 356 | 837 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71863036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32475467 |
GRCz11 | 18 | 32445923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGAAACAGCTTTTCCATGCTCACAGACTTCACAGAAAGAAAATTCT[C/T]AATATAAATTAATTTGCAACATATATCGAGATCTTCTTGTACTGAAAAAT
Long Flanking Sequence:
TTGCTAGTGATTACCACCAGAGCAGAGCACTTGCTTACATAATCAAATATTTTGGCTGGTCTTGGGTGGGAGCTGTGAACAGTGACAATGACTATGGAAACCATGGAATGGCTATATTTCTAAGTACAGCAGAGAAAGAGGGGGTTTGCGTGGAGTACTCTGTGAAATTCCAGAGAACAGAGCCAGAGAAACTGAAAAAGGTGGTAGATACAATAAAAAAAGGCACTTCAAAAGTGATTGTTGCATTTCTTACTGAATTTGAGATGAAAAATCTACTTGAATATTTAATTATTCAGAATGTAACAGGTCTACAAGTAATTGGTGTGGAGGCATGGATAACAGCAAACAGTATGATCAAACCAAATAGTTTTCATGTGCTGGGAGGGTCACTGGGGTTTGCAGTAAAAAAACTCAATATTGAAGGTTTTGAAGATTATGTCACCAAAGCATTCTGGGAAACAGCTTTTCCATGCTCACAGACTTCACAGAAAGAAAATTCT[C/T]AATATAAATTAATTTGCAACATATATCGAGATCTTCTTGTACTGAAAAATGACAATAAAGATGTACCTGAACAAAGATATGCTAGCAATGTCTACAAAGCTGTTTATGCTGTCGCTCATTCACTACACAACATATTAAAGTGTAGAGAAAATGGAGCATGTGAAACAGACATGAAAATACAACCTCAGCAGGTAATAAACAAAAACAATGAATGAATGTTAGGAAGTTAGAGCGCAAGAGGGTAATTTTTAATTTCTGTCTTTTTCTTTTCACTAGGTGGTTGAGGCTCTGCGAAAGGTAAATTTCACCATTAAGATGGGGGACTGTGTGTGGTTTGACAGCACTGGTGCAGTTGTAGCTCAATATGAAGTTGTAAACTGGCAGCCAGACTATAATGGATCGATACAATTCAAACCAGTGGGGTACTATGATGCTTCACTGCCCCCTAATCAGCGCTTTGTGATCAACACTGAAAACATAATCTGGGCTGGAGGACAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41080
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 |
---|---|---|---|---|---|
ENSDART00000059643 | Essential Splice Site | 419 | 837 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71863228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32475659 |
GRCz11 | 18 | 32446115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGAGAAAATGGAGCATGTGAAACAGACATGAAAATACAACCTCAGCAG[G/A]TAATAAACAAAAACAATGAATGAATGTTAGGAAGTTAGAGCGCAAGAGGG
Long Flanking Sequence:
TGAAAAAGGTGGTAGATACAATAAAAAAAGGCACTTCAAAAGTGATTGTTGCATTTCTTACTGAATTTGAGATGAAAAATCTACTTGAATATTTAATTATTCAGAATGTAACAGGTCTACAAGTAATTGGTGTGGAGGCATGGATAACAGCAAACAGTATGATCAAACCAAATAGTTTTCATGTGCTGGGAGGGTCACTGGGGTTTGCAGTAAAAAAACTCAATATTGAAGGTTTTGAAGATTATGTCACCAAAGCATTCTGGGAAACAGCTTTTCCATGCTCACAGACTTCACAGAAAGAAAATTCTCAATATAAATTAATTTGCAACATATATCGAGATCTTCTTGTACTGAAAAATGACAATAAAGATGTACCTGAACAAAGATATGCTAGCAATGTCTACAAAGCTGTTTATGCTGTCGCTCATTCACTACACAACATATTAAAGTGTAGAGAAAATGGAGCATGTGAAACAGACATGAAAATACAACCTCAGCAG[G/A]TAATAAACAAAAACAATGAATGAATGTTAGGAAGTTAGAGCGCAAGAGGGTAATTTTTAATTTCTGTCTTTTTCTTTTCACTAGGTGGTTGAGGCTCTGCGAAAGGTAAATTTCACCATTAAGATGGGGGACTGTGTGTGGTTTGACAGCACTGGTGCAGTTGTAGCTCAATATGAAGTTGTAAACTGGCAGCCAGACTATAATGGATCGATACAATTCAAACCAGTGGGGTACTATGATGCTTCACTGCCCCCTAATCAGCGCTTTGTGATCAACACTGAAAACATAATCTGGGCTGGAGGACAGCTAAAGGTACATGGCCATAACATAATCATACTACTCTTAGGCAGGCATATTTAAATTTAATTAATAATTTAAAAAATATTTGACGAGTAGCTGCAGAGCATCAAGCAAAAACGGAAAGCATTCACACAAAAAGAGACCCTAGCCCATACTAATGAACTACTTTGGTCTAACCAAGTGTTTCAGTATCATAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21144
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059643 | Nonsense | 711 | 837 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71865991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32478422 |
GRCz11 | 18 | 32448878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTCTTATCTGTGTGCTTTGGCTAGCAGTATCTCCTCCATTGCCCTAC[A/T]AAAATACGAAATATTTCAAAGAAAAAATTATTCTTGAGTGCAGTCTGGGT
Long Flanking Sequence:
GTCCAGGGGAATACTGGTCTAATGCTGAGAAAAATAAATGTGTGTTAAAGGCTGTAGAGTTCCTGTCATTCAAAGAACTAATGGGTATAGTTCTAGTCTTTTTCTCACTGTTAGGCGCAGGATTAACCACACTAGTTGCTATTCTGTTTTATAGCAAGAAGGACACTCCAATAGTAAAAGCCAACAACTCAGAGCTGAGCTTCCTGCTACTCTTTTCATTGATGCTATGTTTTCTCTGTTCTCTTACTTTCATTGGTCGCCCCACTGAATGGTCCTGTATGTTGCGCCACACAGCATTTGGGATCACTTTTGTCCTCTGTATCTCCTGTGTTCTGGGGAAAACCATAGTGGTGTTAATGGCCTTTAAGGCTACTCTACCAGGTAGTGATGTTATGAAATGGTTTGGTCCTATACAACAACGACTCAGTGTTCTTGTGATTACAATTGTACAAGTTCTTATCTGTGTGCTTTGGCTAGCAGTATCTCCTCCATTGCCCTAC[A/T]AAAATACGAAATATTTCAAAGAAAAAATTATTCTTGAGTGCAGTCTGGGTTCTACTATAGGTTTTTCTGCTGCACTAGGTTATATAGGTCTTCTGGCTATCCTGTGTTTCATTTTGGCTTTTCTGGCTCGCACACTGCCTGATAAATTCAATGAAGCAAAATTCATCACATTCAGTATGATCATATTCTGTGCTGTATGGATCACATTTATCCCTTCTTATTTAAGTTCTCCTGGAAAACTGACTGTAGCAGTAGAGATATTTGCCATTTTAGCTTCAAGTTTTGGTTTATTATTTTGCATATTTTTACCAAAATGTTATATAATCATGTGCAAGCCTGAACAGAATACAAAGCTGCATATTATTGGTAAGCTCAACAAATAAACAGTTTCTTAAGTCATTCACAATCAATCCTAAAATTAAACAATTGGCTTTTTATGCTTGTAGTTGTGACTTTTTTTATGAAGTAGGAAAGAGCACATAGACATAAAACAGTTCTCC
Associated Phenotype:
Not determined