ZMP
ENSDARG00000088029
Ensembl ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10950 | Nonsense | Available for shipment | Available now |
sa14843 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13020 | Nonsense | Available for shipment | Available now |
sa36681 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2984 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa10950
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 |
---|---|---|---|---|---|
ENSDART00000064153 | Nonsense | 158 | 748 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31401882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33198741 |
GRCz11 | 18 | 33173336 |
KASP Assay ID:
2261-2344.1 (used for ordering genotyping assays)
KASP Sequence:
TTMATTTCATAATTTATGCTTCCTGTTTGCAATAAMTTTTAGGTAAGTTA[T/A]TTTTCAACATGTGCGTGTCTCAGTGATAGAAAAAAATAWCCATYATTTTT
Long Flanking Sequence:
GAAACATGCAAAGGATTAAGTGCACGGGGTAAGTTGTGAATTGATTCAAACATGGAATCATTGGCAATGTTAAGAGCATTATTTTTCTTCTCGTATTTACTGCACAGATTTGACCTACGTGCATTTCGTTGGATTCAGTCAATGATGTTTGCAGTGGATGAAATAAATAAAAATGAGGAGTTGCTTCCTCACATTTCTTTGGGCTATAAAATAATGGATTCTTGTGCTTCACCCACGAACGTTTTACGAGCAGTATTCTCACTGGTAAGTGAGCAGAAGGAGCAGGAATTTACATCTCAGTGTCACCTTCCACTTACAGCTCTTGTTGCTGAATCAGGATCTTCACAGTCTTTAGCTGTTGCCGGAATGCTTGGACCATTTAGAGTGCCCATGGTAATGTCAATCATTCTCGCAGCACACTTGCATTGGTGTTCCTGAAAATGAAATCAGTTCATTTCATAATTTATGCTTCCTGTTTGCAATAACTTTTAGGTAAGTTA[T/A]TTTTCAACATGTGCGTGTCTCAGTGATAGAAAAAAATATCCATCATTTTTCCGCACAATTCCAAGTGACTTCTACCAAGCAAAAGCTTTGGCCTCTCTGGTAAAACAGTTTGGATGGACTTGGATTGGAGCTTTGCAGTCTGACAATGATTATGGGAGAAATGGAATTTCAGCTTTCACAAAGGAAGTGGAAAAAATGGGAGTTTGCATTGCATTTGTCGGCACTATATTAAGAACATATCCCCAAAGTAAAATCACTGAAGTGGTAGAAATGATCAAAGAATCGACAGTAAAAGTCATCCTGGCATTCGTGCCAGAGGGAGATCTCTATCCTCTAATGAAAGAAGTTGTGAACCGGAATATCACAGGAATCCAGTGGATTGCAAGTGAAGCCTGGGTAACAGCAGCAAGACCATCTACCCCTGAAATGTTCAAGTCATTTGGAGGCACCGTAGGATTTGTGGTCAGAAAGATGGCTATGTTAAAACTAAGACCTTACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14843
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 |
---|---|---|---|---|---|
ENSDART00000064153 | Nonsense | 171 | 748 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31401921)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33198780 |
GRCz11 | 18 | 33173375 |
KASP Assay ID:
1641-0494.1 (used for ordering genotyping assays)
KASP Sequence:
TAGGTAAGTTAWTTTTCAACATGTGCGTGTCTCAGTGATAGAAAAAAATA[T/A]CCATYATTTTTCCGCACAATTCCAAGTGACTTCTACCAAGCAAAAGCTTT
Long Flanking Sequence:
ATTGATTCAAACATGGAATCATTGGCAATGTTAAGAGCATTATTTTTCTTCTCGTATTTACTGCACAGATTTGACCTACGTGCATTTCGTTGGATTCAGTCAATGATGTTTGCAGTGGATGAAATAAATAAAAATGAGGAGTTGCTTCCTCACATTTCTTTGGGCTATAAAATAATGGATTCTTGTGCTTCACCCACGAACGTTTTACGAGCAGTATTCTCACTGGTAAGTGAGCAGAAGGAGCAGGAATTTACATCTCAGTGTCACCTTCCACTTACAGCTCTTGTTGCTGAATCAGGATCTTCACAGTCTTTAGCTGTTGCCGGAATGCTTGGACCATTTAGAGTGCCCATGGTAATGTCAATCATTCTCGCAGCACACTTGCATTGGTGTTCCTGAAAATGAAATCAGTTCATTTCATAATTTATGCTTCCTGTTTGCAATAACTTTTAGGTAAGTTATTTTTCAACATGTGCGTGTCTCAGTGATAGAAAAAAATA[T/A]CCATCATTTTTCCGCACAATTCCAAGTGACTTCTACCAAGCAAAAGCTTTGGCCTCTCTGGTAAAACAGTTTGGATGGACTTGGATTGGAGCTTTGCAGTCTGACAATGATTATGGGAGAAATGGAATTTCAGCTTTCACAAAGGAAGTGGAAAAAATGGGAGTTTGCATTGCATTTGTCGGCACTATATTAAGAACATATCCCCAAAGTAAAATCACTGAAGTGGTAGAAATGATCAAAGAATCGACAGTAAAAGTCATCCTGGCATTCGTGCCAGAGGGAGATCTCTATCCTCTAATGAAAGAAGTTGTGAACCGGAATATCACAGGAATCCAGTGGATTGCAAGTGAAGCCTGGGTAACAGCAGCAAGACCATCTACCCCTGAAATGTTCAAGTCATTTGGAGGCACCGTAGGATTTGTGGTCAGAAAGATGGCTATGTTAAAACTAAGACCTTACCTGGAAAACATCAGTCCCTACTCTCCTACACAATCAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13020
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 |
---|---|---|---|---|---|
ENSDART00000064153 | Nonsense | 436 | 748 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31403224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33200083 |
GRCz11 | 18 | 33174678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATACAACCGGTACTGTTATCTAATTYAACTGTATAATTTWTACACAATTT[A/T]AACTAGCTAAATATTGTCATAATTGTAATTCTTTTATAGGAGCAGCAGAC
Long Flanking Sequence:
ATAGCATACTTCAAACGTTTAAATTATACTTCATTCAAAGGTCAGCGATCAGTTGGAAAGAGTGAATTTTATAGATGAATATGGAGAAAATGTGTTCTTTGATGAGAATGGAGACCCGCCTGCATCATATGAGCTCATAAACTGGCAGCTAAATCAGGGAGAGGTGCAACATGTGACTGTGGGCTATTTCAGCAAATCCCCAGATGGAACATATAAACTTACAATTAAAGAGGATAACGTCCACTGGAGCACAGAAAATTTGGTACTTCACCGATTAAAGCATCCTTATTCATTTTAATTTACTATAAATTGGCTAACGTATGATCACTTGACAGATACCCAAAGCAGTGTGCTCAGACACCTGCCCGAAAGGCACAAGGAAAGCACAAATAAAAGGTCGGCCTGTTTGCTGCTTTGACTGCATCCCATGTGCTGATGGTTCAATATCAAATACAACCGGTACTGTTATCTAATTTAACTGTATAATTTTTACACAATTT[A/T]AACTAGCTAAATATTGTCATAATTGTAATTCTTTTATAGGAGCAGCAGACTGCACTCTTTGTCCTAAAGAATACTGGTCAAATGAAAGACGGGACAAGTGTCTTGTGAAAACAATAGAGTTTCTGTCGTATACAGAAACAATGGGAATAATTCTCACTGCTCTATCGCTATTTGGAGCCAGTCTTACAGTTGCAACTATGATTGTCTTCATACACTATAGAGAAACACCAATAGTGAAAGCTAACAACTCAGAGCTGAGCTCACTATTACTCTCTTCGTTGTTCTTTTGTTTCCTTTGTCCTCTTACATTCATTGGTGAGCCGACACATTGGTCATGTATGCTACGTCATACAGCTTTTGGGCTTACTTTTGCTCTCTGCATTTCTTGTGTTTTGGGGAAGACCATAGTAGTTGTCACAGCTTTCAGAGCCACATTACCAGGAAATAAATTGTCTGGTAAGTTTGGGCCAGTACAACAAAGAGCCATCGTGTTCTTATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36681
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064153 | Nonsense | 461 | 748 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31403300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33200159 |
GRCz11 | 18 | 33174754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTCTTTTATAGGAGCAGCAGACTGCACTCTTTGTCCTAAAGAATACT[G/A]GTCAAATGAAAGACGGGACAAGTGTCTTGTGAAAACAATAGAGTTTCTGT
Long Flanking Sequence:
GAATATGGAGAAAATGTGTTCTTTGATGAGAATGGAGACCCGCCTGCATCATATGAGCTCATAAACTGGCAGCTAAATCAGGGAGAGGTGCAACATGTGACTGTGGGCTATTTCAGCAAATCCCCAGATGGAACATATAAACTTACAATTAAAGAGGATAACGTCCACTGGAGCACAGAAAATTTGGTACTTCACCGATTAAAGCATCCTTATTCATTTTAATTTACTATAAATTGGCTAACGTATGATCACTTGACAGATACCCAAAGCAGTGTGCTCAGACACCTGCCCGAAAGGCACAAGGAAAGCACAAATAAAAGGTCGGCCTGTTTGCTGCTTTGACTGCATCCCATGTGCTGATGGTTCAATATCAAATACAACCGGTACTGTTATCTAATTTAACTGTATAATTTTTACACAATTTAAACTAGCTAAATATTGTCATAATTGTAATTCTTTTATAGGAGCAGCAGACTGCACTCTTTGTCCTAAAGAATACT[G/A]GTCAAATGAAAGACGGGACAAGTGTCTTGTGAAAACAATAGAGTTTCTGTCGTATACAGAAACAATGGGAATAATTCTCACTGCTCTATCGCTATTTGGAGCCAGTCTTACAGTTGCAACTATGATTGTCTTCATACACTATAGAGAAACACCAATAGTGAAAGCTAACAACTCAGAGCTGAGCTCACTATTACTCTCTTCGTTGTTCTTTTGTTTCCTTTGTCCTCTTACATTCATTGGTGAGCCGACACATTGGTCATGTATGCTACGTCATACAGCTTTTGGGCTTACTTTTGCTCTCTGCATTTCTTGTGTTTTGGGGAAGACCATAGTAGTTGTCACAGCTTTCAGAGCCACATTACCAGGAAATAAATTGTCTGGTAAGTTTGGGCCAGTACAACAAAGAGCCATCGTGTTCTTATGCACTGCGATTCAAATAGTGATCTGTGCTTTATGGCTTCTAATAAAGCCACCATTTCCTGACAAGGCCCTCAGGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2984
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000064153 | Nonsense | 578 | 748 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 31403650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33200509 |
GRCz11 | 18 | 33175104 |
KASP Assay ID:
554-3339.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGCATTTCTTGTGTTTTGGGGAAGACCATAGTAGTTGTCACAGCTTTC[A/T]GAGCCACATTACCAGGAAATAAATTGTCTGGTAAGTTTGGGCCAGTACAA
Long Flanking Sequence:
CATGTGCTGATGGTTCAATATCAAATACAACCGGTACTGTTATCTAATTTAACTGTATAATTTTTACACAATTTAAACTAGCTAAATATTGTCATAATTGTAATTCTTTTATAGGAGCAGCAGACTGCACTCTTTGTCCTAAAGAATACTGGTCAAATGAAAGACGGGACAAGTGTCTTGTGAAAACAATAGAGTTTCTGTCGTATACAGAAACAATGGGAATAATTCTCACTGCTCTATCGCTATTTGGAGCCAGTCTTACAGTTGCAACTATGATTGTCTTCATACACTATAGAGAAACACCAATAGTGAAAGCTAACAACTCAGAGCTGAGCTCACTATTACTCTCTTCGTTGTTCTTTTGTTTCCTTTGTCCTCTTACATTCATTGGTGAGCCGACACATTGGTCATGTATGCTACGTCATACAGCTTTTGGGCTTACTTTTGCTCTCTGCATTTCTTGTGTTTTGGGGAAGACCATAGTAGTTGTCACAGCTTTC[A/T]GAGCCACATTACCAGGAAATAAATTGTCTGGTAAGTTTGGGCCAGTACAACAAAGAGCCATCGTGTTCTTATGCACTGCGATTCAAATAGTGATCTGTGCTTTATGGCTTCTAATAAAGCCACCATTTCCTGACAAGGCCCTCAGGTATGACCATAAAAAGATCATTTTAGAGTGCAACACTGGCTCGGATGCTGGATTTTATGCAGCTTTAGGATATGTTGGCCTTCTGTCAACAATCTGTTTGATTTTAGCATTTTTAGGAAGAAAACTTCCTGATAATTTTAATGAGGCCAAATTCATCTCATTCAGTATGCTCATATTTTGTGCTGTTTGGGTAACATTTATACCTGCATACATTAGTTCACCTGGCAAGTACACTGTTGCGGTGGAGATTTTTGCCATTTTGTCATCTGCCTTTGGATTGTTGCTATGTATATTTGCACCAAAATGTTTCATTATTCTCATTAAACCAGAGAGAAATACTAGAAAGCATGTCATG
Associated Phenotype:
Not determined