ZMP
ENSDARG00000038532
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21145 | Nonsense | Available for shipment | Available now |
sa41081 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8447 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8621 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21145
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 |
---|---|---|---|---|---|
ENSDART00000088854 | Nonsense | 246 | 840 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71981904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32594107 |
GRCz11 | 18 | 32564563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACAGCTCAGGAGGAGGGGATTTGTGTTGAGTACTCAGAAAAATTCTA[T/A]CGAACAGATCCTGAGAAACTTAGAAAAGTAGTAGACACAATTAAAAACAG
Long Flanking Sequence:
TTCTATGAGTGCAACTATGGCATTGATGAATGGTAAAGAATTTTCTGCTGAGGATAAATGTAACGGACAGTCTGCCATACATGCCATCATAGGAGAAACTGAGTCTTCTGCTACAGTGATTCTGTCCAGAACTACAGGACCTTTTAAAATACCAGTGGTAAGAGACTGTACAGCATAGCCTGAATAGCAAGTCTAATAAAGCCCTACATACTGATGATGGTTTCATAGATTTCTTTGTTTGTTTGGGTTTTTTTTTTACAGATAAGTCACTCAGCCACATGTGAATGTCTTAGCAACAGGAAAAACCATCCCTCTTTCTTTCGAACTATTGCTAGTGATTACCATCAGAGCAGAGCACTTGCATACATAGTCAAGCACTTTGGCTGGTCATGGGTGGGAGCTGTGAACAGTGACAATGACTATGGCAATAATGGAATGGCAATATTTCTAAATACAGCTCAGGAGGAGGGGATTTGTGTTGAGTACTCAGAAAAATTCTA[T/A]CGAACAGATCCTGAGAAACTTAGAAAAGTAGTAGACACAATTAAAAACAGCACTGCAAAAGTAATTGTTGCATTTCTTACCAGTTTGGAAATGGAAAATTTGCTTCAGGAACTAACTAAAGCTAACATTACAGGACTCCAAATTATTGGTGTGGAAGCGTGGATAACAGCAAACAGTTTGCTCACTCCAAACAGCTTTCGTGTTCTGGGAGGATCATTGGGGTTTGCAGTACCAAAGGTCAATATTCAAGGTTTTTCAAACTATGTCATAAAAGATTTCTGGGAAACAGCTTTTCCATGCTCAGAGACTGAGATAAATGTATCTCAATATTCATCATTAAGTTGCAATTCTTATGATGACCTGCTTTTGCTGAAAAATTACAATGAAGATGTGCCTGAACAAAGATATGCAAGCAATGTCTATAAAGCAGTTTATGCTGTGGCTCATGCATTACACAGTCTACTTAAATGTAAAGTAAATGAAGGTTGTAAGAAAGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41081
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 |
---|---|---|---|---|---|
ENSDART00000088854 | Nonsense | 382 | 840 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71982312)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32594515 |
GRCz11 | 18 | 32564971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTGCTTTTGCTGAAAAATTACAATGAAGATGTGCCTGAACAAAGATA[T/A]GCAAGCAATGTCTATAAAGCAGTTTATGCTGTGGCTCATGCATTACACAG
Long Flanking Sequence:
AGTGACAATGACTATGGCAATAATGGAATGGCAATATTTCTAAATACAGCTCAGGAGGAGGGGATTTGTGTTGAGTACTCAGAAAAATTCTATCGAACAGATCCTGAGAAACTTAGAAAAGTAGTAGACACAATTAAAAACAGCACTGCAAAAGTAATTGTTGCATTTCTTACCAGTTTGGAAATGGAAAATTTGCTTCAGGAACTAACTAAAGCTAACATTACAGGACTCCAAATTATTGGTGTGGAAGCGTGGATAACAGCAAACAGTTTGCTCACTCCAAACAGCTTTCGTGTTCTGGGAGGATCATTGGGGTTTGCAGTACCAAAGGTCAATATTCAAGGTTTTTCAAACTATGTCATAAAAGATTTCTGGGAAACAGCTTTTCCATGCTCAGAGACTGAGATAAATGTATCTCAATATTCATCATTAAGTTGCAATTCTTATGATGACCTGCTTTTGCTGAAAAATTACAATGAAGATGTGCCTGAACAAAGATA[T/A]GCAAGCAATGTCTATAAAGCAGTTTATGCTGTGGCTCATGCATTACACAGTCTACTTAAATGTAAAGTAAATGAAGGTTGTAAGAAAGACCTGAAAATACAACCTCAGCAGGTAATGATCGCAATACAAATTGACAATGTAAGAGTGATTGCAAAAAGTGACTTGCTCTCCTGTACATCATTTTCTCAGGTTGTTGACACTCTAAAAGAAATAAATTTCACCATAAATATGGGAGATCGTGTGTGGTTTGACAGCACTGGTGCCACAATAGCCCAATATGAAGTCATAAACTGGCAGCAAGGCTCTGATGGATCAATCCAATTTAAAACAGTGGGATACTTTGATGCCTCACTGCCACATGACCAGCGCTTTGTTCTTAACACTGAAAGTATAATCTGGACTGGAGGACAACTTGAGGCAAATAACAATGCAATATTAACTGATGGAGCTACATATCAATATATAACATTTAGAACAACGACAAATAATTAATATAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8447
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088854 | Nonsense | 538 | 840 | 6 | 6 |
ENSDART00000088854 | Nonsense | 538 | 840 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71983843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32596046 |
GRCz11 | 18 | 32566502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATACTTTTATTTCTAATTGCTGTAATAACTGTAATTTTCTTCCAGATT[C/A]AGTTAACTGCAAACAGTGTCCAGGGGAGTACTGGTCTAATGCTGAGAAAA
Long Flanking Sequence:
AGTAACAAAAAGACTTGGCAAAGAAGTGGAGAAATGTAAATTTACTGAATTTCTGGCACAATTTTAGATTTACTTTGGTTACAGAATTTTTCATTCATCAGTCCACAGTAGTTTCCTTTACCTTTTTATTAGTTCACATATGCCATACTTAGTAATGCTTTTAAAAATTAAAATTTTTAAATTTGTAAATCATACATCTTTCTATGTAGAAGCCAAAGTCTGTGTGTAGTGAGAACTGCCCTGCCGGTACCAGGAAGGCTGTACAGAAAGGACGGCCTGTCTGCTGTTATGACTGTATTCCATGTGCAGATGGAGAAATCAGTAATGACACAGGTAATATTCAGCCTATCTCACATTTTTGAAGAAGATGTTTAAGACTTTTGTTCCTTTTTTATCCCTTTTATTTAACTTTAACAAGCAATGTCTTAACAAATTAACTACATAAAACATTGATACTTTTATTTCTAATTGCTGTAATAACTGTAATTTTCTTCCAGATT[C/A]AGTTAACTGCAAACAGTGTCCAGGGGAGTACTGGTCTAATGCTGAGAAAAATAGATGTGTGTTAAAGACTGTAGAGTTTCTGTCATTCACAGAAGTTATGGGTATAGTTCTAGTCTTTTTCTCACTCTTTGGAGTAGGATTAACTGTGCTGGTTGCCATTCTATTTTACAGCAAGAAAGAGACTCCCATTGTAAAAGCCAACAACTCAGAGTTGAGCTTCTTGCTGCTCTTCTCATTAACTCTGTGTTTTCTCTGTTCACTTACTTTTATTGGTCGACCGACTGAGTGGTCCTGTATGTTGCGTCATACAACTTTTGGGATCACATTTGTCCTATGCATCTCATGTGTTTTAGGAAAAACAGTAGTGGTGTTAATGGCCTTTAGAGCTACACATCCCGGAAAAGATATTATGAAATGGTTTGGTCCTGTACAACAAAGACTTAGTGTTATTGCACTTACCCTTATACAGGTTCTAATTTGTGTGCTTTGGCTAACAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8621
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088854 | Nonsense | 538 | 840 | 6 | 6 |
ENSDART00000088854 | Nonsense | 538 | 840 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 71983843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32596046 |
GRCz11 | 18 | 32566502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATACTTTTATTTCTAATTGCTGTAATAACTGTAATTTTCTTCCAGATT[C/A]AGTTAACTGCAAACAGTGTCCAGGGGAGTACTGGTCTAATGCTGAGAAAA
Long Flanking Sequence:
AGTAACAAAAAGACTTGGCAAAGAAGTGGAGAAATGTAAATTTACTGAATTTCTGGCACAATTTTAGATTTACTTTGGTTACAGAATTTTTCATTCATCAGTCCACAGTAGTTTCCTTTACCTTTTTATTAGTTCACATATGCCATACTTAGTAATGCTTTTAAAAATTAAAATTTTTAAATTTGTAAATCATACATCTTTCTATGTAGAAGCCAAAGTCTGTGTGTAGTGAGAACTGCCCTGCCGGTACCAGGAAGGCTGTACAGAAAGGACGGCCTGTCTGCTGTTATGACTGTATTCCATGTGCAGATGGAGAAATCAGTAATGACACAGGTAATATTCAGCCTATCTCACATTTTTGAAGAAGATGTTTAAGACTTTTGTTCCTTTTTTATCCCTTTTATTTAACTTTAACAAGCAATGTCTTAACAAATTAACTACATAAAACATTGATACTTTTATTTCTAATTGCTGTAATAACTGTAATTTTCTTCCAGATT[C/A]AGTTAACTGCAAACAGTGTCCAGGGGAGTACTGGTCTAATGCTGAGAAAAATAGATGTGTGTTAAAGACTGTAGAGTTTCTGTCATTCACAGAAGTTATGGGTATAGTTCTAGTCTTTTTCTCACTCTTTGGAGTAGGATTAACTGTGCTGGTTGCCATTCTATTTTACAGCAAGAAAGAGACTCCCATTGTAAAAGCCAACAACTCAGAGTTGAGCTTCTTGCTGCTCTTCTCATTAACTCTGTGTTTTCTCTGTTCACTTACTTTTATTGGTCGACCGACTGAGTGGTCCTGTATGTTGCGTCATACAACTTTTGGGATCACATTTGTCCTATGCATCTCATGTGTTTTAGGAAAAACAGTAGTGGTGTTAATGGCCTTTAGAGCTACACATCCCGGAAAAGATATTATGAAATGGTTTGGTCCTGTACAACAAAGACTTAGTGTTATTGCACTTACCCTTATACAGGTTCTAATTTGTGTGCTTTGGCTAACAATAT
Associated Phenotype:
Not determined