ZMP
v2rh14
Ensembl ID:
ZFIN ID:
Description:
vomeronasal 2 receptor, h14 [Source:RefSeq peptide;Acc:NP_001076568]
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 |
---|---|---|---|
sa6525 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36684 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13866 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6525
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 |
---|---|---|---|---|---|
ENSDART00000099139 | Nonsense | 143 | 820 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31570242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33367101 |
GRCz11 | 18 | 33341696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTWAAATATATACATTATATAGGTTAGCTACTAWGCMACATGCTCCTG[T/A]TTAAGTGACCGGAGCAAATACYCMTCTTTCTTCAGAACAATTCCCAGTGA
Long Flanking Sequence:
GATTATTGATTTTAGGATTATTTACTGAATAATAACATTTGCACCACCTTTTCTAGGTTCTATATGGCAAGTTTTCAGCAGGCACAAACTATGGTATATGCCATAAATGAAATCAATAACAATCCTAACCTGTTGCCTAACATCACCCTCGGTTACCATCTGTATGACAATTGTGTGAAGCTTGGAGTTGCATTCAGGTCTGCAACAGCTTTGGTTAGTGGGACAGAGGAATCCTTCAATGTTTTGAACTGCACTGGTCCACCACCCATCATTGGGATTGTGGGGGATCCTGGATCTACTCATTGTATAGCAATCTCCAGTGTGCTGGGATTATTTCGAATACCTATGGTAGGATGTTTTGTATATAAAATTGTATTACCGCCTATAAAAATTGTTAATTGTGTCTGTTCATGTCAAACTGTACTGGCTGTAATGATAACACATTTGTCTTTTTAAAATATATACATTATATAGGTTAGCTACTATGCCACATGCTCCTG[T/A]TTAAGTGACCGGAGCAAATACCCCTCTTTCTTCAGAACAATTCCCAGTGATGCTTTCCAGGTGCGGGCTATGGTTCTGATCTTGAAGCACTTTGGATGGACCTGGGTTGGGCTCCTCTACAGTGATGATGATTATGGCATCAATGCTGCTCAATCTTTCCAAAAGGAAGTGCAGTTGTTTGGAGGTTGTGTTTCTTTTTCTGAAATCCTGCCACTTGATAATAACCACATGGACATCCAGCGTATTGTACAAGTGATTCAGGCCTCTACAGCAATAGTGGTGGTAGTTTTTTCCACAGAAGCCTATCTGCTTTCCTTGATGGACGAGGTGGTTTTGCAGAATGTAACAGGCAGGCAGTGGATTGCAAGTGAAGCTTGGGCCACCTCTTCAGTTTTTCACACTAAGCGTCTTTTGCCTTTCCTGGGAGGCACACTGGGTATTGCCATAAGACGTGGAGAGATCCAGGGACTTCGTGATTTTCTGCTAAGCCTCCACCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36684
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 |
---|---|---|---|---|---|
ENSDART00000099139 | Nonsense | 183 | 820 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31570362)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33367221 |
GRCz11 | 18 | 33341816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTTCTGATCTTGAAGCACTTTGGATGGACCTGGGTTGGGCTCCTCTA[C/A]AGTGATGATGATTATGGCATCAATGCTGCTCAATCTTTCCAAAAGGAAGT
Long Flanking Sequence:
AATCCTAACCTGTTGCCTAACATCACCCTCGGTTACCATCTGTATGACAATTGTGTGAAGCTTGGAGTTGCATTCAGGTCTGCAACAGCTTTGGTTAGTGGGACAGAGGAATCCTTCAATGTTTTGAACTGCACTGGTCCACCACCCATCATTGGGATTGTGGGGGATCCTGGATCTACTCATTGTATAGCAATCTCCAGTGTGCTGGGATTATTTCGAATACCTATGGTAGGATGTTTTGTATATAAAATTGTATTACCGCCTATAAAAATTGTTAATTGTGTCTGTTCATGTCAAACTGTACTGGCTGTAATGATAACACATTTGTCTTTTTAAAATATATACATTATATAGGTTAGCTACTATGCCACATGCTCCTGTTTAAGTGACCGGAGCAAATACCCCTCTTTCTTCAGAACAATTCCCAGTGATGCTTTCCAGGTGCGGGCTATGGTTCTGATCTTGAAGCACTTTGGATGGACCTGGGTTGGGCTCCTCTA[C/A]AGTGATGATGATTATGGCATCAATGCTGCTCAATCTTTCCAAAAGGAAGTGCAGTTGTTTGGAGGTTGTGTTTCTTTTTCTGAAATCCTGCCACTTGATAATAACCACATGGACATCCAGCGTATTGTACAAGTGATTCAGGCCTCTACAGCAATAGTGGTGGTAGTTTTTTCCACAGAAGCCTATCTGCTTTCCTTGATGGACGAGGTGGTTTTGCAGAATGTAACAGGCAGGCAGTGGATTGCAAGTGAAGCTTGGGCCACCTCTTCAGTTTTTCACACTAAGCGTCTTTTGCCTTTCCTGGGAGGCACACTGGGTATTGCCATAAGACGTGGAGAGATCCAGGGACTTCGTGATTTTCTGCTAAGCCTCCACCCAGACAGTAATTTGAGAAATAATATGGTGAAAATCTTCTGGGAAAACATGTTTGAGTGCAGTTTTGATACTGTGGGTAGAAAGGGTGAAACGATGTGTACAGGTCAAGAAGATATCAGGACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13866
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 |
---|---|---|---|---|---|
ENSDART00000099139 | Nonsense | 738 | 820 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31572610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33369469 |
GRCz11 | 18 | 33344064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTATATTGGCATTTTAGCARCAGYAAGTTTTCTCTTAGCCTTCCTGGCA[C/T]GAAATTTACCAGATCATTTTAATGAGGCAAAGTTCATYACTTTTAGCATG
Long Flanking Sequence:
CTGTGGTTGTCATTTTTGCACATCATCGTCACACTCCTGTAGTACGTGCTAACAATTCAGAGCTCAGCTTCCTTCTGCTTGTGTCGCTCAAACTGTGTTTCCTGTGCGTGCTGCTGTTCATTGGCCAGCCACAGTTGTGGACATGTCGGTTAAGACATGCTGTGTTTGGCATTAGCTTTGTCCTGTGCATCTCCAGCATTCTGGTCAAGACTATGGTGGTGATAGCAGTATTCAAGTCCTCTCGACCTGAGGGTAAAAGTGCTATGAAATGGTTTGGTTCACATCAACAAAGATGCACAGTTCTGGTCCTCACTGCACTCCAGGTTGTCATATGTGCAGTCTGGCTAACAAATGCATCCCCAAAACCTTACAAAAACAACCAGTATACAAGCTCCAAAATAGTATATGAATGTACTATTGGCTCAGTGGTTGGTTTTGCAATGCTACTTGGCTATATTGGCATTTTAGCAGCAGTAAGTTTTCTCTTAGCCTTCCTGGCA[C/T]GAAATTTACCAGATCATTTTAATGAGGCAAAGTTCATCACTTTTAGCATGCTCATCTTCTGTGCTGTATGGATTGCATTTGTTCCAGCATATGTGAGCTCTCCAGGAAAATATGCAGTGGCTGTGGAGATATTTGCTATTTTAGCTTCTAGTTTTGGATTGCTGGCTGCCATATTTGCACCAAAATGCTACATTATTATTTTACACCCAGAAAGAAACACTAAAAAAGCCATCATGGGAAGAGCAACCTGAAAGAACATAATTTGTATCATAGACCAGCTTGATCTCACAAGAACATGTAAAAATGTTGCATTTTGCCAGTTTAGTGGCTAATTCGTATGAATTCATACGAGTTCAGTTATTTGAGACATGGCACCTAACCCCACCCCTAAACCCAACCGTCATTGATAGATGAACAAATCATACTAAATTGTACTAATTAGATCGTACGAATTCATATGAATTAGCCACTAAATCAAAAATTTACAAATTGCCTTGAGA
Associated Phenotype:
Not determined