ZMP
v2rh12
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3KQH5]
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 |
---|---|---|---|
sa10737 | Essential Splice Site | Available for shipment | Available now |
sa23327 | Nonsense | Available for shipment | Available now |
sa29061 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10737
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007035 | Essential Splice Site | 153 | 850 | 3 | 6 |
ENSDART00000141838 | Essential Splice Site | 172 | 867 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31615890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33412749 |
GRCz11 | 18 | 33387344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTCATCTGACTAACACTTAATCTGTTCTGCCCTATATATTTTCTAATT[A/G]GATAAGCTACTACGCCACTTGCTCTTGTTTAAGTGACAAKAAAAAGTACC
Long Flanking Sequence:
CCATCAGTGAGATTAATCACAATCCCAACTTGCTGCCAAACATCACACTTGGTTACCAGATCTATGACACTTGTTTAAGGCTTAGAGTGGCATTTCAGGCAGCAACAGCTCTGATAAGTGGGACAGAGGAGACCATCTCTGACTTCAACTGTAAAGGCCCACCACCAGTTATTGGACTCATAGGTGATCCAGGATCTACACATTCTATTGCAATTTCCAGTGTTCTGGGGCTGTTTCGAATGCCTATGGTATGGACCTTAAAAAAGATTCTTGTGGGATTTTTTTCGGGGAGGGCGTCTATTCTGCAACCTTTTTTTATTTGTTTTTATCACATTTTATTTGGCTTTTTTTGTATTTGGCTATATCTACTTTATGATTGATAATAACATAATACAATTTTTCCAAATCTTTATTTTTTGAACTGTGGATTTAGAGCTAAATACTTATTTTGTCTCATCTGACTAACACTTAATCTGTTCTGCCCTATATATTTTCTAATT[A/G]GATAAGCTACTACGCCACTTGCTCTTGTTTAAGTGACAAGAAAAAGTACCCTTCTTTCTTCAGAACAATTCCAAGTGATACCTTCCAAGTGCGGGCTATAGTTCAGACCTTGAGACATTTTGGCTGGACCTGGGTTGGTCTGATCTACAGTAATAATGACTATGGTATCTACGCTGCTCAGTCCTTCCATCAAGAAATGCAGTTGTTTGGACACTGTGTTGCTTTTTCTGAAATCCTGCCCCAAGATAACAACCCCAGAGTTATTGATCACATTATGGGAGTAATTCAGGCCTCTACAGCTAGAGTAGTGGTTGTTTTTTCTGCTTCATCCTTATTGATTCCTTTGATGAACAAGGTAGTGTTGCACAACTTAACAAGCAGGCAGTGGATAGCAAGTGAAGCCTGGGTCACCGCAGCTGTGTTCCGCACACCATATTACCAGCCCTTTCTAAAGGGAACATTGGGCATTGCTATTAGGCGTGGAGAAATCCAGGGTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23327
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 |
---|---|---|---|---|---|
ENSDART00000007035 | Nonsense | 359 | 850 | 3 | 6 |
ENSDART00000141838 | Nonsense | 378 | 867 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31616510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33413369 |
GRCz11 | 18 | 33387964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGTTTGGGTGCAGTTTTGAAACTGGGGATAAAGAGACATTTGGGCAA[C/T]AAATGAAAAAGGTGTGTACAGGACTGGAGGATCTGAGCACTGCAAACACA
Long Flanking Sequence:
TTGGCTGGACCTGGGTTGGTCTGATCTACAGTAATAATGACTATGGTATCTACGCTGCTCAGTCCTTCCATCAAGAAATGCAGTTGTTTGGACACTGTGTTGCTTTTTCTGAAATCCTGCCCCAAGATAACAACCCCAGAGTTATTGATCACATTATGGGAGTAATTCAGGCCTCTACAGCTAGAGTAGTGGTTGTTTTTTCTGCTTCATCCTTATTGATTCCTTTGATGAACAAGGTAGTGTTGCACAACTTAACAAGCAGGCAGTGGATAGCAAGTGAAGCCTGGGTCACCGCAGCTGTGTTCCGCACACCATATTACCAGCCCTTTCTAAAGGGAACATTGGGCATTGCTATTAGGCGTGGAGAAATCCAGGGTCTTCATAGTTTTCTGTTACGCCTTCATCCCAACAGTGACCAAAGAAATAATATAGTGAGAATATTCTGGGAGACCATGTTTGGGTGCAGTTTTGAAACTGGGGATAAAGAGACATTTGGGCAA[C/T]AAATGAAAAAGGTGTGTACAGGACTGGAGGATCTGAGCACTGCAAACACACCTTACACTGATGTTTCAGGATTGAGGGCAACTTATAATGTGTATAAAGCAGTTTATGCCCTGGCCCATGCACTTCATGACCTGATGCAGTGTAAAGAGAAGAGAGGACCATTCAGTGGGAACAGCTGTGCTGACATAACAGATCTAAAACCCTGGCAGGTAAGACCCACAGGTATAGTGAAGAAAAGTTAGCACACACATAATATGTACCTTATGCTCATTTAAATCAGATATATGTATAACATTTGTCCTGTCTACAATCTGTACAGCTTGTTCACTACCTAAAAAAAGTGAATTTCACCACAAGCTTTGGGGATTCTGTATCATTTGACAATAATGGAGATGCTCTAGCCATCTATGATGTGTTGAACTGGCAGCCGAGCTCTGAAGAATCAATTAAACTTCACAATATCGGTGTAGTAAATGAGGTGGCAACAGAAATGGTGCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29061
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 |
---|---|---|---|---|---|
ENSDART00000007035 | Nonsense | 628 | 850 | 6 | 6 |
ENSDART00000141838 | Nonsense | 645 | 867 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 31617629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33414488 |
GRCz11 | 18 | 33389083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTACGTGCCAACAATTCAGAGCTCAGCTTCCTGCTGCTTTTGTCACTC[A/T]AACTGTGTTTCCTGTGTGTGCTGCTGTTCATTGGTCAGCCCCAGTTGTGG
Long Flanking Sequence:
GAAAGAGACGACAGGCATGACTAATTACACATGATGTTACTTTCAGCCCCCACAGTCTGTGTGCAGTGAGAGCTGTCTCCCAGGCACCAGAAGAGCCATGAGGAAGGGCCTTCCTGTCTGCTGTTTTGACTGCCTGATTTGTGGAGATGGTGAAATTTCTAACACAACAGGTGAGAAAATTATTGTATACAAAATTGTATTTTAGAAATAAAAGAGTGAATTAAAAAAAGAGAAAATGAATTAATTTTGTACCAACAGATGCTATTAAGTGCACAGTTTGTCCAGATGAATTTTGGTCCAATCTAAATAAGGATCAATGTGTTCCTAAAGAAATTGATTTTCTATCATATGAGGATCCTCTGGGCATCTCGCTGACCACTACTTCCCTGCTGGGAACCTGTTTTTGTGCTCTTGTGATGATAATTTTTACTTTTCACCGTAACACTCCTATAGTACGTGCCAACAATTCAGAGCTCAGCTTCCTGCTGCTTTTGTCACTC[A/T]AACTGTGTTTCCTGTGTGTGCTGCTGTTCATTGGTCAGCCCCAGTTGTGGACGTGTCAATTAAGACATGCTGTGTTTGGCATAAGCTTTGTCCTGTGCATCTCCAGCATTTTGGTCAAGACTATGGTGGTAATAGCTGTGTTCAAATCCTCTCGGCCTGAGGGCTCAGGAGCAATGAAATGGTTTGGAACAGCACAACAAAGATGCACAGTTCTGGTCCTAACAGCCCTCCAAATTGTAATATGTGCAGTCTGGCTATCAACTTCTTCTCCAACACCCTATAAAAATAACCAGTCTATCCGCTCTAAAATAGTCTATGAATGTGCCATTGGCTCATTGGCTGGGTTTTCTTTGCTGCTGGGATATATAGGATTGTTGGCAGCAATAAGCTTCCTACTAGCCTTTCTGGCTAGAAATCTTCCAGATAATTTTAATGAGGCAAAGTTTATCACTTTTAGTATGCTGATCTTCTGTGCGGTATGGGTTGCATTTGTTCCAGCA
Associated Phenotype:
Not determined