ZMP
olfcd3
Ensembl ID:
ZFIN ID:
Description:
Odorant receptor VR3.13a [Source:UniProtKB/TrEMBL;Acc:Q4VDB2]
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 |
---|---|---|---|
sa18045 | Nonsense | Available for shipment | Available now |
sa25067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36679 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10065 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18045
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059500 | Nonsense | 183 | 850 | 3 | 6 |
ENSDART00000099111 | Nonsense | 102 | 539 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 31321423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33118282 |
GRCz11 | 18 | 33092877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATCAGTCAYTTTGCCACATGTGYCTGCTTGAGTAACAGAAAAAGGTA[T/G]GCATCCTTCTTTAGAACGATCCCCAGTGACTATTACCAAAGCAGAGCACT
Long Flanking Sequence:
TTTGCTCAAACACTGATTTTTGCCATCGAAGAGATTAATAACAACACACAGCTATTGCCTGGTGTGTCTTTGGGCTATAAGATATATGATTCATGTGGCTCAATAGCTCAAGCTATATTCTCAGGCATGGCTTTGATGAATGGTTATGAAGAAACTTTGAGCGATACATCCTGCTCTAGACCACCAGCTGTTAATGCCATTGTAGGAGAGTCAAACTCCTCTCCCACCATAGCCTTGGCTTCTATAGCTGGTCCATTCAGTTTACCTGTTGTAAGAACCCTTGCTTATTGGCTTGTTATTGTGGCAAGTGTTTTTTTTTTCCTTTTTTTTTTTTTCATTAGTTGCACAATCTTTAATGCAAGTATGTAAATTGTATTTACAGTATAATTATATACTGTATATATTACTTTTGATTAAATAAGTGAATAAAATATTCTGTTTCTCCTCTTGCAGATCAGTCACTTTGCCACATGTGCCTGCTTGAGTAACAGAAAAAGGTA[T/G]GCATCCTTCTTTAGAACGATCCCCAGTGACTATTACCAAAGCAGAGCACTGGCTCAGCTTGTTAAGCACTTTGGCTGGACCTGGGTTGGTACAGTCAGGAGTCGCAGTGATTATGGCAATAATGGCATTGCAACATTCGAGGAAGCAGCAAAAAAAGAGGGGATTTGTATTGAATACTCAGAGGCCATATTAAGAACTGATCCACAAGATCAATTTCTGAAGACAGTAGAAGTGATAAAGAAGGGCACTGCGAGGGTTGTGTTAGCTTTTGTTGCATTAAGAGATTTTTACCCACTTTTAAAAGAAATTGCGCAACAAAACATTACAGGGCTGCAGTGGGTTGGCAGTGAATCTTGGATAACATCCCGAACTGTAGCAGAAACAAAGGAATATAGTTTCCTTTCTGGAGCTGTGGGCTTTTCTATAGCAAATGTCAAACTTGTGGGCCTACTAGATTTTCTAGTGAATGTGCACCCTGATCATGAACCGAAAAATAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25067
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 |
---|---|---|---|---|---|
ENSDART00000059500 | Nonsense | 289 | 850 | 3 | 6 |
ENSDART00000099111 | None | None | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 31321107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33117966 |
GRCz11 | 18 | 33092561 |
KASP Assay ID:
554-7897.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTGTTGCATTAAGAGATTTTTACCCACTTTTAAAAGAAATTGCGCAA[C/T]AAAACATTACAGGGCTGCAGTGGGTTGGCAGTGAATCTTGGATAACATCC
Long Flanking Sequence:
TTTTCCTTTTTTTTTTTTTCATTAGTTGCACAATCTTTAATGCAAGTATGTAAATTGTATTTACAGTATAATTATATACTGTATATATTACTTTTGATTAAATAAGTGAATAAAATATTCTGTTTCTCCTCTTGCAGATCAGTCACTTTGCCACATGTGCCTGCTTGAGTAACAGAAAAAGGTATGCATCCTTCTTTAGAACGATCCCCAGTGACTATTACCAAAGCAGAGCACTGGCTCAGCTTGTTAAGCACTTTGGCTGGACCTGGGTTGGTACAGTCAGGAGTCGCAGTGATTATGGCAATAATGGCATTGCAACATTCGAGGAAGCAGCAAAAAAAGAGGGGATTTGTATTGAATACTCAGAGGCCATATTAAGAACTGATCCACAAGATCAATTTCTGAAGACAGTAGAAGTGATAAAGAAGGGCACTGCGAGGGTTGTGTTAGCTTTTGTTGCATTAAGAGATTTTTACCCACTTTTAAAAGAAATTGCGCAA[C/T]AAAACATTACAGGGCTGCAGTGGGTTGGCAGTGAATCTTGGATAACATCCCGAACTGTAGCAGAAACAAAGGAATATAGTTTCCTTTCTGGAGCTGTGGGCTTTTCTATAGCAAATGTCAAACTTGTGGGCCTACTAGATTTTCTAGTGAATGTGCACCCTGATCATGAACCGAAAAATAAACTTTTAAAAGAATTCTGGGAAACAACATTCCAGTGCTCTTTTAATAACAGAGGAAGCGTTGGGTGTACTGGCTCAGAGAAACTAGCAAACTTACAAAATGAATATACTGATGCCTCAGAGCTACGGATAGCCAATAAAGTGTACACAGCAGTGTATGCTGTTGCACATACACTACACAATATATTTCAAGACTTCAAATCAGCCAACAGGAGCAAATTAAAACAACCAACACCTCAAATGGTGGGTGAAAAATTAGATATAGGATATAGGAATAGGATTCAGGGATGAATGAATTTGTCATAATAGTTTTAATATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36679
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 |
---|---|---|---|---|---|
ENSDART00000059500 | Essential Splice Site | 505 | 850 | 4 | 6 |
ENSDART00000099111 | None | None | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 31320371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33117230 |
GRCz11 | 18 | 33091825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCAGGTTAATCAGGAACATGTGCTATGGGCAGATAACAGTAGACAG[G/A]TATTATTTTCTACTGTATCAAAATAAGGTAATGAGAAAATTCTCAAAACA
Long Flanking Sequence:
AAGCGTTGGGTGTACTGGCTCAGAGAAACTAGCAAACTTACAAAATGAATATACTGATGCCTCAGAGCTACGGATAGCCAATAAAGTGTACACAGCAGTGTATGCTGTTGCACATACACTACACAATATATTTCAAGACTTCAAATCAGCCAACAGGAGCAAATTAAAACAACCAACACCTCAAATGGTGGGTGAAAAATTAGATATAGGATATAGGAATAGGATTCAGGGATGAATGAATTTGTCATAATAGTTTTAATATTTCTCCTCAGGTACTGAACTATATGAAAGATGTAAGATTCACTGTCAAAACAGGTGAAGAAATATTTTTTGATACAAGTGGTGATCCAGTGGCAAGATATGATCTTGTGAACTGGCAACCTTCTGGGGATGGAAGTCTGCAGTTTAAAAATGTGGGCATCTATGACAGTTCACTTCCTTCAGAGAAATGTCTTCAGGTTAATCAGGAACATGTGCTATGGGCAGATAACAGTAGACAG[G/A]TATTATTTTCTACTGTATCAAAATAAGGTAATGAGAAAATTCTCAAAACAATCAATTTGGCATATTTGTTTTAAAATATATGACATCAGAGAGTCAAAAAGCTTTTGAAAATACAACAGTATTTAGAAGTATATTACAGTCAGTATATTACATTTAAATATTTAATCATACTCCTATAGGCCTTTTATATGACAGCTTATTTTTTCATAGTTGCCTGTATCCGTGTGCAGTGAGAGCTGCCCCCTTGGAACTAGGAAGGCTGTGCAAAAAGGAAGACCGGTCTGCTGTTTTGATTGTATTCCATGTGCAGATGGAGAAATAAGTAACAACACTGGTAAAGCAGTTCATGCTGGTTAACTCTCAAAAAAGTACTTTGAATTAAAATTTATTGTCCAATCCTCACACTGTTCCTTTTCCCCCCTGACAGACTCTAGTGACTGCTCTCCTTGTGATGAGGAGTACTGGTCAAATGAAAGAAAAGAAAAATGTGTGTTAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10065
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 |
---|---|---|---|---|---|
ENSDART00000059500 | Nonsense | 725 | 850 | 6 | 6 |
ENSDART00000099111 | None | None | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 31319408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33116267 |
GRCz11 | 18 | 33090862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTTKGTTAACTGTCTCTCCTCCATTCCCATATAAGAATTTGAGCTA[T/A]TACAGAGAAAAGATCATCCTGGAATGTAATTTRGGTTCAGCTTTGGGATT
Long Flanking Sequence:
TGGTCAAATGAAAGAAAAGAAAAATGTGTGTTAAAAGTGATCGAATTCCTCTCTTATACTGAAATCATGGGGATGGTGCTTTGTATATTCTCCTTTATTGGATTGTTATTAACAGCAATGGTATCTTTTTTGTTCTATCTTCACAAAGAAACACCTATTGTCAGAGCCAACAACTCAGAACTGAGCTTCCTGCTGCTCTTCTCACTCTCACTGTGTTTTCTTTGTTCACTCACTTTCATTGGTCGTCCCACTGAGTGGTCCTGTATGTTGCGTCACACAGCATTTGGGATCACTTTTGTCCTCTGTATTTCCTGTGTTCTGGGGAAAACAATAGTGGTGTTAATGGCCTTCAGGGCTACACTTCCGGGAAGTAATGTCATGAAATGGTTTGGGCCTACACAACAACGACTCAGTGTTGTTTTTTTAACATTAATACAGGTGATTATCTGTGTTGTTTGGTTAACTGTCTCTCCTCCATTCCCATATAAGAATTTGAGCTA[T/A]TACAGAGAAAAGATCATCCTGGAATGTAATTTGGGTTCAGCTTTGGGATTTTGGGCCGTTCTGGGTTATACTGGCCTGCTATCTGTCTTGTGTTTTATTTTAGCTTTTCTTGCTCGTAAACTCCCTGATAACTTCAATGAAGCCAAGTTCATCACATTTAGTATGCTCATATTTTGTGCTGTTTGGCTCACATTCATTCCAGCTTATGTCAGCTCTCCTGGAAAATTCACAGTAGCAGTGGAGATATTTGCTATCTTATCTTCAAGTTTTGGTTTACTATTTTGCATATTTGCTCCGAAATGTTACATAATTTTACTCAAACCAGAAAAAAACACAAAGAAACAAATGATGGGAAAGTCGTCTTCTAAAACTATTTAAAATCATACAAGTAAACAACATTTTCTGTCTTGTGGTTAGCATTCTTATTTTCAACATAATACTTGTTGATTGTTTTCTTTCTTTATTTAAACTAAGAGGGCACATTGAAACCATGTAGACAT
Associated Phenotype:
Not determined