ZMP
olfcg7
Ensembl ID:
ZFIN ID:
Description:
Novel odorant receptor protein [Source:UniProtKB/TrEMBL;Acc:B8JIF5]
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 |
---|---|---|---|
sa22448 | Nonsense | Available for shipment | Available now |
sa28285 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35664 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13840 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22448
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 |
---|---|---|---|---|---|
ENSDART00000110523 | Nonsense | 227 | 675 | 2 | 5 |
ENSDART00000137393 | Nonsense | 393 | 842 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17692703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32804968 |
GRCz11 | 18 | 32781818 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGATGTGCCTGAACACAGATATTCAAGCCATGTTTATAAAGCAATTTA[T/A]GCAGTAGCTCATTCACTACATAGTCTGCTCAAATGCAAGGAAGGAGAAGA
Long Flanking Sequence:
AATTATGGAATGGCCATATTTCTCGAAACAGCCCAGAAAGAGGGAATTTGCGTGGAGTATTCTGTAAAATTCTACAGAACAGAGACAGAAAAACTAAAAAGAGTGGTAGACACAATTAAAAAAAGCACTGCAAAAGTGATTGTTGCATTTGTTTCATTTATTGAGATGGGCTTATTAATTGAACAGCTAAGTATTCAGAATATTACAGGATTCCAAATAATTGGAGTAGAGGGATGGATAACTTCAAAGAACTACATAACCACAAACAGCTTTCATTCAATGGGAGGTTCACTGGGATTGGCATTGAGAAAAATCCATTTGGAAGGGTTTTTAGATTATGTAACTAAATCGTTTTGGAGCACAGCATTCCCATGCTCACAGACTGAGGGGATTTTGCCTACTGTAGGTTGCAGCAAATATAAGGATCTACTTCCACTGAAAAACTACACTGAAGATGTGCCTGAACACAGATATTCAAGCCATGTTTATAAAGCAATTTA[T/A]GCAGTAGCTCATTCACTACATAGTCTGCTCAAATGCAAGGAAGGAGAAGATTGTGAGAAAGGCCACGCAACACAACCACAGCAGGTTAAATATAAACCACAACCTAATTTTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATACTTGATATTGTATGGATAAATTGTGTTTTTCTTTTCCCAATAGGTGGTTGAGGCTCTAAAAAAAGTTAATTTCACTGTAAAGTTTGGAGATCGTGTGTGGTTTGACCGTACTGGTGCCACAGTAGCCCATTATGAGGTTGTGAACTGGCAGCAGGACACTGATGGATCATTCCAGTTTAAACAAGTAGGATACTATGATGCCTCACTGCCTCCTGACCAGCGCTTTGTTCTCAACATTGAAAGCATCATCTGGCCTGGAGGAAATTTGGAGGTATTTAAATTTTTTGTAACACACTGTGTTTAAAAGTGGCAATTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28285
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, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110523 | Splice Site | None | 675 | None | 5 |
ENSDART00000137393 | Essential Splice Site | 421 | 842 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17692788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32805053 |
GRCz11 | 18 | 32781903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGGAAGGAGAAGATTGTGAGAAAGGCCACGCAACACAACCACAGCAG[G/A]TTAAATATAAACCACAACCTAATTTTATAATATATATATATATATATATA
Long Flanking Sequence:
CAGAAAAACTAAAAAGAGTGGTAGACACAATTAAAAAAAGCACTGCAAAAGTGATTGTTGCATTTGTTTCATTTATTGAGATGGGCTTATTAATTGAACAGCTAAGTATTCAGAATATTACAGGATTCCAAATAATTGGAGTAGAGGGATGGATAACTTCAAAGAACTACATAACCACAAACAGCTTTCATTCAATGGGAGGTTCACTGGGATTGGCATTGAGAAAAATCCATTTGGAAGGGTTTTTAGATTATGTAACTAAATCGTTTTGGAGCACAGCATTCCCATGCTCACAGACTGAGGGGATTTTGCCTACTGTAGGTTGCAGCAAATATAAGGATCTACTTCCACTGAAAAACTACACTGAAGATGTGCCTGAACACAGATATTCAAGCCATGTTTATAAAGCAATTTATGCAGTAGCTCATTCACTACATAGTCTGCTCAAATGCAAGGAAGGAGAAGATTGTGAGAAAGGCCACGCAACACAACCACAGCAG[G/A]TTAAATATAAACCACAACCTAATTTTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACATACTTGATATTGTATGGATAAATTGTGTTTTTCTTTTCCCAATAGGTGGTTGAGGCTCTAAAAAAAGTTAATTTCACTGTAAAGTTTGGAGATCGTGTGTGGTTTGACCGTACTGGTGCCACAGTAGCCCATTATGAGGTTGTGAACTGGCAGCAGGACACTGATGGATCATTCCAGTTTAAACAAGTAGGATACTATGATGCCTCACTGCCTCCTGACCAGCGCTTTGTTCTCAACATTGAAAGCATCATCTGGCCTGGAGGAAATTTGGAGGTATTTAAATTTTTTGTAACACACTGTGTTTAAAAGTGGCAATTGTCTGCTCCCTTATAAATACTGGGCTGTATAAGATTCCCCACAAGTAGCAAAATACACATGGATTTGTTGACTATAAGCTGACAGAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35664
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 |
---|---|---|---|---|---|
ENSDART00000110523 | Essential Splice Site | 371 | 675 | 4 | 5 |
ENSDART00000137393 | Essential Splice Site | 538 | 842 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17694146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32806411 |
GRCz11 | 18 | 32783261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTATGACTGTGTTCCATGTGCAGATGGAGAAATTAGTAATGAGACAG[G/A]TAATTATCACCTCATATCATCAACCGATTAGTTGTACATTTTGTTTTCTT
Long Flanking Sequence:
TTGTTAGTCATATGGCCTGTTGGACTTTTTTGCATTTTTGAGATATATAATAAACAAACTTTAGATTGTTCAGGGACTGGAATACTCCACTAAATTTCTGCATATGTAATCTACATAACAGTACTTTATAAATGAATTTGCACATAAGCCCTACTTACAATGGAATTCATGAACATACTCATTTAACTAAATTAAATTTTAAAAATGTTCATAAAATACTAATGAATTCACAGGGGAGTTTTTGGGTTATTAATTTTAAGTTATATTTTATGTGCAAAGTACTCACAATGTACTAAAGTATATACAAAAATAATAAATTTATGAGAAATGCATGAGGTTCAATGTTTTTAAATGCATGTATTTTTAACACATGAAGAAACCAAGGTCTGTGTGCAGCGAAAGCTGTTCTCCAGGCACCAGAAAGGCTGCTCAGAAAGGAAGACCTGTCTGCTGTTATGACTGTGTTCCATGTGCAGATGGAGAAATTAGTAATGAGACAG[G/A]TAATTATCACCTCATATCATCAACCGATTAGTTGTACATTTTGTTTTCTTCTTTCTCTCTCTTTCTCTCTCTGATCATGACTTTCATTCCAGATTCGGTTAACTGCAAGCAGTGTCCAAGGGAATACTGGTCTAATGGTGAAAAAAATAAATGTGTGTTAAAAGCTATAGAGTTTTTGTCATTCACAGAAATTATGGGTATTGTGTTGGTCTGTTTTTCACTGTTTGGAGTAGGATTAACTGCAGTCGTGGCCATTCTGTTTTGGAGCAAAATGGACACTCCCATTGTAAAAGCCAACAACTCAGAGCTAAGCTTCCTGCTGCTCTTCTCACTGACTCTTTGTTTCCTATGTTCACTTACGTTTATTGGTCGGCCCACTGAGTGGTCCTGTATGTTGCGTCATACTGCCTTTGGGATCACTTTTGTCCTTTGCATCTCCTGTGTTTTAGGGAAAACAATAGTGGTGTTAATGGTTTTCAAGGCTACACTTCCAGGAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13840
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 |
---|---|---|---|---|---|
ENSDART00000110523 | Nonsense | 656 | 675 | 5 | 5 |
ENSDART00000137393 | Nonsense | 823 | 842 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17695092)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 32807357 |
GRCz11 | 18 | 32784207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGGCTTACTTCTCTGCATATTTGCACCTAAATGTTACATAATCATATG[T/A]AAGCCTGAACAAAATACAAAGCAACATGTCATGGGAAAAACATCTTTAAA
Long Flanking Sequence:
TTAGGGAAAACAATAGTGGTGTTAATGGTTTTCAAGGCTACACTTCCAGGAAGTAATGTCATGAAATGGTTTGGGCCTACACAACAACGACTCAGTGTTCTTGCTTTTACATTTATACAGGTACTTATATGTGTGCTTTGGCTTACAATATCACCACCATTTCCTAACAAAAATATGACATATTATAAAGAAAAGATTATTATTGAGTGCAGTCTTGGTTCTACTATAAGTTTCTGGGCTGTTCTTGGTTACATTGGCCTGCTAGCTGTCTTGTGCTTCATTTTGGCTTTTTTGGCTCGCAAACTACCAGATAACTTCAATGAAGCCAAGTTCATCACATTCAGTATGCTTATTTTCTGTGCTGTATGGATCACATTTATTCCAGCTTATGTCAGTTCTCCAGGAAAATTCACAGTAGCTGTGGAAATATTTGCTATCTTAGCCTCTAGTTTTGGCTTACTTCTCTGCATATTTGCACCTAAATGTTACATAATCATATG[T/A]AAGCCTGAACAAAATACAAAGCAACATGTCATGGGAAAAACATCTTTAAAGGTTCAATAACCAGAAAGTAAAGTTTTTTTTTTTGTAGTCAAGATAGTAAGGGAGAACATATGGTGTAGATTTTTTATAACTTGAACAGCATACCATGGTACTAGCAATCTCAATCTTAGTGCTTAATTCCAAAAGAAAGCATAATGTGATGAATCATACACTTAAAATACAATATTTGGATAAAATAAACAACGATTTATAGTGTACATTTTGGGGTATTTAAAGCTAAACAGCACTGAATCTAATTAGGAGTGAATAGGAGGGTTTGGAAATACAGCATATTGAAGATGTTTATCAAAACTTACAATCAAAAGATGATAATTTCTCAGTATCCCTAGTTACATAATTTAGTTTAATCTAGTTGTTATAAATGCATATGTGCTTTGAATTGATGCAATTTAACATCAGTGCTAATATATACCACATACAGAAACCTTTTGGCATTTATC
Associated Phenotype:
Not determined