ZMP
olfcg5
Ensembl ID:
ZFIN ID:
Description:
similar to putative pheromone receptor CPpr4 [Source:RefSeq peptide;Acc:NP_001103413]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1104 | Nonsense | F2 line generated | Not yet available |
| sa30979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1104
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000067567 | Nonsense | 157 | 833 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17904140)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 33016405 |
| GRCz11 | 18 | 32993255 |
KASP Assay ID:
554-1006.1 (used for ordering genotyping assays)
KASP Sequence:
TACATGCTATCATAGGAGAAACTGAGTCTTCTGCCACAGTGATTCTGTCC[A/T]GAACTACAGGACCTTTCAAAATTCCAGTGGTAAGGATCAAAGATTATTAT
Long Flanking Sequence:
TTGGAGACGTAACTATTGGGGGTATTTTTTCAATCCGCAGTGTAGAAATATTACCTTCATTGGAATTTACACAAAAACCCCAGCTTCTGTCATGCTCCAGGTTTGTAACATTGTATTTGGGAAATGATTTCAAGAACATTCCAGAATAAGTACTCAATATTAACATAATTTACTGCATATTATGCTTAGTATGTTGAATTCATGCTTATAAATCAACATAACATCTGAAATATTGTGACAGTGTTAATCTAAGAGATTTCCGGATGGCTCAAATTATGATCTTTGCCATTGAGGAGATTAACAGAAGTGAAAGTTTGCTTCCTAATGTTTCAATTGGTTACAAAATTTATGATAGCTGTGGTTCAAGACTATCTTCTATTAGTGCAACCATGTCACTGATGAATGATCAGGAGTTTCCAAAAGGAAACATATGCAATGGACAATATCCAATACATGCTATCATAGGAGAAACTGAGTCTTCTGCCACAGTGATTCTGTCC[A/T]GAACTACAGGACCTTTCAAAATTCCAGTGGTAAGGATCAAAGATTATTATGCTTGACAATACTTATTGATTAATAAATTAGTCTAATGTATTGGGGGTTTTCTTTTTTAGATAAGTCACTCAGCCACATGCGAATGTCTCAGCAATAGAAGAGATTACCCATCATTCTTCAGGACCATTGCTAGTGATTATCACCAGAGCAGAGCACTTGCATACATTGTAAAATACTTTGGGTGGTCTTGGGTGGGAGCTGTGAACAGTGATAATGACTATGGAAACAATGGAATGGCCATATTTCTTAAAACAGCACAAGAGGAAGGGATTTGTGTGGAGTACTCTGTTAAATTCTACCGAACAGAGCCGGAAAAGCTTCAAAAAGTCGTTGAGACTATGAAAAGAAGCACCACAAAAATAATCATTGCATTTCTATCTCGTGTTGAGATGGTCAATCTACTTGAGGAACTAAGCATTCAGAACATTTCAGGCTTTCAAGTAATTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30979
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 |
|---|---|---|---|---|---|
| ENSDART00000067567 | Nonsense | 713 | 833 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17906314)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 33018579 |
| GRCz11 | 18 | 32995429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGGTTGATAATATCACCTCCATTTCCCTACAAAAATATGAAGTATTA[T/A]AAGGAAAAGATCATTCTTGAATGCAGTCTGGGTGCTACAATATGTTTTTC
Long Flanking Sequence:
TCTAACACTGAGAAAAATAAATGTGTGTTCAAATCTGTAGAGTTTTTGTCATTCACAGAAGTTATGGGTGTAGTGTTAGTCTTTTTCTCACTGTTTGGAGTAGGATTAACTATGCTGGTGGCCATTCTCTTTTACAACAAGAAAGATACTCCCATAGTAAAAGCCAACAACTCAGAGTTGAGCTTCCTGCTGCTCTTCTCACTGACTCTGTGTTTCCTCTGTTCACTTACTTTCATTGGTCGCCCAACTGAGTGGTCCTGTATGTTGCGACACACAACATTTGGGATCACTTTTGTCCTCTGCATCTCCTGTGTTTTAGGGAAAACAATAGTGGTGTTAATGGCCTTCAAAGCTACACTTCCAGGAAGCAATATAATGAAATGGTTTGGGCCTGTACAACAAAGACTTAGTGTTCTTGCCTTTACACTCATACAGGTTATCATCTGTGTGCTTTGGTTGATAATATCACCTCCATTTCCCTACAAAAATATGAAGTATTA[T/A]AAGGAAAAGATCATTCTTGAATGCAGTCTGGGTGCTACAATATGTTTTTCTGCAGTTTTATTTTACATTGGCCTTCTGGCTATCTTATGTTTCATTTTGGCTTTTCTAGCACGTAAGCTCCCTGATAACTTCAATGAAGCCAAATTCATCACCTTTAGTATGCTTATATTCTGTGCTGTATGGATCACATTTATTCCGGCTTATGTTAGTTCTCCTGGGAAATTTACTGTTGCTGTGGAGATATTTGCCATATTGGCCTCAAGCTTTGGTCTACTATTTTGTATATTTGTGCCAAAATGTTATATAATTCTGTTCAAAAATGAACAAAATACAAAACAACATATAATGGGGAAGATAAAGTAAGTCTTTAAAAATATAAATATACTTTTATACTGCATAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAAGTGACTAAGCAGACAAGAAAATGAAATTAATGAATGAATATAT
Associated Phenotype:
Not determined