ZMP
olfcd2
Ensembl ID:
ZFIN ID:
Description:
olfactory receptor C family, d2 [Source:RefSeq peptide;Acc:NP_001074079]
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 |
---|---|---|---|
sa38156 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30347 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38157 | Nonsense | Available for shipment | Available now |
sa30348 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38156
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099219 | Nonsense | 509 | 850 | 4 | 6 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3499 (position 30663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33080233 |
GRCz11 | 18 | 33055100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAACGTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGT[G/T]GATTGGTACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTT
Long Flanking Sequence:
AGTGCTCTATGTACTGGTTCTGAGAAACTTGGAGAGTTGAAGAATGAATATACTGATGTATCAGAGCTACGGATAGAACACAAAGCGTATGCTGCAGTGTATGCAGTTGCACACACACTGCATAATGTTTTTAAAGATGTAAAAGCCCCCAACAACAGCAAAAGAGAGCTACCCACACCACAAAAGGCAATGAATGAATGCATAAATACATGAATAAATAATTACATGAATACTGTAGTAATAAATAAAACAATTATGTTTCTGACCTTTACTGTCAGGTATTGCAGTATATGAGAAATCTGAGTTTCACAATAAAAACAGGTGAGAACATCTTCTTTGATGCAAGTGGAGATCCAGTGGCAAGATATGACCTTGTGAATTGGCAGACTGCTGAGGATGGAAGTCTGCAGTTTAAGCATGTGGGCATCTATGACAGCTCACTGCCTTCAAAGCAACGTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGT[G/T]GATTGGTACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTTGGACAATTTATTGACTTTTTACTTATATTTTATTGTAGTTACCATTGTCCGTGTGCACTGAGAGCTGTCTCCCAGGAACTAGAAAGGCTGTACAAAAAGGACGCCCTGTCTGCTGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGGTAAAATTATACAAGTGAAATAACTGTGATAAAAGTATTATAAAGTATGCACACAGGCCACATGATTCCTGATCCACTCTATATTCCAATAATCTTTTCTGAAAATTCTTTCACAGATTCTAGTGACTGCTTTTCATGTGATTTGGAGTACTGGTCAAATGAAAAGAAAGACAGATGTATATTAAAAGTGGTTGAATTCCTTTCATATGCAGAAATCATGGGGATAATTCTTTGTATTGTCTCTTTCATTGGGTTGCTATTAACAGTAATGGTAACTTGTCTGTTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30347
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 |
---|---|---|---|---|---|
ENSDART00000099219 | Essential Splice Site | 510 | 850 | 4 | 6 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3499 (position 30669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33080239 |
GRCz11 | 18 | 33055106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGTGGATTG[G/A]TACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTTGGACAA
Long Flanking Sequence:
CTATGTACTGGTTCTGAGAAACTTGGAGAGTTGAAGAATGAATATACTGATGTATCAGAGCTACGGATAGAACACAAAGCGTATGCTGCAGTGTATGCAGTTGCACACACACTGCATAATGTTTTTAAAGATGTAAAAGCCCCCAACAACAGCAAAAGAGAGCTACCCACACCACAAAAGGCAATGAATGAATGCATAAATACATGAATAAATAATTACATGAATACTGTAGTAATAAATAAAACAATTATGTTTCTGACCTTTACTGTCAGGTATTGCAGTATATGAGAAATCTGAGTTTCACAATAAAAACAGGTGAGAACATCTTCTTTGATGCAAGTGGAGATCCAGTGGCAAGATATGACCTTGTGAATTGGCAGACTGCTGAGGATGGAAGTCTGCAGTTTAAGCATGTGGGCATCTATGACAGCTCACTGCCTTCAAAGCAACGTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGTGGATTG[G/A]TACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTTGGACAATTTATTGACTTTTTACTTATATTTTATTGTAGTTACCATTGTCCGTGTGCACTGAGAGCTGTCTCCCAGGAACTAGAAAGGCTGTACAAAAAGGACGCCCTGTCTGCTGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGGTAAAATTATACAAGTGAAATAACTGTGATAAAAGTATTATAAAGTATGCACACAGGCCACATGATTCCTGATCCACTCTATATTCCAATAATCTTTTCTGAAAATTCTTTCACAGATTCTAGTGACTGCTTTTCATGTGATTTGGAGTACTGGTCAAATGAAAAGAAAGACAGATGTATATTAAAAGTGGTTGAATTCCTTTCATATGCAGAAATCATGGGGATAATTCTTTGTATTGTCTCTTTCATTGGGTTGCTATTAACAGTAATGGTAACTTGTCTGTTCTATCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38157
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099219 | Nonsense | 535 | 850 | 5 | 6 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3499 (position 30826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33080396 |
GRCz11 | 18 | 33055263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGTCTCCCAGGAACTAGAAAGGCTGTACAAAAAGGACGCCCTGTCTG[C/A]TGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGG
Long Flanking Sequence:
GAGAGCTACCCACACCACAAAAGGCAATGAATGAATGCATAAATACATGAATAAATAATTACATGAATACTGTAGTAATAAATAAAACAATTATGTTTCTGACCTTTACTGTCAGGTATTGCAGTATATGAGAAATCTGAGTTTCACAATAAAAACAGGTGAGAACATCTTCTTTGATGCAAGTGGAGATCCAGTGGCAAGATATGACCTTGTGAATTGGCAGACTGCTGAGGATGGAAGTCTGCAGTTTAAGCATGTGGGCATCTATGACAGCTCACTGCCTTCAAAGCAACGTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGTGGATTGGTACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTTGGACAATTTATTGACTTTTTACTTATATTTTATTGTAGTTACCATTGTCCGTGTGCACTGAGAGCTGTCTCCCAGGAACTAGAAAGGCTGTACAAAAAGGACGCCCTGTCTG[C/A]TGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGGTAAAATTATACAAGTGAAATAACTGTGATAAAAGTATTATAAAGTATGCACACAGGCCACATGATTCCTGATCCACTCTATATTCCAATAATCTTTTCTGAAAATTCTTTCACAGATTCTAGTGACTGCTTTTCATGTGATTTGGAGTACTGGTCAAATGAAAAGAAAGACAGATGTATATTAAAAGTGGTTGAATTCCTTTCATATGCAGAAATCATGGGGATAATTCTTTGTATTGTCTCTTTCATTGGGTTGCTATTAACAGTAATGGTAACTTGTCTGTTCTATCTTCATAAAGAAACACCTATTGTCAGAGCCAACAACTCAGAGCTGAGCTTTTTGCTGCTCTTCTCACTCTCACTGTGTTTTCTCTGTTCACTCACATTCATTGGTCGTCCCACTCAGTGGTCCTGTATGTTGCGTCACACAGCATTTGGGATCACGTTTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30348
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099219 | Essential Splice Site | 552 | 850 | 5 | 6 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3499 (position 30877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33080447 |
GRCz11 | 18 | 33055314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGG[T/C]AAAATTATACAAGTGAAATAACTGTGATAAAAGTATTATAAAGTATGCAC
Long Flanking Sequence:
TAAATAATTACATGAATACTGTAGTAATAAATAAAACAATTATGTTTCTGACCTTTACTGTCAGGTATTGCAGTATATGAGAAATCTGAGTTTCACAATAAAAACAGGTGAGAACATCTTCTTTGATGCAAGTGGAGATCCAGTGGCAAGATATGACCTTGTGAATTGGCAGACTGCTGAGGATGGAAGTCTGCAGTTTAAGCATGTGGGCATCTATGACAGCTCACTGCCTTCAAAGCAACGTCTACAAGTCAATCAGGAAATCATGCTGTGGGCAGGGAAAAGTGGATTGGTACATCAATATTATAATTTTTCCATGAAGGCATCCGGCAAATTTGGACAATTTATTGACTTTTTACTTATATTTTATTGTAGTTACCATTGTCCGTGTGCACTGAGAGCTGTCTCCCAGGAACTAGAAAGGCTGTACAAAAAGGACGCCCTGTCTGCTGTTATGACTGTATTCCATGTGCAGAGGGAGAAATCAGTAACAGCACAGG[T/C]AAAATTATACAAGTGAAATAACTGTGATAAAAGTATTATAAAGTATGCACACAGGCCACATGATTCCTGATCCACTCTATATTCCAATAATCTTTTCTGAAAATTCTTTCACAGATTCTAGTGACTGCTTTTCATGTGATTTGGAGTACTGGTCAAATGAAAAGAAAGACAGATGTATATTAAAAGTGGTTGAATTCCTTTCATATGCAGAAATCATGGGGATAATTCTTTGTATTGTCTCTTTCATTGGGTTGCTATTAACAGTAATGGTAACTTGTCTGTTCTATCTTCATAAAGAAACACCTATTGTCAGAGCCAACAACTCAGAGCTGAGCTTTTTGCTGCTCTTCTCACTCTCACTGTGTTTTCTCTGTTCACTCACATTCATTGGTCGTCCCACTCAGTGGTCCTGTATGTTGCGTCACACAGCATTTGGGATCACGTTTATCCTCTGTATTTCCTGTGTTCTGGGGAAAACAATAGTGGTGTTGATGGCATTC
Associated Phenotype:
Not determined