ZMP
olfcj1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100005028 [Source:RefSeq peptide;Acc:NP_001103761]
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 |
---|---|---|---|
sa22449 | Nonsense | Available for shipment | Available now |
sa17553 | Nonsense | Available for shipment | Available now |
sa35666 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22449
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004952 | Nonsense | 295 | 857 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17921945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33034210 |
GRCz11 | 18 | 33011060 |
KASP Assay ID:
2260-7408.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGATTAAAGAGCTTTATTACCAAAATGTAACTGGTTATCAGTGGGTT[G/T]GAAGTGAGGGTTGGATCACGTACAGATTTCTAGCAACTGCGATTAACTAT
Long Flanking Sequence:
CTGCATACATCAGAATCACATTGTTTTGTGTCTACTGTTACTCTAGTGTGAGTCAGGAATCATTTTTCAAATATTACAGTGATTTAAAACATTTATTTTGTCTTTTTCAGCTTAGCCATTCAGCAACCTGTGCATGTCTCAGTAATAGACAGCAATATCCATCTTTCTTCAGGACCATTCCAAGTGATTACTACCAGAGCAGAGCACTGGTTAAACTGGTCACCTATTTTGGCTGGAAGTGGGTTGGAGCTGTAAGAAGCATGGGAGATTATGGTAACAATGGAATGGCCACTTTTCTAGAAGCAGCTGAGAAAGAGGGTATCTGTGTCGAATACTCTGTGTCCATTTACAGAACAAATTCAAGAGAGAAGATTTTGGAGGTTACAGACATAATTAAAAAATCAACATCTAAAGTCATAGTGGCTTTTGCAGATGGCAACGATTTGGACATGCTGATTAAAGAGCTTTATTACCAAAATGTAACTGGTTATCAGTGGGTT[G/T]GAAGTGAGGGTTGGATCACGTACAGATTTCTAGCAACTGCGATTAACTATGCTGTGGTTGGGGGGGCAATAGGTTTTGCTGTGCCAAACGCTTATATTCCTGGGTTAAAGGAGTTTATTACAGGTAGCCAGCCTTCTTTGAGACCAGGCAACACAGGACTGGTTGAACTTTGGGAAAGTGTGTTTGACTGCACTTTAAATTCACAAACACACAATGCCTCCAAGATATGCAATGGGCAGGAGTCCTTAGCAAATATAAATACACGTTTTACAGATGTGTCTGATGCTAGTCTTTTAAACAATGTCTACAATGCAGTCTACGCCGTTGCTCATGCTGTTGAAGAACTGCTGACTTGTGAGAAAGGGAAGGGGCCATTCCACAAAAAAACATGTGCAGAGAAAGGGAAAATACAGCCTTGGCAGGTGTGTACTACTAAAAGTCATTCTCTGTTATTCAAAGGCTATGGGTATTCAGGTGGAAACTGTTTTATGCAGGTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17553
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004952 | Nonsense | 470 | 857 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17922544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33034809 |
GRCz11 | 18 | 33011659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTTGACAAACATGGTGRCCCAGTTGCACGTTACACACTGGTTAATTG[G/A]CAGATGAGCTATGAAGGAATAATAACATTTGAATCCATTGGCTTGTATGA
Long Flanking Sequence:
CCTGGGTTAAAGGAGTTTATTACAGGTAGCCAGCCTTCTTTGAGACCAGGCAACACAGGACTGGTTGAACTTTGGGAAAGTGTGTTTGACTGCACTTTAAATTCACAAACACACAATGCCTCCAAGATATGCAATGGGCAGGAGTCCTTAGCAAATATAAATACACGTTTTACAGATGTGTCTGATGCTAGTCTTTTAAACAATGTCTACAATGCAGTCTACGCCGTTGCTCATGCTGTTGAAGAACTGCTGACTTGTGAGAAAGGGAAGGGGCCATTCCACAAAAAAACATGTGCAGAGAAAGGGAAAATACAGCCTTGGCAGGTGTGTACTACTAAAAGTCATTCTCTGTTATTCAAAGGCTATGGGTATTCAGGTGGAAACTGTTTTATGCAGGTGCTGTATTATCTAACTCAGGTGAACTTTACGACCAAAAATGGAGAAAATGTTCACTTTGACAAACATGGTGACCCAGTTGCACGTTACACACTGGTTAATTG[G/A]CAGATGAGCTATGAAGGAATAATAACATTTGAATCCATTGGCTTGTATGACGCATCCAAGCCAGAGGGACAAGAGATTCAAATGAGAGATGATATTGAGGCAATCTGGGCAGGAAACCAGAAAAAAGTGAGTTATTAAGGAAGGAAGTAAACTAGTAATCTCCCATAAACCTATATTTTTCTATAGTTCCTCTCAAAACATAATTGTATGTATGTGATTTTGTGTGTAGGTGCCTCTGTCTGTGTGCAGTGAGACTTGCCTTCCAGGCACTCGACAAGCTTTTGTGAAAGGAAAACCTATTTGCTGCTTCGACTGCATTGACTGTGCAGATGGAGAGTTCAGCAACACCACAAGTGAGACGAATAGGCATCTTTTATCAAAAGTGACACTTGTCATTTTGCTGTGTTGATAACCTGAAATCTGTGTGGTTTTTCGTTGTCTTGAAAGTAAGTTGTTTTTCTCTTGAATCTTTCTGTGCTTTCAGATGCAGTTACATGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35666
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004952 | Nonsense | 667 | 857 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 14 (position 17923369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 33035634 |
GRCz11 | 18 | 33012484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCCTGTATGTTGCGTCACACAGCATTTGGGATCACTTTTGTGCTCTG[C/A]ATTTCCTGTGTTCTAGGTAAAACATTAGTTGTTTTAATGGCATTCAGGGC
Long Flanking Sequence:
TGCAGATGGAGAGTTCAGCAACACCACAAGTGAGACGAATAGGCATCTTTTATCAAAAGTGACACTTGTCATTTTGCTGTGTTGATAACCTGAAATCTGTGTGGTTTTTCGTTGTCTTGAAAGTAAGTTGTTTTTCTCTTGAATCTTTCTGTGCTTTCAGATGCAGTTACATGCATACCATGCCCTCTTGAGTACAAATCAAATGGGAATAGAACACAATGTGTCCTCAAAAACATTGAATTCCTGACATTTAATGAAGTAATGGGTAATATACTTGTAACATTTTCTATGTGTGGTGGATGTCTCACAATCACAGTAGGGCTGATTTTTTTCTACCACAGACACACACCAATTGTCAGAGCCAACAACTCAGAGCTGAGCTTCCTGCTGCTTTTCTCGCTCACTTTGTGTTTTCTGTGTTCTCTTACTTTCATCGGTCAGCCCACTGAATGGTCCTGTATGTTGCGTCACACAGCATTTGGGATCACTTTTGTGCTCTG[C/A]ATTTCCTGTGTTCTAGGTAAAACATTAGTTGTTTTAATGGCATTCAGGGCTACACTGCCAGGAAGTAATGTCATGAAATGGTTTGGACCTCCTCAACAGAGATTAAGTGTTTTTGTCTTTACTTTTATACAATTGCTAATTTGCATGCTTTGGTTAACAATGTCACCTCCATTTCCCAACAAAACTACAAACAATTATAAAGACAAAATAATTCTTGAGTGTGATTCAGGTTCAGCTGTTGGCTTCTGGGCTGTACTCAGTTATATTGGCTTTCTGGCTATCTTATGTTTTATTCTAGCTTTTCTTGCCCGCAAGCTGCCTGATAACTTTAATGAAGCCAAATTCATCACATTCAGTATGCTCATATTCTGTGCTGTATGGATCACTTTTATTCCAGCTTATATCAGTTCCCCAGGAAAATTCACTGTAGCCGTGGAGATATTTGCTATTTTAGCATCAAGTTATGGAATGCTCTTTTGTATATTCATTCCTAAATGCTA
Associated Phenotype:
Not determined