Busch Lab

ZMP

olfcj1

Ensembl ID:
ENSDARG00000079954
ZFIN ID:
ZDB-GENE-060503-724
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]

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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