Busch Lab

ZMP

olfch1

Ensembl ID:
ENSDARG00000075988
ZFIN ID:
ZDB-GENE-060503-819
Description:
hypothetical protein LOC100004933 [Source:RefSeq peptide;Acc:NP_001103760]
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
sa13136 Nonsense Available for shipment Available now
sa42369 Nonsense Mutation detected in F1 DNA Not yet available
sa42370 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13136
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
ENSDART00000104792 Nonsense 206 853 3 6
Genomic Location (Zv9):
Chromosome 14 (position 17908693)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 33020958
GRCz11 18 32997808
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATTACTACCAGAGCAGAGCACTGGCACAGTTAGTGAAACACTTCGGGT[G/A]GACCTGGATTGGAGCAGTAAGAAGTGWCAATGACTATGGAAACAATGGCA
Long Flanking Sequence:
CATTTCAATTGGATACCAAATATTTGACAGCTGTGGTTCCACATTAGCCTCTATGAGGTCATCAATGGCTTTGATAAATGGCCAGGAGCTGACAGCAGAACATACCTGCTCTGGAAAACCAGCAGTTAAAGCCATTATTGGAGAATCTGAGTCTTCCACAACTATTGTACTGTCTAGAGCAGCAGGGCCATTCAACATTCCCGTGGTAATTTATGTGTGTTGTATGGTAGAAATCTCTCTCGTTCTCTCTCTCTCTCTCTGTGTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATACAAATAATTGATATGCTCTGTTTGTCAGATTAGCCATTTTGCTACTTGTGCCTGCCTGAGCAGTAGAAAGCAGTTTCCATCTTTCTTCAGAACTATTCCAAGTGATTACTACCAGAGCAGAGCACTGGCACAGTTAGTGAAACACTTCGGGT[G/A]GACCTGGATTGGAGCAGTAAGAAGTGACAATGACTATGGAAACAATGGCATGGCAACATTTGTAGAGGTAGCTGAGAAAGAAGGAGTGTGTATTGAGTATTCAGAGGCCATATCAAGGACAAATTCCAAAGACAAGATTGCCAAGGTTGTTGAAGTAATAAAAAAAGGCACTGCTAAAGTTCTCATGGCATTTCTGGCACAGGGTGAAATGGATGTGTTGTTGGAAGAGCTTATCAGGCAAAATGTCGTTGGACTACAGTGGGTTGGCAGTGAATCTTGGATTACATCAAGTTACTTGGCAACTGAAAGAACTTTAAACATCCTTGGTGGTGCAATTGGCTTTACAATTATCAAGTCAAAAATTCCCGGCCTGAAAGAATTCCTACTTAAAGTTGGTCCATCCCAGAACCTTTCAAATGCTCTTCTTGGGGAATTTTGGGAGATGGTGTTTGGTTGTTGTCTCTCTCCTACAGTCTGCCCTAATTCTGAGCATGCAACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42369
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104792 Nonsense 497 853 4 6
Genomic Location (Zv9):
Chromosome 14 (position 17909653)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 33021918
GRCz11 18 32998768
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAAAGTTCATCACTGTAGGACAATATGATGCCTCGCTATCCAGTGAA[C/T]AGCAGTTTGTCATTAATTCGTTCGATATAATTTGGGCAGGAGACAGTCCC
Long Flanking Sequence:
TCTCTCTCCTACAGTCTGCCCTAATTCTGAGCATGCAACATTTTGTGATGGATCTGAAAATCTAACCAATGTTAGTAATGCGTTCACAGACGTTTCTGAGCTAAGGATTTCAAATAATGTTTATAAGGCAGTCTATGCTATCGCTTATGCACTGCATAACACAATAACTTGCAAAAACTCAAATGGTGGAAATGAAAACATAACATGTGGAGATGTGGATTTATTGGTTTCCAGCCAAGTAAGTAATTCTTGTAAATATTTAGAATACTATGAAATATCTAACACATTTTAACAAAGTAAATAGAACTATAATAATGAAATCACAGGTCCTGCATTCACTTCAAAATGTCAATTTCACAATGGACTCAGGTGAGACAGTGTACTTTGACAAAAATGGGGATCCTATGGCAAAATATGAGCTAGTAAACTGGCAGAAAAATGGAGCAGGGGAAACAAAGTTCATCACTGTAGGACAATATGATGCCTCGCTATCCAGTGAA[C/T]AGCAGTTTGTCATTAATTCGTTCGATATAATTTGGGCAGGAGACAGTCCCACGGTATGTACATAGTAAATGCATTATGTTGAAGTCAACACAAATAAAAAAAATAAAAAAAAGTTGTCCAACAAAGTAAGAATGTGTAAACATGACAGAAACCAATCTCAGTGTGCACTGAGAGCTGCCAGCCAGGATTCAGGCAAGCTGTGATAAAAGGAAGACCAGTATGCTGCTTTGAATGTTTGCAGTGCCCAGCTGGAGAAATTAGCAATACTACTGGTGAGACAACCAGTAACTTGATTCATAAAAACACAAACACCATTTAATGTCAAGTTTTACATTTGATGTGGTGCACAACTAATAGTGTTTTTAATATTTCCTCAATGCCATACTAGAGAATGATGCATGTATTATGATATGTATTTTTTTTTTTATTTGCTATTCATCTCTTTATTTTTGTATTTTTAGATTCAGCTGAATGCATCAAATGTCCATTAGAATACTGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42370
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
ENSDART00000104792 Nonsense 567 853 6 6
Genomic Location (Zv9):
Chromosome 14 (position 17910149)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 33022414
GRCz11 18 32999264
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTTGTATTTTTAGATTCAGCTGAATGCATCAAATGTCCATTAGAATA[C/A]TGGTCAAATAAAAACCACAGCATCTGTGTTCTCAAAAAGGTGGAATTCCT
Long Flanking Sequence:
TGAACAGCAGTTTGTCATTAATTCGTTCGATATAATTTGGGCAGGAGACAGTCCCACGGTATGTACATAGTAAATGCATTATGTTGAAGTCAACACAAATAAAAAAAATAAAAAAAAGTTGTCCAACAAAGTAAGAATGTGTAAACATGACAGAAACCAATCTCAGTGTGCACTGAGAGCTGCCAGCCAGGATTCAGGCAAGCTGTGATAAAAGGAAGACCAGTATGCTGCTTTGAATGTTTGCAGTGCCCAGCTGGAGAAATTAGCAATACTACTGGTGAGACAACCAGTAACTTGATTCATAAAAACACAAACACCATTTAATGTCAAGTTTTACATTTGATGTGGTGCACAACTAATAGTGTTTTTAATATTTCCTCAATGCCATACTAGAGAATGATGCATGTATTATGATATGTATTTTTTTTTTTATTTGCTATTCATCTCTTTATTTTTGTATTTTTAGATTCAGCTGAATGCATCAAATGTCCATTAGAATA[C/A]TGGTCAAATAAAAACCACAGCATCTGTGTTCTCAAAAAGGTGGAATTCCTTTCATTTGAGGAAAACATGGGAATTCTTTTGACTGCATTCTCATTAACTGGGGTTACTTTAACAATTGCAGTTGCGATAGTGTTTTACAAATTTATAGACACACCTCTTGTGAAGGCCAGCAATACAGAACTGAGCTTTTTGTTGCTTTTTTCATTGTCTCTGTGCTTTCTCTGTTCACTTACTTTCATTGGTCGGCCCACTGAGGGGTCCTGTATGTTGCGTCATTCATCATTTGGGGTCACTTTCGCTCTTTGTATGTCTTGTGTTCTGACAAGAACAATAGCCGTGGTAATGGCCTTCAAGACCACAGTGCCTGGTTCAGGGCTTCCTCATTGTTCATTACCTTTACAAAGAATTAGTGTTTTCTGTTGCACTGTTTTTCAGGTGATGATATGTATCCTGTGGCTGGCACTGGCCCGTCCAATGCCATATAAAAATAGCATGTATTC
Associated Phenotype:
Not determined