ZMP

v2rh32

Ensembl ID:

ENSDARG00000040594

ZFIN ID:

ZDB-GENE-050419-41

Description:

vomeronasal 2 receptor, h32 [Source:RefSeq peptide;Acc:NP_001076358]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa5912	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43136	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa5912

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000048182	Nonsense	45	855	1	6

Genomic Location (Zv9):

Chromosome 18 (position 31602604)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33399463
GRCz11	18	33374058

KASP Assay ID:

554-3776.1 (used for ordering genotyping assays)

KASP Sequence:

TTTCAAGTTGAACAGAATGTATAAGGATGGAGATTATATCATTGGAGGCT[T/A]GTTTGAGGTTCAGCACCTCAAAGTATTTCCAGAACTGAGTTTCCGAATGG

Long Flanking Sequence:

GTAAAATAGTGCCATTGTTAATTGAATTTGCAGTGCATGACTGCCACCTAGATCAGATTCGGTGTAGCCTACTTAAAAAACAGTCCCAGCTCTTCCAGCCCATCTCAGTTACCCAAAATAATCTTAGTTTATTATACATGCAAGGGTAATTGAACAATACATTTTTTTTTCATTCTGTACTATCATTCATTAATGGTATTCAAAAGCATAAATAACCTCATAATTACATATAAATGTATGTAACTACATTACAGAACCACCTGTTCTATGGGGTGGGTGGGAGGTGGTGCTATGGCGCATGTCCATATGGCTAATAAATTCAGAAGCTGAAATGGTTTGTGGCTCATAAAAAGATTAATGGAGAGAGATGTGTATCACTCTAAACATCTGCCTGCATCTGTCCTTTATCTTTATTTCTGTCAATTCTGACTCCTGTCAAATCCAGGGACATTTCAAGTTGAACAGAATGTATAAGGATGGAGATTATATCATTGGAGGCT[T/A]GTTTGAGGTTCAGCACCTCAAAGTATTTCCAGAACTGAGTTTCCGAATGGAGCCAGAACAGCCAAAGTGTGAGGAGTAAGTGAACAAATTAAACAATAACAAATTATGTATACTGAAAAAAAAACATGTTTTTTTTTTTTATTTGATTGCATGTCAAATTTATTAAGTACTAAAATCAACTCCTACATAAATTAAATATTGTACAAACTGTACCATAATTCTCAAAGCTGTGATTTTGTTCTGTGTAGTTCCACTGATGTCATTTTGAAAATATTGTTTGCATTTTTACTCTTTATTATTTGTTTCATTCTATGCTTCAGATTCTACATGTCAAGCTTCCAGCAGGCACAGACCATGGTTTTTGCTATAGATGAGATCAATAAGAATCCAAACCTGTTGCCTAACATCACACTTGGTTACCATCTTTATGACAACTGTTTAAAGCTTGTGGTGGCATTTCGGGCTGCTACAACTCTTATTAGTGGGACGGAGGAAACGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43136

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
ENSDART00000048182	Nonsense	338	855	3	6

Genomic Location (Zv9):

Chromosome 18 (position 31603816)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33400675
GRCz11	18	33375270

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTATCCATCGGGGAAAGATCAAAGGACTTCATGAATTTCTGCTACACATA[C/T]AACCTGACAATGATCCAACAAATAACATGGTGAGAATTTTTTGGGAGAAC

Long Flanking Sequence:

ATGCCACATGCTCATGTTTGAGTAACAGGAAAAAGTACCCCTCTTTCTTCAGAACAATCCCCAGTGATGCATTCCAGGTTCGGGCTATGGTTCAGATCTTAAAATATTTTGGATGGACCTGGGTTGGTGTTCTCTATAGTGATGATGACTATGGCATTTATGCTGCTCAGTCCTTCCAGCAGGAAATGCAGCGGTTCAAAGGCTGTGTGGCTTTTTCTGAAATAGTGCCCTATGATAATCATAGGGACATTCAACGCATAGTGGCAGTTATTAAGGCCTCTACAGCCAGAGTAGTCGTGGCTTTCTCAACTGATCTGTTACCCCTGATGGAAGAGCTGTTACAACAAAATGTGACAGGCAGGCAGTGGATTGCAAGTGAGGCATGGTCCACCTCCCCTGTCCTTCATCTTCCACGTTTTGTACCTCTCGTTAGGGGCACGCTTGGCATTGCTATCCATCGGGGAAAGATCAAAGGACTTCATGAATTTCTGCTACACATA[C/T]AACCTGACAATGATCCAACAAATAACATGGTGAGAATTTTTTGGGAGAACATGTTTGGGTGCAGTTTTGAGAAAGGCAACGGGTATGGAGAAAAAATGTGTACAGCACAAGAGGATCTAAACATCACAGTTAATGAATACAATGATGTATCAGAGCTGAGAGCCTCTTATAATGTCTATAAGGCAGTTTATGCACTGGCACATGCACTTCATGATCTTATGCAGTGTGAGGAGGGGAGAGGACCATTCAGTGGGAACAGCTGTGCTGACATAACAAAACTGAAACCTTGGCAGGTTAGACCTGGAGCTTACTGCTCCAAAAATCTACATAAATTACGGAAAACTAATTTGGGGAAAAAAGACAAGCATATGTATGTAAAATATATTTGTTGATATTTGCAGATGGTTCCCTACCTGCAAAAAGTGAACTTCACTACAGGCTTTGGGGATCATGTGTCATTTGATGAGAATGGAGATGCTCTGGCCATTTATGATGTGATG

Associated Phenotype:

Not determined