ZMP

v2rh7

Ensembl ID:

ENSDARG00000056000

ZFIN ID:

ZDB-GENE-050419-265

Description:

pheromone receptor [Source:RefSeq peptide;Acc:NP_001119923]

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
sa36686	Nonsense	Available for shipment	Available now
sa43137	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36686

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059412	Nonsense	328	851	3	7
ENSDART00000059462	Nonsense	311	825	3	6
ENSDART00000147592	Nonsense	328	832	3	6

Genomic Location (Zv9):

Chromosome 18 (position 31751477)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33548336
GRCz11	18	33522931

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCGTGGAGAAATCCAGGGCCTTCATAGTTTTCTGTTACGTCTTCATCCC[A/T]AGAGTGACCAAAGAAATAATATAGTGAGGATATTCTGGGAGACCATGTTC

Long Flanking Sequence:

GTTTAAGTGACAAGAAAAAGTACCCCTCCTTCTTCAGAACAATTCCAAGTGATACCTTCCAGGTGCGAGCTATGGTTCAGACCTTGAGGCATTTTGGCTGGACCTGGGTTGGTCTGATTTACAGTAATAATGACTATGGTATCTACGCAGCTCAGTCCTTTCATCAAGAAATGCAGTTGTTTGGACATTGTGTTGCTTTTTCTGAAATCCTGCCCCAAGATAACAACCCCAGAGTTATTGATCACATTATGGGAGTAATTCAGGCCTCTACAGCTAGAGTAGTGGTTGTTTTTTCAGCTTCATCTGTATTGATACCTTTAATGAATGAGGTGGTGTTACAGAATTTGACAGGCAGGCAGTGGATAGCGAGTGAAGCCTGGGTCACCTCAGCTGTATTTCGCACACCATATTTCCAGCCCTTTCTAAAAGGAACGTTGGGCATTGCTATTAGGCGTGGAGAAATCCAGGGCCTTCATAGTTTTCTGTTACGTCTTCATCCC[A/T]AGAGTGACCAAAGAAATAATATAGTGAGGATATTCTGGGAGACCATGTTCGGGTGCAGTTTTGAAACTGGGGATGAAGTGACATTTGTTCAACAAATGAAAAAGGTGTGTACAGGACAGGAGGACCTGAGCATCACAAACACACCTTACACTGATGTTTCAGGATTGAGAGCACCTTATAATGTGTATAAAGCAGTTTATGCCCTGGCCCATGCACTTCATGACCTGATGCAGTGTAAAGAGAAGAGAGGACCACTCAGTGAGAACAGCTGTGCTGACATAACTGATCTAAAACCCTGGCAGGTAAGACCCACAGGTACAGTGCAGGGGAATGGAATATGGACAAGCACAATATGTGCCTTATAATTATTTAAATGCCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGGCTTGGCATTAAGATTCAGTAGATTTTCAACATACTAGCAACTCACCATTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43137

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059412	Essential Splice Site	428	851	3	7
ENSDART00000059462	Essential Splice Site	411	825	3	6
ENSDART00000147592	Essential Splice Site	428	832	3	6

Genomic Location (Zv9):

Chromosome 18 (position 31751780)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33548639
GRCz11	18	33523234

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACTCAGTGAGAACAGCTGTGCTGACATAACTGATCTAAAACCCTGGCAG[G/A]TAAGACCCACAGGTACAGTGCAGGGGAATGGAATATGGACAAGCACAATA

Long Flanking Sequence:

CTGTATTGATACCTTTAATGAATGAGGTGGTGTTACAGAATTTGACAGGCAGGCAGTGGATAGCGAGTGAAGCCTGGGTCACCTCAGCTGTATTTCGCACACCATATTTCCAGCCCTTTCTAAAAGGAACGTTGGGCATTGCTATTAGGCGTGGAGAAATCCAGGGCCTTCATAGTTTTCTGTTACGTCTTCATCCCAAGAGTGACCAAAGAAATAATATAGTGAGGATATTCTGGGAGACCATGTTCGGGTGCAGTTTTGAAACTGGGGATGAAGTGACATTTGTTCAACAAATGAAAAAGGTGTGTACAGGACAGGAGGACCTGAGCATCACAAACACACCTTACACTGATGTTTCAGGATTGAGAGCACCTTATAATGTGTATAAAGCAGTTTATGCCCTGGCCCATGCACTTCATGACCTGATGCAGTGTAAAGAGAAGAGAGGACCACTCAGTGAGAACAGCTGTGCTGACATAACTGATCTAAAACCCTGGCAG[G/A]TAAGACCCACAGGTACAGTGCAGGGGAATGGAATATGGACAAGCACAATATGTGCCTTATAATTATTTAAATGCCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGGCTTGGCATTAAGATTCAGTAGATTTTCAACATACTAGCAACTCACCATTTTTATTAGCCACAATTTTGTTGTTGAGAAAATATATTTTATATGCAGAAATTTGACTTTGGCATGCTAAAATTGCTTGATTTAAATTATGTGTTATGTCCACAAGTCTCCTTTACTTTGTTTTATTTTACTAAGGGCTCAACACTAAGGATTTACCTTTTTTTCTGGCCACACCAAAATAATTATTCCCATGCCATGCATTTAAAAAAATGTCAAAACAAAGTAAACATAGCTACATACACACACATTTTATTCAACAAAAAATGTTCTTAAATACAATTGACATTTTAAAAAATCATTCTCATGT

Associated Phenotype:

Not determined