ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate phermone receptor protein [Source:UniProtKB/TrEMBL;Acc:A3KQL9]

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]

Allele Name:

sa36682

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050639	Essential Splice Site	151	836	3	12
ENSDART00000131796	None	None	781	None	5

The following genes are also affected by this mutation:

• ENSDARG00000023168

Genomic Location (Zv9):

Chromosome 18 (position 31494349)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33291208
GRCz11	18	33265803

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13250

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050639	None	None	836	None	12
ENSDART00000131796	Nonsense	147	781	2	5

Genomic Location (Zv9):

Chromosome 18 (position 31502017)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33298876
GRCz11	18	33273471

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa23325

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050639	None	None	836	None	12
ENSDART00000131796	Nonsense	170	781	2	5

Genomic Location (Zv9):

Chromosome 18 (position 31502087)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33298946
GRCz11	18	33273541

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa2972

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050639	None	None	836	None	12
ENSDART00000131796	Nonsense	172	781	2	5

Genomic Location (Zv9):

Chromosome 18 (position 31502094)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33298953
GRCz11	18	33273548

KASP Assay ID:

554-3135.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18478

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050639	None	None	836	None	12
ENSDART00000131796	Nonsense	180	781	2	5

Genomic Location (Zv9):

Chromosome 18 (position 31502118)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33298977
GRCz11	18	33273572

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43133

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
ENSDART00000050639	None	None	836	None	12
ENSDART00000131796	Nonsense	184	781	2	5

Genomic Location (Zv9):

Chromosome 18 (position 31502128)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	33298987
GRCz11	18	33273582

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: