ZMP

Ensembl ID:

ZFIN ID:

Description:

Ubr3 protein [Source:UniProtKB/TrEMBL;Acc:Q1JPS8]

Human Orthologue:

UBR3

Human Description:

ubiquitin protein ligase E3 component n-recognin 3 (putative) [Source:HGNC Symbol;Acc:30467]

Mouse Orthologue:

Ubr3

Mouse Description:

ubiquitin protein ligase E3 component n-recognin 3 Gene [Source:MGI Symbol;Acc:MGI:1861100]

Allele Name:

sa17047

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000047723	Nonsense	196	288	5	6
ENSDART00000062336	Nonsense	97	607	3	14
ENSDART00000129091	Nonsense	444	954	8	20
ENSDART00000129693	Nonsense	97	607	3	15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

• ENSDART00000133189

Genomic Location (Zv9):

Chromosome 9 (position 3944302)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	3960681
GRCz11	9	3932210

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa16003

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000047723	None	None	288	None	6
ENSDART00000062336	Nonsense	224	607	6	14
ENSDART00000129091	Nonsense	571	954	11	20
ENSDART00000129693	Nonsense	224	607	6	15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

• ENSDART00000133189

Genomic Location (Zv9):

Chromosome 9 (position 3933145)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	3949524
GRCz11	9	3921053

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa10176

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000047723	None	None	288	None	6
ENSDART00000062336	Essential Splice Site	274	607	7	14
ENSDART00000129091	Essential Splice Site	621	954	12	20
ENSDART00000129693	Essential Splice Site	274	607	7	15

The following transcripts of ENSDARG00000042508 do not overlap with this mutation:

• ENSDART00000133189

Genomic Location (Zv9):

Chromosome 9 (position 3928048)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	3944427
GRCz11	9	3915956

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: