ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate plexin B family [Source:UniProtKB/TrEMBL;Acc:B0V3R5]

Human Orthologue:

PLXNB3

Human Description:

plexin B3 [Source:HGNC Symbol;Acc:9105]

Mouse Orthologue:

Plxnb3

Mouse Description:

plexin B3 Gene [Source:MGI Symbol;Acc:MGI:2154240]

Allele Name:

sa34299

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
ENSDART00000026965	Nonsense	197	2058	1	40
ENSDART00000144838	None	None	1095	None	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

The following genes are also affected by this mutation:

• ENSDARG00000092420

Genomic Location (Zv9):

Chromosome 8 (position 8741508)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8158090
GRCz11	8	8196675

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa21199

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026965	Nonsense	308	2058	1	40
ENSDART00000144838	None	None	1095	None	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

The following genes are also affected by this mutation:

• ENSDARG00000092420

Genomic Location (Zv9):

Chromosome 8 (position 8741841)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8158423
GRCz11	8	8197008

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13997

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
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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
ENSDART00000026965	Essential Splice Site	471	2058	3	40
ENSDART00000144838	None	None	1095	None	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

The following genes are also affected by this mutation:

• ENSDARG00000092420

Genomic Location (Zv9):

Chromosome 8 (position 8760486)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8177068
GRCz11	8	8215653

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa10506

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026965	Nonsense	1119	2058	19	40
ENSDART00000144838	Nonsense	161	1095	3	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

Genomic Location (Zv9):

Chromosome 8 (position 8789184)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8205766
GRCz11	8	8244351

KASP Assay ID:

2260-0147.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11827

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
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Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026965	Essential Splice Site	1391	2058	24	40
ENSDART00000144838	Essential Splice Site	428	1095	7	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

Genomic Location (Zv9):

Chromosome 8 (position 8798334)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8214916
GRCz11	8	8253501

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18565

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026965	Nonsense	1534	2058	27	40
ENSDART00000144838	Nonsense	571	1095	10	23

The following transcripts of ENSDARG00000032990 do not overlap with this mutation:

• ENSDART00000139719

Genomic Location (Zv9):

Chromosome 8 (position 8802163)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	8218745
GRCz11	8	8257330

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: