ZMP

Ensembl ID:

ZFIN ID:

Human Orthologue:

UNC13B

Human Description:

unc-13 homolog B (C. elegans) [Source:HGNC Symbol;Acc:12566]

Mouse Orthologue:

Unc13b

Mouse Description:

unc-13 homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1342278]

Allele Name:

sa44602

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
ENSDART00000064752	None	None	1192	None	31
ENSDART00000128664	Essential Splice Site	89	255	3	7
ENSDART00000131918	Essential Splice Site	73	267	2	8
ENSDART00000140710	None	None	761	None	18

The following transcripts of ENSDARG00000017391 do not overlap with this mutation:

• ENSDART00000144508

Genomic Location (Zv9):

Chromosome 5 (position 20893913)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	18606770
GRCz11	5	19110570

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa9739

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064752	Nonsense	107	1192	3	31
ENSDART00000128664	None	None	255	None	7
ENSDART00000131918	None	None	267	None	8
ENSDART00000140710	Nonsense	84	761	2	18

The following transcripts of ENSDARG00000017391 do not overlap with this mutation:

• ENSDART00000144508

Genomic Location (Zv9):

Chromosome 5 (position 20950970)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	18663827
GRCz11	5	19167627

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14652

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064752	Nonsense	577	1192	14	31
ENSDART00000128664	None	None	255	None	7
ENSDART00000131918	None	None	267	None	8
ENSDART00000140710	Nonsense	552	761	12	18

The following transcripts of ENSDARG00000017391 do not overlap with this mutation:

• ENSDART00000144508

Genomic Location (Zv9):

Chromosome 5 (position 20976737)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	18689594
GRCz11	5	19193394

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: