ZMP

Ensembl ID:

ZFIN ID:

Description:

wnt8-like protein 2 [Source:RefSeq peptide;Acc:NP_001018637]

Human Orthologue:

WNT8A

Human Description:

wingless-type MMTV integration site family, member 8A [Source:HGNC Symbol;Acc:12788]

Mouse Orthologue:

Wnt8a

Mouse Description:

wingless-related MMTV integration site 8A Gene [Source:MGI Symbol;Acc:MGI:107924]

Allele Name:

sa31997

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105649	Nonsense	14	354	1	6
ENSDART00000147756	Nonsense	14	353	1	6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

• ENSDART00000135991

Genomic Location (Zv9):

Chromosome 14 (position 35625712)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	34154989
GRCz11	14	34495303

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11601

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105649	Essential Splice Site	35	354	None	6
ENSDART00000147756	Essential Splice Site	35	353	None	6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

• ENSDART00000135991

Genomic Location (Zv9):

Chromosome 14 (position 35625978)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	34155255
GRCz11	14	34495569

KASP Assay ID:

2260-7758.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa1188

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105649	Essential Splice Site	122	354	4	6
ENSDART00000147756	Essential Splice Site	121	353	4	6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

• ENSDART00000135991

Genomic Location (Zv9):

Chromosome 14 (position 35626323)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	34155600
GRCz11	14	34495914

KASP Assay ID:

554-1097.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa42419

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
ENSDART00000105649	Nonsense	197	354	6	6
ENSDART00000147756	Nonsense	196	353	6	6

The following transcripts of ENSDARG00000078507 do not overlap with this mutation:

• ENSDART00000135991

Genomic Location (Zv9):

Chromosome 14 (position 35627558)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	34156835
GRCz11	14	34497149

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: