ZMP

Ensembl ID:

ZFIN ID:

Description:

helicase SKI2W [Source:RefSeq peptide;Acc:NP_001038366]

Human Orthologue:

SKIV2L

Human Description:

superkiller viralicidic activity 2-like (S. cerevisiae) [Source:HGNC Symbol;Acc:10898]

Mouse Orthologue:

Skiv2l

Mouse Description:

superkiller viralicidic activity 2-like (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1099835]

Allele Name:

sa14407

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089609	Nonsense	153	1249	5	29
ENSDART00000135607	Nonsense	153	743	5	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27404875)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27334987
GRCz11	19	26919210

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14666

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
ENSDART00000089609	Nonsense	569	1249	16	29
ENSDART00000135607	Nonsense	569	743	16	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27396641)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27326753
GRCz11	19	26910976

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43295

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
ENSDART00000089609	Nonsense	587	1249	16	29
ENSDART00000135607	Nonsense	587	743	16	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27396589)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27326701
GRCz11	19	26910924

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa36849

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
ENSDART00000089609	Essential Splice Site	666	1249	17	29
ENSDART00000135607	Essential Splice Site	666	743	17	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27393532)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27323644
GRCz11	19	26907867

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43294

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089609	Nonsense	791	1249	21	29
ENSDART00000135607	None	None	743	None	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27380797)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27310909
GRCz11	19	26895132

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa44917

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089609	Essential Splice Site	833	1249	21	29
ENSDART00000135607	None	None	743	None	19
ENSDART00000136216	None	None	114	None	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27380667)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27310779
GRCz11	19	26895002

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14992

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
ENSDART00000089609	Nonsense	1155	1249	28	29
ENSDART00000135607	None	None	743	None	19
ENSDART00000136216	Nonsense	20	114	1	2

The following transcripts of ENSDARG00000062206 do not overlap with this mutation:

• ENSDART00000145256

Genomic Location (Zv9):

Chromosome 19 (position 27360884)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27290996
GRCz11	19	26875219

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: