ZMP

Ensembl ID:

ZFIN ID:

Description:

phosphatase and tensin homolog A [Source:RefSeq peptide;Acc:NP_957002]

Human Orthologue:

PTEN

Human Description:

phosphatase and tensin homolog [Source:HGNC Symbol;Acc:9588]

Mouse Orthologue:

Pten

Mouse Description:

phosphatase and tensin homolog Gene [Source:MGI Symbol;Acc:MGI:109583]

Allele Name:

hu1864

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
ENSDART00000104735	Nonsense	43	431	2	9
ENSDART00000104738	Nonsense	43	444	2	9
ENSDART00000122209	Nonsense	43	467	2	10
ENSDART00000128958	Nonsense	43	454	2	10

The following transcripts of ENSDARG00000071018 do not overlap with this mutation:

• ENSDART00000134713

Genomic Location (Zv9):

Chromosome 17 (position 23498331)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23648480
GRCz11	17	23668504

KASP Assay ID:

1105-0001.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12727

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104735	None	None	431	None	9
ENSDART00000104738	None	None	444	None	9
ENSDART00000122209	Essential Splice Site	237	467	7	10
ENSDART00000128958	Essential Splice Site	237	454	7	10

The following transcripts of ENSDARG00000071018 do not overlap with this mutation:

• ENSDART00000134713

Genomic Location (Zv9):

Chromosome 17 (position 23492591)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23642740
GRCz11	17	23662764

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa42927

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
ENSDART00000104735	Nonsense	221	431	7	9
ENSDART00000104738	Nonsense	221	444	7	9
ENSDART00000122209	Nonsense	244	467	8	10
ENSDART00000128958	Nonsense	244	454	8	10

The following transcripts of ENSDARG00000071018 do not overlap with this mutation:

• ENSDART00000134713

Genomic Location (Zv9):

Chromosome 17 (position 23489805)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23639954
GRCz11	17	23659978

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39161

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104735	Nonsense	348	431	8	9
ENSDART00000104738	Nonsense	361	444	8	9
ENSDART00000122209	Nonsense	384	467	9	10
ENSDART00000128958	Nonsense	371	454	9	10

The following transcripts of ENSDARG00000071018 do not overlap with this mutation:

• ENSDART00000134713

Genomic Location (Zv9):

Chromosome 17 (position 23485733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23635882
GRCz11	17	23655906

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: