ZMP

Ensembl ID:

ZFIN ID:

Description:

Sister chromatid cohesion protein PDS5 homolog A [Source:UniProtKB/Swiss-Prot;Acc:A1L1F4]

Human Orthologue:

PDS5A

Human Description:

PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:29088]

Mouse Orthologue:

Pds5a

Mouse Description:

PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1

Allele Name:

sa14643

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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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
ENSDART00000033078	None	None	432	None	13
ENSDART00000102654	None	None	1320	None	33
ENSDART00000126785	None	None	1321	None	33
ENSDART00000143014	Essential Splice Site	None	99	1	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22144349)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22679516
GRCz11	1	23370255

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa19496

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
ENSDART00000033078	Nonsense	129	432	4	13
ENSDART00000102654	Nonsense	129	1320	4	33
ENSDART00000126785	Nonsense	130	1321	4	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22117576)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22652743
GRCz11	1	23343482

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa39608

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
ENSDART00000033078	Essential Splice Site	213	432	6	13
ENSDART00000102654	Essential Splice Site	213	1320	6	33
ENSDART00000126785	Essential Splice Site	214	1321	6	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22117045)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22652212
GRCz11	1	23342951

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa32667

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
ENSDART00000033078	Nonsense	281	432	8	13
ENSDART00000102654	Nonsense	281	1320	8	33
ENSDART00000126785	Nonsense	282	1321	8	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22116643)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22651810
GRCz11	1	23342549

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa6583

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
ENSDART00000033078	Nonsense	295	432	9	13
ENSDART00000102654	Nonsense	295	1320	9	33
ENSDART00000126785	Nonsense	296	1321	9	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22116510)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22651677
GRCz11	1	23342416

KASP Assay ID:

554-4962.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa15921

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
ENSDART00000033078	None	None	432	None	13
ENSDART00000102654	Nonsense	767	1320	21	33
ENSDART00000126785	Nonsense	768	1321	21	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22109241)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22644408
GRCz11	1	23335147

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa38264

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
ENSDART00000033078	None	None	432	None	13
ENSDART00000102654	Nonsense	882	1320	24	33
ENSDART00000126785	Nonsense	883	1321	24	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22108575)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22643742
GRCz11	1	23334481

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa16957

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000033078	None	None	432	None	13
ENSDART00000102654	Essential Splice Site	1207	1320	31	33
ENSDART00000126785	Essential Splice Site	1208	1321	31	33
ENSDART00000143014	None	None	99	None	3

The following transcripts of ENSDARG00000055022 do not overlap with this mutation:

• ENSDART00000137145
• ENSDART00000140078
• ENSDART00000142840

Genomic Location (Zv9):

Chromosome 1 (position 22104406)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	22639573
GRCz11	1	23330312

KASP Assay ID:

2259-0554.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: