ZMP

Ensembl ID:

ZFIN ID:

Description:

dynamin-1 [Source:RefSeq peptide;Acc:NP_001025299]

Human Orthologue:

DNM2

Human Description:

dynamin 2 [Source:HGNC Symbol;Acc:2974]

Mouse Orthologue:

Dnm2

Mouse Description:

dynamin 2 Gene [Source:MGI Symbol;Acc:MGI:109547]

Allele Name:

sa20128

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Nonsense	25	755	1	18
ENSDART00000097146	Nonsense	25	872	1	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48319404)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50320544
GRCz11	3	47131184

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa20129

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Essential Splice Site	129	755	3	18
ENSDART00000097146	Essential Splice Site	129	872	3	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48352601)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50353741
GRCz11	3	47164381

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13248

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Nonsense	130	755	4	18
ENSDART00000097146	Nonsense	130	872	4	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48352694)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50353834
GRCz11	3	47164474

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13768

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Nonsense	265	755	6	18
ENSDART00000097146	Nonsense	265	872	6	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48355835)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50356975
GRCz11	3	47167615

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa17720

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Essential Splice Site	331	755	8	18
ENSDART00000097146	Essential Splice Site	331	872	8	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48358454)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50359594
GRCz11	3	47170234

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa9093

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Essential Splice Site	498	755	None	18
ENSDART00000097146	Essential Splice Site	498	872	None	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48368301)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50369441
GRCz11	3	47180081

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa16501

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	None	None	755	None	18
ENSDART00000097146	Essential Splice Site	518	872	14	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48373125)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50374265
GRCz11	3	47184905

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa20130

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Nonsense	594	755	16	18
ENSDART00000097146	Nonsense	598	872	17	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48386994)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50388134
GRCz11	3	47198774

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa15133

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024031	Nonsense	648	755	17	18
ENSDART00000097146	Nonsense	656	872	18	22

The following transcripts of ENSDARG00000069937 do not overlap with this mutation:

• ENSDART00000131421

Genomic Location (Zv9):

Chromosome 3 (position 48389670)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	50390810
GRCz11	3	47201450

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: