ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to H.sapiens DNM1L, dynamin 1-like (DNM1L) [Source:UniProtKB/TrEMBL;Acc:B8JIY8

Human Orthologue:

DNM1L

Human Description:

dynamin 1-like [Source:HGNC Symbol;Acc:2973]

Mouse Orthologue:

Dnm1l

Mouse Description:

dynamin 1-like Gene [Source:MGI Symbol;Acc:MGI:1921256]

Allele Name:

sa34505

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092024	Essential Splice Site	82	675	None	17
ENSDART00000137808	None	None	108	None	3
ENSDART00000142061	Essential Splice Site	82	479	None	11

The following transcripts of ENSDARG00000063159 do not overlap with this mutation:

• ENSDART00000138422

Genomic Location (Zv9):

Chromosome 8 (position 53254755)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	50997280
GRCz11	8	50986302

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa7622

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 > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092024	Missense	308	675	9	17
ENSDART00000137808	None	None	108	None	3
ENSDART00000142061	Missense	293	479	8	11

The following transcripts of ENSDARG00000063159 do not overlap with this mutation:

• ENSDART00000138422

Genomic Location (Zv9):

Chromosome 8 (position 53276942)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	51019467
GRCz11	8	51008489

KASP Assay ID:

554-4358.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa21391

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
ENSDART00000092024	Nonsense	409	675	10	17
ENSDART00000137808	None	None	108	None	3
ENSDART00000142061	Nonsense	394	479	9	11

The following transcripts of ENSDARG00000063159 do not overlap with this mutation:

• ENSDART00000138422

Genomic Location (Zv9):

Chromosome 8 (position 53282830)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	51025355
GRCz11	8	51014377

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa41302

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
ENSDART00000092024	Nonsense	578	675	15	17
ENSDART00000137808	Nonsense	11	108	1	3
ENSDART00000142061	None	None	479	None	11

The following transcripts of ENSDARG00000063159 do not overlap with this mutation:

• ENSDART00000138422

Genomic Location (Zv9):

Chromosome 8 (position 53290095)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	51032620
GRCz11	8	51021642

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13350

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
ENSDART00000092024	Essential Splice Site	657	675	16	17
ENSDART00000137808	Essential Splice Site	90	108	2	3
ENSDART00000142061	None	None	479	None	11

The following transcripts of ENSDARG00000063159 do not overlap with this mutation:

• ENSDART00000138422

Genomic Location (Zv9):

Chromosome 8 (position 53291589)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	51034114
GRCz11	8	51023136

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: