ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to vertebrate low density lipoprotein-related protein 1B (Deleted in tumors) (

Human Orthologue:

LRP1B

Human Description:

low density lipoprotein receptor-related protein 1B [Source:HGNC Symbol;Acc:6693]

Mouse Orthologue:

Lrp1b

Mouse Description:

low density lipoprotein-related protein 1B (deleted in tumors) Gene [Source:MGI Symbol;Acc:MGI:21511

Allele Name:

sa15111

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
ENSDART00000004416	Nonsense	481	4616	9	91
ENSDART00000133385	Nonsense	491	2895	9	54

Genomic Location (Zv9):

Chromosome 22 (position 14816729)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14647277
GRCz11	22	14671852

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa24113

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
ENSDART00000004416	Essential Splice Site	622	4616	11	91
ENSDART00000133385	Essential Splice Site	632	2895	11	54

Genomic Location (Zv9):

Chromosome 22 (position 14810947)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14641495
GRCz11	22	14666070

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa24112

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Essential Splice Site	695	4616	12	91
ENSDART00000133385	Essential Splice Site	705	2895	12	54

Genomic Location (Zv9):

Chromosome 22 (position 14807602)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14638150
GRCz11	22	14662725

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14370

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
ENSDART00000004416	Essential Splice Site	957	4616	18	91
ENSDART00000133385	Essential Splice Site	967	2895	18	54

Genomic Location (Zv9):

Chromosome 22 (position 14774501)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14605049
GRCz11	22	14629624

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43799

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
ENSDART00000004416	Essential Splice Site	1411	4616	25	91
ENSDART00000133385	Essential Splice Site	1421	2895	25	54

Genomic Location (Zv9):

Chromosome 22 (position 14751545)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14582093
GRCz11	22	14606668

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa8556

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Nonsense	1416	4616	26	91
ENSDART00000133385	Nonsense	1426	2895	26	54

Genomic Location (Zv9):

Chromosome 22 (position 14748597)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14579145
GRCz11	22	14603720

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa24111

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
ENSDART00000004416	Essential Splice Site	1752	4616	31	91
ENSDART00000133385	Essential Splice Site	1762	2895	31	54

Genomic Location (Zv9):

Chromosome 22 (position 14724762)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14555310
GRCz11	22	14579885

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11357

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
ENSDART00000004416	Nonsense	2199	4616	40	91
ENSDART00000133385	Nonsense	2209	2895	40	54

Genomic Location (Zv9):

Chromosome 22 (position 14701391)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14531939
GRCz11	22	14556514

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12158

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
ENSDART00000004416	Nonsense	2526	4616	46	91
ENSDART00000133385	Nonsense	2536	2895	46	54

Genomic Location (Zv9):

Chromosome 22 (position 14656320)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14486868
GRCz11	22	14511443

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa3167

Status:

F2 line generated
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
ENSDART00000004416	Nonsense	2578	4616	47	91
ENSDART00000133385	None	2583	2895	47	54

Genomic Location (Zv9):

Chromosome 22 (position 14653090)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14483638
GRCz11	22	14508213

KASP Assay ID:

554-2797.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa32392

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Nonsense	2704	4616	50	91
ENSDART00000133385	Nonsense	2681	2895	50	54

Genomic Location (Zv9):

Chromosome 22 (position 14640829)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14471377
GRCz11	22	14495952

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa37467

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Essential Splice Site	2769	4616	52	91
ENSDART00000133385	Essential Splice Site	2745	2895	52	54

Genomic Location (Zv9):

Chromosome 22 (position 14631517)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14462065
GRCz11	22	14486640

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43798

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Nonsense	2816	4616	53	91
ENSDART00000133385	Nonsense	2792	2895	53	54

Genomic Location (Zv9):

Chromosome 22 (position 14629677)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14460225
GRCz11	22	14484800

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa753

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
ENSDART00000004416	Essential Splice Site	3178	4616	59	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14604112)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14435019
GRCz11	22	14459594

KASP Assay ID:

554-0660.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa1481

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Nonsense	3363	4616	64	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14598984)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14429891
GRCz11	22	14454466

KASP Assay ID:

554-1406.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Stage	Entity	Quality	Tag
Larval:Day 5 ZFS:0000037	whole organism ZFA:0001094	quality PATO:0000001	normal PATO:0000461

Allele Name:

sa13305

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
ENSDART00000004416	Nonsense	3595	4616	69	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14566981)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14397888
GRCz11	22	14422463

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa10588

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
ENSDART00000004416	Nonsense	3815	4616	74	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14552620)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14383527
GRCz11	22	14408102

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa37466

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
ENSDART00000004416	Essential Splice Site	4048	4616	78	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14546528)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14377435
GRCz11	22	14402010

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa17465

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004416	Essential Splice Site	4088	4616	None	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14543229)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14374136
GRCz11	22	14398711

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa19282

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
ENSDART00000004416	Nonsense	4206	4616	82	91
ENSDART00000133385	None	None	2895	None	54
ENSDART00000004416	Nonsense	4206	4616	82	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14534644)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14365551
GRCz11	22	14390126

KASP Assay ID:

2261-6565.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa12543

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
ENSDART00000004416	Nonsense	4206	4616	82	91
ENSDART00000133385	None	None	2895	None	54
ENSDART00000004416	Nonsense	4206	4616	82	91
ENSDART00000133385	None	None	2895	None	54

The following genes are also affected by this mutation:

• ENSDARG00000094171

Genomic Location (Zv9):

Chromosome 22 (position 14534644)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14365551
GRCz11	22	14390126

KASP Assay ID:

2261-6565.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: