ZMP

Ensembl ID:

ZFIN ID:

Description:

Novel protein similar to human amyotrophic lateral sclerosis 2 (Juvenile) chromosome region, candida

Human Orthologue:

ALS2CR8

Human Description:

amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 8 [Source:HGNC Symbol;Acc:14

Mouse Orthologue:

Carf

Mouse Description:

calcium response factor Gene [Source:MGI Symbol;Acc:MGI:2182269]

Allele Name:

sa21447

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000017932	Essential Splice Site	191	657	5	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Essential Splice Site	195	477	5	10

The following transcripts of ENSDARG00000019950 do not overlap with this mutation:

• ENSDART00000132770

Genomic Location (Zv9):

Chromosome 9 (position 13510107)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	13262672
GRCz11	9	13233875

KASP Assay ID:

554-6613.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa9357

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
ENSDART00000017932	Nonsense	246	657	6	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Nonsense	250	477	6	10
ENSDART00000017932	Nonsense	246	657	6	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Nonsense	250	477	6	10

The following transcripts of ENSDARG00000019950 do not overlap with this mutation:

• ENSDART00000132770

Genomic Location (Zv9):

Chromosome 9 (position 13511504)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	13264069
GRCz11	9	13235272

KASP Assay ID:

2260-1593.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa18940

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
ENSDART00000017932	Nonsense	246	657	6	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Nonsense	250	477	6	10
ENSDART00000017932	Nonsense	246	657	6	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Nonsense	250	477	6	10

The following transcripts of ENSDARG00000019950 do not overlap with this mutation:

• ENSDART00000132770

Genomic Location (Zv9):

Chromosome 9 (position 13511504)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	13264069
GRCz11	9	13235272

KASP Assay ID:

2260-1593.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa41376

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
ENSDART00000017932	Nonsense	372	657	9	14
ENSDART00000140269	None	None	162	None	4
ENSDART00000141705	Nonsense	376	477	9	10

The following transcripts of ENSDARG00000019950 do not overlap with this mutation:

• ENSDART00000132770

Genomic Location (Zv9):

Chromosome 9 (position 13515138)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	13267703
GRCz11	9	13238906

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa15446

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
ENSDART00000017932	Nonsense	633	657	13	14
ENSDART00000140269	Nonsense	138	162	3	4
ENSDART00000141705	None	None	477	None	10

The following transcripts of ENSDARG00000019950 do not overlap with this mutation:

• ENSDART00000132770

Genomic Location (Zv9):

Chromosome 9 (position 13522719)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	13275284
GRCz11	9	13246487

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: