ZMP

Ensembl ID:

ZFIN ID:

Description:

Nuclear prelamin A recognition factor [Source:UniProtKB/Swiss-Prot;Acc:Q6DHP6]

Human Orthologue:

NARF

Human Description:

nuclear prelamin A recognition factor [Source:HGNC Symbol;Acc:29916]

Mouse Orthologue:

Narf

Mouse Description:

nuclear prelamin A recognition factor Gene [Source:MGI Symbol;Acc:MGI:1914858]

Allele Name:

sa35338

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007053	Splice Site, Nonsense	20	465	3	12
ENSDART00000142716	Splice Site, Nonsense	20	131	3	5

The following transcripts of ENSDARG00000024184 do not overlap with this mutation:

• ENSDART00000147618

Genomic Location (Zv9):

Chromosome 12 (position 34960155)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33364264
GRCz11	12	33465247

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa27988

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
ENSDART00000007053	Nonsense	74	465	4	12
ENSDART00000142716	Nonsense	74	131	4	5

The following transcripts of ENSDARG00000024184 do not overlap with this mutation:

• ENSDART00000147618

Genomic Location (Zv9):

Chromosome 12 (position 34960497)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33364606
GRCz11	12	33465589

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa22143

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
ENSDART00000007053	Nonsense	122	465	5	12
ENSDART00000142716	Nonsense	122	131	5	5

The following transcripts of ENSDARG00000024184 do not overlap with this mutation:

• ENSDART00000147618

Genomic Location (Zv9):

Chromosome 12 (position 34960716)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33364825
GRCz11	12	33465808

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa6266

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
ENSDART00000007053	Essential Splice Site	176	465	6	12
ENSDART00000142716	None	None	131	None	5

The following transcripts of ENSDARG00000024184 do not overlap with this mutation:

• ENSDART00000147618

Genomic Location (Zv9):

Chromosome 12 (position 34962478)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33366587
GRCz11	12	33467570

KASP Assay ID:

554-5169.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: