ZMP

Ensembl ID:

ZFIN ID:

Description:

Sodium channel modifier 1 [Source:UniProtKB/Swiss-Prot;Acc:Q2YDS5]

Human Orthologue:

SCNM1

Human Description:

sodium channel modifier 1 [Source:HGNC Symbol;Acc:23136]

Allele Name:

sa42749

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
ENSDART00000004284	Nonsense	98	249	4	8
ENSDART00000132351	Nonsense	96	247	4	8

The following transcripts of ENSDARG00000003027 do not overlap with this mutation:

• ENSDART00000133965

Genomic Location (Zv9):

Chromosome 16 (position 31934983)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	29754346
GRCz11	16	29688969

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa14725

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
ENSDART00000004284	Nonsense	101	249	4	8
ENSDART00000132351	Nonsense	99	247	4	8

The following transcripts of ENSDARG00000003027 do not overlap with this mutation:

• ENSDART00000133965

Genomic Location (Zv9):

Chromosome 16 (position 31934974)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	29754337
GRCz11	16	29688960

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype: