ZMP

Ensembl ID:

ZFIN ID:

Description:

hypothetical protein LOC447883 [Source:RefSeq peptide;Acc:NP_001004622]

Human Orthologue:

FAM3C

Human Description:

family with sequence similarity 3, member C [Source:HGNC Symbol;Acc:18664]

Mouse Orthologue:

Fam3c

Mouse Description:

family with sequence similarity 3, member C Gene [Source:MGI Symbol;Acc:MGI:107892]

Allele Name:

sa10699

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:

G > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067354	Essential Splice Site	42	241	3	9
ENSDART00000138851	Essential Splice Site	42	192	4	9
ENSDART00000138946	Essential Splice Site	42	79	4	5
ENSDART00000145334	Essential Splice Site	55	183	5	9

The following transcripts of ENSDARG00000045824 do not overlap with this mutation:

• ENSDART00000146689

Genomic Location (Zv9):

Chromosome 25 (position 20226811)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19638788
GRCz11	25	19736739

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa44286

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067354	Splice Site, Nonsense	107	241	5	9
ENSDART00000138851	Splice Site, Nonsense	107	192	6	9
ENSDART00000138946	None	None	79	None	5
ENSDART00000145334	Splice Site, Nonsense	120	183	7	9

The following transcripts of ENSDARG00000045824 do not overlap with this mutation:

• ENSDART00000146689

Genomic Location (Zv9):

Chromosome 25 (position 20227325)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19639302
GRCz11	25	19737253

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa38061

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067354	Nonsense	140	241	6	9
ENSDART00000138851	Nonsense	140	192	7	9
ENSDART00000138946	None	None	79	None	5
ENSDART00000145334	Nonsense	153	183	8	9

The following transcripts of ENSDARG00000045824 do not overlap with this mutation:

• ENSDART00000146689

Genomic Location (Zv9):

Chromosome 25 (position 20228707)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19640684
GRCz11	25	19738635

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa44287

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
ENSDART00000067354	Nonsense	142	241	6	9
ENSDART00000138851	Nonsense	142	192	7	9
ENSDART00000138946	None	None	79	None	5
ENSDART00000145334	Nonsense	155	183	8	9

The following transcripts of ENSDARG00000045824 do not overlap with this mutation:

• ENSDART00000146689

Genomic Location (Zv9):

Chromosome 25 (position 20228711)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	19640688
GRCz11	25	19738639

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: