ZMP

Ensembl ID:

ZFIN ID:

Description:

hypothetical protein LOC777608 [Source:RefSeq peptide;Acc:NP_001071184]

Human Orthologue:

FHDC1

Human Description:

FH2 domain containing 1 [Source:HGNC Symbol;Acc:29363]

Mouse Orthologue:

Fhdc1

Mouse Description:

FH2 domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2684972]

Allele Name:

sa24875

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100367	None	None	755	2	12
ENSDART00000136393	Missense	34	826	2	12

The following transcripts of ENSDARG00000069129 do not overlap with this mutation:

• ENSDART00000131394

Genomic Location (Zv9):

Chromosome 10 (position 26835157)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	26239014
GRCz11	10	26200727

KASP Assay ID:

554-7723.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa11455

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100367	Essential Splice Site	286	755	9	12
ENSDART00000136393	Essential Splice Site	357	826	9	12

The following transcripts of ENSDARG00000069129 do not overlap with this mutation:

• ENSDART00000131394

Genomic Location (Zv9):

Chromosome 10 (position 26828995)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	26232852
GRCz11	10	26194565

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa34913

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100367	Nonsense	305	755	10	12
ENSDART00000136393	Nonsense	376	826	10	12

The following transcripts of ENSDARG00000069129 do not overlap with this mutation:

• ENSDART00000131394

Genomic Location (Zv9):

Chromosome 10 (position 26828862)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	26232719
GRCz11	10	26194432

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa10115

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
ENSDART00000100367	Nonsense	435	755	12	12
ENSDART00000136393	Nonsense	506	826	12	12

The following transcripts of ENSDARG00000069129 do not overlap with this mutation:

• ENSDART00000131394

Genomic Location (Zv9):

Chromosome 10 (position 26826498)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	26230355
GRCz11	10	26192068

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa21745

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100367	Nonsense	537	755	12	12
ENSDART00000136393	Nonsense	608	826	12	12

The following transcripts of ENSDARG00000069129 do not overlap with this mutation:

• ENSDART00000131394

Genomic Location (Zv9):

Chromosome 10 (position 26826191)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	26230048
GRCz11	10	26191761

KASP Assay ID:

2260-3302.1 (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: