ZMP

Ensembl ID:

ZFIN ID:

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:

sa7389

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121612	Missense	209	916	5	11
ENSDART00000141628	Missense	209	916	6	12

The following transcripts of ENSDARG00000090527 do not overlap with this mutation:

• ENSDART00000132321

Genomic Location (Zv9):

Chromosome 14 (position 18718943)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	14513396
GRCz11	14	14818959

KASP Assay ID:

554-4321.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa42377

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
ENSDART00000121612	Nonsense	758	916	11	11
ENSDART00000141628	Nonsense	758	916	12	12

The following transcripts of ENSDARG00000090527 do not overlap with this mutation:

• ENSDART00000132321

Genomic Location (Zv9):

Chromosome 14 (position 18727189)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	14521642
GRCz11	14	14827205

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: