ZMP

Ensembl ID:

ZFIN ID:

Description:

hypothetical protein LOC100006550 [Source:RefSeq peptide;Acc:NP_001077051]

Human Orthologues:

PRSS21, PRSS38, PRSS42, PRSS44, PRSS45, PRSS50

Human Descriptions:

protease, serine, 21 (testisin) [Source:HGNC Symbol;Acc:9485]
protease, serine, 38 [Source:HGNC Symbol;Acc:29625]
protease, serine, 42 [Source:HGNC Symbol;Acc:30716]
protease, serine, 44 [Source:HGNC Symbol;Acc:37324]
protease, serine, 45 [Source:HGNC Symbol;Acc:30717]
protease, serine, 50 [Source:HGNC Symbol;Acc:17910]

Mouse Orthologues:

Prss21, Prss38, Prss41, Prss42, Prss43, Prss44, Prss45, Prss46, Prss50

Mouse Descriptions:

protease, serine, 21 Gene [Source:MGI Symbol;Acc:MGI:1916698]
protease, serine, 38 Gene [Source:MGI Symbol;Acc:MGI:2685095]
protease, serine, 41 Gene [Source:MGI Symbol;Acc:MGI:1918253]
protease, serine, 42 Gene [Source:MGI Symbol;Acc:MGI:2665280]
protease, serine, 43 Gene [Source:MGI Symbol;Acc:MGI:2684822]
protease, serine, 44 Gene [Source:MGI Symbol;Acc:MGI:1920586]
protease, serine, 45 Gene [Source:MGI Symbol;Acc:MGI:3605764]
protease, serine, 46 Gene [Source:MGI Symbol;Acc:MGI:1921556]
protease, serine, 50 Gene [Source:MGI Symbol;Acc:MGI:2447303]

Allele Name:

sa33141

Status:

Mutation detected in F1 DNA
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Availability:

Not yet available

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079323	Essential Splice Site	82	313	3	6

The following transcripts of ENSDARG00000056773 do not overlap with this mutation:

• ENSDART00000140034

Genomic Location (Zv9):

Chromosome 3 (position 19447465)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	19410500
GRCz11	3	19560240

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: