ZMP

LOC571079

Ensembl ID:

ENSDARG00000052064

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]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa10791	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10791

Status:

Available for shipment
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Availability:

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Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104453	Nonsense	159	621	2	14

Genomic Location (Zv9):

Chromosome 25 (position 19235479)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	18647456
GRCz11	25	18745407

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATATGTCTAGCAGATGAAAACAGCAACTTCCCTCGTGGCACCAAMAGCTG[G/A]GTCGCAGGCTGGGGGGATATTGGARTTTTGGGCACAGGTGGTATAAGAGG

Long Flanking Sequence:

GACGTCCAAACCCCACATTAAATCCTCGCATTGTGGGTGGTGTGAATGCAACTCATGGCGCGTGGCCGTGGATGGTCAGTCTGCAGGGCAGATATGGCCATTTTTGTGGCGGCTCCCTCATCAACAATCAATGGGTGCTGACAGCAGCTCACTGCATTGTTGAGTAAGACACCTCAACTATAATCAATGGCCTTATTTGGTTGGTGGAAATGTTCTTTAAGTACCATTTTTGTTACTCTTGTTTTTTTCTTTCTTGTACACAGTCAAACCCCATCCAGCATAATTGTGTACTTAGGAAAGTGGAGAAGTTATGTAGCTGATGTCAATTCAATCTCCAGAACTATCAGACACATCATTCCCCATCCCTCCTACAGTAACATAACTAAAGATAATGACATCGCTCTGCTGCAGCTGACATCTACAGTCCAATATACTGACTACATTAAACCCATATGTCTAGCAGATGAAAACAGCAACTTCCCTCGTGGCACCAACAGCTG[G/A]GTCGCAGGCTGGGGGGATATTGGAGTTTTGGGCACAGGTGGTATAAGAGGCAGAACCACAGTGTCTGTGCCTTTACCTCATCCTGGCATTCTGCAAGAGGCTGAGCTTAAAGTGTACAGTAATGCAGACTGCAATAATATTTGTCATGGACGGATCACCCCCAACATGATTTGTGCTGGTACACGTCCTGGAGGCAAAGCAACCTTTTCTGTATGATGATCAATGAGATTGTTCTTGTCAAGATACTCCATATGCACACACCTAAACACACTGCAAACTTGAATGTCCAACCAGACTGACTGTATGTTGTCTCTGTTTGATGAGACAAACACAATACACCAAAACAGTAACTGAATAACCTAATCTTTCTCTGTATAGGGGGACTCTGGTGGTCCACTGATGACTAAGTGTTCAGTGTGGGTTCAGGCTGGTGTTCTCAGTCATGGTTATGGATGCGCACAGCCCAATCTTCCTGAGGTGTTCATTCGTGTCTCAGAGTA

Associated Phenotype:

Not determined