zgc:162180

Ensembl ID:

ENSDARG00000070713

ZFIN ID:

ZDB-GENE-070424-25

Description:

hypothetical protein LOC799770 [Source:RefSeq peptide;Acc:NP_001082915]

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	Consequence	Status	Availability
sa40743	Nonsense	Mutation detected in F1 DNA	Not yet available
sa26787	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa40743

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004240	Nonsense	9	387	1	8

Genomic Location (Zv9):

Chromosome 6 (position 39016895)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39088495
GRCz11	6	39086031

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCAGGAGAAGAGATAGCTGGTGAAGATGTGGAGGTTCACTTGTGTCAGTT[T/A]AGCGCTGCTCTTGTGTGTTCAAGGTAAGGGACTCTATTTGATGTTTATGA

Long Flanking Sequence:

TCTTAAAGAGACAGCTCATCCAAAAGTAGAAATTGTATTTTTTTTACATTCTTTTATTATTGCTGGGAGTGACAAAATGTCTACTAGCAAAGGTGTCATTCTTGACCAATTCAACCTCTGAAAGTCAGAAACAAGTTTTGGAACTGGTTTTGGAACAAAATGTCCAATTGCTGTAGTTTTGGGTGAACTATCCCTTGGAGACTTAGCATTAACACCCTGCAGAACAAAACTTAATCTTTGAAAACAAAACCTGCTTAAAATCTGTGTTCAGAGAATTAACTTCCAGAATACATGTCTAATAGGTCTGCCTTGTAAAAACAGGGTGAGAAAAAAAACTGATTAAAGCGCCATTAAAGTAATTAGAAGAGTGACGAGCAGAGACTGGAGAAGTGGATATAAAAAGGGTTTGTGAGAGCAGAGAGAAACAAATCCATCATCTGCAATCATCCTGCAGGAGAAGAGATAGCTGGTGAAGATGTGGAGGTTCACTTGTGTCAGTT[T/A]AGCGCTGCTCTTGTGTGTTCAAGGTAAGGGACTCTATTTGATGTTTATGAAAGAGTTTTTATCATTACACTGTAAAAGTGATCAGTTACTTTAATTTAAAAAAGTGAGTAGACCCGTTGCCTTGAAAGCCACAAGTTGATTTTACTTAAAGTCAGTAAACCCATTGACTTATTTCAAGTTTTATAATGGACCCTTTTCACAAGACTGTTGTGACACGTTTAATGGTCATCAGCATCTTAAATACTTTAAAGATTTTAAAATTTAGATTTAAAAAAAAAATGTATGCACATTTAGATGTATTTATGATACATTAAATCTTCTTTGCAAATTAAAAAACAAATTACCGCTTGTGCGAGATGTTTTAAATGCAGGTTGTATTTTCAGGACAGTAAATTTGATGCTGTTCTCTCTTCTATATTTTTAGTTTTTCTGAAAGTCTTGGTAACACCACTGTCAAGGTTTTCTTTTATTATTTCAGCAAATAGGATTGTAAAAAAATA

Associated Phenotype:

Not determined

Allele Name:

sa26787

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004240	Essential Splice Site	383	387	8	8

Genomic Location (Zv9):

Chromosome 6 (position 39021804)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39093404
GRCz11	6	39090940

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATAGTAGAAAATACAAGACGTCCTTCATCTGTTTGTTTTTGTGTCTCTGC[A/G]GTGGATCAAAGAGGGTAAACTCTTGGTCAACACAAGCTTCTCTGTGACGG

Long Flanking Sequence:

ACTGCATTACCTACTTCTACTATTTCAACTGCATCCCCAACTACTACTACTACCACAAAAATTTCCACGATCTCATCTGCATCTACTAAACCACCTACTACCTCACAAACTTCTACAACAACTACTACGAATTTAAGACCTCCGCCCAATCAGAGTAACTCTCTTGCTTATTTTCATATACAAAATTGTACCTATTTAACACTTACTGTCTTTTTAATGACACTTGTTTTTATATTTTTTGCATGTTTGTTTTAGCCTCAATCTCTTGTCGCAAGAGATGTGGTGAAAAATACGACATCCGCAACCGCTGCAACTGCAATAATCGCTGCCACAAAAACTGCTGCTGGGATTATGAAAAGAAATGCAGTAAGTTCAAATAATCCTGTGGTTCTTTATGGTGTTTATAGTGGTGTAAGACTGAAATCACTGATCATGCGTGTTACAACAGTAATAGTAGAAAATACAAGACGTCCTTCATCTGTTTGTTTTTGTGTCTCTGC[A/G]GTGGATCAAAGAGGGTAAACTCTTGGTCAACACAAGCTTCTCTGTGACGGCTTCTCTCTATGTGTCTTTTCATGTTCTTCATGCATTCTGTATGATGTCAAGTACAGTTTACAGAATAAATAAATAAATAAATTTTATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTTTAAATCAGCTCAGCATTTATATTATTTTCTTCTCTTGACTAAAGATTTCAAGTCAAATGTCAAATAAGTACCTTCATTTACAAATTCTTGTATAACATAAAACATAAATATGAATGTAATTTCTGTCTTGTTTTCTATTTATCTGTTATCTGTCATGATTAAAGAAATACTTTGCATCATTTTTCTTGTAAAGTGTCTTGCTGTACTAAATTACACCAACAGGGGGCATTTGTTTGCATCTAATAAATAATGAGGACAGTCAAGTACAAAGAATAAAGAATTTAAAGAC

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details