zgc:100868

Ensembl ID:

ENSDARG00000004748

ZFIN ID:

ZDB-GENE-040801-33

Description:

hypothetical protein LOC554458 [Source:RefSeq peptide;Acc:NP_001003526]

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
sa5731	Essential Splice Site	F2 line generated	Not yet available
sa33262	Nonsense	Mutation detected in F1 DNA	Not yet available
sa13737	Nonsense	Available for shipment	Available now
sa33261	Essential Splice Site, Missense	Mutation detected in F1 DNA	Not yet available
sa40129	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa5731

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013553	Essential Splice Site	None	551	3	11
ENSDART00000135192	Essential Splice Site	81	498	3	10
ENSDART00000013553	Essential Splice Site	None	551	None	11
ENSDART00000135192	Essential Splice Site	81	498	None	10

Genomic Location (Zv9):

Chromosome 3 (position 39481583)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	39344943
GRCz11	3	39486801

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTCTCATTAACAACCAATGGATTCTGACTGCAGCCCATTGCTTTCCCAAG[T/G]ATAAAGWCAGGCAACAAGTCCTTTCAAAATACTGTATGTCATTTACCTGA

Long Flanking Sequence:

AGACAAGCAAAACATATGGTCTTGTTTTAAGTAATAGGACAATATTAAGTTTTTCCTTAAAACAAGATTATTTTGCTTATCCCACTGGCAGATTATTTTTGCTTGTTTTAATATATTAATATATATATATATATATATATATATTAAATCTAACATTGGGTTACGACAGCCCAGCACTTTTTAAAATCATTTTGCTGAATTTATTAGTAACTCAGTCTGTATGTTGTTTTCTAGGGTGTGACGCACAACTAGATGGTAACCAGTTTTTCAACACATCACTTAAAATAGCCAGATTGTAGTGTTTCTGTGGCTAAAATGTGCATTTTTTATTGTCAGTGTGTGGTACGGCACCTCTCAACTCAAGGATAGTGGGAGGACAGAATGCACCGGTTGGCGCTTGGCCATGGCAGGTCAGTCTTCAAAGAGACGGCAGCCATTTCTGTGGTGGATCTCTCATTAACAACCAATGGATTCTGACTGCAGCCCATTGCTTTCCCAAG[T/G]ATAAAGACAGGCAACAAGTCCTTTCAAAATACTGTATGTCATTTACCTGATGTGGTTAACAGTTGTTGTCATTTTCCAGCCCTTCGACGACTGGTCTACTTGTATATTTGGGCCTACAAAAACTAGCATCATTTGAATCATACTCGATGTCCAGTGCTGTCTCCAATATCATAAAACATCCAAACTACAATAGTGATACTGAAGACAATGACATCACTCTTCTGCAACTGGCCTCAACAGTGAGCTTTTCGAACTACATCAGACCTATCTGTCTGGCTGCATCCGACAGTACTTTCTTCAATGGAACTTTGGTCTGGATCACTGGATGGGGGAACACTGCCACAGGCGGTAAGCATTTACTTTTACTCTTTTCAATCAGAGTTAGAACATACAGTGTACTCCTGCAGTAGATGACACGGGCTGTTTCTTTTTTCTCTCAGTCAGCCTACCTTCCCCGGGGACTCTACAAGAAGTGCAAGTGCCGATTGTTGGAAACAGGA

Associated Phenotype:

Not determined

Allele Name:

sa33262

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
ENSDART00000013553	Nonsense	152	551	6	11
ENSDART00000135192	Nonsense	255	498	6	10

Genomic Location (Zv9):

Chromosome 3 (position 39478522)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	39341882
GRCz11	3	39483740

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTGTGAGTTTTGGTACAGGCTGTGCTCAACCAAACTTCCCTGGTGTGTA[T/A]ACCAGGGTGTCTAAATATCAGAGCTGGATCCAGCAGAGAATCACCACCAC

Long Flanking Sequence:

AACTGATATCAGGACAACTATTCCAGAGTTTAGGGGCCAGATATTAAAATGCTCAACCTCCTACAACTTTATTGTGTAATAATCACTTTATAGAAACTACACAGAACCCTCATGAAAGTTCTTAAGATAGACATACTGTACATATGATGAATGTTCATCCAGCTTCCAGCCATACTGGTTTTACATTCGATGACAAGTTTTAGAAAGAAAAAGTACCGCTGAATGCTTCAGGCCATTTCCCTGACAGAACACAGCTGACACTGTAAACTTGCATTGACAAGAATATATTCACACTATTCCTTCATATTATATTTTACAGCTGCAACCTTCAGCTGGAGTAGATCTGCAGAATGGTTTTTACACCTAGTCACTAACTCCCTCTTCATTCGACAGGGTGACTCTGGTGGTCCAATGGTCAGCAAACAGGGCTCAGTTTGGATCCAGTCTGGAATTGTGAGTTTTGGTACAGGCTGTGCTCAACCAAACTTCCCTGGTGTGTA[T/A]ACCAGGGTGTCTAAATATCAGAGCTGGATCCAGCAGAGAATCACCACCACCCAGCCAGGCTTTGTCATGTACAATTCCAATGGTACTGATGGTGACCTGAGTGTAAACTGCCCTGGTCTCCCCACCATTCCCCCCACCACAGCTTCTACAACACAAACAACTACAATGTCAACTACGACTGTCGCACGTAAGTTTTTTTTAAGTAATCCAAATAAACATTCAGAGACTTTTACTGTATATTACTGGTGAGATCAATTCTGCTTTTGGTATCACTTTAGTGATGGTCCATTTGACGCATTTTGTTGAATTTAAGTTACATTGCATCTACATGCCAACTAATTCTCATTAGATTACATGTAGATTGTTAGGTTGGGGTTAGGGTTAGAGTACTTGCAAAGTTTCTTACCGCCAATGATGTCTGTTGAAGCAGCATTATCAGCAGACATTAGCTGACAATCCTCAAATAAGAACATGTTTTAGTCAACAAAATGTGCAACAAG

Associated Phenotype:

Not determined

Allele Name:

sa13737

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
ENSDART00000013553	Nonsense	389	551	9	11
ENSDART00000135192	Nonsense	492	498	9	10

Genomic Location (Zv9):

Chromosome 3 (position 39474718)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	39338078
GRCz11	3	39479936

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGGAAACTCATCCTCAAACAACAGTATTTGTACAACTGCTTTCGACTTA[C/T]AACAGGCAAGTTGTTTCTGSTTTTGTTTTGACTTTTTNGGTGAATAAAAT

Long Flanking Sequence:

TGATGATAAGTTAAAAGATTTGATTGAGTAGAGATCTTTTGTTGTTGGTTTTCAGCTCCACCAATGCCACAGGATGGACTGTTGTCCTGGGCCGACTCAATCAGAACAGCTCCAACCCCAATGAGGTCTCCATCAAAGTGGCAAATTTCTCAATGAGCAACAATTCGGGTAACAACGTTGCCGTCCTGCAGTTGGCGGTTACACCAAACTTCACCAATTACATTCAGCCCATATGTGTGGACTTGGGAGGCAACAATGTTGACGCCAACACTCAATGCTGGGCAGCAGGATGGGGATCAGGAGCAGGAGGAGGTGAGCTCAATATCTGTGGCCATGCTATGCTAATCACGAAACCTCATTTACTTAGATTTTTAAACAAATCTTCTCCATTTGAATGTGTTTTTATAGTGAATCAAACTCTTCAGCAATACCAGACTTCTATTGTGAGCTGTGGAAACTCATCCTCAAACAACAGTATTTGTACAACTGCTTTCGACTTA[C/T]AACAGGCAAGTTGTTTCTGGTTTTGTTTTGACTTTTTTGGTGAATAAAATTACTTAAGGAGAGGGCTATAACCATGGTGGACATTGAACAGAACAAGTATCAAATTACTAAACTGTAAAAGTGACAGTGACCGTGAGTCCAGCTCAGTTAATGTAGAAGGTTTGAATGGAGAAAGAGGGAAGGGTTCGCATGAAAACGGGAGTATCATTACGTGCACTACAGCTGTTTTTTACACCGCAACACAGATGGTGATTCGCAGAGCAGCATTTACAGTGGATCTAAGAGCTGTGTGGACGATTTTCAGTCCATATTATTGTAGTGATATAATTTAGTAACTAAATCATTTTGACTAAGGTATGTCTTTAACTGAAAGAGTACTGCTGACGATAACTAACCATCTGAATAAACATAAACAAAGAACACTGATCACACACTTACCAAATTAGAGACAGGAAAATCAACACCAGCTGGAACCACATCTTTATTTTAAAGAAGATTAG

Associated Phenotype:

Not determined

Allele Name:

sa33261

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 > T

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013553	Missense	392	551	10	11
ENSDART00000135192	Essential Splice Site	494	498	10	10

Genomic Location (Zv9):

Chromosome 3 (position 39470209)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	39333569
GRCz11	3	39475427

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATGAAGGTAATAATCCTCTTCACTGTGTGTCTTTCACTCTCTTAGGGT[G/T]TTCAAGGTGGTCCACTGATGTGTTTGGTGGGTCAGTCATGGATCCATATT

Long Flanking Sequence:

TCTGAGTTTTGGAAATCACCCCCACTTTGGTAAACACTGGACTAGATTGCTGGTGATTGTGACATTAAAATCCACTTAAATTTGTAGTTAACTTAATTCCCAGCAAGCATTTTTGCATTTAATAGACGCTTAATTGACATCTAAACGTAGACAGCTTGGCTAAAACAAGGCCCGTCAGTGAAAATCTAATAGACATCTAAGAACAGCTCAAAACTAGACTAGTCGTCAAATAGACAGATTAGACAGACTTGATATATGTAGTCATTCATTTCTTTTTATTTGATGACTAATATAGTTTTGGCCTATTTTTAGATCGATTAGATTTTCACTGACAGCCCAAATTTAGACTTGTTTTAGCCAGTAGACATCTATTAGACATCTTTTAAAAAAAATAAAAAACGCTTGCTGGGTTTCTTCATGTATTGCCAACACAAATCGATTTTTTACAGTGTATGAAGGTAATAATCCTCTTCACTGTGTGTCTTTCACTCTCTTAGGGT[G/T]TTCAAGGTGGTCCACTGATGTGTTTGGTGGGTCAGTCATGGATCCATATTGCAGTATTAACCATATCGAACAGCAACTCAAACAGCAGCATCTCTAACAGTACTCTGAACAACAGTACTCTCAATAACTGCACCGTCAACAACAGCACCGTCAACAACTGCACTGTCAATAACAGCACTGTCAATAACAGCACAAGCAGCACAGGCAGCAAAGGTGCTGACTTGTACTTCCCTGTTAAGGCTCAGGGTGTCCAGATCTTCACTAAAACCTCCAGCTTTTCCACATTCCTGACAGCTGTGATCAGTTCCTTCCCTCAAAAAGCTACAAACACTACAAGTGCAAGTACAAGCGCTCCTTCTGCAAGCACCTCAAATACAACCCAGTCTAATGGCTCACCAGCATCTTTTTCCTCCTGCTATACAGTTTCTGTTTTATTCTCCTCACTTCTAACTCTCCAAATCTTTCACAAGAGCATCTTTTGAGGAAAAACGGCTCACTGT

Associated Phenotype:

Not determined

Allele Name:

sa40129

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000013553	Essential Splice Site	None	551	None	11
ENSDART00000135192	None	None	498	10	10

Genomic Location (Zv9):

Chromosome 3 (position 39469449)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	39332809
GRCz11	3	39474667

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTACACAAGTTTTTTTTTTTTTTTTAAACAGATTTAACAGTTTATCTTG[T/A]GTTTCACAAATTTTGGTAACACTTTATTTTGATGGTCCATTTGAGTATTA

Long Flanking Sequence:

CACTAAAACCTCCAGCTTTTCCACATTCCTGACAGCTGTGATCAGTTCCTTCCCTCAAAAAGCTACAAACACTACAAGTGCAAGTACAAGCGCTCCTTCTGCAAGCACCTCAAATACAACCCAGTCTAATGGCTCACCAGCATCTTTTTCCTCCTGCTATACAGTTTCTGTTTTATTCTCCTCACTTCTAACTCTCCAAATCTTTCACAAGAGCATCTTTTGAGGAAAAACGGCTCACTGTTAGAGTGAATGTGAAATATCCAGACCCATATTAATATGTTTTTCAGTATGCCCCATGACTGATTAGATTGTCATACATTTAGCATTCAAGGCTTTTGTGGAGCATATTCAGTACTAGACAAATGTGAATGTTAATTGATAAGTCAGACCATGAAGATGTTGAGTGTTTGTATACTGTGCAATTACACAAAAAAAATCTGTTAAATAACAGTTACACAAGTTTTTTTTTTTTTTTTAAACAGATTTAACAGTTTATCTTG[T/A]GTTTCACAAATTTTGGTAACACTTTATTTTGATGGTCCATTTGAGTATTAGTAGGCTATCTGCGTAATATCTGCTGATACTGCTCCCTCAACAGACATTTAACTGACTGTAAGAAACTTGCAAGTACGAGTCAAACCTACAATAACCACAACCTAACAGTCTACTTATAATCTAATGAGAATTAATTGCAATGTAACTTAAATTCTACAAACGGACCCTCAAAATAAAGTGTGACCCAAGTGTTTTCCATTTATTTCCGGCTCTAAGTTGCATTATGGGATGTTTATCACTGCTTTTGAAATTGACAATTCAACTTAGCGGTTTAACAAAGTGACTTTTATTGACATTTTAGTCGTTTGAAATGTATAAGAAATAATATAAAAAAATAATTAATAAATAATTATTTTATAACATAATAGAAAACATGTCACTTTAAACTATTAAATATATTAATCAAAGTAATGTATTTTAACTTTTCAAGTTGTTGAAAGAATGAAGCA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details