Busch Lab

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 are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa10791 Nonsense Available for shipment Available now
sa44273 Nonsense Mutation detected in F1 DNA Not yet available
sa44272 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38050 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10791
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:
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

Mutation Details

Allele Name:
sa44273
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104453 Nonsense 192 621 2 14
Genomic Location (Zv9):
Chromosome 25 (position 19235382)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 18647359
GRCz11 25 18745310
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCAGAACCACAGTGTCTGTGCCTTTACCTCATCCTGGCATTCTGCAA[G/T]AGGCTGAGCTTAAAGTGTACAGTAATGCAGACTGCAATAATATTTGTCAT
Long Flanking Sequence:
CCATTTTTGTGGCGGCTCCCTCATCAACAATCAATGGGTGCTGACAGCAGCTCACTGCATTGTTGAGTAAGACACCTCAACTATAATCAATGGCCTTATTTGGTTGGTGGAAATGTTCTTTAAGTACCATTTTTGTTACTCTTGTTTTTTTCTTTCTTGTACACAGTCAAACCCCATCCAGCATAATTGTGTACTTAGGAAAGTGGAGAAGTTATGTAGCTGATGTCAATTCAATCTCCAGAACTATCAGACACATCATTCCCCATCCCTCCTACAGTAACATAACTAAAGATAATGACATCGCTCTGCTGCAGCTGACATCTACAGTCCAATATACTGACTACATTAAACCCATATGTCTAGCAGATGAAAACAGCAACTTCCCTCGTGGCACCAACAGCTGGGTCGCAGGCTGGGGGGATATTGGAGTTTTGGGCACAGGTGGTATAAGAGGCAGAACCACAGTGTCTGTGCCTTTACCTCATCCTGGCATTCTGCAA[G/T]AGGCTGAGCTTAAAGTGTACAGTAATGCAGACTGCAATAATATTTGTCATGGACGGATCACCCCCAACATGATTTGTGCTGGTACACGTCCTGGAGGCAAAGCAACCTTTTCTGTATGATGATCAATGAGATTGTTCTTGTCAAGATACTCCATATGCACACACCTAAACACACTGCAAACTTGAATGTCCAACCAGACTGACTGTATGTTGTCTCTGTTTGATGAGACAAACACAATACACCAAAACAGTAACTGAATAACCTAATCTTTCTCTGTATAGGGGGACTCTGGTGGTCCACTGATGACTAAGTGTTCAGTGTGGGTTCAGGCTGGTGTTCTCAGTCATGGTTATGGATGCGCACAGCCCAATCTTCCTGAGGTGTTCATTCGTGTCTCAGAGTATAAGCAATGGATTACAGGCAATGTCGGTGGAAACCTGCCTGGATTTGTCCTCTTTGACCCAAGATGTTCTCTTCGCAGTAAGATTCCACATCCTTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44272
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104453 Essential Splice Site 300 621 7 14
Genomic Location (Zv9):
Chromosome 25 (position 19231716)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 18643693
GRCz11 25 18741644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATATTTAAACAATGCAGCTTAAACAGTCATAATTTCAGGTTTGTGTTT[C/T]GAAAAAAGATTTAGAAATAAAACAACGGAAAAAGAGCCTGGGAACTCAAA
Long Flanking Sequence:
GGTAAAAATCATTTAATGTAAAAAAAAATGGAATTCAAAAATCAATTTCGAATTGTAATATTTCAGAATACATTTAATTGAATTAAATAAACATGATCATATAAAACCCTGTATTCTTTTAATGATGTATATTGTTTTTTGCATAACATGCAGATGTGTTATCATTGCTTTATTTTTAATTTGGTTTAGTTTATTATGTTTCAGTTTAATGTCAAATGTGTCATTTTCATTCACTGGTATTTTAAGACACTATACTATATTTCACCATAGGTTTTTGAAGTTTCTTGTTGGACAGAGTCAATATTTGGTCCCGCAAGCTCCTGTGCAGGTTTTAACTCCGAGACTCGAGTCTGAGGGTTTCAGGTTTACAGCAGCTTTTTTCAGCTGTGGCTTTTATCCACCGCTCTTCAAATGTGCTGGCATTCAAATGAGCCAAACAGAATACACAGAATATATTTAAACAATGCAGCTTAAACAGTCATAATTTCAGGTTTGTGTTT[C/T]GAAAAAAGATTTAGAAATAAAACAACGGAAAAAGAGCCTGGGAACTCAAATGACTGTTGTCTTGCCTTCAGCTGATATAAGCTCAGTATCTTCACATGCTACATCAGAGCTAACGCTAACTTATGCTTCACACAACTGATCGCGTACACATTGTGTCTGGATCAAGAAAGACAGATTAAAAAAAGAACAAAAGAAAATTATACTAAAAGTGTAATGTAAAAACTATTGACTATAAAACAATATTTTCCTCATGTCAAAATATGCACATGTACAATGCATATCATCGTCGTTTACTTTAATATGTGTTGTTTATTTAATCTGAATGTTGAGTGTATGAATTATTACTTCAAATATACACACAGGGGTATTTAATTATTCATTTTTGGATAAAAAAAAATGGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTTACTAACATAAACTAATCATGAACAACACATGAACAGCATTTATTAATCATAATTGAACATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38050
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
ENSDART00000104453 Essential Splice Site 432 621 12 14
Genomic Location (Zv9):
Chromosome 25 (position 19220790)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 18632767
GRCz11 25 18730718
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACTAAACATTAGCCACTTGTAATTCATTGTGTTCTTCATGGTCCGTA[T/A]TCAGTGTCATCACGTCGAGTGTGCTTGTGTACTTGGGAAGAAGGACACAA
Long Flanking Sequence:
AATGTCCTAATTCAAACACAAACCCATTGCATTGTGCGTAGTTTTAAAGAAGCAAAAGCTCCTGCTCTTCCTATTGTTTTCCCTAGTGTACTTTCCCATGTAAATTGGATGAGCTTATTTTGCAATTGATAGTTTGATGAAAAAGAAGAAGCCAGTACTGTACATACAGAGTCTCAAAGAAATCATTTAAGTAGTCGAAAGCTGAGAAAATTATAATTTAAAACACCAATTGAAAACATAAATGTCTCTCTTTCAGTTTGTGGACGTCGGCATTTAAACGCTCGTATTGTGGGCGGGGAGGATGCACCTAAGGAGGCGTGGCCATGGACAGTTAGTCTTCACAGCCCCAGATATAATGGTCATTTTTGCGGCGGTTCCCTGATCAGCAGTGAATGGGTGCTTTCGGCTGCTCACTGTTTCTCCAGGTCAGAACTGCATAAACACACATTCCTCACTAAACATTAGCCACTTGTAATTCATTGTGTTCTTCATGGTCCGTA[T/A]TCAGTGTCATCACGTCGAGTGTGCTTGTGTACTTGGGAAGAAGGACACAACAGGGAGTTCATGACCATGAAGTCAACAGAACAATAAGTGAGCTCTTCATTCACCCTTCCTACAGCAGCGATTACTACAACAATGATATTGCTCTCCTGCATCTGTCCGCTTCAGTCAGCTTTAACAAATATATTAGACCTGTGTGTTTAGCAGCAGAAAACAGCAGCTTTCCTTCAGGCACCAGCAGCTGGATCACAGGCTGGGGACAAACAGCAGCTGGAGGTAGAGTATCACACCAAATAACCTAGTTACATTTTAAGATAAAGCGCCCTCTAGTAGATGTAAAAATAATGACAGATATGTATAATCAGCATAAGCATTCAAAATGCAGGTACTGTCCATTTAAAGTCAACATGAAATGGAAGTTAAAGTACACTTGAAATTGAAACTAACCATATGGATTTTAGGGCTGCAACAAACGATTATTTAAATAATCGATTAATCTGGCG
Associated Phenotype:
Not determined