Busch Lab

ZMP

LOC100333187

Ensembl ID:
ENSDARG00000071841
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa13026 Nonsense Available for shipment Available now
sa15454 Nonsense Available for shipment Available now
sa44750 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13026
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000106572 Nonsense 33 282 1 4
Genomic Location (Zv9):
Chromosome 12 (position 4887284)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4170006
GRCz11 12 4206771
KASP Assay ID:
2260-4854.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTGTCTGCTGGTAATGTTMCCTGGCCTTGGMAAGCCGATCTGTACTA[T/G]TTTGGGTATCGCCTTTGTGGAGGATCCCTCATCAGCCACRAGTGGGTGCT
Long Flanking Sequence:
GGAGGGAGACGCGAGATTACCGGGAGATCATCACTCGTTTGCGGGCATCCGGAGACTCGCGAAACTTCCCGCCCTACTCATAATTCTCTCTTCATATAGCCGTAAGCTTATTACATATCCATAAAACACTGTGATTTAACCACGCTTGGATCGGATCGCTTTCTCACTGTAATCGAACCGCTCCAGGGTTCGTTTCAATCGAGCCGACCACCTCACTCAGGCGATCTCGGAGCGATTACTTTGGTGTGGAACAGAGCGCGATTGCCCTGTTCACATATGCCAAACGAACCGCGCTAACTGGGCAAACGAGATACGTTCCTAAACAAAAGTGTAGGTGTGAAAGCACCCTATAAGTTTAAAAATCTGTCAAATTTCACAAATTATTTACATTTCTGGCTATTCTCCACAGCACAGAGTTGTGGAGTTTCTCCACTAAACTCTCCAGGTGGGAATGTGTCTGCTGGTAATGTTACCTGGCCTTGGCAAGCCGATCTGTACTA[T/G]TTTGGGTATCGCCTTTGTGGAGGATCCCTCATCAGCCACGAGTGGGTGCTCACTGCAGCTCACTGCGTTTACTACATGTAAGAACACAAAATAGCATGTGGTTTAATGTGAGTTATCATTAAAGCAAGCGCACTGAAGGTTTTTGCTTTCTCATCCAGACCTAAAAGTTACATCACTGTCTATCTGGGTAGAAACAGCCAAAACGCTTCGGACTCCAACGCAAATAGGGTTACCCTGAGTGCCCAGTCTATCATTATACATCCAGACTTTGACTCCCTTCAGTTCACCAATGACATCGCCTTGCTGAGACTTGCTAAACCAGTGAACTTCACCAGCTCCATCAGCCCCATCTGCCTGGCTGCTAATGACAGCGTCTTTCACAACGGCACCACCTGCTGGGCCACTGGGTGGAGCTATAATCAAGGTAATGATCATCAGTTTCACTACATGTACTATAGGGAACAAAACAAATGCCAAAAGTATTTGTTGAATAGCACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15454
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000106572 Nonsense 33 282 1 4
Genomic Location (Zv9):
Chromosome 12 (position 4887284)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4170006
GRCz11 12 4206771
KASP Assay ID:
2260-4854.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTGTCTGCTGGTAATGTTACCTGGCCTTGGCAAGCCGATCTGTACTA[T/G]TTTGGGTATCGCCTTTGTGGAGGATCCCTCATCAGCCAYRAGTGGGTGCT
Long Flanking Sequence:
GGAGGGAGACGCGAGATTACCGGGAGATCATCACTCGTTTGCGGGCATCCGGAGACTCGCGAAACTTCCCGCCCTACTCATAATTCTCTCTTCATATAGCCGTAAGCTTATTACATATCCATAAAACACTGTGATTTAACCACGCTTGGATCGGATCGCTTTCTCACTGTAATCGAACCGCTCCAGGGTTCGTTTCAATCGAGCCGACCACCTCACTCAGGCGATCTCGGAGCGATTACTTTGGTGTGGAACAGAGCGCGATTGCCCTGTTCACATATGCCAAACGAACCGCGCTAACTGGGCAAACGAGATACGTTCCTAAACAAAAGTGTAGGTGTGAAAGCACCCTATAAGTTTAAAAATCTGTCAAATTTCACAAATTATTTACATTTCTGGCTATTCTCCACAGCACAGAGTTGTGGAGTTTCTCCACTAAACTCTCCAGGTGGGAATGTGTCTGCTGGTAATGTTACCTGGCCTTGGCAAGCCGATCTGTACTA[T/G]TTTGGGTATCGCCTTTGTGGAGGATCCCTCATCAGCCACGAGTGGGTGCTCACTGCAGCTCACTGCGTTTACTACATGTAAGAACACAAAATAGCATGTGGTTTAATGTGAGTTATCATTAAAGCAAGCGCACTGAAGGTTTTTGCTTTCTCATCCAGACCTAAAAGTTACATCACTGTCTATCTGGGTAGAAACAGCCAAAACGCTTCGGACTCCAACGCAAATAGGGTTACCCTGAGTGCCCAGTCTATCATTATACATCCAGACTTTGACTCCCTTCAGTTCACCAATGACATCGCCTTGCTGAGACTTGCTAAACCAGTGAACTTCACCAGCTCCATCAGCCCCATCTGCCTGGCTGCTAATGACAGCGTCTTTCACAACGGCACCACCTGCTGGGCCACTGGGTGGAGCTATAATCAAGGTAATGATCATCAGTTTCACTACATGTACTATAGGGAACAAAACAAATGCCAAAAGTATTTGTTGAATAGCACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44750
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
ENSDART00000106572 Nonsense 260 282 4 4
Genomic Location (Zv9):
Chromosome 12 (position 4882407)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4165129
GRCz11 12 4201894
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCGAATTCCAAAGCTGGATCCTAAATAATGTTAACGGGTCAGACATC[G/T]GATTGGAAACTTTTAAATCTGACGGTGAAGACAAAGACAACAGCTTTCTG
Long Flanking Sequence:
ACCACAGCAGAATGAACCGCCAATTATTCCAGCATCCACACTCATACACTATAGCTAATTTAAACTGTGTTAAACAAATGCTGGAATAGTTGGCGGTTCATTCCACTGTGGCGACCCCTGATAAATAAGGCATTAGGTCAAAGGAAAATTAATGAATGACGAGGCTGAATTATATAATTAAATTAATGTATAATAAGAGACAGATGCTTATCATGGAAGCAAACAAAAACATAATCGTGTTGAAACAGAACAAACTAATAATAATTAAACAAAAGTCCACTTTATGTGATACTTTCACAGTTTTAATTGTATGTCATGTCTCCCGCTTTCTTTTTTAGGGACAATTAGGTGATCCTTTACAGTGTATGCAGGGATCTGTGTGGATCTTAGCTGGTGTTACTAATTTTGGGTTTTGCGGCACTGGAGTTGCACCTGACGTTTATTCTAAAGTATCCGAATTCCAAAGCTGGATCCTAAATAATGTTAACGGGTCAGACATC[G/T]GATTGGAAACTTTTAAATCTGACGGTGAAGACAAAGACAACAGCTTTCTGTGCAATGGAGAAGATACAGGTAAGAGCGAAAACAGCTAACAATCAATAGTAACCTAATAGTAACCTATCACAACAGAGAGCACAATTAGTCATTTTTTAAATAAATGTTCAATTTATTTAACTTTTTTTTTAAAAGATTGTAAACTTCATAGTTTAAATTGTGAATAAACACTTTTACATAATAATCATGAGCCTTAAAAAGAAAACAAATTTTGGGAAGTGTTGAAAATCAGAAATAGTTGTGTCAAAGGTGAAACAGTTTAAAATGTCTTTGACAACTTGTGGTGTAGTCCTAACAAAAAAGGTGGTGTACTATTACCCTCCACCCCAAATATTTAAAGTAGGCAAAGAAACGACGGAAGTCAGTGGTTTTTTTAATCATTAGCAATATTTATTTATCAACACAAGTAACCTGTAACTTTTAACTTCCACAGAAGAAAAAAACAAAAA
Associated Phenotype:
Not determined