Busch Lab

ZMP

ENSDARG00000070897

Ensembl ID:
ENSDARG00000070897
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 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24687 Nonsense Available for shipment Available now
sa24686 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa24687
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104449 Nonsense 160 257 2 5
Genomic Location (Zv9):
Chromosome 25 (position 25790945)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 24991010
GRCz11 25 25086194
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGCTTAAAGTGTACAGTAATGCAGACTGTAATAGTATTTGTCATGGA[C/T]GAATCAACCCCAACATGATTTGTGCTGGTACACGAAGTGGAGGCAAAGCA
Long Flanking Sequence:
CGTCAAGTAAGTAAGACACGTCAAACACAAACTATAATAAATTACCTTGTTTGTTGGTGGAAATGTTCATGTATCAGTTTTTCCATCTCTTGTTTTCTTTTTCTGTATACAGCTTAACTAGGTCCAACATGCTTGTATACTTGGGAAAGTGGAGACGTTATGCAGCTGATGTCAATGAAATCACCAGAACTGTCAGCAACATCATTCCACATCCTTCCTACAATAGCACAACTTATGATAATGACATTGCTCTGCTGCAGCTGTCATCTACAGTCCACTATTCTGACTACATTAAACCCGTTTGTTTAGCAGATGAGCAAAGCAACTTCCCTCCTGGCACCAGGAGCTGGGCCACAGGCTGGGGGCGTATCGGAGTTTCAGGCAAAGGTGGTATAAGAGGCAGAACCACAGTGTCTGTGCCTTTACCTCCTCCTGGGATTCTGCAAGAGGTTAAGCTTAAAGTGTACAGTAATGCAGACTGTAATAGTATTTGTCATGGA[C/T]GAATCAACCCCAACATGATTTGTGCTGGTACACGAAGTGGAGGCAAAGCAACCTTTTCTGTATGATAATCAATAAGATTATTCTAATCAAGACATTATTCTTCTGTATATGCACACACCTAAACACACTGCAAACCTGAATCTCCAACCAGTCTGACTGTATGTTGTCTCTATTTGATGACACAAAAACAATAAACTAAATCAGTAACTGCATAACATAATCTCTCTCTGTAGGGGGACTCTGGTGGTCCACTGGTGAGTAAGCAGTGTTCAGTGTGGGTTCAGGCTGGTGTTGTCAGTCATGGGTATGGATGCGCACAGCCTAATCTTCCTGAGGTGTTCATCCGTGTCTCAGAGTATAAACAATGGATTACAGCCGCTGTTGGTGGAAACCTGCCTGGATTTGTCCACTTTGACCCAACATGTTTACTTCCTAGTAAGATTCTTCTCCTCATGCCTACACACACGCATATACACAAATTGTACAATAACACACATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24686
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
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104449 Essential Splice Site 247 257 4 5
Genomic Location (Zv9):
Chromosome 25 (position 25790414)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 24991541
GRCz11 25 25086725
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACAATAACACACATATTTTTACTAATGTTTGTTTATGTATTTTGTGT[A/T]GACAATTGCGTTAAACTCAGAAATTGCTTTGGGTAATTAAAACTGCTGCA
Long Flanking Sequence:
CACGAAGTGGAGGCAAAGCAACCTTTTCTGTATGATAATCAATAAGATTATTCTAATCAAGACATTATTCTTCTGTATATGCACACACCTAAACACACTGCAAACCTGAATCTCCAACCAGTCTGACTGTATGTTGTCTCTATTTGATGACACAAAAACAATAAACTAAATCAGTAACTGCATAACATAATCTCTCTCTGTAGGGGGACTCTGGTGGTCCACTGGTGAGTAAGCAGTGTTCAGTGTGGGTTCAGGCTGGTGTTGTCAGTCATGGGTATGGATGCGCACAGCCTAATCTTCCTGAGGTGTTCATCCGTGTCTCAGAGTATAAACAATGGATTACAGCCGCTGTTGGTGGAAACCTGCCTGGATTTGTCCACTTTGACCCAACATGTTTACTTCCTAGTAAGATTCTTCTCCTCATGCCTACACACACGCATATACACAAATTGTACAATAACACACATATTTTTACTAATGTTTGTTTATGTATTTTGTGT[A/T]GACAATTGCGTTAAACTCAGAAATTGCTTTGGGTAATTAAAACTGCTGCAGTGATTTCATACTCTGGTGAGTCCACACATACATACCCCCACACAAACATATATATATATATATATATATATATATATATATATATATATATATAATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGGTTCTCATTT
Associated Phenotype:
Not determined