ZMP
zgc:101791
Ensembl ID:
ZFIN ID:
Description:
transmembrane protease serine 2 [Source:RefSeq peptide;Acc:NP_001008623]
Human Orthologue:
TMPRSS2
Human Description:
transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:11876]
Mouse Orthologue:
Tmprss2
Mouse Description:
transmembrane protease, serine 2 Gene [Source:MGI Symbol;Acc:MGI:1354381]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21790 | Nonsense | Available for shipment | Available now |
sa34966 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21790
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126157 | Nonsense | 318 | 486 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 39999258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 38780733 |
GRCz11 | 10 | 38724140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGGGCTGGACGGTGTATGCTGGATATCTGACCCAATCAGAGATGGCGT[C/A]GGCCTCCGGAAACTCTGTAAACCGAATTGTCATTCATGATTTCAACCCAA
Long Flanking Sequence:
TACTCACCCGGTTGATTACATTAATAATTAGCAACATTTTTTGCATGACTAGGCAAGGCAAACTTTATTTATAGAGCACAATTATACACTAAAGGGTTGTATATAATCTGGCAATATGTGTACAGTAAAAGCATGTCCTTCAGTAAAAACCTTCAGAATAAAGATATGAATTAAGTTGTGGAGAAGTGTTCTGTATATTAAAGCTGATAAAGTTGCAATTTATGGCTCAGTGCAAGAGAAAAACTGCCTTAATTTGTTTTTTAATTGAAACCTACAAACAAAAATTGATAAAGTGTGCCAAAATAAAGGATTAAAGGTATATTGATTGATACAAAACATACAATCATGTTTTGGATGTTTTGTTTTCACAAGAGGTGGGAAAAGTCTCTCCCCTAAACACACTTATGATGAGCTCTAATGAAGGAAAAACATGTGCAGGTTTTCAAATCCAGGGGGCTGGACGGTGTATGCTGGATATCTGACCCAATCAGAGATGGCGT[C/A]GGCCTCCGGAAACTCTGTAAACCGAATTGTCATTCATGATTTCAACCCAAACACCAATGAGAATGATATCGCACTAATGAGGCTAAACACAGCACTCACTATTTCAAGTAAGACTGAATTTTCATGTTTCCCAGCCAATAAGAATGTCCTTTGAGAATTATTCCTTAGTTAAAGTTAAAGAATGTTTGATTAATGCCATGTCATTTTAGAATTATTTGTGTGCCCTCATAGTGTTAATAGTGATCAATTTTTCTTTATATTTTCACTTTTATGTTTGATTCAAGTTTTTATTTTAATTTTAGTAATTTTTTTATGTGAAAAAAAAATATTCAGCTTACTTGGTTTAATTAATATAAGTGCCTTTACTCTGGTTTTGTGTTCCTATCCAATATATATTTTTTCAGTTATATTTTGTTAATTTTTGTTGACAACAAAATGTAATAGTTTGTAATTAAAAATTATGCATATACTATATTTTATTTTACTGTAATGATTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34966
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126157 | Essential Splice Site | 433 | 486 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 39996253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 38783738 |
GRCz11 | 10 | 38727145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCATGATCTGTGCTGGAAAGCTGGCAGGCGGCGTGGACTCCTGTCAG[G/A]TCAGAAACGCAAACAATAGCTGCCCCATCAGATCTGTAAAGCTGATTATG
Long Flanking Sequence:
CATTTTCCTTCGGCTTAGTCCCTTTATTCATCAGGGGTCACCACAGTGGAATGAACCGCCAACTTATTCAGCATATGTTTTACACAGCGGATGCCCTTCCGACCACAACCCAGTACTGGGACACACCCATACACTCTCACATTCACACACATAATGCACGGCCAATTTAGTTCTTTCAATTCACATATAGCGCAGGTCTTTAGACTGTGGGGGGAAACCAGACACCAAGAGGAAACCCAAACAAGCACAGGGACAAACTCCACACAGAAATGCCAGCTGATTTGGAATTCACCTGCAGTATTGATTAAAACTTTTAGTTGAAGCGTGCATATGAAAATCAAATGTGTTTCTTTAAAGGCTCTTCCTCAGCAACCCTACAAGAGGCCAAAATCCAGCTGATCGACAGCACGATTTGTAACAGCCGGCCTGTGTATAACGGACTGATCACCGACACCATGATCTGTGCTGGAAAGCTGGCAGGCGGCGTGGACTCCTGTCAG[G/A]TCAGAAACGCAAACAATAGCTGCCCCATCAGATCTGTAAAGCTGATTATGAACTCTTATGAACTTATTTTGGTTCATTTATTTCTAGCAACATCTGCATTAAAAACTGACAGGCAGCAATTAAAATATCATTACCACATGCAGGGTTCTGATTGGCTGATGACTATTCTTGTGCAGTTATTTTCAGATAAATGCACAGCTAAAGTAGTACCAGGCAGGTCTTGACCACATTACAGGTTCATATCAGTACGCTGAATGATTTCAGATATTTCATAGCTATAACAGTCGGAAATCACATTACAACGAAACCGAATGCTTTAAGTTAGTTGTGTAAAAAGTGTGTTTGTGAATAAATTGATGGCCCTTCGTCAGTTAATCTTTGCATATAATGAATTGCATTAATGGCCGTTATTATTGTGCAATTCTAAACCAAACCTCTAGACCTGCTCATGATCCTCTGCCAATTCTTATGTAGAGCAGTGTAAATGTACTGTATATACA
Associated Phenotype:
Not determined