ZMP
TMPRSS7
Ensembl ID:
Description:
transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:30846]
Human Orthologue:
TMPRSS7
Human Description:
transmembrane protease, serine 7 [Source:HGNC Symbol;Acc:30846]
Mouse Orthologue:
Tmprss7
Mouse Description:
transmembrane serine protease 7 Gene [Source:MGI Symbol;Acc:MGI:2686594]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9804 | Nonsense | Available for shipment | Available now |
sa45011 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24499 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9804
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129558 | Nonsense | 502 | 785 | 14 | 19 |
ENSDART00000130197 | Nonsense | 501 | 780 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 24 (position 22455634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21702512 |
GRCz11 | 24 | 21847686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTATGTTCTGTAATTAATATGTTTGATGTGCAGAGACTAGCTGTTCT[G/T]GAGTCAGTTATCAGTGTGACAATGGAGCCTGCATTCTTAAGAAAAATGCA
Long Flanking Sequence:
AATTTTAGCACTTCCTTAATACTTAGACAAAATATGAACAGTAAAAATGGTGTCACTTTTACCATTTTAATTTAAATGTGAATTCATCATTAGGAAGTGCGTTCAAAGAGATTTGTTTTTGCAAATTTGGCAATAAATATCTGTTAGAAAAACTATGTAGGCTTGTACACCAAGTAAAGCAGGAAGAAATAAAGAAAAAGAAGTCTTCAATGATTGAGAACAATGCATTTTTATAATATCAAATGAGTATTTCTATGAATATTCAGCGTTTTATCATACGTTACGTTATCTCTGTTCCACAGCTAAACCTCCTAAATTCTGTGGTGGTACATCCCCTTTGCACCCATTATACATTTGTAATGGAGAGATGGACTGTTCCAGTGGTAAAGATGAGACAAACTGTACTCAGGGTAATGTGAAAGCTAAAAAATCTGACTTTAAGATGTGTCAGTTGTATGTTCTGTAATTAATATGTTTGATGTGCAGAGACTAGCTGTTCT[G/T]GAGTCAGTTATCAGTGTGACAATGGAGCCTGCATTCTTAAGAAAAATGCAAAATGTGATGGCTTTCCTGACTGCTTTGACCAGAGCGATGAAAAGAACTGTGGTAAGTTTTACTGTGGTAACATCCATTCAGATAATCACTCTTGATACTGGTTTGCAGACATAAAATGAAAGAGAACTGATTTTTCATAGTTTTATGTTTGTTTTAGAGGTATTTTATAATTAATTAAATTCCATTTAAACTAAAAAAATGTCATAGGAACCAAACAATGAGCATTAAAGTAGCTTTAAATCAGATGTAAATCATAAAATTAAAGACACTTGGAGAAATCGTTCACTTATTTTTATATATATAAATGTAAAATCTGTTTCATGGTTCACATTTATTATTCTTACTTTGTAAACAAATTGCATCCTAATGTCATATTGCTGCACATCCTTTAAAGAGTGTCCAAAAGTTTAATTAAGGGAACCAGTGTTTCATGAATGACTGACTAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45011
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129558 | Essential Splice Site | 594 | 785 | 16 | 19 |
ENSDART00000130197 | Essential Splice Site | 589 | 780 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 24 (position 22453617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21700495 |
GRCz11 | 24 | 21845669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTGATGTGTGGCTTATTTCCGCAGCACACTGTTACAGCAAAGAAAG[G/T]TGAGAAACATCAGATGCATCTATAAATCATTGAAAATCAACATTTAATAC
Long Flanking Sequence:
TAGACAGACAGACGGACTACCAGACAGACAAATAGTTGGATAGATGGATGGATAGACAGACAGACGGACTACCAGACAGACAAATAGTTGAATGAATGGATGGATAGATGGATGGATGGATGGATTGATAGATAGAGACGGACAGATGGACAGACAGACAGATTGAAAGATAGACAGACAGAGACAGACAGACAGGCATACAGACAGACAGACATACAGACAAAACAGTCTCAATCTCACACTTAATCTCACCTTTGTCACACACACATGCTTTTGTCTTACATTTCCGTATGATTTGTAGCCTGTGGCAAACCCACCCATGTAAAACGTGTATTAGATGGCACCAGCCCTCAGCAGCGTATTGTGGGTGGAGTCAATGCTGTGGAGGGGGAGTGGCCATGGCAGGTCAGCATGCATTTTTCTGGTCAGCTGTATTGTGGAGCTTCAGTCCTCTCTGATGTGTGGCTTATTTCCGCAGCACACTGTTACAGCAAAGAAAG[G/T]TGAGAAACATCAGATGCATCTATAAATCATTGAAAATCAACATTTAATACATTTTGTTAGTGTTTTCATACAGCATGTGTGATCTTTGATGCTTTCAGGTTGGCAGATCCACGTATGTGGATGGCTCATTTGGGAATGCTGAACCAGGGCAGTGCCAAGCATGTGGCCGAGATCCGTCGAATTGTGGTGCATGAGTACTACAATGCAAGAAATTTTGACTATGATATTGCCCTCCTGCAGTTGAAGAAGGTCTGGCCAAGCGGACTGGAACAATATATCCAGCCTGTGTGCCTGCCGGCCCCATCCCAAACCTTTACTGAGGGACACCGCTGCTGGGTGACTGGCTGGGGTTATCGTTCTGAACAGGGTAACAATCTCAAAATCAAGGAGAAACCATGTGCTCCGCTGTTTAAATTTAAACATTTTAAATACGTCTGCATTTAGTGAAACATACAGTTTAAACAGTACTACTGAGAAGTGTCATTTTTAACATTTTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24499
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129558 | Essential Splice Site | 594 | 785 | 17 | 19 |
ENSDART00000130197 | Essential Splice Site | 589 | 780 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 24 (position 22453520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21700398 |
GRCz11 | 24 | 21845572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACATTTTGTTAGTGTTTTCATACAGCATGTGTGATCTTTGATGCTTTC[A/G]GGTTGGCAGATCCACGTATGTGGATGGCTCATTTGGGAATGCTGAACCAG
Long Flanking Sequence:
GGATGGATAGATGGATGGATGGATGGATTGATAGATAGAGACGGACAGATGGACAGACAGACAGATTGAAAGATAGACAGACAGAGACAGACAGACAGGCATACAGACAGACAGACATACAGACAAAACAGTCTCAATCTCACACTTAATCTCACCTTTGTCACACACACATGCTTTTGTCTTACATTTCCGTATGATTTGTAGCCTGTGGCAAACCCACCCATGTAAAACGTGTATTAGATGGCACCAGCCCTCAGCAGCGTATTGTGGGTGGAGTCAATGCTGTGGAGGGGGAGTGGCCATGGCAGGTCAGCATGCATTTTTCTGGTCAGCTGTATTGTGGAGCTTCAGTCCTCTCTGATGTGTGGCTTATTTCCGCAGCACACTGTTACAGCAAAGAAAGGTGAGAAACATCAGATGCATCTATAAATCATTGAAAATCAACATTTAATACATTTTGTTAGTGTTTTCATACAGCATGTGTGATCTTTGATGCTTTC[A/G]GGTTGGCAGATCCACGTATGTGGATGGCTCATTTGGGAATGCTGAACCAGGGCAGTGCCAAGCATGTGGCCGAGATCCGTCGAATTGTGGTGCATGAGTACTACAATGCAAGAAATTTTGACTATGATATTGCCCTCCTGCAGTTGAAGAAGGTCTGGCCAAGCGGACTGGAACAATATATCCAGCCTGTGTGCCTGCCGGCCCCATCCCAAACCTTTACTGAGGGACACCGCTGCTGGGTGACTGGCTGGGGTTATCGTTCTGAACAGGGTAACAATCTCAAAATCAAGGAGAAACCATGTGCTCCGCTGTTTAAATTTAAACATTTTAAATACGTCTGCATTTAGTGAAACATACAGTTTAAACAGTACTACTGAGAAGTGTCATTTTTAACATTTTATGTACAGTAATAACAGGCCGTAGCCAGCCTGGTAAAATGGGTGGTTTTCTATTTAATTATAAGATTTAATTACTGCATTTAGTGACATTTTAAGCACTAT
Associated Phenotype:
Not determined