ZMP
tmprss13b
Ensembl ID:
ZFIN ID:
Description:
Novel transmembrane protease serine family protein [Source:UniProtKB/TrEMBL;Acc:A5PF55]
Human Orthologue:
TMPRSS13
Human Description:
transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:29808]
Mouse Orthologue:
Tmprss13
Mouse Description:
transmembrane protease, serine 13 Gene [Source:MGI Symbol;Acc:MGI:2682935]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16531 | Essential Splice Site | Available for shipment | Available now |
sa31465 | Nonsense | Available for shipment | Available now |
sa13510 | Nonsense | Available for shipment | Available now |
sa8506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16531
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084839 | Essential Splice Site | 5 | 475 | None | 13 |
ENSDART00000084841 | Essential Splice Site | None | 279 | None | 16 |
ENSDART00000133437 | Essential Splice Site | 5 | 239 | None | 8 |
The following transcripts of ENSDARG00000077573 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 39500699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37300068 |
GRCz11 | 5 | 37900221 |
KASP Assay ID:
2259-6225.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCTACCTGACCGCTTWAAACSGATACTCACATATGGAGCACAAACAGG[T/C]ACAAATATTGTTTTAAACAAACATAGAAAAAACAACTTTTACATTTTAGT
Long Flanking Sequence:
TAAAGAAACTCTTAAAGGAACCATTTGAAAGTAAATAGTAGTACATTTCCATTTTTGAGTGAATTATCCAGCCTGATATGTGTTGAATTATCTCTTCAACATATATGACGCTCACACTTTCCTTTGTTTATTTTGAAGTTGTGTGGATTGTTGTGTGAAATGGGATTCATACTTGTGTGATCGAGGACAACATTATGATGCAGCAATGATTATTCATCTATGATGAAAGCAGCTGACAGAATGTTCTCTGTGTGTGTTTCTATGGACATGTTGTTTAGAAACTCTATTTGAGAAGGCTGACTGTAAAACCTGTTGAACAGGTGAAAGAGTGGGAGAGGATGACATGAGTTACTGCAGGCTGAGCCCGTCCCGCTCTGATCATGTAAGAGGTGTGCCACTAGCAGGTGGATGACAGAGAACAAATCTATAGCTGAAGAAGAGTACAGGTAGAGGCTACCTGACCGCTTTAAACGGATACTCACATATGGAGCACAAACAGG[T/C]ACAAATATTGTTTTAAACAAACATAGAAAAAACAACTTTTACATTTTAGTCCTTATTTCAGGTGTGTGATTAGGTCAGTCGGTTGAAGAGTTTGATATAACTTTGATTTTCTTGTTTTATTTGTACTCTATCAGAAATAATGGTACAAAAGCTGTCATAAAAGGACTATATTAAATGTATATACTGTACATAAGTTCATATATAAGTAATTAAAAAGAAAAAAAGTGGGATGATTTAAAAAGATGCTGGTACATTGACAGCTTTAGTATCTTTATTTCTGATTGTTCATTTTATTTTGACCATTGAGCGAATGGCACTGAAATTCCATTTGAGTGAAATTCTGATCTTTATCTGAATGCTTTTCTTTCTGTGATCAGCTTGTCGTCAGTAGTTGTCATTGTTGTGTCCGAATCGGCAGTTGGATTAGTTGACTTGTATCCATAGTTACTGTTACTAATTATTAACATATATAGAATTAGTAACATAGCTGGTTGCCGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31465
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084839 | Nonsense | 12 | 475 | 2 | 13 |
ENSDART00000084841 | None | None | 279 | 2 | 16 |
ENSDART00000133437 | Nonsense | 12 | 239 | 2 | 8 |
The following transcripts of ENSDARG00000077573 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 39497319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37296891 |
GRCz11 | 5 | 37897044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATACAATCTCTTTTTTCACGAATACAGACTGAGGCTCCTCCCTCATA[T/A]GACTCTGTGGTGACTCAGAACATCACACCTCCACCTTCATATCCCAGTCT
Long Flanking Sequence:
ATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATACATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAGAAAGAGAGACAGATAGTAGATTTTATTATATTAAATGATTAAATAATTAACATAAATATATTGTGAATGTAATTCAGTGAATGAACAGTGTTACTAGATCTGCATATTTTTTTTGCTCGCTGCTTTTATACAATCTCTTTTTTCACGAATACAGACTGAGGCTCCTCCCTCATA[T/A]GACTCTGTGGTGACTCAGAACATCACACCTCCACCTTCATATCCCAGTCTACAAATATTGTCGACCACTCAAGTCCAACCGTACTACATACCTCAGCCATTACCTCAAATTCCTGCTCCCCATGTAGTAGAGACAAGTAAAACTTAATAACACAAACTACCTACAAACACATCTCAAAATCGTAGTCAGTGAGTTGAAGTTGAGCAATAATCACCATTGCTGTTTCCTTCCAGCAGTCCCACAACAGAGAACTCAAGCTGTCTCATACAGGAGCAAAAGGTGTTGCTATGGAGGATCCACTGGCATTGCTGCTGTAGTTGTCCTGGTTGTAATTGCTGTGTATCTGGGAGGTAAGCATATTATATGTAATTATGTTACATACTGTCTCTGATTAGCATCATATTCGCTAATCTTAGGTTGTATACAATGCGTCTTTTTCTCTTAAATGTGTAAACTTTTACATTTTTTGTAACCAGGGCTTGCACTTTAAAAAGATATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13510
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 |
---|---|---|---|---|---|
ENSDART00000084839 | Nonsense | 262 | 475 | 8 | 13 |
ENSDART00000084841 | Nonsense | 69 | 279 | 8 | 16 |
ENSDART00000133437 | None | None | 239 | None | 8 |
The following transcripts of ENSDARG00000077573 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 39493723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37293379 |
GRCz11 | 5 | 37893532 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGGTCACTGGCCATGGCAGGCCAGTCTGCATTTTCAAGGAAAGCACT[C/A]MTGTGGAGGATCTCTGGTGGCTCCAGACTTTATCATCACTGCTGCTCACT
Long Flanking Sequence:
CAGCAAAGATAAAAGAAATTAGTTATTAGAAATTATTTATTAAAACGATTATGTTTTTAAAATGGCTTCTGTCTATTAAACAGCACTTAGAAACATTGGGAACAGAAATTAAACTTTTACTGGAGGGCTAATAATTTTGCCTTCAACTGTATAAAATGTAATGTTTTACAATTTGGCCAATTTAAATGATGATAGATGTAGGGGAACAAACGGCACTATGTATTTATGCTGTGTGTGTGTGTGTGTGTGTAACAGTGTTGTTGTTGTAATTGTAGTTCATCGTGTCCCGATCAGCAGAGTGTGTCCCTGCAGTGCTGCGGTGAGAAGTTTACACCGATGCCACATGTTAATGCTTCTTGATAATGCTATCTAAGTCTAAACAGTCTCTTCCTGATCAGATTGTGGAAGGCCACCAGTTTCATCAAGGATTATTGGGGGAAGCGTGGCTGCTGAGGGTCACTGGCCATGGCAGGCCAGTCTGCATTTTCAAGGAAAGCACT[C/A]ATGTGGAGGATCTCTGGTGGCTCCAGACTTTATCATCACTGCTGCTCACTGCTTCCCCAAGTTAGTACACCGTATATTAGACAGATGGACAGAAGAGTTGATGACAAGTCTACATGTTAGACACAATGTCGTAGTCTGTAGTTATAAATAATATTAATAAACAATTTAGGAAATACTATCAAAAATGGCTGTATGAACAGATAAATTAATATGCTTTTCCCCCTCTTCTTAGAGAAACATCTGGCTCTCAGTTGCCTAGTAACTGGAAAGTGTACATAGGTTTCGTGTCCCAGCTCAAGCTGCCCAGTCCGTATTATGTAAAGGAAATCATTTTACATGAAAAGTACAACCCAACAACAAAAAACTATGACATCGCCTTGCTGAAACTCAATAAACCTGCCAGTGAGTTTGAGCTGCACACAGAGCTGCAAATAATTAACCCATATCCTTCTCTCCTGTTTTGCTTTTGAGTGTCTCTCATTTGGCAAAAGATTAACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8506
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084839 | Nonsense | 310 | 475 | 9 | 13 |
ENSDART00000084841 | Nonsense | 114 | 279 | 10 | 16 |
ENSDART00000133437 | None | None | 239 | None | 8 |
The following transcripts of ENSDARG00000077573 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 39493406)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37293062 |
GRCz11 | 5 | 37893215 |
KASP Assay ID:
2259-6223.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGTGTACATAGGTTTCGTGTCCCAGCTCAAGCTGCCCAGYCCGTATTA[T/A]GTAAAGGAAATCATTTTACATGAAAAGTACAACCCAACAACAAAAAACTA
Long Flanking Sequence:
CGGTGAGAAGTTTACACCGATGCCACATGTTAATGCTTCTTGATAATGCTATCTAAGTCTAAACAGTCTCTTCCTGATCAGATTGTGGAAGGCCACCAGTTTCATCAAGGATTATTGGGGGAAGCGTGGCTGCTGAGGGTCACTGGCCATGGCAGGCCAGTCTGCATTTTCAAGGAAAGCACTCATGTGGAGGATCTCTGGTGGCTCCAGACTTTATCATCACTGCTGCTCACTGCTTCCCCAAGTTAGTACACCGTATATTAGACAGATGGACAGAAGAGTTGATGACAAGTCTACATGTTAGACACAATGTCGTAGTCTGTAGTTATAAATAATATTAATAAACAATTTAGGAAATACTATCAAAAATGGCTGTATGAACAGATAAATTAATATGCTTTTCCCCCTCTTCTTAGAGAAACATCTGGCTCTCAGTTGCCTAGTAACTGGAAAGTGTACATAGGTTTCGTGTCCCAGCTCAAGCTGCCCAGTCCGTATTA[T/A]GTAAAGGAAATCATTTTACATGAAAAGTACAACCCAACAACAAAAAACTATGACATCGCCTTGCTGAAACTCAATAAACCTGCCAGTGAGTTTGAGCTGCACACAGAGCTGCAAATAATTAACCCATATCCTTCTCTCCTGTTTTGCTTTTGAGTGTCTCTCATTTGGCAAAAGATTAACTTTGTGTGTGTGTGTGGTTCAGAAATATTATACAAGTAAATTTTGATCATTTGCATCTTAAAATGTTTGTTTTTAAAGATTTTCTCTTTTTTTTCCTTCTTTTTCTGATTCTTAATTTATTTATCTATGAAATATTTCTATGAAAAAATATGCTGCCTATATACTTTACACTCACTGGCCACTTTATAAGGTACATATTACATATTACTCATCGTCACGTTCAGCAAAGATGATTCAAGCTTTATGACATGGCACGTTATCCTGCTGGAAGTAGTTTTCAGAAGATGTGTTCATAAAGTGATGGACATGGACAGCAACAA
Associated Phenotype:
Not determined