Busch Lab

ZMP

tmprss13b

Ensembl ID:
ENSDARG00000077573
ZFIN ID:
ZDB-GENE-090309-2
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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