ZMP
tysnd1
Ensembl ID:
ZFIN ID:
Description:
peroxisomal leader peptide-processing protease [Source:RefSeq peptide;Acc:NP_001122182]
Human Orthologue:
TYSND1
Human Description:
trypsin domain containing 1 [Source:HGNC Symbol;Acc:28531]
Mouse Orthologue:
Tysnd1
Mouse Description:
trypsin domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1919017]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5862 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12043 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5862
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110157 | Essential Splice Site | 393 | 521 | 3 | 4 |
ENSDART00000124122 | Essential Splice Site | 393 | 565 | 3 | 5 |
ENSDART00000146097 | Essential Splice Site | 393 | 521 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 30362488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30008436 |
GRCz11 | 13 | 30138886 |
KASP Assay ID:
554-3830.1 (used for ordering genotyping assays)
KASP Sequence:
AGTGTTTTTATCCCTGTGMAGCGGCTGACATATTGCTGTTGKGTTTGCTT[A/C]GGTGAGGATGTGGTYGTTGTGGGTTATGGAGCTTTAGGGAGCCGCTGCGG
Long Flanking Sequence:
GGGATGTTATGAGCTAAATAAAATCTAAATTACTACATATAAATGTATTATGAGGTAAAATTTAAATCAAAGTTAATACAAAAACAATGTAGATCATAAAGCCTTAATTATGAGTTTAAAAATGTTATAATTGACAAAAAAGGACCAGTACGAGACTTGTCAGTGTCACATTAATAACTTGGTATTAATCTAAGTGTATCTTATTATTTTTTATAATCATTAGGATTTGACTTTAACTGGGTATTTCATAATTTGACTGTATATCACAATATGGCTTCATTTAATTGTATATGACACCTCATTTTTATCAAGTTGTATACTCATTTTCCTCTTAGAATTATGTGGCATATCATCATTTTAACTTTTTATTAAATCTTTTAATATGTCATAATTTCGCTTTGTCAATTTTGCCTTTTTTTTCTCTCATAATTTAGAATTTGTATTCAACAAAGTGTTTTTATCCCTGTGAAGCGGCTGACATATTGCTGTTGTGTTTGCTT[A/C]GGTGAGGATGTGGTTGTTGTGGGTTATGGAGCTTTAGGGAGCCGCTGCGGCCCATCACTGACCTCAGGTATCTTATCCAGAGTCATTACCCATCAGTCTCAGCCTGTGATGCTGCAGACCACATGTGCAGTGCAGTCAGGAGCCAGCGGAGGTGCTGTGATTCGTTCTGACACCGGGGAATTACTAGGTAATCAGGGGTCTGATTTCTAAAATTTGCATAGAAAACTTCCTAAAAGTGAACAAACACTAGAATAAATTTAGGTGTATTTATTAATAATGAATTATGGCTCAGATAAGGCTCATATAATTATTTAAAGTAGTTCAATCAAGTCAATATTTAATTTAGATATGTTTACTTAGAATTTACTGCGTACAATCTCCTGTCAAGTTTGTTTTTTATAGATAAAAACATTGCGTGGGACTGGTGCACACACATTTCCACCCCGTAAACCATGTATAAAATACTACAAAAATATTACAGATACAGTTGAAGTCTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12043
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 |
---|---|---|---|---|---|
ENSDART00000110157 | Nonsense | 470 | 521 | 4 | 4 |
ENSDART00000124122 | Nonsense | 470 | 565 | 4 | 5 |
ENSDART00000146097 | Nonsense | 470 | 521 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 30359784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30005732 |
GRCz11 | 13 | 30136182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAGGTATTGTGTCCAGCAACACTCGAGACTATGCAGCAAAAGTGACGTA[T/A]CCACACCTGAACTTCAGCATCCCGGTGACTCTTCTGGAGCCTCTGCTCAG
Long Flanking Sequence:
ACAAATGCATTAATAAAATCCAAAGTTGTGCTTGTTTACATTAGTTAATGCACTGTGAGTAACATGAACGAACGCTATTTAACTTAACATTAACTCACAAAGATGAATAAATACCAAAATATATCTGTTACTAATAATTTATGTTAGGAAATACATAATCTACATTAACTAATGGATCATTATTTTAAAGTGTAACCATGAAATTAACTAATCATTTTAAAGCACCTAGTTTACTTGCTTTTCTAAAGTAAAGTGAACTAAACGCTTTTTACAGTGTAGTAGAGATTAAATATACAATAATTTCTCTAGCCAGAAGGCGGCGCCACATGACCATTAAATATTTTTCTTGAATCACAGCAAACCAGTCCTCCTGACAATATCTTGACTAAATCACGTGTTCATGAGCAGAATTATACTTAAATATGCTGTTTTATCTTATATATCCTATTATTAGGTATTGTGTCCAGCAACACTCGAGACTATGCAGCAAAAGTGACGTA[T/A]CCACACCTGAACTTCAGCATCCCGGTGACTCTTCTGGAGCCTCTGCTCAGACGCTTTGCTCAAACTGGAGACGCTGCTGTGTTTAATGTCTTAGACAGTGCAGTGGAGGATGTGAGGAAGGTATGGAGACTACAAAATATTCAGAGCAAGCTTTAATCAGTCCCCAAAATATACTACTAATAAAATAAATATGCAGATGGTATAAACTGTGATGCTTAAGATAGAAAAAATGAATTAAAAAGCGATAGAATTATATTTAAACAAAGTTATGTGTATAAGTTTGATTAAAGCTCACAGAAAATCAGACTTCAATTCCTTTTGCTGCCTAAACTGAGCTTTTATTAGACACATGCAAGTGATCATAATGACTGGTCAGTGTAGGTTAAAAAATGCTGTTGACATTCTTCAGCCGTAAACAATTATGTATTATTTTATAAAACGATTTAGGATATAAATGTTTATAAATTCTTAAACAGTTTAACGAAATAAAAATATGTTTG
Associated Phenotype:
Not determined