ZMP
ticrr
Ensembl ID:
ZFIN ID:
Description:
Treslin [Source:UniProtKB/Swiss-Prot;Acc:Q6DRL4]
Human Orthologue:
C15orf42
Human Description:
chromosome 15 open reading frame 42 [Source:HGNC Symbol;Acc:28704]
Mouse Orthologue:
5730590G19Rik
Mouse Description:
RIKEN cDNA 5730590G19 gene Gene [Source:MGI Symbol;Acc:MGI:1924261]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa440 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa8433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa440
Status:
Confirmed mutation in F2 line
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067056 | Nonsense | 253 | 1823 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 31308426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 29875787 |
GRCz11 | 25 | 30318794 |
KASP Assay ID:
554-0292.1 (used for ordering genotyping assays)
KASP Sequence:
ACTACACTGGCATAGAGACTCTGATGGAACGTCTTGGGCTGGTTGGTGGA[C/T]AGGTGGTGCCAATGTTGTCTCCTTGTTTACCACTGATGGACCAGCATCCT
Long Flanking Sequence:
TTTAGAACAGGCCCGCGGGCACCATCTTGGTGACCCCTGCTTTAGAGTTTCCACATTTTTCTGAACTCTAGTGTGGTTAACTTTAATCAAGACTTGATATTGCAGATCCTGCAATGTGACTATTGTGGATGTGCAAACTGCAGTATTGATACTGAAATAATATGTGGTGTAGCCCTACTTTACATGTTTTAGGGTTTTTTGTACGCAAAATAATCATTTAGCAAAACGTTAAAAACCGATAGCCATTGACTTTCATAGTTTTTCATAGGATGTCAATGAATATGAATTTCCAGTGTGTTCAACAGAAAAAAAGTGTTTGGATTCGCTTAAGGGTCGTTTAGGTCTTCATTTATGGGTGAACTATCCCCTTTATGCTCCAATTTTTTAAATGACTGTTCATTTTCTCTTTTTTTTTTTTTTTTCCAAACCAGGCTGATCATGTGGCGAAGGACTACACTGGCATAGAGACTCTGATGGAACGTCTTGGGCTGGTTGGTGGA[C/T]AGGTGGTGCCAATGTTGTCTCCTTGTTTACCACTGATGGACCAGCATCCTAAAATGAACTCTTTACTGGCTTTGGGAGTGGATGCATTTCCAATAGATTCCACAAATAGCTACCTTCACTTGTCTAAAAGAATGCAGCAACAATTGTTTCCTCCACTAGGAGCATCTTTTTCCTGGATTGCAGGTAAACGTATAAAATTGGTATAGTATTTTTAAAATAGTATTTTTTATAGGGATGCTCTGATTGATCAGCCGGAGATTGGTATCGGCTGATATGATAATCACTTTTAATGATCGTATCAGTAGTCGCTGAGCTGAGGTTCGTTCTTCGTACGAGGATTGCTCAGTTAGCTTGATTTGGGTATTGACGACACGATCCAGGATTGTTTCGTTCTTCAAAACTAATCAAAGAGTTGTTGTCATAGCAACAGTTCCGGTAGCTCAAACCTGGTCTGGAGCAGGCTCATTTCATATAAACAAGATTAGATCTGCCCAGTTCAA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 4 ZFS:0000036 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Larval:Day 4 ZFS:0000036 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Larval:Day 4 ZFS:0000036 |
inner ear ZFA:0000217 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Larval:Day 4 ZFS:0000036 |
integument ZFA:0000368 |
detached from PATO:0001453 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa8433
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067056 | Nonsense | 1303 | 1823 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 31321001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 29888362 |
GRCz11 | 25 | 30331369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAATCCGGGTCCTTTCCTTTTTGCAATTCTCYATTGAAACCAAATATA[C/T]AAAAAACAATACAAAGCCCCATCCYAACACACAGAATGTGCACTCGCTCT
Long Flanking Sequence:
AGACACCCATGAAAAGCCCACTGAAGGGGATACTCAAGACTCCGATTAAAAAAAGCCTCTTGGATTGTGTTTCTCCAAATGGTGCTTGGCTGAGGAGCCCAGGTTGTAAAACACCAAAGAAGTGTGTGACATGGTCTCCATCGCCACGGAAACCTGTGCCAGAAAACCAGGTCAATGTGCCAGATTCTCCGGTGTTTGCAAAAAGACACTCACCAAGGCTGGTTACACCTGGCAAAAATAGCAGCCCAGAGGAAAAAATTGTTTTTAAAACGCCTGACAAGGTGCCCCAAAGGAAATCTAAGACATCTCCTGAAATTATTCTCAGGAGACTTGAAATTCCTGTAAATATTGACCCTGAAACATGTAAGTCTATTACGAGGTCAGGAAAGATAAGAACACTGAGCTTACCTTACAAAACAAGTAAAGGGTCAGATGAGTTTTTACCTCAGTCTGAATCCGGGTCCTTTCCTTTTTGCAATTCTCCATTGAAACCAAATATA[C/T]AAAAAACAATACAAAGCCCCATCCCAACACACAGAATGTGCACTCGCTCTGGTAACACACCCGTGAAAGAGTCTTGTTCACCCTCTAGCAACTCTCAGGGCATAACAGGTACTAGCCCTTCACCTCGTAAAAGTCTGTCTTCGACTGTAGCAAAATCAAGTCCATCACCATCCTTTGGTCCATCTAGATCGGGTGTCAGCAATCAAAATAATTCATCCATCAGTAATGTGGAAAAGCATACAGATGATAATGAATTAATTGTGCAAAACAAGGCCAACGATGAAAAAGCAGAAGAGGCATCATCTTCTGACTCCCAGCAGTTTGATTGCTCTGAATTCAGCATTACAACAGATGATGAAAGCATTGACATATCAGAGGCCGCAGTGGTGAAGACCCAGCTTGTTGGAGGCATCAAGATGAATATTGCATTCTCAAGGAAACCCTCTAAATCAGACGTTTTTGAATTTGAGGGCAAACAAACTACCTCGACTGGTACACCA
Associated Phenotype:
Not determined