ZMP
thoc5
Ensembl ID:
ZFIN ID:
Description:
THO complex subunit 5 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6NY52]
Human Orthologue:
THOC5
Human Description:
THO complex 5 [Source:HGNC Symbol;Acc:19074]
Mouse Orthologue:
Thoc5
Mouse Description:
THO complex 5 Gene [Source:MGI Symbol;Acc:MGI:1351333]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37987 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37988 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37987
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055845 | Essential Splice Site | None | 684 | 1 | 20 |
| ENSDART00000126611 | None | None | 705 | None | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 3816238)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 3634163 |
| GRCz11 | 25 | 3759822 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAAATTCACGTTTAAATAACACAGTAGGACAAATTCAGTCAATAAAGG[T/G]GAGGTTTATGCTTTCTTTTTTATCTAGGCGTCTTATTTGAACACAACACT
Long Flanking Sequence:
ATATTTGATACGATTTCAACTTCCCCAAAGGTGAGCTTCCTTCAGGATAGCTACTTTCAAAATAAAGGTCTAATGCTGAAAGCGCAGGAAAGGTTTTAATTAAACTGTGACAATCACTATATTTTGTGCTACATATTTTCAAGAATCTAGTAATTCAAAAAAATTTAAATATCAAATTAAAATATGCACTATGCATTTGTTATTCATTTATGATGCATTAGTAACTTGAAAAGACAAAGCTTTGCAAAAAGGATTTATTCAATTTAAATGCATTACCTATTATTACATATTATTTTGATAATTTTATGTGCAGCTAATCATTTTTAGCTGAAATCGTTTTGTCGCGTTTAGAGATCTTTTATTATGTAACCAGGCAGCGGACGTGCTGTCTGTTGTTTCCTCCACGCACCAGCCTGCCCGCTTCTGCTGCATGAATGACAACGGCTAATAATTAAATTCACGTTTAAATAACACAGTAGGACAAATTCAGTCAATAAAGG[T/G]GAGGTTTATGCTTTCTTTTTTATCTAGGCGTCTTATTTGAACACAACACTATGCGTATCTTGCGTTTAAAGCTATCTGCTGTTACTTCAAGAAGCTAATGTTAACCGGATAGCAAAAAGTTAGACAGATCAGCGATGTTTTATTAATATTTATGTAGTTTCATTAATTTTTGTTATTTTTTAAATTCAAAATTTACTTTTGTTTTAAATTTGCTGTATTTAAAATGTATGTTGAGTCACAAATTATAAACAGTTATGAATTACTGCGCTATTTATTACATGCTTCATATGTAAATAAACTAATAAATGTTTATTTGTATTACTTTTGAGTATTTAAGCTATGCAATTGTAGTTTTGTTTCGTACTGTCTATTTTTTATATAGATAGATAGATAGATAGATAGATAAATTGGTTGATAGTTATTTATAGTGCTCAGCATATATAAGTACACTCCTCACAAATCTCTCTTTTAAGTTAATATTACATTTTTAATAGGAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37988
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055845 | Essential Splice Site | 323 | 684 | 10 | 20 |
| ENSDART00000126611 | Essential Splice Site | 344 | 705 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 3830963)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 3648888 |
| GRCz11 | 25 | 3774547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGATGATGAAAGTGATTCAGATGCGGAAGAGGAGCAGCAGAACACGG[T/C]CAGGCTGCGTTTTTATGTCCTCCATGTTTATTATCTTCTAGCTGATGTGT
Long Flanking Sequence:
AGGCTCGAACCTGCGACCTTCTTGCTGTGAGGCGACAGCACTGCCTACTGTGCCACTGCATCGCCTTTAAAATGCTTTAGATTATGTAATATGCATTACGCTTTAATGCTTTTGACGTTGAAACAAGCAGTGTGTTAAAACATGTAGCAACATGCTAGAATGTATTGGCGAAATGTTTAAAAATGCACAGAAATATGCTAGCAACATGATGAAACCTGTTTAAAAAAGTTGCTTAATTCTCTCAATCTGTCTGTATCGATCTAGACAAAAATCTGACTGTCAGCATCCGCGGAGACGTGGATGAAGCTAAAGCTCTTTCCAGACCGCCTGAAGACTCACAAGGTGTGTGTGTGTGTGTTCACTCTGTTTAATAAATGTTTGTGATGTTCAAGTCTTGTTCAAGTCTTTGTGAAGTTCAAGTTAAGTCTTATATTTCGCATCCGTTTCTGTCTCAGATGATGAAAGTGATTCAGATGCGGAAGAGGAGCAGCAGAACACGG[T/C]CAGGCTGCGTTTTTATGTCCTCCATGTTTATTATCTTCTAGCTGATGTGTGCTAATGTTGTCGTTTCCGCTCCGTGTGTTCAGAAGCGCAGACGGCCAACTGTAGGAGTTCAGCTGGATGACAAGAGGAAGGAGATGCTGAGACGCCACCCGCTCTCACTCGGCATCGACCTCAAGTGTAAAGGTGAGAGGAAAAGCACACAACAGGGGAGCCTTTACACTTCTGGGCTTCTCAGCACTGGAAGTTCTTATGGTTGGGTAAACTTATGCTGTGTTCACACCATACACAGCATGCATAAATAAATCACACTATTTGTGTTTAAATAGACGTGGGGTCAATTTGAGTTTACTTCATTCGCGCATCAAATTCACTTTATTCACACGTCAAATTCGCTTTGTTTGCGCGTCAAATTGACTTCACGATAGATGCGGATTTGCGTTATAGGCAGGGCTTCTATTTGCCCGGTGACTCTAGCTTCATTGCTAAATGGTTAACATAGA
Associated Phenotype:
Not determined