ZMP
si:ch211-255l12.1
Ensembl ID:
ZFIN ID:
Description:
probable ATP-dependent RNA helicase DHX34 [Source:RefSeq peptide;Acc:NP_001121805]
Human Orthologue:
DHX34
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 34 [Source:HGNC Symbol;Acc:16719]
Mouse Orthologue:
Dhx34
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 34 Gene [Source:MGI Symbol;Acc:MGI:1918973]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5915 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23373 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5915
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 |
|---|---|---|---|---|---|
| ENSDART00000086943 | Nonsense | 266 | 1150 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 42986425)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 44576316 |
| GRCz11 | 18 | 44569770 |
KASP Assay ID:
554-3804.1 (used for ordering genotyping assays)
KASP Sequence:
CCACCAAACTGCTGTTCCTCACYGAGGGMCTGCTGCTCMGGCAGATCCAG[C/T]AGGACGCGTCGCTGGGCCAGTACCAGGTGCTGATCGTAGACGAGGTGCAC
Long Flanking Sequence:
GATGATAGTAAGATTGGTGGATGGATAGTAAGATATTTAGATGGATGGATGATTGTAAGATGGATGGATGAATGGCTGGATAGTAAGATGGGTGGATGGATAGGTGGATGGATGGATAGTAAGATATATAGATGGATGGATGATTGTTTGTAAGATGGTTGGATGGATGAATGGCTGGATAGTAAGATGGGTGGATGGATAGTAAGATATATAGATGGAAGGATGATAGTAAGACGGATGGATTGATAGTATGATGGGTTGATGGACAGGTGGATGAATTGATAGTGAGATAGATGGATGGATGGATGGATGGATGGATGGAAGAAAGAAATAAAGAAACTGCAATAATATTGTAAGCTAGTTATGGGTTTATTTTAAAAATAGTGTGATCAAGTGTTTTCCCTCTTCAGGTCGGGTACCAGATCCGCTTTGAGACGAGCCGCACCCTAGCCACCAAACTGCTGTTCCTCACCGAGGGCCTGCTGCTCAGGCAGATCCAG[C/T]AGGACGCGTCGCTGGGCCAGTACCAGGTGCTGATCGTAGACGAGGTGCACGAGCGACACCTCCACTGTGACTTCCTACTGGGAGTTCTGCGCTCCCTGTTGTCTCTGCGTCCTGACCTGCGGCTCGTGCTCATGTCGGCCACCATCAACATCAAGCTCTTCTCCAGCTACTTCAATGACGCTCCTGTGCTGCAGGTGCCAGGCAGACTCTTCCCCATTCAGGTCAGTTCACTTATGATGTTCATAACATTATGTACACCAACATGACTGCTTTATACATGAATAGATTTGAGATGTAATAATTAAATTTGGCAAATATTATATCACAGTACTCAAAAACAAATATCACAGGTGCATATTTTGCCAGTATTGTGCGTTCATGCAGACTTGCAGTGTTCATGCATGTTTGTTTTTAAATTGCTGACTCTGTAAGTTTCTCATTTGCGTATATGCACAGGTAATCTACCAGCCTATTCCTCCAGAAGAGCAGGTGTCACGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23373
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 |
|---|---|---|---|---|---|
| ENSDART00000086943 | Essential Splice Site | 997 | 1150 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 43001455)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 44591346 |
| GRCz11 | 18 | 44584800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAGAGAAGCTCTGTGAGGGACTTGTGCGGTTTCTGCTGTACACTGAGG[T/C]AGTGACGTAAACACTGTAATGATGAGTGTGTATTACAACTGCATGATTAA
Long Flanking Sequence:
CCCTGATTTATCATGAGGTGCCAAACATAATTTTTACCCTTTTTCACTTCCAGCAGCAACCCATTAACTCATGAACCCCAAGGGCTGGGAAACACCCATACACTCTTTCATTTACACATACTCATACAGGCCAAGTTTATCCAATTCACTTAATTGGACTTATTTGTTTTACTTTTCTTATTTTTCTTATTTTAATCCAACTTTGAATCTCTGGCAGGCTCTGCTGCTGGTGGCCAACTCGGTGAACAGTAATGCGGACTGCACGCGGTTGGTGGTGGACGGCTGGCTGGAACTGAGCTTGACTGATGGAGACGCGGCTCTAAAGGTGCTCTCCTCGGCCCTCAGTCTGCGGGCGGAATGGGAAAGGCTGCTTCAGGCTCAGCTCAGACAGAGCGGGTCTTGTTCCTCTGCTGGATTCGGCTCAAGTGGACCAAGAGTGTCCCGCAGAGAACTAGAGAAGCTCTGTGAGGGACTTGTGCGGTTTCTGCTGTACACTGAGG[T/C]AGTGACGTAAACACTGTAATGATGAGTGTGTATTACAACTGCATGATTAATCGTTGAAAGACCCACAAAATTTGAATAATACATGATCACAGTTTGCATGTTTATTAGACGATGGCCACAGCTATACATTCAGATCTGTGTTTGACCCAAAGAGAGCATGTATGATTATTAAACTGTGGCTGTTTTATTCTGTTTAACGTTATTTTTGAGGTACAAACAATCAAATAGTCAAATATGTGTATGTGATATTGCAATAATTGAATATTTGCATGACTCTGGTTTTTTCTGATAGGTTAATTATAGTTTGAAGCGTCTAACGGCGCTGCAGTCACAGAACCTGTATATCGGACCTCAGCAGGATCCGGATCTTTCTTCAGCTGCAGCTATCGGTTCTCTGTTTCCTGGGATGAAGGCAGAACCAGATCCCATTAAAGGAGGCCTGCGTTTGTGCAGCTACTTCACATACAACTGTCTCTGTGTAAGTACTGTTGTGTTTTTTG
Associated Phenotype:
Not determined