ZMP
dhx16
Ensembl ID:
ZFIN ID:
Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 16 [Source:RefSeq peptide;Acc:NP_956318]
Human Orthologue:
DHX16
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 16 [Source:HGNC Symbol;Acc:2739]
Mouse Orthologue:
Dhx16
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 16 Gene [Source:MGI Symbol;Acc:MGI:1916442]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35958 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39062 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42595 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35958
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006288 | Essential Splice Site | None | 1054 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 34229739)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35075515 |
| GRCz11 | 15 | 34933484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGCATACATGTTGTTGTAAGAGAAAGCGTGTGGAGAGACAACTAAACG[T/A]AAGTTTAGCGTTTCCAGTGTTAATGTTTAAGTTTGTGAACCAGTATACTG
Long Flanking Sequence:
TACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACATACATATATATATATATAAAACGTTACTGCAATATTCTGTTTTACAAACTGTACAGACGTGTATCCCATTTTTTCCTAGTTATATGCGTTACTACACTAAACATTCTGTTGCATTAAAATTTTGTCGAAACGCAAATTTTTATAAAATAATAACATTTAAAACCCAAAGGGAAAAATAGTATAATTACATGGCCATAATACCAAACCAGCTAATAAGAGCTAGAAAATTTGTCCCAGTTAACGCCAACTACTGAACAAGAGTACTTTTCTTTCCAGTTTTCTACCTTTCGTCTTTTTTGTGTCCACGCCGGCCAAACCATGAATGGGTTTTTCTGTGACTTTTATTTTGACAGAACCAACACTGTGACCCGGAAGTCGCATACATGTTGTTGTAAGAGAAAGCGTGTGGAGAGACAACTAAACG[T/A]AAGTTTAGCGTTTCCAGTGTTAATGTTTAAGTTTGTGAACCAGTATACTGCTTGTATCGAGTCCGTATTTTTATATATATCTTCTAAGCACGTCAATAAATTAAAATAATGAATGTGCAGTGTTGACCTGCTTTAGTTGTCTGCAGTAGTCACACTTTTGGTTTTAACTTAGCAGCTAACATAGCTTCTAACGTTACTCAGGATATTTCATGTAGTCCTCATTTTCGTATGAAATAAATCACGGCTTAATTTATTAAAATACGACGTTCAAGTATTGATGTAAAGTTGGTTTTATATACGCACATTCGTTCAGTGATAACTTGTGATGTGCTCCTTATATTGTTTACCATGGTAACTTACTTTGAGAATGACTTAAAACAACATTAACACTAATTATCTGACTGTGAACAATGTTGTACTCTGTCATTGGCTGCTAATATGATTTCACTATTTAGTATTCGCAAAGAATATATGAAATCATATTATTATAGGGAGAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39062
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006288 | Essential Splice Site | 66 | 1054 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 34226780)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35072556 |
| GRCz11 | 15 | 34930525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACATTGATCAAAGAATCACAGCGTTTGCACATGAGTTGTACGACAAGG[T/A]ATGTTTTTTAAGGTCAATACACAGAATGTTAATGTAATACTTGAATTTAC
Long Flanking Sequence:
CAATCTGAGACCCACTTTAAATCAGATATCACTCAGCTAGTGGAGAGCGCTGATTTTTTTAAGAAAACAGACCTTAAACGCACCGGATTTTGCATTGGCATTCAATTCGCAGGAAGCGCTTAACCCAGGTTAATGGAAAATTAAAAGTCCTATTAGCATGCTTCGGCATACACCCCATTAGTTTGATCAAGTGTGTTAATTAGGTGTCAAACTCCGCCAGTTTAGCTTTAACCCTGTGATCTAGTAAATCTAGTTGTTATTGAAACTAACACATGTTTTTTTGTTTTTTTTTGTAGTCACAATGGCCAATCTGGAACAGTGGGTTAGTGACCAGCTCCATGACATCCTGGGTTTAAGTGACCGATATGTGGCCCAGTTCATGATCGGACTGGTTCAGAAGTCGTCTGGACCTCAGGATTTTGTGTCTCGGCTTCAGGACACTGGAACTATTGACATTGATCAAAGAATCACAGCGTTTGCACATGAGTTGTACGACAAGG[T/A]ATGTTTTTTAAGGTCAATACACAGAATGTTAATGTAATACTTGAATTTACTGTGAAAGTATAATGAGCTTCCTTTTCAGGCTCCCAAAAAGCATGTGGTTGAAAAACCTGCTCGAGCAATCGAACGTCAGGTCATGGAGATGGAGAGAAAGAACAGAACCTACACCCTTCTGGAGGACAGCGAGAGCGATGGAGAGGCAGCCAGAGAAGGAGGAAAGGAGAAGAAAAGCAAAGAACGAGACAAAGGAAAGAAGAGGAAACATCTCAGACAGAAACGAGACGAAAGTCCATCGTCCAGTGAAGAGGACAAGAAAAAGAGGTGATTATGTTCTGTCTTTTTTTGTACACTGCAGGGGTCAGCTTTTGTTGTGTTTATTTGTACTTTGAGTAAATAAGTAAATGAATGAATGCATTAGGGTTGTGCGATTTAAGGAAATATAATAAATGCTATTTTATTTATTTATTTTTTCTCTCTCCCTGATTTAATTTTGCGGTTTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42595
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 |
|---|---|---|---|---|---|
| ENSDART00000006288 | Nonsense | 364 | 1054 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 34220975)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 35066751 |
| GRCz11 | 15 | 34924720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCCAGACAAGAGCGCGAACGGCGGATCAAGGAGGAGCAGGAGAGATAC[C/T]AGCTCATTTTAGAGGAAGAGGAGATGATCACCTTCGTCAGCACCGCAATT
Long Flanking Sequence:
TGGTTCGGACCAAAGCCAGCAGTATGTTGTGAAAACGACCCAAAGACGGCAGGAGATGCAACAATGTATCATTTATTACCCTTGGTCCGGACCAAATGAAGCGAACTACAGATGTGAAAGCACCCTTAATCTACCATTTTAGGTCATTAATATGTAAAGAATAAAGTACATCCAGGTGGTTATTATCTTAAAATCTGAAACATAATTGGTTTGCTGACATATTCAGGAATTTTAAATATCTATTTTTTTAGTATTTACAATGTCATTTCTGTTGTTAAAATGATAAGTAAATAGCATAATTAAACTTGACTGTTTTCATCTTTGTCCAAACATTGCAGTCGATTCCTCAAAAAGACATGGATCTGGAGTTTGAGGAGACTCCCAGAGAGGGCGGTGGAGAGCAGGGCCGATGGGAGGAGGCACGAGTGGCCACTGCCACACTGCAGTTTGGGGCCAGACAAGAGCGCGAACGGCGGATCAAGGAGGAGCAGGAGAGATAC[C/T]AGCTCATTTTAGAGGAAGAGGAGATGATCACCTTCGTCAGCACCGCAATTACCATGAAGGGAACGCTGTCAGAGAAGGTTGACATTATTTATGGTTGTTTTTCTGTACCACTGCATCCCAAATGGCACACTATGCACTTATACACAGTGTACTTATGCACTTACTCACTCAACAGCATTCATTCGTTAGTTTTCCTTCAGCTTAGTCCCTTATTTATCAGGGGAATGAACCACCAATATTTCAGCATATGTTTCATGCAGCGGATGCCCTTCCAGCAACAACCCAGTACTGGGAAACACTCATACACACTCATTCACACTCATATACGGCGGTTTATTTCTGTTCATCCAATTCACCTTTACTGCATGTCTTTAAAACCCACACAAACACAGGGAGAACATGCAAACTGCACACAGAAATGCCAACTGGCCCAGCCGGGACGGGAACCAGCGACCTTCTTACTATGAGGCAACAGTACTAACTAATACTAATACTAGCCA
Associated Phenotype:
Not determined