ZMP
ddx49
Ensembl ID:
ZFIN ID:
Description:
probable ATP-dependent RNA helicase DDX49 [Source:RefSeq peptide;Acc:NP_938179]
Human Orthologue:
DDX49
Human Description:
DEAD (Asp-Glu-Ala-Asp) box polypeptide 49 [Source:HGNC Symbol;Acc:18684]
Mouse Orthologue:
Ddx49
Mouse Description:
DEAD (Asp-Glu-Ala-Asp) box polypeptide 49 Gene [Source:MGI Symbol;Acc:MGI:2136689]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa4404 | Nonsense | F2 line generated | Not yet available |
sa24887 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa4404
Status:
F2 line generated
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007204 | Nonsense | 162 | 468 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 6960684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 6868178 |
GRCz11 | 11 | 6878017 |
KASP Assay ID:
554-3504.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTTTTGACAGATCATGGATGAAGCTGATCGTCTTCTGGAGCAGGGYTG[T/A]ACTGATTTTACTAAAGATTTAGAGGTCATTCTCAGTGCGGTGCCAGYAAA
Long Flanking Sequence:
TTTATAGTCTATTCAAGTCTATACAAAATGTAGCATTTCAATCAGAACCTATACTCATATGTTTGAGAAATAACAAAAATAGGAGCTTAATTTTAACCTTTATTTTACATCTGCAGAGTTGTGAGAAAATCGTGATCGTTGTTTTAAACAATAAAACTGCGATTCTCATTTTTGCCAGAATGGTGTAGCCTGAATAACTGTACTGTCTAGAATCATATATGTATTAAATAGATATTTTTTTCTTTTTTCTTCCATTAGACATGGTTACTCAGGGTTTGGAGTTGTCAAAAAAGCCACATGTTGTTGTTGCCACACCGGGACGACTTGCTGATCACATTCGCAGCTCTGACACAATTAACCTGAACAGAATCCAATTTCTAGTAAGACGATCATTTTGTCTGCCTTCAAGCTTTTTTTTTAATATCAAAGCAGTTTTGATGTAATTAACGTGTCTTTTGACAGATCATGGATGAAGCTGATCGTCTTCTGGAGCAGGGCTG[T/A]ACTGATTTTACTAAAGATTTAGAGGTCATTCTCAGTGCGGTGCCAGTAAAGCGGCAGACTCTTCTGTTCAGTGCCACGCTCACAGACACGCTGCAGCAGCTGCAGAGCATCGCTATGAACAGGCCCTTCTTCTGGGAGCATAAATCAGAGTAAGACACTGTCAGACGTGTGTTAGGCGAATGAAGATATGTAAAGTGCTGAATTAATTTTTTTTTATGAAATTTGGCTTCTGCTGGTTTCAAATCAGGAACCAGAAATGTTAGTGGCTGGTGTTAGGCTTCTGGCAGTGTAAAATGTTCTTTTTCAAATAATTGCTTAACTTTTTATTACAGAAATTGACCTTAAATTATCATGATATTACTAGTTAAATTGAAACACTTTGCAATAAATTATCATTAGTGCATTTTAGTTAGTTAATTAATTAAAATCAACACTCAGAAATGGCCATATCATAGGTGTGTGTTAAAGGGAATACAAATAAATACAACTGAATTCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24887
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007204 | Essential Splice Site | 310 | 468 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 6956803)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 6864297 |
GRCz11 | 11 | 6874136 |
KASP Assay ID:
554-7791.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCTCTAATTTGGTTCTCTTTTCTGTGCTTGTTCTGTTCTTAACTGA[A/G]GGGGTTTGGATATTCCCACAGTTCAAGTTGTTATTAATCACAACACACCC
Long Flanking Sequence:
TGGTAATTTTCAAAAACCCATAATAGGGGCTCTTTAATAAATGTTCATTCTCAGTTCATGTTAGTAAATCTATAAATTAGCATTAACTAAAGCAGCCTTATTGTAAAGTGTAAAAATCATTTAAATAGTATCTAAAATGACATTGTTATGCAGTATTGTTGTTCTAATGTTCCAGGAGCTGTCAGATACTCACTATGATGCTGCGGGAATTCAATTTCCCAACCATCTCTCTGCACTCAATGATGAAGCAGGTAAGTGATGTAGTTAAAATTGATTCTTACTCCGTCCCTAATGTCTGTACTAATGCTTTTTCTCTTTTACAGAGACAGCGTTTTGCCAACCTTGCAAAATTCAAGTCTAACGTCTTCAAAATTCTCATAGCCACAGATGTTGCTGCCAGGTACAGAAAACACTTCTCAACACAACTCGCCAGTGTCTGTAATCTCTTTGCCTTTCTCTAATTTGGTTCTCTTTTCTGTGCTTGTTCTGTTCTTAACTGA[A/G]GGGGTTTGGATATTCCCACAGTTCAAGTTGTTATTAATCACAACACACCCGGTTTGCCAAAAATCTACATCCACAGAGTAGGACGAACCGCTCGAGCTGGTGAGTTTGCATATGTTAACAACATAATTGAAAGCCTGTTTGAATGAAGCAATTGTTTTTATAAGTCGTAAATCAGCCGTTATTGTTTTTCTCTAGAATAAATTATTAACAGCAGGTATTGGCTTCTACTAATAATATATACATTTAATTTGTCTAAAATCAAAATGTTCGATGTTTAATTTGCTCGTTCATATTGTTATTCTGATGCTGTGTTCACGCCAGACTCGGCACTCGTGATTAAATCCTGCTATTCTTGCGTAAATGAACATTTAGAGTTTACCCATTTCATTCATGCGTCTAATTTGCTTCATTCGTGTGTCAAATTCACTTCACAATAGAAGTGGATTCGCTTTATGGGTGGGGCTTCTGTCTACCCAGTGATACTAGCTACGTTGCTAAAT
Associated Phenotype:
Not determined