Busch Lab

ZMP

ddx49

Ensembl ID:
ENSDARG00000012899
ZFIN ID:
ZDB-GENE-031030-3
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.
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.
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