ZMP
zgc:193690
Ensembl ID:
ZFIN ID:
Description:
ATP-dependent RNA helicase DDX19A [Source:RefSeq peptide;Acc:NP_001122187]
Human Orthologues:
DDX19A, DDX19B
Human Descriptions:
DEAD (Asp-Glu-Ala-As) box polypeptide 19A [Source:HGNC Symbol;Acc:25628]
DEAD (Asp-Glu-Ala-As) box polypeptide 19B [Source:HGNC Symbol;Acc:2742]
DEAD (Asp-Glu-Ala-As) box polypeptide 19B [Source:HGNC Symbol;Acc:2742]
Mouse Orthologues:
Ddx19a, Ddx19b
Mouse Descriptions:
DEAD (Asp-Glu-Ala-Asp) box polypeptide 19a Gene [Source:MGI Symbol;Acc:MGI:99526]
DEAD (Asp-Glu-Ala-Asp) box polypeptide 19b Gene [Source:MGI Symbol;Acc:MGI:2148251]
DEAD (Asp-Glu-Ala-Asp) box polypeptide 19b Gene [Source:MGI Symbol;Acc:MGI:2148251]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24391 | Nonsense | Available for shipment | Available now |
sa24390 | Essential Splice Site, Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24391
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102886 | Nonsense | 176 | 471 | 7 | 12 |
ENSDART00000134461 | Nonsense | 176 | 492 | 7 | 12 |
ENSDART00000146835 | Nonsense | 160 | 168 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 37202115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 37001343 |
GRCz11 | 23 | 37104005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTTCCCCCACATATGAGCTGGCTCTGCAGACGGGCAAAGTCATCGAG[C/T]AGATGGGCAAATTTTATCCGGAAGTCACACTGGCATATGCAGTTCGAGGA
Long Flanking Sequence:
ATTCATATAAACTCTGTCATCTCGTCATGATCAATCCCATGATCCCCAACGCTCCACTAGTGTTTGAAGGGGAAAGCGCAGTTGCGTTTTACTGGATCCCAATCTTCATATTTTGCGATGTCGTGTATCAACGTCGATGTGTGCAGGCGAAAGATCCGAACACAAAACGAATCATTCATTCGACTCCGAGTCTACTCTTTCCTTGAAGAATCAGTAGTTTTAAACATGGTGCACTTTCAGATTTAAACCTCAGCTGGATGTTTTCATTCACTTAGTGCTGTGTTACTGAATGGAAGGTCTGTTTTAAAATCCCATAGGGGCTCTTTAACTAAATCTGCAAAATATCTTTGCAATAACTCACAAAGTCAAAGGAATGAGTTTTCTTTTGAGCATGAGGTGTGATGTACAGTACATGTTATTAATTCACCGTGTCTGTCTTCCAGTGTTTGTGCATTTCCCCCACATATGAGCTGGCTCTGCAGACGGGCAAAGTCATCGAG[C/T]AGATGGGCAAATTTTATCCGGAAGTCACACTGGCATATGCAGTTCGAGGACATAGAAGTAAGCGTCTTTAAATAAAGCCTCTGAACCTTGTGATATGTAAATGCATGACGACTGCTGTGTTGTGTGTCAGTGGAGCGTGGCGTAAGGATCAAGGATCAGATCGTCATCGGCACACCTGGAACGGTTCTGGACTGGTGCATTAAGCTGAAACTCATAGACCCCAAAAAGATCAAAGTGTTTGTTCTGGACGAGGCCGATGTCATGATCGCCACACAGGGACACCAGGACCAGAGCATTCGCATTCAGAGGTCAGCTTTCCCTAATGTTTCAGAACGTGCTTTGACACCGAGCAAATGTGGACTGTTAAATATATGGATATTAGTTAATAATTAATAACCTGAATGTAAAACGCATTCCTTTGCAATGCCCTATTTTTAATGCTATGATTTTTTTTATCTGGAGAGGAATTCGTTTAAAATGTAAGCCCTTTCAAAATTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24390
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:
G > A
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102886 | Splice Site | None | 471 | None | 12 |
ENSDART00000134461 | Essential Splice Site | 453 | 492 | 11 | 12 |
ENSDART00000146835 | None | None | 168 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 37196946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36996174 |
GRCz11 | 23 | 37098836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCAGCGCAGCATGGAGATTCTCAAGACATACGAGAGGCATTTTGGCAA[G/A]TCTTTTTCATCATTAAAATAAATAGTTAACCCAATTTTACTTAATATTGT
Long Flanking Sequence:
ATTGGGGGAAAAAAATAAACTGGGGGGGGCTAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTACATTTATATAGATATATAGATACATACATACATAAATACATATAAAAAATACCCATGCACACGTATTTATATACATCTATATAAAGAGAGAGAGAGAGAGAGAGATTTTTTTTTTATGTGTGCACGATTAGCAGTGCTATATGGCTGTATATCAGCACTGGTGGGAGGCATGCGCCTTTCAGTTTGTAAGTCATGCATTCTGCCATGTTCCTTAATCAAGCTACTGACCCACAGGTATTGATGTTGAACAAGTGTCGGTGGTGATCAACTTTGACCTTCCCCTGGACAAAGATAGCAATCCAGACAACGAGACATACCTCCACCGGATTGGCAGGACTGGGCGGTTTGGCAAGAGAGGACTCGCCATCAACATGGTGGACAGTCAGCGCAGCATGGAGATTCTCAAGACATACGAGAGGCATTTTGGCAA[G/A]TCTTTTTCATCATTAAAATAAATAGTTAACCCAATTTTACTTAATATTGTACCTGATTTAAAATGAATAAGTTAGGGAATATTGAGCTACTCCCCAAAAAAGTAACTAGTTACTTTTAATAGTAAGAAATAAGTTACGTTACTTTTGCTTTACTTTTTCTGACCTGGCTGTGACTTATCTCTTTTAGGACTTGCCAAGTATTTTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTTTTTAAATAGAGGAGCTCTGCAATTAACAGACTGTATAACCATCATTTACCTTCATTAAAAAAAAAAGCGTTAATGGAACACATTTTTAAAAAAAAGTAATGTAGGATAATGTTATCCTCAGAGAACTTCCTGACCCCAGAGCTCTACATGCTGTATATACAGATTAATGAAAGTTTAAAGCAATGTGTTTGCTCCTTTTGTCTTATTAATAAGTAAAATCACTGTCCAATCAGATGATCCTCTTTTCCTTTTCTTCCATGT
Associated Phenotype:
Not determined