ZMP
im:7153552
Ensembl ID:
ZFIN ID:
Human Orthologue:
DHX8
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 8 [Source:HGNC Symbol;Acc:2749]
Mouse Orthologue:
Dhx8
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 8 Gene [Source:MGI Symbol;Acc:MGI:1306823]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22114 | Nonsense | Available for shipment | Available now |
sa22113 | Nonsense | Available for shipment | Available now |
sa44765 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6254 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13601 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22114
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066282 | Nonsense | 89 | 1210 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 29157934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27495543 |
GRCz11 | 12 | 27586903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCGTCTCATTCAAACAATGCGCCCTCCTGCAAAAGCATCTACCAGT[A/T]AAGGTAAGTGCATTTTGGATCAGTTTACAGAATAGCAGCTCATATTGATT
Long Flanking Sequence:
ATTGGCAGCTAATATGATTTCACTATTTAGAATTTGCAAAAAATAATTTTCTGAAATTATATTATTAAGGAGAACGTTCGAATATCTTAATATAAAATCAACCTTACCTCAATTCAGGTTAGTCCCTGATTTATCCTGGGTCACCACAGCGGAATGGACCAGCAATTAAATTTACTTGATAAATTTAACAAACCACTAAAGAAGTCTGTGTTAACAGTTCGTTGCTTTTTATGTCTTCCAGCTGAGTTTGTAATCAGTCTTGCTGAGAAAAACACAGCCTTTGATGGATTTAAGTCAGCACTGGTTAAGAATGGAGCAGATTTCACGGTAAATAATATAAATTAATCATTAAATAATATCATTGTACTAGGTTTCATAATCTTTGTTGCAGTTGTGGGACTAATTAAGCCAATTTGACCTGTCTTTTTTAGGATTCACTCATCGGCAATTTGCTTCGTCTCATTCAAACAATGCGCCCTCCTGCAAAAGCATCTACCAGT[A/T]AAGGTAAGTGCATTTTGGATCAGTTTACAGAATAGCAGCTCATATTGATTTCACCAACATTTTTAAGCGAGTCAGGCTTTTTGCATTTTTCTTGCCATATTGTGATATTAAATTATTATTGTTTTTTTTAATTGTCATGTTTTATGTGATTTTATGTTTTATGTACAGCCTCTTTTCCTGCGGCTAAGCCAAAAAATGAAAAAGACAAGCTGAAAGAGCTTTTCCCAGCTCTCTGCAGACCTGATAATCCTACTACCAGGGTACTTATTTATAATTTACCTTAATGCATACATATTTGGCTTATTTAGGTGAAAAATGTCACATTTTGGTGTCTATTCCAAGTTATAATATTATATAAATTAATTATTAATGTTATATTCATAGTAGGGCTGCACAATATATTGTTTCAGCATCGATATTGCAATGTGATCATTCGCAATAGTCACATCATGAGTATATGCAATGTTGAGTCTGGATTATATTGGATCATTTTGCAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22113
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066282 | Nonsense | 597 | 1210 | 13 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 29151227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27488836 |
GRCz11 | 12 | 27580196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCAGGGAAGACCACTCAGATCACACAATACCTGGCAGAAGCAGGATA[C/A]ACCACACGAGGGAAGATTGGGTGCACACAACCCAGAAGAGTGGCTGCTAT
Long Flanking Sequence:
GGTCTGCTATCGAGGCAGATGGTGACTGGCTTGCACATAACAACACTATCTCTGCTTCTCATATGCCCTCTGGCCTTGTATGAGCTCAAGTCTATTACTGTCTTTGTTCGTCCATAACAAATGCTTTTTCTTGTCTTCACACAGTTGACGGCAGGCAGATTGCTGCCAACATGAGGGGCATAGGTATGATGCCCAATGATATCCCTGAATGGAAGAAACATGCTTTTGGTGGCAACAAGGCCTCCTATGGAAAAAAGACGCAACTTTCTATTCTGGAGCAGAGAGAGAGTCTTCCCATCTACAAGCTGAAAGAGCAGCTCATTCAGGTGGGACTCAATAGTGATGGGGATATTTGTGCCAGATTTCAGTTTAGTTCTGTCCATATATTCAACCATTGTGTTTTTACAGGCTGTCCATGACAATCAGATCCTGATTGTTATTGGTGAGACAGGCTCAGGGAAGACCACTCAGATCACACAATACCTGGCAGAAGCAGGATA[C/A]ACCACACGAGGGAAGATTGGGTGCACACAACCCAGAAGAGTGGCTGCTATGTCTGTGGCTAAAAGAGTGTCTGAAGAGTACGGTTGTTGTTTAGGTCAAGAGGTAGGTCATTACTAGGAATGGTGAAAAATAGTTTTTGTTAAATAGTTTTTTCAATTAACAATTAAAAAAAAGTGGTCAATTCAATATTGATATTTATTTGTAAGTGGGCTTATTCTGTATTATGGAGGGCTGTGCAATTAATCAAAATTGAATAGTAATCATGATATGAAACATTGTGATTTAGCAAATCGCAAAAGGCTGTGATATGAATACTATAGAAATATAACATAAATATGGACCTGAGAACAGGTGTCTATTTCTGTGTGACTTTATTGCCAGTCAATTAAATGAGGAAAATATCGTTTTGCCTAATCAACATTGCTTAAACCATACTAGTTAATACAGCCCACCATTTAGGATGCATCAATATTAGTCAGAGAACTATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44765
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 |
---|---|---|---|---|---|
ENSDART00000066282 | Essential Splice Site | 693 | 1210 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 29147607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27485216 |
GRCz11 | 12 | 27576576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGAGAGGACCATCCACACAGACGTGCTCTTCGGCCTTCTCAAGAAGG[T/A]ACAATTCACATTTTAGACTTTGTTAGTCAGTCTCTATACTGTTCAGAATT
Long Flanking Sequence:
ATGTGTTGAAAAAAATCTTCTCTCCGTTAAACATAAATTGGGGGAAAAAATAAACGGGGATTAATAATTCAGGGGGCTAATAATTCTGACCTCAACTGTACATGCTTGTACCCGTATGCCTAAAATAAAGTGTTCTGTGATCCCTTTTAGAAATATCAATAGCCTTTGCAAGCTAGTTTTCAATTAATGAATTTGGGACAATTCGAATCATTACTCATCCCTAGTTTATACTACAAGTATTTTGACAGTATAGACAACAATTTACAAACATTTCAATATAACGTTCTGAGCATTCATTTTTGTGCCTGCACAGGTTGGCTACACCATCCGTTTTGAGGACTGCACTAGTCCTGAGACAGTCATTAAATACATGACGGACGGTATGCTGTTAAGAGAGTGTCTTATTGACCCTGATCTGGGCCAGTATGCCATCATTATGCTGGATGAGGCCCATGAGAGGACCATCCACACAGACGTGCTCTTCGGCCTTCTCAAGAAGG[T/A]ACAATTCACATTTTAGACTTTGTTAGTCAGTCTCTATACTGTTCAGAATTCTGAATGTTGGAGTATTGTTTAAAATATTGTTTAAAATACCAACTATTGTTAGTGTTTTTTTAAGGAAATTACTCTTTTACTTTCTTTTATTTTACACTGTCTTGTTTTTCTTTCCTTTTTTGATTATTTAGACTGTACAGAAACGAACTGACATGAAGCTCATTGTGACATCTGCCACACTGGATGCCGTGAAATTCTCACAGTACTTTTATGAAGCACCTATTTTTACAATCCCTGGTCGTACATACCCGGTAGAGGTTTTGTATACAAAAGAACCTGAAACTGACTATCTGGATGCCAGTCTGATCACAGTCATGCAGATTCACCTCACTGAACCTCCAGGTAAGCTTTCAAACACAATTCTACAAAACAAAATTATTAAATTTGAAAAACAGTTCCAATTAATAAAAATTATTAATTGTGCAGGTGATATCTTGGTGTTCCTGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6254
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066282 | Nonsense | 746 | 1210 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 29147266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27484875 |
GRCz11 | 12 | 27576235 |
KASP Assay ID:
554-5406.1 (used for ordering genotyping assays)
KASP Sequence:
CGTACATACCCGGTAGAGGTTTTGTATACAAAAGAACCTGAAACTGACTA[T/A]CTGGATGCCAGTCTGATCACAGTCATGCAGATTCACCTCACTGAACCTCC
Long Flanking Sequence:
GCACTAGTCCTGAGACAGTCATTAAATACATGACGGACGGTATGCTGTTAAGAGAGTGTCTTATTGACCCTGATCTGGGCCAGTATGCCATCATTATGCTGGATGAGGCCCATGAGAGGACCATCCACACAGACGTGCTCTTCGGCCTTCTCAAGAAGGTACAATTCACATTTTAGACTTTGTTAGTCAGTCTCTATACTGTTCAGAATTCTGAATGTTGGAGTATTGTTTAAAATATTGTTTAAAATACCAACTATTGTTAGTGTTTTTTTAAGGAAATTACTCTTTTACTTTCTTTTATTTTACACTGTCTTGTTTTTCTTTCCTTTTTTGATTATTTAGACTGTACAGAAACGAACTGACATGAAGCTCATTGTGACATCTGCCACACTGGATGCCGTGAAATTCTCACAGTACTTTTATGAAGCACCTATTTTTACAATCCCTGGTCGTACATACCCGGTAGAGGTTTTGTATACAAAAGAACCTGAAACTGACTA[T/A]CTGGATGCCAGTCTGATCACAGTCATGCAGATTCACCTCACTGAACCTCCAGGTAAGCTTTCAAACACAATTCTACAAAACAAAATTATTAAATTTGAAAAACAGTTCCAATTAATAAAAATTATTAATTGTGCAGGTGATATCTTGGTGTTCCTGACGGGTCAGGAGGAGATTGACACGGCTTGTGAGATCCTTTATGAAAGAATGAAATCTCTCGGTCCTGATGTTCCAGAGCTGATCATTCTCCCAGTCTACTCTGCCCTGCCCAGTGAAATGCAGACCAGGATCTTTGACCCAGCACCACCTGGAAGTAGAAAGGTACCATCTGTTGTTTCTCCATTCTTTGGTCACCTCAAACATTAATCTAGAATTCCCAGAAAATTTCTATTACATGATTTTAATTCACATTAACAAACCATTCTGCTTTTTCTGTGCTGTTCTTAGGTGGTCATTGCTACAAACATTGCTGAGACCTCTTTGACAATTGATGGGATCTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13601
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 |
---|---|---|---|---|---|
ENSDART00000066282 | Nonsense | 1060 | 1210 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 29144069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27481678 |
GRCz11 | 12 | 27573038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACAACAAGTTTTYYAACCCCTGGTGTTACGAGAACTTCATTCAAGYC[C/T]GATCTCTYCGACGTGCACAGGATATCCGCAAACAGATGCTGGGCATCATG
Long Flanking Sequence:
ACAGTTATGCTGGCTTCATACCAAATGTGAATTCATACCAAACGTGTATGCATGAGTAGATTACATACAAAGTCAATGCAAACACGGGATTAAAAGTGAATTTCTGCAGAGCGGTGCAGATGAGACCAATTTTGCAATGCATTTGCTGCGATCTTGCATAAATTTGCCTTAATCATGTCTTCTCTGCCATTTAAAAAAAAAAATTTAAATTAGTGAGGTGAAAAACATCCCGCAACTGACCTAGAGTAATTGATGTGATTCGAATGCTCTTGTCAGGTTTGTTGTGAACTTGACATTATATCATTACATAGAGTTTAAGGTATCCAAGTAGACTGATCCTAAAATGATTTCAATCTCAGGACAAACAAGCTCTGGCAGACCAGAAGAAGGCCAAGTTTCACCAGCCTGAGGGAGACCACCTGACTTTGTTGGCTGTCTATAACTCCTGGAAGAACAACAAGTTTTCCAACCCCTGGTGTTACGAGAACTTCATTCAAGCC[C/T]GATCTCTCCGACGTGCACAGGATATCCGCAAACAGATGCTGGGCATCATGGACAGGTGAGGGGATCAGAACTTTATACAGGCTTGGTTGTGCTTTTTAAATTAAATTGGATTGTGATAGGCTTTTAATATTATAAATATTTTTTTTAGCTTTTAAAAATGCGGCAATTTGCATAATCACAGCCTCTAACAACCTGTCTACACGTGACAATGCAGATTAAACCACTTTACATTTTTTAGTTAATTTGTTTTAATAAAAGAATACTTTTATCATGCAGAATATGCAAAGTTTTTTAGCATTTATATTGTACGGTGACATATATTTTAAAGCCACTTAACTAATTGAATTAATGTCAGTGAAGTGAAACATGCTGAGTACTTTCATTACCAAAAATAAAACTAATAAGAAAACGCATTTAATAAGTTTAATTTAAAAACAATATCAAGAGAAGTGATATTAAACTTTACAGAAACCCATGGCCCAAAATAATAAAATGAGATC
Associated Phenotype:
Not determined