ZMP
si:dkey-119o24.1
Ensembl ID:
ZFIN ID:
Description:
probable ATP-dependent RNA helicase DHX36 [Source:RefSeq peptide;Acc:NP_001122016]
Human Orthologue:
DHX36
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 36 [Source:HGNC Symbol;Acc:14410]
Mouse Orthologue:
Dhx36
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 36 Gene [Source:MGI Symbol;Acc:MGI:1919412]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41078 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21142 | Essential Splice Site | Available for shipment | Available now |
sa21143 | Nonsense | Available for shipment | Available now |
sa14771 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41078
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 |
---|---|---|---|---|---|
ENSDART00000109467 | Essential Splice Site | 466 | 1037 | 10 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 71121715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31734146 |
GRCz11 | 18 | 31712951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAATATCATGAGAGCTGGCCCTGCTATGCCCGTACACTTAGAGATCGG[T/A]AAGTCTTTTACTTTTTTCTGTTCTAGTTTTCCTAAAAAAAATCATGCTTA
Long Flanking Sequence:
GCTCATAATCAATCATAAAGCCCTCAGGCTGCAGGAATTAGGAGGTTTGCTGAGGGTCACAGCTGTTGTGCAGTGAGAATGATTCATAAATCCATATGAAACAGTCCCTTAAAAGTCACGTCTCGCTTTCAGTTTCAGGCTTTGGCGCGTTTTGCACTCAAACACAAGCGCCAAAGCCCAAGTGAACCGCGAGCCCAATTCAGTGCACTCACTCTTCTCAAACGATCCAGGAAACGGGCCTGGGCATGGTAAAGATAGCATAGTGTGAGTAGGCCCTGTGTTGCAGCTCAATAGTCGTGGTATTGAAATTGATCACACTGAATTATGGGGTTGTCTAAATTTTAACTTTGATTCACAGATTCCAGCCACGGTACAAGCAACGTAAACCACATTATAGGAAAAGGAATAATCATGGCTCAAGTGCACGGCCTGAGAAAGGCAAAATAGAGGCCAAATATCATGAGAGCTGGCCCTGCTATGCCCGTACACTTAGAGATCGG[T/A]AAGTCTTTTACTTTTTTCTGTTCTAGTTTTCCTAAAAAAAATCATGCTTAATGACAACAATTATTTTATGCTTTGAAATGTACAAACATTCAATTAAATTATATATTTTCCAACTGCACTGTAGTAAGACACATTTGCATCATCATTTGCATTTGCATCATCAGCTAGGTTGACATACACAAGCATTTAATTTCTGTAAAAAATTTATTTACTAGTGAGGCTGATGTTAGAGTTGCTGTTATGTTATCTTTTGAAATGGCAAAATTTAGAATTGACTGTTGCAAACTGTAATGCTGCCTGACCTCTTTCTTATGTGATTGGCAGATTTTCAGACACTACCATTGAAGTGCTGGGTATGATGGATGATGATGACAACATCGATCTGGAGCTTACTGCTGCGCTGATTCGTCACATTGCGGTGAATGAGAATGTGAGTGCTTTTCCTGTGCTCATGTTTCTGTATATATGAGTGGGTTTTTTTGTGTATTGCTGTGGGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21142
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109467 | Essential Splice Site | 552 | 1037 | 13 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 71149740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31762171 |
GRCz11 | 18 | 31741078 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCATCCCTCTCCACTCTCTGATGCCCACGGTCTCTCAAACCCAAGTTA[G/A]TAAGCTGTGACCAGCTCTCTGCCTTGCACAACAACCTTAAAATGAAATGT
Long Flanking Sequence:
ACTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATGTACAGACACATGCATACATACATACATACATACATGTGTGTGTGTGTGTATTATTTGATTGAATATCACAGTAGGGTTTAACACTCACATTATGCTTTGTATTTATTAAAATACTAATAATGTTTCTGAGACATTTATTTAATCTATTTGCAAATTCTGTACATTTAATCAATGTCGTTGTTAAAAGAACAACAAAATGAATCATTGAATAATGTGGCATAGTCTGAAAGTAAAGAACTTTAAGGTATAGTGTTAGTATTACTTCCATGTCTTACCATTGACACAAAGGTTTAGAAATATTTGGCCAAAGGATTAGTCTTTATGTTTAGGTAATTATGTTTAACAAATTTTCTTGAATATCTGCTCTCTTTTAGATCGGTTTATCATCATCCCTCTCCACTCTCTGATGCCCACGGTCTCTCAAACCCAAGTTA[G/A]TAAGCTGTGACCAGCTCTCTGCCTTGCACAACAACCTTAAAATGAAATGTTTCTCTTACATCTGCCAGCAAAATTGAAATAGCTCTGTCTGAAGCCAAATACTAGAAACTTTAAAAGAGCTTTTATTTACATTAGTTTCTCTTTTTCCTCAGGTTTTCAAAAAGCCACCCCCGGGAGTGCGCAAGATTGTAATTGCTACTAACATTGCAGAAACCAGGTGTGTTTTATTTGTTTAGGTTTTTATGTGTTTGTTTTCAGCTTTTTTATCGATTGTCTTGGATGACACGATGGAAACATCATTTATCATATTTGTTTGACAATAACATTAAGTGCATTTACATTGATCATCCAAATGAGATTTATATAGGAATCACATTTCGGTGGCACAAAAAAAAGATGAAATTACAACCATACAAAAGTGTTTCGCTTTAGATGGAAATAAATGAAGACCGCGTTTAGTAACACCTACTCTAAGTCTAACATTTGTACTGTGAAAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21143
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109467 | Nonsense | 635 | 1037 | 16 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 71174191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31786622 |
GRCz11 | 18 | 31765286 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCATTTGTTTTGTTTTTGTTTGATTAGAGTGTCCCCAGGAAAATGCTA[T/A]CATCTGTATAATGGACTCAGGGCCAGCCTCTTGGATAACTACCAGTTACC
Long Flanking Sequence:
ATTTCTAAATGTATAGCCACTTCATGCTGATTGATTACAACATAAAGTGGATTTGAGTGACTCAGTGAATATTAATAGCATTTTTTAATAGTGTTTTTTTGGTGTTGTTTTTTACCATTGAAATGGTTTACAGTGTACAGTTATGCAAGTTGTGAACAGAACCATGCTTTATTATATGCGCTAAATGAATGCATTAAAGGGTTAGTTCAACCAAAAATAAAAAATGTACTCTCTATTTACTTTAATGCAAAACAAAAGATATGTAATCGTTTTGTAAATGTTTTGTACCCACCTGATACTATCTCGAAATTATTACAAATTTAATTGTTTATATAAACTTTTATTTAAGAACATTTATTAAATTACATTTAAGCAGTGGCAATTTGCATAAGTCAAACAGACTTCCCTAATAAAATCAGTATAATAATAATATTACTTGTATTTGCTACATCTCATTTGTTTTGTTTTTGTTTGATTAGAGTGTCCCCAGGAAAATGCTA[T/A]CATCTGTATAATGGACTCAGGGCCAGCCTCTTGGATAACTACCAGTTACCTGAGATCCAACGCACTCCACTGGAAGAGCTTTGCTTACAAATTAAGGTCTGAGCTTTTAAGGAAAACTAAAATTAAAAAAATTGCAGTTTCGGCATACTTTAGATCAGTCATAGAATGAATGAATGATTGATTGATTGATTGATTGATTGATTGATTAAATAAAAAAAATCTTGATAAATTTAAATGAATTAAGGTAATATATTCAGTAATTAAAATGTATAAATTAATAAAAAATATAATAATTGATTTTTATTTCACTTTTGCAGCAAAATATGGGTTGTCTTTAAAATTGCATATGTATTTACAAGCTCCCATAAATGAGCACCTCATAAAATACATATGCAATACCTACTTTACAAATATGTTTTGAACAAACACTTAAATAGTTACTTTAGATCAAACACACTTCACTGGCATTGTAAGCTTGTATGTGTGAGCTTTTCAGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14771
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109467 | Essential Splice Site | 972 | 1037 | 25 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 71254671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31867102 |
GRCz11 | 18 | 31837558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTATGATCAWATTTCACAGGTTTGATTTTTTTTTTTTTCTGAAAATTT[A/G]GGACCTGAAAAAGGAGTTGGATGTATTACTGGAGGAAAAGATAAAGAGTC
Long Flanking Sequence:
AGAAATGAAATCATACTTTTCCCCTAGGGTATAAAATATATCCAAATTAAATTGCAAGCCAGCAGGCTAATTAATAAGGGATGCCCAAACTTTTGCATAAAACTGTATTTGTGACATTATTTTGTTTGTTCTAAATTTTATTTCCAATGAATTAATTAAATGTTTTTTTTTTATAACACTTCATTGATATGTAAAAAAGATATTTGTGATTTGAGTTATTTTTTTTATAAAAACGTTTGTAAATAAAAATATATTTCCATTCTAAAGATCTTCCTCTATGACTGCACTGAGGTATCTCCATTTTCATTGCTGTTCTTTGGAGGGAATATTTCTATCCAGAGAGACCAGGACCAGGATACGATTGCAGTGGATGAGTGGATTGTGTTTCAGTCCCCAGGGCGCATTGCCCACCTTGTCAAGGTGAGCATTAACTCGACATGTTTCTAGAAAAATTATGATCAAATTTCACAGGTTTGATTTTTTTTTTTTTCTGAAAATTT[A/G]GGACCTGAAAAAGGAGTTGGATGTATTACTGGAGGAAAAGATAAAGAGTCCACATCCTGTGGACTGGAAAGACCAGCAGTCGAAAGATTGTGCAGTAATCTCTGCCATAATCGACCTCATCACTACACAGGAAACCCCTGCTGGAGACCCCTCGAAAGATAGCCAACCTGTGTATCAACGATCAGATTGTTTATTTGAATGATATTTAGGTTTGATATAGCCTGCAGACAGTGCTCTACTGTCTCGATACTGTCTGAACACAGTCTTATACTCTTTTTCAATATTTCCAGTTGTAATAACTTCCTACAGCATTAGAAGATATTTTTTTCATATTATTATTATTATTTATTGGGGTTAATTATCATATGCTATTCTAATCAGTTATACATTAAATTGTCAAAGTTTCATATATTCTGTTTTTCTATGGGGGACGGATTATTTTGATAGGCACATAAGGGACATATGGGTAAAAGGTTTAAGGTATTAACAGTATTTGCAGT
Associated Phenotype:
Not determined