ZMP
si:dkey-15f17.9
Ensembl ID:
ZFIN ID:
Description:
Putative ATP-dependent RNA helicase TDRD9 [Source:UniProtKB/Swiss-Prot;Acc:B8A4F4]
Human Orthologue:
TDRD9
Human Description:
tudor domain containing 9 [Source:HGNC Symbol;Acc:20122]
Mouse Orthologue:
Tdrd9
Mouse Description:
tudor domain containing 9 Gene [Source:MGI Symbol;Acc:MGI:1921941]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2676 | Nonsense | F2 line generated | Not yet available |
sa17024 | Essential Splice Site | Available for shipment | Available now |
sa22335 | Nonsense | Available for shipment | Available now |
sa38952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35527 | Splice Site, Nonsense | Available for shipment | Available now |
sa4512 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2676
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 |
---|---|---|---|---|---|
ENSDART00000019202 | Nonsense | 84 | 1342 | 3 | 35 |
ENSDART00000124958 | Nonsense | 84 | 1344 | 3 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31628674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31274622 |
GRCz11 | 13 | 31405072 |
KASP Assay ID:
554-2480.1 (used for ordering genotyping assays)
KASP Sequence:
AACCTTTGATTTATAGGTCCAGGAACAAGCCCTCCTTCACTGGCCAGTTA[T/A]GAGTATCCAATTCTACCAATTACTAAGAACAGACAAGAGGTACTGTACAT
Long Flanking Sequence:
TGTTCTTTCATCAGGTGACCGCATGTAAAGAGATGACTAAAACCGAGGACTCTAGAAATGAACAGATCAAATCTATTTCCGGCTCTTAATGCAGATGTTTAACTTCTGTCTTTCACGTGATGAACGAACAACTCAATCCTGATAGAAGACTTGGAAAAAAGGAACTAATCTTCGCAAATGAATGAATCCCTCCCTGAGAGGACTCATCTTTTTCGAGTCATACAAAAGATTCGTTCAAAATGCACGAATCATTCAAGAACGAACCATCACTACTTCCTAAGATGTTTTTCTGATGCTGATATTTAAAGTGGACATTAGAAAAACATTACAAAAATGCTGTTTATGAGCAATTGTATAATTCACTAAAATTGCGGTCAATAATCAAATATTGTGCTACATTTACTGGAATCTATTGCATAGCTTATATTTAAGTTTAATCTGTTGTAATACAACCTTTGATTTATAGGTCCAGGAACAAGCCCTCCTTCACTGGCCAGTTA[T/A]GAGTATCCAATTCTACCAATTACTAAGAACAGACAAGAGGTACTGTACATGCATGCATACACACAAATATATTCGCTATTCAGAAGATTTCACTATATCTCATGTCTGATTATGTTGGGTGTATTTCCCTTTTATGTGTTTATAAAAGTCCCTCTGTTTGTGTATGTAGTTGGTGTCTCTGATTGAGAATAACTCTGTGGTCATCATTCGTGGAGCGACCGGCAGTGGGAAAACCACCCAGCTGCCACAGTTCATTCTGGATCACTATGCAGAGAGAAACATACCCTGTAATCTGGTGGTCACTCAGCCTCGCAAAATTGGAGCCACAAGCATCGCCCGTTGGGTGGCACGTGAGCGCAAATGTACTCTGGGAAGCTTGGTGGGGTATCAGGTGTGAGATGCATGGCATACAATCTCTTTTCCATAACAGTATGAAAATAATATAGATATTAAATGGAATGGGAATTAATTTGCATAAGAATTTAAACTAGTGTATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17024
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019202 | Essential Splice Site | 171 | 1342 | 4 | 35 |
ENSDART00000124958 | Essential Splice Site | 171 | 1344 | 4 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31629067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31275015 |
GRCz11 | 13 | 31405465 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGGCACGTGAGCGCAAATGTACTCTGGGAAGCTTGGTGGGGTATCAGG[T/A]GTGAGATGCATGGCATACAATCTCTTTTCCATAACAGTATGAAAATAATA
Long Flanking Sequence:
CTACATTTACTGGAATCTATTGCATAGCTTATATTTAAGTTTAATCTGTTGTAATACAACCTTTGATTTATAGGTCCAGGAACAAGCCCTCCTTCACTGGCCAGTTATGAGTATCCAATTCTACCAATTACTAAGAACAGACAAGAGGTACTGTACATGCATGCATACACACAAATATATTCGCTATTCAGAAGATTTCACTATATCTCATGTCTGATTATGTTGGGTGTATTTCCCTTTTATGTGTTTATAAAAGTCCCTCTGTTTGTGTATGTAGTTGGTGTCTCTGATTGAGAATAACTCTGTGGTCATCATTCGTGGAGCGACCGGCAGTGGGAAAACCACCCAGCTGCCACAGTTCATTCTGGATCACTATGCAGAGAGAAACATACCCTGTAATCTGGTGGTCACTCAGCCTCGCAAAATTGGAGCCACAAGCATCGCCCGTTGGGTGGCACGTGAGCGCAAATGTACTCTGGGAAGCTTGGTGGGGTATCAGG[T/A]GTGAGATGCATGGCATACAATCTCTTTTCCATAACAGTATGAAAATAATATAGATATTAAATGGAATGGGAATTAATTTGCATAAGAATTTAAACTAGTGTATTGTTTATAAATTCCTCATTCCTACAGTATATATCTTGAATCCTGCAGTATAAAAATGTCAACTTTTAAAATTAAGAGTGTTAGCTATTAGACTGACTTAATGCAATAAGCATTAAGCGTTGTATAAATCTTTCTCTCTCTCTAGGTGGGTTTGGAGAAGATGGCCACAGAACACACCAAGCTGATTTATGTGACCACAGGAGTCTTACTGCAGAAATTAGTGTCATCCAAAACACTCACCGAATACTCGCACATCTTCATAGATGAGGTACACAAATAATCTGCAAGATATACAGTAATGGTAAAATGTCTGGAGTCTGCATGTTTTGAAAAGTCTTACCAAAGCTGCATGTTTAATCACAAATACTGTGAAACTGTAATATTGAGAATACTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22335
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 |
---|---|---|---|---|---|
ENSDART00000019202 | Nonsense | 495 | 1342 | 14 | 35 |
ENSDART00000124958 | Nonsense | 497 | 1344 | 14 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31633014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31278962 |
GRCz11 | 13 | 31409412 |
KASP Assay ID:
2260-6604.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTGATTTGAATTGCAGCGGTCACCGTTGGCCAGTACCTTGT[T/A]GAAGGTAAAGTTGTTGGATATGGGGGATCCTCGCTCGGTTCTCTCCACAG
Long Flanking Sequence:
ATGTTAAATACGGTGGGTGTTGCTTTTATTTATCATTCTTTAAGGTCATCTTATTGTAAGAAGTATAAATTATGCCTTGTTTTGTGTGTGTTGTGCAGTGATTGACTTCTGCCTTGTGCGTCAGTTGGCATGTGATAAGGAAACCAATTACAGATGTCTCCGTATCACATGGGCATCCAAGACCAGTTGCAACCAGCGTCGGGGTATCACTTCATTTCTTTTTAAAGGCCACTGATTCTTATTTTTTTTGTTGTCTTATTTTGATTTTGTATCTGTTCTTGTGTGTTTTCCAAGGACGTGCCGGACGAGTCTCTAAAGGCTTCTGTTACCGGTTGGTGACGAGACATTTCTGGGAGAATGAGATTCCAAATTTCTCAATTCCAGAGATGCTGGTATGGGGATGACCACGTCTATCCATAATAGCAACACTTGAGCAGATTTACATAAGTGTGTGTGTGTGTGATTTGAATTGCAGCGGTCACCGTTGGCCAGTACCTTGT[T/A]GAAGGTAAAGTTGTTGGATATGGGGGATCCTCGCTCGGTTCTCTCCACAGCCCTCACACCACCCATCCTCGGTGACATCGAAAGGACCGTCCTGCAGCTCAAACAGGTCAGTACAGTTGATTTATTTATTTTTTTTATTGAACCAGCTTTGACATTGTTGAATAAAGTTACAACGTTGAAGTTCTAACCTCACTTTAAAATTTGCATCATTCATAACGGCAAACGGAGAAAAATTTTGTATCACATTTTTGAGCATTTAGTAGTTTGATAATTTTAGCAGGATCTTGTCTAAATGCATTGAAAGTGATTCTGAAGATTTTTATTTTGGCAGTATTTTAGTATAATTTAATTATATTGCTATATATTTTAGTAATTTGTTGAATTTTCTTTTTATCATATCAGTTTCTTGTTTGTTTATATAGATTTTTATGCTTAGATTTATTTTGTTTATATAAAACTTTGTTACACTTCTACCCAGTAATAGTAATAGTTTCAGCGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38952
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 |
---|---|---|---|---|---|
ENSDART00000019202 | Nonsense | 746 | 1342 | 22 | 35 |
ENSDART00000124958 | Nonsense | 748 | 1344 | 22 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31637594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31283542 |
GRCz11 | 13 | 31413992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTCTCTCTCAGATTCGGAATTTGCCTCCGTTTGCATTCCTGTGCTA[T/A]AAGCAGCTGCAGTCACTGTTTCGTCAATGTGGACAGGTCAAGTCAATCGC
Long Flanking Sequence:
GACCACAATTCTGGTACCATTGTCTACTAACAATAGTTAGATGTAGATGGGTGTGGTGCAGTGGACTATATACACAATGCTAAGAGCTTTAATTTGAGTACAACTGTACAAATCTTATTTGTACTTTCCTGTCTTCACTGTTCTATTAAAATAATACAAAGCAATAGTTAACATATTTTTCTGTATTTATTAAAAGGTGAATAATTACTGTTATTGTGAAACAACATTTTTATATAAACATTGCTGAGCATTGTTTAGATTTTATAAATGAGTTTATAGATCACTTCCTGCATCTTTCAATGGCATAGGCAGTTAACAAGTATTGAACTTAAGAAATATAAAAATTAACTTAGACCTTTTTTTTTTTTTTAAGTTAATTTACTTTTTTTTTTTTTAAAGTTAATTTATTACATATTTATGAGCTTGTATAGAGTTGGTCTCGGCTCTAACTCCTTTCTCTCTCAGATTCGGAATTTGCCTCCGTTTGCATTCCTGTGCTA[T/A]AAGCAGCTGCAGTCACTGTTTCGTCAATGTGGACAGGTCAAGTCAATCGCCTTTGATGGATCGAGGTAACTTGAATACAGAAACACAATGTATTTTGTATGGAAAAATAAACACAACTGCAACATTATATCTAAAAATGTAAAAAAGTTGGAATTTTGTGTTTGAAATTCACAATATTGGTAATCTCAAAAATAGCAGATGTCAGAGTTTAAGTCAGAAGTACAATGGTCACTTTCACTTATGCAATGAGTAGTCAAAATTGTGACATAAGAAGTCAAAGTTACTGTTTGATTTTATTGCAGAGCTTATGTGGAGTTTCACCGCTCGTGTGTGAGGGAGTCCGGTGTGTTACATGAGGTGTTATTGGCATTGCTGAGATCACGACACACCCCTGCACTCCACCTGCAGGTGCACCATGCAGACGAGGTGGAGTTCCATGCTAAAGGAAAGCCCATTGCCCACCTGCGTTACACAAGGTACCCACAAGCTCACACAGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35527
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019202 | Splice Site, Nonsense | 863 | 1342 | 24 | 35 |
ENSDART00000124958 | Splice Site, Nonsense | 865 | 1344 | 24 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31638247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31284195 |
GRCz11 | 13 | 31414645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATCCCGAGAAACTTCCAACCAGCCGAGATTTCGTCATCAACATTACT[G/T]AGGTGAAAATACTACACATGAAAGTCCTCTCAAATAGGCTTAACCACATG
Long Flanking Sequence:
ATTTTGTGTTTGAAATTCACAATATTGGTAATCTCAAAAATAGCAGATGTCAGAGTTTAAGTCAGAAGTACAATGGTCACTTTCACTTATGCAATGAGTAGTCAAAATTGTGACATAAGAAGTCAAAGTTACTGTTTGATTTTATTGCAGAGCTTATGTGGAGTTTCACCGCTCGTGTGTGAGGGAGTCCGGTGTGTTACATGAGGTGTTATTGGCATTGCTGAGATCACGACACACCCCTGCACTCCACCTGCAGGTGCACCATGCAGACGAGGTGGAGTTCCATGCTAAAGGAAAGCCCATTGCCCACCTGCGTTACACAAGGTACCCACAAGCTCACACAGATCTGAACCAGAGATGTGTAGTTATTTAACAGAAGTCTCTCTCTCAGGGTTAACGTGGATGTTCAGAGCCACACTGTGTCACCTGTTGGAGTTCTGAGCAGCAGTGTGAATCCCGAGAAACTTCCAACCAGCCGAGATTTCGTCATCAACATTACT[G/T]AGGTGAAAATACTACACATGAAAGTCCTCTCAAATAGGCTTAACCACATGCCCTCCAACTGTTAGTCTGCTGTAAGTGAAAGATGAGAGGAGGAGCGCAAAAATACCCCCCCCCATACTTAATATTTCATTTTATTTGGAAATTGTCACGTAGGACTGCTTAAGAGGTGAAGACAAAAGGACAAGATCCAAATGCATTTAATGGTTGGATTGTCGTGCAGATAAACAGGTGGTAAAATAAGGAACATTTAAAATATTCATACAGACACAAGGTCAACTCAAATCGGGCATCCAAATGCAAAGTATTAAATAAACAAACAAAAATATAACCAGAGGCAAGGCTATGGTACACAACACATGACACAAATTAAAGTCTTATAACTGAACTAATGTGTGCAGGGTGCATATATAGTCCAAACAACCCTTGATGAAAGGTGTCAGCTGCATGTGTGTGATTAGTCGAAAGTGGACACCAGTGTGTGTATAGTGGTATGTAGGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4512
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019202 | Nonsense | 1222 | 1342 | 32 | 35 |
ENSDART00000124958 | Nonsense | 1224 | 1344 | 32 | 35 |
Genomic Location (Zv9):
Chromosome 13 (position 31644902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31290850 |
GRCz11 | 13 | 31421300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACCTGCTTTACTGGAGCTCTGTGTGGACTGGGCTGGAACTCTGTTTCC[C/T]AAGAGGCAGTGCTTCCTGAACATGACATTGAGATTGCATTTGACGTCAAG
Long Flanking Sequence:
AGAATAAATGTCAATTTCTTTATTAATGATTATGGCTAGTTTGATATGTCAAATCATATGATAAAAGTTGACTTAATTGAACCACTTTAAATTAAGTTAATATGTTTACTTAGAATTTACAAGGTGTGCACGCTCTCCCATCAAGTATGTTTTTTTAAGCTTTATAACTTGTGCTTGAGAAATGGCATACTCACCTTTACTCCCCATTTTGTGCATTTTTGAATGAAACATGGTCTTTGAATAATGATGTTCATTTAGTCTCATGAGTCACAATAATCAGTTCATGCCAACTGTACCACATTTTCACAACCACAAGGTGTTAAATCTTGTGTACAAAAAACTCACCTTACATGGTTAGTCATGAAATTGCAGGCCACACTTATACTTCATTTGAATGTAAAAATCAGCATTTAATGCATGCACACTTCCTTTGCAGTACTAATGAGGACAGGACCTGCTTTACTGGAGCTCTGTGTGGACTGGGCTGGAACTCTGTTTCC[C/T]AAGAGGCAGTGCTTCCTGAACATGACATTGAGATTGCATTTGACGTCAAGTTTGAAATTGAAGACATCACAGAGGTATGTTTTGATATACGAGTGTGCGTATTTCTGTGTGTAGGCTGAGGAGATTATTAGTGTGGCAATGAAATAAACATTCTGGAAAGACAATAATATTTGACACTGTATATGGCCAGAAAGCACAACTCAAGTAAATCAAAAATATTTAAATGTTTTTTCCAGAACATTTGACTTTGACTTTTTAACTTTAAAAAAATGTCAGTACAGCATCACTCAAGTAACTCCATTCTAAACAAAGAAACCATTCAGTTAAATAAAGCTCTACTCCAAGTACACCACACAACGGTTAATGCAAAAAACTCCCCATATATTCAGAAACACTGTACATTAAGAAACCAGGTAAATTTCCTTGTAGAATGTAGCCATTTAGGTAGAGAAGTTCACTTCAAATTACTAATTGTAAGCCAGGGGTTCTCAATCTCGGTC
Associated Phenotype:
Not determined