ZMP
TDRD6 (2 of 2)
Ensembl ID:
Description:
tudor domain containing 6 [Source:HGNC Symbol;Acc:21339]
Human Orthologue:
TDRD6
Human Description:
tudor domain containing 6 [Source:HGNC Symbol;Acc:21339]
Mouse Orthologue:
Tdrd6
Mouse Description:
tudor domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:2679727]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36303 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22990 | Nonsense | Available for shipment | Available now |
sa42863 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39141 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13845 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42864
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 309 | 1388 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6376316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6455252 |
GRCz11 | 17 | 6612482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGATGGGTCTCCATGTGCAACAAAAGGTAGCGACGGGAAATGGTAC[C/T]GATCGGTTCTTCAGCAGAATGACATCTCAGATGTTGTCAAGGTCTTTCAT
Long Flanking Sequence:
CGGGTGCTTCAAAGTTCATCAGATCTTTGTGTGGGAAAAACATCTCTGGATGTGTTCAGGATGTGATAATGCCATCCCGGATCATTCTTCTTGATGTTCCAAGCATATCCAAACAAATGTATGAATTCGGGTTTGCTAAAAATACGCCTTGTAAAAATTTCAAAATCCTTGTAACGTATTCACTGCATTTGCCAAGAAGTCCCTCCATCCAAACTGACCTTTTGACTACAAATGGTCAGCAGGAGCATGCCAGTAATTCAGATAGGTTGTGGCAGTACTTGTATCCAGAGTTGTCGCCTGGAACAATTGAGATTGTAACTGTAACACAAGTTGTTCATCCATTGAAGATCTATTGCAAACTGTGTGTCTTTTCACAAGAGCTCAAGAAACTAAGCGTTCAGCTCTATGAACACTATGAAGATGCATTCTCTGCTCAAATCCCAGTACCACTGTGTGATGGGTCTCCATGTGCAACAAAAGGTAGCGACGGGAAATGGTAC[C/T]GATCGGTTCTTCAGCAGAATGACATCTCAGATGTTGTCAAGGTCTTTCATGTTGATTATGGAATTGGTGATTTTGTTAAACTCTCCAACATCAGACCATTGTCCGCAAGATTCTTCCACTTGCCTGTTGTCACCTATGGATGCTCTTTGCATGGTGTAATTGACAAAGGTGTTGGATGGCGGACAGATCAGATAGATTATCTGAAATCTGTCATACTGGATCAAATCCTTGTTGGAAAGTTCGAGCACTACAGTGTGAGTGAGGGTGTCTATTATATAACACTGTATGGAAATGACAATGTGAATGTGAACCTAACCTTTGGTCACAAAGAGCATTGTTTGGCAGTGAACGAGAAGATGTGTGGGGATCCAACTCTTGATACTCTAAACAAAGTGACATATGGCAATATGCATGGCAGAAATGATTCTCTACAATCTCTCCATTCAGCTCATTTAACTGAGTGCTCCAGTTCTGTTGAAGATGTTAATGTAGTCGGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36303
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 375 | 1388 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6376116)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6455052 |
GRCz11 | 17 | 6612282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGGTGTAATTGACAAAGGTGTTGGATGGCGGACAGATCAGATAGATTA[T/G]CTGAAATCTGTCATACTGGATCAAATCCTTGTTGGAAAGTTCGAGCACTA
Long Flanking Sequence:
CCCTCCATCCAAACTGACCTTTTGACTACAAATGGTCAGCAGGAGCATGCCAGTAATTCAGATAGGTTGTGGCAGTACTTGTATCCAGAGTTGTCGCCTGGAACAATTGAGATTGTAACTGTAACACAAGTTGTTCATCCATTGAAGATCTATTGCAAACTGTGTGTCTTTTCACAAGAGCTCAAGAAACTAAGCGTTCAGCTCTATGAACACTATGAAGATGCATTCTCTGCTCAAATCCCAGTACCACTGTGTGATGGGTCTCCATGTGCAACAAAAGGTAGCGACGGGAAATGGTACCGATCGGTTCTTCAGCAGAATGACATCTCAGATGTTGTCAAGGTCTTTCATGTTGATTATGGAATTGGTGATTTTGTTAAACTCTCCAACATCAGACCATTGTCCGCAAGATTCTTCCACTTGCCTGTTGTCACCTATGGATGCTCTTTGCATGGTGTAATTGACAAAGGTGTTGGATGGCGGACAGATCAGATAGATTA[T/G]CTGAAATCTGTCATACTGGATCAAATCCTTGTTGGAAAGTTCGAGCACTACAGTGTGAGTGAGGGTGTCTATTATATAACACTGTATGGAAATGACAATGTGAATGTGAACCTAACCTTTGGTCACAAAGAGCATTGTTTGGCAGTGAACGAGAAGATGTGTGGGGATCCAACTCTTGATACTCTAAACAAAGTGACATATGGCAATATGCATGGCAGAAATGATTCTCTACAATCTCTCCATTCAGCTCATTTAACTGAGTGCTCCAGTTCTGTTGAAGATGTTAATGTAGTCGGACCTTCCAAAGCTGAAGGAAACCTACAGTCTACAAAGGGAGGCTACACACTGAATGCTGCAACAACTTCACCTCTTCAGACCGATGCATATGTCGATGTACCACCCAAAATTAAAGTGGGTGCCAAGATGAAGCTACACATAACCTGTGTGCAAAGCGTGAACCAGTTTTATGGCCATTTTGCACAAAATACTGACGCCGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22990
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 |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 531 | 1388 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6375648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6454584 |
GRCz11 | 17 | 6611814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAAGATGAAGCTACACATAACCTGTGTGCAAAGCGTGAACCAGTTTTA[T/A]GGCCATTTTGCACAAAATACTGACGCCGTAACAAAAATGACCAAAGATAT
Long Flanking Sequence:
GGTGTTGGATGGCGGACAGATCAGATAGATTATCTGAAATCTGTCATACTGGATCAAATCCTTGTTGGAAAGTTCGAGCACTACAGTGTGAGTGAGGGTGTCTATTATATAACACTGTATGGAAATGACAATGTGAATGTGAACCTAACCTTTGGTCACAAAGAGCATTGTTTGGCAGTGAACGAGAAGATGTGTGGGGATCCAACTCTTGATACTCTAAACAAAGTGACATATGGCAATATGCATGGCAGAAATGATTCTCTACAATCTCTCCATTCAGCTCATTTAACTGAGTGCTCCAGTTCTGTTGAAGATGTTAATGTAGTCGGACCTTCCAAAGCTGAAGGAAACCTACAGTCTACAAAGGGAGGCTACACACTGAATGCTGCAACAACTTCACCTCTTCAGACCGATGCATATGTCGATGTACCACCCAAAATTAAAGTGGGTGCCAAGATGAAGCTACACATAACCTGTGTGCAAAGCGTGAACCAGTTTTA[T/A]GGCCATTTTGCACAAAATACTGACGCCGTAACAAAAATGACCAAAGATATTCAACAGCTGTGCCGCAAACGTCCACAAGCAAAGTTTTCAATTTCCCCGAAGATGATGTGTCTTGCTAAATTTTCAGATGGGCAGTGGCACAGAGGACAAATTGAATCTGTGCATCCAAAAATACTTGTCCAATTTGTAGACTACGGTGACCTGGTGGTTGTCGATAAATCTGATATTCTACCATTTCCTCCAAATGCGAATGCAATTGCATCTCTTCCCATTCAGGCTGTTCAGTTTGAACTTTTCAATGTAGCATTACCTGAGCCGTGTGAGCTTAATGAGTGGTTCAAAAACTACGCCACAGACTGCATGTTCAATGTAGTTGTGAAGCTAAATTCTTCAGGCAAACTGTCAGTGGAGATGTATGATGACAAAACAAACCTCAACTTAAAAATTAAAGACCTGTGGAGCAAGACCAAAAGAAACGAGTCAATCAACACCAAAGGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42863
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 788 | 1388 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6374144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6453080 |
GRCz11 | 17 | 6610310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCACAAGAAATTGGAAACAGTAGTCACACGAAAGCAATCCAGCCAGAT[C/T]AGTTACGCCAAGGTGGAATTTGTTTGGCTCGCTTTTCTGACCAGCTCTGG
Long Flanking Sequence:
TTATTGACTTTGGGAATGAAGTGACACTCCTGCCCACTAAAATAAAGCAACTTGACAAGCAGTTCCTTAGCACTCCCAGGCTCAGTATTCAATGCATGCTTGAGGATGGAAAGAGACGAGGAAAAAGAGACTGGACCCAGGAGGAGATAATGACTTTCAAAGAGGCAGCAGGTGAAAATGGTGAAAAGAAAATTCAATGCAAGTTCATTCAAGAAGATGCAAATTGTTGGCTTGTAAGTTTAGAACACCAGGAAGGATGGTTTACTGTCAAATCAGATGCTCAAAGCGAATCCCAAGTACACTGCATTAAAAATACCCAGCCTTTAACTTTCAAGAAGCCAGCTGTAACTCCAGGACAAACTGTAGAGGCATATGCTTCATCTATCGTCGGACCAAATTACTTCTGGTGCCAGTTCAAAAACTCAGAGATTCTTGACAAAATCTCACTGCTTGCACAAGAAATTGGAAACAGTAGTCACACGAAAGCAATCCAGCCAGAT[C/T]AGTTACGCCAAGGTGGAATTTGTTTGGCTCGCTTTTCTGACCAGCTCTGGTACAGAGCACAGGTTATCAATACCCATGAAAAGGTCTCTGTTCTTTTTATAGATTATGGAAATGAGTCTGAAATTGATTTTAACTCCATAAAGGCCCTGCCAACCAAGCTGCTGGAAAGCCCACCACAAGCCTTTCTATGTCAGTTGCAAGTTTTGGGGTCTGTAGAGGGCACATGGAGCGACAGTGCAGCTGATAAATTCTTTGAGATTCTAGTGGATGAACCTTTAAAAGTGACTGTTCAGAATATGGTGGTGACCCCTAACCCTACAATGTGTCCTCAGTTTAGTGTCCTTGTTGAATGCAAGGAGCTGATCGTTAATGATCTTATGAAAGATTTCTTGTCTGATCCCAAACCTCAAGTCTCTAGTAAGGGGTCCATGGCAAAAACCAATGCAGGGAAGGACGATTTTGGTGTAACTAACTCTGAAGCTGTCCAGAAAAATAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39141
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 1120 | 1388 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6373146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6452082 |
GRCz11 | 17 | 6609312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGACGAACATCTGCTGTCATACCCAAGGTTCAGCATTCACTGCAGCTA[T/G]AGTTTAAATGACCAATTCAAGGGAATGAAGAAGCAGGAAATTCTCTTCAA
Long Flanking Sequence:
ACACCCAACCTTAACTCTAGTACAACACCATCAATTGATGATGTCAACAATTCAGCAGCATTGACCACAGGTGTAAACATGATGGATCCTGAATCAATGCAGTCTTTTCCTCGATCTGTAGATCTTCCCCAACGTGTGATACAACCAGGTACAATGTCTGAAGTATATATTTCACACATCAATAACCTGAGAAGTTTTTACGTGCAACTCAAAGAGGATGAGAATACGCTCTTCTCCCTCACCGAGTCATTGAATTCCCATCAACCATCAGAGAAAGATGAAATGCATGGATTGAGTGTTCAGCAGGGAAGTTTGGTGAAAGCCATGTTTCCTGAAGATGATTCCTGGTATCGTGCTGTTGTGAAATGTGCTCCTGAAAATGACATGGTCTTTGTAGAGTTCATAGATTTTGGCAATGAGGCAATGGTTTCTTCCCTTAAAATTTGCAGACTTGACGAACATCTGCTGTCATACCCAAGGTTCAGCATTCACTGCAGCTA[T/G]AGTTTAAATGACCAATTCAAGGGAATGAAGAAGCAGGAAATTCTCTTCAAAGAAGTGCTTGGTGGAGCTGGTGAAAACACCCTCTCTTGCAGTTTTATCAAAAAAGATGACATTGCTTGGGAAGTTACAATGACTCCCTGTGAAGGCACATCTGATTCGTTCAGTAAGAAATGGGATCAGTTAGACTTGAATGCATTATCAGTCGTCACCAAACCAGTTAAGGAGACATTCAATTTTCTTTTCAAGAAACCAGATGTTTCTTTGGGACAAACCATTGAAGCTTTTGCGTCATGCATTGTTGGACCTGATTATTTTTGGTGCCAGTTTTCGAACTCTGAAATACTTGACCACATCACACAAGTTGCTCAAGAATGTGGAAATTCCAGTGAAACGCAGCCAATTCTACTGGATAATTTGGATTCTGGAAGTCCATGCCTGGCTCGCTTTTGTGATGACCAGATGTGGTACCGTGCACAAGTTATTAAGAAGTGCACAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13845
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129555 | Nonsense | 1338 | 1388 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 6372494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6451430 |
GRCz11 | 17 | 6608660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGTGTCGGTTGGAAGGATTTAATCCCTCTGGAGGATYGTGGGATAGT[G/T]AGGCTACTGATAACTTCTACGAACTCTTGGTGGATAAACCTCTGAAAGTG
Long Flanking Sequence:
CTGATTCGTTCAGTAAGAAATGGGATCAGTTAGACTTGAATGCATTATCAGTCGTCACCAAACCAGTTAAGGAGACATTCAATTTTCTTTTCAAGAAACCAGATGTTTCTTTGGGACAAACCATTGAAGCTTTTGCGTCATGCATTGTTGGACCTGATTATTTTTGGTGCCAGTTTTCGAACTCTGAAATACTTGACCACATCACACAAGTTGCTCAAGAATGTGGAAATTCCAGTGAAACGCAGCCAATTCTACTGGATAATTTGGATTCTGGAAGTCCATGCCTGGCTCGCTTTTGTGATGACCAGATGTGGTACCGTGCACAAGTTATTAAGAAGTGCACAAACACAGTATCTGTACTTTTTGTTGACTTTGGAAATGAGTCTGAAGCCAGTGAAGGTTCTGTAAAAGCACTACCTTGTGACTTGCTGGAAAGTCCACCTCAAGCTTTCCTGTGTCGGTTGGAAGGATTTAATCCCTCTGGAGGATCGTGGGATAGT[G/T]AGGCTACTGATAACTTCTACGAACTCTTGGTGGATAAACCTCTGAAAGTGAGTGTGCAGTGTATTGATGATTCAGTGGAACCTAACAGTCCTCCATATTATGTTAAAGTTGAGTCTTCGCAAAGTCTTGTAAATGAGCTCATGGCAAAGTTTTGGAGTAATTGCACTCACCATGATCAAAACTCTGCTGAGGTGATTGAATCCTGTGAAAAAGATGTGGGATCAGCACCTGTTGATCAGTCTATTTCAGAGGATAAAACAAGTGAGTGTCTTGCGATCTCTACTGAGGATAATCACACAAGTGTACCTACCTGTCCTGAACTACACAGAGATAATCCATTGATGGAAAATGGTAACTTGCATAATGTACCTGAAAACGAAGTGGATGATAAGATTGTTGGAGCAGATGTGATTGCTACTACAACAAATTCTGATGTTGCTGCTAATGATCCTGCAAATTCAGATTTGGAAATTCAAGAAGGTTATCATGAGCCTGACGGA
Associated Phenotype:
Not determined