ZMP
si:dkey-30j22.9
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RHL8]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9787 | Nonsense | Available for shipment | Available now |
sa43494 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3060 | Nonsense | F2 line generated | Not yet available |
sa23764 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9787
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102504 | Nonsense | 266 | 1281 | 1 | 3 |
ENSDART00000124497 | Nonsense | 281 | 1623 | 1 | 2 |
ENSDART00000141627 | None | None | 337 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 35470906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35543419 |
GRCz11 | 20 | 35446298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGTTTTCTCTCAGGAGCTGAAAAAGTTGACTGAACAGATCACTCAGTA[T/G]TACGAGGGAAGAGTAGGAAGYTATTTTGCAAGAGCTGAGARTTTGGGCAG
Long Flanking Sequence:
AGTGACTTTTTCTATCTTCCTCCTGAAGTTGAATTCTGCATTCTTGCCAATGCCTTACCACTATCTCCTGAAAACAATTGGTCCTCAATGGCCTTAGAGTTTATGAAGACCTTCTGTGGTCGAAGAGTCAATGCCACCGTTCAAGATGTTCTTGTAGCTCATCGAACATTCCTTCTTGACATTCCTTGTCTGTCAAGGCAGATGTTTGAAATGGGCTTTGCAAAGAAATTGTACAGTGATCAGTTCATGGAGTTTGTTGTGAGATCTTTGCAGGCCAGCACCGGAACTAGCGATCTTAAGAGAATTTCCTCCATTAGAACCAAACCAGTTGAGATCATTGAGCAAAAGGAAAAGCAGCAGGCCTACATGTTTCCTGAGCTGCAGACCGATACTGTAGAGACTGTTGTTATCACTGAGGTAACAAGTCCATTTCGAATATTCTGTCAGCTTAAGGTTTTCTCTCAGGAGCTGAAAAAGTTGACTGAACAGATCACTCAGTA[T/G]TACGAGGGAAGAGTAGGAAGCTATTTTGCAAGAGCTGAGAATTTGGGCAGCCCATGTGCATCAAGAGGAAGTGATGGCAAATGGTATCGTTCTGTGCTGCAGCAAGTCATGTCTGCAAACAATGTGGTTGAGGTTTTGCATGTGGATTATGGGAAGAAACAATTTGTACAAGTTGAGAATGTCAAGCCACTTGCCTCTGAATTCTTCAGAATGCCGGTTGTAACATATGTTTGCTCTCTGCATGGAATTGTTGACAAAGGTGTTGGTTGGACTGCTTCACAGATTGACTACCTGAAATCTCTGTTGCTCAATCGCACAGTGATTGCCAAGTTTCAGTATCAAAGCCTTTCTGAGGGTGTCCACTATGTAACACTTTATGGAGAGGAGAACACAAACATAAACAAATTGTTTGAACTGAAACCAAAATGTTCACTGGACTCTGACATGACTCTTGCAGATTTCGCTGTTCAGAAGAGCCCATCATCTCAGAAGAGCAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43494
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 |
---|---|---|---|---|---|
ENSDART00000102504 | Nonsense | 281 | 1281 | 1 | 3 |
ENSDART00000124497 | Nonsense | 296 | 1623 | 1 | 2 |
ENSDART00000141627 | None | None | 337 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 35470950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35543463 |
GRCz11 | 20 | 35446342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTATTACGAGGGAAGAGTAGGAAGCTATTTTGCAAGAGCTGAGAATT[T/A]GGGCAGCCCATGTGCATCAAGAGGAAGTGATGGCAAATGGTATCGTTCTG
Long Flanking Sequence:
TGCCAATGCCTTACCACTATCTCCTGAAAACAATTGGTCCTCAATGGCCTTAGAGTTTATGAAGACCTTCTGTGGTCGAAGAGTCAATGCCACCGTTCAAGATGTTCTTGTAGCTCATCGAACATTCCTTCTTGACATTCCTTGTCTGTCAAGGCAGATGTTTGAAATGGGCTTTGCAAAGAAATTGTACAGTGATCAGTTCATGGAGTTTGTTGTGAGATCTTTGCAGGCCAGCACCGGAACTAGCGATCTTAAGAGAATTTCCTCCATTAGAACCAAACCAGTTGAGATCATTGAGCAAAAGGAAAAGCAGCAGGCCTACATGTTTCCTGAGCTGCAGACCGATACTGTAGAGACTGTTGTTATCACTGAGGTAACAAGTCCATTTCGAATATTCTGTCAGCTTAAGGTTTTCTCTCAGGAGCTGAAAAAGTTGACTGAACAGATCACTCAGTATTACGAGGGAAGAGTAGGAAGCTATTTTGCAAGAGCTGAGAATT[T/A]GGGCAGCCCATGTGCATCAAGAGGAAGTGATGGCAAATGGTATCGTTCTGTGCTGCAGCAAGTCATGTCTGCAAACAATGTGGTTGAGGTTTTGCATGTGGATTATGGGAAGAAACAATTTGTACAAGTTGAGAATGTCAAGCCACTTGCCTCTGAATTCTTCAGAATGCCGGTTGTAACATATGTTTGCTCTCTGCATGGAATTGTTGACAAAGGTGTTGGTTGGACTGCTTCACAGATTGACTACCTGAAATCTCTGTTGCTCAATCGCACAGTGATTGCCAAGTTTCAGTATCAAAGCCTTTCTGAGGGTGTCCACTATGTAACACTTTATGGAGAGGAGAACACAAACATAAACAAATTGTTTGAACTGAAACCAAAATGTTCACTGGACTCTGACATGACTCTTGCAGATTTCGCTGTTCAGAAGAGCCCATCATCTCAGAAGAGCAAGATTTCAAGGACAACCGAGAGCACACACATTAACGAGACCTACTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3060
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 |
---|---|---|---|---|---|
ENSDART00000102504 | Nonsense | 380 | 1281 | 1 | 3 |
ENSDART00000124497 | Nonsense | 395 | 1623 | 1 | 2 |
ENSDART00000141627 | None | None | 337 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 35471246)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35543759 |
GRCz11 | 20 | 35446638 |
KASP Assay ID:
554-2708.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTGAAATCTCTGTTGCTCAATCGCACAGTGATTGCCAAGTTTCAGTAT[C/T]AAAGCCTTTCTGAGGGTGTCCACTATGTAACACTTTATGGAGAGGAGAAC
Long Flanking Sequence:
AGCAAAAGGAAAAGCAGCAGGCCTACATGTTTCCTGAGCTGCAGACCGATACTGTAGAGACTGTTGTTATCACTGAGGTAACAAGTCCATTTCGAATATTCTGTCAGCTTAAGGTTTTCTCTCAGGAGCTGAAAAAGTTGACTGAACAGATCACTCAGTATTACGAGGGAAGAGTAGGAAGCTATTTTGCAAGAGCTGAGAATTTGGGCAGCCCATGTGCATCAAGAGGAAGTGATGGCAAATGGTATCGTTCTGTGCTGCAGCAAGTCATGTCTGCAAACAATGTGGTTGAGGTTTTGCATGTGGATTATGGGAAGAAACAATTTGTACAAGTTGAGAATGTCAAGCCACTTGCCTCTGAATTCTTCAGAATGCCGGTTGTAACATATGTTTGCTCTCTGCATGGAATTGTTGACAAAGGTGTTGGTTGGACTGCTTCACAGATTGACTACCTGAAATCTCTGTTGCTCAATCGCACAGTGATTGCCAAGTTTCAGTAT[C/T]AAAGCCTTTCTGAGGGTGTCCACTATGTAACACTTTATGGAGAGGAGAACACAAACATAAACAAATTGTTTGAACTGAAACCAAAATGTTCACTGGACTCTGACATGACTCTTGCAGATTTCGCTGTTCAGAAGAGCCCATCATCTCAGAAGAGCAAGATTTCAAGGACAACCGAGAGCACACACATTAACGAGACCTACTCTGACCTTAAAGTGAACAAACCTGTCTTTTTCACAGAAACTCTCACACCTAACTCTACACACATGGCTGTTGTGCAGCATGTTGACAGCCCTGGAAAGTTTTGGATTCAAACACAGCGTTATGCTGATGAGTTCGATCTGCTAATGAATGGCCTTGGAAATCTGTACAGTGATCCAACAAGCACTGAATCATTGATTAGAAAGCCTGTTGTTGGTCTCATCTGTGCAGCTAAAGCACAAGATGGTGTGTTCTACAGAGCGGCTGTCTATAAGGTGATTGACAAGACAGCAGAAGTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23764
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 |
---|---|---|---|---|---|
ENSDART00000102504 | Nonsense | 546 | 1281 | 2 | 3 |
ENSDART00000124497 | Nonsense | 567 | 1623 | 2 | 2 |
ENSDART00000141627 | None | None | 337 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 35471792)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35544305 |
GRCz11 | 20 | 35447184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTTCCTCGACTATGGCAACACAGAAGTTGTTGATAGTTTTAACCTT[C/T]GACAGCTGCCTTTAAGATTCCAGCAGCTACCAGCTGTGGCAGTAAAATGC
Long Flanking Sequence:
AGAACACAAACATAAACAAATTGTTTGAACTGAAACCAAAATGTTCACTGGACTCTGACATGACTCTTGCAGATTTCGCTGTTCAGAAGAGCCCATCATCTCAGAAGAGCAAGATTTCAAGGACAACCGAGAGCACACACATTAACGAGACCTACTCTGACCTTAAAGTGAACAAACCTGTCTTTTTCACAGAAACTCTCACACCTAACTCTACACACATGGCTGTTGTGCAGCATGTTGACAGCCCTGGAAAGTTTTGGATTCAAACACAGCGTTATGCTGATGAGTTCGATCTGCTAATGAATGGCCTTGGAAATCTGTACAGTGATCCAACAAGCACTGAATCATTGATTAGAAAGCCTGTTGTTGGTCTCATCTGTGCAGCTAAAGCACAAGATGGTGTGTTCTACAGAGCGGCTGTCTATAAGGTGATTGACAAGACAGCAGAAGTTTACTTCCTCGACTATGGCAACACAGAAGTTGTTGATAGTTTTAACCTT[C/T]GACAGCTGCCTTTAAGATTCCAGCAGCTACCAGCTGTGGCAGTAAAATGCTCTTTACATGGTGTTAAACCCAGATTGAAACTCTGGGAGGAGAGAGCTACGTTGTTCTTTTCAAAACTTGTCAGAGACAGAATCATTGATTTGCATGTACAGGACAAACAACAAGACACTCACATTGTTCAGTTGGTGGACCCAAGTTTGGATGGAGAAAAGGATGTGAGCAAGTTATTGTGCAATGCAGGTTTTGCTGTAAGTGAAAAGAGCATTGTGGATTATTCAGCTACAAGATCTTGTGGTTTGAAAACCACCCATGCATCTGGCGTATTCTTGACAGGCACTCAACCCCAAACACCTTGCAGTTCTTCTGTTGTAATGGACAGTGCATCTGCTTTCAAGGAGTACTTGTTTCCAATTGGAAGTTCACTGGAAGTAACTGTGTCCTACATTGAGAATCCAAATGACTTCTGGTGTCAAAAGGCCAGAAATGCAGCATGCTTAGAA
Associated Phenotype:
Not determined