ZMP
zgc:77174
Ensembl ID:
ZFIN ID:
Description:
Tudor domain-containing protein 3 [Source:UniProtKB/Swiss-Prot;Acc:Q6NYG6]
Human Orthologue:
TDRD3
Human Description:
tudor domain containing 3 [Source:HGNC Symbol;Acc:20612]
Mouse Orthologue:
Tdrd3
Mouse Description:
tudor domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2444023]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35158 | Essential Splice Site | Available for shipment | Available now |
sa41916 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21978 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35158
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028955 | Essential Splice Site | 348 | 734 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 43879189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 42506474 |
GRCz11 | 11 | 42798555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAGCCCAGAGCAGCCCCAGTGGAGCAGAGCCGCCCGCCGCCCCGAGG[T/C]AAAAACCTGCAGATGGTTATAAACGAAAAATAACCAGAGAGCAACTTCAC
Long Flanking Sequence:
CAATCCTTGAGAACGCCTCAAGTGCCCAAAAATTGTACGGTGGGCTTTTATTTATAATTATATGGCATTATTTGTCTCTAATGCGAGTAGAGAAGCGAACGCTTGCCTTTTACTGGACAGAAGTCAAGTGGGTGGCTGATGTAAGCACCGATGGATAACCCCACTTGTGTTTTGTTTTGATTGCAGTCGTATTTCCGTGTTTTTGTGCTTCAGTGGTGCTCTGCGTGTTTTCTGCGTCTGTACTTTTGTCCTTGCGTGATGGATTTTAATGGAGTGCTGGATGACCCTTAAGATTTCTGTGTTCTGCTGTTTTTTTGCCTCTTCAAGGTTGATGAGCGAGCTTTGAGGGACATCATGGAGATGGGCTTTAACCGAGAGGCGGCCAGACAGGCTCTGCTAGATAACAATAATAACCTTGAAGTGGCCCTTAACCTCCTGCTAACCAGAGCAAACCAGCCCAGAGCAGCCCCAGTGGAGCAGAGCCGCCCGCCGCCCCGAGG[T/C]AAAAACCTGCAGATGGTTATAAACGAAAAATAACCAGAGAGCAACTTCACACAGGTGTCAGCATGATGCAGCACTCTTCATTTTAATGTCCAATACTGATGACATTTTAAAATTGTTCTTCATTTTTTGCCCTCCTGTGCAATACTTTTTTATTTTCCAAGCAATATTTAACAGATTAAAGACATTTTTTACTGCATTTCCTATGCTATTTATTTTGTTTTTATTTTGAACATAATTAAAGCAGTTGTTAATTTTTTAAAACCCTTTTAAGGTCAATATTATTAGCCCCCTGGAGGCTATATTTTTTTTGATTGTCTACCAAATAAGTCATCATTACAATGACTTGCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAGAATATCTAGTCAAATATTATGTGCTGTCATCATGGCAAATATAAAATAAATCAGTTAATAGAAATGAGTTATTAAAACTATTATAATTAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41916
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028955 | Nonsense | 507 | 734 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 43889926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 42517211 |
GRCz11 | 11 | 42809292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCAAGTCCAGAGAGCAGCAGGGTGCGTCTGGAAAGGAGCTTAATAAA[G/T]AGCAGGATGGCACAGGACCTGCTTCATTTAGGAAAAACCAATCAAACGGA
Long Flanking Sequence:
TAATAAATAAGTGATTATAAATAAGCAGCTAGTTACTCATTTATTGAGCTAAAAGTCTAAGTTAATGGTTTTTAATAGCATGAATTGTACCTTAAAATAAAGTGTGATTATTTTATTTCCTTCATATTTTTCTCAATAACCCTCCAGACTCAAAGCCTTCACAACAAGACCACCAAACCAAGATGAACTTCTCTAACTCTGATCAAATGTCCAGAGATGCAGGACAGTTTAAACCTCCTCCCCGAAACGATGGAAGATCACAGAGAAACGACAGACCTCCACGTTTCCAGAAAGACGGAGACTTTCCCAAACCCACCCCAGCCTCGTCCAGCTTCTCCCAGCCGCAGAAATGGAGGGACGGAGAGCGAACGGGACGAGGAGGAGGACCAGAGCGATGGAAAAACGAGAGTCAGGATGCTAGAAATGCACCGTTATCATACAACTCCAGCTTCTCCAAGTCCAGAGAGCAGCAGGGTGCGTCTGGAAAGGAGCTTAATAAA[G/T]AGCAGGATGGCACAGGACCTGCTTCATTTAGGAAAAACCAATCAAACGGACCTGCGCCACCCAAATTCTCAACCCCTGCTGATCCCAAAATGAGAAATGAGCCGAACAACAGAAGGAAAGGCAGGCCGGAAAGACCCAATTCAGGGTACTTTGAGCATTCCCAGGATGCATTGGGAAAAAAAGACTTTCAGGATGAAGGTCAGTTTGTTAAAGTGGGCCCAGTTTCAAACACGCCGCTTCCTAATGGGGATTTAGAACACAGACGAACTGGTCCAATCAAACCACATTTTTCAGCCCCGCCTCCAAGGCAAACAAATATGCATAACCCCGCCTCCAAGAGGAGATCTGGCCCAATCAAAGGTCCGAGAGACTCGGTGGACATAAATAATTTTGTGAACTGGAAAGCGGGTGATCAGTGTCTGGCGCTCTACTGGGAAGACAATAAGGTCAGTGATAGTGTGCGTTTATGCAGCCCACTTTATACTTCTTTATTTTTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21978
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 |
---|---|---|---|---|---|
ENSDART00000028955 | Nonsense | 717 | 734 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 43895523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 42522808 |
GRCz11 | 11 | 42814889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTATGAAAATTCTCTTGAGTTTCGAAGAGGAGGAGATGGACAACCT[C/T]GACGCTCTCGACCGACACAACAATATTACCAACCGCCTCGTGCAAGAGAC
Long Flanking Sequence:
CAAAAATAAGACAAATAAGACTTTCTCTAGAAGAAAAAATATTATAGGAAATACTTTGGAAAAATGTAAATAATAGGAAAATACATATTAAAAAAGTCAAAGGAAGGCGAATAATTGCGACTTCAACTGTATATTCTTTTTATAGTTTCATATATTTATTTTAATGTGATTTTATTTGTATTTTTAATTGGTTAATTTTAATGTAATATTTGTTGATTTTTTTTGTTTTCTAGTTTATTATTAAAACTATTAAAAGTGATACATTTTTATTTATTTATGTTTATTTATATCCAGCTTACTGTTGTTTTTTAGGTAGTCCTTTGAGTAACTTTTATGATACACATGTTCAAAATTGGCACATTCTAGTGATGTTGAATGATCTAATAAACAGTTTGTCTTGTGTTTGCTGCTCTCATTTCTTGTTAATTTCTCCACAGGATGATGAAGATATTTACTATGAAAATTCTCTTGAGTTTCGAAGAGGAGGAGATGGACAACCT[C/T]GACGCTCTCGACCGACACAACAATATTACCAACCGCCTCGTGCAAGAGACTGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAACCTTTCCCTAGCGTTTGATTTGCTCAAGAAAAAAAAAACAACTAATGCTCTTCTGGTAAACACAAACACACTTATGTCAGGTCTAGCGCAGGTTTACGGCTGTTACTTTAGGCCCTTTTAGCATCGTGTAGATACTGTAGAACAATATAAATGCAACATGATGTTCTCTCCCTATGCAGGTAATCATCATCTCGTTATCCACAAGTAAACGACTCTAATTGGAGAAAATGACATGCGGTTTGTATCATTATTGACGGCTGAATATATGGCAAATGCTGACAGCGTGAATGTTTCCTGAATTGTTTTGATTTGTGATTATTTTCATGGAAATGAAGCCCTAATTATTATTATTACAATTACAAAAGAAGTAAAATATTTATT
Associated Phenotype:
Not determined