ZMP
tacc3
Ensembl ID:
ZFIN ID:
Description:
transforming acidic coiled-coil-containing protein 3 [Source:RefSeq peptide;Acc:NP_997746]
Human Orthologue:
TACC3
Human Description:
transforming, acidic coiled-coil containing protein 3 [Source:HGNC Symbol;Acc:11524]
Mouse Orthologue:
Tacc3
Mouse Description:
transforming, acidic coiled-coil containing protein 3 Gene [Source:MGI Symbol;Acc:MGI:1341163]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14332 | Essential Splice Site | Available for shipment | Available now |
sa38959 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14332
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002750 | Essential Splice Site | 98 | 942 | None | 17 |
ENSDART00000122810 | Essential Splice Site | 98 | 259 | None | 4 |
ENSDART00000145884 | Essential Splice Site | 98 | 228 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 36291234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35763803 |
GRCz11 | 13 | 35889635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTAATGGACAAATATGCTAAYGTGTAAAACCTCCTTTTGTGTTTTTC[A/T]GGAGTTCATTGATGAATAACACTCACACCACACCAATTGACATAGAATGT
Long Flanking Sequence:
TTTTATTTATATTAATTTCCACCAAAGGCACTTCTTCGAACAGACCCAGAGACTTCTGGTGTAAAATGATGGGTAAAACATAATGATCCTGTTTCCAAATAATATTAACATGGGTTTTCAAAAATTTTGTCTGAAAGCTGTAAACTTGCTTGGGATGTATTCACGGTGAAAGGACATATTTCTTTCAAATCTTTCACAATATAATGATTCAACTTTATAATTGAATCCACATATCATGTTTGACCTGTGGTGCATGCTCAAATAGGATTCCTATTTGACATTACTTTTTCTTCTTGACTATTGTTGATGCCCACATTGCAAAACAATATTTCAGTGCTAAAACAATATTTTGTCAACTTTAATGTACCACTCTAATAGTACAAGGTATTCATAAGAAAACTAGGTTAAAGATTAATTTTTAAAATATTTTTATGTAAGCCTCTTAACCTGTTTTTAATGGACAAATATGCTAACGTGTAAAACCTCCTTTTGTGTTTTTC[A/T]GGAGTTCATTGATGAATAACACTCACACCACACCAATTGACATAGAATGTAACAGTGTTGCTTTACCTGATGATGACATGCCTGTTCAGAGCAGAGGGGCCTATTCCTTTGATCTTGACAATATTGATGCCATCAACCCTTTCCAGGGCTCCAATAAAATGGCGAATTCCCCACCTAAATCTTCTGCTTTTACGGAGGCGGCAACATCAGAGCTTGTAGAGTCTAACACAACCATAGCCCCTGTTTCTGCACCCCAGGTAGAGGTAGAGACAGAGGCAGAAGTGACTGACAGTGCATTTGAAGAAGCTGTCCCATCAGTGGAGAATTCCCTTGCAGAATGCTCTGCCAACATCTCATCGACAGAGGGCAACGTAGCCCCTGTTCTTGCACCTCAGGCTGAAGTTCCAGAGGTGACTGAAAGTGCACTTGATGAGACTCTCCCATTTGTGCCATCAGTGGAGAATTCCCTTGCAGAATGCTCGGCCAACCTCTCTTCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38959
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002750 | Essential Splice Site | 879 | 942 | 15 | 17 |
ENSDART00000122810 | None | None | 259 | None | 4 |
ENSDART00000145884 | None | None | 228 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 36284757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35757326 |
GRCz11 | 13 | 35883158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGCGTTATCAAGCTCTTAAAGCCCACGCTGAGGAGAAACTAGAACA[G/A]TATGTGCTCTGTCATGTCTCAAATGTTGCCTTACAAACTTAAAAATACAA
Long Flanking Sequence:
CTTCTTTTCTCAGGTTTATAATGTCAGAATTTGAGACCACCATCACTCAAATCACCGGTATGAAATATTGTTTTAAGCCTAAATTTTAAAGGCAGACCTTAATCATTTTAAAAGCAGACAGTTGGATATTTAAACATTCTTGTGTGTTTAAAGATGAGCACAAACAGAAAGAAGCATTGGCTAAAATGGAGATGGAGAGAGTTCTTGAAGAAAAAGATCAGCTGGCCAAAGATTTGAATGAGTTGGAGCGATCGTTCTCCTCAGTCGTCAAACGTCTTGACAGATGCAAGGAAGTTATTGAGGGATTTAAAAAGGTTGGTATAGAAACTTACCATCTGTGTTGGTAATTTTTGGTAACCATTTTAGTGAATCATGTTCCCTTCTCCACTGTAGAATGAGGAGACCCTGAAGCAATATGCTAAGAACTGCATGGACAGACTGCAGAAAGAGGAAAAGCGTTATCAAGCTCTTAAAGCCCACGCTGAGGAGAAACTAGAACA[G/A]TATGTGCTCTGTCATGTCTCAAATGTTGCCTTACAAACTTAAAAATACAACAAATAATGAAGATTGGTTACATATGATTGGATATATCCCTAATGGTGCTGTTGTTGTTTCAGAGCAAATAAAGCCATAGCCGAGGTCCGCACTAAACAAGGTGCAGAGGTGGCGGCGCTACAGGTACAGCTCAAGAGAGAGCAGCTGAAGGTTCAGTCCCTAGAGAAGGATCTGGAACAAAAGGTACATATACAGGCTGTAAACTGTTCAATTTGAATTTGTTCATTGTTTTGAATTATAAGGTTATTGCAAAAGCCCCTTTCACACAGTGATATTGGTAAATATCTAGAAAATTTCCAGAACAATTTTACTGGAAAATTCAAAAAAGCGCAGTTCACACAGGCAAGGATGATGCAGATTATTTCCGGAATAGACCATTCACACATCCATTCCAAAATATCGGTAAATTCTGACATGATTAACCAGAAATGAGCCCTAAACAACTGGGC
Associated Phenotype:
Not determined