Busch Lab

ZMP

tacc3

Ensembl ID:
ENSDARG00000005454
ZFIN ID:
ZDB-GENE-050522-327
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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