ZMP
tube1
Ensembl ID:
ZFIN ID:
Description:
tubulin epsilon chain [Source:RefSeq peptide;Acc:NP_957279]
Human Orthologue:
TUBE1
Human Description:
tubulin, epsilon 1 [Source:HGNC Symbol;Acc:20775]
Mouse Orthologue:
Tube1
Mouse Description:
epsilon-tubulin 1 Gene [Source:MGI Symbol;Acc:MGI:1919174]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43359 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43360 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43359
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064562 | None | None | 271 | None | 9 |
| ENSDART00000064565 | None | None | 271 | 9 | 13 |
| ENSDART00000124476 | Nonsense | 296 | 471 | 9 | 12 |
| ENSDART00000132669 | Nonsense | 296 | 470 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 292306)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 282901 |
| GRCz11 | 20 | 271536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGAATGAGATAGCCATGAACCTGGTCCCTTTCCCACGTTTACACTA[C/A]CTTGTGTCCAGCCTGACTCCTCTCTACACACTGGCTGATGTCAGTGTGCC
Long Flanking Sequence:
TTCTGACACCAGATCAACAACTAGAAGACCTGTTATTATCTGATGTTCATAAAACCTGTTGACAATGCATTTGTCCGGTAGTGTAGTACTTTTTGTTTTTTCATAGTTTTGAAATAACCTGAAGGTAAATAATCTTGACGATTTCTGTTCTTGTTCTCTGCTGTTGTTCTAGTCTCTGGTTGATATTGTCGGTAAGATAAAACACATGTCCAACACTGGCAAACCAGGCTGTGCTATCAAGAAGGACAGTACCATCATCTCTGGACAAGGAGGGGTGGTGAAGGTGGAGAAGCCCTTTGATGCCATGAACAACATTGTGGCCAATCTGCTTCTTAATATTACCAGGTGCTAAATCCTCTGCTAATACATTTTCAACTTAATAGAGATGTGATTACTCATAAAGTTGTTTTTATTCTTAGTTCAGCGCGGTTTGAGGGCTCTCTCAACATGGATCTGAATGAGATAGCCATGAACCTGGTCCCTTTCCCACGTTTACACTA[C/A]CTTGTGTCCAGCCTGACTCCTCTCTACACACTGGCTGATGTCAGTGTGCCACCCCGCAGGTACGTTTGCAGTCAATCGTTTATGCAGGGGAAAAGTACTGGGAATTTACCCCTAAAAAAAGAGCGGAAACTGTAGAGCAAAGCAGAATATATTTCCTGTTTCCAATTATGTTTGATTGGAAACTGTGAAACCATTGAGATCTTATTTAAGGCTAGGACACACCAAGCCAACGGCTACTAGTGCAGACAAAACTGTACTGTCGCCTCATGTTGCCATCCAGTAGCTCAGAGTTTGTCCAGTCTGTAGAGTTTATAGTAAAATATCTTGCAGCTTTTGGATGCCCTTTATGACATATTCCATCAAAATAGAAGTAAAATAACATACGTTATGTGTTTATTAAAAAAAATATATATATATTTGCATGTTGTGACTTTTTATATTTTCAGTTAAATAAAAGACTATTTTCCAAATCATTATTAGGAATATTTTCCATTCATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43360
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 |
|---|---|---|---|---|---|
| ENSDART00000064562 | None | None | 271 | None | 9 |
| ENSDART00000064565 | None | None | 271 | 12 | 13 |
| ENSDART00000124476 | Nonsense | 428 | 471 | 12 | 12 |
| ENSDART00000132669 | Nonsense | 427 | 470 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 295227)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 285822 |
| GRCz11 | 20 | 274457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAATGGTGTTTGTTGTGCCCCTACCCCACAGGCTCATTTGCATCATTA[T/A]CTAGCCGTTGATGGCATGGAGCAGTCTGGATTCACTGAAGCGCTGTCATC
Long Flanking Sequence:
ATTTATATACATATTGACCACATGGAAGGGACTATTTCAGGTTTTTACAGTTTAAATCTTATACTCAGATGTACTCGTTCATATTTTTACTTTATGTAGAGCTATTTGGAGCACATGTTTGGTTACTGATGGAAAAAATATGAAATATATATGAATAAACTACAAAACAAAACAGAGATTCATTTCAAAAACGAATGATTACATGCCCAACACAAAATACTACAATAAAATGCTAAATATAAACCACTCTGACACCAAGCTTTTATTCACGATTTTGATCATAAATATAATGAAAAAGTATTGCAGTAAACAATGCATATTGTTATATATATATAATATAACAACATGCATTGTTTATATATATATATAGTTATATTGCACAGCTCTGTCACAGATTATGGAATGTTGACATGTTCTTGTGCACGGTGCAGATATTCTGAAGCTCTGTATGTTAATGGTGTTTGTTGTGCCCCTACCCCACAGGCTCATTTGCATCATTA[T/A]CTAGCCGTTGATGGCATGGAGCAGTCTGGATTCACTGAAGCGCTGTCATCAATCTCAACACTTATTGAAGACTACACACACCTGGAATGCCCTCTCATGCCAAACGCCCCCAGACTCACCATGGCCACCTGACCTGTGTGTATATTAGACATTTCTTATCCATCTACCTATATCTGAGTAATCGAGGAAGTGAATTTACTTCACTTTGCAGATTAATAATGATTTAATCAGCTGAAGTTTGAAGAACCACGCTGTTTTAATCTTCTAAGCAAGGACTTATGCGGTCCTGGTGACATCTTGTGGATGGACAATGTCAACTGTCTTTGACTAATAGACGCCACCGCACTGTCTCTCAGAAATTGTAAATATTTTCAAATAGGCACCATTATAAATAAACTGCATAGTTGCAATCTAAACAACTACATTCTCCACTAAAAAAGCATTAAAAGTACATTGTGTTGTCCAATAGCTGCAATATTTATCAAACTGTAAAGTGTCCT
Associated Phenotype:
Not determined