ZMP
tbca
Ensembl ID:
ZFIN ID:
Description:
tubulin-specific chaperone A [Source:RefSeq peptide;Acc:NP_957348]
Human Orthologue:
TBCA
Human Description:
tubulin folding cofactor A [Source:HGNC Symbol;Acc:11579]
Mouse Orthologue:
Tbca
Mouse Description:
tubulin cofactor A Gene [Source:MGI Symbol;Acc:MGI:107549]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29516 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa37230 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29516
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023997 | Nonsense | 7 | 108 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 7485054)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7807521 |
| GRCz11 | 21 | 7545189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCTTTTAACGATTTCAAACTGCACGGACAATGGCTGATCCAAGAATA[C/T]GACAAATAAAAATCAAGACGGGTGTGGTGAAACGGTAAGCAGACAGAACG
Long Flanking Sequence:
TAACAGGCCGGTTGCATGTTTGATTTAATAATAGCAACATAATTGACATATGAGTTTTGAATTAGGCTATATTGCAAAGAATTAGCTATAAACCTGTAAAATAGACTATGAAACGATGTTACTAAATTAAATAGTGTATGATATTATTTGATTATATTTAAATGATCAAAGTGCAGATAAACANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAGCTTTATTATAACTTCTTGTGAAGTGATGTGATTTCTGATCTGCCTTGAACGCGCTGTCTAATCTGCGCATGCGCGAGGTTTATGCTGCGTGTTGTAGTGTCATTGCTAACAGGCTAAGTTCTGCTGCTCGCATCTCTCGTAATAAACATTTTATCCGCGTTTCCTTGCCTTTTAACGATTTCAAACTGCACGGACAATGGCTGATCCAAGAATA[C/T]GACAAATAAAAATCAAGACGGGTGTGGTGAAACGGTAAGCAGACAGAACGGTCTTATTTTATGTACTAATGTCTTTAGGGTAAGGCCGCGGATTCGCCGCGGCACACGACAAACAGTCGCCGCAAATGCGCGCCCTACTGCTGCAGAATCTGTAACTCTAGTCCAGGGCTCTGACAGCTGCTGGGGGTTTAGCCAGATGTCAAGTTCACTTCTCCAGTCACTTTCAGTGCCGTGAAAACTATTGAAATGCAATTCATTACGGTTATTACAGGTTGATATTTGTGCATGGGATTAATTTGTTGTTACAAAACATAAGTACACATCAAAATGAGGTGTTGAATGAAGAATCTGAGGTGAGCAAATGCCCTGTGCAATACATATTTCTATACACTGTCAAGCTAGAAGGTGATTAATTTATTTATTTAGTGTTAATATTTAACTTTTTTTTTTTTTTTAGGAGTGACTATATGTAGTTAAATGTAGGAAATTTATATGACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37230
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023997 | Nonsense | 8 | 108 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 7485057)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 7807524 |
| GRCz11 | 21 | 7545192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTTAACGATTTCAAACTGCACGGACAATGGCTGATCCAAGAATACGA[C/T]AAATAAAAATCAAGACGGGTGTGGTGAAACGGTAAGCAGACAGAACGGTC
Long Flanking Sequence:
CAGGCCGGTTGCATGTTTGATTTAATAATAGCAACATAATTGACATATGAGTTTTGAATTAGGCTATATTGCAAAGAATTAGCTATAAACCTGTAAAATAGACTATGAAACGATGTTACTAAATTAAATAGTGTATGATATTATTTGATTATATTTAAATGATCAAAGTGCAGATAAACANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAGCTTTATTATAACTTCTTGTGAAGTGATGTGATTTCTGATCTGCCTTGAACGCGCTGTCTAATCTGCGCATGCGCGAGGTTTATGCTGCGTGTTGTAGTGTCATTGCTAACAGGCTAAGTTCTGCTGCTCGCATCTCTCGTAATAAACATTTTATCCGCGTTTCCTTGCCTTTTAACGATTTCAAACTGCACGGACAATGGCTGATCCAAGAATACGA[C/T]AAATAAAAATCAAGACGGGTGTGGTGAAACGGTAAGCAGACAGAACGGTCTTATTTTATGTACTAATGTCTTTAGGGTAAGGCCGCGGATTCGCCGCGGCACACGACAAACAGTCGCCGCAAATGCGCGCCCTACTGCTGCAGAATCTGTAACTCTAGTCCAGGGCTCTGACAGCTGCTGGGGGTTTAGCCAGATGTCAAGTTCACTTCTCCAGTCACTTTCAGTGCCGTGAAAACTATTGAAATGCAATTCATTACGGTTATTACAGGTTGATATTTGTGCATGGGATTAATTTGTTGTTACAAAACATAAGTACACATCAAAATGAGGTGTTGAATGAAGAATCTGAGGTGAGCAAATGCCCTGTGCAATACATATTTCTATACACTGTCAAGCTAGAAGGTGATTAATTTATTTATTTAGTGTTAATATTTAACTTTTTTTTTTTTTTTAGGAGTGACTATATGTAGTTAAATGTAGGAAATTTATATGACAAATAT
Associated Phenotype:
Not determined