ZMP
tbcb
Ensembl ID:
ZFIN ID:
Description:
tubulin folding cofactor B [Source:RefSeq peptide;Acc:NP_997940]
Human Orthologue:
TBCB
Human Description:
tubulin folding cofactor B [Source:HGNC Symbol;Acc:1989]
Mouse Orthologue:
Tbcb
Mouse Description:
tubulin folding cofactor B Gene [Source:MGI Symbol;Acc:MGI:1913661]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43153 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43153
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 |
---|---|---|---|---|---|
ENSDART00000078053 | Nonsense | 45 | 246 | 3 | 7 |
ENSDART00000132577 | Nonsense | 45 | 72 | 2 | 2 |
The following transcripts of ENSDARG00000068404 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 35603992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 37283148 |
GRCz11 | 18 | 37264156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTCAATGAACCTAACTTGTATATTTGTTTTTCAGAGTAAACTGGAGT[T/A]GATTGTGGGCACTCCAGCTAGTTGTATGGACCTAGATCTGTTCAGCTCCT
Long Flanking Sequence:
ATTAAATGAATTTGATACATAATCATTCAGTTTAATTTTTAAACTAATATTAACAATCAGTACTTAAATAAATCAGTTTTTTTTTCTCACAGTTGATTTTGTTTCATTAAGCAATTTTTACTAATATGACTTTACGCAAATGAGGACGTTGCTAAACCTTTTGATCACAAACATTTTGCCACCAAATGCAAAACTTTGCTATTGATTGTAAAGTTATTAGCATAACATTATTGTAATTCAATCAAACATTTTTGTTTGGGTGAACATAAACATTTTGTAAACAAACAAAAATTCCACAGGAACATAAAAGTTTAGCAAGAGAACATTTTTTTTTGTTTGTTTTCAAACCATCCCAAGCTATATTAATATTAAGAAAATGAATTTCGTTCTGAGAGTGAATTACATCCACAAATTGCTTGAGTCATTTTGAAATCACATTGATGTTTTAGTATGGTCAATGAACCTAACTTGTATATTTGTTTTTCAGAGTAAACTGGAGT[T/A]GATTGTGGGCACTCCAGCTAGTTGTATGGACCTAGATCTGTTCAGCTCCTCAGACAAGTTCCTTCAGAAACTAGATAACAATGAAGCTCTGCTGGGCTCCTATCATGTGGATGATGACTGCAGAATACATGTGGGTATTTACTCTTTTTGACACCTCGTCTACAAAGTGAACAACATGACACATTTAGAACATGTGAAAGGATGCGAGTTCGTCCTAAATTTCCACAGTGTGTCACATTCATGGGTTGTTATATGTTGGTGTCCCTGGAATATCTTTTCACTCTGGAAATTTAGTCAAAACCTTATTCCTATCCCTAAACCTGGACCATCCACTTGTTAAGTCATGACGTATAGACTACTGTTTCCGGGTCCAAGCTGCTACTCATTTGTCCTGTGATAATACTCGAATGTGACCACTTTTTAGTTATATCACACATTAAATAGATTTTTATATAAAATCATGGTGTACACGACAGTCTCTGGACTTGCTGCATCACAGA
Associated Phenotype:
Not determined