ZMP
cct8
Ensembl ID:
ZFIN ID:
Description:
T-complex protein 1 subunit theta [Source:RefSeq peptide;Acc:NP_957356]
Human Orthologue:
CCT8
Human Description:
chaperonin containing TCP1, subunit 8 (theta) [Source:HGNC Symbol;Acc:1623]
Mouse Orthologue:
Cct8
Mouse Description:
chaperonin containing Tcp1, subunit 8 (theta) Gene [Source:MGI Symbol;Acc:MGI:107183]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41662 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34906 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41662
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009477 | Essential Splice Site | 127 | 546 | 4 | 15 |
The following transcripts of ENSDARG00000008243 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 25973619)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 25377476 |
| GRCz11 | 10 | 25339323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGAGCTTGCAGAGGAGCTACTGAGAATGGGTCTTTCAGTTTCAGAG[G/T]TCAGCCAACAACAGAACTAATGCACTGTGTCTCTATTTATGTTTAATTCC
Long Flanking Sequence:
CACTGTGTATAGATACTGTGAAAGAATTGTGATTGGGCCCAAGACCAAAGAATCCCTGAGAATTGTGATTGGGCCTAAAACAATATTTTGCCCCTTGATTAAGTCCTATAGATGTTGAAATTTAATTAGATTGGATTATTTTTTGTAGTGTAAATGATCATGCTTATTAATCTTTATACAGGTATGAACAAAATGGTCATCAACCACTTGGAGAAACTGTTTGTCACTAATGATGCTGCAACTATTCTGAGAGAGCTGGAGGTACATATTAGTAATCATAGCTATGCATGCATTAATATAAATAATTTAGAATACTATTTATATCTCTCTCTTTTTTTCCTTCCCCCAAGGTTCAGCACCCAGCAGCCAAAATGATAGTGATGGCGTCCCACATGCAGGAGCAGGAAGTAGGCGATGGCACAAACTTTGTTCTGGTGTTTGCTGGAGCTCTGCTGGAGCTTGCAGAGGAGCTACTGAGAATGGGTCTTTCAGTTTCAGAG[G/T]TCAGCCAACAACAGAACTAATGCACTGTGTCTCTATTTATGTTTAATTCCACTTATTTTTTGTTATTTAATATATTTGAGATTCTAAATGTGTAACAATTGTGCAAAATACCCAAGTTTAGAAACAGATTTTTTTTTTCTTTAAAACGGATTTAAAAGGTTGTATGTTAATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATGTATATGTAAAACATTTTTTAAATCAAATTATATTAGGTCTAAATTCCCTTTTCAAGTTGAAATCATTTTCAAACACGATAGATTTGATAACTAATTTCTACTAATTTACTAATGTTTTTGCCATGATGACAGTACATAATATTTTACTAGTTTTTTTTGGGGGGGGATGCTAGTGTTCAGCTAAAAGTGCAATTTAAAGGCTTAACTAGGTTTGGTTAAATGGGCAAGTCTCTGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34906
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009477 | Essential Splice Site | 314 | 546 | None | 15 |
The following transcripts of ENSDARG00000008243 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 25970476)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 25374333 |
| GRCz11 | 10 | 25336426 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATATGGCTCTTCATTATGCCAACAAGTACAAGCTCATGGTGGTCAGG[T/C]AAGAAAAAGACTGATCCGGATCACTTCATCATCCAGGTTGTTTCAAAATA
Long Flanking Sequence:
GAAACTTGCAACGGTTGCCTCACCTCAGAGCTCTTCTAAATGGTCCAATGCTGTGGAACTGACAGGGATGAGCTGTGCTATGTGTGAAAGCTGAAGTTCTTTCAACTTGACGCGTCTAAAAAGACGTGAGTTTAATGGTCACACAAGTCCATGTTTACATTGAAAACCATTAAAAAGCAGCACGGTAGAAAGGAAAATGCATTCTGTGTGAACGACCTGACAGTTTCTTTTTCTTTCTATGATGTTCAAAATTGTGAAGTTATCATTGTTTTCTTTTGATCTGTAGCTCAATTTGATTAATTCTTTGTGATGTTTCATAGGGAACAGTACTTATCAAGAATGCAGATGAGCTCATGAATTTCAGCAAAGGAGAGGAGGACCTGATGGAGGCCCAGGTGAAGGCTATTGCGGATTCAGGGGCCAGTGTGGTTGTGACTGGGGGCAAAGTCGCTGATATGGCTCTTCATTATGCCAACAAGTACAAGCTCATGGTGGTCAGG[T/C]AAGAAAAAGACTGATCCGGATCACTTCATCATCCAGGTTGTTTCAAAATATTTTTGATTTGTTAAATGTATGAAATTTATGGTTTTTTTTTTTTTTGTACCAAGGCTTAACTCAAAATGGGACCTCAGAAGACTATGCAAAACTGTCGGAGCCACAGCATTGCCCAGACTGGTGAGCTTAGATTGTATTAGTGGCCATTTGTGTGAAGCAATGAGTTAGTGATAAACCAGATGGTGTTGTCAGATATTGTGTTCAATCTAAATGCTGTTTATTTTGGCTGGGACAAACAGACTTCCCCTACCCCAGAAGAGATGGGACGCTGTGACAGTGTTTACCTGTCTGAGGTTGGAGATACACAGGTTGTGGTCTTCAAACATGGTAAGGAAAATAGTATGCTTCATCCTGTGTTTACAAATTACACATGTACAAGTTATGTGGATTGGTGTGTGCTTACCTTTGATTAAATGTTTGTGGACAGTAATATTTTTCTAAGAAAGTAA
Associated Phenotype:
Not determined