ZMP
cct7
Ensembl ID:
ZFIN ID:
Description:
T-complex protein 1 subunit eta [Source:RefSeq peptide;Acc:NP_775355]
Human Orthologue:
CCT7
Human Description:
chaperonin containing TCP1, subunit 7 (eta) [Source:HGNC Symbol;Acc:1622]
Mouse Orthologue:
Cct7
Mouse Description:
chaperonin containing Tcp1, subunit 7 (eta) Gene [Source:MGI Symbol;Acc:MGI:107184]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21108 | Nonsense | Available for shipment | Available now |
| sa21107 | Essential Splice Site | Available for shipment | Available now |
| sa2381 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa21108
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006802 | Nonsense | 86 | 547 | 3 | 11 |
| ENSDART00000014899 | Nonsense | 91 | 422 | 3 | 9 |
The following transcripts of ENSDARG00000007385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60630929)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 59849894 |
| GRCz11 | 7 | 60155131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGTTGTGCATCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCT[C/T]AAGATGCTGAGGTAAGATGACCTCTTCATTTTTATGGATTTAGTCCAATA
Long Flanking Sequence:
AGATTATAATAATCTGCATAATATGGAGAATGTCAGTATTATTATATATGTGTACTAGTTTGGTTTTCTCTTAAGAGTACTAAAATTAGTTGTCATTAAAAAAGGCGACGTATTAATGATAATGCATTAATTCTTGAATTTTTTCCTACAGTCCACTCCAGTCATCCTCTTGAAAGAGGGCACAGACACCTCTCAGGGGGTCCCACAACTGGTCAGCAACATAAATGCCTGCCAGGTTGTGGCAGAGGCTGTGCGGACCACCCTTGGCCCCCGTGGCATGGACAAGCTTGTGGTGGATAACCGAGGTTAGTCAGCAATTCTGTATTTTAAATAGAAGTGTTGTTATAACTGTAAAGATATAAGTTGCACATTAATGTGATGCCCTGTCGTTTAATGCTTTTACAGGCAAAGCCACTATTTCTAATGATGGAGCCACAATTCTGAAGCTTTTGGATGTTGTGCATCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCT[C/T]AAGATGCTGAGGTAAGATGACCTCTTCATTTTTATGGATTTAGTCCAATAGTTTTCTAGACACAAAAATAACGGAATTAGGGCTGTGTGATTAATCAAAATCGAATCACACTCGCGATTACCAAAAAAAAGAGGCTGCGATATAAAATATGTATTGTTTAATTTCCCCTCCCATTGCAAACGCAAGCATAGTGAATGTTAGTGATGCCCACAAAAAAAAAAAAACAGGAAAGCGTGGACGAGTGGGATGCTGTCTGCTGCTTCAGAAGCATTAATAGATTAATTAATATCAAAGAAAAGCAGGACATCGGCAATATGGGATAATTTTGGTTTCAAAGTCACAAAAAATTCAAGTTTAATGTTTTCACAACTTCATCTGTATTTCGTGTGCATTCACAGCTTACTATACAGGTATGTATGTCGTGTGTGGTGACTGACTGTTATGTACTATAAAAATATAATTTGTCATTTCATTTTTATAGGACAGTTATATATAGATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21107
Status:
Available for shipment
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:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006802 | Essential Splice Site | 89 | 547 | None | 11 |
| ENSDART00000014899 | Essential Splice Site | 94 | 422 | None | 9 |
The following transcripts of ENSDARG00000007385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60630916)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 59849881 |
| GRCz11 | 7 | 60155118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCTCAAGATGCTGAGG[T/G]AAGATGACCTCTTCATTTTTATGGATTTAGTCCAATAGTTTTCTAGACAC
Long Flanking Sequence:
CTGCATAATATGGAGAATGTCAGTATTATTATATATGTGTACTAGTTTGGTTTTCTCTTAAGAGTACTAAAATTAGTTGTCATTAAAAAAGGCGACGTATTAATGATAATGCATTAATTCTTGAATTTTTTCCTACAGTCCACTCCAGTCATCCTCTTGAAAGAGGGCACAGACACCTCTCAGGGGGTCCCACAACTGGTCAGCAACATAAATGCCTGCCAGGTTGTGGCAGAGGCTGTGCGGACCACCCTTGGCCCCCGTGGCATGGACAAGCTTGTGGTGGATAACCGAGGTTAGTCAGCAATTCTGTATTTTAAATAGAAGTGTTGTTATAACTGTAAAGATATAAGTTGCACATTAATGTGATGCCCTGTCGTTTAATGCTTTTACAGGCAAAGCCACTATTTCTAATGATGGAGCCACAATTCTGAAGCTTTTGGATGTTGTGCATCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCTCAAGATGCTGAGG[T/G]AAGATGACCTCTTCATTTTTATGGATTTAGTCCAATAGTTTTCTAGACACAAAAATAACGGAATTAGGGCTGTGTGATTAATCAAAATCGAATCACACTCGCGATTACCAAAAAAAAGAGGCTGCGATATAAAATATGTATTGTTTAATTTCCCCTCCCATTGCAAACGCAAGCATAGTGAATGTTAGTGATGCCCACAAAAAAAAAAAAACAGGAAAGCGTGGACGAGTGGGATGCTGTCTGCTGCTTCAGAAGCATTAATAGATTAATTAATATCAAAGAAAAGCAGGACATCGGCAATATGGGATAATTTTGGTTTCAAAGTCACAAAAAATTCAAGTTTAATGTTTTCACAACTTCATCTGTATTTCGTGTGCATTCACAGCTTACTATACAGGTATGTATGTCGTGTGTGGTGACTGACTGTTATGTACTATAAAAATATAATTTGTCATTTCATTTTTATAGGACAGTTATATATAGATGCAATAGTTGCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2381
Status:
F2 line generated
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006802 | Essential Splice Site | 262 | 547 | 7 | 11 |
| ENSDART00000014899 | None | None | 422 | None | 9 |
The following transcripts of ENSDARG00000007385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60626107)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 59845072 |
| GRCz11 | 7 | 60150309 |
KASP Assay ID:
554-3299.1 (used for ordering genotyping assays)
KASP Sequence:
CTAATATAAATGAANTTAGTTGTTTACCCTTGTTTTAATGTGGCTGTTTGC[A/T]GGACTATCAGGCCATTGTTGATGCTGAATGGAACATCCTGTATGATAAAC
Long Flanking Sequence:
GATGATGGAAGAAATCGCACCTAAATGCTTTTATGGGTTAAGGTTTAATCTTTTTGGCTGTTCTGACCTGTGACTCAAAAAATTGAAGTGTGATCTGAACTGGAGATGTGTTTTCTGTTACACCACCATTTAAAGGACAAGTTCATGTTTTGATTTCAAAGATATTAAAATGTCATATTTCAAAATTGCAAAAGTGGGCGTTTATGTATGTATATGACAAAATGGGTATACCATGAACAGTACATCTCCTGGTAAAGGTTATGACCAACTCTAATAATAACCTTTCTCTCACCGCTGGCATAACTTTGCTTGTGCATATTTCAATATTCTGCATGCAACACAAATGCTTGACACATAAAATGTTTTTTAAATAAGTACAGCTCTCTGCGATATAGATATCACATATACTATTATTCCAATAAATATAGTTTTAGCATATATTGTGCAGCCCTAATATAAATGAATTAGTTGTTTACCCTTGTTTTAATGTGGCTGTTTGC[A/T]GGACTATCAGGCCATTGTTGATGCTGAATGGAACATCCTGTATGATAAACTGGAGAAGATCCACAAATCTGGCGCTAAAGTTGTGCTGTCCAAGCTGCCCATTGGAGATGTAGCCACACAGTACTTTGCAGACAGAGATCTGTTCTGTGCAGGCCGCGTCGTGGAGGAAGATCTCAAAAGAACTATGATGGTATACTGTTTTTGGTTGTTTTTCTTGTCTATTATGACAGTCAGTATGTCTTCTGTCATTCAGTTTTTAGTCTGTCTTTGTGTACTTTTAAAGTTGATATAACGCATTGCAGTCATAAAACATTTTGGTAGTCTAACCTAAAATTTAGCGCCCCCACGTTCCATGGATTTGAACACTTGTTAACTAACAAGTTTTATTTTGTGCTTTCTAGGCTTGTGGTGGCTCCATTCAGACCAGTGTTGGTTCCCTGACTGATGATGTTCTTGGCCAGTGTGAGCTATTTGAAGAAGTGCAGGTTGGAGGAGAGAGG
Associated Phenotype:
Not determined