cct7

Ensembl ID:
ENSDARG00000007385
ZFIN ID:
ZDB-GENE-020419-7
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 Estimate
sa21108 Nonsense Available for shipment Available now
sa21107 Essential Splice Site Available for shipment Available now
sa2381 Essential Splice Site F2 line generated During 2016

Mutation Details

Allele Name:
sa21108
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TGGATGTTGTGCATCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCT[C/T]AAGATGCTGAGGTAAGATGACCTCTTCATTTTTATGGATTTAGTCCAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21107
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Essential Splice Site
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCCTGCAGCCAAGACTCTGGTGGACATTGCTAGATCTCAAGATGCTGAGG[T/G]AAGATGACCTCTTCATTTTTATGGATTTAGTCCAATAGTTTTCTAGACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2381
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
A > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006802 Essential Splice Site 262 547 7 11
ENSDART00000014899   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
KASP Assay ID:
554-3299.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CTAATATAAATGAANTTAGTTGTTTACCCTTGTTTTAATGTGGCTGTTTGC[A/T]GGACTATCAGGCCATTGTTGATGCTGAATGGAACATCCTGTATGATAAAC
Associated Phenotype:
Not determined

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