Busch Lab

ZMP

cct6a

Ensembl ID:
ENSDARG00000021252
ZFIN ID:
ZDB-GENE-011018-2
Description:
T-complex protein 1 subunit zeta [Source:RefSeq peptide;Acc:NP_958447]
Human Orthologues:
CCT6A, CCT6B
Human Descriptions:
chaperonin containing TCP1, subunit 6A (zeta 1) [Source:HGNC Symbol;Acc:1620]
chaperonin containing TCP1, subunit 6B (zeta 2) [Source:HGNC Symbol;Acc:1621]
Mouse Orthologues:
Cct6a, Cct6b
Mouse Descriptions:
chaperonin containing Tcp1, subunit 6a (zeta) Gene [Source:MGI Symbol;Acc:MGI:107943]
chaperonin containing Tcp1, subunit 6b (zeta) Gene [Source:MGI Symbol;Acc:MGI:1329013]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa9774 Essential Splice Site Available for shipment Available now
sa16648 Nonsense Available for shipment Available now
sa10117 Essential Splice Site Available for shipment Available now
sa37375 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9774
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
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009484 Essential Splice Site 205 531 6 15
ENSDART00000137630 Essential Splice Site 205 531 6 15
ENSDART00000141067 Essential Splice Site 160 242 5 7
Genomic Location (Zv9):
Chromosome 21 (position 40520579)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 41818198
GRCz11 21 41831408
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGGTGGAGATTATGGAGAKKAAACACAAAACCGACAGTGATACTCAG[T/A]AAGACTCATAGCATTGTGTGCGGTCTCATGTCRATGTTAGACAACATTAA
Long Flanking Sequence:
TCATGCATAACTATATGGAAGCATGCACAGGAACATGTTGTTAGTGCTGCTCTACAAATTTCGAGAGTTTTGAAACTGAAGTTTTGCTATGTCACTAGCGACATAATGTTGCTGTTCTTGAAGCAGTTACACTTAAAACTTCATTGTAAGTATAGAGGGTGCTGAGGGAATCAGATTCAGCTAATTCACACATGCTTTATTAGCTCTTTCTCTCTCTACAATCTGCTTTAGTCTGCATAATAATATCCCAAACTTTTAATGTTAGCTACAAAACGATGTTCTGGAGTTTTGCAAGCTTGGGATGATATGCATGCCATGACTCCATTGTTGTGATCTAATAATTAAATAGTGCATATGTGTATCGTCTATTCAAATGTTTTCCTGTTTGTCTTCAGGCTGTAGTGGATGCTGTACTGGCCATAAGGAAACCCAACGAGCCCATTGACCTCTACATGGTGGAGATTATGGAGATGAAACACAAAACCGACAGTGATACTCAG[T/A]AAGACTCATAGCATTGTGTGCGGTCTCATGTCGATGTTAGACAACATTAATTAATCCAAATTATCCATTAAACAAATTAAATTAAACAAAAATTATCCAATTATAAACCATCTTGAGTTGAAGGTGTTCAGAAATGTGCAAATTGATGGCAAACACTTTGGACTTTTGTTTGTGTTTTAAATTTCAATCTCACTATTAGATAGCACAGTGGAGAAGGGAAGAAATTAACAAATGAACAACTCGCATCCAGGTTGAAAGTCAGTTCAGTTCTTCATCCATTTCATTCCCTCACAGAATCTGCTCACACAGAAATTTGCTGATTCCTGCCAGTGTTTAAGCCCATAATCAGTACTCTTTAATCCTAACAAAACATTGACCGTGCAGTTAAATTACAAATTTTAAACAAACTACAAATCAAAAAGGAACAATACAAATTAAAGAAGGCTCTTTAATAGAGTATTTGCACATTTGCAATGTCCGCTGCTAATAAAAAAAAACCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16648
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009484 Nonsense 237 531 7 15
ENSDART00000137630 Nonsense 237 531 7 15
ENSDART00000141067 Nonsense 192 242 6 7
Genomic Location (Zv9):
Chromosome 21 (position 40517909)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 41815528
GRCz11 21 41828738
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAAGAAGAGAAYAGAAGAKGCTTTCATTCTCACSTGCAACGTTTCCT[T/A]GGAATACGAGAAAACGTGAGCTTTATTCATTGYAGATTAYTGTGTGTTGC
Long Flanking Sequence:
AACTATGAGGTAAACACAAAACAAAACTTACCATCCGGAGCTCCTTCACGGGACTCCACACTTGTAAACAATCGCTCGCGCCATTCGCGCTGCTCTCGGTCCCGCCCAGACTCGTCATCGCTACCAAGCCGACCAATTAGTTACATTTTTTGAGAGGTGCACGTCAGCGACGGCCACGGCGAAGGGCTATGCGTCAGCGCCGTAGCATACGCTGGCGTTTGACGCAGAAGTATAAATCAGCCTTTACTGTTACTCGTAGAAGACCACGGCCAGAAATGTTTACTTTTTTATTGGAACAAAAAATAATACAATTGTGGAACAAATAGGAGGGTTGCCATTTGTTAAGTGTTAAATTTCTTACTACTGTTATCGTTTAGTCAATTTTCTTTTTTTATTTATTTTTAGACTGATCAGAGGGTTGGTGTTGGACCACGGAGCCAGACATCCTGACATGAAGAAGAGAATAGAAGATGCTTTCATTCTCACCTGCAACGTTTCCT[T/A]GGAATACGAGAAAACGTGAGCTTTATTCATTGTAGATTACTGTGTGTTGCTGGTCGTCAGTTTATCAGCAAAACTATAATCACACTGTCTGTGTTCACAGCGAAGTGAACTCCGGGTTTTTCTACAAGAGCGCAGACGAGAGAGACAAGCTGGTGAAAGCTGAGAGGAAGTTCATTGAAGATCGTGTGATGAAAATAATCGACCTGAAGAATAAAGTGTGCGCTGATAATAAAAAGGGCTTTGTGGTCATCAATCAGAAGGTAACGGATAGGTTTTTGGAAAATATTAAAGCATTTTTTTGGTTGCTTTATTTTGATGGTCTGTTTGTTGAGTTAGGTTACATTGCATCTACATGCCAACCAATTCTCAATAGATTATAGGTAGACTGTTAGGTTAGGGATAGGGTTAGTGTAAGTTGAAATGTACTTGCAAAGTTTCTTATAGTCAGTTAAATGTCTGTTTAGCAGCAGATATTAGGCATACAGTCTACTAATACTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10117
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
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009484 Essential Splice Site 323 531 9 15
ENSDART00000137630 Essential Splice Site 323 531 9 15
ENSDART00000141067 None None 242 None 7
Genomic Location (Zv9):
Chromosome 21 (position 40516351)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 41813970
GRCz11 21 41827180
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGGGCATTGTGGCTCTGCGCCGTGCAAAGAGACGGAATATGGAAAGG[T/C]AAAGGTGGCACTGCTGCCAATTTCTGATTTACCTGCTTGAATCCTTTCTT
Long Flanking Sequence:
GATAAGAGTACACTTTCTAAAACTGCATTTAAAGACATCCAGGTTCACACTTTGATTAAACTAAGCTCTCAATTTACATATTTGATGTTCATATTTAACAGTTGTTGAATTTTTTCATAAAGCGGTGGTCAGATATTACAATTTAAAAAATTGAGTGGTGGGAGCTTAAATTAAATATAATTTGACTACAGTGTTAAAACCACTGCTTTAAATGCATTGAGAATTTTGTGGCCATTGGTACTTTGTTCAAGCTATACTCTCTGGCAATTTAAGAAAGCTTAGATTAAAACTAAATCAGGAATCACAATGAAACTGCCAAAATAACACACACATTTATTAGATTATCTGTCTTTTAACTGTCAAGCTACATGGCTGGCTAATTAAATTGCTTAACCCAAGTTATTTCTTTTACACAGGGTATTGATCCATTCTCTCTGGATGCGCTGGCCAAAGAGGGCATTGTGGCTCTGCGCCGTGCAAAGAGACGGAATATGGAAAGG[T/C]AAAGGTGGCACTGCTGCCAATTTCTGATTTACCTGCTTGAATCCTTTCTTTTCCCTCAAAATAATAAAATGATGTGGATTGCTTTGTGTTTACATGTCTGTAATGCACTTTAATGATGCGGCTAAAACCGGCATACTCCACACGTCTTATTTTGATTTCTTTTTAGTCCGATTATGACCTTAATCTGATTAAATAAATCAAAAATTGATTTCTACATGGTAGATTCTTAATCAGAGTATTGTCTTAAATTAAAATTTAATTATTGGTGTCCATGTAAACGTAGTCAGTTTCACAAGCAGTTTGTGAAACATTTTGGAAACAGGAGATGGACTCCTGGTCTAATGCGCCATCTGGCTTGAGAAACTCGTTCTCAAAGACTGACTTTAAGATATTATTTGGGTAGCACACATATTCTGAATGCCTTCGGCAGAATTCAAAGGAGCCATTTTAATCTAGATAAAAAAAATAGTATGTATGTATATATATGTATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37375
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009484 Nonsense 396 531 11 15
ENSDART00000137630 Nonsense 396 531 11 15
ENSDART00000141067 None None 242 None 7
Genomic Location (Zv9):
Chromosome 21 (position 40514947)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 41812566
GRCz11 21 41825776
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACAAGCACACCCTGACACAGATCAAAGACGCAGTGAGAGACGGACTC[A/T]GAGCTGTCAAAAACGCCATTGAAGATGGTAGGATATCAAACCATACAACA
Long Flanking Sequence:
GGCTATCGAATGTATCGACCATATTTTGTTAAGAAACGGCAAACACTGCTGTCAGTGCTGTTATTTAAAAATGTGCAAAATAATGTTTTTTGTATATTTAGTATTATAGTATTATTAATTTTGATTAAACCAGAAGAAGAAAATGCCAAATTTTTAATTGAAAAAAAAAAAATTTTTTTTAATCATTCCAAATGTTATCTTCCCATAAGGCTGACTCTGGCATGTGGTGGTGTAGCAATGAACTCTGTGGAGGATCTCACGCCAGAGTGTTTGGGACACGCTGGTCTTGTGTACGAGTACACACTGGTGAGTTCAGAAAAATTGTTAAAATATGCAGACTATTAGTTCCGCTTTACTCAAGCTTGACTTTTTTGTATTAGGGTGAGGAGAAATTCACGTTCATTGAGAACTGTAGCAACCCTCGTTCTGTGACCCTGCTGGTGAAAGGCCCAAACAAGCACACCCTGACACAGATCAAAGACGCAGTGAGAGACGGACTC[A/T]GAGCTGTCAAAAACGCCATTGAAGATGGTAGGATATCAAACCATACAACAGCACACACACTTTGGCTGCACAATATATGGTATCGCAATGTGTGCATCCGTAATAGTCGCATCAGAAGATAAGCAACGTTGAGTTTGAATCATAGTTAACCAGGAGCCACAGAACACATGTGATTTGTAGAGTCCCTGCTTAGTTTAACCATAATTTAGAGTAAATGCTTATCGTTTGCATGTGTTTTTAAGGCCTGTGAGCATTTCAGGAGAGTCCTAAACATTTGGGAGCATGCAATTATGATGTCTGGTGGTGTGACAAAGATGAATTGTATTTCATTATTTACATGGTTTATGCTAAAAATGTTTGTCTTGTTTTTATTTTGGTCTTTTTTCTAGTCCAAATATTTAAGTTTAGATTTTTTTTACTTGCAATTATTAAGTTTATTTCAAAATGTGCATGTAAATGTGTATATATAAAACATAAGTAGCCTGACTCTATTGCGTTCA
Associated Phenotype:
Not determined