ZMP
cct6a
Ensembl ID:
ZFIN ID:
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]
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]
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 |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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