ZMP

cct3

Ensembl ID:

ENSDARG00000016173

ZFIN ID:

ZDB-GENE-020419-5

Description:

T-complex protein 1 subunit gamma [Source:RefSeq peptide;Acc:NP_775357]

Human Orthologue:

CCT3

Human Description:

chaperonin containing TCP1, subunit 3 (gamma) [Source:HGNC Symbol;Acc:1616]

Mouse Orthologue:

Cct3

Mouse Description:

chaperonin containing Tcp1, subunit 3 (gamma) Gene [Source:MGI Symbol;Acc:MGI:104708]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1761	Essential Splice Site	Available for shipment	Available now
sa28686	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa1761

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003752	Essential Splice Site	47	543	3	14

The following transcripts of ENSDARG00000016173 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 16 (position 32723902)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	30462417
GRCz11	16	30420344

KASP Assay ID:

554-1754.1 (used for ordering genotyping assays)

KASP Sequence:

CCATAGCAGACATCATCAGGACATGCCTAGGACCAAGGGCTATGATGAAG[G/A]TGCGCTTAAGATGTTCACGTTATCATTTTCCCAAGTGAATCTTTGTTATA

Long Flanking Sequence:

CTGGCATTGTAGTTTCTATATAACGGACGCTTTAAAAGAATGAATTAGTTAGCATCAGGCTAACAGCAGTGCGTAGAGGGTGGGCTTACTAAAGCTGCACCCTTTTCGTGTTAAGGAACAGATTTGTTGTATTGTTTTTCAGTTGTCTTGGCTTGGTGTTAGGTTTTAAGGCAGTGAATGTTATTTGAATTTTTTTAGTGAATGAAGAGTTTAGAGTTCATCATATGAAGAAGCAGATTTAATGCCCATTGGCTCTGTTTTTGGTACAGGTCAGAACATCAAGAGAGAATCTGGACGGAAGGTCCAGATTGGAAACATCTCTGCGGCTAAGGTGAGTCTATGTTTAGTTTATTGTATATATATGTATTTTTTTGTTATTGCAACGTTGCCTACATGTCACATAAATCATATCACCAACCTGACTTGCAGTCTTCTGTTCCCTTTTTTAGACCATAGCAGACATCATCAGGACATGCCTAGGACCAAGGGCTATGATGAAG[G/A]TGCGCTTAAGATGTTCACGTTATCATTTTCCCAAGTGAATCTTTGTTATAGAAAGAGATAAAAATATGTTTTGTCTGCAGATGCTGCTGGATCCCATGGGTGGTATCGTCATGACCAATGATGGCAATGCCATTTTGAGAGAGGTGATTTGAACCCTGCTACATTATCTGTGAGTTGTTAAATGAAATCTGTATCTTGATTTTAATTAATGTTAAATTGTTTCATGTGGACTTTAGATCCAGGTCCAGCATCCTGCTGCCAAGTCCATGATTGAGATTAGCCGCACACAGGATGAAGAAGTTGGAGATGGGACCACCTCTGTCATCATTCTAGGTGAGGGTCTTCTTTTTTTACTGTGCATTGCTCTTTGGATCTGGTATTATTATGTATTTAAATGCAACTTTTGTTGACAGTTTTGCCATTGTCTAAATCACTTTTGCATGAGCATTTTATGCATTATTATAGATAATATTTCTGTAGAATTTTTAAAATCATATCAG

Associated Phenotype:

Data not yet available

Mutation Details

Allele Name:

sa28686

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:

T > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003752	Missense	56	543	4	14

The following transcripts of ENSDARG00000016173 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 16 (position 32723796)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	30462311
GRCz11	16	30420238

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATAAAAATATGTTTTGTCTGCAGATGCTGCTGGATCCCATGGGTGGTA[T/A]CGTCATGACCAATGATGGCAATGCCATTTTGAGAGAGGTGATTTGAACCC

Long Flanking Sequence:

CGTGTTAAGGAACAGATTTGTTGTATTGTTTTTCAGTTGTCTTGGCTTGGTGTTAGGTTTTAAGGCAGTGAATGTTATTTGAATTTTTTTAGTGAATGAAGAGTTTAGAGTTCATCATATGAAGAAGCAGATTTAATGCCCATTGGCTCTGTTTTTGGTACAGGTCAGAACATCAAGAGAGAATCTGGACGGAAGGTCCAGATTGGAAACATCTCTGCGGCTAAGGTGAGTCTATGTTTAGTTTATTGTATATATATGTATTTTTTTGTTATTGCAACGTTGCCTACATGTCACATAAATCATATCACCAACCTGACTTGCAGTCTTCTGTTCCCTTTTTTAGACCATAGCAGACATCATCAGGACATGCCTAGGACCAAGGGCTATGATGAAGGTGCGCTTAAGATGTTCACGTTATCATTTTCCCAAGTGAATCTTTGTTATAGAAAGAGATAAAAATATGTTTTGTCTGCAGATGCTGCTGGATCCCATGGGTGGTA[T/A]CGTCATGACCAATGATGGCAATGCCATTTTGAGAGAGGTGATTTGAACCCTGCTACATTATCTGTGAGTTGTTAAATGAAATCTGTATCTTGATTTTAATTAATGTTAAATTGTTTCATGTGGACTTTAGATCCAGGTCCAGCATCCTGCTGCCAAGTCCATGATTGAGATTAGCCGCACACAGGATGAAGAAGTTGGAGATGGGACCACCTCTGTCATCATTCTAGGTGAGGGTCTTCTTTTTTTACTGTGCATTGCTCTTTGGATCTGGTATTATTATGTATTTAAATGCAACTTTTGTTGACAGTTTTGCCATTGTCTAAATCACTTTTGCATGAGCATTTTATGCATTATTATAGATAATATTTCTGTAGAATTTTTAAAATCATATCAGAAATTGCAATAATTCTCATGACAAGGATGAAAAACTATACCCTCTTCTGGGAAAATGCTGAATATTTTAATATATATATATTATTCACAGATTCACAAGATATTTA

Associated Phenotype:

Not determined