ZMP

ccdc126

Ensembl ID:

ENSDARG00000062695

ZFIN ID:

ZDB-GENE-060503-11

Description:

coiled-coil domain-containing protein 126 [Source:RefSeq peptide;Acc:NP_001038868]

Human Orthologue:

CCDC126

Human Description:

coiled-coil domain containing 126 [Source:HGNC Symbol;Acc:22398]

Mouse Orthologue:

Ccdc126

Mouse Description:

coiled-coil domain containing 126 Gene [Source:MGI Symbol;Acc:MGI:1889376]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43261	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36822	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43261

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090942	Nonsense	56	166	2	3
ENSDART00000134650	Nonsense	34	144	3	4

Genomic Location (Zv9):

Chromosome 19 (position 20656223)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	20589603
GRCz11	19	20173926

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGAGCAGTGCAGAGCTCCGTCAACAGATCCTTGAGCTCAGCCATCGCTA[T/A]GTCAAAGTCCTTAGTGAGGAAAACCAGAACCCCTCGGGACCCCATGGCAC

Long Flanking Sequence:

TGCCTGTAAGAAGTTTTGTATTATTCTGACAAAGAGAAAAAAATCTATTTTTTTATCTCATTTTACTGATCTTGCTTGTTTTGTTGTGTGTTTTGTATTTTTACAGGAATGTCTTTGATCTGAAGCCCACTGCTCAAGACAATTCAATCACCATCTCAATTTCCTAGACAAGACAGTTAAGCAAATTCACAAGATAACTCAACATTAACCGCCACTCCATTTATTCAAGACATAAATATTCCCAGCCTTCAACCTGACACTTTCTGTAAAAAACAAAGACTTGACCCCGCCCTGTCCCCTTAACCCAGGTCCCATCAGACCTGCAGCTCTGCCATGCTGGGCTGTCTCCTGCGGAGGAGCATGTCTCACAGGCTCAGTGTGTTTCTGGTGCTCTTTGGCTTGGTCTGGTGTCTCCTGCTACTTCACTACACTGTCACACAACCACGGCGCCAGAGCAGTGCAGAGCTCCGTCAACAGATCCTTGAGCTCAGCCATCGCTA[T/A]GTCAAAGTCCTTAGTGAGGAAAACCAGAACCCCTCGGGACCCCATGGCACCTCAATGGCAGGATATGGTAAGGATTGGATTACCATCATGTGGTTACAAACTTGAATTCCATTTGATAAAGTTGAAAAGCATCATAATTCATCCTAATGTAGTCTATTTAGTAATAAAATCTTTGGAGACATAAAGTAATTTTGTGATTTAAAAAAAAAGTCAGAAATTGATACCTGTGGCTTATGTTGTATTTCCTGTGTTTTCTAAATAATTGCCTGTATTTTCTTGATGAACTTTATTTTGTTTATTTCCATTGTTTGGGTTATGTCCATAGTTTTTGTTGTGGACTAACATTGGAAAAAAGTACATCAATTGTTTTGACATTTATTTATTAAGGTTAGTGGCATTATAATGTTAAAATTAACTTTAATTGGTGAGCATGTGTTAAAATATTTAAAACTTTACAACATGAGTGGGGAAAAACCTTATATATTTAGATGTATTAAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36822

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 > G

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090942	Splice Site, Nonsense	78	166	2	3
ENSDART00000134650	Splice Site, Nonsense	56	144	3	4

Genomic Location (Zv9):

Chromosome 19 (position 20656289)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	20589669
GRCz11	19	20173992

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGGAAAACCAGAACCCCTCGGGACCCCATGGCACCTCAATGGCAGGATA[T/G]GGTAAGGATTGGATTACCATCATGTGGTTACAAACTTGAATTCCATTTGA

Long Flanking Sequence:

TGATCTTGCTTGTTTTGTTGTGTGTTTTGTATTTTTACAGGAATGTCTTTGATCTGAAGCCCACTGCTCAAGACAATTCAATCACCATCTCAATTTCCTAGACAAGACAGTTAAGCAAATTCACAAGATAACTCAACATTAACCGCCACTCCATTTATTCAAGACATAAATATTCCCAGCCTTCAACCTGACACTTTCTGTAAAAAACAAAGACTTGACCCCGCCCTGTCCCCTTAACCCAGGTCCCATCAGACCTGCAGCTCTGCCATGCTGGGCTGTCTCCTGCGGAGGAGCATGTCTCACAGGCTCAGTGTGTTTCTGGTGCTCTTTGGCTTGGTCTGGTGTCTCCTGCTACTTCACTACACTGTCACACAACCACGGCGCCAGAGCAGTGCAGAGCTCCGTCAACAGATCCTTGAGCTCAGCCATCGCTATGTCAAAGTCCTTAGTGAGGAAAACCAGAACCCCTCGGGACCCCATGGCACCTCAATGGCAGGATA[T/G]GGTAAGGATTGGATTACCATCATGTGGTTACAAACTTGAATTCCATTTGATAAAGTTGAAAAGCATCATAATTCATCCTAATGTAGTCTATTTAGTAATAAAATCTTTGGAGACATAAAGTAATTTTGTGATTTAAAAAAAAAGTCAGAAATTGATACCTGTGGCTTATGTTGTATTTCCTGTGTTTTCTAAATAATTGCCTGTATTTTCTTGATGAACTTTATTTTGTTTATTTCCATTGTTTGGGTTATGTCCATAGTTTTTGTTGTGGACTAACATTGGAAAAAAGTACATCAATTGTTTTGACATTTATTTATTAAGGTTAGTGGCATTATAATGTTAAAATTAACTTTAATTGGTGAGCATGTGTTAAAATATTTAAAACTTTACAACATGAGTGGGGAAAAACCTTATATATTTAGATGTATTAAACTTTTAAATAACAATAATTTCTAAAATGTTATAAATTAGGGCTGTACAATGTATCATTTCAACATCGA

Associated Phenotype:

Not determined