ZMP

ccdc24

Ensembl ID:

ENSDARG00000038793

ZFIN ID:

ZDB-GENE-050327-18

Description:

coiled-coil domain-containing protein 24 [Source:RefSeq peptide;Acc:NP_001014330]

Human Orthologue:

CCDC24

Human Description:

coiled-coil domain containing 24 [Source:HGNC Symbol;Acc:28688]

Mouse Orthologue:

Ccdc24

Mouse Description:

coiled-coil domain containing 24 Gene [Source:MGI Symbol;Acc:MGI:2685874]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32956	Essential Splice Site, Missense	Mutation detected in F1 DNA	Not yet available
sa45107	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa32956

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 > C

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056656	Essential Splice Site	203	229	None	7
ENSDART00000114573	Essential Splice Site	203	397	None	8
ENSDART00000132221	Missense	204	210	6	6
ENSDART00000134024	Essential Splice Site	203	280	None	8

Genomic Location (Zv9):

Chromosome 2 (position 33152553)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	33451460
GRCz11	2	33434678

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTGACTGAAGAATCTGAAGCTTTGAGAAAAGATGTGCAGGCCTTGCAGG[T/C]AAGGGCTTATTTTGACGTTAATTACTGGTTTTGATTGCAACATCGATTTC

Long Flanking Sequence:

AGTTTTCATTTAAAAAATAGATTTTAAAAAAAAGATTCTTTAAAGAAATTTTCTCTAAAAAAGGTTGTTTTATGACATCCCTGTCAATACCAACCTGATCTTGCTAGAAAAAGTATTTTTTAAAAGTGTTTTACCTACAGTATTGGTGGAAAAGTGGCTAATTTGTATAAACTCATATGATTTCGTTCCTACAAAAAAAAAAAAAAAACTAAAAAAGAATGAGCAAATCTTGCAAAAATCTGCTAATGAATATGTAATTTTCATATGAATTAGCCACTAAATCAAAAAGTTACAATTTCCCATAAGAGAGTTTCGAGAAAACACCATTTTACTTCCACCTGGCCCCTTTTTAAAATATTTTCTGAGAGACTTACACTTTGTGACTGTTGATTCAAACTTATGCATATGCTGGCTTTCTAAAAGAGGGCTTTGTTTGCCTGACAGGTCAGTCCTGACTGAAGAATCTGAAGCTTTGAGAAAAGATGTGCAGGCCTTGCAGG[T/C]AAGGGCTTATTTTGACGTTAATTACTGGTTTTGATTGCAACATCGATTTCAGGATTACTTTAATAACATGCTATGATTCTGGATCTGAAGAGAGGAGGAATGTACAAAACAATGCCTCTGAGCGCTTGTTTTTCATATGTGAAGCACTTTTCTTTTGTGGTTTCTACAGTGTTTTAAGTCAGATCAGGTTTTAAATTCCTTTTTATATGGGTAAATAAGCATCGCAAAATAAAAAAAAAACCACGTTGTGTTTTCATAATGCAAGTTAGTCCATTGTTATGGTGCAGTATATTATGGCCTGTTTCCACTGAGTGGTACAGTATGGGCTGGTATGGGTCACCTTTATGAGGCTTGTGTTTCCACTGCCAAAAAGGTACCAATGGTGGACATGGCGTATGACAGAAAGTTTCAGTCAACGTTATTCTCACTTGAGAAAATGTCAAAGCTGAATGTTCATATATCATATGAGAAGCACTTCTCACCAAACAGAGGCTTTATAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45107

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:

G > A

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000056656	Nonsense	228	229	6	7
ENSDART00000114573	Splice Site	None	397	None	8
ENSDART00000132221	None	None	209	None	6
ENSDART00000134024	Splice Site	None	280	None	8

Genomic Location (Zv9):

Chromosome 2 (position 33143582)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	33442489
GRCz11	2	33425707

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTACTCAGACAGAGCCTGTGTGCCCTGAACCCACATTAGCAGGTACATG[G/A]AGTTAATCCTGACAAATGACATTGGTTTCATGGCAGTTTTTTGGAGCAGC

Long Flanking Sequence:

TTATTTGATCAATTACAATTATTTAAAAGAAATATAAAAACTTTTTAGATTTTTTTTTCTTAAAACAAGCTAAATAATCTGCCAATCGGGTAAGGTAAATAATCTTAATTTCCACTTTGAAATGTAGATATTTGGACTAGAAGCAAGGCAAAAATTCCATGTAAGAACAACTTTTTTTTTGGTATAAATTGTAAAAATAATTAAATACAGGTCATTTCTCAATCAAAAGTGCTTTAAAGGGTCTGTGGCTCATTCTTTTATTTGTGCTGTTGAACTGTTTCATAAACACAATATGACGTGGAGATGTGTGATATGGCTGTATATCAGCACAGCTGTGATCACCTATAGTAAAAGCGTATATATTCTGTATATATTTAATGGTGTAAGTTGACGACTGTGGATTGATTTGTTTTGTTTCATTCACAGGAAAACCTTGAGGCTGAGCGAGTCAGTACTCAGACAGAGCCTGTGTGCCCTGAACCCACATTAGCAGGTACATG[G/A]AGTTAATCCTGACAAATGACATTGGTTTCATGGCAGTTTTTTGGAGCAGCCCTTTACATCTTTCTTCATAAACATTGCATCATAATGCCCATTTTATTTGAAATCTTTTCTCCAAATGTGATCTTTTTTGAATTGTGTATTACTACCATCTAGTGGTTCACCACTGAATTCTTATCCACTCCGTTCCACAGCTCAATAAAGAATGATCAAGGTTACTATCCTCAGTCTTTTCAGAGCAGAATACTTTTCAATTGAAGTAATAAAGCAGAATTTCTTTTATTTCTTGATTTTTTTTCAGGGTCATTATGAAAAGGTTTATCCTGGAGCAAAACTACCTTTAATTGATTCCTTGTCTTTCAGAGCTCAAAGAAGAACGGAGACTAATTCAGAGGGATCTGAATGTTCAGGGTTCAATGAGCTGCTCCTACAAATCAAACAATCGGAGTACCAGAAACCCACAAAAACACACAAGGTCAGTACACATTTCTAGAACAAGACTT

Associated Phenotype:

Not determined