ZMP

ccdc75

Ensembl ID:

ENSDARG00000026892

ZFIN ID:

ZDB-GENE-040718-89

Description:

Coiled-coil domain-containing protein 75 [Source:UniProtKB/Swiss-Prot;Acc:Q6DGZ0]

Human Orthologue:

CCDC75

Human Description:

coiled-coil domain containing 75 [Source:HGNC Symbol;Acc:26768]

Mouse Orthologue:

Ccdc75

Mouse Description:

coiled-coil domain containing 75 Gene [Source:MGI Symbol;Acc:MGI:1858435]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42309	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa28210	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa10202	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa42309

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

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000034541	Essential Splice Site	17	262	1	8

Genomic Location (Zv9):

Chromosome 13 (position 51223159)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	49934256
GRCz11	13	50247499

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGCTGATGATGAAGATGATTACATGTCTGACGCTTTCCTCAACCAAATG[T/C]GAGTTTAAGAATTGACGTTTTTAGCGTCATACTTGTACAGTCAGAGTGAG

Long Flanking Sequence:

CACCTGGGGTAAGGACTTTCCTCCTACCTGGAGATGGCAAACCACCAATATAATTTTTGCAATAACAATTTATTTATTTATTTATTATTATTATTTATTTTTTTGCTGCTGAATAACAGAACTTCAAATAAAAATCGTATACAGTAATATTACTTATAATATTATAAAAGTTATATTATATATGTTATATTATATATAATATAACTTAAATTAGTTAAAAAAAATCTGAATTTATTTTAATATATAAAAATAACAAAACTAAATTTGTATTAAAAATGTTGATAAAAGTTTGTTCGCTGTTCACTGTGTCCGTCTAATAGGAACTCAATCCTCTTTCTTCTGCGTTCCAGTCGGACACATTTACTGGAAGGAACAACAAAGGGGATCAGAGAGAAATTTCATTGCTATTTCAATTAATATTTGTATTTAGAAGCTGAATAATTGTACAAATGGCTGATGATGAAGATGATTACATGTCTGACGCTTTCCTCAACCAAATG[T/C]GAGTTTAAGAATTGACGTTTTTAGCGTCATACTTGTACAGTCAGAGTGAGTGCGTTTTCTCAGATGTAAACACGAATGAACGCAAAGTTATTTATGCCAAATAAATCAGTTGATTATATATTGTAGCTATATTTCATGGTTAATTAGTGAAAATTCGTTGAGAAATCTTATAAAAGCGCTGTTAATAAAAGTATAGAGAGTTATACATGACGAAACGTTATTTAGGAAATTATGTGCTATTTTGATAGATATTAATAACATTCGACATATAAATAACCTGTATGACACTAGTTAAATGTGCTTGGAAACATGAAATATTGCAGGAAATACAAATATATAAGCTCAGACGTGTCTTTGTTATTTTAGTATCACTCGTTTTTCTATAATATGCAGTTTATTTTTATGTGATAGACTTATGAAGTTTTTAAATATTAATTATTAAGAATTAATGTGTAGCACACATTACAAATAAGGTACAATAGCAAATAAATACAACAGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28210

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000034541	Essential Splice Site	107	262	3	8

Genomic Location (Zv9):

Chromosome 13 (position 51220182)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	49931279
GRCz11	13	50244522

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTGCAGGTGCTGGACGGGTCGAGCCGGTTCCTCTCAACATCAAAACAGG[T/G]CAGGAATATTCTGATTTTCGCATTATTAGTTATTTATGACATTGAGCTGT

Long Flanking Sequence:

TTATTGGCCACTTTTAGGGCAAACAAAATCCCCTTAATAGTGGACAATGAAGTTTAAAGTAACAGTAAGTATAGATTAACAGTAAATTGACTAAACATTTAACAAAATAACAGCCAATTTTAATTAATATTTGATGCTCTTCCAGCTCAGATGTTCGTCCTGGTGTCCCGATGGTCAAGCGTGTGAAGGAGGCTATAAAGAAAGAGGCTTTACATAAAGAAAAAAATATTCAAAACCGGCAGAAGAGCTTCAAAGAGCAGGAGAAGGAGAGTCGAGAAGCTGCGCTGCAGAGCTCCATAGGCAGCCAAAATAAAGGCTTCGCTCTGCTGCAGAAGATGGGATATAAGGCAGGACAGGGCCTGGGCAAAGAGGGTCAGTGATGGAGACTTTTATTTATAGTCCAGAAATACCCAAAACATAAGAGAGATTTGTTGATTAAAATATGATCATGCTGCAGGTGCTGGACGGGTCGAGCCGGTTCCTCTCAACATCAAAACAGG[T/G]CAGGAATATTCTGATTTTCGCATTATTAGTTATTTATGACATTGAGCTGTAAATGTTTCTGGTTGCATAACACAGTTCAAGAAGTATTCACCCTCCTGATAGTTTTCTATTTCTTATTTTTCCCAAAAGATGTTGAACAGATCCAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAACTCTTATTTGTTTTATTTCGACTAGAATAAAAGCAGTTTTTAATTGTTTTGAACCCATTTTAAGGTCAATATTATTAGCTCCCTTAAGCAATATTTGTTTTGGATTGTCTGCAGACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATTCTAGTATCTTGTAGACTATCTAGTCTAATATTATTTACTGTCATCATGGCAAAGTTCAAATAAATCAGTTATTAGAAATTCTCCCTGCGTTGGCGTGGGTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa10202

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
ENSDART00000034541	Nonsense	252	262	8	8

Genomic Location (Zv9):

Chromosome 13 (position 51212129)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	49923226
GRCz11	13	50236469

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCACTGACATTTTCYCATTCAACAGATGAAGAGGATTTGGGTACRAATTG[T/A]CCTGGAGACACGGCAGCGGATCATGATGATWRAAACAACACAAATGCTTT

Long Flanking Sequence:

CAGCATATGTTTTAAACAGCGGATGCCCCTCCAGCTGCAACCCAGTACTGGGAAACACCCATACTCTTTCACATTCACACACTCATACGCTACGGCCAATGTAGTTCATCAATTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGGTAAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGAAATTCGAGCCAGCAACCTTCTTGCTGTGAGGCGACAGAGCTAACCACTGAGCCACCGAAATATTTCACAATATTTACCATTATTCATGTTTGCCCTCAGCCTTTAGATAAGCTGCAGTTTCTCACCTCATATCTGCGGGGAGTTCATTATTACTGCATCTGGTGCGGCACGGCATATAACGGTGAGAAGTGTTCACAAATCATCATTTATTTGATCAGTTAAATATTTTAATCAGCAAGCACTGACATTTTCTCATTCAACAGATGAAGAGGATTTGGGTACGAATTG[T/A]CCTGGAGACACGGCAGCGGATCATGATGATTGAAACAACACAAATGCTTTGCTTTTAGGGTTTCTTTTCATAGCTGTGTGTAATATTTATGTTTTCTTGTTGCTTCATTAAATATTGCAGTGATGTTTTGTTTAAAATGGTGTGATATGACTATTGACCATGATGCATCATGTAATTTTTTTTATGTAAATGAATATCAAACAAATACAAAAATGTGTGGTTGCATAATTATTCTTTCCATTATGTTTGTACAATCCATTCCAGGGTGTGGTGATTTGTGTGACAGCTCTGTGCTAGTTATAGATGAACAAATGCTAATTACTTAACAGGCAATATTACTTCCCAGTAATACTCCAGGGAAAATACCAGTCAGACTAAAGCATATCTAAATATTTAGATGTTCTCGAGTTTTGTAGGAAAAGTATATTTAAATTTTAATTCATATCTAAATACTTAGAGTTGGTCTTGGGTTTTGTAGGAAAAACTTAATACAATGTACT

Associated Phenotype:

Not determined