CCDC150

Ensembl ID:
ENSDARG00000090935
Description:
coiled-coil domain containing 150 [Source:HGNC Symbol;Acc:26834]
Human Orthologue:
CCDC150
Human Description:
coiled-coil domain containing 150 [Source:HGNC Symbol;Acc:26834]
Mouse Orthologue:
Ccdc150
Mouse Description:
coiled-coil domain containing 150 Gene [Source:MGI Symbol;Acc:MGI:1925266]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa28525 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa28525
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128136 Essential Splice Site 305 964 6 24
Genomic Location (Zv9):
Chromosome 15 (position 39803340)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 41320047
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACTCATCAGAGACGGACGAGACCTCCGAGCAGCTGCAGATCAAGTGCAGG[T/C]ATGCAAACACACACACATGCAATCTGTTTGGTGTTGTATAATTATGTTAG
Associated Phenotype:
Not determined

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