LOC100007472

Ensembl ID:
ENSDARG00000055720
Human Orthologue:
CCDC41
Human Description:
coiled-coil domain containing 41 [Source:HGNC Symbol;Acc:17966]
Mouse Orthologue:
Ccdc41
Mouse Description:
coiled-coil domain containing 41 Gene [Source:MGI Symbol;Acc:MGI:1924298]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa40283 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa40283
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:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078101 Nonsense 566 685 13 16
Genomic Location (Zv9):
Chromosome 4 (position 19062204)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 20405539
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATCTTTTGGTCTGTTTTCTTATCCAGAGGAAAACAATGACTGAACTGAAA[G/T]AAAACAAACTCAAAGACAAGATTCAGCTCCTGGAAGCCAAGATAGCAGAA
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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