LOC797675

Ensembl ID:
ENSDARG00000086728
Human Orthologue:
CXorf58
Human Description:
chromosome X open reading frame 58 [Source:HGNC Symbol;Acc:26356]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa24751 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa24751
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 2014.
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126599 Nonsense 9 253 1 6
Genomic Location:
Chromosome Zv9_scaffold3516 (position 60876)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGCTAAATTGTTCTTTATGATTCAGAATGCAGAGTTATGAGGATTGTGCC[A/T]GAAAAATACAGGCGTGTTGGAGATCATTCAGAGACAGGCGACTCTTCAGA
Associated Phenotype:
Not determined

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