CXorf57 (2 of 2)

Ensembl ID:
ENSDARG00000036575
Description:
chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:25486]
Human Orthologue:
CXorf57
Human Description:
chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:25486]
Mouse Orthologue:
D330045A20Rik
Mouse Description:
RIKEN cDNA D330045A20 gene Gene [Source:MGI Symbol;Acc:MGI:2147848]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa20896 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa20896
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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053138 Nonsense 398 809 6 15
Genomic Location:
Chromosome 7 (position 20571314)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CAGAGATGGAGGAGTATCGCTGGATCCAGATGGTGGACCGGACATCAGAC[C/T]AGCCAATCATGATCAAACTTTTCTCCACATCACAGCCTGATGTTCAGAGC
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/6286dqtd