CLSPN

Ensembl ID:
ENSDARG00000087655
Description:
claspin [Source:HGNC Symbol;Acc:19715]
Human Orthologue:
CLSPN
Human Description:
claspin [Source:HGNC Symbol;Acc:19715]
Mouse Orthologue:
Clspn
Mouse Description:
claspin homolog (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:2445153]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa36922 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa36922
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 > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127822 Essential Splice Site 45 279 2 6
Genomic Location (Zv9):
Chromosome 19 (position 49561230)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AATGGAGGAGCCTGTGATTGACAACAACAAGCGCACTGAGGACCAGCAAG[G/A]TAAGATGATACTAAAGGTCCAAATCTGAATTTATTAATGTCAAAGATCTA
Associated Phenotype:
Not determined

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