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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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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 2018 |
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 2018.
- 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)
- Other Location(s):
-
Assembly Chromosome Position GRCz11 19 47840274 - 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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