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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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dcaf13
- Ensembl ID:
- ENSDARG00000002267
- ZFIN ID:
- ZDB-GENE-040426-703
- Description:
- DDB1- and CUL4-associated factor 13 [Source:UniProtKB/Swiss-Prot;Acc:Q803X4]
- Human Orthologue:
- DCAF13
- Human Description:
- DDB1 and CUL4 associated factor 13 [Source:HGNC Symbol;Acc:24535]
- Mouse Orthologue:
- Dcaf13
- Mouse Description:
- DDB1 and CUL4 associated factor 13 Gene [Source:MGI Symbol;Acc:MGI:2684929]
Alleles
There is 1 allele of this gene:
Allele name | Consequence | Status | Availability Estimate |
---|---|---|---|
sa25029 | Essential Splice Site | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa25029
- 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:
- T > G
- Consequence:
- Essential Splice Site
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015139 | Essential Splice Site | 417 | 445 | 10 | 11 |
The following transcripts of ENSDARG00000002267 do not overlap with this mutation:
- Genomic Location (Zv9):
- Chromosome 16 (position 47490924)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 16 44689120 GRCz11 16 44655836 - KASP Assay ID:
- 554-7743.1 (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- TGAAGCAGAAGAGAGAGCTGAAGGAAATGAAGGAAGCACGCCGCAGGAAG[T/G]AAGTTCCCTTCAGAAAATGTTAATGTTTTTATAGTTTTCACAGTACTGGG
- Associated Phenotype:
- Not determined
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