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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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dcst2
- Ensembl ID:
- ENSDARG00000088693
- ZFIN ID:
- ZDB-GENE-070809-6
- Human Orthologue:
- DCST2
- Human Description:
- DC-STAMP domain containing 2 [Source:HGNC Symbol;Acc:26562]
Alleles
There is 1 allele of this gene:
| Allele name | Consequence | Status | Availability Estimate |
|---|---|---|---|
| sa36162 | Essential Splice Site | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa36162
- 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 |
|---|---|---|---|---|---|
| ENSDART00000122082 | Essential Splice Site | 483 | 652 | 9 | 15 |
| ENSDART00000122082 | Essential Splice Site | 483 | 652 | 9 | 15 |
- Genomic Location (Zv9):
- Chromosome 16 (position 30977890)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 16 28815028 GRCz11 16 28749651 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- TGTCTCGTGAAGCCTTCGGAGCCTGATTACATGAGATACCTGCTCATTGG[T/G]AAAACTACAATTCGAAGTATTATGTACTTATATTGCACATGCGGTCATCA
- Associated Phenotype:
- Not determined
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