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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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ENSDARG00000069026
- Ensembl ID:
- ENSDARG00000069026
Alleles
There is 1 allele of this gene:
| Allele name | Consequence | Status | Availability Estimate |
|---|---|---|---|
| sa36968 | Nonsense | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa36968
- 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:
- C > T
- Consequence:
- Nonsense
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100098 | Nonsense | 24 | 268 | 1 | 3 |
- Genomic Location (Zv9):
- Chromosome 20 (position 7174321)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 20 7009805 GRCz11 20 6999694 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- ACTGCAAGGAGCTCGAGACTCTCTTCCAGAAGTACAACCTGAAGCTGGAG[C/T]AAACCGCCACGCTCAAAGCGCTGGCCATCCTCATCCTCGCCGCGTCCGCG
- Associated Phenotype:
- Not determined
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