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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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ENSDARG00000078024
- Ensembl ID:
- ENSDARG00000078024
Alleles
There is 1 allele of this gene:
| Allele name | Consequence | Status | Availability Estimate |
|---|---|---|---|
| sa43759 | Nonsense | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa43759
- 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 |
|---|---|---|---|---|---|
| ENSDART00000113811 | Nonsense | 384 | 426 | 6 | 6 |
- Genomic Location (Zv9):
- Chromosome 22 (position 4437335)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 22 4411749 GRCz11 22 4796124 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- CAGGGTATGTTGACAGGCTCCTGCAGCTATTGTTTGACTGTGTGCTAGAG[C/T]AGCCCCAGCTGTTCCAGGACAAGCTTTTGCAAATTCAAGTTCCTGAACAC
- Associated Phenotype:
- Not determined
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