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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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ENSDARG00000079047
- Ensembl ID:
- ENSDARG00000079047
Alleles
There is 1 allele of this gene:
| Allele name | Consequence | Status | Availability Estimate |
|---|---|---|---|
| sa43766 | Nonsense | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa43766
- 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:
- Nonsense
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110947 | Nonsense | 18 | 245 | 1 | 3 |
- Genomic Location (Zv9):
- Chromosome 22 (position 8404390)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 22 8336651 GRCz11 22 8366497 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- GTTGGAGAATCAGTCACTCTAGAAATACAGAGAAGCGGGGACATCGAGTG[G/A]AAGTTTAGATCCCACAACATTCTTATAGCTTACATCAGCAGAGATGAAAT
- Associated Phenotype:
- Not determined
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