LOC796113

Ensembl ID:
ENSDARG00000087319
Human Orthologue:
CECR6
Human Description:
cat eye syndrome chromosome region, candidate 6 [Source:HGNC Symbol;Acc:1844]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa40248 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa40248
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 2017.
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123953 Nonsense 173 395 1 1
Genomic Location (Zv9):
Chromosome 4 (position 11375640)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 12312267
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCCATTTTTGGATGCAACCTCGGCGAGTTTACCTTCGCCTACCTTGCATG[G/A]CTGATCTACGTGATCGCGTCCACCCCAAAAGTGGTGCTCGTGTTGGAAAC
Associated Phenotype:
Not determined

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