LOC100329514

Ensembl ID:
ENSDARG00000092276
Human Orthologue:
PARP6
Human Description:
poly (ADP-ribose) polymerase family, member 6 [Source:HGNC Symbol;Acc:26921]
Mouse Orthologue:
Parp6
Mouse Description:
poly (ADP-ribose) polymerase family, member 6 Gene [Source:MGI Symbol;Acc:MGI:1914537]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa44332 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa44332
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 > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000146765 Essential Splice Site 27 606 1 21
Genomic Location (Zv9):
Chromosome 25 (position 30110873)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 28690322
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGGACTCGGATGGTGACAGTGATGGTGAAGATTTCTTCTATGGTGCCCAG[G/T]TAAGCATACTGAGAAATAATCTACTGGGAAAACGAGCTAAATCTGCTAAA
Associated Phenotype:
Not determined

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