LOC100151337

Ensembl ID:
ENSDARG00000071319
Human Orthologue:
NARF
Human Description:
nuclear prelamin A recognition factor [Source:HGNC Symbol;Acc:29916]
Mouse Orthologue:
Narf
Mouse Description:
nuclear prelamin A recognition factor Gene [Source:MGI Symbol;Acc:MGI:1914858]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa35336 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa35336
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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105374 Nonsense 268 465 8 11
Genomic Location (Zv9):
Chromosome 12 (position 34656806)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 33369277
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CGCACTTAAATGATTGTTTGGTTTTAGGAGAGATTCTCCACCTGATGGAA[C/T]AAAGCAAAGTCACTGTTGAGGAAGTGGACTCTGCTCCTTTGGATCATGTG
Associated Phenotype:
Not determined

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