PHF13

Ensembl ID:
ENSDARG00000078021
Description:
PHD finger protein 13 [Source:HGNC Symbol;Acc:22983]
Human Orthologue:
PHF13
Human Description:
PHD finger protein 13 [Source:HGNC Symbol;Acc:22983]
Mouse Orthologue:
Phf13
Mouse Description:
PHD finger protein 13 Gene [Source:MGI Symbol;Acc:MGI:2446217]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa38210 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa38210
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
ENSDART00000114111 Nonsense 270 319 4 4
Genomic Location (Zv9):
Chromosome Zv9_NA732 (position 87739)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 41771133
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CATGTTTCTGCATGAAGCCATTTGCCGGCCGGGCGATGATCGAATGCAAC[C/T]AGTGCAATACGTGGATCCATCTTTCATGTGCCAAAATCCGCAAGTCCAAC
Associated Phenotype:
Not determined

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