GPC5

Ensembl ID:
ENSDARG00000088858
Description:
glypican 5 [Source:HGNC Symbol;Acc:4453]
Human Orthologue:
GPC5
Human Description:
glypican 5 [Source:HGNC Symbol;Acc:4453]
Mouse Orthologue:
Gpc5
Mouse Description:
glypican 5 Gene [Source:MGI Symbol;Acc:MGI:1194894]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa44411 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa44411
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:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125684 Essential Splice Site 175 268 3 5
Genomic Location (Zv9):
Chromosome Zv9_NA503 (position 153433)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 2868163
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCCTCTGCAGACGGACGGGCCTGCTGGAACGGAGACGACGTGGCCAGAAG[G/A]TACAAATAAGTCAACTTTTGCCTCTTGGTTTCTTTCTCTCTGATTTAAAT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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