PLEKHG5

pleckstrin homology and RhoGEF domain containing G5

Relationship to CMT

CMTRIdSMA AR 2 subtypes 1p36.31
First described 2007
Subtypes2
SubtypeInheritanceClassOMIMSentinel Publication
SubtypedSMA-4 Inheritanceautosomal recessive ClassdSMA OMIM611067 Sentinel Publication
2007 · 10.1086/518900
SubtypeCMTRIC Inheritanceautosomal recessive ClassCMTRI OMIM615376 Sentinel Publication
2013 · 10.1093/hmg/ddt274

ClinVar Variants

Pathogenic and likely pathogenic variants in PLEKHG5, as classified in ClinVar, are read live from NCBI.

Reported in CMT
Reported in Other Diseases

Reported in a disease other than CMT. Listed apart rather than counted as CMT variants.

Variants w/o a Recorded Disease

Pathogenic or likely pathogenic in ClinVar, submitted without a disease recorded.

What the review stars mean

Review stars are ClinVar’s measure of how well a classification is supported: four for a practice guideline, three for an expert panel review, two for agreement among multiple submitters, and one for a single submitter with criteria provided. A record with no criteria provided earns no stars and is not indexed.

Only aggregate germline records are indexed. Uncertain and conflicting classifications are not. Experts in CMT makes no claim to the accuracy of ClinVar data. This index is provided for informational purposes only.

Gene Function

PLEKHG5 functions as a guanine exchange factor (GEF) for RAB26 and thus regulates autophagy of synaptic vesicles in axon terminal of motoneurons (By similarity). Involved in the control of neuronal cell differentiation. Plays a role in angiogenesis through regulation of endothelial cells chemotaxis. Also affects the migration, adhesion, and matrix/bone degradation in macrophages and osteoclasts Source: UniProt

Indexed Identifiers

No HGNC Aliases
hgnc_idHGNC:29105
ensembl_gene_idENSG00000171680
coords_grch38chr1:6467122-6520074
coords_grch37chr1:6526152-6580121
entrez_id57449
omim_gene611101
uniprot_idsO94827
refseq_accessionNM_020631
mane_refseqNM_020631.6
mane_ensemblENST00000377728.8

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