FARP1 FERM, ARH/RhoGEF and pleckstrin domain protein 1
Gene ID: 10160, updated on 27-Aug-2024Gene type: protein coding
Also known as: CDEP; GLCC1; PLEKHC2; PPP1R75; FARP1-IT1
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- Go to complete Gene record for FARP1
- Go to Variation Viewer for FARP1 variants
Summary
This gene encodes a protein containing a FERM (4.2, exrin, radixin, moesin) domain, a Dbl homology domain, and two pleckstrin homology domains. These domains are found in guanine nucleotide exchange factors and proteins that link the cytoskeleton to the cell membrane. The encoded protein functions in neurons to promote dendritic growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. GeneReviews: Not available | |
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. GeneReviews: Not available | |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. GeneReviews: Not available | |
Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13). GeneReviews: Not available | |
Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. GeneReviews: Not available | |
Genome-wide meta-analysis identifies new susceptibility loci for migraine. GeneReviews: Not available | |
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. GeneReviews: Not available | |
Voxelwise genome-wide association study (vGWAS). GeneReviews: Not available |
Genomic context
- Location:
- 13q32.2
- Sequence:
- Chromosome: 13; NC_000013.11 (98142589..98455176)
- Total number of exons:
- 30
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for FARP1 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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