FAXC failed axon connections homolog, metaxin like GST domain containing
Gene ID: 84553, updated on 17-Jun-2024Gene type: protein coding
Also known as: C6orf168; dJ273F20
- See all available tests in GTR for this gene
- Go to complete Gene record for FAXC
- Go to Variation Viewer for FAXC variants
Summary
Predicted to be integral component of membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| A genome-wide association study of behavioral disinhibition. GeneReviews: Not available |
Genomic context
- Location:
- 6q16.2
- Sequence:
- Chromosome: 6; NC_000006.12 (99271161..99350056, complement)
- Total number of exons:
- 9
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for FAXC variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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