Gene Gene information from NCBI Gene database.
Entrez ID 84553
Gene name Failed axon connections homolog, metaxin like GST domain containing
Gene symbol FAXC
Synonyms (NCBI Gene)
C6orf168dJ273F20
Chromosome 6
Chromosome location 6q16.2
miRNA miRNA information provided by mirtarbase database.
253
miRTarBase ID miRNA Experiments Reference
MIRT024842 hsa-miR-215-5p Microarray 19074876
MIRT026241 hsa-miR-192-5p Microarray 19074876
MIRT046397 hsa-miR-15b-5p CLASH 23622248
MIRT042924 hsa-miR-324-3p CLASH 23622248
MIRT709478 hsa-miR-3620-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5TGI0
Protein name Failed axon connections homolog
Protein function May play a role in axonal development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17172 GST_N_4 117 212 Glutathione S-transferase N-terminal domain Domain
PF17171 GST_C_6 263 326 Glutathione S-transferase, C-terminal domain Domain
Sequence
MHWGVGFASSRPCVVDLSWNQSISFFGWWAGSEEPFSFYGDIIAFPLQDYGGIMAGLGSD
PWWKKTLYLTGGALLAAAAYLLHELLVIRKQQEIDSKDAIILHQFARPNNGVPSLSPFCL
KMETYLRMADLPYQNYFGGKLSAQGKMPWIEYNHEKVSGTEFIIDFLEEKLGVNLNKNLG
PHERAISRAVTKMVEEHFYWTLAYCQWVDNLN
ETRKMLSLSGGGPFSNLLRWVVCHITKG
IVKREMHGHGIGRFSEEEIYMLMEKDMRSLAGLLGDKKYIMGPKLSTLDATVFGHLAQAM
WTLPGTRPERLIKGELINLAMYCERI
RRKFWPEWHHDDDNTIYESEESSEGSKTHTPLLD
FSFYSRTETFEDEGAENSFSRTPDTDFTGHSLFDSDVDMDDYTDHEQCK
Sequence length 409
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CIRRHOSIS OF LIVER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LATE-ONSET ALZHEIMER'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROLIFERATIVE DIABETIC RETINOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations