Gene Gene information from NCBI Gene database.
Entrez ID 84915
Gene name Family with sequence similarity 222 member A
Gene symbol FAM222A
Synonyms (NCBI Gene)
C12orf34
Chromosome 12
Chromosome location 12q24.11
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT024272 hsa-miR-215-5p Microarray 19074876
MIRT026251 hsa-miR-192-5p Microarray 19074876
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.
Q5U5X8
Protein name Protein FAM222A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15258 FAM222A 30 161 Protein family of FAM222A Family
Sequence
MLACLQRTQNAPGQHLACPSKSLELRKCEAVASAMHSSRYPSPAELDAYAEKVANSPLSI
KIFPTNIRVPQHKHLSRTVNGYDTSGQRYSPYPQHTAGYQGLLAIVKAAVSSSSTAAPAG
PAKSVLKSAEGKRTKLSPAAVQVGIAPYPVPSTLGPLAYPK
PPEAPAPPPGLPAAATAAS
VIPLPGRGLPLPPSNLPSIHSLLYQLNQQCQAPGAAPPACQGMAIPHPSPAKHGPVPSFP
SMAYSAAAGLPDCRKGTELGQGATQALTLAGAAKPAGYADSGLDYLLWPQKPPPPPPQPL
RAYSGSTVASKSPEACGGRAYERASGSPLNCGVGLPTSFTVGQYFAAPWNSVLVTPTSDC
YNPAAAVVVTELGPGAARELAGPPADALSGLPSKSVCNTSVLSSSLQSLEYLINDIRPPC
IKEQMLGKGYETVAVPRLLDHQHAHIRLPVYR
Sequence length 452
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormal brain morphology Likely pathogenic rs763757845 RCV000454202
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 31994347
Neoplasm Metastasis Associate 31994347