Gene Gene information from NCBI Gene database.
Entrez ID 84886
Gene name Chromosome 1 open reading frame 198
Gene symbol C1orf198
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q42.2
miRNA miRNA information provided by mirtarbase database.
459
miRTarBase ID miRNA Experiments Reference
MIRT019596 hsa-miR-340-5p Sequencing 20371350
MIRT022692 hsa-miR-124-3p Microarray 18668037
MIRT024382 hsa-miR-215-5p Microarray 19074876
MIRT026464 hsa-miR-192-5p Microarray 19074876
MIRT038936 hsa-miR-31-3p CLASH 23622248
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 IEA
GO:0005829 Component Cytosol IDA
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.
Q9H425
Protein name Uncharacterized protein C1orf198
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15797 DUF4706 31 134 Domain of unknown function (DUF4706) Family
Sequence
MASMAAAIAASRSAVMSGNRPLDDRERKRFTYFSSLSPMARKIMQDKEKIREKYGPEWAR
LPPAQQDEIIDRCLVGPRAPAPRDPGDSEELTRFPGLRGPTGQKVVRFGDEDLTWQDEHS
APFSWETKSQMEFS
ISALSIQEPSNGTAASEPRPLSKASQGSQALKSSQGSRSSSLDALG
PTRKEEEASFWKINAERSRGEGPEAEFQSLTPSQIKSMEKGEKVLPPCYRQEPAPKDREA
KVERPSTLRQEQRPLPNVSTERERPQPVQAFSSALHEAAPSQLEGKLPSPDVRQDDGEDT
LFSEPKFAQVSSSNVVLKTGFDFLDNW
Sequence length 327
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
VENOUS THROMBOEMBOLISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Venous Thromboembolism Venous thromboembolism Pubtator 31420334 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations