Gene Gene information from NCBI Gene database.
Entrez ID 400757
Gene name Chromosome 1 open reading frame 141
Gene symbol C1orf141
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1p31.3
miRNA miRNA information provided by mirtarbase database.
15
miRTarBase ID miRNA Experiments Reference
MIRT839736 hsa-miR-1246 CLIP-seq
MIRT839737 hsa-miR-3163 CLIP-seq
MIRT839738 hsa-miR-4668-3p CLIP-seq
MIRT839739 hsa-miR-4694-3p CLIP-seq
MIRT839740 hsa-miR-520d-5p CLIP-seq
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.
Q5JVX7
Protein name Uncharacterized protein C1orf141
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15078 DUF4545 1 116 Domain of unknown function (DUF4545) Family
PF15078 DUF4545 112 391 Domain of unknown function (DUF4545) Family
Sequence
MAEKILEKLDVLDKQAEIILARRTKINRLQSEGRKTTMAIPLTFDFQLEFEEALATSASK
AISKIKEDKSCSITKSKMHVSFKCEPEPRKSNFEKSNLRPFFIQTNVKNKE
SESTAQIEK
KPRKPLDSVGLLEGDRNKRKKSPQMNDFNIKENKSVRNYQLSKYRSVRKKSLLPLCFEDE
LKNPHAKIVNVSPTKTVTSHMEQKDTNPIIFHDTEYVRMLLLTKNRFSSHPLENENIYPH
KRTNFILERNCEILKSIIGNQSISLFKPQKTMPTVQRKDIQIPMSFKAGHTTVDDKLKKK
TNKQTLENRSWNTLYNFSQNFSSLTKQFVGYLDKAVIHEMSAQTGKFERMFSAGKPTSIP
TSSALPVKCYSKPFKYIYELNNVTPLDNLLN
LSNEILNAS
Sequence length 400
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
22
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
ANKYLOSING SPONDYLITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOIMMUNE DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOIMMUNE THYROID DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CELIAC DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Pneumonia Associate 28302172
★☆☆☆☆
Found in Text Mining only
Sarcoidosis Associate 26051272
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Uveomeningoencephalitic Syndrome Associate 32437414
★☆☆☆☆
Found in Text Mining only