C1orf141 (chromosome 1 open reading frame 141)

Gene
Gene miRNA Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
400757
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 1 open reading frame 141
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C1orf141
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p31.3
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all(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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Other IDs Protein Associated diseases
UniProt ID 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
AISKIKEDKSCSITKSKMHVSFKCEPEPRKSNFEKSNLRPFFIQTNVKNKESESTAQIEK
KPRKPLDSVGLLEGDRNKRKKSPQMNDFNIKENKSVRNYQLSKYRSVRKKSLLPLCFEDE
LKNPHAKIVNVSPTKTVTSHMEQKDTNPIIFHDTEYVRMLLLTKNRFSSHPLENENIYPH
KRTNFILERNCEILKSIIGNQSISLFKPQKTMPTVQRKDIQIPMSFKAGHTTVDDKLKKK
TNKQTLENRSWNTLYNFSQNFSSLTKQFVGYLDKAVIHEMSAQTGKFERMFSAGKPTSIP
TSSALPVKCYSKPFKYIYELNNVTPLDNLLNLSNEILNAS
Sequence length 400
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (6)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Crohn Disease Crohn's disease or Leprosy (opposite effect), Crohn's disease N/A N/A GWAS
Inflammatory Bowel Disease Inflammatory bowel disease, Inflammatory bowel disease (MTAG) N/A N/A GWAS
Leprosy Leprosy N/A N/A GWAS
Psoriasis Psoriasis N/A N/A GWAS
Show/Hide Text Mining Associations (3)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Pneumonia Associate 28302172
Sarcoidosis Associate 26051272
Uveomeningoencephalitic Syndrome Associate 32437414