Gene
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.
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.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
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
AISKIKEDKSCSITKSKMHVSFKCEPEPRKSNFEKSNLRPFFIQTNVKNKE
SESTAQIEK
KPRKPLDSVGLLEGDRNKRKKSPQMNDFNIKENKSVRNYQLSKYRSVRKKSLLPLCFEDE
LKNPHAKIVNVSPTKTVTSHMEQKDTNPIIFHDTEYVRMLLLTKNRFSSHPLENENIYPH
KRTNFILERNCEILKSIIGNQSISLFKPQKTMPTVQRKDIQIPMSFKAGHTTVDDKLKKK
TNKQTLENRSWNTLYNFSQNFSSLTKQFVGYLDKAVIHEMSAQTGKFERMFSAGKPTSIP
TSSALPVKCYSKPFKYIYELNNVTPLDNLLN
LSNEILNAS
Sequence length 400
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 26301688
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs869025224 26301688
Common variable immunodeficiency Common Variable Immunodeficiency rs72553883, rs121908379, rs104894650, rs587776775, rs398122863, rs398122864, rs397514332, rs397514331, rs727502786, rs727502787, rs72553882, rs869320688, rs869320689, rs869320754, rs773694113
View all (35 more)
26301688
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
26301688
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac Disease 26301688 ClinVar
Crohn disease Crohn Disease 26974007, 17435756, 26192919, 17804789, 30500874, 18587394, 26301688, 23850713, 17068223, 17554300 ClinVar
Leprosy Leprosy 22019778, 25642632 ClinVar, GWAS
Sarcoidosis Sarcoidosis 26051272 ClinVar, GWAS
Associations from Text Mining
Disease Name Relationship Type References
Pneumonia Associate 28302172
Sarcoidosis Associate 26051272
Uveomeningoencephalitic Syndrome Associate 32437414