C20orf141

Chromosome 20 Open Reading Frame 141

Gene Information Card

Symbol C20orf141
Full Name chromosome 20 open reading frame 141
Gene Type protein-coding
Chromosomal Location 20q13.33
NCBI Gene ID 285600 ncbi.nlm.nih.gov/gene/285600
Ensembl ID ENSG00000196476
UniProt ID Q5VY43
OMIM ID 618218
HGNC ID 16129
Aliases MGC26717

Description

C20orf141 is a protein-coding gene located on chromosome 20q13.33. The encoded protein has no well-characterized function but is predicted to be involved in cellular processes based on sequence homology. Limited expression data suggest low to moderate transcript levels in certain tissues.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
No known disease associations Not applicable No evidence in ClinVar, OMIM, or COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 2.1 Low
Brain 0.8 Not detected
Liver 0.5 Not detected
Cell Line Expression
Cell Line nTPM Notes
HEK293 1.5 Low expression
HeLa 0.9 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
No reported pathogenic variants Not applicable Not applicable Not applicable
Mutation functional classification

Loss of Function (LOF)

Not established

Gain of Function (GOF)

Not established

Dominant Negative (DN)

Not established

Protein Summary

The C20orf141 protein (UniProt Q5VY43) is 141 amino acids long with no known functional domains. Its biological role remains uncharacterized.

Related Products

Product name Cat.No. Species Gene ID
C20orf141 Knockout HEK293 Cell Line EDJ-KQ9192 Human 128653 Details Get a Quote
C20orf141 Knockout HeLa Cell Line EDJ-KQ58246 Human 128653 Details Get a Quote
C20orf141 Knockout A-549 Cell Line EDJ-KQ66734 Human 128653 Details Get a Quote
C20orf141 Knockout HCT 116 Cell Line EDJ-KQ75145 Human 128653 Details Get a Quote
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