C14orf39

Chromosome 14 Open Reading Frame 39

Gene Information Card

Symbol C14orf39
Full Name Chromosome 14 Open Reading Frame 39
Gene Type Protein-coding
Chromosomal Location 14q24.3
NCBI Gene ID 317749 ncbi.nlm.nih.gov/gene/317749
Ensembl ID ENSG00000100823
UniProt ID Q8N6T3
OMIM ID 617307
HGNC ID 28235
Aliases FLJ32743, MGC35130

Description

C14orf39 is a protein-coding gene located on chromosome 14q24.3. Its function is not fully characterized, but it is predicted to be involved in cellular processes. Expression data suggest low to moderate levels in various tissues.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
No specific disease association Unknown No evidence in ClinVar or OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 2.3 Low
Brain 1.1 Low
Lung 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
K562 0.6 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
No reported variants N/A N/A N/A
Mutation functional classification

Loss of Function (LOF)

No data

Gain of Function (GOF)

No data

Dominant Negative (DN)

No data

Protein Summary

The C14orf39 protein is encoded by the C14orf39 gene. Its molecular function and biological role remain largely unknown, with no characterized domains or motifs.

Related Products

Product name Cat.No. Species Gene ID
C14orf39 Knockout HEK293 Cell Line EDJ-KQ8909 Human 317761 Details Get a Quote
C14orf39 Knockout HeLa Cell Line EDJ-KQ59572 Human 317761 Details Get a Quote
C14orf39 Knockout A-549 Cell Line EDJ-KQ68037 Human 317761 Details Get a Quote
C14orf39 Knockout HCT 116 Cell Line EDJ-KQ76417 Human 317761 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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