Identity
HGNC
LOCATION
14q23.1
LOCUSID
ALIAS
POF18,SPGF52,Six6os1
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 317761
MIM: 617307
HGNC: 19849
Ensembl: ENSG00000179008
Variants:
dbSNP: 317761
ClinVar: 317761
TCGA: ENSG00000179008
COSMIC: C14orf39
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34718620 | 2022 | Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia. | 7 |
| 35305148 | 2022 | In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia. | 3 |
| 34718620 | 2022 | Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia. | 7 |
| 35305148 | 2022 | In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia. | 3 |
| 33508233 | 2021 | Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans. | 28 |
| 33508233 | 2021 | Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans. | 28 |
Citation
Dessen P
C14orf39 (chromosome 14 open reading frame 39)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/60941/c14orf39-(chromosome-14-open-reading-frame-39)
