SEPTIN14 (septin 14)

2014-11-01  

Identity

HGNC
SEPTIN14
LOCATION
7p11.2
LOCUSID
346288
ALIAS
14-Sep
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 346288
MIM: 612140
HGNC: 33280
Ensembl: ENSG00000154997

Variants:

dbSNP: 346288
ClinVar: 346288
TCGA: ENSG00000154997
COSMIC: SEPTIN14

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000154997ENST00000388975Q6ZU15

References

Pubmed IDYearTitleCitations
377124362023X-ray structure of the metastable SEPT14-SEPT7 coiled coil reveals a hendecad region crucial for heterodimerization.0
377124362023X-ray structure of the metastable SEPT14-SEPT7 coiled coil reveals a hendecad region crucial for heterodimerization.0
322491552020Expression and localization of Septin 14 gene and protein in infertile men testis.6
322491552020Expression and localization of Septin 14 gene and protein in infertile men testis.6
271156722016SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.8
271156722016SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.8
179221642007Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin.25
179221642007Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin.25

Citation

Dessen P

SEPTIN14 (septin 14)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73123/cancer-prone-explorer/js/lib/bootstrap.min.js