FIGN (fidgetin, microtubule severing factor)

2015-02-01  

Identity

HGNC
LOCATION
2q24.3
LOCUSID
ALIAS
-

Other Information

Locus ID:

NCBI: 55137
MIM: 605295
HGNC: 13285
Ensembl: ENSG00000182263

Variants:

dbSNP: 55137
ClinVar: 55137
TCGA: ENSG00000182263
COSMIC: FIGN

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000182263ENST00000333129Q5HY92
ENSG00000182263ENST00000409634B8ZZS6

Expression (GTEx)

0
5
10
15
20
25

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.85
192400612009Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.75
226729012012Human Fidgetin is a microtubule severing the enzyme and minus-end depolymerase that regulates mitosis.20
196806352009Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients.15
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.11
283027522017Lower Circulating Folate Induced by a Fidgetin Intronic Variant Is Associated With Reduced Congenital Heart Disease Susceptibility.3
285342412017A Genetic Variant in FIGN Gene Reduces the Risk of Congenital Heart Disease in Han Chinese Populations.3

Citation

Dessen P

FIGN (fidgetin, microtubule severing factor)

Atlas Genet Cytogenet Oncol Haematol. 2015-02-01

Online version: http://atlasgeneticsoncology.org/gene/54988/fign