Identity
HGNC
LOCATION
1p22.2
LOCUSID
ALIAS
MER3,POF9,SEC63D1,Si-11,Si-11-6,helicase
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: 164045
MIM: 615684
HGNC: 20193
Ensembl: ENSG00000162669
Variants:
dbSNP: 164045
ClinVar: 164045
TCGA: ENSG00000162669
COSMIC: HFM1
RNA/Proteins
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35486194 | 2022 | Identification of a new splice-acceptor mutation in HFM1 and functional analysis through molecular docking in nonobstructive azoospermia. | 2 |
| 35526155 | 2022 | Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees. | 9 |
| 35881270 | 2022 | Novel pathogenic splicing variants in helicase for meiosis 1 (HFM1) are associated with diminished ovarian reserve and poor pregnancy outcomes. | 2 |
| 35486194 | 2022 | Identification of a new splice-acceptor mutation in HFM1 and functional analysis through molecular docking in nonobstructive azoospermia. | 2 |
| 35526155 | 2022 | Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees. | 9 |
| 35881270 | 2022 | Novel pathogenic splicing variants in helicase for meiosis 1 (HFM1) are associated with diminished ovarian reserve and poor pregnancy outcomes. | 2 |
| 34429122 | 2021 | Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia. | 11 |
| 34429122 | 2021 | Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia. | 11 |
| 31279343 | 2019 | A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency. | 18 |
| 31279343 | 2019 | A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency. | 18 |
| 26679638 | 2016 | Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women. | 15 |
| 26679638 | 2016 | Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women. | 15 |
| 24597873 | 2014 | Mutations in HFM1 in recessive primary ovarian insufficiency. | 59 |
| 24597873 | 2014 | Mutations in HFM1 in recessive primary ovarian insufficiency. | 59 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
Citation
Dessen P
HFM1 (helicase for meiosis 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64250/hfm1-(helicase-for-meiosis-1)
