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: 125150
MIM: 614535
HGNC: 26993
Ensembl: ENSG00000214941
Variants:
dbSNP: 125150
ClinVar: 125150
TCGA: ENSG00000214941
COSMIC: ZSWIM7
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34402903 | 2022 | ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency. | 10 |
| 35218660 | 2022 | Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency. | 0 |
| 36202298 | 2022 | A novel homozygous variant in homologous recombination repair gene ZSWIM7 causes azoospermia in males and primary ovarian insufficiency in females. | 2 |
| 34402903 | 2022 | ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency. | 10 |
| 35218660 | 2022 | Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency. | 0 |
| 36202298 | 2022 | A novel homozygous variant in homologous recombination repair gene ZSWIM7 causes azoospermia in males and primary ovarian insufficiency in females. | 2 |
| 33713115 | 2021 | A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination. | 8 |
| 33713115 | 2021 | A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination. | 8 |
Citation
Dessen P
ZSWIM7 (zinc finger SWIM-type containing 7)
Atlas Genet Cytogenet Oncol Haematol. 2008-07-01
Online version: http://atlasgeneticsoncology.org/gene/50269/zswim7
